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MINAMI HidetoGraduate School of Engineering / Department of Chemical Science and EngineeringProfessor
Researcher basic information
■ Research Keyword■ Research Areas
■ Committee History
- Jun. 2024 - Present, 高分子学会関西支部, 副支部長
- Jun. 2022 - Present, 日本接着学会, 理事
- Oct. 2019 - Present, 日本ゴム協会, サタデーセミナー運営委員長
- Jun. 2019 - Present, 日本ゴム協会, 関西支部 副支部長
- 2019 - Present, 高分子学会, 代議員
- Jun. 2018 - Present, 高分子学会関西支部, 常任幹事
- 2012 - Present, 近畿化学協会, 重合工学部会幹事
- 2010 - Present, 色材協会, 理事
- 2008 - Present, 高分子ミクロスフェア研究会, 運営委員
- 2008 - Present, 色材協会, 関西支部運営委員
- Jun. 2022 - Jun. 2024, 日本接着学会, 関西支部支部長
- Oct. 2022 - Oct. 2023, 日本化学会, 代議員
- 2016 - May 2022, 日本接着学会, 関西支部幹事 副支部長
- 2012 - May 2022, 日本接着学会, 評議員
- Nov. 2019 - Oct. 2020, 日本化学会, 代議員
Research activity information
■ Award- Feb. 2024 色材協会, 色材協会功績賞
- May 2021 日本ゴム協会, 第13回日本ゴム協会科学技術奨励賞, 高分子微粒子の構造制御とその機能化に関する研究
- Feb. 2016 Japan Society of Colour Material, 2015 Most Accessed Review Award of Japan Society of Colour Material (2016), Preparation of Composite Particles Utilizing Hydrogen Bonding Interaction一般社団法人・色材協会が発行している『色材協会誌』の中で、2015年に最もダウンロードが多かった総説論文に対して授与されるOfficial journal
- Nov. 2010 社団法人 色材協会, 2010年度色材協会研究発表会最優秀ポスター賞, SaPSeP法によるイオン液体含有カプセル粒子の合成
- Jul. 2008 Prague Meeting on Macromolecules 48th Microsymposium: Polymer Colloids: From Design to Biomedical and Industrial Applications (2008), First Prize for Poster Contest, Preparation of Polystyrene/Polyacrylic acid Composite particles in Ionic liquids
- Jun. 2005 日本接着学会, 第43回年次大会ベストポスター賞, SaPSeP法を用いた重付加反応による硬化剤内包型マイクロカプセルの調製
- May 2005 高分子学会, Award for Encouragement of Research in Polymer Science, ミクロンサイズの単分散中空橋かけ粒子の創製
- Abstract Micrometer-sized, monodispersed silicone hollow particles are functional materials with properties attributed to both their hollow structure and the silicone composition. However, there are few reports on their preparation. We have successfully prepared these particles by combining an original suspension polymerization technique, the self-assembling phase-separated polymer method, with a molecular diffusion method. The resulting particles exhibit heat resistance owing to the silicone matrix and maintain their hollow structure even after heating to 900 °C.Oxford University Press (OUP), Dec. 2024, Chemistry Letters, 54(1) (1)Scientific journal
- Abstract Single hollow particles are used in various fields, particularly in thermal insulation materials, owing to their low thermal conductivity attributed to encapsulated air properties. “The self‐assembling phase separated polymer (SaPSeP) method” is an original hollowing method that is proposed by this laboratory 25 years ago. Most hollow particles prepared by the SaPSeP method have carbon, oxygen, and hydrogen polymer shells, which lack sufficient heat resistance. In this study, hollow particles with a silicone shell, which is highly heat‐resistant, are prepared using the SaPSeP method using a trimer of 3‐methacryloxypropylmethyldimethoxysilane (MPDS). The MPDS trimer (3MPDS) is synthesized through the sol–gel reaction of MPDS with a basic aqueous solution. Additionally, hollow particles are prepared using a new silicone oligomer composed of MPDS and dimethoxymethylvinylsilane (DMVS). Both hollow particles prepared from 3MPDS and from a new silicone oligomer composed of MPDS and DMVS showed high heat resistance. They maintained their hollow structure even when exposed to temperatures up to 900 °C.Wiley, Dec. 2024, Macromolecular Reaction EngineeringScientific journal
- American Chemical Society (ACS), Nov. 2024, ACS Applied Materials & Interfaces, 16(46) (46), 64058 - 64064Scientific journal
- Circular dichroism (CD) studies on poly(1,4‐phenylene)s bearing a chiral side chain in the aggregated conditions were carried out. Little CD was observed in a solution form, while addition of a poor solvent into the polyphenylene solution induced aggregation and a strong CD was observed, accordingly. Applying the controlled degree of polymerization (DP) of poly(1,4‐phenylene) in the use of bidentate diphosphine Chiraphos as a ligand for the nickel catalyst, the relationship of DP with CD strength was studied to reveal to show the highest CD at the DP = 84 (gabs = ca. 2 x 10–2). It was also found that the related aggregation was observed in good solvent 1,2‐dichloroethane upon standing the solution at 4 °C for 3–23 days to observe gabs = ca. 10–1. Studies on the substituent effect of poly(1,4‐phenylene) suggested that CD behaviors were dependent on the type of non‐chiral substituent on the aromatic ring as well as the side‐chain chirality.Wiley, 2024, Chem. Eur. J., 30(35) (35), e202400706[Refereed]Scientific journal
- Abstract Hollow polyimide (PI) particles were successfully prepared using chemical imidization with acetic anhydride and pyridine as the chemical imidization reagents. The imidization reagents were added to the dispersion in which N,N-dimethylformamide (DMF) droplets with dissolved poly(amic acid) (PAmA, the precursor of PI) were dispersed in a cyclohexane medium. In the absence of poly(n-butyl methacrylate) (P[n-BMA]) in PAmA/DMF droplets, approximately 10% of the PI particles had hollow structures. Conversely, in the presence of a small amount of P(n-BMA) in PAmA/DMF droplets (0.2∼1 wt%), all PI particles had hollow structures. The P(n-BMA) would affect the phase separation of the PI in the droplets, thereby promoting the formation of a hollow structure.Corresponding, Oxford University Press (OUP), Dec. 2023, Chemistry Letters, 53(2) (2), English[Refereed]Scientific journal
- Elsevier BV, Oct. 2023, Sensors and Actuators B: Chemical, 393, 134133 - 134133, English, Co-authored internationally[Refereed]Scientific journal
- A novel sandwich detection was demonstrated for 0.01 wt% pork adulteration within 30 min, using PSA-imprinted polymer nanogels to capture PSA and anti-PSA antibody complexed with-Fc-domain imprinted fluorescent polymer nanogels to detect PSA.Royal Society of Chemistry (RSC), Aug. 2023, Nanoscale, 15(37) (37), 15171 - 15178, English[Refereed]Scientific journal
- Elsevier BV, Jul. 2023, Colloids and Surfaces A: Physicochemical and Engineering Aspects, 668, 131447 - 131447, English, Co-authored internationally[Refereed]Scientific journal
- Iodine transfer polymerization was used to synthesize micrometer-sized block copolymer particles using methyl methacrylate (MMA) and vinyl acetate (VAc) in a microsuspension system. Three morphologies were obtained after hydrolysis, depending on the block ratio.Corresponding, Royal Society of Chemistry (RSC), Jun. 2023, Polymer Chemistry, 14(26) (26), 3126 - 3135, English[Refereed]Scientific journal
- Springer Science and Business Media LLC, Apr. 2023, Journal of Polymer Research, 30(3) (3), English, Co-authored internationally[Refereed]Scientific journal
- Wiley, Apr. 2023, Polymer International, 72(4) (4), 424 - 433, Co-authored internationally[Refereed]Scientific journal
- Elsevier BV, Apr. 2023, Surfaces and Interfaces, 37, 102738 - 102738, English, Co-authored internationally[Refereed]Scientific journal
- The morphologies of polypropylene (PP)/polystyrene (PS) composite particles obtained using different type of the initiator in the seeded emulsion polymerization of styrene with multi-hollow PP seed particles.Corresponding, Royal Society of Chemistry (RSC), Jan. 2023, Polymer Chemistry, 14(3) (3), 352 - 358, English[Refereed]Scientific journal
- The inclusion of mesoporous H2N-SiO2 support in H2N-SiO2/Ni/PPy nanocomposite particles improved their electrochemical performance, suitable for energy storage devices.Royal Society of Chemistry (RSC), Nov. 2022, New Journal of Chemistry, 46(45) (45), 21798 - 21811, English, Co-authored internationally[Refereed]Scientific journal
- Corresponding, American Chemical Society (ACS), Aug. 2022, ACS Applied Polymer Materials, 4(8) (8), 5619 - 5625, English[Refereed]Scientific journal
- Elsevier BV, Aug. 2022, Colloids and Surfaces A: Physicochemical and Engineering Aspects, 647, 129044 - 129044, English, Co-authored internationally[Refereed]Scientific journal
- Corresponding, American Chemical Society (ACS), Jun. 2022, Langmuir, 38(23) (23), 7341 - 7345, English[Refereed]Scientific journal
- American Chemical Society (ACS), Apr. 2022, ACS Omega, 7(15) (15), 13010 - 13021, English, International magazine[Refereed]Scientific journal
- Corresponding, Springer Science and Business Media LLC, Apr. 2022, Colloid and Polymer Science, 300(4) (4), 365 - 373, English, International magazine[Refereed]Scientific journal
- Springer Science and Business Media LLC, Apr. 2022, Colloid and Polymer Science, 300(4) (4), 279 - 296, English, International magazine, Co-authored internationally[Refereed]Scientific journal
- Schematic of the behaviors of iodine species in the microsuspension polymerization of vinyl acetate (VAc) in an aqueous medium.Corresponding, Royal Society of Chemistry (RSC), Feb. 2022, Polymer Chemistry, 13(5) (5), 640 - 648, International magazine[Refereed]Scientific journal
- Corresponding, American Chemical Society (ACS), Aug. 2021, Langmuir, 37(34) (34), 10388 - 10393, English[Refereed]Scientific journal
- Corresponding, American Chemical Society (ACS), Aug. 2021, Langmuir, 37(31) (31), 9371 - 9377, English[Refereed]Scientific journal
- Corresponding, Wiley, May 2021, Journal of Applied Polymer Science, 138(19) (19), 50397 - 50397, English[Refereed]Scientific journal
- Elsevier BV, May 2021, Colloids and Surfaces A: Physicochemical and Engineering Aspects, 617, 126403 - 126403, English, Co-authored internationally[Refereed]Scientific journal
- Near-infrared (NIR) light irradiation induced the transformation of polypyrrole (PPy) to nitrogen-containing carbon (NCC) material due to its light-toheat photothermal property. The temperature of the PPy increased over 700 degrees C within a few seconds by the NIR laser irradiation, and elemental microanalysis confirmed the decreases of hydrogen and chloride contents and increases of carbon and nitrogen contents. Monodispersed polystyrene (PS)-core/PPy shell particles (PS/PPy particles) synthesized by aqueous chemical oxidative seeded polymerization were utilized as a precursor toward monodispersed NCC capsules. When the NIR laser was irradiated to the PS/PPy particles, the temperature rose to approximately 300 degrees C and smoke was generated, indicating that the PS component forming the core was thermally decomposed and vaporized. Scanning electron microscopy studies revealed the successful formation of spherical and highly monodispersed capsules, and Fourier transform infrared spectroscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy studies confirmed the capsules consisted of NCC materials. Furthermore, sunlight was also demonstrated to work as a light source to fabricate NCC capsules. The size and thickness of the capsules can be controlled between 1 and 80 pm and 146 and 231 nm, respectively, by tuning the size of the original PS/PPy particles and PPy shell thickness.American Chemical Society (ACS), Apr. 2021, Langmuir, 37(15) (15), 4599 - 4610, English[Refereed]Scientific journal
- Corresponding, American Chemical Society (ACS), Mar. 2021, Langmuir, 37(10) (10), 3158 - 3165, English, Co-authored internationally[Refereed]Scientific journal
- Elsevier BV, Jan. 2021, Carbohydrate Polymers, 251, 117024 - 117024, English, Co-authored internationally[Refereed]Scientific journal
- Corresponding, American Chemical Society (ACS), Dec. 2020, ACS Omega, 5(51) (51), 33047 - 33052, English[Refereed]Scientific journal
- Corresponding, American Chemical Society (ACS), Dec. 2020, Macromolecules, 53(24) (24), 11027 - 11032, English[Refereed]Scientific journal
- In this study, we report the preparation of hollow cellulose particles via a solvent-releasing method with the ionic liquid 1-ethyl-3-methylimidazolium acetate ([Emim]Ac). A dispersion comprising [Emim]Ac droplets with dissolved cellulose and a hexane medium containing a stabilizer was poured into a large amount of acetone (precipitant), resulting in the precipitation of cellulose and the formation of solid cellulose particles with a hollow structure. We found that the formation of the hollow structure resulted from the equilibrium phase separation. Porous structures were also obtained using ethanol or t-butanol as a precipitant, where cellulose immediately precipitated (i.e., exhibited non-equilibrium phase separation). In the case where acetone was used as the precipitant, the diffusion rate of [Emim]Ac from the droplets into the precipitant was relatively low that is, the precipitation of cellulose was delayed, which allowed the cellulose to be phase-separated into a thermodynamically stable structure (equilibrium phase separation), resulting in the formation of the hollow structure.American Chemical Society, Nov. 2020, Langmuir, 36(46) (46), 14076 - 14082, EnglishScientific journal
- Corresponding, Royal Society of Chemistry (RSC), Oct. 2020, Polymer Chemistry, 11(39) (39), 6328 - 6334
Composite particles consisting of elastic silicone and glassy poly(methyl methacrylate) were prepared. The morphology of the particles could be alternated between sea-island and core–shell structures by controlling the annealing temperature.
[Refereed]Scientific journal - Corresponding, Oct. 2020, Langmuir, 36, 11957 - 11962, English[Refereed]Scientific journal
- Corresponding, Sep. 2020, Macromol. Rapid Commun., 41, 2000141 - 2000147, Co-authored internationally[Refereed]
- Aug. 2020, Langmuir, 36, 8668 - 8679, EnglishPreparation and morphology control of poly(ionic liquid) particles[Refereed][Invited]Scientific journal
- The self-assembly of block copolymers has attracted attention for many decades because it can yield polymeric nanoobjects with a wide range of morphologies. Membrane emulsification is a fairly novel technique for preparation of various types of emulsions, which relies on the dispersed phase passing through a membrane in order to effect droplet formation. In this study, we have prepared polymeric nanoparticles of different morphologies using self-assembly of asymmetric block copolymers in connection with membrane emulsification. Shirasu Porous Glass (SPG) membranes has been employed as the membrane emulsification equipment, and poly (oligoethylene glycol acrylate)-Trans Tech Publications, Ltd., Jul. 2020, Materials Science Forum, 1000, 324 - 330, English, Co-authored internationally
block -poly (styrene) (POEGA-b -PSt) copolymers prepared via RAFT polymerization. It has been found that a number of different morphologies can be achieved using this novel technique, including spheres, rods, and vesicles. Interestingly, the results have shown that the morphology can be controlled not only by adjusting experimental parameters specific to the membrane emulsification step such as membrane pore size and pressure, but also by changing the nature of organic solvent. As such, this method provides a novel route to these interesting nanoobjects, with interesting prospects in terms of exercising morphology control without altering the nature of the block copolymer itself.[Refereed]Scientific journal - Jul. 2020, Materials Chemistry and Physics, 249, 122957 - 122967, English, Co-authored internationallyNickel decorated melamine–formaldehyde resin/polyaniline composites for high specific capacitance[Refereed]Scientific journal
- Corresponding, Jun. 2020, Macromol. Rapid Commun., 41, 2000271 - 2000276, EnglishPreparation of Poly(ionic liquid) Particles with Anionic Side-Chain by Dispersion Polymerization[Refereed]Scientific journal
- Jun. 2020, Materialia, 11, 100676 - 100685, English, Co-authored internationallyCationic polyelectrolyte grafted mesoporous magnetic silica composite particles for targeted drug delivery and thrombolysis[Refereed]Scientific journal
- Apr. 2020, Carbohydrate Polymers, 233, 115842 - 115850, English, Co-authored internationallyAg impregnated sub-micrometer crystalline jute cellulose particles: catalytic and antibacterial properties[Refereed]
- We reported the preparation of porous cellulose particles by the solvent-releasing method, in which a solution of cellulose, dissolved in 1-butyl-3-methylimidazolium chloride and N,N'-dimethylformamide, was dropped into a large amount of 1-butanol using a syringe. The obtained particles had a high specific area because of their porous structure. Herein, to functionalize the cellulose particles, carboxylate groups are introduced into their porous structure by 2,2,6,6-tetramethylpiperidine-1-oxyl-mediated oxidation and ion exchange of carboxylate groups to Ag cations is conducted. Composite cellulose/Ag particles were synthesized by the reduction reaction using the carboxylate groups as a scaffold without free silver nanoparticles in the medium. The obtained composite particles exhibited a high catalytic ability, which was evaluated by examining the reduction of 4-nitrophenol. Moreover, we determined that the catalytic efficiency was maintained for at least three cycles by immobilizing Ag on cellulose particles.Corresponding, AMER CHEMICAL SOC, Feb. 2020, ACS Omega, 5(4) (4), 1919 - 1926, English[Refereed]Scientific journal
- Corresponding, Dec. 2019, ACS Sustainable Chem. Eng., 7, 19157 - 19166, English, Co-authored internationally[Refereed]Scientific journal
- Nov. 2019, ACS Appl. Mater. Interfaces, 11, 48450 - 48458, English, Co-authored internationallyAmbient Temperature Waterborne Polymer/rGO Nanocomposite Films: Effect of rGO Distribution on Electrical Conductivity[Refereed]Scientific journal
- Nov. 2019, Cellulose, 26, 8713 - 8727, English, Co-authored internationally[Refereed]Scientific journal
- To prepare cross-linked silicone (silicone rubber) particles in an aqueous medium, we investigated two synthesis methods involving a miniemulsion system. The first method was based on cationic ring-opening polymerization of cyclic siloxane, which is a common synthetic route for linear silicone oil and uses octamethylcyclotetrasiloxane (D-4) as the monomer and dimeric D-4 (bis-D-4) as the cross-linker. Although this method produces silicone particles, the particles do not remain in the particulate state after drying because of low cross-linking density. The polymerization mechanism of this method was also investigated, which proceeds under the ring-opening reaction of D-4 in monomer droplets and upon polycondensation of hydrolyzed D-4, which occurs in the water phase (ie, outside the monomer droplets). This mechanism implied that introducing the cross-linking structure into particles is difficult because of the low solubility of bis-D-4 in water. To overcome these difficulties, we demonstrated a second method of preparing silicone particles based on the thiol-Michael addition reaction between thiol-terminated silicone oil and triacrylate in miniemulsion systems. Transmission electron microscopy images indicated that the silicone particles obtained in the particulate state upon drying and the aggregates of these particles showed elasticity.Corresponding, WILEY, Nov. 2019, Polym. Adv. Technol.,, 30(12) (12), 3003 - 3010, English[Refereed]Scientific journal
- Nov. 2019, Ind. Eng. Chem. Res., 58, 21165 - 21170, English, Co-authored internationally[Refereed]Scientific journal
- Composite particles were prepared by the seeded polymerization of an ionic liquid monomer ([2-(methacryloyloxy)ethyl]trimethylammonium bis(trifluoromethanesulfonyl)amide) ([MTMA][TFSAD in the presence of poly(methyl methacrylate) (PMMA) particles. The obtained particles have a core-shell morphology: PMMA core and P([MTMA][TFSA]) shell. To change the composite particle morphology from core-shell to Janus, we used the solvent-absorbing/releasing method with methyl isobutyl ketone, which is a suitable solvent for PMMA and P([MTMA]-[TFSA]) with nonionic surfactants (polyoxyethylene nonylphenyl ether, Emulgen 950) and Li[TFSA]. Based on the ultrathin cross-section observations, we found the core-shell PMMA/P([MTMA][TFSA]) composite particle morphology changed to a Janus structure. Moreover, anion exchange occurred in the obtained Janus particles. When using LiBr, we obtained PMMA hemisphere particles because of the changes in the PIL hemisphere polarity via anion exchange and dissolution in water. On the contrary, the use of poly(sodium styrenesulfonate) maintained the Janus structure because of ionic cross-linking and the changes in the PIL hemisphere to hydrophilic properties, which became swollen with medium water.Corresponding, AMER CHEMICAL SOC, Nov. 2019, Ind. Eng. Chem. Res., 58(46) (46), 20996 - 21002, English[Refereed]Scientific journal
- Sep. 2019, Colloids Surfaces B: Biointerface,, 181, 85 - 93, English, Co-authored internationally[Refereed]Scientific journal
- Jun. 2019, J. Polym. Eng., 39, 671 - 678, English[Refereed]Scientific journal
- Jun. 2019, Electrochimica Acta, 308, 115 - 120, English[Refereed]Scientific journal
- In this study, cylindrical polystyrene particles were applied as a particulate stabilizer to prepare a Pickering emulsion of decane (oil)/water. Unlike the spherical particles that are typically used in Pickering emulsions, the cylindrical particles enhanced the emulsion's stability (up to 1 year). Furthermore, the cylindrical particulate stabilizer enabled a stable emulsion across a wide range of pH. Notably, unique adsorption behavior of the cylindrical particles on an oil droplet was observed, in which the cylindrical particles connected head to head to form a network that acted as a cage around the oil droplet. (C) 2019 Elsevier Inc. All rights reserved.Corresponding, ACADEMIC PRESS INC ELSEVIER SCIENCE, May 2019, J. Colloid Interface Sci.,, 522, 230 - 235, English[Refereed]Scientific journal
- May 2019, J. Appl. Polym. Sci.,, 136, 47524 - 47538, English[Refereed]Scientific journal
- Apr. 2019, Macromolecules,, 52, 2965 - 2974, English[Refereed]Scientific journal
- Apr. 2019, Nanoscale, 11, 6566 - 6570, English[Refereed]Scientific journal
- Polystyrene/graphene oxide (PSt/GO) nanocomposite latexes have been prepared by Pickering miniemulsion polymerization in the presence of the conventional surfactant sodium dodecyl sulfate (SDS) in order to investigate its influence on the polymerization mechanism. Miniemulsion polymerization of styrene can be conducted successfully using GO as the sole surfactant, but the polymerization rate is very low. In the presence of SDS, a significant rate enhancement is observed. It has been clarified that the presence of SDS leads to additional nucleation pathways besides monomer droplet nucleation, namely nucleation involving free GO sheets in the aqueous phase as well as homogeneous nucleation. These mechanistic pathways are consistent with the rate enhancement and the increase in molecular weight as well as experimentally observed particle distributions in the presence of SDS. The present results represent a significant step forward in terms of our understanding of the fundamental polymerization mechanism of this Pickering miniemulsion system, which will aid in the preparation of advanced nanocomposite materials based on polymers and graphene (oxide).Royal Society of Chemistry, Jun. 2018, Polymer Chemistry, 9(24) (24), 3368 - 3378, English[Refereed]Scientific journal
- Porous γ-alumina (γ-Al2O3) is one of widely used ceramic materials. To maximize the application potentials attempt was made to prepare multifunctional γ-Al2O3 ceramic composite particles following magnetization and then seeded polymerization with epoxide functional glycidyl methacrylate (GMA). γ-Al2O3 particles were first prepared by a modified sol-gel approach and then doped with variable content Fe3O4 nanoparticles. At higher Fe3O4 content the magnetite nanoparticles were oriented into needle like hairy structure basically grown from the surface of γ-Al2O3 particles. Before the seeded polymerization the magnetic γ-Al2O3 particles were modified with SiO2 layer to improve the compatibility with the PGMA layer. The produced multifunctional ceramic particles were named as γ-Al2O3/Fe3O4/SiO2/PGMA nanocomposite because one of the phases constituting Fe3O4 was in nano-size range. The produced nanocomposite particles possessed superparamagnetic properties and could be isolated from the dispersion medium by external magnetic field. Fourier Transform IR (FTIR) and X-ray photoelectron spectroscopic (XPS) data revealed that final nanocomposite particles contained reactive epoxide groups on or near the surface. The produced multifunctional γ-Al2O3 ceramic nanocomposite particles can be useful in biotechnology, catalysis and adsorbents for pollutant removal.Elsevier Ltd, Mar. 2018, Ceramics International, 44(4) (4), 3951 - 3959, English[Refereed]Scientific journal
- In this investigation, epoxide (oxirane), a cyclic ether with a three-atom ring, functional semi-interpenetrating polymer network (semi-IPN) hydrogel microspheres composed of temperature-sensitive poly(N-isopropylacrylamide-N,N-methylene-bis-acrylamide) (P(NIPAM-MBAAm)) and P(NIPAM-glycidyl methacrylate) (P(NIPAM-GMA)) are prepared. We called these microspheres as P(NIPAM-MBAAm)/P(NIPAM-GMA). The microspheres exhibited temperature-sensitive volume phase transition at a temperature range of 33–35°C. The chemical bonding of anticancer drugs with the epoxide ring increased the absorption capacity but their release is affected, as the temperature is decreased below the volume phase transition, studied under an in vitro condition suitable for application in the treatment of cancer cells. The epoxide functionality of semi-IPN hydrogel microspheres is also utilized to isolate inorganic nanoparticles, using Fe3O4 nanoparticles as an example, simply by blending the hydrogel and magnetic (Fe3O4) dispersions. The presence of strained oxirane ring derived from GMA segment induced high affinity for semi-IPN hydrogel microspheres toward magnetic Fe3O4 nanoparticles and eventually reduced the colloidal stability.John Wiley and Sons Inc., Feb. 2018, Advances in Polymer Technology, 37(1) (1), 94 - 103, English[Refereed]Scientific journal
- 2018, Colloids Surfaces A: Physicochem. Eng. Aspects, 555, 80 - 87, English[Refereed]Scientific journal
- 概要Corresponding, AMER CHEMICAL SOC, 2018, Langmuir, 34(50) (50), 15490 - 15494, English[Refereed]Scientific journal
- 2018, Soft Matter, 14, 5469 - 5479, English[Refereed]Scientific journal
- 2018, Polymer Composites, 39, 4628 - 4636, English[Refereed]Scientific journal
- A facile and novel approach to prepare monodisperse polystyrene (PS) particles having a cylindrical shape was discovered. Spherical PS particles prepared by dispersion polymerization were stirred in a polyvinylpyrrolidone (PVP) aqueous solution for several hours using a magnetic stirrer at room temperature. In the presence of PVP, the spherical PS particles deformed into cylindrical shapes following stirring; however, the particles did not deform in the absence of PVP. The deformation rate of the particles was affected by the molecular weight of the dissolved PVP. This stirring method is not only highly efficient and high yielding, but also applicable to other materials such as polymethyl methacrylate. Moreover, the cylindrical particles were successfully applied as particulate surfactants in a Pickering emulsion system, which exhibited excellent stability in comparison to a system using spherical particles as a surfactant. In the first case, the emulsion was left standing for more than 4 months.Corresponding, WILEY-V C H VERLAG GMBH, 2018, Angew. Chem. Int. Ed, 57(31) (31), 9936 - 9940, English[Refereed]Scientific journal
- Nickel oxide (NiO) nanoparticles are useful in many catalysis reactions because of large surface area, high adsorptive properties, fast diffusivities, low cost and additionally they possess special electric and magnetic properties. However, the application of bare NiO nanoparticles often suffers from poor colloidal stability and weak chemical inertness. To overcome the disadvantages this investigation described the preparation of a novel three-layered NiO/SiO2/poly(glycidyl methacrylate) nanocomposite particles abbreviated as NiO/SiO2/PGMA. The epoxide functionality derived from PGMA on the surface of NiO nanoparticles is expected to increase the absorption capacity of the substrate, a prime requirement for high catalytic performance. The formation of nanocomposite particles is confirmed by Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), transmission electron microscope (TEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD) and thermogravimetric analyses (TGA). The produced NiO/SiO2/PGMA nancomposite particles possess core-shell type morphology with porous shell structure. The UV light driven photocatalytic degradation of congo red (CR), a water soluble azo dye, in presence of NiO/SiO2/PGMA nanocomposite particles is evaluated in terms of degradation efficiency and kinetics. Degradation efficiency decreased with the increase of initial CR concentration and a maximum efficiency of 100% is attained within 10 min when 10 mL of 40 mg L-1 CR aqueous solution is irradiated in presence of 0.01 g of NiO/SiO2/PGMA nanocomposite photocatalyst.ELSEVIER SCIENCE BV, Sep. 2017, COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 529, 783 - 792, English[Refereed]Scientific journal
- Membrane emulsification entails the use of two immiscible liquids for preparation of oil-in-water or water-in-oil emulsions of well-defined droplet size. In this work, we have developed a novel approach for preparation of polymeric nano-objects of various morphologies based on self-assembly of diblock copolymers in tandem with microporous membrane technology (Shirasu porous glass (SPG) membranes). Diblock copolymers poly(oligoethylene glycol acrylate)-b-poly(styrene) (POEGA-b-PSt) comprising different block lengths were prepared by RAFT polymerization. Self-assembly using SPG membrane technology was subsequently conducted by first dissolving the polymer in tetrahydrofuran, followed by continuous passage of this copolymer solution through the membrane pores into the aqueous phase. The results indicate that it is possible to conveniently tune the nano-object morphology via the process parameters of pressure and pore size for a given formulation. The technique also holds promise with regards to high throughput, in particular in the case of vesicles.ROYAL SOC CHEMISTRY, Aug. 2017, REACTION CHEMISTRY & ENGINEERING, 2(4) (4), 451 - 457, English[Refereed]Scientific journal
- Disk-like cellulose particles were facilely prepared by stirring a dispersion of spongy cellulose particles that were prepared with a solvent-releasing method (SRM) with a magnetic stir bar. The obtained particles were thick and disk-like and retained their spongy structure in the wet state. The thick, disk-like particles became thinner in a specific direction upon drying because of capillary force. In contrast, when the same procedure was conducted using cellulose particles with dense structures, the particle shapes were not deformed, and disk-like shapes did not appear. Moreover, when the stirring was carried out using a shaking bath or a touch mixer, the shape transformation was not observed. These results suggest that the spongy structure of the cellulose particles would be a pseudo-plasticization state, which can cause the cellulose particles to deform. The disk-like particles formed as a result of the grinding of spongy cellulose particles between the stir bar and the vial. The number of disk-like particles and the degree of deformation increased with increasing of the stirring time, the speed and the contact area.Corresponding, SPRINGER, Aug. 2017, CELLULOSE, 24(8) (8), 3111 - 3118, English[Refereed]Scientific journal
- This investigation describes the preparation of magnetically doped degradable microcrystalline cellulose (MCC) nanocomposite particles with application potential in biotechnology, solid support for biomolecule/water purification, oil recovery from water and beyond. MCC was first extracted from cotton wool, the most abundant biocompatible polymer, by sulfuric acid hydrolysis and the effect of acid strength was examined. The size of the elongated fiber structure was reduced with increasing acid strength. MCC particles extracted by treatment with 70% sulfuric acid were used to prepare magnetic MCC nanocomposite particles. The nanocomposite particles named as MCC/Fe3O4 were prepared via in situ co-precipitation of Fe+3/Fe+2 from their alkaline solution. The precipitated Fe3O4 nanoparticles are expected to be bonded with MCC particles via hydrogen bonding. The nanocomposite dispersion was colloidally stable and the particles responded when external magnetic field was applied. It was possible to control the magnetic property by regulating the content of iron oxide. (C) 2017 Elsevier Ltd. All rights reserved.ELSEVIER SCI LTD, Aug. 2017, CARBOHYDRATE POLYMERS, 170, 72 - 79, English[Refereed]Scientific journal
- Magnetic particles have attracted much interest because they can be easily guided under the influence of magnetic field and are considered suitable in biomedical as well as in separation technology. In this work, magnetite (Fe3O4) loaded cross-linked polystyrene (PS) composite particles are prepared by a novel suspension polymerization of styrene and divinylbenzene (DVB) in presence of nanosized iron oxide (Fe3O4) particles dispersed in n-octane. The structure and surface properties are systematically characterized using FTIR, scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and thermogravimetric analyses (TGA). The morphology and surface structure reveal that Fe3O4 nanoparticles are mostly dispersed within the P(S-DVB) copolymer layer. Finally the applicability of Fe3O4/P(S-DVB) composite polymer particles as adsorbent for toxic element like trivalent arsenic (As) has been investigated. Fe3O4/P(S-DVB) composite polymer particles exhibited good sorption efficiency compared to reference P(S-DVB) copolymer particles.SPRINGER, Jul. 2017, MACROMOLECULAR RESEARCH, 25(7) (7), 671 - 679, English[Refereed]Scientific journal
- A convenient and industrially scalable method for synthesis of homogeneous nanocomposite films comprising poly(styrene-stat-butyl acrylate) and nanodimensional graphene oxide (GO) or reduced GO (rGO) is presented. Importantly, the nanocomposite latex undergoes film formation at ambient temperature, thus alleviating any need for high temperature or high pressure methods such as compression molding. The method entails synthesis of an aqueous nanocomposite latex via miniemulsion copolymerization relying on nanodimensional GO sheets as sole surfactant, followed by ambient temperature film formation resulting in homogeneous film. For comparison, a similar latex obtained by physical mixing of a polymer latex with an aqueous GO dispersion results in severe phase separation, illustrating that the miniemulsion approach using GO as surfactant is key to obtaining homogeneous nanocomposite films. Finally, it is demonstrated that the GO sheets can be readily reduced to rGO in situ by heat treatment of the film. (C) 2017 Wiley Periodicals, Inc.WILEY, Jul. 2017, JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 55(14) (14), 2289 - 2297, English[Refereed]Scientific journal
- Emulsion polymerization of styrene was conducted using a biosurfactant (i.e., sodium surfactin, hereinafter 30 called just "surfactin") having very low critical micelle concentration (CMC, 2.9 X 10(-3) rnmol/L) and biodegradability characteristics. The nucleation mechanism was investigated by comparing with a conventional surfactant sodium dodecyl sulfate) system. Unlike the emulsion polymerization systems using conventional surfactants, nucleation mechanisms changed above CMC in the presence of a biosurfactant. At low concentrations of surfactin (above CMC), the polystyrene (PS) particles are likely generated via a soap-free emulsion polymerization mechanism. In contrast, at high surfactin concentrations, the PS particles would be synthesized by following a micellar nucleation mechanism. However, the slope (0.23) of the log N-p versus log C-s plot (N-p: number of particles; C-s: concentration of surfactin) did not obey the Smith Ewart theory (0.6), this probably being produced by the high adsorbability of surfactin.Corresponding, AMER CHEMICAL SOC, Jun. 2017, LANGMUIR, 33(23) (23), 5814 - 5818, English[Refereed]Scientific journal
- Composite particles comprising poly(2-phenylethyl methacrylate) (PPhEMA) and imidazolium-based poly(ionic liquid)s were prepared by suspension polymerization of 1-vinyl-3-ethylimidazolium bis(trifluoromethanesulfonyl)amide as an ionic liquid monomer with dissolved PPhEMA. Not only PPhEMA exhibits lower critical solution temperature (LCST) behavior in 1-vinyl-3-ethylimidazolium bis(trifluoromethanesulfonyl)amide but also the polymer blend in the bulk state exhibited LCST behavior. However, the composite polymer particles obtained after polymerization at 70 degrees C maintained a homogeneous inner structure after heat treatment as the polymerization temperature was greater than the LCST in this system due to the formation of a cross-linked structure during polymerization. When the composite particles were prepared by suspension polymerization at 30 degrees C, their inner morphology changed from homogeneous to phase separated during the subsequent heat treatment. Moreover, the morphology transformation of the composite particles was dependent on the PPhEMA molecular weight. Copyright (c) 2016 John Wiley & Sons, Ltd.Corresponding, WILEY, Apr. 2017, POLYMERS FOR ADVANCED TECHNOLOGIES, 28(4) (4), 470 - 475, English[Refereed]Scientific journal
- Flattened cross-linked hollow poly(divinylbenzene) (PDVB) particles with encapsulated n-hexadecane (HD) were successfully prepared through suspension polymerization using the self -assembling of phase-separated polymer (SaPSeP) method, in which the solid dispersion medium was gelled by gellan gum and compressed. The solid phase induced by gellan gum can be easily changed to a liquid state by heating, allowing the obtained particles to be easily recovered after polymerization. When the polymerization was conducted in the solid dispersion medium without compression, spherical hollow PDVB/HD composite particles were obtained. In contrast, when the polymerization was conducted with the compression of the solid dispersion medium, flattened hollow PDVB/HD composite particles were obtained. The shape of the flattened hollow polymer particles was controlled by changing the compression ratio of the solid phase, and the size could also be controlled by changing the DVB/HD droplet size using the Shirasu porous glass membrane-emulsification technique. Furthermore, flattened hollow particles larger than 20 mu m in size were obtained, but it was difficult to obtain spherical hollow particles of such large size using the SaPSeP method.AMER CHEMICAL SOC, Feb. 2017, LANGMUIR, 33(6) (6), 1541 - 1546, English[Refereed]Scientific journal
- Dispersion polymerization of L-lactide was proceeded in various ionic liquids. Ionic liquids as 1-Hexyl-3-methylimidazolium bis (trifluormethylsulfonyl) imide, [HMIM] [TFSI], 1-Butyl-3-methylimidazolium bis (trifluoromethylsulfonyl) imide, [BMP] [TFSI], and N,N,N-Trimethyl-N-Propylammonium Bis (trifloromethanesulfonyl) imide, [TMPA] [TFSI], were employed as reaction medium that dissolved both of lactide and stabilizer (polyvinylprrolidone). Sn-supported on bentonite was used as a ring opening catalyst of L-lactide. Gel Permeation Chromatography result showed that poly-(L-lactic acid) were formed in ionic liquids [HMIM] [TFSI] and [BMP] [TFSI] with molecular weight as 19390 and 20844, respectively.AMER INST PHYSICS, 2017, PROCEEDINGS OF THE 3RD INTERNATIONAL SYMPOSIUM ON APPLIED CHEMISTRY (ISAC) 2017, 1904, 020037(1 - 8), English[Refereed]International conference proceedings
- We have reported cellulose particles with a spongy structure that we prepared by the solvent releasing method (SRM) from cellulose droplets composed of cellulose, 1-butyl-3-methylimidazoliumchrolide ([Bmim] Cl), and N,N-dimethylformamide (DMF). The spongy structure collapsed as the medium evaporated, resulting in dense cellulose particles. In this study, we encapsulated the hydrophilic and hydrophobic fluorescent substances in these particles to investigate the use of such particles in potential applications that require encapsulating of substances (e.g., drug delivery). Wet cellulose particles retained their spongy structure in both hydrophobic and hydrophilic media. When the spongy cellulose particles were dispersed in a solution containing nonvolatile solutes, these solutes were driven into the cellulose particles as media evaporated. Subsequently, the cellulose particles collapsed and encapsulated the nonvolatile solutes. Regardless of whether the solute was hydrophilic or hydrophobic, the encapsulation efficiency exceeds 80%. The maximum loading reflected the saturated solubility of solute in solution that filled the cellulose beads. Moreover, the encapsulated solute was released by dispersing the cellulose beads in the solvent, and the rate of release of the encapsulated solute could be controlled by coating the cellulose beads with a conventional polymer.Corresponding, AMER CHEMICAL SOC, Jan. 2017, ACS APPLIED MATERIALS & INTERFACES, 9(1) (1), 944 - 949, English[Refereed]Scientific journal
- Magnetic conducting nanoparticles with reactive functional groups are attractive materials for applications in electromagnetic interference shielding, magneto-optical storage, biomedical sensing, gas and humidity sensors, flexible electronics etc. The objective of this work was to prepare carboxyl functionalized polypyrrole (PPy) nanocomposite particles having good magnetic properties. Electromagnetic PPy nanostructures, abbreviated as PPy/-Fe2O3, were first prepared by a chemical one-step method. In this reaction process FeCl3 is used as an oxidant for the polymerization of pyrrole and as a source of Fe3+ for the formation of -Fe2O3. The formation of -Fe2O3 is also aided by the initial presence of Fe2+, and p-toluenesulfonic acid (p-TSA) acted as a dopant. The effects of different stabilizers on the stability and morphology of PPy/-Fe2O3 particles were evaluated. The presence of citric acid/sodium dodecyl sulfate during chemical oxidative polymerization produced a relatively stable PPy/-Fe2O3 colloidal emulsion. PPy/-Fe2O3/poly(methylmethacrylate-methacrylic acid) (PPy/-Fe2O3/P(MMA-MAA)) nanocomposite polymer particles were then prepared by the seeded copolymerization of MMA and MAA in the presence of magnetic PPy/-Fe2O3 nanocomposite seed particles. The structure and morphology of the prepared nanocomposites were confirmed by different instrumental techniques such as Fourier transform IR spectroscopy, UV-visible spectroscopy, electron micrographs, XRD and X-ray photoelectron spectroscopy. The electrical and magnetic properties were also investigated. The carboxyl functional electromagnetic PPy nanocomposite polymer particles should be useful for the immobilization of drugs or biomolecules to design electrically stimulated drug delivery systems for modulating the activities of nerve, cardiac, skeletal muscle and bone cells. (c) 2016 Society of Chemical IndustryWILEY-BLACKWELL, Oct. 2016, POLYMER INTERNATIONAL, 65(10) (10), 1179 - 1186, English[Refereed]Scientific journal
- A combination of maghemite polypyrrole (PPy/gamma-Fe2O3) and stimuli-responsive properties in the same hydrogel microspheres is expected to enhance their application potential in various fields such as tissue engineering, regenerative medicine, biosensors, biomedical applications and removal of heavy metals from waste water, catalysis etc. In this investigation a simple two step process is used to prepare conductive stimuli-responsive polypyrrole (PPy) composite hydrogel particles with strong magnetic properties. Poly(styrene-methacrylic acid-N-isopropylacrylamide-polyethelene glycol methacrylate) or P(S-NIPAM-MAA-PEGMA) hydrogel seed particles are first prepared by soap-free precipitation copolymerization. The copolymer hydrogel particles exhibited both temperature- and pH-responsive volume phase transition. Conductive P(S-NIPAM-MAA-PEGMA)/PPy/gamma-Fe2O3 nanocomposite hydrogel particles are then prepared by seeded chemical oxidative polymerization of pyrrole in the presence of P(S-NIPAM-MAA-PEGMA) hydrogel seed particles using FeCl3 as a oxidant and p-toluene sulfonic acid (p-TSA) as a dopant. In the reaction system FeCl3 functioned as a source of Fe(III) for the formation of gamma-Fe2O3. This reaction also requires the initial presence of Fe(II) provided by the addition of FeCl2. The size and size distribution, surface structure, and morphology of the prepared conductive composite hydrogel particles are confirmed by FTIR, electron micrographs, X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and UV-visible spectroscopy. The performance of nanocomposite hydrogel particles has been evaluated for the removal of hexavalent chromium (Cr) ions from water. (C) 2016 Elsevier B.V. All rights reserved.ELSEVIER SCIENCE BV, Aug. 2016, JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS, 412, 15 - 22, English[Refereed]Scientific journal
- We report a new paradigm for the synthesis of metal organic framework (MOP) crystals with controlled thickness by utilizing interfacial self-assembly of frameworks on metal ion-doped polymer precursors. The approach involves preparation of metal ion-doped polymer precursors through ion-exchange reactions and synthesis of MOF crystals by immersion into solutions containing organic ligands. The thickness of the resulting MOF crystals can be readily controlled by the number of doped-metal ions in the polymer precursors. MOF crystals could be very important and potentially useful for applications, and the present approach based on interfacial self-assembly could significantly advance MOF crystal preparation techniques.AMER CHEMICAL SOC, May 2016, CRYSTAL GROWTH & DESIGN, 16(5) (5), 2472 - 2476, English[Refereed]Scientific journal
- Poly(ionic liquid) (PIL) particles with a single-hollow structure are prepared by suspension polymerization from monomer droplets consisting of the hydrophobic ionic liquid monomer [2-(methacryloyloxy)ethyl]trimethylammonium bis(trifluoromethanesulfonyl)amide, ethylene glycol dimethacrylate, and n-butyl acetate containing dissolved poly(n-butyl methacrylate). The obtained PIL hollow particles' shells can be changed from hydrophobic to hydrophilic by anion exchange using a LiBr/ethanol solution. In the case of hydrophilic PIL hollow particles, the water-soluble fluorescent materials can penetrate into the hollow structure, whereas in the case of hydrophobic PIL hollow particles, penetration of the fluorescent materials is restricted. In addition, the encapsulated water-soluble materials can be preserved into the hollow part by changing the shell property of the PIL particle encapsulated with the water-soluble materials from hydrophilic to hydrophobic.Corresponding, AMER CHEMICAL SOC, Mar. 2016, LANGMUIR, 32(10) (10), 2331 - 2337, English[Refereed]Scientific journal
- The preparation of polymer nanoparticles containing reduced graphene oxide nanosheets (rGO) within their interior has been conducted by radical polymerization in aqueous miniemulsion employing the nonionic surfactant Tween 80. Polymerizations were conducted using the ionic liquid monomer 1-vinyl-3-ethylimidazolium bis(trifluoromethanesulfonyl)amide ( [Veim] [TFSA]) as well as mixtures of this monomer with ethyl methacrylate (EMA). [Veim] [TFSA] plays an important role in that it provides stabilization of rGO monomer dispersions, presumably via pi-pi interactions between rGO and [Veim][TFSA]. If the EMA: [Veim] [TFSA] ratio is too high, rGO precipitates during preparation of the monomer phase of the miniemulsion. Interestingly, it was demonstrated that addition of a small amount of the homopolymer of [Veim] [TFSA] leads to significantly improved rGO stability (more so than the effect of [Veim] [TFSA] monomer), thus enabling preparation of polymer nanoparticles containing higher amounts of EMA.Corresponding, AMER CHEMICAL SOC, Feb. 2016, MACROMOLECULES, 49(4) (4), 1222 - 1228, English[Refereed]Scientific journal
- Polymeric nanoparticles containing reduced graphene oxide (rGO) nanosheets have been prepared by aqueous miniemulsion radical polymerization of methyl methacrylate (MMA) utilizing poly(ionic liquid) (PIL) as stabilizer to effectively disperse the rGO nanosheets in the monomer phase. The PIL that gave the best results in terms of rGO dispersibility was a block copolymer of the ionic liquid monomer 1-(2-methacryloyloxyethyl)- 3-butylimidazolium bis(trifluoromethanesulfonyl) amide ([Mbim][TFSA]) and MMA, the concept being that the MMA units impart solubility in the MMA monomer droplets whereas the IL units act as adsorption sites for rGO. The rGO dispersibility in vinyl monomer was demonstrated to be superior using the above PIL block copolymer compared to the corresponding statistical copolymer or PIL homopolymer. Overall, the approach developed demonstrates how PILs can be employed to conveniently switch (turn ON/OFF) the dispersibility of PIL/rGO via anion exchange reactions, which can be an efficient strategy for synthesis of polymer/rGO nanocomposite materials.Corresponding, ROYAL SOC CHEMISTRY, 2016, SOFT MATTER, 12(17) (17), 3955 - 3962, English[Refereed]Scientific journal
- Seeded dispersion polymerization of an ionic liquid monomer ([2-(methacryloyloxy)ethyl]trimethylammonium bis(trifluoromethanesulfonyl)amide) ([MTMA][TFSA]) was carried out in the presence of poly(methylmethacrylate) (PMMA), poly(ethyl methacrylate) (PEMA), and poly(t-butyl methacrylate) (PtBMA) as seed particles in a methanol/water mixture. For PMMA and PEMA seed particles, composite particles with poly(ionic liquid) (PIL) were obtained. In contrast, for PtBMA seed particles, secondary nucleated PIL particles were formed and no PtBMA/PIL composite particles were obtained. These results were also predicted by theoretical consideration based on the spreading coefficients calculated from the interfacial tensions. Moreover, we showed that anion exchange of the PIL-core in the PIL/cross-liked PMMA core-shell composite particles from TFSA to Br and FeCl4 anions can be used to modify the properties of only the core component of the composite particles.Corresponding, ROYAL SOC CHEMISTRY, 2016, RSC ADVANCES, 6(37) (37), 31574 - 31579, English[Refereed]Scientific journal
- We prepared a heterogeneous double-network (DN) ionogel containing a low-molecular-weight gelator network and a polymer network that can exhibit high ionic conductivity and high mechanical strength. An imidazolium-based ionic liquid was first gelated by the molecular self-assembly of a low-molecular-weight gelator (benzenetricarboxamide derivative), and methyl methacrylate was polymerized with a cross-linker to form a cross-linked poly(methyl methacrylate) (PMMA) network within the ionogel. Microscopic observation and calorimetric measurement revealed that the fibrous network of the low-molecular-weight gelator was maintained in the DN ionogel. The PMMA network strengthened the ionogel of the low-molecular-weight gelator and allowed us to handle the ionogel using tweezers. The orthogonal DNs produced ionogels with a broad range of storage elastic moduli. DN ionogels with low PMMA concentrations exhibited high ionic conductivity that was comparable to that of a neat ionic liquid. The present study demonstrates that the ionic conductivities of the DN and single-network, low-molecular-weight gelator or polymer ionogels strongly depended on their storage elastic moduli.AMER CHEMICAL SOC, Oct. 2015, ACS APPLIED MATERIALS & INTERFACES, 7(41) (41), 23346 - 23352, English[Refereed]Scientific journal
- Encapsulation of nickel oxide (NiO) particles is of great interest to the researchers as such modification produces remarkable improvement in properties and versatility in application potential. In this investigation, nano-sized NiO particles were first prepared by calcination of nickel hydroxide precursor obtained using a simple liquid-phase process. The produced NiO particles were stabilized with oleic acid and then treated with tetraethylorthosilicate to produce NiO/SiO2 composite seed particles. Finally tri-layered inorganic/organic composite particles were prepared by seeded copolymerization of styrene and 2-hydroxyethyl methacrylate (HEMA) in the presence of NiO/SiO2 composite seed particles. The produced composite particles named as NiO/SiO2/P(S-HEMA) were colloidally stable, and the obtained particles were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy and thermogravimetric analyses. Copyright (C) 2015 John Wiley & Sons, Ltd.WILEY-BLACKWELL, Sep. 2015, POLYMERS FOR ADVANCED TECHNOLOGIES, 26(9) (9), 1047 - 1052, English[Refereed]Scientific journal
- Metal nanocrystal/metal-organic framework core/shell nanostructures have been constructed using metal ion-trapped nanocrystals as scaffolds through a selective self-assembly of framework components on the nanocrystal surfaces. The resulting nanostructures exhibit unique catalytic activity toward nitrophenol analogs. (C) 2015 Elsevier Inc. All rights reserved.ACADEMIC PRESS INC ELSEVIER SCIENCE, Aug. 2015, JOURNAL OF COLLOID AND INTERFACE SCIENCE, 451, 212 - 215, English[Refereed]Scientific journal
- This contribution reports the precipitation copolymerization of lauryl methacrylatedivinylbenzene (LMADVB) in stable isolated droplets dispersed in water. The droplets contain either n-hexadecane (HD) or HDtoluene (HDT) or toluene as a nonsolvent for the resulting P(LMADVB) copolymer. The polymerization proceeds smoothly with an appreciably high content of DVB without the formation of coagulum and thus proves the quite high stability of the droplet reactors. The differences in the interaction between the nonsolventcopolymer combinations allow the variation of the internal morphology of the particles between core and shell type, highly porous, and solid sphere. (C) 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 41881.WILEY-BLACKWELL, Apr. 2015, JOURNAL OF APPLIED POLYMER SCIENCE, 132(16) (16), 41881 - 7, English[Refereed]Scientific journal
- Preparation of Thermosensitive “Snowman-like” Composite Gel Particles Incorporating an Ionic Liquid概要発行機関名, 2015, J. Adhesion Soc. Jpn, 51, 225 - 226, English[Refereed]Scientific journal
- The influence of the structure of ionic liquids on the crystallinity of aluminum hydroxide (Al(OH)(3)) prepared by a sol-gel process with aluminum isopropoxide (Al(OPri)(3)) in imidazolium-based ionic liquids was investigated. When Al(OH)(3) was prepared in ionic liquids having long alkyl chains, such as 1-butyl-3-methylimidazolium salts and 1-methyl-3-octylimidazolium salts, highly crystalline products were obtained. In contrast, Al(OH)(3) obtained using the 1-ethyl-3-methylimidazolium salt was an amorphous material, indicating that hydrophobic interaction of the alkyl tail of the imidazolium cation of the ionic liquid strongly affects the crystallinity of sol-gel products and the local structure of the ionic liquid. Moreover, the crystallinity of Al(OH)(3) prepared in ionic liquids increased relative to the amount of additional water (ionic liquid/water = 1.28/2.0-3.5/0.2, w/w). In the case of addition of a small amount of water (ionic liquid/water = 3.5/0.2, w/w), the product was amorphous. These results implied that the presence of an ionic liquid and a sufficient amount of water was crucial for the successful synthesis of sol-gel products with high crystallinity. H-1 NMR analyses revealed a shift of the peak associated with the imidazolium cation upon addition of water, which suggested that the molecular orientation of the ionic liquid was similar to that of a micelle.Corresponding, ROYAL SOC CHEMISTRY, 2015, PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 17(28) (28), 18705 - 18709, English[Refereed]Scientific journal
- 2015, J. Adhesion Soc. Jpn, 51, 233 - 234, EnglishControl of Morphology of ‘Rattle’-like Particles Prepared by One-step Suspension Polymerization[Refereed]Scientific journal
- Janus particles with two hemispheres having different stabilizers, a polystyrene (PS) phase stabilized by poly(acrylic acid) (PAA) (PSPAA) and a poly(methyl methacrylate) (PMMA) phase stabilized by poly(vinylpyrrolidone) (PVP) (PMMA(PVP)), were synthesized by the solvent-absorbing/releasing method of PSPAA/PMMA(PVP) composite particles with a core-shell structure. The PSPAA/PMMAPVP composite particles were prepared by seeded dispersion polymerization of MMA using PVP as stabilizer in the presence of PS seed particles stabilized by PAA. We also demonstrated the facile formation of the colloidal chains via hydrogen bonding interaction between different stabilizers.Corresponding, AMER CHEMICAL SOC, Jan. 2015, LANGMUIR, 31(2) (2), 674 - 678, English[Refereed]Scientific journal
- Interpenetrating polymer network (IPN) hydrogel microspheres composed of temperature-sensitive crosslinked poly(N-isopropylacrylamide) (PNIPAM) and pH-sensitive crosslinked poly(methacrylic acid) (PMAA) are prepared by sequential polymerization method. The IPN hydrogel microspheres are characterized for their temperature- and pH-responsive behaviors by measuring the variation of hydrodynamic diameters. The results showed that these hydrogel microspheres exhibited both temperature- and pH-sensitive volume phase transitions. The structure and properties are systematically characterized using FTIR, H-1-NMR, transmission electron microscope (TEM), scanning electron microscope (SEM), differential scanning calorimetry (DSC) and thermo-gravimetric analyses (TGA). IPN hydrogel microspheres are then magnetically doped by in-situ formation of Fe3O4 nanoparticles. The adsorption/desorption of various dyes and subsequent separation of dye loaded magnetic hydrogel microspheres from the aqueous medium are studied under the influence of magnetic field. (C) 2014 Elsevier B.V. All rights reserved.ELSEVIER SCIENCE BV, Oct. 2014, COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 459, 39 - 47, English[Refereed]Scientific journal
- Multiple polymer particles encapsulated in a polymer shell are applied in electrophoretic ink. We demonstrate a simple one-step polymerization of polymer capsules containing small particles (rattle-like particles). In the obtained capsules, encapsulated particles independently dispersed and moved in response to the electric field.ROYAL SOC CHEMISTRY, Sep. 2014, CHEMICAL COMMUNICATIONS, 50(69) (69), 9921 - 9924, English[Refereed]Scientific journal
- Emulsion polymerization of ionic liquid monomer [2-(methacryloyloxy)ethyl]trimethylammonium bis(trifluoromethanesulfonyl)amide ([MTMA][TFSA]) was performed. In the presence of potassium persulfate and sodium dodecyl sulfate as the ionic initiator and emulsifier, respectively, the system was colloidally unstable and coagulated, owing to anion exchange between the ionic liquid monomer and ionic emulsifier. When a nonionic initiator and emulsifier were used (2,2'-azobis 2-methyl-[1,1-bis(hydroxymethyl)-2-hydroxyethylpropionamide]; VA-080, polyoxyethylenesorbitan monooleate; Tween 80, respectively), a stable emulsion was obtained without coagulation, and the zeta potential of the prepared particles exhibited a high positive charge. Utilizing this surface charge, poly([MTMA][TFSA]) (PIL) particles were then successfully prepared via emulsifier-free emulsion polymerization without an ionic initiator. Moreover, the contact angle of water on the PIL emulsion film (emulsifier-free emulsion polymerization) was found to be similar to 70 degrees (static measurement), indicating that the surface of the PIL film was relatively hydrophobic. The retreating contact angle (similar to 28 degrees) also indicated water wettability. However, when water was dropped on the PIL film just after the water already on the surface had completely retreated, the PIL film was instantaneously hydrophobic again. This result suggests that responsiveness of the PIL emulsion film was switchable between hydrophobic (in air) and hydrophilic (in water).Corresponding, AMER CHEMICAL SOC, Apr. 2014, LANGMUIR, 30(12) (12), 3406 - 3412, English[Refereed]Scientific journal
- Cellulose is a ubiquitous natural fiber used in various industrial materials and applications. We prepared micron-sized cellulose particles by the solvent releasing method (SRM) in which cellulose-[Bmim]Cl-N,N-dimethylformamide (DMF) droplets are dispersed in hexadecane (HD) containing dissolved surfactant. The dispersion is then poured into a large amount of 1-butanol. Since 1-butanol is miscible with HD, [Bmim]Cl, and DMF but not with cellulose, the cellulose particles precipitate out. FOR and H-1 NMR analyses confirmed that this technique precipitated cellulose and completely removed [Bmim]Cl and DMF from the cellulose-[Bmim]Cl-DMF droplets. Interestingly, the obtained cellulose particles were almost the same size as the original droplets (cellulose, 7 wt%), indicating a microporous structure of the cellulose particles with a large medium content. Although the microporous structure collapsed as the medium evaporated, it was maintained by a freeze-drying technique. (C) 2013 Elsevier Inc. All rights reserved.Corresponding, ACADEMIC PRESS INC ELSEVIER SCIENCE, Mar. 2014, JOURNAL OF COLLOID AND INTERFACE SCIENCE, 418, 126 - 131, English[Refereed]Scientific journal
- Large polystyrene particles stabilized by polyvinylpyrrolidone (PVP) (PSPVP)-core/small silica particles (SiO2)-corona raspberry-like composite particles were successfully prepared by heterocoagulation technique utilizing hydrogen bonding interaction between the pyrrolidone group of PVP and the silanol group of SiO2. The coverage of the SiO2 corona particles on the PSPVP core particle could be controlled by changing the pH of dispersions and the molecular weight of PVP. Moreover, heterocoagulation of large poly(methyl methacrylate) particles stabilized by PVP and small SiO2 particles was also carried out, resulting in formation of raspberry-like composite particles. These results suggested that raspberry-like particles composed of various polymer particles and inorganic particles could be prepared by heterocoagulation technique utilizing hydrogen bonding interaction.Japan Society of Colour Material, 2014, 色材協会誌, 87(10) (10), 356 - 360, Japanese[Refereed][Invited]Scientific journal
- In this study, reversible addition fragmentation chain transfer (RAFT) miniemulsion polymerization using a novel type of amphiphilic RAFT agent was investigated. The novel amphiphilic RAFT agent has a specific chemical structure in which a hydrophilic poly(ethylene glycol) chain is directly bonded to the "Z-group" position, and not the leaving group (R group), of the thiocarbonylthio group (RAFT group). As a result, the RAFT groups are localized at the interface of the water/monomer droplets (polymer particles) throughout the polymerization, unlike with a conventional amphiphilic RAFT agent. Polystyrene (PS) particles with a broad molecular weight distribution and 69% degree of livingness were successfully prepared using the novel RAFT agent in a manner similar to that for a conventional RAFT system. Notably, after the completion of polymerization, the RAFT groups could be easily removed from the dispersed PS particles via treatment with an excess of potassium persulfate, because the RAFT groups only exist near the particle surfaces.AMER CHEMICAL SOC, Jan. 2014, MACROMOLECULES, 47(1) (1), 130 - 136, English[Refereed]Scientific journal
- Boron nitride (BN) was prepared by the dehydrogenation of ammonia borane (AB) in an ionic liquid (1-butyl-3-methylimidazolium tetrafluoroborate, [Bmim][BF4]) at 300 C-degrees, which is lower than the temperature of the general preparation method of BN and below the decomposition temperature of polystyrene (PS). The reaction was performed at 120 degrees C for 10 h under atmospheric pressure, and the product material was subsequently heated at 300 degrees C for 24 h under reduced pressure in [Bmim][BF4]. The reaction rate and final conversion increased when [Bmim][BF4] was used as the medium as compared to those observed in the bulk system (in the absence of the solvent system). Moreover, PS/BN composite particles were successfully prepared by dehydrogenation in [Bmim][BF4] in the presence of cross-linked PS seed particles. Transmission electron microscopy images of ultrathin cross-sections of the composite particles confirmed the core-shell morphology of the particles with a PS core and a BN shell.Corresponding, ROYAL SOC CHEMISTRY, 2014, RSC ADVANCES, 4(17) (17), 8605 - 8611, English[Refereed]Scientific journal
- Microencapsulated ionic liquids represent a novel type of material with high potential for various applications in chemical synthesis, catalysis or separation processes. We present a detailed morphological analysis of this material by means of two imaging techniques, i.e., scanning transmission X-ray microspectroscopy (STXM) and transmission electron microscopy (TEM). While TEM can be utilized only in the dry state, STXM offers access to high-resolution imaging in liquid surroundings. In either case prolonged illumination leads to degradation of the stabilizing polymer. We discuss potential scenarios, e.g., formation of perforations within the polymer shell, to explain the experimental findings.ROYAL SOC CHEMISTRY, 2014, RSC ADVANCES, 4(7) (7), 3272 - 3277, English[Refereed]Scientific journal
- Seeded dispersion polymerization of the ionic-liquid monomer ([2-(methacryloyloxy)ethyl]trimethylammonium bis(trifluoromethanesulfonyl)amide) ([MTMA][TFSA]) was performed in ethanol by using either polystyrene (PS) or poly(methyl methacrylate) (PMMA) particles as seeds. In the presence of PS seed particles, secondary nucleated poly(ionic liquid) (PIL) particles were formed, and no PS/PIL composite particles were observed. In the case of PMMA seeds particles, the diameters of the obtained particles increased compared to those of PMMA seed particles (without formation of particles that were formed as byproducts), which indicates that the PMMA/PIL composite particles were successfully prepared. Transmission electron microscopy studies of ultrathin cross sections of the PMMA/PIL particles revealed that the obtained particles had a sea-island structure consisting of PIL domains. These results are consistent with the theoretical considerations based on the spreading coefficients calculated from the interfacial tensions. © 2013 American Chemical Society.Corresponding, Sep. 2013, Langmuir, 29(36) (36), 11284 - 11289, English[Refereed]Scientific journal
- Considering the application potentials of organic materials possessing both conducting and ferromagnetic functions in various electronic devices, an attempt was made to prepare conducting polyaniline (PANI) layered magnetic nano composite polymer particles. Two routes were used to modify magnetic Fe3O4 core particles. In one route, seeded emulsion polymerization of methyl methacrylate (MMA) was carried out in presence of nano-sized Fe3O4 core particles. In another route, cross-linker ethyleneglycol dimethacrylate (EGDM) was used in addition to MMA. The modified composite particles were named as Fe3O4/PMMA and Fe3O4/P(MMA-EGDM), respectively. Finally, seeded chemical oxidative polymerization of aniline was carried out in the presence of Fe3O4/PMMA and Fe3O4/P(MMA-EGDM) composite seed particles to obtain Fe3O4/PMMA/PANI and Fe3O4/P(MMA-EGDM)/PANI composite polymer particles. The modification of Fe3O4 core particles was confirmed by electron micrographs, FTIR, UV-visible spectra, X-ray photoelectron spectra, X-ray diffraction pattern and thermogravimetric analyses. A comparative study showed that crosslinking of intermediate shell improved the magnetic susceptibility and electrical conductivity of PANI layered magnetic nano composite particles. © 2013 John Wiley & Sons, Ltd.Aug. 2013, Polymers for Advanced Technologies, 24(8) (8), 740 - 746, English[Refereed]Scientific journal
- The solubility behavior of poly(ionic liquid) (PIL) particles, which were prepared by dispersion polymerization of ([2-(methacryloyloxy)ethyl]trimethylammonium bis(trifluoromethanesulfonyl)amide), [MTMA][TFSA], was observed in detail. The solubility of PILs was varied by changing the counter anion. A PIL with [TFSA] anion does not dissolve in polar solvents such as ethanol however, a PIL with Br anions does dissolve in ethanol. Upon the addition of LiBr to ethanol solution at high concentrations (> 2.5. wt.%), the PIL particles dissolved from their outer surface and the counter anions [TFSA] were replaced with Br anions on the particle surfaces. On the other hand, in the case of the ethanol solutions at low LiBr concentrations (< 2.5. wt.%), a specific solubility behavior was observed: domains inside the PIL particles were generated before their dissolution, most likely due to osmotic pressure. Moreover, PIL particles having hollow structures were prepared using this specific solubility behavior. © 2013 Elsevier Inc.Corresponding, May 2013, Journal of Colloid and Interface Science, 398, 120 - 125, English[Refereed]Scientific journal
- Magnetically modified functional particles are emerging as one of the most promising candidate in numerous multidisciplinary applications. In this research, a simple process has been developed to prepare magnetically modified aminated silica (SiO2) particles. Herein, submicron-sized SiO2 particles were modified with poly(methylmethacrylate-methacrylic acid) by seeded polymerization without any stabilizer. The carboxyl groups localized near the particles surface were then covalently linked with ethylene diamine to prepare aminated composite particles. Iron ions were then precipitated on the surface of aminated composite particles to obtain magnetically doped functional SiO2 particles. The preparation of such particles was confirmed by scanning electron microscopy, Fourier transform infrared, 1H NMR, X-ray photoelectron spectroscopy and thermogravemetric analyses. Relative measurement of adsorption study of different biomolecules suggested that magnetically doped functional silica particles are comparatively hydrophobic. Copyright (c) 2012 John Wiley & Sons, Ltd.WILEY-BLACKWELL, Feb. 2013, POLYMERS FOR ADVANCED TECHNOLOGIES, 24(2) (2), 174 - 180, English[Refereed]Scientific journal
- Large polystyrene particles stabilized by poly(acrylic acid) (PAA) (L-PSPAA) (as the core) and small polystyrene particles stabilized by poly(vinyl pyrrolidone) (PVP) (S-PSPVP) (as the corona) were successfully used to prepare raspberry-like particles by a heterocoagulation technique utilizing the hydrogen bonding interaction between PAA and PVP. The coverage of L-PSPAA by S-PSPVP could be controlled by adding PVP homopolymer to the L-PSPAA dispersion and by changing the molecular weight of the stabilizers. Moreover, the heterocoagulation of large poly(methyl methacrylate) particles stabilized by PAA (L-PMMAPAA) and S-PSPVP particles was also accomplished, resulting in the formation of L-PMMAPAA-core/S-PSPVP-corona raspberry-like composite particles. These results suggested that the raspberry-like particles composed of various polymer particles could be formed by the heterocoagulation technique utilizing the hydrogen bonding interaction. © 2012 American Chemical Society.Jan. 2013, Langmuir, 29(2) (2), 554 - 560, English[Refereed]Scientific journal
- Encapsulation of ionic liquid, 1-hexyl-3-methylimidazolium bis(trifluoromethane sulfonyl)amide ([Hmim][TFSA]), was carried out by microsuspension polymerization of ethylene glycol dimethacrylate (EGDM) utilizing the self-assembling of phase-separated polymer method, which had been proposed by us for the preparation of hollow polymer particles. After the optimization of the polymerization conditions, ionic liquid-encapsulated polymer particles, which have smooth surface morphology and a single hollow structure, were successfully prepared. Encapsulation efficiency of [Hmim][TFSA] was significantly improved from about 20-70 % by changing the shell polymer from polyEGDM homopolymer to poly(EGDM-butyl methacrylate) (50/50, w/w) copolymer, which was likely to have relatively low affinity for [Hmim][TFSA]. Additionally, ionic liquid-encapsulated polymer particles displaying ionic conductivity were successfully prepared using triethylene glycol dimethacrylate as divinyl monomer instead of EGDM.SPRINGER, Jan. 2013, COLLOID AND POLYMER SCIENCE, 291(1) (1), 45 - 51, English[Refereed]Scientific journal
- Composite gel particles consisting of 2-phenylethyl methacrylate (PhEMA)-vinyl toluene (VT) copolymer (P(PhEMA-VT)) and poly(methyl methacrylate) (PMMA) were prepared by seeded polymerization of MMA in the presence of P(PhEMA-VT)/1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl) amide ([Bmim] [TFSA], IL) gel particles, in which P(PhEMA-VT) exhibited lower critical solution temperature (LCST)-type phase transition behavior in IL. The particles obtained at 70 degrees C (above the LCST) adopted a phase-separated snowman-like shape and clearly exhibited volume-phase transition behavior in which the P(PhEMA-VT) phase reduced in size and the PMMA phase increased in size above the LCST. The P(PhEMA-VT) phase exhibited LCST-type volume-phase transition behavior and separation of IL occurred. In contrast, the PMMA phase was swollen with IL separated from the P(PhEMA-VT) phase, in which the PMMA phase could act as a preserver of IL. Interestingly, the composite gel particles exhibited similar volume-phase transition behavior in both air and vacuum without leakage of IL from the gel particles, which should be free-standing thermosensitive gel particles.Corresponding, ROYAL SOC CHEMISTRY, 2013, SOFT MATTER, 9(6) (6), 1761 - 1765, English[Refereed]Scientific journal
- Various nonspherical polystyrene (PS) particles were prepared by slow evaporation of toluene (used common good solvent) from homogeneous PS/hexadecane (HD)/toluene droplets dispersed in surfactant aqueous solutions at room temperature, followed by the rapid removal of HD from PS/HD particles with various phase-separated morphologies. The morphology of PS/HD particles was controlled by tuning the interfacial tension with various types of surfactants. Hemispherical PS particles with flat surfaces were obtained from phase-separated PS/HD/toluene droplets having a Janus structure, when polyoxyethylene nonylphenyl ether with an average ethylene oxide chain length of 30.8 was used as the surfactant. Polymer Journal (2012) 44, 1112-1116; doi:10.1038/pj.2012.71; published online 23 May 2012NATURE PUBLISHING GROUP, Nov. 2012, POLYMER JOURNAL, 44(11) (11), 1112 - 1116, English[Refereed]Scientific journal
- Iodine transfer dispersion polymerization (dispersion ITP) with CHI3 and reversible chain transfer-catalyzed dispersion polymerization (dispersion RTCP) with N-iodosuccinimide of methyl methacrylate were performed successfully in supercritical carbon dioxide medium. Both polymerizations proceeded smoothly to similar to 80% conversion in 6 h and yielded the polymeric product as a powder after venting the reactor. In both syntheses, the number-average molecular weights (M-n) increased with greater conversion. The ratio (M-w/M-n) was maintained at comparatively low values throughout the polymerizations; the values of M-w/M-n were lower in the dispersion RTCP (1.3-1.4) than the dispersion ITP (1.5-1.7). A chain extension test using styrene indicated that the poly(methyl methacrylate) prepared by dispersion ITP and dispersion RTCP had high degrees of livingness (71 and 74%, respectively). Polymer Journal (2012) 44, 1082-1086; doi:10.1038/pj.2012.78; published online 23 May 2012NATURE PUBLISHING GROUP, Nov. 2012, POLYMER JOURNAL, 44(11) (11), 1082 - 1086, English[Refereed]Scientific journal
- It is known that it is difficult to polymerize carboxylic acid-based monomer by atom transfer radical polymerization (ATRP) in polar solvents due to the protonation of ligand caused by acidic dissociation of the monomer. In this study, precipitation reverse ATRP of acrylic acid (AA) was carried out in supercritical carbon dioxide (scCO(2)), which is a nonpolar solvent to dissolve transition metal complexes, at 30 MPa and 45 degrees C. The polymerization proceeded smoothly and the conversion reached 86% for 3 h. After vending of scCO(2), a dry poly(acrylic acid) (PAA) powder was obtained. Weight-average molecular weight and polydispersity of the methylated PAA, which were measured by gel-permeation chromatography after methyl esterification, were 3.5 x 10(4) and 2.07, respectively, indicating that the precipitation reverse ATRP proceeded with a bad control manner. However, chain extension of the methylated PAA with styrene was possible by ATRP in a bulk system. Moreover, PAA-b-polystyrene was successfully prepared in scCO(2) directly by two-step ATRP, although its molecular weight distribution was broad. (C) 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 50: 2578-2584, 2012Lead, WILEY-BLACKWELL, Jul. 2012, JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 50(13) (13), 2578 - 2584, English[Refereed]Scientific journal
- Micron-sized monodisperse poly(ionic liquid) (PIL) particles, poly([2-(methacryloyloxy)ethyl]trimethylammonium bis(trifluoromethanesulfonyl)amide), were prepared by dispersion polymerization at 70 degrees C in methanol with poly(vinylpyrrolidone) as a stabilizer. The obtained particle size could be controlled by addition of ethanol to the methanol medium while maintaining narrow monodispersity. The PIL particles exhibit unique properties; they can be observed by scanning electron microscopy without platinum coating, which is generally used to avoid an electron charge. Moreover, the solubility of the PIL particles can be easily changed by changing the counter anion, similar to the process for ionic liquids.WILEY-V C H VERLAG GMBH, Jul. 2012, MACROMOLECULAR RAPID COMMUNICATIONS, 33(13) (13), 1130 - 1134, English[Refereed]Scientific journal
- Highly crystalline magnesium hydroxide (Mg(OH)(2)) was obtained by sol-gel process using magnesium nitrate (Mg(NO3)(2)) with ammonium hydroxide (NH4OH) in a hydrophilic ionic liquid, 1-butyl-3-methylimidazolium chloride ([Bmim]Cl) as a medium. Crystallite size of Mg(OH)(2) obtained in [Bmim]Cl was larger than that obtained in 2-propanol (used as a medium for comparison), which indicates that [Bmim]Cl worked as a template. The obtained Mg(OH)(2) was transformed to magnesium oxide (MgO) by heat treatment under atmospheric pressure. After heat treatment, crystallite size of the MgO obtained in [Bmim]Cl was also larger than that obtained in 2-propanol, reflecting the crystallinity of Mg(OH)(2) before heat treatment. Polystyrene (PS)/Mg(OH)(2) composite particles were successfully prepared by seeded dispersion sol-gel process in [Bmim]Cl in the presence of PS seed particles. The composite particles had smooth surfaces and core shell morphology consisting of PS core and Mg(OH)(2) shell having high crystallinity. The Mg(OH)(2) content of the composite particles calculated from the weight loss measured by thermogravimetry (17 wt %) agreed well with the theoretical value (19 wt %). Using 2-propanol as a medium, secondary nucleation of Mg(OH)(2) was observed, and composite particles were not obtained. It was clarified that the core-shell structure was consistent with the predicted morphology from the viewpoint of the spreading coefficients calculated from the interfacial tensions.AMER CHEMICAL SOC, Jul. 2012, JOURNAL OF PHYSICAL CHEMISTRY C, 116(27) (27), 14568 - 14574, English[Refereed]Scientific journal
- We have successfully demonstrated the preparation of poly(n-butyl acrylate)-b-polystyrene particles without any coagulation by two-step emulsifier-free, organotellurium-mediated living radical emulsion polymerization (emulsion TERP) using poly(methacrylic acid) (PMAA)methyltellanyl (TeMe) (PMAA30-TeMe) (degree of polymerization of PMAA, 30) and 4,4'-azobis(4-cyanovaleric acid) (V-501). The final particle size was similar to 30 nm and second particle nucleation was not observed throughout the polymerization. Mn increased linearly in both steps with conversion and blocking efficiency was similar to 75%. PDI was improved by increasing radical entry frequency into each polymer particle due to an increase of the polymerization temperature. (c) 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012WILEY-BLACKWELL, May 2012, JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 50(10) (10), 1991 - 1996, English[Refereed]Scientific journal
- Submicrometer-sized, polystyrene (PS) particles with controlled molecular weight distribution (MWD), were successfully obtained directly as powder state by iodine transfer dispersion polymerization (dispersion ITP) and reversible chain transfer catalyzed dispersion polymerization (dispersion RTCP) in supercritical carbon dioxide (scCO(2)) for the first time. These dispersion polymerizations proceeded similarly reaching 80% conversion in 21 h. In the dispersion ITP, the number-average molecular weight (M-n) nonlinearly increased with the conversion, which were always higher than theoretical values, and the MWD at each conversion was comparatively narrow (M-w/M-n = 1.5-1.7) throughout polymerization. In the dispersion RTCP, M, also nonlinearly increased with increasing conversion and M-w/M-n values were in the range of 1.3-1.5, which were lower than those of the dispersion ITP. In chain extension tests in bulk systems, the degrees of livingness of PS prepared by the dispersion ITP and the dispersion RTCP in scCO(2) systems were, respectively, estimated to be 56% and 48%. From these results, while more investigation is necessary, it was concluded that both polymerizations with scCO(2) proceeded in a partly controlled manner. (C) 2012 Elsevier Ltd. All rights reserved.ELSEVIER SCI LTD, Mar. 2012, POLYMER, 53(6) (6), 1212 - 1218, English[Refereed]Scientific journal
- Iodine transfer polymerization (ITP) with CHI3 as transfer agent and reversible chain transfer catalyzed polymerization (RTCP) with N-iodosuccinimide (NIS) as catalyst of methyl methacrylate (MMA) were successfully applied to aqueous microsuspension systems (respectively, microsuspension ITP and microsuspension RTCP). Both microsuspension ITP and RTCP proceeded smoothly without induction period and with a controlled/living manner. Polydispersity index (PDI, M-w/M-n.) of the microsuspension RTCP was smaller than that of the microsuspension ITP, and it was larger than RTCP in a bulk system (bulk RTCP). The difference seems to be based on that NIS would partly react with water dissolved in the MMA phase, and formed succinimide, which is a low controllable catalyst in comparison with NIS. With decreasing particle (monomer droplet) size, the polymerization rate increased, and a reasonable control was maintained throughout the polymerization based on the segregation effect.AMER CHEMICAL SOC, Mar. 2012, MACROMOLECULES, 45(5) (5), 2286 - 2291, English[Refereed]Scientific journal
- The phase-transfer behavior of poly(acrylic acid) (PAA) particles from the hydrophobic ionic liquid N,N-diethyl-N-methyl-N-(2-methoxyethyl)ammonium bis(trifluoromethanesulfonyl)amide phase to the water phase in the particle state, which we reported previously, was examined in more detail. PAA particles were prepared in the ionic liquid 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide ([Bmim][TFSA]) and the organic solvent chloroform and were extracted. The transfer of PAA particles to water in the particle state was also observed in [Bmim][TFSA] systems. In contrast, the transfer phenomenon was not observed in the chloroform system. It was clarified that water/oil interfacial tension gamma(wo) is an important parameter in the extraction of PAA in the particle state from the viewpoint of free energy. When the cationic surfactant tetradecyltrimethylammonium bromide, aqueous solution was used as the extraction medium, the PAA particles were extracted in the particle state from chloroform to water, in which gamma(wo) became as low as that of the ionic liquid. This suggests that the phase-transfer phenomenon of PAA particles in the particle state was induced by the ionic liquid's unique property of low interfacial tension with water despite its high hydrophobic character.AMER CHEMICAL SOC, Feb. 2012, LANGMUIR, 28(5) (5), 2523 - 2528, English[Refereed]Scientific journal
- We demonstrated a successful preparation of poly(methyl methacrylate) (PMMA)-b-poly(benzyl methacrylate) (PBzMA) particles in aqueous media by two-step reversible chain transfer catalyzed polymerization (RTCP) with N-iodosuccinimide as a catalyst at 70 degrees C. The polymerization smoothly proceeded, and the number-average molecular weight (M-n) increased linearly with conversion, which agreed with the theoretical molecular weight (M-n,M-th). The molecular weight distribution at each conversion was narrow (polydispersity index approximate to 1.4). Approximately 88% PMMA chains became PMMA-b-PBzMA at 64% conversion, which was a relatively high value.ROYAL SOC CHEMISTRY, 2012, POLYMER CHEMISTRY, 3(6) (6), 1394 - 1398, English[Refereed]Scientific journal
- Aug. 2011, Polymer, Vol 52, No.13, pp. 2729-2734, EnglishEmulsifier-Free, Organotellurium-Mediated Living Radical Emulsion Polymerization of Styrene: Initial Stage of Polymerization[Refereed]Scientific journal
- Nitroxide-mediated radical polymerization (NMP) in microemulsion (microemulsion NMP) of n-butyl acrylate (BA) has been carried out at 100 degrees C using N-tert-butyl-N-(1-diethylphosphono-2,2-dimethylpropyl) nitroxide (SG1), 2,2'-azoisobutyronitrile (AIBN), and the cationic emulsifier tetradecyltrimethylammonium bromide (TTAB). At [SG1](0)/[AIBN](0) of 1.68 (molar ratio), the polymerization exhibited classical trend marks of a controlled/living system with the molecular weight distribution (MWD) shifting to higher molecular weights with increasing conversion and a linear increase in number-average molecular weight (M-n) vs conversion. Bulk NMP carried out under the same conditions (without water and TTAB) proceeded at an extremely high rate without control/livingness. From these results, it is concluded that the confined space effect (compartmentalization) operates in the microemulsion NMP; in other words, it is a useful tool to prepare nanosized monomer-solubilized micelles for regulation and improvement of NMP.AMER CHEMICAL SOC, Jul. 2011, MACROMOLECULES, 44(14) (14), 5599 - 5604, English[Refereed]Scientific journal
- Polystyrene (PS)/aluminum hydroxide (Al(OH)(3)) composite particles were successfully prepared by the sol-gel process of aluminum isopropoxide (Al(OPr')(3)) in a hydrophilic ionic liquid, 1-butyl-3-methylimidazolium tetrafluoroborate ([Bmim][BF4]) using ammonium hydroxide (NH4OH) as a catalyst in the presence of PS seed. Transmission electron microscopy observation of ultrathin cross sections of the composite particles revealed that the composite particles had a core-shell morphology consisting of a PS core and a Al(OH)(3) shell having high crystallinity. nucleated Al(OH)(3) could be reduced by dropwise addition of NH4OH. Moreover, PS/eta-Al2O3 successfully prepared by heat treatment of PS/Al(OH)(3) at 300 degrees C in N-2 atmosphere, which is temperature of PS.Corresponding, AMER CHEMICAL SOC, Apr. 2011, LANGMUIR, 27(8) (8), 4474 - 4480, English[Refereed]Scientific journal
- AMER CHEMICAL SOC, Nov. 2010, MACROMOLECULES, 43(21) (21), 8703 - 8705, English[Refereed]Scientific journal
- Sep. 2010, Macromolecules, Vol 43, ,No.18, pp. 7465-7471, EnglishEmulsifier-Free, Organotellurium-Mediated Living Radical Emulsion Polymerization: Particle Formation[Refereed]Scientific journal
- Highly crystalline Al(OH)(3) particles were successfully prepared by the sol gel process of aluminum isopropoxide (Al(OPri)(3)) in a hydrophilic ionic liquid (IL), 1-butyl-3-methylimidazolium tetrafluoroborate ([Bmim][BF4]) at 30 degrees C using NH4OH as catalyst. Moreover, crystalline alumina particles were prepared from the Al(OH)(3) particles by heat treatment at 300 degrees C. When 2-propanol was used as medium for comparison, obtained particles were low crystalline AlO(OH). This difference seemed to arise from the difference in the local structure of Al(OPri)(3) in IL.Corresponding, CHEMICAL SOC JAPAN, Jul. 2010, CHEMISTRY LETTERS, 39(7) (7), 741 - 743, English[Refereed]Scientific journal
- Mushroom-like Janus poly(methyl methacrylate) (PMMA)/poly(styrene-2-(2-bromoisobutyryloxy)ethyl methacrylate)-graft-poly(2-(dimethylamino)ethyl methacrylate) (PDM) particles synthesized in our previous report(27) were applied as particulate surfactants. The PDM moiety at the one side of the Janus particles reversibly exhibited the volume phase transition in response to pH and temperature in an aqueous medium; that is, the surface property of the Janus particles comprising both PDM and PMMA reversibly changed between amphiphilic and hydrophobic based on the nature of PDM. Consequently, 1-octanol-in-water emulsion droplets stabilized by the amphiphilic Janus particles coalesced in the alkaline region and at 60 degrees C around neutral pH because of desorption of the hydrophobized Janus particles from the interface to the oil phase.AMER CHEMICAL SOC, Jul. 2010, LANGMUIR, 26(14) (14), 11732 - 11736, English[Refereed]Scientific journal
- Micrometer-sized, monodisperse, "hamburger-like" polystyrene (PS)/poly(2-ethylhexyl methacrylate)/decane composite particles were obtained by seeded dispersion polymerization of 2-ethylhexyl methacrylate with PS seed particles in the presence of decane. The morphological stability of the hamburger-like particles was investigated based on thermodynamic and kinetic aspects. The hamburger-like morphology was maintained at 60 A degrees C (above glass transition temperature (T (g))) for at least 1 week in spite of less thermodynamic stability than hemispherical morphology. T (g) of the particles gradually increased throughout the polymerization due to monomer consumption. Geometric calculation result indicates that the degree of reduction of the interfacial free energy at the early stage of the morphological development is significantly low. From these results, it is concluded the morphological stability of the hamburger-like particles is considerably high because the development from hamburger-like to hemispherical morphologies is retarded by the gradual increase in viscosity inside the particles and the significantly lower interfacial free energy reduction.SPRINGER, Jun. 2010, COLLOID AND POLYMER SCIENCE, 288(8) (8), 879 - 886, English[Refereed]Scientific journal
- The polymerization rate, control/livingness, and particle morphology in seeded activators generated by electron transfer for the atom-transfer radical polymerization of styrene with PiBMA-Br macroinitiator particles were investigated at 70, 90, and 110 degrees C. At 110 degrees C, the polymerization proceeded quickly until 60% conversion was reached, but control/livingness was not observed. This seems to be the reason for the high activation rate and spontaneous initiation of styrene, which significantly increased the radical concentration, resulting in a number of radical terminations. As a result, the block copolymer was not sufficiently formed, leading to a sea-island structure. However, at 70 and 90 degrees C, the polymerizations were almost complete in 14 and 7 h, respectively. Control/livingness was maintained, resulting in PiBMA-b-PS. As a result, onionlike multilayered particles were successfully synthesized. These polymerization behaviors were discussed from the viewpoint of the radical concentration and propagation rate coefficient at various temperatures.AMER CHEMICAL SOC, May 2010, LANGMUIR, 26(10) (10), 7029 - 7034, English[Refereed]Scientific journal
- Apr. 2010, Langmuir, Vol 26. No. 9, pp. 6303-6307, EnglishPreparation of Poly(acrylic acid) Particles by Dispersion Polymerization In an Ionic Liquid[Refereed]Scientific journal
- Microilleter-sized, monodisperse dimple and hemispherical polystyrene (PS) particles were successfully prepared by heating (55-70 degrees C) of spherical PS particles dispersed in methanol/water media (40/60 to 80/20, w/w) in the presence of decane droplets, and subsequent cooling down to room temperature. Decane was absorbed by the PS particles during the heating process. Decane-absorbed PS particles phase-separated into PS and decane phases in the inside during the cooling process, and eventually dimple and/or hemispherical particles were formed by removal of the decane phase from phase-separated PS/decane particles by evaporation. The size of the dimple, which is determined by the volume of decane phase-separated from decane-absorbed PS particles during the cooling process, increased with increases in the heating temperature and the methanol content.AMER CHEMICAL SOC, Mar. 2010, LANGMUIR, 26(6) (6), 3848 - 3853, English[Refereed]Scientific journal
- Micrometer-sized, monodisperse polystyrene (PS)/poly(styrene-co-sodium styrene sulfonate) (P(S-NaSS))/poly(n-butyl methacrylate) (Pn-BMA) composite particles having a 'golf ball-like' shape were prepared by seeded dispersion polymerization of n-butyl methacrylate with PS-core/P(S-NaSS)-shell seed particles with various shell thicknesses in the presence of dodecane droplets in a methanol/water (80/20, w/w) medium, followed by evaporation of the dodecane. The effects of the hydrophilic P(S-NaSS)-shell properties of seed particles on the formation of golf ball-like particles were investigated on the basis of thermodynamic and kinetic considerations. The dimples at the surface formed by the volume reduction of Pn-BMA/dodecane domains were deep when PS/P(S-NaSS) seed particles, the hydrophilic shell of which was thick, were used, whereas PS/P(S-NaSS)/Pn-BMA composite particles, the P(S-NaSS) hydrophilic shell of which was thin, exhibited a polyhedral shape. This is attributed to the fact that the molecular weight of the shell moiety comprising P(S-NaSS) was reduced by lowering the monomer concentration to decrease shell thickness, which seems to result in an increase in the mobility of Pn-BMA/dodecane domains at the particle surface. On the basis of this finding, when the molecular weight of the shell moiety of the seed particle was increased, golf ball-like particles were formed, even if the shell thickness of seed particles was thin. Polymer Journal (2010) 42, 66-71; doi:10.1038/pj.2009.313SOC POLYMER SCIENCE JAPAN, Jan. 2010, POLYMER JOURNAL, 42(1) (1), 66 - 71, English[Refereed]Scientific journal
- Utilizing the thermal stability of ionic liquid, micrometer-sized Nylon-6 particles were successfully prepared by hydrolytic polymerization of epsilon-caprolactam at high temperature with polyvinyl pyrrolidone as stabilizer in ionic liquids, 1-butyl-3methyl imidazolium tetrafluoroborate, [Bmirn][BF(4)] and N,N-diethyl-N-methyl-N-(2-methoxyethyl)ammonium bis(trifluoro-methanesulfonyl)amide, [DEME][TFSA]. The obtained particles had a unique shape because Nylon-6 is a crystalline polymer. Viscosity-average molecular weights of Nylon-6 prepared in [Bmirn][BF(4)] and [DEME][TFSA] at 180 degrees C for 48 h were 4200 and 2200, respectively.WILEY-V C H VERLAG GMBH, 2010, MACROMOLECULAR SYMPOSIA, 288, 49 - 54, English[Refereed]International conference proceedings
- Synthesis of multilayered composite polymer particles comprising mainly poly(iso-butyl methacrylate)block-polystyrene (PiBMA-b-PS) has been carried out by the use of two-step activator generated by electron transfer for atom transfer radical polymerization (AGET ATRP) in aqueous microsuspension. PiBMA-Br macroinitiator seed particles were prepared in the first step, followed by swelling with styrene and second step (seeded) polymerization. The blocking efficiency in the second step was found to be crucial with regards to the resulting particle morphology. A disordered sea-island morphology was obtained when the blocking efficiency was 47% (73% conversion), whereas a blocking efficiency of 61% (71% conversion) resulted in the formation of multilayered particles. High blocking efficiency can be achieved by careful adjustment of the activation rate by proper choice of polymerization temperature and amount of reducing agent (ascorbic acid). (C) 2009 Published by Elsevier Ltd.ELSEVIER SCI LTD, Jul. 2009, POLYMER, 50(14) (14), 3182 - 3187, English[Refereed]Scientific journal
- The thermal properties of n-hexadecane (HD) encapsulated in crosslinked capsule particles containing a water and/or air domain were studied from the viewpoint of heat-storage applications. The capsule particles were prepared by the microsuspension polymerization of divinylbenzene at 70 degrees C with the self-assembling of phase-separated polymer method that we developed. In the differential scanning calorimetric thermograms, pure HD had a single solidification temperature (T(s)) peak at 15 degrees C, whereas the encapsulated HD containing a water domain had two peaks at 6 and 1 degrees C. That is, the encapsulated HD containing the water domain required a longer time and lower temperature to complete the solidification than pure HD, which was negative for heat-storage applications. However, once the particles were dried and the water domain was replaced with air, the problem with the partially lowered T, improved. The air domain was also found in the encapsulated HD core after solidification because of the shrinkage of HD. The presence of the air domain did not affect the thermal stability of the encapsulated HD. (C) 2009 Wiley Periodicals, Inc. J Appl Polym Sci 112: 3257-3266, 2009JOHN WILEY & SONS INC, Jun. 2009, JOURNAL OF APPLIED POLYMER SCIENCE, 112(6) (6), 3257 - 3266, English[Refereed]Scientific journal
- Preparation and Characterization of Stimuli-Responsive Composite Polymer Particles Bearing Fluorescein Sodium (FNa)A synthetic route for the preparation of dye labelled stimuli-responsive composite polymer particles is presented. Polystyrene (PS) particles were first prepared by dispersion polymerization in ethanol media in presence of fluorescein sodium dye. The incorporation of dye in PS particles was confirmed by UV-visible absorption spectra, fluorescence measurement and H-1 NMR spectra. Then PS/poly(2-dimethylaminoethyl methacrylate-N-isopropyl acrylamide-ethylene glycol dimethacrylate)[PS/P(DM-NIPAM-EGDM)] composite polymer particles were prepared by seeded copolymerization. Adsorption behavior of surfactants and macromolecules on composite polymer particles were investigated at different temperatures and pH values. Results indicated that PS/P(DM-NIPAM-EGDM) composite polymer particles bearing FNa has strong pH-dependent adsorption characteristics. The temperature-responsive property has however been reduced as compared to the previously reported bare PS/P(DM-NIPAM-EGDM) composite polymer particles.M D PUBLICATIONS, Apr. 2009, JOURNAL OF POLYMER MATERIALS, 26(2) (2), 215 - 225, English[Refereed]Scientific journal
- Organotellurium-mediated living radical polymerization (TERP) of n-butyl acrylate (BA) in emulsifier-free emulsion polymerization system was carried out for the first time, using the in situ nucleation technique via self-assembly of the propagating amphiphilic polymer chains derived from water-soluble TERP agent, poly(methacrylic acid)-methyltellanyl, with water-soluble thermal initiator, 4,4'-azobis(4-cyanovaleric acid), as a radical source at 60 degrees C. The polymerization proceeded with high control/livingness to high conversion without coagulation, resulting in nanosized poly(BA) particles. The difference in the stirring rates of the polymerization system, where the whole monomer dispersed as droplets at a high rate or it existed as an upper layer on the aqueous medium at a low rate, had a great influence both on the rate of polymerization and on the degree of the control/livingness. On both of them, the polymerization with the high stirring rate gave more desirable results than those with the low rate.AMER CHEMICAL SOC, Mar. 2009, MACROMOLECULES, 42(6) (6), 1979 - 1984, English[Refereed]Scientific journal
- Submicron-sized monodisperse PS particles were prepared by dispersion polymerization of styrene in ionic liquids with poly(vinylpyrrolidone) as stabilizer. Seeded dispersion polymerization of MMA was subsequently carried out with PS seeds in [Bmim][BF(4)] to prepare PS/PMMA composite particles. Observation of the obtained particles of ultrathin cross-sections with a scanning and transmission electron microscope revealed that no secondary nucleation occurred during the seeded dispersion polymerization and that the particles have a core-shell morphology consisting of a PS core and a PMMA shell. Successful preparation of PS/PMMA composite particles in an ionic liquid has thus been demonstrated. Moreover, PS/PAA (PS-core/PAA-shell) composite particles were prepared by seeded dispersion polymerization in [DEME][TFSI], illustrating that hydrophobic/hydrophilic composite particles can be readily prepared in the ionic liquid.WILEY-V C H VERLAG GMBH, 2009, MACROMOLECULAR SYMPOSIA, 281, 54 - 60, English[Refereed]International conference proceedings
- Hollow polymer particles with multiple holes in the shell were prepared by aqueous microsuspension polymerization of micrometer-sized, monodisperse divinyl-benzene/n-hexadecane droplets in the presence of sodium dodecyl sulfate (SDS) at concentrations above 4 mM utilizing the Self-assembling Phase-Separated Polymer (SaPSeP) method developed by the authors. The total surface area of the holes per particle increased with an increase in the SDS concentration. At [SDS] = 10 mM, "flower-like" non-spherical particles were formed.SPRINGER, Nov. 2008, COLLOID AND POLYMER SCIENCE, 286(13) (13), 1561 - 1567, English[Refereed]Scientific journal
- To prepare cured epoxy resin particles encapsulating a curing agent (diamine), the self-assembly of phase-separated polymer (SaPSeP) method was developed to be applicable to polyaddition reaction of a stoichiometrically imbalanced system. The SaPSeP method was developed by the authors for preparation of micrometer-sized, hollow cross-linked polymer particles by radical polymerization based on the self-assembly of phase-separated polymer at the inner interface of particles. Although a polyaddition reaction, in general, requires that the reactants are in stoichiometric balance for the cure reaction to proceed well, diamine was successfully encapsulated within a cured epoxy resin shell by utilizing the SaPSeP method regardless of stoichiometric imbalance. The results provide further Support of the previously proposed SaPSeP mechanism for the formation of hollow particles. Moreover. Such diamine Capsules can be employed in one-component epoxy adhesives.AMER CHEMICAL SOC, Sep. 2008, LANGMUIR, 24(17) (17), 9254 - 9259, English[Refereed]Scientific journal
- Micrometer-sized, monodisperse, hollow polystyrene (PS)/poly(ethylene glycol dimethacrylate) (PEGDM) composite particles with a single hole in the shell were prepared by seeded polymerization using (ethylene glycol dimethacrylate/xylene)-swollen PS particles in the presence of sodium dodecyl sulfate (SDS). Single holes were observed at SDS concentrations above 3 mM, much lower than in the PS/polydivinylbenzene (PDVB) system previously reported (above 45 mM). Phase separation inside droplets occurred at lower conversion in the PEGDM system than the PDVB system. Phase separation in the droplet at the early stage of the polymerization is an important factor for the formation of the single hole in the shell.SPRINGER, Sep. 2008, COLLOID AND POLYMER SCIENCE, 286(11) (11), 1335 - 1341, English[Refereed]Scientific journal
- Submicron-sized monodisperse polystyrene (PS) particles were successfully prepared by dispersion polymerization of styrene in an ionic liquid, N,N-diethyl-N-methyl-N-(2-methoxyethyl)ammonium bis(trifluoromethanesulfonyl)imide ([DEME][TFSI]) at 70 degrees C with poly(vinyl pyrrolidone) (PVP) as a stabilizer. At the optimum PVP and styrene concentrations with regard to preparation of stable polymer particles, the number-average diameter and coefficient of variation were 350 nm and 5.7%, respectively. The particle size increased with a decrease in the PVP concentration and an increase in the styrene concentration. Moreover, we succeeded in producing PS particles by thermal polymerization in the absence of a radical initiator at 130 degrees C in [DEME][TFSI] using a conventional reactor (not autoclave) utilizing the advantages of non-volatility and thermal stability of the ionic liquid.WILEY-BLACKWELL, Apr. 2008, MACROMOLECULAR RAPID COMMUNICATIONS, 29(7) (7), 567 - 572, English[Refereed]Scientific journal
- From the viewpoint of heat storage application, encapsulation of n-hexadecane (HD) was carried out by microsuspension copolymerizations of divinylbenzene (DVB) and acrylic monomers (butyl acrylate, BA; ethyl acrylate, EA) utilizing the self-assembling of phase-separated polymer (SaPSeP) method proposed by the authors. The heat of solidification (H-s) of encapsulated HD in the micron-sized, cross-linked particles was determined by the differential scanning calorimeter (DSC). H-s of the encapsulated HD in poly(DVB) particles was much lower than that of pure HD, but it was increased with BA or EA content copolymerized up to that of pure HD. Such an influence of encapsulation on the H-s was discussed.SPRINGER, Feb. 2008, COLLOID AND POLYMER SCIENCE, 286(2) (2), 217 - 223, English[Refereed]Scientific journal
- Direct atom transfer radical polymerization (ATRP) of iso-butyl methacrylate in microemulsion has been performed successfully for the first time. ATRP was performed at 40 degrees C with different emulsifier systems: i) the cationic emulsifier n-tetradecyltrimethylammonium bromide (TTAB); and ii) mixed emulsifier systems based on TTAB and the non-ionic emulsifiers Emulgen 911 or Emulgen 931. All polymerizations proceeded in a controlled/living fashion, and the microemulsions were transparent with particle diameters less than 15 nm. The emulsifier system TTAB/Emulgen 911 exhibited better control than TTAB only. This is proposed to be caused by complex formation between Emulgen 911 in the organic phase and CuBr(2) (the deactivator), thus reducing the extent of exit of CuBr2 to the aqueous phase.. The more hydrophilic Emulgen 931 did not lead to improved control.WILEY-BLACKWELL, Dec. 2007, MACROMOLECULAR RAPID COMMUNICATIONS, 28(24) (24), 2354 - 2360, English[Refereed]Scientific journal
- Micrometer-sized silica-stabilized polystyrene latex particles and submicrometer-sized polystyrene - silica nanocomposite particles have been prepared by dispersion polymerization of styrene in alcoholic media in the presence of a commercial 13 or 22 nm alcoholic silica sol as the sole stabilizing agent. Micrometer-sized near-monodisperse silica-stabilized polystyrene latexes are obtained when the polymerization is initiated with a nonionic AIBN initiator. These particles are stabilized by silica particles that are present on the latex surface at submonolayer concentration. The total silica content is no greater than 1.1 wt %, which corresponds to a silica sol incorporation efficiency of less than 1.3%. Reduction of the initial silica sol concentration led to a systematic increase in the mean latex diameter. In contrast, submicrometer-sized polystyrene-silica nanocomposite particles are obtained when the polymerization is initiated with a cationic azo initiator. The silica contents of these nanocomposite particles are significantly higher, ranging up to 29 wt %. Zeta potential measurements, XPS, and electron spectroscopy imaging by transmission electron microscopy (ESI/TEM) studies reveal a well-defined core - shell morphology for these particles, whereby the core is polystyrene and the shell comprises the silica sol. After calcination, these nanocomposite particles can form hollow silica capsules. Variation of the initial silica sol and initiator concentration has relatively little effect on the final particle size and silica content of these polystyrene - silica nanocomposite particles, but indicates silica sol incorporation efficiencies up to 72%.AMER CHEMICAL SOC, May 2007, CHEMISTRY OF MATERIALS, 19(10) (10), 2435 - 2445, English[Refereed]Scientific journal
- 2007, Macromolecules, 40, 3062-3069, EnglishAtom transfer radical polymerization in miniemulsion: partitioning effects of Copper(I) and Copper(II) on polymerization rate, livingness, and molecular weight distribution[Refereed]Scientific journal
- Nitroxide-mediated controlled/living dispersion polymerization of styrene in supercritical carbon dioxide (scCO(2)) has been performed successfully to high conversion using N-tert-N-butyl-N-[1-diethylphosphono-(2,2-dimethylpropyl)] nitroxide (SG1) and a poly(dimethylsiloxane-b-methyl methacrylate) stabilizer at 110 degrees C. The molecular weight distributions were narrow (M-w/M-n = 1.12-1.43), and the number-average molecular weight (M-n) values agreed well with theory. A large excess of free SG1 was required to obtain satisfactory control in the dispersion polymerization, possibly due to SG1 partitioning. The critical degree of polymerization at which the polymer precipitates (J(crit)) was determined as 28 by visual observation using a novel approach. Polymerizations conducted in solution ( toluene) proceeded at a similar rate (similar to 20% faster) to those in scCO(2). The number of chains increased with conversion in both dispersion and solution, with the greater increase being observed in the dispersion system.AMER CHEMICAL SOC, Oct. 2006, MACROMOLECULES, 39(20) (20), 6853 - 6860, English[Refereed]Scientific journal
- Morphology of composite particles prepared by two-step dispersion polymerization in supercritical carbondioxideRecently, in addition to water, there is increasing interest in carrying out chemical reactions and extractions in environmentally benign solvents such as supercritical carbon dioxide (scCO2. The use of scCO2 as a medium for polymerizations has several potential advantages: low cost, no toxicity, eases of medium removal and recycling and marked variations of solubility power, viscosity and polarity by relatively small changes in temperature and pressure without altering medium composition We have successfully produced PMMA particles by dispersion polymerizations in scCO 2 with PDMS-based azoinitiator as an inistab (an initiator + a colloidal stabilizer). Control of morphology is one of the functionalization of particles in their applications. To our knowledge, the first report on the preparation of composite particles by seeded dispersion polymerization in scCO2 was reported by DeSimone. However, several aspects remain to be clarified. In this study, micron-sized PMMA/PS composite particles having "a gradient sea-islands structure" were prepared by two-step dispersion polymerization in scCO2.2006, Polymer Preprints, Japan, 55(2) (2), 3746 - 3747, JapaneseInternational conference proceedings
- Preparation of polymer particles by dispersion polymerization in an ionic liquidIn the last decade, there has been increasing interest in the use of ionic liquids, which are salts that melt at ambient temperature, for electrochemical and separations processes and as media for chemical and biochemical synthesis. The unique properties exhibited by ionic liquids can lead to differing solvent behavior, and differing chemical reaction. Ionic liquids are considered as environmental friendly solvents due to their low vapor pressures, chemical and thermal stability, and non-flammability. In the field of polymer chemistry, application of ionic liquids as solvents for polymerization processes is gradually receiving increased attention. However, to our knowledge preparation of polymer particles in an ionic liquid has not been reported. In this presentation, preparation of polystyrene (PS) particles was demonstrated for the first time in dispersion polymerization of styrene in an ionic liquid, N,N-diethyl-N-methyl-N-(2-methoxyethyl) ammonium bis(trifluoromethanesulfonyl) imide (DEMMA][TFSI]). At the optimum PVP and styrene concentrations, submicron-sized, monodisperse PS particles were successfully prepared. Moreover, we succeeded in producing PS particles by thermal polymerization (i.e. in the absence of a radical initiator) at 130°C in [DEMMA][TESI] with conventional reactor (not autoclave) utilizing the advantages of non-volalitv and thermal stabilitv.2006, Polymer Preprints, Japan, 55(2) (2), 4156 - 4157, JapaneseInternational conference proceedings
- Nitroxide-mediated radical dispersion polymerization of styrene in supercritical carbon dioxideSupercritical carbon dioxide (scCO2) has attracted attention as a benign, inexpensive, non-flammable and widely available polymerization medium. Nitroxide-mediated controlled/living radical dispersion polymerizations of styrene have been successfully carried out in scCO2 at 110°C based on the N-tert-butyl-N-(1-diethylphosphono-2,2-dimethylpropyl) nitroxide (SG1). Colloidal stabilization was achieved by using either (i) a poly(dimethylsiloxane-b-methyl methacrylate) stabilizer, or (ii) a poly(dimethylsiloxane) based alkoxyamine inistab, which operates as initiator and stabilizer simultaneously. The polymerizations proceeded in a controlled/living fashion with low polydispersities and number-average molecular weights increasing with conversion close to the theoretical values. The polymeric products were recovered as powders at high conversion after venting of the CO2. The particle diameters were measured to be approximately 150 nm by dynamic light scattering after re-dispersal in n-hexane.2006, Polymer Preprints, Japan, 55(2) (2), 3748 - 3749, EnglishInternational conference proceedings
- Preparation and thermodynamic stability of disc-like polymer particlesPolymer particles produced by heterogeneous polymerization are normally spherical. However, in the course of investigations on the synthesis of composite particles, various nonspherical particles have been prepared with properties different from those of spherical particles. It is important to be able to control such nonspherical shapes from an applications point of view. In this study, micron-sized, monodisperse polymer particles having unique "disc-like" shapes were prepared by seeded dispersion polymerization of 2-ethylhexyl methacrylate (EHMA) with polystyrene seed particles in the presence of saturated hydrocarbon droplets in methanol/water. Particle shapes could be controlled by the polymerization conditions. Thermodynamic consideration of particle stabilities indicated that a "hamburger- like" morphology, which is a precursor of the disc like particles, was in fact less stable than a hemispherical morphology. The hamburger-like morphology changed to a hemispherical morphology by heating at 150°C.2006, Polymer Preprints, Japan, 55(1) (1), 1327, JapaneseInternational conference proceedings
- Dispersion polymerization of methyl methacrylate in scCO2 using PDMS-b-PMMA as stabilizerWe report the preparation of PMMA particles by dispersion polymerization of MMA in scCO2 with PDMS-b-PMMA as stabilizer, prepared by control/living radical polymerization. PDMS-b-PMMA was found to be an effective stabilizer in scCO2, leading to excellent PMMA yield and monodisperse PMMA particles. Futhermore, monodisperse PMMA/PS composite polymer particles were prepared by seeded dispersion polymerization of styrene in scCO2 with PDMS-b-PMMA as stabilizer. They had a sea-islands morphology with a high number of PS domains dispersed in a continuous PMMA phase.2006, Polymer Preprints, Japan, 55(1) (1), 145, JapaneseInternational conference proceedings
- Effect of temperature in seeded ATRP; experiment and simulationAtom transfer radical polymerization (ATRP) of styrene using a poly(iso-butyl methacrylate) macroinitiator and dNbpy ligand have been carried out in emulsion (seeded ATRP) and bulk at various temperatures. It was found that the rate of polymerization was higher in emulsion than in bulk, due to partitioning of CuIIBr2 (deactivator) between the particles and the aqueous phase, resulting in a lower CuIIBr 2 concentration at the locus of polymerization. The magnitude of the increase in the rate of polymerization was in quantitative agreement with simulations based on literature values of partition coefficients of Cu IIBr2.2006, Polymer Preprints, Japan, 55(1) (1), 144, JapaneseInternational conference proceedings
- Effect of emulsifier in microemulsion atom transfer radical polymerizationPoly(iso-butyl methacrylate) nanoparticles having narrow molecular weight distribution were successfully prepared by microemulsion ATRP of iso-butyl methacrylate with cationic and nonionic emulsifiers. In the case of the polymer particles prepared using Emulgen 911 (polyoxyethylene nonyl phenyl ether), which has a low HLB value, the molecular weight distribution was narrower than when using Emulgen 931, which has a high HLB value. This result seems to be related to the incorporation of nonionic emulsifier into the polymer particles.2006, Polymer Preprints, Japan, 55(1) (1), 485, JapaneseInternational conference proceedings
- 2006, Macromol. Theory and Simul, 15, 608-613, EnglishComartmentalization in Atom Transfer Radical Polymeriztion (ATRP) in Dispersed Systems[Refereed]Scientific journal
- Nov. 2005, Colloid and Polymer Science, 284,327-333, EnglishProduction of poly(methyl methacrylate) particles by dispersion polymerization with organic peroxide in the presence of trimethylsiloxy terminated poly(dimethylsiloxane) in supercritical carbon dioxide[Refereed]Scientific journal
- Oct. 2005, Langmuir, 21,5655-5658, 8703 - 8708, EnglishPreparation of hollow polymer particles with single hole in the shell by SaPSeP[Refereed]Scientific journal
- Aug. 2005, Colloid Polym. Sci., 283,1041-1045, 793 - 798, EnglishMicron-sized, Monodisperse, Snowman/Confetti-shaped Polymer Particles by Seeded Dispersion Polymerization[Refereed]Scientific journal
- Jun. 2005, Polymer, 46,1051-1056, EnglishProduction of cured epoxy resin particles having one hollow by polyaddition reaction[Refereed]Scientific journal
- Jun. 2005, Polymer, 46,1045-1049, 1045 - 1050, EnglishPreparation of block copolymer particles by two-step atom transfer radical polymerization in aqueous media and its unique morphology[Refereed]Scientific journal
- Jun. 2005, Macromolecular Rapid Communications, 26,955-960, 955 - 960, EnglishNitroxede-Mediated Controlled/Living Free Radical Copolymerization of Styrene and Divinylbenzene in Aqueous Miniemulsion[Refereed]Scientific journal
- Preparation of cross-linked polymer particles encapsulating n-hexadecane by SaPSeP methodRecently, we proposed the technique to prepare about micron-sized, monodisperse, cross-linked polymer particles having one hollow by suspension polymerization for DVB/toluene droplets dissolving polystyrene (PS) and benzoyl peroxide, and suggested the formation mechanism. When the droplets did not contain PS, no hollow particle was obtained. The polymer dissolved in the droplets was needed to promote phase separation of PDVB prepared during the polymerization. The method is named the "self assembling of phase separation polymer (SaPSeP)" method. Moreover, hollow particles were obtained with no PS using nonsolvent of PDVB, ex. n-hexadecane, in place of toluene. In a series of this study, the PDVB/HD particles having a water-domain were observed. In this research, in order to clarify the diffusion mechanism of water and formation mechanism more in detail, we will try to produce PDVB/HD particles having hollow structure by SaPSeP method.2005, Polymer Preprints, Japan, 54(1) (1), 1083, JapaneseInternational conference proceedings
- The synthesis of high light scattering polymer particles by suspension polymerizationPolymer particles with internal hollow(s) are used as hinding or opacifying agents in coating and molding compositions. Recently, monodisperse, cross-linking polymer particles about 5 μ m in sized with one hollow at the center were produced by seeded polymerization of highly [divinylbenzene (DVB)/toluene]-swollen polystyrene (PS) particles prepared by the dynamic swelling method (DSM). On the basis of the same formation mechanism, hollow polymer particles were also produced earlier by suspension polymerization of divinylbenzene (DVB)/toluene droplets dissolving polystyrene (PS) and benzoyl peroxide (BPO), though they were polydisperse. In this presentation, in order to enhance the light scattering ability of the polymer particles having one hollow structure, we try to prepare hollow PS/polydivinylbenzene (PDVB) composite particles containing titanium oxide (TiO2) by the suspension polymerization.2005, Polymer Preprints, Japan, 54(1) (1), 1082, JapaneseInternational conference proceedings
- Preparation of hollow polymer particles with single hole in the shellThe influence of emulsifier on the shell formation of the hollow polymer particles prepared by the SaPSeP method, which was proposed by the authors for the preparation of micron-sized hollow polymer particles, was investigated. A single hole was observed in the shell of the hollow particles prepared by seeded polymerization of micron-sized, monodisperse divinylbenzene/p-xylene droplets in the presence of dodecylbenzenesulfonic acid sodium salt (SDBS), which were prepared by the dynamic swelling method. The fraction of the hollow particles having the single hole and the area of the hole increased with the SDBS concentration. In the cases of SDBS, n-tetradecyltrimethylammonium bromide and Emulgen 911 (polyoxyethylene lauryl ether), the similar phenomena to SDS were observed.2005, Polymer Preprints, Japan, 54(1) (1), 1081, JapaneseInternational conference proceedings
- Preparation of epoxy resin microcapsules by SaPSeP method wfth polyaddition reaction and its applicationPolymer particles are used as films in many industrial fields, in painting, printing etc. Moreover, in recent years significant attention has turned to direct application of particles, as exemplified in the biomedical field and in microelectronics. We had suggested a novel swelling method of seed polymer particles with a large amount of monomer which was named the "dynamic swelling method" in order to prepare polymer particles having more than 5 um-size. Moreover, the technique was developed to prepare about 5-um-sized, monodisperse, cross-linked polymer particles having one hollow by seeded polymerization and the formation mechanism was suggested. The method is named the "Self-assembling of Phase Separated Polymer (SaPSeP)" method The SaPSeP method was developed to be applicable to polyaddition reaction system of epoxy resin with diamine. Cured epoxy resin particles having one hollow were successfully prepared by the polyaddition reaction in the dispersed system In this presentation, we try to preparing cued epoxy resin particles encapsulating curing agent (diamin) by polyaddition reaction in suspension system and the mechanism of the SaPSeP method more in detail is discussed.2005, Polymer Preprints, Japan, 54(2) (2), 2997 - 2998, JapaneseInternational conference proceedings
- Poly(i-butyl methacrylate)-polystyrene block copolymer was successfully prepared in an aqueous medium by two-step atom transfer radical polymerization (ATRP), mini-emulsion- and seeded-ATRP, in which ethyl 2-bromoisobutyrate/CuBr/4,4'-dinonyl-2,2'-dipyridyl initiator system was used. The block copolymer had narrow molecular weight distribution (Mw/Mn=1.1) and the number-average molecular weight measured by gel permeation chromatography agreed with the calculated value.SPRINGER, May 2004, COLLOID AND POLYMER SCIENCE, 282(7) (7), 747 - 752, English[Refereed]Scientific journal
- Poly(methyl methacrylate) (PMMA) particles were produced by dispersion polymerization of methyl methacrylate in the presence of mercaptopropyl terminated poly(dimethylsiloxane) (MP-PDMS) in supercritical carbon dioxide at about 30 MPa for 24 h at 65 degreesC. The particle diameter could be controlled in a size range of submicron to micron by varying MP-PDMS concentration. The MP-PDMS worked as not only a chain transfer agent but also a colloidal stabilizer, which was named "transtab."SPRINGER-VERLAG, Apr. 2004, COLLOID AND POLYMER SCIENCE, 282(6) (6), 569 - 574, English[Refereed]Scientific journal
- Production of poly(methyl methacrylate) particles by dispersion polymerization with aminopropyl-terminated poly (dimethylsiloxane) stabilizer in supercritical carbon dioxideMicron-sized poly(methyl methacrylate) particles were produced by dispersion polymerization of methyl methacrylate with aminopropyl-terminated poly(dimethylsiloxane) as a colloidal stabilizer in supercritical carbon dioxide at about 30 MPa for 24 h at 65 degreesC.SPRINGER-VERLAG BERLIN, 2004, AQUEOUS POLYMER DISPERSIONS, 124, 121 - 125, English[Refereed]International conference proceedings
- Production of hallow particles by suspension polymerization of divinylbenzene with nonsolventSuspension polymerization for divinylbenzene droplets including n-hexadecane as a non-solvent for polydivinylbenzene (PDVB) was carried out. The hollow particles were produced under conditions where phase separation in the droplet occurred at an early stage of polymerization. The time when phase separation begins, depends on both the content of n-hexadecane and the crosslinking reaction of PDVB. Phase separation behavior during polymerization is discussed by means of phase diagrams.SPRINGER-VERLAG BERLIN, 2004, AQUEOUS POLYMER DISPERSIONS, 124, 54 - 59, English[Refereed]International conference proceedings
- Micron-sized, monodisperse polymer particles having reversibly transformable shapesMicron-sized, monodisperse, cross-linked, hollow polymer particles having transformable shapes were produced by seeded polymerization of (divinylbenzene/vinylbiphenyl/xylene)-swollen polystyrene particles prepared utilizing the dynamic swelling method. The influence of the shell strength, which was controlled by shell thickness, cross-linking density and solvent-release temperature, on shape transformation of the hollow particles between sphere and non-sphere, respectively, based on the absorbed and release of solvent was discussed in comparison with a theoretical pressure-buckling relationship.SPRINGER-VERLAG BERLIN, 2004, AQUEOUS POLYMER DISPERSIONS, 124, 42 - 46, English[Refereed]International conference proceedings
- Dispersion atom transfer radical polymerization of methyl methacrylate with bromo-terminated poly(dimethylsiloxane) in supercritical carbon dioxidePoly(dimethylsiloxane)-block-poly(methyl methacrylate) particles were successfully prepared by dispersion atom transfer radical polymerization of methyl methacrylate with bromo-terminated poly(dimethylsiloxane) as inistab ((i) under bar(n) under bar(i) under bar tiator + (s) under bar(t) under bar(a) under bar(b) under bar ilizer) in supercritical carbon dioxide medium (scCo(2)). The block copolymers had narrow molecular weight distributions (M-w/M-n approx. 1.25), indicating that the polymerization in scCO(2) was conducted in a controlled manner.VSP BV, 2004, DESIGNED MONOMERS AND POLYMERS, 7(6) (6), 553 - 562, English[Refereed]Scientific journal
- Polyacrylonitrile particles were produced by precipitation polymerization of acrylonitrile (AN) without any colloidal stabilizer in supercritical carbon dioxide as a polymerization medium at about 30 MPa for 24 h at 65 degreesC at different initiator concentrations (0.8-45.2 mmol/l) and at different AN concentrations (10-40% w/v). An increase in the initiator concentration led to increases in the conversion and in the degree of coagulation and to a decrease in the molecular weight. At AN concentration of 20% w/v, micron-sized, relatively monodisperse polyacrylonitrile particles with clean and uneven surfaces were produced.SPRINGER-VERLAG, Oct. 2003, COLLOID AND POLYMER SCIENCE, 281(10) (10), 964 - 972, English[Refereed]Scientific journal
- The effects of viscosity within a droplet and its size on the production of hollow particles by suspension polymerization for divinylbenzene/toluene droplets dissolving polystyrene were studied. When the viscosity was low at the beginning of the phase separation during the polymerization, the poly(divinylbenzene) microgel could adsorb at the interface of the droplet and hollow particles were obtained. Even if the viscosity in the droplet was low, when the droplet size was large, hollow particles were not obtained because the microgel had to move a long distance to be adsorbed at the interface of the droplets.SPRINGER-VERLAG, Apr. 2003, COLLOID AND POLYMER SCIENCE, 281(4) (4), 302 - 307, English[Refereed]Scientific journal
- Thermodynamic simulation of the morphology of monomer-adsorbed, cross-linked polymer particles prepared by the dynamic swelling method which the authors proposed was conducted to clarify its thermodynamic stability from the viewpoint of the total interfacial free energy. By comparing it with experimental results reported in previous articles, it was found that the morphology was controlled thermodynamically. Snowman-shaped composite polymer particles having different morphologies were prepared by seeded polymerization of the monomer-adsorbed, cross-linked polymer particles, in which the polymer particles had different cross-linking densities.SPRINGER-VERLAG, Mar. 2003, COLLOID AND POLYMER SCIENCE, 281(3) (3), 246 - 252, English[Refereed]Scientific journal
- Micron-sized, monodisperse, non-spherical polymer particles with "rugby ball" and "red blood corpuscle" -like shapes were produced by seeded polymerization of the dispersion of (divinylbenzene/ vinylbiphenyl/xylene)-swollen polystyrene particles prepared by utilizing the dynamic swelling method which the authors proposed in 1991. Their non-spherical shapes were based on buckling of the shell of the resultant hollow particles. In this article, the reversible shape transformation of the hollow composite polymer particle between spherical and such non-spherical shapes was studied in detail by controlling the shell strength. A part of the shell was buckled by external pressure which was caused by evaporation of xylene from the hollow when the shell had the tensile modulus below the critical value calculated from the pressure-buckling relationship of a spherical shell proposed by Uemura. The plasticization of the shell by a good solvent was one of key factors for the shape transformation.SPRINGER-VERLAG, Mar. 2003, COLLOID AND POLYMER SCIENCE, 281(3) (3), 214 - 219, English[Refereed]Scientific journal
- Phase-separation behavior within polymerizing divinylbenzene/ toluene droplet dissolving polystyrenes (PS) was investigated to clarify the formation mechanism of the hollow polymer particles by suspension polymerization. No hollow particles were obtained at a low content of low-molecular-weight PS where phase separation occurred at high conversion. On the other hand, hollow particles were obtained at a high content of high-molecular-weight PS where phase separation occurred at low conversion. The phase separation in an early stage of the polymerization, which was promoted by the presence of PS and cross-links of polydivinylbenzene, was a key factor for the formation of the hollow structure.SPRINGER-VERLAG, Feb. 2003, COLLOID AND POLYMER SCIENCE, 281(2) (2), 123 - 129, English[Refereed]Scientific journal
- 2003, Colloid Polym. Sci.,, 89(3), 706-710, EnglishProduction of polystyrene/poly(ethylene glycol dimethacrylate) composite particles encapsulating hinokitiol[Refereed]Scientific journal
- Kobe University, 2003, Mem.Grad.School Sci. & Technol., Kobe Univ., 21-A 1-13, 1 - 13, EnglishPreparation of polymer particles by dispersion and precipitation polymerizations in supercritical carbon dioxide using small-scale high-pressure reactors[Refereed]Scientific journal
- 2003, J. Appl. Polym. Sci.,, 88(2), 428-433, EnglishPreparation of micron-sized, monodisperse, magnetic polymer particles[Refereed]Scientific journal
- Suspension polymerizations for ethylene glycol dimethacrylate (EGDM)/toluene droplets dissolving styrene-methyl methacrylate copolymers with different compositions were carried out. Hollow particles were obtained independent of the copolymer composition. In suspension copolymerizations for EGDM/divinyl benzene/toluene droplets dissolving poly(methyl methacrylate), hollow particles were produced at high EGDM content, but not at low EGDM content. Preferential adsorption of the polymer formed by the suspension polymerizations at the interfaces of the droplets over the (co)polymers preliminarily dissolved therein was one of the key factors for the formation of the hollow structure. © 2002 Wiley Periodicals, Inc. J. Appl. Polym. Sci.Oct. 2002, Journal of Applied Polymer Science, 86(5) (5), 1087 - 1091, English[Refereed]Scientific journal
- Springer Science and Business Media LLC, Aug. 2002, Colloid & Polymer Science, 280(8) (8), 765 - 769, English[Refereed]Scientific journal
- Springer Science and Business Media LLC, Apr. 2002, Colloid & Polymer Science, 280(4) (4), 310 - 315, English[Refereed]Scientific journal
- Wiley, Feb. 2002, Journal of Applied Polymer Science, 83(9) (9), 2013 - 2021, English[Refereed]Scientific journal
- Springer Science and Business Media LLC, Feb. 2002, Colloid & Polymer Science, 280(2) (2), 183 - 187, English[Refereed]Scientific journal
- Polydivinylbiphenyl particles were produced by precipitation polymerization of divinylbiphenyl without any stabilizer in supercritical carbon dioxide as polymerization medium at ca. 30 MPa for 24 h at 65 °C at different initiator concentrations (0.5-58.1 mmol l-1). The conversions in all polymerization systems were relatively high. An increase in initiator concentration led to increases in the degree of coagulation and in the amount of low-molecular-weight byproducts and to a decrease in the amount of vinyl groups in the particle.2002, Colloid and Polymer Science, 280(12) (12), 1084 - 1090, English[Refereed]Scientific journal
- Springer Science and Business Media LLC, Oct. 2001, Colloid & Polymer Science, 279(10) (10), 976 - 982, English[Refereed]Scientific journal
- A series of monomer-adsorbed, crosslinked polystyrene/polydivinylbenzene composite particles having snowmanlike shapes were prepared by the dynamic swelling method that the authors had proposed in 1991. The morphology of the snowman-shaped particles was estimated with the contact angle of the monomer phase on the polymer particle. Influences of the kind of monomers and polyvinyl alcohol colloidal stabilizer on the morphology were obviously observed and discussed from the viewpoint of thermodynamic stability.Sep. 2001, Journal of Polymer Science, Part A: Polymer Chemistry, 39(18) (18), 3106 - 3111, English[Refereed]Scientific journal
- Springer Science and Business Media LLC, Jan. 2001, Colloid & Polymer Science, 279(1) (1), 77 - 81, English[Refereed]Scientific journal
- Suspension polymerizations for divinylbenzene/toluene droplets dissolving styrene (S)-methyl methacrylate copolymers having different compositions were carried out. Hollow particles were produced not with the copolymers having low S contents but with those having high S contents. © WILEY-VCH Verlag GmbH.2001, Macromolecular Symposia, 175, 321 - 328, English[Refereed]Scientific journal
- Micron-sized, monodispersed, electrically conductive polystyrene (PS)/polyaniline (PAn) composite particles were produced by chemical oxidative seeded dispersion polymerization of aniline at 0 °C with 1.37-μm-sized, monodispersed PS seed particles in HCl aqueous solution, where the pH value was kept at 2.5 with a pH stat. The composite particles consisted of a PS core and a PAn shell. A pellet of the composite particles had a conductivity of 3.4 × 10-3 S/cm.2001, Colloid and Polymer Science, 279(2) (2), 139 - 145, English[Refereed]Scientific journal
- Suspension polymerizations for divinylbenzene (DVB)/toluene droplets dissolving polystyrene (PS) having different end groups were carried out. Hollow polymer particles were not obtained with PS having polar sulfate end groups, which were prepared by emulsifier-free emulsion polymerization with potassium persulfate initiator. On the other hand, they were obtained with PS having low polarity isobutyronitrile end groups, which were prepared by solution polymerization with 2,2′-azo-bis (isobutyronitrile) initiator. The interfacial tensions between the water and xylene/toluene (1/1, w/w) mixture solution of PS having polar groups was smaller than that having low polarity groups. From these results, it is concluded that the preferential adsorption of PDVB molecules formed by the suspension polymerization at the interface of the droplets over PS molecules, which depended on the kind of the end groups, is one of the key factors for the formation of the hollow structure.2001, Colloid and Polymer Science, 279(5) (5), 519 - 523, English[Refereed]Scientific journal
- Micron-sized, monodisperse, "rugby-ball-like" polymer particles were produced by seeded polymerization for the dispersion of (divinylbenzene/vinylbiphenyl/xylene)-swollen polystyrene particles prepared by utilizing the dynamic swelling method which the authors proposed in 1991. The shape of the composite polymer particle was reversibly transformed between a rugby-ball-like shape and a spherical one by absorbing/releasing toluene.2001, Colloid and Polymer Science, 279(9) (9), 931 - 935, English[Refereed]Scientific journal
- Lead, Wiley, Dec. 2000, Journal of Polymer Science Part A: Polymer Chemistry, 38(23) (23), 4238 - 4246, English[Refereed]Scientific journal
- Springer Science and Business Media LLC, Oct. 2000, Colloid & Polymer Science, 278(10) (10), 919 - 926, English[Refereed]Scientific journal
- Springer Science and Business Media LLC, Mar. 2000, Colloid & Polymer Science, 278(3) (3), 275 - 279, English[Refereed]Scientific journal
- Suspension polymerizations for divinylbenzene/toluene droplets dissolving different kinds of methacrylate and acrylate homopolymers were carried out. Hollow polymer particles were produced not with high polarity polymers but with low polarity polymers. The results indicate that the preferential adsorption of the homopolymers having high polarity at the interface of the droplets depresses the formation of the hollow structure. A minimum polymer concentration was necessary to produce hollow particles.D. Steinkopff-Verlag, 2000, Colloid and Polymer Science, 278(7) (7), 659 - 664, English[Refereed]Scientific journal
- Micron-sized monodispersed polymer particles having a 'red blood corpuscle-shape' were produced effectively at the completion of the seeded polymerization for the dispersion of highly (divinylbenzene/toluene)-swollen polystyrene particles prepared in an ethanol/water medium by utilizing the dynamic swelling method under optimum ratios of xylene/divinylbenzene and vinyltoluene/divinylbenzene.John Wiley and Sons Ltd, 2000, Macromolecular Symposia, 150, 201 - 210, English[Refereed]International conference proceedings
- Springer Science and Business Media LLC, Sep. 1999, Colloid & Polymer Science, 277(9) (9), 895 - 899, English[Refereed]Scientific journal
- Elsevier BV, Aug. 1999, Colloids and Surfaces A: Physicochemical and Engineering Aspects, 153(1-3) (1-3), 405 - 411, English[Refereed]Scientific journal
- Micron-sized, monodispersed highly styrene-'adsorbed' particles having snow-man shape were prepared by the dynamic swelling method (DSM) with tightly cross-linked polymer seed particles as follows. First, 3.8 μm-sized monodispersed polystyrene (PS)/poly(divinylbenzene) (PDVB) (PS/PDVB = 1/10 wt. ratio) composite particles produced by seeded polymerization utilizing DSM were dispersed in an ethanol/water (6/4, w/w) solution dissolving styrene monomer, and poly(vinyl alcohol) as a stabilizer. Second, water was subsequently added to the dispersion with a micro-feeder at a rate of 2.88 ml/h at room temperature. The cross-linked seed particles adsorbed a large amount of styrene onto the surfaces and resulted in monodispersed highly styrene-'adsorbed' snow-man shape particles having about 10 μm in diameter.Oct. 1998, Colloid and Polymer Science, 276(10) (10), 887 - 892, English[Refereed]Scientific journal
- Polymer particles having single hollow in the inside were successfully prepared by suspension polymerization for divinylbenzene/toluene droplets dissolving polystyrene (PS) in an aqueous solution of poly(vinyl alcohol). Such a hollow polymer particle was not obtained without PS. The hollow structure was affected by the molecular weight and the concentration of PS.Jul. 1998, Colloid and Polymer Science, 276(7) (7), 638 - 642, English[Refereed]Scientific journal
- Recently, the authors reported that micron-sized mono-dispersed cross-linked polymer particles having a single hollow in the inside were produced by seeded polymerization for the dispersion of (toluene/divinylbenzene)-swollen polystyrene (PS) particles prepared utilizing the dynamic swelling method which the authors had proposed. In this article, the particles at various conversions of the seeded polymerization were observed with an optical microscope in detail. From the obtained results, the formation mechanism of the hollow structure is suggested as follows. As seeded polymerization proceeds, polydivinylbenzene (PDVB) molecules precipitated in the swollen particle are trapped near the interface and gradually pile at the inner surface, which results in a cross-linked PDVB shell. PS which dissolves in the swollen particles is repelled gradually to the inside. After the completion of the polymerization, toluene in the hollow evaporates by drying, and PS clings to the inner wall of the shell uniformly.Springer Verlag, 1997, Colloid and Polymer Science, 275(10) (10), 992 - 997, English[Refereed]Scientific journal
- Springer Science and Business Media LLC, May 1996, Colloid & Polymer Science, 274(5) (5), 433 - 438, English[Refereed]Scientific journal
- 4 μm-sized monodispersed cross-linked polymer particles having hollow structure were produced as follows. First, 1.7 μm-sized monodispersed polystyrene (PS) seed particles produced by dispersion polymerization were dispersed in ethanol/water (7/3, w/w) solution in which divinylbenzene (DVB), benzoyl peroxide (BPO), poly(vinyl alcohol), and toluene was dissolved. The PS seed particles were swollen with DVB, toluene and BPO maintaining high monodispersity throughout the dynamic swelling process where water was slowly added continuously. And then, the seeded polymerization of the (toluene/DVB)-swollen PS particles was carried out.John Wiley and Sons Ltd, 1996, Macromolecular Symposia, 101, 509 - 516, English[Refereed]Scientific journal
- Sep. 2020, PHAM TECH JAPAN, 36(9) (9), 177 - 181, JapanesePreparation of Free-standing Composite Gel Particles Incorporating Ionic Liquids Having Thermosensitivity[Invited]Introduction scientific journal
- Japan Society of Colour Material, Oct. 2019, Journal of the Japan Society of Colour Material, 92(10) (10), 299 - 303, Japanese
A facile and novel approach of preparing monodisperse polystyrene (PS) particles having a "cylindrical" shape was discovered. The proposed synthetic method involved dispersion polymerization of the spherical PS particles stirred in a polyvinylpyrrolidone (PVP) aqueous solution for several hours using a magnetic stirrer. In the presence of PVP, the spherical PS particles deformed into cylindrical shapes following stirring; however, the particles did not deform in the absence of PVP. The deformation rate of the particles was affected by the molecular weight of dissolved PVP. This stirring method is not only highly efficient and provides high yield, but is also applicable to other materials such as polymethyl methacrylate (PMMA). Moreover, cylindrical polystyrene particles were applied as a particulate stabilizer to prepare a Pickering emulsion of decane (oil)/water. Unlike the spherical particles that are typically used in Pickering emulsions, the cylindrical particles enhanced the emulsion's stability (up to 1 year). Furthermore, the cylindrical particulate stabilizer enabled a stable emulsion across a wide range of pH. Notably, unique adsorption behavior of the cylindrical particles on an oil droplet was observed, in which the cylindrical particles connected head to head to form a network that acted as a cage around the oil droplet.
[Invited]Introduction scientific journal - Aug. 2019, HIGH POLYMERS, JAPAN, 68(8) (8), 422 - 426, JapaneseRecent Trends on Synthesis of Functional Polymer Particles[Invited]Introduction scientific journal
- Japan Society of Colour Material, 2016, 色材協会誌, 89(7) (7), 219 - 224, Japanese
Ionic liquids that are mostly composed of organic ions are found as molten salts at room temperature and have been the subject of research in various fields due to their low vapor pressures, high thermal stability, and non-flammability. Ionic liquids also exhibit characteristics, such as ionic conductivity and CO2 solubility, which are expected to be useful for the development of functional materials. Poly(ionic liquid)s (PILs) are polymer materials that combine the mechanical stability and processability of polymeric materials with the unique properties of ionic liquids. PILs are prepared by the polymerization of ionic liquid containing vinyl and (meth)acrylate groups on the cationic or anionic components of the liquid. They can have various applications such as sorbents of CO2, polymer electrolytes, and microwave absorbing materials. In this review, we introduce mainly our work on the preparation of PILs as particle state.
[Invited]Introduction scientific journal - シーエムシー出版, Nov. 2015, ファインケミカル : 調査・資料・報道・抄録, 44(11) (11), 47 - 54, JapanesePreparation of Functional Polymer Particles by Controlled Living Radical Polymerizations
- 2015, 高分子学会予稿集(CD-ROM), 64(2) (2)低分子ゲル・高分子ゲル複合型新規ヘテロダブルネットワークイオン液体ゲルの開発
- 2015, 化学工学会秋季大会研究発表講演要旨集(CD-ROM), 47th高導電性を有するダブルネットワークイオン液体ゲルの開発
- 2014, 化学工学会秋季大会研究発表講演要旨集(CD-ROM), 46th低分子ゲル・高分子ゲル共存型新規ヘテロダブルネットワークイオン液体ゲルの開発
- 2014, 高分子学会予稿集(CD-ROM), 63(2) (2)低分子ゲル・高分子ゲル混在型新規ヘテロダブルネットワークイオノゲルの調製
- 2014, C&I Commun, 39(4) (4), Japanese分散安定剤の水素結合を利用した高分子粒子の高次構造化[Invited]Introduction scientific journal
- 日本塗装技術協会, 2014, 塗装工学, 49(6) (6), 207 - 215, Japanese機能性微粒子材料の創成[Invited]Introduction scientific journal
- 2014, PHARM TECH JAPAN, 30(14) (14), 133 - 138, Japanese階層構造制御による高分子微粒子の機能化[Invited]Introduction scientific journal
- The Adhesion Society of Japan, May 2013, Journal of The Adhesion Society of Japan, 49(5) (5), 148 - 156, Japanese[Invited]Introduction scientific journal
- 日本接着学会, Jul. 2010, 日本接着学会誌, Vol 46, ,No.8, pp. 276-281(7) (7), 276 - 281, Japanese超臨界二酸化炭素流体中での高分子(微粒子)の合成Report scientific journal
- Feb. 2010, HIGH POLYMERS, JAPAN, 58(2) (2), 78 - 81, JapaneseControlled / Living Radical Polymerization in Aqueous Dispersed Systems[Invited]
- 電気化学会溶融塩委員会, 2009, Molten Salts, 52(1) (1), 22 - 28, JapanesePreparation of polymer particles in ionic liquid[Invited]
- WILEY-V C H VERLAG GMBH, Feb. 2008, MACROMOLECULAR RAPID COMMUNICATIONS, 29(3) (3), 264 - 264, EnglishOthers
- 色材協会, May 2005, 色材協會誌, 78(5) (5), 240 - 242, Japanese神戸大学 : 大学院自然科学研究科分子物質科学専攻・工学部応用化学科Others
- 日本接着学会, Oct. 2004, 日本接着学会誌 = Journal of the Adhesion Society of Japan, 40(11) (11), 530 - 532, Japanese水媒体ナノリアクター中でのリビングラジカル重合による精密高分子合成Introduction scientific journal
- 26 Jun. 2003, 日本接着学会年次大会講演要旨集, 41, 55 - 56, JapaneseMorphology structure of polystyrene/poly(methyl methacrylate) composite particles having a dent
- Aug. 2002, 日本接着学会誌 = Journal of the Adhesion Society of Japan, 38(8) (8), 319 - 320, Japanese神戸大学大学院自然科学研究科分子集合科学専攻・工学部応用化学科高分子コロイド研究室(大久保正芳研究室)Others
- 05 Jul. 2001, 日本接着学会年次大会講演要旨集, 39, 41 - 42, JapaneseProduction of Poly(acrylonitrile) Particles by Precipitation Polymerization of Acrylonitrile in Supercritical Carbon Dioxide
- 22 Jun. 2000, 日本接着学会年次大会講演要旨集, 38, 101 - 102, JapanesePreparation of anomalous particles by post-treatment using various polymers
- Apr. 2000, 化学と工業 = Chemistry and chemical industry, 53(4) (4), 517 - 517, Japaneseモノマー滴からポリマー粒子へ-ミニエマルション重合系における粒径保持〜Introduction scientific journal
- 25 Jun. 1998, 日本接着学会年次大会講演要旨集, 36, 219 - 220, JapaneseMonomer Adsorption on the Surface of Micron-sized Monodispersed, Tightly Cross-linked Polymer Seed Particles Utilizing the Dynamic Swelling Method
- Joint work, 第2部第20章「コロイド粒子の1~2次元配列・凝集」, 近代科学社Digital, Apr. 2024, ISBN: 476496077X分散・凝集の応用 濃厚分散系の技術
- Joint work, 「不均一反応場におけるリビングラジカル重合」「総説」「不均一系の重合の制御―乳化・分散・懸濁重合」「微粒子の制御―均一微粒子の合成」「ポリマーコロイド」, エヌ・ティー・エス, Dec. 2023, Japanese, ISBN: 9784860438715ラジカル重合ハンドブック
- Contributor, 3章7節「微粒子」, 朝倉書店, Nov. 2022, Japanese, ISBN: 9784254252729高分子材料の事典
- Joint work, 「天然由来の界面活性剤サーファクチンの応用展望について」第3章 第4節, 技術情報協会, Jul. 2021, Japanese, ISBN: 9784861048531【水】と機能性ポリマーに関する材料設計,最新応用
- Single work, 株式会社エヌ・ティー・エス, Dec. 2018, Japanese, 概要, ISBN: 9784860435356「刺激応答性高分子ハンドブック」第3章第6節 不均一重合による刺激応答性高分子微粒子の設計Scholarly book
- Single work, 株式会社シーエムシー, Aug. 2018, Japanese, 概要, ISBN: 9784781313368「リビングラジカル重合―機能性高分子の合成と応用展開―」第II編第6章リビングラジカル重合を用いた機能性高分子微粒子の合成Scholarly book
- Single work, 丸善出版, Apr. 2018, Japanese, 概要, ISBN: 9784621302910「第4版現代界面コロイド化学の基礎」第4章高分子微粒子Scholarly book
- Single work, 株式会社シーエムシー, Nov. 2015, Japanese, 概要, ISBN: 9784861045462ファインケミカル特集:リビングラジカル重合の最新動向「リビングラジカル重合を用いた機能性高分子微粒子の合成」Scholarly book
- Joint work, 株式会社技術情報協会, Oct. 2014, Japanese, ISBN: 9784861045462エマルションの特性評価と新製品開発、品質管理への活用Scholarly book
- Joint work, Yonsei University Press, Oct. 2013, English, ISBN: 9788968500442Emulsion Polymerization and Functional Polymeric Microspheres –Science and Technology- Chapter 6“Syntheses of Poly(acrylic acid) and Poly(acrylic acid)/Polystyrene Composite Particles in an Ionic Liquid”Scholarly book
- Joint work, Yonsei University Press, Oct. 2013, English, ISBN: 9788968500442Emulsion Polymerization and Functional Polymeric Microspheres –Science and Technology- Chapter 4“Glass transition temperatures of polymer particles with incorporated nonionic emulsifier prepared by emulsion polymerizations in emulsion and dry states”Scholarly book
- Single work, 株式会社エヌ・ティー・エス, Dec. 2011, Japanese「イオン伝導体の材料技術と測定方法」第2章 第2節「イオン液体におけるカプセル化・高機能ポリマー微粒子化」Scholarly book
- Joint work, 株式会社エヌ・ティー・エス, Sep. 2010, Japanese「新訂版ラジカル重合ハンドブック」第2編 第1章 第7節「不均一系反応場におけるリビングラジカル重合」Scholarly book
- 広島ゴム技術員会2月例会, Feb. 2020, Japanese, 広島ゴム技術員会, 広島, Domestic conference高分子微粒子の構造設計とそれに基づくコロイド構造体の形成[Invited]Invited oral presentation
- 重合工学レクチャーシリーズNo.7, Jan. 2020, Japanese, 近畿化学協会重合工学部会, 大阪, Japan, Domestic conference高分子微粒子の構造制御による機能化[Invited]Invited oral presentation
- The 16th Pacific Polymer Conference (16PPC), Dec. 2019, English, Pacific Polymer Federation, Singapore, Singapore, International conferencePreparation of Polystyrene Having a “Cylindrical” Shape[Invited]Invited oral presentation
- 2nd G'L'owing Polymer Symposium in KANTO, Nov. 2019, English, 高分子学会関東支部, 東京, Japan, International conferenceMorphology Control of Cellulose ParticlesOral presentation
- 第28回ポリマー材料フォーラム, Nov. 2019, Japanese, 高分子学会, 名古屋, Japan, Domestic conference高分子微粒子のモルフォロジー制御とその機能[Invited]Invited oral presentation
- 第28回ポリマー材料フォーラム, Nov. 2019, Japanese, 高分子学会, 名古屋, Domestic conferenceSynthesis of Poly(ionic liquid) and Application to an AdhesivePoster presentation
- 37th Australasian Polymer Symposium (37APS), Nov. 2019, English, Royal Australian Chemical Institute, Sunshine Coast,, Australia, International conferencePreparation of Cylindrical Polystyrene Particles and Its Adsorption Behavior[Invited]Invited oral presentation
- 2019年度色材研究発表会, Oct. 2019, Japanese, 色材協会, 東京, Japan, Domestic conferencePreparation of Cylindrical PS/P(S-MMA) Janus Particles by Stirring MethodPoster presentation
- 2019年度色材研究発表会, Oct. 2019, Japanese, 色材協会, 東京, Japan, Domestic conferenceTwo-Dimensional Colloidal Structure Utilizing Disc-like ParticlesPoster presentation
- 第68回高分子学会討論会, Sep. 2019, Japanese, 高分子学会, 福井, Domestic conferenceInfluence of Precipitation Solvent on Morphology of Cellulose Particles by Solvent Releasing MethodPoster presentation
- 第68回高分子学会討論会, Sep. 2019, Japanese, 高分子学会, 福井, Japan, Domestic conferencePreparation of silicone/polymer composite particlesPoster presentation
- 第68回高分子学会討論会, Sep. 2019, Japanese, 高分子学会, 福井, Japan, Domestic conferenceMorphology Control of Janus Particles and Colloidal Structure Utilizing Hydrogen Bonding InteractionsOral presentation
- 第68回高分子学会討論会, Sep. 2019, Japanese, 高分子学会, 福井, Japan, Domestic conference, Co-authored internationallyPreparation of Polymer Particles Containing Reduced Graphene Oxide Using Block Copolymer[Invited]Invited oral presentation
- 2019年度膜工学サロン, Sep. 2019, Japanese, 先端膜工学研究推進機構, 神戸, Domestic conference高分子(複合)微粒子の構造制御とその機能化[Invited]Invited oral presentation
- 第65回高分子研究発表会(神戸), Jul. 2019, Japanese, 高分子学会関西支部, 神戸, Domestic conferencePreparation of Cylindrical Janus Particles by Stirring MethodOral presentation
- 第65回高分子研究発表会(神戸), Jul. 2019, Japanese, 高分子学会関西支部, 神戸, Japan, Domestic conferenceTwo-Dimensional Colloidal Structure Using Disc-like ParticlesOral presentation
- 第65回高分子研究発表会(神戸), Jul. 2019, Japanese, 高分子学会関西支部, 神戸, Japan, Domestic conference2官能シリコン化合物を用いた単分散微粒子の合成および粒径制御Oral presentation
- The International Polymer Colloid Group (IPCG) Conference 2019, Jun. 2019, English, International Polymer Colloids Group, Singapore, Singapore, International conferenceEffect of Kind of Precipitation Solvent on Morphology of Cellulose ParticlesPoster presentation
- The International Polymer Colloid Group (IPCG) Conference 2019, Jun. 2019, English, International Polymer Colloids Group, Singapore, Singapore, International conferencePreparation of microcapsules with hemisphere silica particlesPoster presentation
- The International Polymer Colloid Group (IPCG) Conference 2019, Jun. 2019, English, International Polymer Colloids Group, Singapore, Singapore, International conferencePreparation of Cylindrical Shape ParticlesPoster presentation
- The International Polymer Colloid Group (IPCG) Conference 2019, Jun. 2019, English, International Polymer Colloids Group, Singapore, Singapore, International conferenceSynthesis of Poly(ionic liquid) Particles and Application to a Metal-plastic AdhesivePoster presentation
- The International Polymer Colloid Group (IPCG) Conference 2019, Jun. 2019, English, International Polymer Colloids Group, Singapore, Singapore, International conferencePreparation of silicone/polymer composite particles with various morphologiesPoster presentation
- 第54回高分子の基礎と応用講座, Jun. 2019, Japanese, 高分子学会関西支部, 大阪, Japan高分子合成と反応(1) -高分子の生成反応,合成法-[Invited]Invited oral presentation
- 第57回日本接着学会年次大会, Jun. 2019, Japanese, 日本接着学会, 福岡, Japan, Domestic conferencePreparation of Building Block Particles Having Different Stabilizer and Colloidal StructurePoster presentation
- 第57回日本接着学会年次大会, Jun. 2019, Japanese, 日本接着学会, 福岡, Japan, Domestic conferenceSynthesis of monodisperse particles using bi-functional silicon compoundPoster presentation
- 第162回ラドテック研究講演会, Jun. 2019, Japanese, ラドテック研究会, 大阪, Japan, Domestic conference高分子微粒子の構造制御および微粒子構造体[Invited]Invited oral presentation
- 第68回高分子学会年次大会, May 2019, English, 高分子学会, 大阪, Domestic conferenceFormation Mechanism of Cellulose Particles Having Hollow StructureOral presentation
- 第68回高分子学会年次大会, May 2019, Japanese, 高分子学会, 大阪, Domestic conferencePreparation of silicone/polymer composite particles by seeded polymerizationOral presentation
- 第68回高分子学会年次大会, May 2019, Japanese, 高分子学会, 大阪, Domestic conferenceSynthesis of Poly(ionic liquid) and Application to an AdhesivePoster presentation
- 第68回高分子学会年次大会, May 2019, Japanese, 高分子学会, 大阪, Japan, Domestic conferenceMorphology Control of Building Block Particles and Colloidal StructurePoster presentation
- 第68回高分子学会年次大会, May 2019, Japanese, 高分子学会, 大阪, Japan, Domestic conferenceColloidal Structure of Disc-like ParticlesPoster presentation
- 第68回高分子学会年次大会, May 2019, Japanese, 高分子学会, 大阪, Japan, Domestic conferencePreparation of Janus Particles Having a Cylindrical Shape by Stirring MethodPoster presentation
- 第68回高分子学会年次大会, May 2019, Japanese, 高分子学会, 大阪, Japan, Domestic conferenceMorphology Control and Functionalization of Polymer Particles[Invited]Invited oral presentation
- 第99回日本化学会春季年会, Mar. 2019, Japanese, 日本化学会, 神戸, Domestic conference銀ナノ粒子を含有したセルロース粒子の作製Oral presentation
- 高分子学会「Webinar2018」, Feb. 2019, Japanese, 高分子学会, 東京, Domestic conferenceソフトマター“高分子微粒子”の構造設計とその機能Public discourse
- 2th SPSJ International Polymer Conference (IPC2018), Dec. 2018, English, 高分子学会, 広島, International conferencePreparation of Silicone Particles by Click Reaction and Silicone/Polymer Composite Particles by Seeded PolymerizationPoster presentation
- 2th SPSJ International Polymer Conference (IPC2018), Dec. 2018, English, 高分子学会, 広島, International conferencePreparation of Functionalized Cellulose ParticlesPoster presentation
- 1st G'L'owing Polymer Symposium in KANTO, Dec. 2018, English, 高分子学会関東支部, 東京, International conferenceMorphology Control of Cellulose Particles Having Porous StructureOral presentation
- 1st G'L'owing Polymer Symposium in KANTO, Dec. 2018, English, 高分子学会関東支部, 東京, International conferenceA Facile Preparation of Cylindrical Polymer Particle and Its Absorption at InterfaceOral presentation
- 2th SPSJ International Polymer Conference (IPC2018), Dec. 2018, English, 高分子学会, 広島, International conferenceA Facile Preparation of Cylindrical Particles and Its ApplicationPoster presentation
- 第20回高分子ミクロスフェア討論会, Nov. 2018, Japanese, 高分子ミクロスフェア研究会, 岡山, Domestic conference沈殿重合による単分散なポリアクリル酸微粒子の作製Oral presentation
- 第21回NICガーデンレクチャー, Nov. 2018, Japanese, 日華化学, 福井, Domestic conference高分子微粒子の構造設計およびコロイド構造体Invited oral presentation
- 基礎セミナー「接着技術に必要な基礎を学ぶ」, Nov. 2018, Japanese, 日本接着学会関西支部, 大阪, Domestic conference高分子微粒子の基礎Public discourse
- 第20回高分子ミクロスフェア討論会, Nov. 2018, Japanese, 高分子ミクロスフェア研究会, 岡山, Domestic conferenceシリンダー状高分子粒子の合成とその応用Oral presentation
- 第20回高分子ミクロスフェア討論会, Nov. 2018, Japanese, 高分子ミクロスフェア研究会, 岡山, Domestic conferenceイオン液体を利用したセルロース微粒子の形態制御Oral presentation
- 第27回ポリマー材料フォーラム, Nov. 2018, Japanese, 高分子学会, 東京, Domestic conferenceTEMPO酸化を利用した機能性セルロース粒子の作製Poster presentation
- Joint Lecture Series between Jagielonian University and Kobe University, Nov. 2018, English, Jagielonian University, Cracow, Poland, International conferencePreparation of functional polymer particles and colloidal building blocks[Invited]Invited oral presentation
- International Conference on Emerging Advanced Nanomaterials (ICEAN) 2018, Nov. 2018, English, Global Innovative Centre for ADVANCED NANOMATERIALS, Newcastle, Australia, International conferencerGO Nanocomposite Films via Miniemulsion PolymerizationOral presentation
- 2018年度色材研究発表会, Oct. 2018, Japanese, 色材協会, 大阪, Domestic conference水素結合を利用した粒子構造体に向けたヤヌス粒子のモルフォロジー制御Poster presentation
- 2018年度色材研究発表会, Oct. 2018, Japanese, 色材協会, 大阪, Domestic conferenceThiol-ene反応によるシリコーン粒子及びシリコーン/汎用ポリマー複合粒子の作製Poster presentation
- 第67回高分子学会討論会, Sep. 2018, Japanese, 高分子学会, 北海道, Domestic conference粒子構造体形成に向けたヤヌス粒子のモルフォロジー制御Poster presentation
- 第67回高分子学会討論会, Sep. 2018, Japanese, 高分子学会, 北海道, Domestic conference中空構造を有するセルロース微粒子のモルフォロジー制御Poster presentation
- 第69回コロイドおよび界面化学討論会, Sep. 2018, Japanese, 日本化学会コロイドおよび界面化学部会, 筑波, Domestic conference単中空構造を有するセルロース微粒子の合成Poster presentation
- 第67回高分子学会討論会, Sep. 2018, Japanese, 高分子学会, 北海道, Domestic conferenceクリック反応を用いたシリコーン粒子の合成とシリコーン/ポリベンジルメタクリレート複合粒子の作製Poster presentation
- 第67回高分子学会討論会, Sep. 2018, Japanese, 高分子学会, 北海道, Domestic conferenceイオン液体ポリマーを用いたフッ素樹脂/金属の接着Poster presentation
- 第64回高分子研究発表会(神戸), Jul. 2018, Japanese, 高分子学会関西支部, 神戸, Domestic conferenceヤヌス粒子のモルフォロジー制御とその粒子構造体Oral presentation
- 第64回高分子研究発表会(神戸), Jul. 2018, Japanese, 高分子学会関西支部, 神戸, Domestic conferenceイオン液体ポリマーを利用した異種材料接着への応用Oral presentation
- 第64回高分子研究発表会(神戸), Jul. 2018, Japanese, 高分子学会関西支部, 神戸, Domestic conferenceThiol-ene反応を用いたシリコーン粒子の作製Oral presentation
- IUPAC MACRO2018, Jul. 2018, English, IUPAC, Cairns, Australia, International conferencePreparation of Poly(ionic liquid) Particles Having Cationic Exchange Property by Dispersion PolymerizationPoster presentation
- IUPAC MACRO2018, Jul. 2018, English, IUPAC, Cairns, Australia, International conferencePreparation of Janus particles composed of hydrophobic and hydrophilic polymerOral presentation
- IUPAC MACRO2018, Jul. 2018, English, IUPAC, Cairns, Australia, International conferenceApplication of Spongy Cellulose Particles as MicrocapsulePoster presentation
- IUPAC MACRO2018, Jul. 2018, English, IUPAC, Cairns, Australia, International conferenceA Facile Method for Preparation of Monodisperse Cylindrical Polystyrene ParticlesPoster presentation
- 第53回高分子の基礎と応用講座, Jun. 2018, Japanese, 高分子学会関西支部, 大阪, Domestic conference高分子合成と反応(1)高分子の構造と生成反応,合成法の特徴Public discourse
- 第56回日本接着学会年次大会, Jun. 2018, Japanese, 日本接着学会, 東京, Domestic conferenceイオン液体ポリマー微粒子の合成とカチオン交換による粒子の機能化Poster presentation
- 第56回日本接着学会年次大会, Jun. 2018, Japanese, 日本接着学会, 東京, Domestic conferenceイオン液体ポリマーの接着剤への応用Poster presentation
- 第67回高分子学会年次大会, May 2018, English, 高分子学会, 名古屋, Domestic conference棒状ポリスチレン粒子の作製とその界面吸着挙動Oral presentation
- 第67回高分子学会年次大会, May 2018, Japanese, 高分子学会, 名古屋, Domestic conferenceカチオン交換性イオン液体ポリマー微粒子の合成Poster presentation
- 第67回高分子学会年次大会, May 2018, Japanese, 高分子学会, 名古屋, Domestic conferenceTEMPO酸化を利用した機能性セルロース粒子の作製Poster presentation
- The 6th Asian Symposium on Emulsion Polymerization and Functional Polymeric Microspheres, Mar. 2018, English, ASEPFPM, 福井, International conferencePreparation of Polymer Particles Containing Reduced Graphene Oxide Stabilized by Poly(ionic liquid)[Invited]Invited oral presentation
- The 6th Asian Symposium on Emulsion Polymerization and Functional Polymeric Microspheres, Mar. 2018, English, ASEPFPM, 福井, International conferenceApplication of Spongy Cellulose Particles to EncapsulationPoster presentation
- The 6th Asian Symposium on Emulsion Polymerization and Functional Polymeric Microspheres, Mar. 2018, English, ASEPFPM, 福井, International conferenceA Facile Method for Preparation of Monodisperse Cylindrical Polystyrene ParticlesPoster presentation
- Energy Materials Nanotechnology Meeting, Dec. 2017, English, Energy Materials Nanotechnology Meeting, Orlando, USA, International conferenceFormation of Colloidal Chain Using Hydrogen-bonding Interaction[Invited]Invited oral presentation
- First Materials Research Society of Thailand International Conference, Nov. 2017, English, Materials Research Society of Thailand, Chiang Mai,Thailand, International conferenceColloidal structure using hydrogen bonding interaction between colloidal stabilizerKeynote oral presentation
- 2017年度色材研究発表会, Oct. 2017, Japanese, 色材協会, 東京, Domestic conference銀ナノ粒子を含有したセルロース粒子の作製Poster presentation
- 2017年度色材研究発表会, Oct. 2017, Japanese, 色材協会, 東京, Domestic conferenceイオン液体ポリマーを分散剤とした還元型酸化グラフェン含有汎用性高分子微粒子の合成Poster presentation
- The 3rd International Symposium on Applied Chemistry (ISAC 2017), Oct. 2017, English, Indonesian Institute of Sciences, Jakarta, Indonesia, International conferenceDispersion polymerization of L-lactide utilizing ionic liquids as reaction mediumPoster presentation
- 第66回高分子学会討論会, Sep. 2017, Japanese, 高分子学会, 愛媛, Domestic conference新規な単分散棒状粒子の作製Poster presentation
- 第66回高分子学会討論会, Sep. 2017, Japanese, 高分子学会, 愛媛, Domestic conference塩添加により開口部を形成するカプセル粒子の作製Oral presentation
- 第66回高分子学会討論会, Sep. 2017, Japanese, 高分子学会, 愛媛, Domestic conferenceセルロース/銀複合粒子の作製Poster presentation
- 第66回高分子学会討論会, Sep. 2017, Japanese, 高分子学会, 愛媛, Domestic conferenceイオン液体ポリマー微粒子の合成とカチオン交換による金属イオンの担持Oral presentation
- 第68回コロイドおよび界面化学討論会, Sep. 2017, Japanese, 日本化学会コロイドおよび界面化学部会, 神戸, Domestic conferenceイオン液体ポリマーを分散剤として用いた還元型酸化グラフェン含有高分子微粒子の合成Poster presentation
- 第66回高分子学会討論会, Sep. 2017, Japanese, 高分子学会, 愛媛, Domestic conferenceアニオン交換を利用したポリイオン液体中空粒子の機能化Oral presentation
- 第68回コロイドおよび界面化学討論会, Sep. 2017, Japanese, 日本化学会コロイドおよび界面化学部会, 神戸, Domestic conferenceTEMPO酸化を利用したセルロース/銀複合粒子の作製Poster presentation
- 第63回高分子研究発表会(神戸), Jul. 2017, Japanese, 高分子学会関西支部, 神戸, Domestic conference金属酸化物を内包したポリイオン液体中空粒子の合成Oral presentation
- 第63回高分子研究発表会(神戸), Jul. 2017, Japanese, 高分子学会関西支部, 神戸, Domestic conferenceアニオン部を主鎖とするイオン液体ポリマー微粒子の合成Oral presentation
- 第63回高分子研究発表会(神戸), Jul. 2017, Japanese, 高分子学会関西支部, 神戸, Domestic conferenceTEMPO酸化を利用したセルロース粒子の機能化Oral presentation
- The International Polymer Colloids Group Conference 2017, Jun. 2017, English, The International Polymer Colloids Group, Arantzazu, Spain, International conferenceSynthesis of Polymer Nanoparticles Containing Reduced Graphene Oxide Utilizing Poly(ionic liquid) as StabilizerPoster presentation
- The International Polymer Colloids Group Conference 2017, Jun. 2017, English, The International Polymer Colloids Group, Arantzazu, Spain, International conferencePreparation of Poly(ionic liquid) Hollow Particles with Switchable PermeabilityPoster presentation
- The International Polymer Colloids Group Conference 2017, Jun. 2017, English, The International Polymer Colloids Group, Arantzazu, Spain, International conferenceEncapsulatiion Strategy Using Spongy Cellulose ParticlesPoster presentation
- The International Polymer Colloids Group Conference 2017, Jun. 2017, English, The International Polymer Colloids Group, Arantzazu, Spain, International conferenceA Simple Method to Synthesize Monodisperse Cylindrical Particles by PolystyrenePoster presentation
- 第66回高分子学会年次大会, May 2017, Japanese, 高分子学会, 千葉, Domestic conference単分散な棒状ポリスチレン粒子の作製Poster presentation
- 第66回高分子学会年次大会, May 2017, Japanese, 高分子学会, 千葉, Domestic conference多孔質構造セルロース粒子を利用したカプセル化Poster presentation
- 第66回高分子学会年次大会, May 2017, Japanese, 高分子学会, 千葉, Domestic conference塩刺激開口部を有するカプセル粒子の作製Poster presentation
- 第55回日本接着学会年次大会, May 2017, Japanese, 日本接着学会, 大阪, Domestic conferenceポリイオン液体中空粒子に対する磁性の付与Poster presentation
- CAMD Seminar, Mar. 2017, English, University of New South Wales, Sydney, Australia, International conferenceRAFT Polymerization in a Miniemulsion System using a Novel Type of Amphiphilic RAFT AgentInvited oral presentation
- 5th International Conference on Multifunctional, Hybrid and Nanomaterials, Mar. 2017, English, Elsevier Ltd, Lisbon, Portugal, International conferencePreparation of cellulose/polymer composite beads using ionic liquidPoster presentation
- Chemistry Seminar of UTAS, Feb. 2017, English, University of Tasmania, Tasmania, Australia, International conferencePreparation of Functional Polymer ParticlesInvited oral presentation
- International Polymer Conference 2016, Dec. 2016, English, 高分子学会, 福岡, International conferenceSynthesis of Polymer Particles Containing Reduced Graphene Oxide Utilizing Poly(ionic liquid) as StabilizerPoster presentation
- International Polymer Conference 2016, Dec. 2016, English, 高分子学会, 福岡, International conferencePreparation of Silicone Particles via Ring-opening Polymerization of Cyclic Siloxane in Aqueous MediumPoster presentation
- KCPC seminar, Dec. 2016, English, University of Sydney, Sydney, Australia, International conferencePreparation of functional polymer colloidInvited oral presentation
- International Polymer Conference 2016, Dec. 2016, English, 高分子学会, 福岡, International conferenceMechanism of Emulsion Polymerization with Bio-SurfactantPoster presentation
- International Polymer Conference 2016, Dec. 2016, English, 高分子学会, 福岡, International conferenceA Facile Method to Prepare Cylindrical Particles by PolystyrenePoster presentation
- 第19回高分子ミクロスフェア討論会, Nov. 2016, Japanese, 高分子ミクロスフェア研究会, 千葉, Domestic conference微細多孔質構造を有するセルロース粒子の形態制御Oral presentation
- 第19回高分子ミクロスフェア討論会, Nov. 2016, Japanese, 高分子ミクロスフェア研究会, 千葉, Domestic conference汎用ポリマー/イオン液体ポリマー複合粒子のモルフォロジィ制御Oral presentation
- 第19回高分子ミクロスフェア討論会, Nov. 2016, Japanese, 高分子ミクロスフェア研究会, 千葉, Domestic conference生物由来界面活性剤を使用した乳化重合Oral presentation
- 第19回高分子ミクロスフェア討論会, Nov. 2016, Japanese, 高分子ミクロスフェア研究会, 千葉, Domestic conference水媒体不均一系でのシリコーン粒子の作製Oral presentation
- 第19回高分子ミクロスフェア討論会, Nov. 2016, Japanese, 高分子ミクロスフェア研究会, 千葉, Domestic conferenceカプセル内ゾルゲル反応によるシリカ内包粒子の生成機構Oral presentation
- 36th Australasian Polymer Symposium, Nov. 2016, English, The Royal Australian Chemical Institute, Lorne, Australia, International conferencePreparation of Polymeric Particles Containing Reduced Graphene Oxide by Miniemulsion PolymerizationKeynote oral presentation
- 2016年度色材研究発表会, Oct. 2016, Japanese, 色材協会, 大阪, Domestic conference溶剤吸収放出法を利用したイオン液体ポリマー複合粒子のモルフォロジィ制御Poster presentation
- 2016年度色材研究発表会, Oct. 2016, Japanese, 色材協会, 大阪, Domestic conference多孔質構造セルロース粒子を用いたカプセル化Poster presentation
- 2016年度色材研究発表会, Oct. 2016, Japanese, 色材協会, 大阪, Domestic conferenceポリイオン液体中空粒子を用いた無機物質の導入Poster presentation
- 第65回高分子討論会, Sep. 2016, Japanese, 高分子学会, 横浜, Domestic conference微細多孔質セルロース粒子の形態制御Poster presentation
- 第65回高分子討論会, Sep. 2016, Japanese, 高分子学会, 横浜, Domestic conference多孔質セルロース粒子を用いたカプセル化Oral presentation
- 第65回高分子討論会, Sep. 2016, Japanese, 高分子学会, 横浜, Domestic conference磁性を有するポリイオン液体中空粒子の合成Poster presentation
- 第65回高分子討論会, Sep. 2016, Japanese, 高分子学会, 横浜, Domestic conferenceひとつもしくは複数のシリカ粒子を内包したポリマーカプセルのワンポット作製Invited oral presentation
- 第65回高分子討論会, Sep. 2016, Japanese, 高分子学会, 横浜, Domestic conferenceイオン液体ポリマーを分散剤として用いた還元型酸化グラフェン含有汎用性高分子微粒子の合成Oral presentation
- 第14回ゾルゲル学会討論会, Aug. 2016, Japanese, ゾルゲル学会, 東京, Domestic conferenceシリカ粒子内包ポリマーカプセルの生成機構Poster presentation
- 第62回高分子研究発表会(神戸), Jul. 2016, Japanese, 高分子学会関西支部, 神戸, Domestic conference微細多孔質構造セルロース粒子を利用したカプセル化Oral presentation
- 第62回高分子研究発表会(神戸), Jul. 2016, Japanese, 高分子学会関西支部, 神戸, Domestic conference刺激応答開閉カプセル粒子の合成Oral presentation
- 第62回高分子研究発表会(神戸), Jul. 2016, Japanese, 高分子学会関西支部, 神戸, Domestic conferenceイオン液体ポリマーを用いた還元型酸化グラフェン含有高分子微粒子の合成Oral presentation
- ACA(Asian Conference on Adhesion)2016(第54回日本接着学会年次大会), Jun. 2016, English, 日本接着学会, 東京, International conferenceMorphology Control of Poly(ionic liquid) Composite ParticlesPoster presentation
- 第65回高分子学会年次大会, May 2016, Japanese, 高分子学会, 神戸, Domestic conference微細多孔質構造を有するセルロース粒子の作製Poster presentation
- 第65回高分子学会年次大会, May 2016, Japanese, 高分子学会, 神戸, Domestic conference汎用ポリマー/イオン液体ポリマー複合微粒子のモルフォロジィ制御Poster presentation
- 第65回高分子学会年次大会, May 2016, Japanese, 高分子学会, 神戸, Domestic conference生物由来界面活性剤を用いた乳化重合Poster presentation
- 第65回高分子学会年次大会, May 2016, Japanese, 高分子学会, 神戸, Domestic conference水媒体不均一系での開環重合によるシリコーン粒子の作製Poster presentation
- Seminar of Materials Science and Engineering, Apr. 2016, English, 高分子学会, 北京,中国, International conferencePreparation of functional polymer particles and formation of colloidal structuresInvited oral presentation
- 第117回黒鉛化合物研究会, Jan. 2016, Japanese, 黒鉛化合物研究会, 神戸市, Domestic conference高分子微粒子の構造制御とその機能化[Invited]Invited oral presentation
- 日本ゾルゲル学会第13回討論会, Nov. 2015, Japanese, 日本ゾルゲル学会, 札幌市, Domestic conferenceひとつもしくは複数のシリカ粒子を内包したポリマーカプセルの作製Poster presentation
- 「微粒子セミナー」, Oct. 2015, Japanese, 日本接着学会関西支部, 大阪市, Domestic conference有機高分子微粒子合成の基礎[Invited]Invited oral presentation
- 2015年度 色材研究発表会, Oct. 2015, Japanese, 色材協会, 習志野市, Domestic conference新規な生物由来界面活性剤を使用したスチレンの乳化重合Poster presentation
- 第40回高分子同友会総合講演会(アンコール講演会), Oct. 2015, Japanese, 高分子同友会, 東京都, Domestic conference高分子微粒子の構造設計とその機能化[Invited]Invited oral presentation
- 2015年度 色材研究発表会, Oct. 2015, Japanese, 色材協会, 習志野市, Domestic conferenceミニエマルション系でのカチオン開環重合によるシリコーン粒子の作製Poster presentation
- The 5th Asian Symposium on Emulsion Polymerization and Functional Polymeric Microspheres (ASEPFPM2015), Oct. 2015, English, Chinese Academy of Sciences, 蘇州,中国, International conferencePreparation of Poly (ionic liquid) Hollow Particles Having Permeability-Switchable ShellOral presentation
- The 5th Asian Symposium on Emulsion Polymerization and Functional Polymeric Microspheres (ASEPFPM2015), Oct. 2015, English, Chinese Academy of Sciences, 蘇州,中国, International conferencePreparation of Janus Particles with Different Stabilizers and Formation of Colloidal Chains[Invited]Invited oral presentation
- The 5th Asian Symposium on Emulsion Polymerization and Functional Polymeric Microspheres (ASEPFPM2015), Oct. 2015, English, Chinese Academy of Sciences, 蘇州,中国, International conferenceOne-Pot Synthesis of Organic/Inorganic Composite Microcapsules by Sol-Gel Process inside a Polymer CapsuleOral presentation
- The 5th Asian Symposium on Emulsion Polymerization and Functional Polymeric Microspheres (ASEPFPM2015), Oct. 2015, English, Chinese Academy of Sciences, 蘇州,中国, International conferenceMorphology Control of Cellulose Particles Having Spongy StructureOral presentation
- 第64回高分子討論会, Sep. 2015, Japanese, 高分子学会, 仙台市, Domestic conference低分子ゲル・高分子ゲル複合型新規ヘテロダブルネットワークイオン液体ゲルの開発Poster presentation
- 第64回高分子学会討論会, Sep. 2015, Japanese, 高分子学会, 仙台市, Domestic conference新規な両親媒性可逆的付加開裂連鎖移動(RAFT)剤を用いた水媒体不均一重合[Invited]Invited oral presentation
- 化学工学会第47回秋季大会, Sep. 2015, Japanese, 化学工学会, 札幌市, Domestic conference高導電性を有するダブルネットワークイオン液体ゲルの開発Poster presentation
- 第64回高分子学会討論会, Sep. 2015, Japanese, 高分子学会, 仙台市, Domestic conferenceポリメタクリル酸メチル/ポリイオン液体複合粒子のモルフォロジィ制御Poster presentation
- 第64回高分子学会討論会, Sep. 2015, Japanese, 高分子学会, 仙台市, Domestic conferenceポリマーカプセル内ゾルゲル反応によるシリカ内包粒子の作製[Invited]Invited oral presentation
- 第64回高分子学会討論会, Sep. 2015, Japanese, 高分子学会, 仙台市, Domestic conferenceポリイオン液体中空粒子の作製及びカプセル特性評価Oral presentation
- 第64回高分子学会討論会, Sep. 2015, Japanese, 高分子学会, 仙台市, Domestic conferenceイオン液体を用いて作製した多孔質セルロース粒子の形態制御Poster presentation
- 第64回高分子学会討論会, Sep. 2015, Japanese, 高分子学会, 仙台市, Domestic conferenceイオン液体モノマーを利用した複合高分子微粒子の合成とアニオン交換による機能化Oral presentation
- Malaysian Scientific Association, Sep. 2015, English, Kuala Lumpur, Malaysia, International conferencePREPARATION OF JANUS PARTICLES WITH DIFFERENT STABILIZERS AND FORMATION OF ONE-DIMENSIONAL PARTICLE CHAINS[Invited]Invited oral presentation
- 第61回高分子研究発表会(神戸), Jul. 2015, Japanese, 高分子学会関西支部, 神戸市, Domestic conference汎用ポリマー/イオン液体ポリマー複合粒子のモルフォロジィ制御Oral presentation
- 第61回高分子研究発表会(神戸), Jul. 2015, Japanese, 高分子学会, 神戸市, Domestic conference低分子ゲル・高分子ゲル混在型新規ヘテロダブルネットワークイオン液体ゲルの開発Poster presentation
- 第61回高分子研究発表会(神戸), Jul. 2015, Japanese, 高分子学会関西支部, 神戸市, Domestic conference多孔質セルロース粒子の形態制御Oral presentation
- 第61回高分子研究発表会(神戸), Jul. 2015, Japanese, 高分子学会関西支部, 神戸市, Domestic conference新規な生物由来界面活性剤を用いた乳化重合Oral presentation
- 第33回関西界面科学セミナー 界面科学・分散技術の基礎と最先端研究, Jul. 2015, Japanese, 日本化学会 コロイドおよび界面化学部会, 大阪市, Domestic conference界面・分散を利用してつくる:高分子粒子の設計[Invited]Invited oral presentation
- 第61回高分子研究発表会(神戸), Jul. 2015, Japanese, 高分子学会関西支部, 神戸市, Domestic conferenceミニエマルション系イオン重合によるシリコーン粒子の作製Oral presentation
- 第61回高分子研究発表会(神戸), Jul. 2015, Japanese, 高分子学会関西支部, 神戸市, Domestic conferenceイオン液体ポリマー中空粒子の作製及びカプセル特性評価Poster presentation
- IPCG Polymer Colloids Conference 2015, Jul. 2015, English, International Polymer Colloids Group, New Hampshire, USA, International conferenceColloidal building blocks using hydrogen bonding interactions between stabilizers[Invited]Invited oral presentation
- 兵庫県立大学講演会, Jun. 2015, Japanese, 兵庫県立大学, 姫路市, Domestic conference高分子微粒子構造体の作製[Invited]Invited oral presentation
- IPCG Polymer Colloids Conference 2015, Jun. 2015, English, International Polymer Colloids Group, New Hampshire, USA, International conferencePreparation of polymer particles containing reduced graphene oxide using ionic liquid monomerPoster presentation
- IPCG Polymer Colloids Conference 2015, Jun. 2015, English, International Polymer Colloids Group, New Hampshire, USA, International conferenceMorphology Control of ‘Rattle’-like Polymer Particles Prepared by Suspension PolymerizationPoster presentation
- IPCG Polymer Colloids Conference 2015, Jun. 2015, English, International Polymer Colloids Group, New Hampshire, USA, International conferenceMorphology control of Silica particles prepared by sol-gel process in polymer capsulePoster presentation
- 第64回高分子学会年次大会, May 2015, Japanese, 高分子学会, 札幌, Domestic conference乳化重合を用いたイオン液体ポリマー微粒子の合成とそのフィルム表面物性Oral presentation
- 第64回高分子学会年次大会, May 2015, Japanese, 高分子学会, 札幌, Domestic conference異なる分散安定剤を有したヤヌス粒子の作製及び一次元粒子配列制御Oral presentation
- 第64回高分子学会年次大会, May 2015, Japanese, 高分子学会, 札幌, 概要, Domestic conferenceカプセル内ゾルゲル反応によるシリカ内包粒子の生成メカニズムPoster presentation
- 第64回高分子学会年次大会, May 2015, Japanese, 高分子学会, 札幌, Domestic conferenceイオン液体を利用したセルロース粒子の作製とその複合化Poster presentation
- 高分子同友会勉強会, Feb. 2015, Japanese, 高分子同友会, 大阪市, Domestic conference高分子微粒子の構造設計とその機能化[Invited]Invited oral presentation
- 日本接着学会関西支部「微粒子セミナー」, Nov. 2014, Japanese, 日本接着学会関西支部, 大阪市, Domestic conference有機高分子微粒子合成の基礎[Invited]Invited oral presentation
- 第18回高分子ミクロスフェア討論会, Nov. 2014, Japanese, 高分子ミクロスフェア研究会, 福井市, Domestic conference微細構造セルロース粒子を利用した複合粒子の作製Oral presentation
- 第18回高分子ミクロスフェア討論会, Nov. 2014, Japanese, 高分子ミクロスフェア研究会, 福井市, Domestic conference水素結合を利用した一次元粒子配列制御Oral presentation
- 第18回高分子ミクロスフェア討論会, Nov. 2014, Japanese, 高分子ミクロスフェア研究会, 福井市, Domestic conference新規な可逆的付加開裂連鎖移動(RAFT)剤を用いたミニエマルション重合Oral presentation
- 第18回高分子ミクロスフェア討論会, Nov. 2014, Japanese, 高分子ミクロスフェア研究会, 福井市, Domestic conference懸濁重合法を用いたイオン液体ポリマー中空粒子の作製Oral presentation
- 第3回A-STEP発新技術説明会, Nov. 2014, Japanese, JST, 東京都, Domestic conferenceセルロース微粒子/複合粒子材料の創成Oral presentation
- 第18回高分子ミクロスフェア討論会, Nov. 2014, Japanese, 高分子ミクロスフェア研究会, 福井市, Domestic conferenceカプセル内ゾルゲル反応によるシリカ内包粒子の作製と形態制御Oral presentation
- Workshop on Polymer Nanoparticles, Seil-Assembly and Colloids, Nov. 2014, English, University of New South Wales, Sydney, Australia, International conferencePreparation of poly(ionic liquid) particles by emulsion polymerization” Workshop on Polymer NanoparticlesPoster presentation
- Workshop on Polymer Nanoparticles, Seil-Assembly and Colloids, Nov. 2014, English, University of New South Wales, Sydney, Australia, International conferenceMorphology control of polymeric nanoparticles using membrane emulsification” Workshop on Polymer NanoparticlesPoster presentation
- 2014年度色材研究発表会, Oct. 2014, Japanese, 色材協会, 名古屋, Domestic conferenceポリイオン液体中空粒子の作製とその機能変換Poster presentation
- 2014年度色材研究発表会, Oct. 2014, Japanese, 色材協会, 名古屋, Domestic conferenceセルロース/汎用ポリマー複合粒子の合成Poster presentation
- 第63回高分子討論会, Sep. 2014, Japanese, 高分子学会, 長崎市, Domestic conference分散安定剤間の水素結合を利用した一次元粒子配列制御Poster presentation
- 第63回高分子討論会, Sep. 2014, Japanese, 高分子学会, 長崎市, Domestic conference低分子ゲル・高分子ゲル混在型新規ヘテロダブルネットワークイオノゲルの調製Poster presentation
- 化学工学会 第46回秋季大会, Sep. 2014, Japanese, 化学工学会, 福岡市, Domestic conference低分子ゲル・高分子ゲル共存型新規ヘテロダブルネットワークイオン液体ゲルの開発Poster presentation
- 第63回高分子討論会, Sep. 2014, Japanese, 高分子学会, 長崎市, Domestic conference温度により形状を変化させるイオン液体含有自立ゲル粒子の作製[Invited]Invited oral presentation
- 第1回関西ものづくり技術シーズ発表会, Sep. 2014, Japanese, 近畿経済産業局, 大阪市, Domestic conferenceセルロース(複合)粒子の作製とその構造制御Oral presentation
- 第63回高分子討論会, Sep. 2014, Japanese, 高分子学会, 長崎市, Domestic conferenceシリカ内包カプセル粒子の形態制御とそのメカニズムPoster presentation
- 第63回高分子討論会, Sep. 2014, Japanese, 高分子学会, 長崎市, Domestic conferenceRattle-likeカプセル粒子の作製[Invited]Invited oral presentation
- 5th World Congress on Adhesion and Related Phenomena, Sep. 2014, English, 日本接着学会, 奈良市, International conferenceRAFT Polymerization in a Miniemulsion System using a Novel Type of Amphiphilic RAFT AgentOral presentation
- 5th World Congress on Adhesion and Related Phenomena, Sep. 2014, English, 日本接着学会, 奈良市, International conferenceControl of Morphology of ‘Rattle’-like Particles Prepared by One-step Suspension PolymerizationPoster presentation
- 第60回高分子研究発表会(神戸), Jul. 2014, Japanese, 高分子学会, 神戸市, Domestic conference低分子・高分子共存型新規ヘテロダブルネットワークゲルの開発Poster presentation
- 第60回高分子研究発表会(神戸), Jul. 2014, Japanese, 神戸, Domestic conferencePreparation of polymer particles with encapsulated silicaOral presentation
- 第60回高分子研究発表会(神戸), Jul. 2014, Japanese, 神戸, Domestic conferenceイオン液体ポリマーをシェルとする中空粒子の作製Oral presentation
- 第63回高分子学会年次大会, May 2014, Japanese, 高分子学会, 名古屋市, Domestic conference汎用高分子/イオン液体ポリマー複合微粒子の合成とその構造制御Poster presentation
- 第63回高分子学会年次大会, May 2014, Japanese, 高分子学会, 名古屋市, Domestic conference小粒子内包カプセル粒子の一段階作製Poster presentation
- 色材講演会, Oct. 2013, Japanese, 大阪市, Domestic conference機能性粒子材料の創生[Invited]Invited oral presentation
- 色材協会創立85周年記念会議, Oct. 2013, English, 東京都, International conferencePreparation of quaternary ammonium-based poly(ionic liquid) particles by emulsion polymerizationPoster presentation
- 色材協会創立85周年記念会議, Oct. 2013, English, 東京都, International conferencePreparation of one-dimensional particle array utilizing hydrogen bonding interactionPoster presentation
- 色材協会創立85周年記念会議, Oct. 2013, English, 東京都, International conferenceOne-step synthesis of “rattle”-like particle (particles-encapsulated particle) by suspension polymerizationPoster presentation
- 第62回高分子討論会, Sep. 2013, Japanese, 高分子学会, 金沢市, Domestic conference新しい重合性界面活性剤を用いた難溶性ナノ材料可溶化技術の開発Oral presentation
- 日本セラミックス協会 第26回秋季シンポジウム, Sep. 2013, Japanese, 長野市, Domestic conferenceイオン液体不均一系での高分子/無機酸化物複合粒子の合成[Invited]Invited oral presentation
- 第64回コロイドおよび界面化学討論会, Sep. 2013, Japanese, 名古屋市, Domestic conferenceイオン液体中でのゾル-ゲル反応を利用したコアシェル型有機/無機複合粒子の合成Poster presentation
- 第59回高分子研究発表会(神戸), Jul. 2013, Japanese, 神戸市, Domestic conference乳化重合によるイオン液体ポリマー微粒子の合成Poster presentation
- 住友化学講演会, Jul. 2013, Japanese, 宝塚市, Domestic conference中空高分子微粒子の合成とその中空構造を利用した機能化[Invited]Invited oral presentation
- 第59回高分子研究発表会(神戸), Jul. 2013, Japanese, 神戸市, Domestic conference高分子分散安定剤間の水素結合を利用した粒子配列制御Oral presentation
- 第20回クロマトグラフィーシンポジウム, Jun. 2013, Japanese, 神戸市, Domestic conference高分子微粒子存在下での脱水素反応を利用した高分子/窒化ホウ素複合粒子の合成Poster presentation
- 第20回クロマトグラフィーシンポジウム, Jun. 2013, Japanese, 神戸市, Domestic conference塩溶液中における四級アンモニウム系イオン液体ポリマー微粒子の特異な溶解挙動Poster presentation
- 第20回クロマトグラフィーシンポジウム, Jun. 2013, Japanese, 神戸市, Domestic conferenceシード分散重合法を用いた汎用高分子/イオン液体ポリマー複合微粒子の合成Poster presentation
- 第20回クロマトグラフィーシンポジウム, Jun. 2013, Japanese, 神戸市, Domestic conferenceイオン液体を利用した多孔性セルロース微粒子の形成機構Poster presentation
- IPCG Research Conference 2013, Jun. 2013, English, 上海,中国, International conferenceSpecific Solubility Behavior of Poly(Ionic Liquid) Particles by Changing the Counter AnionPoster presentation
- 第20回クロマトグラフィーシンポジウム, Jun. 2013, Japanese, 神戸市, Domestic conferenceSaPSeP法を利用した小粒子内包カプセル粒子の作製Poster presentation
- IPCG Research Conference 2013, Jun. 2013, English, 上海,中国, International conferencePreparation of Raspberry-like Particles Utilizing Hydrogen Bonding Interaction between Polymeric StabilizersPoster presentation
- IPCG Research Conference 2013, Jun. 2013, English, 上海,中国, International conferencePreparation of Poly(ionic liquid)/Commodity Polymer Composite Particles by Seeded Dispersion PolymerizationPoster presentation
- IPCG Research Conference 2013, Jun. 2013, English, 上海,中国, International conferencePreparation of Hollow Polymer Particles with Encapsulated Small Particles by Suspension PolymerizationPoster presentation
- IPCG Research Conference 2013, Jun. 2013, English, 上海,中国, International conferencePreparation of Boron Nitride and Polystyrene/Boron Nitride Composite Particles by Dehydrogenation Reactions in Ionic LiquidsPoster presentation
- IPCG Research Conference 2013, Jun. 2013, English, 上海,中国, International conferenceOne-pot Synthesis of Polymer Particles with Encapsulated Hollow Silica ParticlesPoster presentation
- IPCG Research Conference 2013, Jun. 2013, English, 上海,中国, International conferenceMorphology Control of Cellulose Particles Utilizing an Ionic LiquidPoster presentation
- 第62回高分子学会年次大会, May 2013, Japanese, 京都市, Domestic conference水素結合を利用した有機/無機複合ラズベリー状粒子の作製Oral presentation
- 第62回高分子学会年次大会, May 2013, Japanese, 京都市, Domestic conferenceマイクロカプセル内ゾルゲル反応によるシリカ粒子内包ポリマー粒子の作成Poster presentation
- 第62回高分子学会年次大会, May 2013, Japanese, 京都市, Domestic conferenceアニオン交換を利用したイオン液体ポリマー微粒子の特異な溶解挙動Poster presentation
- 化学工学会 第78年会, Mar. 2013, Japanese, 化学工学会, 大阪大学, Domestic conference重合性界面活性剤による難溶性材料可溶化技術の開発Oral presentation
- 昭和電工講演会, Dec. 2012, Japanese, たつの市, Domestic conference高分子微粒子の合成とその構造設計Public discourse
- The 9th SPSJ International Polymer Conference (IPC2012), Dec. 2012, English, 神戸市, International conferencePreparation of Polystyrene/Highly Crystalline Magnesium Hydroxide Composite Particles having Core-Shell Morphology by Seeded Dispersion Sol-Gel Process in an Ionic LiquidOral presentation
- The 9th SPSJ International Polymer Conference (IPC2012), Dec. 2012, English, 神戸市, International conferencePreparation of micron-sized monodisperse poly(ionic liquid) particlesPoster presentation
- 第17回高分子ミクロスフェア討論会, Nov. 2012, Japanese, 仙台市, Domestic conference分散重合によるイオン液体ポリマー微粒子の合成とその特異な溶解挙動Oral presentation
- 第17回高分子ミクロスフェア討論会, Nov. 2012, Japanese, 仙台市, Domestic conference分散安定剤水素結合を利用したヘテロ凝集法による異形高分子粒子の作製Oral presentation
- 工学フォーラム2012, Nov. 2012, Japanese, 神戸市, Domestic conference大学シーズからベンチャー起業~材料系研究からの挑戦[Invited]Invited oral presentation
- 第17回高分子ミクロスフェア討論会, Nov. 2012, Japanese, 仙台市, Domestic conference多数の小粒子を内包したカプセル粒子の作製Oral presentation
- 第17回高分子ミクロスフェア討論会, Nov. 2012, Japanese, 仙台市, Domestic conference感温性を有する複合ゲル粒子の作製Oral presentation
- 第17回高分子ミクロスフェア討論会, Nov. 2012, Japanese, 仙台市, Domestic conferenceイオン液体を利用したセルロース微粒子の作製Oral presentation
- 2012年度色材研究発表会, Sep. 2012, Japanese, 堺市, Domestic conference溶媒吸収放出法を利用した微細構造を有するセルロース微粒子の作製Poster presentation
- 第61回高分子学会討論会, Sep. 2012, Japanese, 名古屋市, Domestic conference固相分散系での扁平高分子粒子の合成Poster presentation
- 第61回高分子学会討論会, Sep. 2012, Japanese, 名古屋市, Domestic conferenceマイクロサスペンション重合による小粒子内包カプセル粒子の作製Poster presentation
- 化学工学会 第44回秋季大会, Sep. 2012, Japanese, 化学工学会, 仙台市, Domestic conferenceはがれない界面活性剤による表面改質技術の開発Poster presentation
- 2012年度色材研究発表会, Sep. 2012, Japanese, 堺市, Domestic conferenceシリカ内包ポリマーカプセル粒子のワンポット作製Poster presentation
- 2012年度色材研究発表会, Sep. 2012, Japanese, 堺市, Domestic conferenceイオン液体中における脱水素反応を利用した有機/無機複合粒子の合成Poster presentation
- 第61回高分子学会討論会, Sep. 2012, Japanese, 名古屋市, Domestic conferenceイオン液体を利用したセルロース微粒子の作製と形態制御Poster presentation
- 第61回高分子学会討論会, Sep. 2012, Japanese, 名古屋市, Domestic conferenceイオン液体を含有した自立型温度応答性複合ゲル粒子の作製Oral presentation
- 2012年度色材研究発表会, Sep. 2012, Japanese, 堺市, Domestic conferenceイオン液体ポリマーを用いた複合高分子微粒子の合成Poster presentation
- 第58回高分子研究発表会(神戸), Jul. 2012, Japanese, 神戸市, Domestic conference溶媒吸収放出法によるセルロース微粒子の形態制御Oral presentation
- 第58回高分子研究発表会(神戸), Jul. 2012, Japanese, 神戸市, Domestic conference小粒子内包カプセル粒子の作製Oral presentation
- 積水IM研究会, Jul. 2012, Japanese, 京都市, Domestic conference高分子微粒子材料の設計と機能化Public discourse
- 7月創造例会, Jul. 2012, Japanese, 姫路市, Domestic conference高分子微粒子の合成とその構造設計[Invited]Invited oral presentation
- 第57回高分子夏季大学, Jul. 2012, Japanese, 大津市, Domestic conference固相分散系での非真球中空高分子粒子の合成Poster presentation
- 第57回高分子夏季大学, Jul. 2012, Japanese, 大津市, Domestic conferenceシード分散重合法を用いたイオン液体ポリマー複合微粒子の合成Poster presentation
- 第58回高分子研究発表会(神戸), Jul. 2012, Japanese, 神戸市, Domestic conferenceシード分散重合法によるポリイオン液体複合微粒子の合成Oral presentation
- 第57回高分子夏季大学, Jul. 2012, Japanese, 大津市, Domestic conferenceイオン液体を利用した微細構造を有するセルロース微粒子の作製Poster presentation
- 第58回高分子研究発表会(神戸), Jul. 2012, Japanese, 神戸市, Domestic conferenceイオン液体を媒体としたコア-シェル型ポリスチレン/窒化ホウ素複合粒子の合成Oral presentation
- 第50回日本接着学会年次大会, Jun. 2012, Japanese, 福島市, Domestic conference分散重合による汎用高分子/イオン液体ポリマー複合微粒子の合成Poster presentation
- 第50回日本接着学会年次大会, Jun. 2012, Japanese, 福島市, Domestic conference分散安定剤水素結合を利用したラズベリー状異形粒子の合成Oral presentation
- 花王株式会社化学品研究所セミナー, Jun. 2012, Japanese, 和歌山市, Domestic conference高分子微粒子材料の合成とその構造制御Public discourse
- 第50回日本接着学会年次大会, Jun. 2012, Japanese, 福島市, Domestic conferenceカプセル粒子内ゾルゲル反応によるシリカ内包粒子の作成Oral presentation
- 第50回日本接着学会年次大会, Jun. 2012, Japanese, 福島市, Domestic conferenceイオン液体中におけるポリスチレン/窒化ホウ素複合粒子の合成Poster presentation
- IUPAC World Polymer Congress (MACRO2012), Jun. 2012, English, Virginia, USA, International conferencePreparations of polystyrene/magnesium hydroxide composite particles by seeded dispersion sol-gel process in an ionic liquidPoster presentation
- IUPAC World Polymer Congress (MACRO2012), Jun. 2012, English, Virginia, USA, International conferencePreparations of micron-sized monodsperse poly(ionic liquid) particles by dispersion polymerizationPoster presentation
- 第61回高分子学会年次大会, May 2012, Japanese, 横浜市, Domestic conference超臨界二酸化炭素媒体におけるメタクリル酸メチルの可逆移動触媒分散重合(dispersion RTCP)Oral presentation
- 第61回高分子学会年次大会, May 2012, Japanese, 横浜市, Domestic conference高分子分散安定剤間の水素結合を利用したラズベリー状粒子の作製Poster presentation
- 第61回高分子学会年次大会, May 2012, Japanese, 横浜市, Domestic conferenceマイクロカプセル内でのゾルゲル反応によるシリカ内包ポリマー粒子の作成Oral presentation
- 第92回日本化学会春季年会, Mar. 2012, Japanese, 日本化学会, 横浜市, Domestic conferenceイオン液体を媒体としたシード分散ゾル-ゲル反応によるポリスチレン/水酸化マグネシウム複合粒子の合成Oral presentation
- 「ナノ構造・物性」第4回研究会, Jan. 2012, Japanese, 神戸大学自然科学系先端融合研究環, 神戸市, Domestic conference無乳化剤TERP乳化重合:粒子形成機構Oral presentation
- 「ナノ構造・物性」第4回研究会, Jan. 2012, Japanese, 神戸大学自然科学系先端融合研究環, 神戸市, Domestic conferenceシェルに開口部を有するカプセル微粒子の作製Oral presentation
- 「ナノ構造・物性」第4回研究会, Jan. 2012, Japanese, 神戸大学自然科学系先端融合研究環, 神戸市, Domestic conferenceイオン液体中でのポリスチレン/水酸化マグネシウム複合粒子の合成Oral presentation
- 第2回イオン液体討論会, Dec. 2011, Japanese, イオン液体研究会, 京都市, Domestic conferenceイオン液体中でのゾル-ゲル反応による有機/無機複合粒子の合成とその機構Poster presentation
- 高分子講演会(東海)〜高分子微粒子の精密合成と機能性材料への応用〜, Dec. 2011, Japanese, 高分子学会東海支部, 津市, Domestic conferenceイオン液体を利用した機能性高分子微粒子の機能化Invited oral presentation
- WINPTech2011, Dec. 2011, English, 神戸大学連携創造本部イノベーション推進部門, 神戸市, International conferencePreparation of Poly(ionic liquid) Particles by Dispersion PolymerizationPoster presentation
- the 4th Asian Symposium on Emulsion Polymerization and Functional Polymeric Microspheres (ASEPFPM2011), Dec. 2011, English, ASEPFPM, 香港,中国, International conferencePreparation of Functional Polymer Particles Using Ionic LiquidsInvited oral presentation
- WINPTech2011, Dec. 2011, English, 神戸大学連携創造本部イノベーション推進部門, 神戸市, International conferenceFree-standing Thermosensitive Composite Gel Particles Including Ionic LiquidPoster presentation
- 2011年度色材研究発表会, Nov. 2011, Japanese, 色材協会, 東京都, Domestic conference分散重合法によるイオン液体ポリマー微粒子の合成Poster presentation
- 2011年度色材研究発表会, Nov. 2011, Japanese, 色材協会, 東京都, Domestic conference水素結合を利用したヘテロ凝集法によるラズベリー状粒子の作製Poster presentation
- 2011年度色材研究発表会, Nov. 2011, Japanese, 色材協会, 東京都, Domestic conference自立型温度応答性複合ゲル粒子の作製Poster presentation
- 第60回高分子学会討論会, Sep. 2011, Japanese, 高分子学会, 岡山市, Domestic conference超臨界二酸化炭素媒体における可逆移動触媒重合(dispersion RTCP)によるPMMA-b-PS粒子の作製Poster presentation
- 第60回高分子学会討論会, Sep. 2011, Japanese, 高分子学会, 岡山市, Domestic conference水分散系における選択的表面開始制御/リビングラジカル重合によるキノコ状粒子の合成Poster presentation
- 第60回高分子学会討論会, Sep. 2011, Japanese, 高分子学会, 岡山市, Domestic conference開口部を有するポリジビニルベンゼン中空高分子微粒子の作製Oral presentation
- 第60回高分子学会討論会, Sep. 2011, Japanese, 高分子学会, 岡山市, Domestic conferenceシード分散ゾルゲル法による有機/無機複合粒子合成におけるイオン液体の効果Oral presentation
- 第60回高分子学会討論会, Sep. 2011, Japanese, 高分子学会, 岡山市, Domestic conferenceイオン液体をカプセル化した微粒子の応用展開Oral presentation
- 第60回高分子学会討論会, Sep. 2011, Japanese, 高分子学会, 岡山市, Domestic conferenceIn-situミセル核形成による制御/リビング乳化重合(emulsion TERP)Oral presentation
- 第57回高分子研究発表会(神戸), Jul. 2011, Japanese, 高分子学会関西支部, 神戸市, Domestic conference溶媒吸収放出法を利用したセルロース微粒子の作製Poster presentation
- 第57回高分子研究発表会(神戸), Jul. 2011, Japanese, 高分子学会関西支部, 神戸市, Domestic conference分散重合を用いたイオン液体ポリマー微粒子の合成Oral presentation
- 第57回高分子研究発表会(神戸), Jul. 2011, Japanese, 高分子学会関西支部, 神戸市, Domestic conferenceイオン液体を含有した感温性ゲル粒子の作製Oral presentation
- IPCG Polymer Colloids Conference 2011, Jul. 2011, English, IPCG Group, New Hampshire; US, International conferencePreparation of Polystyrene/Magnesium Oxide Composite Particles in an Ionic LiquidPoster presentation
- IPCG Polymer Colloids Conference 2011, Jul. 2011, English, IPCG Group, New Hampshire; US, International conferencePreparation of Ionic Liquid-encapsulated Polymer ParticlesPoster presentation
- IPCG Polymer Colloids Conference 2011, Jul. 2011, English, IPCG Group, New Hampshire; US, International conferenceEmulsifier-Free, Organotellurium-Mediated Living Radical Emulsion Polymerization (Emulsion TERP) of Methyl MethacrylatePoster presentation
- IPCG Polymer Colloids Conference 2011, Jul. 2011, English, IPCG Group, New Hampshire; US, International conferenceEmulsifier-Free, Organotellurium-Mediated Living Radical Emulsion Polymerization: Initial Stage of PolymrtizationPoster presentation
- 第49回日本接着学会年次大会, Jun. 2011, Japanese, 日本接着学会, 豊田市, Domestic conference原子移動ラジカル重合法によるパラフィン内包カプセル粒子の合成Oral presentation
- 第49回日本接着学会年次大会, Jun. 2011, Japanese, 日本接着学会, 豊田市, Domestic conferenceミクロンサイズで単分散なイオン液体ポリマー粒子の合成Poster presentation
- 第49回日本接着学会年次大会, Jun. 2011, Japanese, 日本接着学会, 豊田市, Domestic conferenceシード分散ゾル-ゲル反応によるポリスチレン/酸化マグネシウム複合粒子の合成Poster presentation
- 第49回日本接着学会年次大会, Jun. 2011, Japanese, 日本接着学会, 豊田市, Domestic conferenceイオン液体感温性高分子をシェルとしたカプセル高分子微粒子の合成Oral presentation
- 第60回高分子学会年次大会, May 2011, Japanese, 高分子学会, 大阪市, Domestic conference無乳化剤TERP乳化重合によるポリメタクリル酸メチル粒子の合成Oral presentation
- 第60回高分子学会年次大会, May 2011, Japanese, 高分子学会, 大阪市, Domestic conference無乳化剤TERP乳化重合における重合初期の重要性Oral presentation
- 第60回高分子学会年次大会, May 2011, Japanese, 高分子学会, 大阪市, Domestic conference超臨界二酸化炭素媒体における窒素化合物を触媒として用いたメタクリル酸メチルの可逆移動触媒重合Poster presentation
- 第60回高分子学会年次大会, May 2011, Japanese, 高分子学会, 大阪市, Domestic conference架橋ポリアクリル酸微粒子の抽出挙動におけるイオン液体の影響Poster presentation
- 第60回高分子学会年次大会, May 2011, Japanese, 高分子学会, 大阪市, Domestic conferenceイオン液体中におけるポリスチレン/酸化マグネシウム複合粒子の合成Poster presentation
- ナノ学会 「ナノ構造・物性」部会 第3回研究会, Mar. 2011, Japanese, ナノ学会, 神戸市, Domestic conference無機複合粒子の合成Oral presentation
- ナノ学会 「ナノ構造・物性」部会 第3回研究会, Mar. 2011, Japanese, ナノ学会, 神戸市, Domestic conferenceSaPSeP法を用いたイオン液体含有感温性高分子微粒子の合成Oral presentation
- The 2010 International Chemical Congress of Pacific Basin Societies (Pacifichem 2010), Dec. 2010, English, 日本化学会, ハワイ, USA, International conferencePreparation of Poly(acrylic acid) by atom transfer radical polymerization in Supercritical Carbon DioxideOral presentation
- The 2010 International Chemical Congress of Pacific Basin Societies (Pacifichem 2010), Dec. 2010, English, 日本化学会, ハワイ, USA, International conferencePreparation of ionic liquid-encapsulated polymer particlesPoster presentation
- The 2010 International Chemical Congress of Pacific Basin Societies (Pacifichem 2010), Dec. 2010, English, 日本化学会, ハワイ, USA, International conferenceOrganic Composite Particles in an Ionic LiquidPoster presentation
- The 2010 International Chemical Congress of Pacific Basin Societies (Pacifichem 2010), Dec. 2010, English, 日本化学会, ハワイ, USA, International conferencePreparation of Block Copolymer Particles by Emulsifier-Free; organotellurium-Mediated Living Radical Emulsion PolymerizationOral presentation
- The 2010 International Chemical Congress of Pacific Basin Societies (Pacifichem 2010), Dec. 2010, English, 日本化学会, ハワイ, USA, International conferencePreparation of "mushroom-like" nonspherical polymer particles by controlled/living radical polymerization in aqueous dispersed systemsOral presentation
- The 2010 International Chemical Congress of Pacific Basin Societies (Pacifichem 2010), Dec. 2010, English, 日本化学会, ハワイ, USA, International conferenceEmulsifier-free; organotellurium-mediated living radical emulsion polymerization at high monomer concentrationPoster presentation
- 第16回高分子ミクロスフェア討論会, Nov. 2010, Japanese, 高分子ミクロスフェア研究会, 福井市, Domestic conference有機テルル化合物を用いたスチレンの制御/リビング乳化重合Oral presentation
- 第16回高分子ミクロスフェア討論会, Nov. 2010, Japanese, 高分子ミクロスフェア研究会, 福井市, Domestic conference水媒体不均一重合における滴中での相分離構造を利用した異形高分子微粒子の作製Oral presentation
- 2010年度 色材研究発表会, Nov. 2010, Japanese, 色材協会, 東京都, Domestic conference水媒体不均一系における窒素化合物を触媒として用いた可逆移動触媒重合Poster presentation
- 第16回高分子ミクロスフェア討論会, Nov. 2010, Japanese, 高分子ミクロスフェア研究会, 福井市, Domestic conference感温性を有するイオン液体含有高分子粒子の合成Oral presentation
- 第16回高分子ミクロスフェア討論会, Nov. 2010, Japanese, 高分子ミクロスフェア研究会, 福井市, Domestic conferenceイオン液体中におけるポリスチレン/アルミナ複合粒子の合成Oral presentation
- 2010年度 色材研究発表会, Nov. 2010, Japanese, 色材協会, 東京都, Domestic conferenceイオン液体中におけるアルミナ粒子の合成Poster presentation
- 第16回高分子ミクロスフェア討論会, Nov. 2010, Japanese, 高分子ミクロスフェア研究会, 福井市, Domestic conferenceイオン液体中での分散重合により作製した架橋ポリアクリル酸粒子の水抽出挙動Oral presentation
- 2010年度 色材研究発表会, Nov. 2010, Japanese, 色材協会, 東京都, Domestic conferenceSaPSeP法によるイオン液体含有カプセル粒子の合成Poster presentation
- 第56回高分子研究発表会(神戸), Jul. 2010, Japanese, 高分子学会, 神戸市, Domestic conference超臨界二酸化炭素媒体中における窒素化合物を触媒として用いた制御/リビングラジカル重合(RTCP)による高分子微粒子の合成Oral presentation
- はりま産学交流会 創造例会, Jul. 2010, Japanese, はりま産学交流会, 姫路市, Domestic conference機能性高分子微粒子 イオン液体を利用してInvited oral presentation
- 第56回高分子研究発表会(神戸), Jul. 2010, Japanese, 高分子学会, 神戸市, Domestic conferenceマイクロサスペンション重合により誘起される相分離構造を利用した半球状高分子微粒子の合成Oral presentation
- 第56回高分子研究発表会(神戸), Jul. 2010, Japanese, 高分子学会, 神戸市, Domestic conferenceイオン液体中での分散重合により作製したポリアクリル酸粒子の水抽出挙動Oral presentation
- 43rd IUPAC World Polymer Congress (MACRO2010), Jul. 2010, English, IUPAC, Glasgow; UK, International conferenceEmulsifier-Free; Organotellurium-Mediated Living Radical Emulsion Polymerization: Particle FormationPoster presentation
- 43rd IUPAC World Polymer Congress (MACRO2010), Jul. 2010, English, IUPAC, Glasgow; UK, International conferenceAtom Transfer Radical Polymerization of Acrylic Acid by Use of Supercritical Carbon Dioxide as mediumPoster presentation
- 第48回日本接着学会年次大会, Jun. 2010, Japanese, 日本接着学会, 大阪市, Domestic conference水分散系での二段階制御/リビングラジカル重合による特異なモルフォロジィを有する高分子微粒子の合成Oral presentation
- 第48回日本接着学会年次大会, Jun. 2010, Japanese, 日本接着学会, 大阪市, Domestic conferenceイオン液体中での架橋ポリアクリル酸の合成Oral presentation
- 第59回高分子学会年次大会, May 2010, Japanese, 高分子学会, 横浜市, Domestic conference発芽状の特異形態を有する中空高分子微粒子の生成Poster presentation
- 第59回高分子学会年次大会, May 2010, Japanese, 高分子学会, 横浜市, Domestic conference超臨界二酸化炭素媒体中でのゲルマニウム化合物を触媒として用いた制御/リビングラジカル重合によるポリスチレン粒子の合成Oral presentation
- 平成22年度色材セミナー, May 2010, Japanese, 色材協会, 大阪市, Domestic conference環境適応媒体中での高分子微粒子の創製Invited oral presentation
- 第59回高分子学会年次大会, May 2010, Japanese, 高分子学会, 横浜市, Domestic conferenceヘキサデカンを内包したポリエチレングリコールジメタクリレートカプセル粒子の作製とその熱物性Poster presentation
- 第59回高分子学会年次大会, May 2010, Japanese, 高分子学会, 横浜市, Domestic conferenceイオン液体中での無機/有機複合粒子の合成Poster presentation
- 第59回高分子学会年次大会, May 2010, Japanese, 高分子学会, 横浜市, Domestic conferenceイオン液体を内包した高分子微粒子の合成Poster presentation
- 第59回高分子学会年次大会, May 2010, Japanese, 高分子学会, 横浜市, Domestic conferenceSaPSeP法を利用したイオン液体含有感温性高分子微粒子の合成Poster presentation
- 日本化学会第90春季年会, Mar. 2010, Japanese, 日本化学会, 東大阪市, Domestic conferenceイオン液体中における無機粒子の作製Oral presentation
- ナノ学会 「ナノ構造・物性」部会 第2回研究会, Jan. 2010, Japanese, ナノ学会 「ナノ構造・物性」部会, 神戸市, Domestic conferenceイオン液体を用いた高分子微粒子の創製と機能化[Invited]Invited oral presentation
- 第18回ポリマー材料フォーラム, Nov. 2009, Japanese, 高分子学会, 東京都, Domestic conference窒素化合物を用いたメタクリル酸メチルの制御リビングラジカルマイクロサスペンション重合Poster presentation
- 第73会関西高分子若手研究会, Nov. 2009, Japanese, 高分子学会関西支部, 豊中市, Domestic conference高分子微粒子の機能化〜イオン液体を利用して〜[Invited]Invited oral presentation
- 第18回ポリマー材料フォーラム, Nov. 2009, Japanese, 高分子学会, 東京都, Domestic conferenceSaPSeP法を利用したイオン液体内包導電性カプセル粒子の合成Poster presentation
- 第58回高分子学会討論会, Sep. 2009, Japanese, 高分子学会, 熊本市, Domestic conference開口部を有するミクロンサイズの単分散中空橋架け高分子微粒子の作製Oral presentation
- 第58回高分子学会討論会, Sep. 2009, Japanese, 高分子学会, 熊本市, Domestic conferenceイオン液体媒体下でのコア・シェル構造を有する複合高分子微粒子の合成Oral presentation
- 東海高分子研究会講演会(夏期合宿), Sep. 2009, Japanese, 高分子学会東海支部, 岐阜市, Domestic conferenceイオン液体を利用した機能性微粒子の創製[Invited]Invited oral presentation
- 3rd Asian Symposium on Emulsion Polymerization and Functional Polymeric Microspheres, Sep. 2009, English, ASEPFPM, South Korea, Jeju, International conferencePreparation of Poly(acrylic acid) Particles by Dispersion Polymerization in Ionic LiquidOral presentation
- 3rd Asian Symposium on Emulsion Polymerization and Functional Polymeric Microspheres, Sep. 2009, English, ASEPFPM, South Korea, Jeju, International conferenceMorphology of Block Copolymer Particles Synthesized by Two-step AGET ATRP in Aqueous Dispersed Systems: Effect of Polymerization TemperaturePoster presentation
- 第55回高分子研究発表会(神戸), Jul. 2009, Japanese, 高分子学会関西支部, 神戸市, Domestic conference超臨界二酸化炭素中でのゲルマニウム化合物を用いた制御リビングラジカル分散重合Poster presentation
- 第55回高分子研究発表会(神戸), Jul. 2009, Japanese, 高分子学会関西支部, 神戸市, Domestic conferenceイオン液体中での無機粒子・無機有機複合粒子の合成Oral presentation
- 第55回高分子研究発表会(神戸), Jul. 2009, Japanese, 高分子学会関西支部, 神戸市, Domestic conferenceイオン液体を含有した感温性高分子微粒子の合成Poster presentation
- 第58回高分子学会年次大会, May 2009, Japanese, 高分子学会, 神戸市, Domestic conference各重合温度におけるシード乳化AGET ATRP法によるブロックポリマー微粒子の作製とその異相構造Poster presentation
- 第58回高分子学会年次大会, May 2009, Japanese, 高分子学会, 神戸市, Domestic conference開口部を有するポリスチレンポリエチレングリコールジメタクリレート中空橋架け高分子微粒子の作製Poster presentation
- 第58回高分子学会年次大会, May 2009, Japanese, 高分子学会, 神戸市, Domestic conferenceイオン液体中でのシード分散重合によるポリアクリル酸ポリスチレン複合高分子微粒子の合成Poster presentation
- 第58回高分子学会年次大会, May 2009, Japanese, 高分子学会, 神戸市, Domestic conferenceSaPSeP法を利用したイオン液体内包カプセル粒子の合成Poster presentation
- The 2nd international symposium on advanced particles (ISAP2009), Apr. 2009, English, 第2回先端粒子国際シンポジウム, 横浜市, International conferencePreparation of Nylon-6 Particles in Ionic LiquidsOral presentation
- 高分子材料開発のための俯瞰的シンポジウム, Jan. 2009, Japanese, 京都大学桂キャンパス, Domestic conference機能性高分子微粒子の合成とその応用Invited oral presentation
- 第168回溶融塩委員会, Jan. 2009, Japanese, 神戸大学瀧川記念学術交流会館, Domestic conferenceイオン液体を反応媒体とする高分子微粒子の創製Invited oral presentation
- 2008年度高分子計算機科学研究会・高分子ナノテクノロジー研究会 合同討論会, Dec. 2008, Japanese, 東京工業大学, Domestic conference環境適応型媒体中での高分子微粒子の創製Invited oral presentation
- 第15回高分子ミクロスフェア討論会, Nov. 2008, Japanese, 神戸大学, Domestic conference超臨界CO2中でのポリアクリル酸粒子の合成Oral presentation
- 第15回高分子ミクロスフェア討論会, Nov. 2008, Japanese, 神戸大学, Domestic conferenceイオン液体中でのポリアクリル酸粒子の合成Oral presentation
- Asia Polymer Symposium (APOSYM/2008), Oct. 2008, English, 済南大学(中国), International conferencePreparation of Onion-like Multilayered PiBMA-b-PS Particles by Seeded Emulsion Polymerization with AGET ATRPPoster presentation
- 22th Seminar of Advanced Particle Handling Science, Oct. 2008, English, 大阪工業大学大阪センター, International conferencePreparation of Micron-sized, Monodisperse Functional Hollow Polymer ParticlesInvited oral presentation
- Asia Polymer Symposium (APOSYM/2008), Oct. 2008, English, 済南大学(中国), International conferencePreparation of Micrometer-sized, Monodisperse, Hollow Polystyrene/Poly(ethylene glycol dimethacrylate) Particles with a Single Hole in the ShellPoster presentation
- Asia Polymer Symposium (APOSYM/2008), Oct. 2008, English, 済南大学(中国), International conferencePreparation of Composite Polymer Particles by Seeded Dispersion Polymerization in Ionic LiquidsOral presentation
- Asia Polymer Symposium (APOSYM/2008), Oct. 2008, English, 済南大学(中国), International conferenceEffect of the particle size on the shell formation mechanism of hollow poly(divinyl benzene) particles with multiple holes in the shellPoster presentation
- 第57回高分子学会討論会, Sep. 2008, Japanese, 大阪市立大学, Domestic conferenceイオン液体中での加水分解重合によるナイロン6粒子の合成Oral presentation
- 第57回高分子学会討論会, Sep. 2008, Japanese, 大阪市立大学, Domestic conferenceイオン液体を媒体とした分散重合によるポリアクリル酸粒子の合成Poster presentation
- 第54回高分子研究発表会(神戸), Jul. 2008, Japanese, 兵庫県中央労働センター, Domestic conference水媒体不均一系制御/リビングラジカル重合法による多層構造を有するブロックポリマー微粒子の合成Poster presentation
- 第54回高分子研究発表会(神戸), Jul. 2008, Japanese, 兵庫県中央労働センター, Domestic conferenceイオン液体を内包したカプセル粒子の合成Poster presentation
- Polymer Colloids: From Design to Biomedical and Industrial Applications, Jul. 2008, English, Prague,Institute of Macromolecular Chemistry AS CR, International conferencePreparation of polystyrene/poly(acrylic acid) composite particles by seeded dispersion polymerization in an ionic liquidOral presentation
- 第57回高分子学会年次大会, May 2008, Japanese, 横浜, Domestic conference開口部を有するポリスチレン/ポリエチレングリコールジメタクリレート中空高分子微粒子の作製Poster presentation
- 第57回高分子学会年次大会, May 2008, Japanese, 横浜, Domestic conferenceマイクロサスペンション重合法による開口部を有する中空高分子微粒子の合成Poster presentation
- 関西H&I研究会 第16回研究会, Mar. 2008, Japanese, 岡山, Domestic conferenceイオン液体中での高分子微粒子の創製Invited oral presentation
- 第10回環太平洋高分子国際会議, Dec. 2007, English, 神戸, International conferencePreparation of Composite Polymer ParticlesPoster presentation
- 第10回環太平洋高分子国際会議, Dec. 2007, English, 神戸, International conferenceNitroxide-Mediated Precipitation Polymerization of Styrene inPoster presentation
- 第56回高分子討論会, Sep. 2007, Japanese, 名古屋,日本, Domestic conference水媒体不均一系における原子移動ラジカル重合の速度論Oral presentation
- 第56回高分子討論会, Sep. 2007, Japanese, 名古屋,日本, Domestic conference完全水媒体不均一系原子移動ラジカル重合によるブロックポリマー微粒子の合成とそのモルフォロジィOral presentation
- 第56回高分子討論会, Sep. 2007, Japanese, 名古屋,日本, Domestic conferenceイオン液体中での機能性高分子微粒子の創製Oral presentation
- 第53回高分子研究発表会(神戸), Jul. 2007, Japanese, 神戸, Domestic conference超臨界二酸化炭素媒体中での感温性高分子の合成Poster presentation
- 第1回 日本材料学会分子動力学部門委員会, Jul. 2007, Japanese, 神戸,日本, Domestic conference機能性高分子微粒子の創製とその応用Invited oral presentation
- 第53回高分子研究発表会(神戸), Jul. 2007, Japanese, 神戸, Domestic conference開口部を有する中空橋かけ高分子微粒子の合成Oral presentation
- 第53回高分子研究発表会(神戸), Jul. 2007, Japanese, 高分子学会, 兵庫県中央労働センター,神戸市, Domestic conferenceマイクロサスペンション重合法による開口部を有する高分子微粒子の合成Poster presentation
- 第53回高分子研究発表会(神戸), Jul. 2007, Japanese, 神戸, Domestic conferenceイオン液体中における水溶性高分子微粒子の合成Poster presentation
- 第53回高分子研究発表会(神戸), Jul. 2007, Japanese, 神戸, Domestic conferenceイオン液体中におけるナイロン粒子の合成Poster presentation
- 神戸大学大学院工学研究科機械工学専攻材料物理コロキウム, Jun. 2007, Japanese, 神戸大学, Domestic conference機能性高分子微粒子の合成とその応用Invited oral presentation
- 2007 Gordon Research Conference, Jun. 2007, English, USA, International conferenceCompartmentalization and partitioning effect in microemulsion ATRPOral presentation
- 第56回高分子学会年次大会, May 2007, Japanese, 京都, Domestic conferenceミニエマルション系での原子移動ラジカル重合における銅触媒の分配及びコンパートメンタリゼーション効果Poster presentation
- 第56回高分子学会年次大会, May 2007, Japanese, 京都, Domestic conferenceマイクロエマルション系での原子移動ラジカル重合におけるノニオン性乳化剤の影響Poster presentation
- 第56回高分子学会年次大会, May 2007, Japanese, 京都, Domestic conferenceSaPSeP法による開口部を有する単中空高分子微粒子の作製Poster presentation
- The Spring meeting of the Polymer Society of Korea, Apr. 2007, English, Jeju, Korea, International conferencePreparation of polymer particles in environmentally friendly media[Invited]Invited oral presentation
- 神戸大学東京フェア, Jan. 2007, Japanese, 東京, Domestic conference環境適応型微粒子材料の創製技術の開発Poster presentation
- Max-Planck-Institute of Colloids and Interfaces, Dec. 2006, English, Potsdam, International conferenceInfluence of Emulsifier on Shell Formation of Hollow Polymer ParticlesInvited oral presentation
- 第15回ポリマー材料フォーラム, Nov. 2006, Japanese, 千里ライフサイエンスセンター, Domestic conference相分離自己組織化(SaPSeP)法を用いた高光散乱TiO2含有複合中空高分子微粒子の合成Poster presentation
- 第15回ポリマー材料フォーラム, Nov. 2006, Japanese, 千里ライフサイエンスセンター, Domestic conference相分離自己組織化(SaPSeP)法を用いたマイクロサスペンション重合による単中空高分子微粒子の合成Poster presentation
- 第14回高分子ミクロスフェア討論会, Nov. 2006, Japanese, 繊協ビル8階繊協閣ホール, Domestic conference水媒体不均一系での制御リビングラジカル重合におけるコンパートメンタリゼーション効果Oral presentation
- 第14回高分子ミクロスフェア討論会, Nov. 2006, Japanese, 繊協ビル8階繊協閣ホール, Domestic conferenceイオン液体を媒体とした分散重合による高分子微粒子の作製Oral presentation
- 第14回高分子ミクロスフェア討論会, Nov. 2006, English, 繊協ビル8階繊協閣ホール, Domestic conferenceTEMP-Mediated Cross-linking Radical Polymerization of Styrene and Divinylbenzene in MiniemulsionOral presentation
- 第55回高分子学会討論会, Sep. 2006, Japanese, 富山, Domestic conference超臨界二酸化炭素媒体中での二段階分散重合により作製した複合高分子微粒子のモルフォロジィOral presentation
- 第59回コロイドおよび界面化学討論会, Sep. 2006, Japanese, 北海道, Domestic conference中空微粒子創製法とその応用Invited oral presentation
- 第55回高分子学会討論会, Sep. 2006, Japanese, 富山, Domestic conferenceイオン液体中での分散重合による高分子微粒子の合成Oral presentation
- 第55回高分子学会討論会, Sep. 2006, English, 富山, Domestic conferenceNitroxide-Mediated Radical Dispersion Polymerization of Styrene in Supercritical Carbon DioxideOral presentation
- International Symposium on Radical Polymerization: Kinetics and Mechanism (SML'06), Sep. 2006, English, イタリア, International conferenceEffect of nonionic emulsifier on molecular weight distribution in atom transfer radical polymerization in microemulsionPoster presentation
- International Symposium on Radical Polymerization: Kinetics and Mechanism (SML'06), Sep. 2006, English, イタリア, International conferenceAtom transfer radical polymerization in aqueous heterogeneous systems: Deactivator partitioning between oil and aqueous phaseOral presentation
- 第52回高分子研究発表会(神戸), Jul. 2006, Japanese, 神戸, Domestic conferenceイオン液体中における高分子微粒子の合成Oral presentation
- Asia Polymer Symposium (APOSYM/2006), Jun. 2006, English, 韓国, International conferencePreparation of polystyrene particles in an ionic liquidPoster presentation
- Asia Polymer Symposium (APOSYM/2006), Jun. 2006, English, 韓国, International conferencePolyaddition reaction of epoxy resin with the SaPSeP method for the preparation of micron-sized, cross-linked capsule particleOral presentation
- 第55回高分子学会年次大会, May 2006, Japanese, Nagoya, Japan, Domestic conference超臨界二酸化炭素中でのPDMS-PMMAブロックコポリマーを分散安定剤とするメタクリル酸メチルの分散重合Invited oral presentation
- 第55回高分子学会年次大会, May 2006, Japanese, 名古屋, Domestic conference原子移動制御/リビングラジカルシード乳化重合における温度の影響とシミュレーションOral presentation
- 第55回高分子学会年次大会, May 2006, Japanese, 名古屋, Domestic conference原子移動制御/リビングマイクロエマルション重合における界面活性剤の影響Poster presentation
- 第55回高分子学会年次大会, May 2006, Japanese, Nagoya, Japan, Domestic conference円盤状高分子微粒子の合成とその熱力学的安定性Poster presentation
- 工学フォーラム2005, Dec. 2005, Japanese, 神戸大学, ホテルオークラ神戸, Domestic conference環境適応型微粒子材料の創製技術の開発Poster presentation
- 2005年度 色材研究発表会, Oct. 2005, Japanese, 大阪府立労働センター, Domestic conference高光散乱能を有するTiO2含有複合中空高分子微粒子の合成Oral presentation
- 第54回高分子学会討論会, Sep. 2005, Japanese, 山形大学, Domestic conferenceSaPSeP法を用いた重付加反応によるマイクロカプセルの合成とその応用Oral presentation
- 第51回高分子研究発表会(神戸), Jul. 2005, Japanese, 兵庫県中央労働センター, Domestic conference水媒体不均一系原子移動型制御/リビングラジカル重合Poster presentation
- 第51回高分子研究発表会(神戸), Jul. 2005, Japanese, 兵庫県中央労働センター, Domestic conferenceミクロンサイズの単分散な磁性カプセル粒子の合成Poster presentation
- 2005 Gordon Research conference, Jul. 2005, English, USATilton school, International conferenceSeeded ATRP in aqueous heterogeneous mediumPoster presentation
- 第51回高分子研究発表会(神戸), Jul. 2005, Japanese, 兵庫県中央労働センター, Domestic conferenceSaPSeP法による単中空高分子微粒子の合成Poster presentation
- 第51回高分子研究発表会(神戸), Jul. 2005, English, 兵庫県中央労働センター, Domestic conferencePendant Reactivities and Crosslinking in TEMPO-Mediated Radical Copolymerization of Styrene and Divinylbenzene in Miniemulsion and BulkPoster presentation
- 2005 Gordon Research conference, Jul. 2005, English, USATilton school, International conferenceMicroemulsion atom transfer radical polymerizationPoster presentation
- 第43回日本接着学会年次大会, Jun. 2005, Japanese, 関西大学, Domestic conference超臨界二酸化炭素媒体中での制御/リビングラジカル重合を用いたブロックポリマー微粒子の合成Poster presentation
- 第43回日本接着学会年次大会, Jun. 2005, Japanese, 関西大学, Domestic conferenceSaPSeP法を用いた重付加反応による硬化剤内包型マイクロカプセルの調整Poster presentation
- 第54回高分子学会年次大会, May 2005, Japanese, 横浜, Domestic conference懸濁重合法による高光散乱性高分子微粒子の合成Poster presentation
- 第54回高分子学会年次大会, May 2005, Japanese, 横浜, Domestic conference開口部を有する中空高分子微粒子の合成Poster presentation
- 第54回高分子学会年次大会, May 2005, Japanese, 高分子学会, 横浜国際会議場, Domestic conferenceSaPSeP法によるヘキサデカン内包中空高分子微粒子の作製Poster presentation
- 第2回ミクロスフェア国際討論会 2005, 2005, English, 不明, 不明, International conferencePreparation of micron-sized, cured epoxy resin capsules by polyaddetion reaction using the SaPSeP methodOral presentation
- 第2回ミクロスフェア国際討論会 2005, 2005, English, 不明, 不明, International conferenceNitroxide-Mediated Controlled/Living Free Radical Copolymerization of Styrene and Divinylbenzene in Aqueous MiniemulsionOral presentation
- 工学フォーラム2004, Dec. 2004, Japanese, 神戸大学, 神戸市産業振興センター, Domestic conference環境適応型微粒子材料の創製技術の開発Poster presentation
- International Symposium on Polymers in Dispersed Media (PDM 2004), Apr. 2004, English, Lyon, International conferenceProduction of cured epoxy resin particles having one hollow by polyaddition reactionPoster presentation
- 第13回高分子ミクロスフェア討論会, 2004, Japanese, 不明, 不明, Domestic conference超臨界二酸化炭素を重合媒体とするシード重合による複合高分子微粒子の合成とその異相構造Oral presentation
- 第50回高分子研究発表会, 2004, Japanese, 不明, 神戸, Domestic conference単中空高分子微粒子のシェル層形成に及ぼす乳化剤の影響Oral presentation
- 第13回高分子ミクロスフェア討論会, 2004, Japanese, 不明, 不明, Domestic conference水媒体不均一系制御/リビングラジカル重合法を用いたブロックコポリマー微粒子の合成における銅粉及び重合温度の影響Oral presentation
- 第53回高分子学会年次大会, 2004, Japanese, 不明, 不明, Domestic conference水媒体不均一系制御/リビングラジカル重合による異相構造を有する高分子微粒子の合成Oral presentation
- 機能分子化学教室 新化学セミナー(第16回), 2004, Japanese, 不明, 不明, Domestic conference「中空高分子微粒子の創製とその応用」-インテリジェント化の追求-Oral presentation
- 第13回高分子ミクロスフェア討論会, 2004, Japanese, 不明, 不明, Domestic conferenceミニエマルション重合法による磁性高分子微粒子の合成Oral presentation
- 第53回高分子学会年次大会, 2004, Japanese, 不明, 不明, Domestic conferenceミクロンサイズの単分散な中高分子微粒子の合成Invited oral presentation
- International Symposium on Polymers in Dispersed Media, 2004, English, 不明, 不明, International conferenceProduction of cured epoxy resin particles having one hollow by polyaddition reactionOral presentation
- International Symposium on Polymers in Dispersed Media, 2004, English, 不明, 不明, International conferencePreparation of block copolymer particles by two-step atom transfer radical polymerization in aquious mediumOral presentation
- Asia Polymer Symposium(APOSYM/2004), 2004, English, 不明, 不明, International conferenceInfluence of Emulsifier on Shell Formation of Hollow Polymer Particles by SAPSeP MethodOral presentation
- 第52回高分子学会年次大会, 2003, Japanese, 高分子学会, 山口大学, Domestic conference軟X線顕微鏡を利用した多層構造を有する複合高分子微粒子の観察Oral presentation
- 第52回高分子学会年次大会, 2003, Japanese, 高分子学会, 山口大学, Domestic conference超臨界二酸化炭素媒体中でのアクリロニトリルーブタジエン共重合体粒子の合成Oral presentation
- 第49回高分子研究発表会, 2003, Japanese, 高分子学会関西支部, 兵庫県民会館, Domestic conference重付加反応による中空高分子微粒子の合成Oral presentation
- 第12回ポリマー材料フォーラム(2003), 2003, Japanese, 高分子学会, 千里ライフサイエンスセンター, Domestic conference可変形状を有するミクロンサイズの単分散な中空粒子の作製Oral presentation
- 第41回日本接着学会年次大会, 2003, Japanese, 日本接着学会, 関西大学, Domestic conferenceへこみを有するポリスチレン/ポリメタクリル酸メチル複合微粒子の異相構造Oral presentation
- 第49回高分子研究発表会, 2003, Japanese, 高分子学会関西支部, 兵庫県民会館, Domestic conferenceサブミクロンサイズの単中空橋架け高分子微粒子の合成Oral presentation
- Gordon Research Conference, 2003, English, 未記入, 未記入, International conferenceVarious Factors Affecting on the Production of PS/PBMA Composite Particles having Hamburger-like Morphology by Seeded PolymerizationOral presentation
- Gordon Research Conference, 2003, English, 未記入, 未記入, International conferenceProduction of Poly(Methyl Methacrylate) Particles by Dispersion Polymerization in the Presence of Trimethylsiloxy Terminated Poly(Dimethylsiloxane) in Supercritical Carbon DioxideOral presentation
■ Research Themes
- 日本学術振興会, 科学研究費助成事業, 基盤研究(C), 神戸大学, 01 Apr. 2020 - 31 Mar. 2023微細多孔質セルロース中空粒子の創製と高機能化本研究では,一つのカプセル材で水溶性/油溶性物質どちらも内包可能な新規なカプセル材料の創出を目的に,セルロース粒子に特に中空構造の導入を目指している。初年度は,特に中空構造を有するセルロース粒子の作製法の確立を目指した。2年度である今年度は,微細構造をカプセル壁に有したセルロース中空粒子作製に取り組み,セルロースの析出挙動について検討を行った。 1. セルロースの析出挙動:ILとDMFからなるセルロース懸濁滴(媒体はヘキサン)を用いて,すべての溶剤を混和する1-ブタノールと,ILだけはほとんど溶解しないアセトンをセルロース析出溶媒として用いた。ILとDMFがそれらと混和すると同時に,セルロースが析出し微細構造を形成する。これまで電子顕微鏡にて観察してきたセルロース粒子は,表面に膜を張っていたが,薄膜形成がセルロース析出時なのか,乾燥時なのかはっきりしていなかった。本検討により,膜形成が析出時であることが明らかとなった。 2. セルロースの化学修飾(フッ素成分の導入):無水メタクリル酸と多孔質セルロース粒子のヒドロキシ基を反応させることで、メタクリロイル基が導入されたセルロース粒子を作製し,次に含フッ素チオールとのチオール・エン反応を実施し、フッ素化セルロース粒子を作製した。FT-IR やEDXを用いて,メタクリロイル基やフッ素基の導入を確認した。また,2段階の修飾反応過程での微細構造の消失を懸念したが,凍結乾燥後の未修飾の微細セルロース粒子の比表面積は140 m2/g程度であったのに対し,同程度を維持していた。微細構造は乾燥にて簡単に破壊され緻密粒子となるが,興味深いことに,フッ素化セルロース粒子は自然乾燥においても100m2/g程度の高い比表面積を保持していた。接触角測定でも強い疎水性を示した。
- 日本学術振興会, 科学研究費助成事業, 基盤研究(A), 神戸大学, 01 Apr. 2019 - 31 Mar. 2023難治癌バイオマーカー同定のためのエクソソーム自動センシングアレイシステムの開発
- 科学研究費補助金/基盤研究(B), Apr. 2017 - Mar. 2020, Principal investigatorCompetitive research funding
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research, Grant-in-Aid for Scientific Research (B), Kobe University, 01 Apr. 2013 - 31 Mar. 2018Development of Controlled/Living Radical Polymerization in Aqueous Dispersed Systems and Synthesis of Functional Polymer ParticlesWe have tried to apply controlled/living radical polymerization (CLRP), which has been so far mainly developed in homogeneous systems, to aqueous dispersed systems and gotten better harvests than expected. Especially, development of emulsifier-free emulsion polymerization, synthesis of high molecular weight (>10e6), monodisperse polystyrene particles, Syntheses of Janus type nonspherical polymer particles by applying CLRP at the limited locus of polymerization at a particle surface, high performance heat storage microcapsule particles, micrometer-size hydrophilic polymer particles without submicrometer-size byproduct particles, and polymer particles having biosensor functionality have been successfully conducted. These results will contribute to overcoming the long-standing problem and creation of novel functional polymer particles.
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research (B), Grant-in-Aid for Scientific Research (B), Kobe University, 01 Apr. 2014 - 31 Mar. 2017Seeded dispersion polymerization of ionic liquid monomer was carried out in the presence of poly(methylmethacrylate) (PMMA) as seed and composite particles with poly(ionic liquid) (PIL) were obtained. Moreover, we showed that anion exchange of the composite particles can be used to modify the properties of only the PIL component of the composite particles. PIL particles with a single-hollow are also prepared by suspension polymerization from monomer droplets consisting of the ionic liquid monomer, ethylene glycol dimethacrylate, and n-butyl acetate. The obtained particles can be changed from hydrophobic to hydrophilic by anion exchange. Moreover, Janus particles with two hemispheres having different stabilizers, a polystyrene (PS) phase stabilized by poly(acrylic acid) and a PMMA phase stabilized by poly(vinyl pyrrolidone), were able to be synthesized. The facile formation of the colloidal chains via hydrogen bonding interaction between different stabilizers were demonstrated.Competitive research funding
- 科学研究費補助金/基盤研究(B), Apr. 2014 - Mar. 2017, Principal investigatorCompetitive research funding
- 学術研究助成基金助成金/国際共同研究加速基金(国際共同研究強化), 2016 - 2017, Principal investigatorCompetitive research funding
- 科学研究費補助金/萌芽研究, Apr. 2012 - Mar. 2014, Principal investigatorCompetitive research funding
- 研究成果最適展開支援プログラム フィージビリティスタディステージ 探索タイプ, 2013, Principal investigatorA-STEP「高次構造セルロース微粒子材料の創成とその物性評価」Competitive research funding
- 科学研究費補助金/基盤研究(B), 2011, Principal investigatorCompetitive research funding
- 科学研究費補助金/基盤研究(A), 2010Competitive research funding
- 科学研究費補助金/挑戦的萌芽研究, 2009, Principal investigatorCompetitive research funding
- 科学研究費補助金/萌芽研究, 2008Competitive research funding
- 科学研究費補助金/若手研究(B), 2007, Principal investigatorCompetitive research funding
- 科学研究費補助金/萌芽研究, 2005Competitive research funding
- 科学研究費補助金/基盤研究(A), 2005Competitive research funding
- 科学研究費補助金/若手研究(B), 2005, Principal investigatorCompetitive research funding
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research, Grant-in-Aid for Scientific Research (A), Kobe University, 2002 - 2004Preparation of hollow polymer particles encapsulating functional substance and its applicationPolymer particles with hollow structures have gotten a lot of attention in many industrial fields. Such particles are used as microcapsules, weight-saving or thermal insulation agents, and are applied to hiding or opacifying agents in coating and molding compositions because of their high light-scattering ability. We had succeeded in preparing micron-sized, monodisperse, crosslinking polymer particles having a single hollow at the center by seeded polymerization. Similar hollow polymer particles were produced by suspension polymerization for divinylbenzene (DVB)/toluene droplets dissolving polystyrene though they were polydisperse. The formation of the hollow structure is based on the self- assembling of phase separated polymer at the interface of the droplet. The method is named the Self-assembling of Phase Separated Polymer (SaPSeP) method. In this research, in order to clarify the formation mechanism of hollow particles by the SaPSeP method in more detail, the effects of phase separation of PDVB in the droplets, viscosity within the droplet and its size on the formation of the hollow structure were discussed. The phase separation in the early stage was required point for the formation of the hollow structure. Since the viscosity in the droplet is low at the low conversion, the PDVB can move and adsorb at the interface of the droplet. The mobility of PDVB microgels after the phase separation in polymerizing droplet was important factor for the formation of the hollow structure. The SaPSeP method was developed to produce composite particles encapsulating hinokitiol or magnetite. Moreover, the method was applied to the polyaddition reaction in a suspension system. The polyaddition reaction system satisfied the required conditions for the preparation of hollow particle by the SaPSeP method. In actual, cured epoxy resin particles having one hollow at the center were successfully prepared after evaporation of toluene.
- 日本学術振興会, 科学研究費助成事業, 若手研究(B), 神戸大学, 2002 - 2003水媒体系化学酸化重合法による機能性高分子微粒子の創製当研究室では一貫して機能性高分子微粒子の合成とその応用に関する研究に取り組んでいるが,そのほとんどがビニルモノマーを対象とし,乳化重合,分散重合,懸濁重合を駆使して行ってきた。さらに,非ビニルモノマーに着目し,すでにサブミクロンサイズのポリスチレン微粒子の水分散系で非ビニルモノマーであるグルタルアルデヒドのアルドール縮合重合を行い,粒子表面にアルデヒド基を有する高分子微粒子の新合成法を確立し,国内外で高い評価を受けている。本研究の目的はアニリンなどの非ビニルモノマー水媒体化学酸化重合法により新しい機能性高分子微粒子合成法を確立することである。さらに,エポキシ基,イソシアネート基などを有する非ビニルモノマーの重付加反応による機能性微粒子の合成も取り上げ,非ビニルモノマーの水媒体における機能性高分子微粒子の創製を目指す。 本年度は,非ビニルモノマーとしてエポキシ樹脂とアミンによる重付加反応を利用した機能性微粒子の合成を検討した。具体的には,当研究室で先に提起している相分離を利用した中空化技術をエポキシ樹脂とアミンに適用し,エポキシ樹脂による非ビニル中空粒子の合成に成功した。これらの結果は,水媒体系における非ビニルモノマーによる機能性高分子微粒子の合成法に関して重要な結果であり,現在論文作成中である。さらに,昨年度の検討課題である化学酸化シード分散重合から作製された導電性を有するミクロンサイズの単分散な中空粒子の合成法に関しても,まもなく投稿予定である。
- 日本学術振興会, 科学研究費助成事業, 萌芽研究, 神戸大学, 2001 - 2002磁性を有するミクロンサイズの単分散高分子微粒子の創製本研究では申請者らが既に合成に成功しているミクロンサイズで単分散な中空高分子微粒子合成技術をもとに,磁性体が強固な高分子でカプセル化され,かつ単分散であるという磁性体含有機能性複合微粒子の合成方法を確立することを目指している。昨年度は,申請者らが独自に提起している動的膨潤法(DSM)と呼称する新規なモノマー吸収法を用いてミクロンサイズの単分散滴を作製し,そのシード重合を行うことにより得られるミクロンサイズの単分散中空高分子微粒子を用い,ペンタカルボニル鉄を中空部に含有させて200℃で熱処理を行うことにより,磁性粒子の合成を支持する結果が得られている。 本年度は,得られた磁性を有する複合粒子の詳細な解析を行った。具体的には内部異相構造の解明には超薄切片を作製し,電子顕微鏡を用いて観察した結果,すべての粒子の中空粒子内壁に処理前には観察されなかったコントラストの高い部分が観察され,X線回折及びX線マイクロアナライザーによる元素分析の結果,磁性体であるFe_3O_4であることがわかった。さらに熱重量分析の結果より,粒子重量の49%を占める量の磁性体を含有していることが明らかになった。また,得られた磁性粒子表面にが多量の残存ビニル基を有していることを利用し,濃硫酸で処理することにより粒子表面に硫酸基を導入することを検討した。その結果,X線光電子分光法,及び等温滴定型熱量計により硫酸基が粒子表面上に0.7μmol/m^2と高効率に導入されていることを明らかにした。
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research, Grant-in-Aid for Scientific Research (B), Kobe University, 2000 - 2001Development of Production of Functional Polymer Particles in Supercritical Carbon DioxideRecently, in addition to water, there have been increasing interests in supercritical carbon dioxide (scCO_2) as environmentally favorable media. The use of scCO_2 as medium for polymerizations has several potential advantages : low cost, low toxicily, eases of medium removal and recycling, and marked variations of solubility power, viscosity and polarity by relatively small changes in temperature and pressure without altering medium composition. The papers describing the dispersion polymerization of vinyl monomers such as methyl methacrylate (MMA) and styrene in scCO_2 have been published in the past eight years. Some fluorinated polymers and poly(dimethylsiloxane) (PDMS)-based polymers have been identified as being soluble in CO_2 or CO_2-philic and have been used as colloidal stabilizers, and there has been increasing interest on the colloidal stabilizers which are effective in scCO_2. In general, PDMS-based polymers may have advantages over fluorinated polymers from the viewpoints that PDMS-based polymers are much less expensive and their solubility in conventional organic solvents makes the characterization of the products obtained easy. In this research, PMMA particles could be produced by dispersion polymerization of MMA in scCO_2 using PDMS-based azoinitiator as inistab (initiator + stabilizer). Production of PMMA particles by the dispersion polymerization of MMA in scCO_2 in the presence of amino propyl terminated PDMS as colloidal stabilizer was also succeeded. Moreover, polydivinylbiphenyl particles were produced by precipitation polymerization of divinylbiphenyl without any stabilizer in scCO_2 at ca. 30 MPa for 24 h at 65℃. The effects of initiation rate of polymerization on the conversion, the fluidity of powder, the degree of coagulation/ the amount of low molecular weight by-products, and the amount of vinyl groups in the particles were examined.
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