2021/08/06 更新

写真a

ヤマウチ タケシ
山内 健
YAMAUCHI Takeshi
所属
教育研究院 自然科学系 生産デザイン工学系列 教授
自然科学研究科 材料生産システム専攻 教授
工学部 工学科 教授
職名
教授
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外部リンク

学位

  • 博士(農学) ( 1994年3月   筑波大学 )

研究キーワード

  • Functional Materials

  • 人工筋肉

  • センサ・アクチュエータ

  • バイオTRIZデータベース

  • バイオミメティックス

  • 材料科学

研究分野

  • ナノテク・材料 / ナノ材料科学

  • 人文・社会 / 科学教育

  • ものづくり技術(機械・電気電子・化学工学) / バイオ機能応用、バイオプロセス工学

  • 情報通信 / 情報学基礎論

  • ナノテク・材料 / 構造材料、機能材料

経歴(researchmap)

  • 京都大学   エネルギー理工学研究所   客員准教授

    2009年4月 - 2010年3月

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  • レディング大学 バイオミメティックセンター 研究員

    2000年 - 2001年

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経歴

  • 新潟大学   工学部 工学科   教授

    2017年4月 - 現在

  • 新潟大学   自然科学研究科 材料生産システム専攻   教授

    2010年4月 - 現在

  • 新潟大学   自然科学研究科 材料生産システム専攻   教授

    2010年4月 - 現在

  • 新潟大学   材料開発工学   教授

    2010年4月 - 2017年3月

  • 新潟大学   自然科学研究科 材料生産システム専攻   准教授

    2004年4月 - 2010年3月

学歴

  • 筑波大学

    - 1994年

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  • 筑波大学   農学研究科   応用生物化学

    - 1994年

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    国名: 日本国

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  • 茨城大学   理学部   化学

    - 1989年

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    国名: 日本国

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  • 茨城大学

    - 1989年

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所属学協会

 

論文

  • Hyaluronic acid-poly(vinyl alcohol) composite cryo-gel for biofunctional material application 査読

    山内 健

    Polymers for Advanced Technologies   2018年10月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  • Logic gate aggregation of poly (N-isopropylacrylamide) nanogels with catechol substituents that respond to body heat 査読

    山内 健

    Polymer Journal   50   503 - 510   2017年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  • Graphene Materials, A Novel Grafting of Polymers onto the Surface of Graphene Oxide 査読

    山内 健

    Graphene Materials   1 - 25   2017年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  • Fabrication of a poly(dimethylsiloxane) microstructured surface imprinted from patterned silicon wafer with a self-cleaning property 査読

    Shingo Tamesue, Eri Takahashi, Shunsuke Kosugi, Kazuhiro Fukami, Tetsu Mitsumata, Norio Tsubokawa, Tetsuo Sakka, Takeshi Yamauchi

    Polymer Journal   48 ( 7 )   835 - 838   2016年7月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    A study was conducted to fabricate a microstructure on a poly(dimethylsiloxane) (PDMS) surface using a porous silicon wafer as a mold. The microstructured PDMS surfaces were deposited with gold and imaged using scanning electron microscopy (SEM). The average height and width of the microrods measured using scanning electron microscopy imaging were 10 and 8 μm. The results show that the water contact angle was 103° on the flat surface and 131° on the microstructured surface, resulting in the microstructure increased hydrophobicity.

    DOI: 10.1038/pj.2016.34

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  • Highly Tolerant and Durable Adhesion between Hydrogels Utilizing Intercalation of Cationic Substituents into Layered Inorganic Compounds 査読

    Shingo Tamesue, Kento Yasuda, Shingo Noguchi, Tetsu Mitsumata, Takeshi Yamauchi

    ACS MACRO LETTERS   5 ( 6 )   704 - 708   2016年6月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:AMER CHEMICAL SOC  

    Adhering hydrogel systems are important particularly in the medical field because they can be used as adhesives cross linking between living tissues. In this research, hydrogels including cationic substituents prepared via free-radical polymerization were brought into contact after applying an aqueous dispersion of the layered inorganic compound Micromica to their surfaces. As a result, the hydrogels adhered to each other due to the intercalation of cationic substituents included in the gel networks into the interlayers of Micromica. As the water content ratio of hydrogels decreased, the adhesive strength came to be higher, and finally the adhesively bonded joint supported a tensile load of 10 kg. Moreover, it was confirmed that the adhered hydrogels have high tolerance toward various environments, such as high or low temperatures and solvents.

    DOI: 10.1021/acsmacrolett.6b00337

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  • Photoelectric properties of C-60-poly(ethylene glycol) and poly(3,4-ethylenedioxythiophene) composite gel prepared via a low-temperature organic-solvent process 査読

    Zhang Huiqiu, Masaru Ichinose, Hideaki Takahashi, Shingo Tamesue, Tetsu Mitsumata, Masayuki Yagi, Norio Tsubokawa, Takeshi Yamauchi

    POLYMER JOURNAL   48 ( 2 )   163 - 168   2016年2月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:NATURE PUBLISHING GROUP  

    C-60 fullerene derivatives, which are formed by grafting polymer chains on a C-60 fullerene, can improve the solubility of C-60 in solvents. These derivatives are able to composite with various functional polymers to form interpenetrating network gel structures. In this study, a composite gel composed of the C-60 fullerene derivatives and poly(3,4-ethylenedioxythiophene)(PEDOT) was prepared using a low-temperature organic-solvent process, and its photoelectric properties were evaluated. Furthermore, the poly(ethylene glycol) (PEG) radicals were successfully trapped in the fullerene (C-60), which worked as a cross-linking point to yield the C-60-PEG gel. Then, PEDOT was composited with the gel using chemical oxidative polymerization to form the C-60-PEG/PEDOT gel. The structure of the film prepared using this composite material was identified. The C-60-PEG/PEDOT film had an amorphous network structure and the UV response was much higher than that of the C-60-PEG gel. In addition, it was estimated that PEDOT was synthesized inside the C-60-PEG gel and formed nanoscale junctions between C-60 and PEDOT, which was beneficial for the movement of electrons and holes. The photocurrent was observed by irradiating the C-60-PEG/PEDOT gel electrode with UV or simulated sunlight. The power conversion efficiency (PCE) was calculated as 1.2 x 10(-3)%. Therefore, it is expected that the C-60-PEG/PEDOT material is applicable for the photoelectric field, such as solar cells.

    DOI: 10.1038/pj.2015.65

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  • Synthesis of Monodisperse Hydrophobic Silicone Particles in the Submicron Size 査読

    山内 健

    Journal of the Japan Society of Colour Material   89 ( 4 )   107 - 112   2016年

  • Various Actuating Motions of Conducting Polymers Actuators on Inorganic Conductive Substrate Formed from Polypyrrole and Gold 査読

    Shingo Tamesue, Genki Endo, Ryota Ishizaki, Tetsu Mitsumata, Norio Tsubokawa, Takeshi Yamauchi

    CHEMISTRY LETTERS   44 ( 12 )   1700 - 1702   2015年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:CHEMICAL SOC JAPAN  

    In order to create more flexible and robust soft actuators, organic/inorganic hybrid actuating fibers were prepared by coating gold fibers in polypyrrole using electropolymerization. The linear, coiled, and helical hybrid fibers were prepared by deforming gold fibers in advance. The obtained fibers exhibit various actuating motions, such as bending, stretching, and rotating motions, due to shrinking and expanding of polypyrrole by doping and de-doping of lithium cations. Merit of the actuating fibers prepared in this research is that the fibers are thin and can be easily combined. Hence, the actuating forces of the fibers caused by doping and de-doping can be amplified by combining the fibers. As a result, heavier weights could be lifted, proportional to the number of fibers combined.

    DOI: 10.1246/cl.150851

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  • Preparation of poly(N-isopropylacrylamide)-terminated carbon nanotubes and determining their aggregation properties in response to infrared light and heating 査読

    Shingo Tamesue, Suguru Hasegawa, Ryota Ishizaki, Kumi Hashimoto, Tetsu Mitsumata, Norio Tsubokawa, Takeshi Yamauchi

    POLYMER JOURNAL   47 ( 10 )   709 - 712   2015年10月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:NATURE PUBLISHING GROUP  

    DOI: 10.1038/pj.2015.47

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  • Preparation of Porous Poly(pyrrole) Utilizing Agar Particles as Soft Template and Evaluation of Its Actuation Property 査読

    Kentaro Obata, Shingo Tamesue, Kumi Hashimoto, Tetsu Mitsumata, Norio Tsubokawa, Takeshi Yamauchi

    MACROMOLECULAR MATERIALS AND ENGINEERING   300 ( 8 )   766 - 771   2015年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:WILEY-V C H VERLAG GMBH  

    Porous poly(pyrrole) (PPy) films are prepared by utilizing agar particles (APs) of various average diameters as templates. The size of the APs can be regulated by the concentration of agar during preparation, and these APs can be removed easily from PPy films by heating up to 90 degrees C after formation of the films by electropolymerization because agar shows a thermally reversible sol-gel transition. The pores in the surface of PPy films can be controlled by the size of APs utilized as templates. The porous PPy films have higher mechanical strength and exhibit the more dynamic actuating behavior than the flat PPy films. Moreover, spring-like actuating motion is induced by the presence of pores in the surface of helically shaped PPy films.

    DOI: 10.1002/mame.201500047

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  • Easy preparation and characterization of conducting polymer-low molecular weight organogel system 査読

    Rie Yamazaki Kuwahara, Hodaka Yamagishi, Kurni Hashimoto, Shingo Tamesue, Takeshi Yamauchi, Norio Tsubokawa

    POLYMER   61   99 - 107   2015年3月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:ELSEVIER SCI LTD  

    Novel organogel system was successfully prepared from organically dispersed polyaniline (PANI) and a low molecular weight organogel system. Organogelator, consisting of cholesteryl hydrogen succinate (CHS) and 1,10-diaminodecane, and organically well-dispersible PANI were synthesized. PANI-containing toluene gels showed thermal reversibility and thixotropic behavior. Viscoelastic measurements demonstrated that PANI-containing toluene gels show rapid and repeated thixotropic behavior. A ballpoint pen refill was packed with PANI-containing toluene gel just like a gel ink, lines similar to the ones produced by ballpoint pen were successfully produced. In addition, PANI-organogelator composites of arbitrary shape were easily prepared by means of toluene evaporation from toluene gel. "Dried" PANI composites showed electrical conductivity. Compared with the neat PANI, the electrical conductivity of the PANI-organogelator composite is hardly affected by about 10 weight% of organogelator in the composite. (C) 2015 Elsevier Ltd. All rights reserved.

    DOI: 10.1016/j.polymer.2014.12.059

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  • Effect of Plasticizer on the Magnetoelastic Behavior for Magnetic Polyurethane Elastomers 査読

    Yukio Kimura, Shunta Kanauchi, Mika Kawai, Tetsu Mitsumata, Shingo Tamesue, Takeshi Yamauchi

    CHEMISTRY LETTERS   44 ( 2 )   177 - 178   2015年2月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:CHEMICAL SOC JAPAN  

    Magnetic polyurethane elastomers containing various plasticizers were synthesized, and the effect of plasticizers on the magnetoelastic behavior has been investigated. The storage modulus for magnetic elastomers at 0 mT decreased with plasticizer content, whereas the storage modulus at 500 mT dramatically increased. The increment in the storage modulus by magnetic fields increased with plasticizer content indicating a well-developed chain structure of magnetic particles. It was found that the on-field storage modulus can be scaled by the off-field modulus independently of the kind of plasticizers.

    DOI: 10.1246/cl.140932

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  • Grafting of polymers onto graphene oxide by cationic and anionic polymerization initiated by the surface-initiating groups 査読

    Kazuhiro Nagata, Takashi Kawahara, Kumi Hashimoto, Kazuhiro Fujiki, Shingo Tamesue, Takeshi Yamauchi, Norio Tsubokawa

    COMPOSITE INTERFACES   22 ( 1 )   25 - 37   2015年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:TAYLOR & FRANCIS LTD  

    The grafting of polymers onto graphene oxide (GO) was achieved by two process: (1) cationic polymerization initiated by carboxyl (COOH) groups on GO and (2) anionic alternating copolymerization of epoxides with cyclic acid anhydrides initiated by potassium carboxylate (COOK) groups on GO. The cationic polymerizations of isobutyl vinyl ether and N-vinylcarbazole were successfully initiated by COOH groups on GO to give the corresponding polymer-grafted GO. The cationic polymerization was considered to be initiated by proton addition from COOH groups to monomer and propagation of polymer cation proceeds with carboxylate anion as a counter ion. It was found that the corresponding polymer was successfully grafted onto GO based on the termination reaction of growing polymer cation and surface counter carboxylate anion. On the other hand, the anionic ring-opening alternating copolymerization of epoxide and cyclic acid anhydrides were also initiated by COOK groups on GO, which were previously introduced onto GO by the neutralization of COOH groups with KOH. During the anionic ring-opening copolymerization of styrene oxide (SO) with phthalic anhydride (PAn) and maleic anhydride (MAn), the corresponding polyesters, poly(SO-alt-PAn) and poly(SO-alt-MAn), were successfully grafted onto GO, based on the propagation of the polyesters from COOK groups. The grafting of polymers onto GO during the above cationic and anionic polymerizations was confirmed by thermal decomposition gas chromatogram/mass spectrum. The untreated GO in THF was immediately precipitated within 15min. On the contrary, these polymer-grafted GOs gave stable dispersions in THF and no precipitation of polymer-grafted GOs was observed even after oneweek.

    DOI: 10.1080/15685543.2015.982482

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  • バイオTRIZを活用した酵素複合導電性高分子の作製とバイオセンサへの応用 査読

    山内 健, 網田英里子, 鈴木貴司, 為末真吾, 三俣哲, 坪川紀夫, 小林秀敏

    材料試験技術   60 ( 3 )   159 - 163   2015年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

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  • Easy preparation of graphene-based conducting polymer composite via organogel 査読

    山内 健

    Colloid and Polymer Science   1 - 11   2015年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1007/s00396-015-3539-2

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  • 再現HAZ鋼材の4点曲げ疲労き裂進展試験 査読

    小林秀敏, 誉田登, ジョイ・ア・カ・ステプ, 堀川敬太郎, 山内健

    材料   64 ( 4 )   323 - 329   2015年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.2472/jsms.64.323

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  • Modification of dispersibility of nanodiamond by grafting of polyoxyethylene and by the introduction of ionic groups onto the surface via radical trapping 査読

    I. Cha, K. Hashimoto, K. Fujiki, T. Yamauchi, N. Tsubokawa

    MATERIALS CHEMISTRY AND PHYSICS   143 ( 3 )   1131 - 1138   2014年2月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:ELSEVIER SCIENCE SA  

    To improve the dispersibility of polycrystalline nanodiamond (ND) in solvents, the grafting of polymers and introduction of ionic groups onto ND surface via radical trapping by ND surface were investigated. The grafting of polyoxyethylene (POE) onto ND surface by trapping of POE radicals formed by the thermal decomposition of POE macro azo-initiator (Azo-POE) was examined. The polymer radicals formed by the thermal decomposition of Azo-POE were successfully trapped by ND surface to give POE-grafted ND. The effect of temperature on the grafting of POE onto ND was discussed. In addition, the introduction of cationic protonated amidine groups onto ND was achieved by the trapping of radicals bearing protonated amidine groups formed by thermal decomposition of 2,2'-azobis(2-methylpropionamidine)dihydrochloride (AMPA). The anionic carboxylate groups was introduced onto ND surface by the trapping of the radicals bearing carboxyl groups formed by thermal decomposition of 4,4'-azobis(4-cyonovaleric acid) (ACVA) followed by the treatment with NaOH aqueous solution. The dispersibility of ND in water was remarkably improved by the grafting of POE, based on the steric hindrance of polymer chains and by the introduction of ionic groups, based on the ionic repulsion, onto ND surface. (C) 2013 Elsevier B.V. All rights reserved.

    DOI: 10.1016/j.matchemphys.2013.11.013

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  • Grafting of polymers onto graphene oxide by trapping of polymer radicals and ligand-exchange reaction of polymers bearing ferrocene moieties 査読

    I. Cha, Y. Yagi, T. Kawahara, K. Hashimoto, K. Fujiki, S. Tamesue, T. Yamauchi, N. Tsubokawa

    COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS   441   474 - 480   2014年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:ELSEVIER SCIENCE BV  

    It was found that graphene oxide (GO) acts as a strong radical scavenger and undergoes a ligand-exchange reaction with ferrocene. Then, the grafting of polymers onto GO was examined by two processes: (1) trapping of polymer radicals by GO and (2) ligand-exchange reaction of polycondensed aromatic rings of GO with ferrocene moieties of a copolymer. It was found that poly(ethylene glycol) (PEG) radicals formed by thermal decomposition of Azo-PEG, which contains thermally decomposable azo linkage in the main chain, were successfully trapped by GO to give PEG-grafted GO: the percentage of PEG grafting was determined to be 15.4%. On the other hand, by heating of GO with copolymers containing vinyl ferrocene (Vf) moieties, such as poly(Vf-co-methyl methacrylate) and poly(Vf-co-styrene), in the presence of AlCl3 and Al powder as catalyst, the corresponding copolymer was grafted onto the GO based on the ligand-exchange reaction of ferrocene moieties of these copolymers with polycondensed aromatic rings of GO: the percentage of grafting of poly(Vf-co-methyl methacrylate) onto GO reached to 54.2%. The grafting of these polymers onto the GO surface was confirmed by XRD and thermal decomposition GC-MS. PEG-grafted and poly(Vf-co-MMA)-grafted GO gave a stable dispersion in organic solvents of grafted polymer. (C) 2013 Elsevier B.V. All rights reserved.

    DOI: 10.1016/j.colsurfa.2013.10.002

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  • 純アルミニウムA1050のリン酸-硫酸系電解研磨における電解条件が表面構造と光沢度に及ぼす影響 査読

    中野信男, 西山 聖, 山内 健, 坪川 紀夫

    表面技術   65 ( 7 )   318 - 324   2014年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.4139/sfj.65.318

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  • 純アルミニウムA1050の電解研磨におけるフッ化水素酸溶液を使用した後処理条件が光沢度と表面構造に及ぼす影響 査読

    中野信男, 西山聖, 山内 健, 坪川紀夫

    材料試験技術   7 ( 59 )   117 - 123   2014年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

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  • Hydrophobicity Enhancement of the Polyvinyl Alcohol/Rice Starch/Silk Fibroin Films by Glycerol 査読

    Pusita Kuchaiyaphum, Takeshi Yamauchi, Ruangsri Watanesk, Surasak Watanesk

    ADVANCED RESEARCH IN MATERIAL SCIENCE AND MECHANICAL ENGINEERING, PTS 1 AND 2   446-447   360 - +   2014年

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    記述言語:英語   掲載種別:研究論文(国際会議プロシーディングス)   出版者・発行元:TRANS TECH PUBLICATIONS LTD  

    Eco-friendly films have been prepared using various biopolymers and their properties have been improved in order to meet the requirements for appropriate applications. However, the frequently encountered weakness of the properties of most biopolymer film is its water solubility. In this study, the polyvinyl alcohol/rice starch/silk fibroin (PVA/RS/SF) films were modified by the addition of glycerol aiming to increase the hydrophobicity of the films. Some properties of the modified films including water contact angle, degree of swelling and water solubility were compared with the unmodified PVA/RS/SF film. Results from the contact angle measurement showed that the films with glycerol could be transformed to be hydrophobic after soaking in ethanol medium. The increase in soaking time tends to increase the hydrophobicity of the films. However, at about 60 min soaking, the water contact angles on the films were quite constant with the values of about 107.9 +/- 5.2 degrees comparing with 65.3 +/- 2.4 degrees of the ethanol-untreated PVA/RS/SF films. In addition, the ethanol-treated glycerol-modified films also show higher degree of swelling with constant solubility and better mechanical properties.

    DOI: 10.4028/www.scientific.net/AMM.446-447.360

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  • Assembly of stimulus-sensitive gel particles with DNA-dye complexes 査読

    Takashi Nishiyama, Yoshiharu Kagami, Takeshi Yamauchi, Norio Tsubokawa

    POLYMER JOURNAL   45 ( 6 )   659 - 664   2013年6月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:NATURE PUBLISHING GROUP  

    In this study, an assembly of stimulus-sensitive gel particles with DNA-dye complexes was investigated for application in optical-sensing devices. This composite material of stimulus-sensitive gels and DNA detects external stimuli as a photo-signal. An assembly of the composite gel particles with DNA-dye complexes would be expected to achieve high responsiveness and to quickly detect environmental information as a photo-signal, because the porous structure produced by its interparticle spaces decreases with the relaxation time of the three-dimensional network structure. Poly(acrylic acid) (PAAc) gel particles with DNA were prepared by emulsion polymerization and the gel particles were assembled by a crosslinking reaction between the gel particles that utilized glutaraldehyde. It was possible to prepare the assembly of PAAc gel particles with DNA in sheet and block shapes by utilizing shaped forms for this synthesis process. The swelling ratio of the assembly increased with the pH, and the assembly reached equilibrium swelling in approximately 180 s. The response speed of the assembly was improved to more than 30 times faster than that of a typical PAAc block gel. Furthermore, the assembly of PAAc gel particles with DNA-ethidium bromide complexes detected pH information in an external solution as an optical signal.

    DOI: 10.1038/pj.2012.169

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  • Immobilization of flame-retardant onto silica nanoparticle surface and properties of epoxy resin filled with the flame-retardant-immobilized silica (2) 査読

    Takashi Kawahara, Akira Yuuki, Kumi Hashimoto, Kazuhiro Fujiki, Takeshi Yamauchi, Norio Tsubokawa

    REACTIVE & FUNCTIONAL POLYMERS   73 ( 3 )   613 - 618   2013年3月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:ELSEVIER SCIENCE BV  

    To prepare silica nanoparticle having flame-retardant activity, immobilization of flame-retardant onto the surface was investigated. The immobilization of phosphorous flame-retardant was achieved by two-step reactions: (1) introduction of cyclotriphosphazene (PH) groups onto silica nanoparticle by the reaction of terminal amino groups of the surface with hexachlorocyclotriphosphazene and (2) immobilization of bis(4-aminophenoxy)phenyl phosphine oxide (BAPPO) onto silica having PH groups by the reaction of PH groups on the surface with BAPPO. The immobilization of BAPPO was confirmed by FT-IR and thermal decomposition GC-MS. The composite of epoxy resin filled with BAPPO-immobilized silica (Silica-PH-BAPPO) was successfully prepared by heating in the presence of curing agents. Thermal decomposition temperature and glass transition temperature of the epoxy resin filled with Silica-PH-BAPPO was higher than that of epoxy resin filled with untreated silica, free HCTP and BAPPO. Moreover, flame-retardant property of epoxy resin filled with Silica-PH-BAPPO was estimated by limiting oxygen index (LOI). The LOI value of epoxy resin filled with Silica-PH-BAPPO was higher than that of epoxy resin filled with untreated silica, free HCTP and BAPPO. This may be due the fact that char yield of the epoxy resin filled with Silica-PH-BAPPO was higher than that filled with free flame-retardant. (C) 2013 Elsevier Ltd. All rights reserved.

    DOI: 10.1016/j.reactfunctpolym.2013.01.001

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  • Application of hydrogen gas sensor utilizing polymerized gel with ionic liquid as a solvent 査読

    山内 健

    Electrochemical Society Transactions   50 ( 12 )   231 - 236   2013年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1149/05012.0231ecst

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  • Bio-TRIZを導入した高分子ゲルバイオリアクターの開発 査読

    山内 健

    高分子論文集   70 ( 7 )   331 - 336   2013年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1295/koron.70.331

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  • Preparation of stimulus-sensitive gel particles with a DNA-dye complex and their pH sensitivity 査読

    Takashi Nishiyama, Yoshiharu Kagami, Takeshi Yamauchi, Norio Tsubokawa

    POLYMER JOURNAL   44 ( 5 )   396 - 400   2012年5月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:NATURE PUBLISHING GROUP  

    In this study, stimulus-sensitive gel particles with DNA dye complexes were prepared. This composite has potential use in optical micro-sensors because it can change its dye concentration in response to stimuli by intercalating dye into DNA. Poly(acrylic acid) (PAAc) gel particles containing DNA were synthesized by emulsion polymerization and immersed in ethidium bromide (EtBr) solution to form DNA EtBr complexes by intercalating dyes in the double-stranded structure. The pH response characteristics were measured in buffer solution with an optical and fluorescence microscope, and the dye entrapment of the composite was evaluated with a UV-Visible spectrophotometer. As a result, the EtBr was immobilized in PAAc gel particles containing DNA, and its volume could be varied by changing the pH in buffer solution. Furthermore, by forming the gel in a particle shape, the PAAc gel reached equilibrium swelling in about 60s. The fluorescence intensity of PAAc gel particles embedded with DNA EtBr complexes displayed high-sensitivity and was found to exponentially decrease as a function of pH. Polymer Journal (2012) 44, 396-400; doi:10.1038/pj.2011.142; published online 25 January 2012

    DOI: 10.1038/pj.2011.142

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  • Suface grafting of polymers onto nanodiamond by ligand-exchange reaction of ferrocene moieties of polymers with polycondensed aromatic rings of the surface 査読

    I. Cha, K. Shirai, K. Fujiki, T. Yamauchi, N. Tsubokawa

    DIAMOND AND RELATED MATERIALS   20 ( 3 )   439 - 444   2011年3月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:ELSEVIER SCIENCE SA  

    To improve the dispersibility of nanodiamond (ND) in solvents and polymer matrices, the grafting of copolymers containing vinyl ferrocene (Vf) onto the surface by a ligand-exchange reaction with ferrocene moieties of the copolymer and polycondensed aromatic rings of ND surface was investigated. The copolymer containing Vf was prepared by the radical copolymerization of Vf with vinyl monomers, such as methyl methacrylate (MMA), styrene (St), and N-isopropylacrylamide (NIPAM), using 2, 2'-azobisisobutyronitrile as an initiator. It was found that by heating of ND with poly(Vf-co-MMA), poly(Vf-co-St), and poly(Vf-co-NIPAN) in the presence of AlCl3 and Al powder as catalysts, the corresponding copolymer was successfully grafted onto the surface. On the contrary, in the absence of AlCl3, no grafting of these copolymers was observed. The grafting of polymers onto the ND surface was confirmed by FT-IR. These polymer-grafted NDs were found to give stable dispersions in solvents for the grafted polymer. In addition, the dispersibility of poly(Vf-co-NIPAM)-grafted ND uniformly dispersed in water below 32 degrees C but precipitated above the temperature. Therefore, it was concluded that the dispersibility of ND in water could be controlled by the temperature of water. (C) 2011 Elsevier B.V. All rights reserved.

    DOI: 10.1016/j.diamond.2011.01.014

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書籍等出版物

  • Materials, Modeling, Applications, and Future Prespectives,

    山内 健( 担当: 共著 ,  範囲: Thermo-Driven Soft Actuators-Electromagnetic Heating Soft Actuators)

    Springer Japan  2016年6月 

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  • トコトンやさしいバイオミメティックスの本

    山内 健, 小林秀敏( 担当: 分担執筆 ,  範囲: 生物から技術矛盾解決のヒントを探る「バイオTRIZって何?」”)

    日刊工業新聞  2016年3月 

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  • バイオTRIZ:生物の不思議を工学に移転する技術―その3 局所性質原理

    山内 健, 小林秀敏( 担当: 共著)

    Public engagement with nano-based emerging technologies newsletter  2014年10月 

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  • バイオTRIZ:生物の不思議を工学に移転する技術―その2 相変化原理―

    山内 健, 小林秀敏( 担当: 共著)

    Public engagement with nano-based emerging technologies newsletter  2014年8月 

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  • 導電性ポリマー材の高機能化と用途開発最前線

    山内 健, 坪川紀夫( 担当: 共著 ,  範囲: 酵素固定化カーボンブラックと導電性高分子との複合化)

    NTS出版  2014年7月 

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  • バイオTRIZ:生物の不思議を工学に移転する技術―その1 分割原理―

    山内 健, 小林秀敏( 担当: 共著)

    Public engagement with nano-based emerging technologies newsletter  2014年6月 

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  • モミジバノ展開特性

    小林秀敏, 山内 健( 担当: 共著)

    Public engagement with nano-based emerging technologies newsletter  2014年4月 

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  • 生物の不思議を工学に移転する技術-バイオTRIZ という技法

    山内 健, 小林秀敏( 担当: 共著)

    Public engagement with nano-based emerging technologies newsletter  2013年8月 

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MISC

  • Sugar-binding property of magnetite particles modified with dihydroxyborylphenyl groups via graft polymerization of acrylic acid

    M Shimomura, T Abe, Y Sato, K Oshima, T Yamauchi, S Miyauchi

    POLYMER   44 ( 14 )   3877 - 3882   2003年6月

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    記述言語:英語   出版者・発行元:ELSEVIER SCI LTD  

    In order to combine sugar-binding property and magnetism, dihydroxyborylphenyl (DHBP) groups were attached to magnetite particles via graft polymerization of acrylic acid. The graft polymerization was carried out in a redox system consisting of mercapto groups introduced onto the surfaces of magnetite particles and ceric ions. DHBP groups were attached through amide linkages by the condensation reaction of 3-aminophenylboronic acid with carboxyl groups of the grafted poly(acrylic acid). Complexation of the attached DHBP groups was examined with various sugars and compared with that of the free phenylboronic acid. The attached DHBP groups gave a large value of binding constant K for the complexation with adenosine having a pair of cis-OH groups, whereas the K values for the DHBP groups with adenosine phosphates were extremely small. With respect to the complexation. with 2 -deoxyadenosine, cooperative interaction of neighboring DHBP groups was suggested. Although the value of acidity index pK(a) of the attached DHBP was larger than that of free phenylboronic acid, the pK(a) value was decreased by coexistent basic groups. (C) 2003 Elsevier Science Ltd. All rights reserved.

    DOI: 10.1016/S0032-3861(03)00327-6

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  • Sugar-binding property of magnetite particles modified with dihydroxyborylphenyl groups via graft polymerization of acrylic acid

    M Shimomura, T Abe, Y Sato, K Oshima, T Yamauchi, S Miyauchi

    POLYMER   44 ( 14 )   3877 - 3882   2003年6月

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    記述言語:英語   出版者・発行元:ELSEVIER SCI LTD  

    In order to combine sugar-binding property and magnetism, dihydroxyborylphenyl (DHBP) groups were attached to magnetite particles via graft polymerization of acrylic acid. The graft polymerization was carried out in a redox system consisting of mercapto groups introduced onto the surfaces of magnetite particles and ceric ions. DHBP groups were attached through amide linkages by the condensation reaction of 3-aminophenylboronic acid with carboxyl groups of the grafted poly(acrylic acid). Complexation of the attached DHBP groups was examined with various sugars and compared with that of the free phenylboronic acid. The attached DHBP groups gave a large value of binding constant K for the complexation with adenosine having a pair of cis-OH groups, whereas the K values for the DHBP groups with adenosine phosphates were extremely small. With respect to the complexation. with 2 -deoxyadenosine, cooperative interaction of neighboring DHBP groups was suggested. Although the value of acidity index pK(a) of the attached DHBP was larger than that of free phenylboronic acid, the pK(a) value was decreased by coexistent basic groups. (C) 2003 Elsevier Science Ltd. All rights reserved.

    DOI: 10.1016/S0032-3861(03)00327-6

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  • Electrical and Mechanical Characteristics of Compounds Containing of Fractionated poly (3-hexylthiophene) and Conducting Particles

    Journal of Applied polymer Science   85, 1429   2002年

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  • Selective 3-O-and/or 6-O-Glycosidation of Unprotected O-and S-Glycosides promoted an Intramoleculatly Coordinated Arylbronic Compound

    Bulletin of the chemical Society of JAPAN   75(6), 1319   2002年

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  • Electrical and Mechanical Characteristics of Compounds Containing of Fractionated poly (3-hexylthiophene) and Conducting Particles

    Journal of Applied polymer Science   85, 1429   2002年

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  • Selective 3-O-and/or 6-O-Glycosidation of Unprotected O-and S-Glycosides promoted an Intramoleculatly Coordinated Arylbronic Compound

    Bulletin of the chemical Society of JAPAN   75(6), 1319   2002年

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  • きのこ(Grifola frondosa)存在下におけるアクリルアミドの重合

    高分子論文集   58(5), 227   2001年

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  • Covalent immobi-lization of glucose on film prepared by electro-chemical copolymerization of thiophene-3-acetic acid and 3-methylthiophene for glucose sensing

    Polymer Journal   Vol. 33, No. 8, pp.629‐631   2001年

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  • Covalent immobilization of glucose oxidase on film prepared by electrochemical copolymerization of thiophene-3-acetic acid and 3-methylthiophene for glucose sensing

    M Shimomura, N Kojima, K Oshima, T Yamauchi, S Miyauchi

    POLYMER JOURNAL   33 ( 8 )   629 - 631   2001年

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    記述言語:英語   出版者・発行元:SOC POLYMER SCIENCE JAPAN  

    DOI: 10.1295/polymj.33.629

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  • Temperature-conductivity characteristics of the composites consisting of fractionated poly(3-hexylthiophene) and conducting particles

    YW Liu, K Oshima, T Yamauchi, M Shimomura, S Miyauchi

    JOURNAL OF APPLIED POLYMER SCIENCE   77 ( 14 )   3069 - 3076   2000年9月

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    記述言語:英語   出版者・発行元:WILEY-BLACKWELL  

    Poly (3-hexylthiophene) (P3HT) synthesized by oxidative polymerization was fractionated by molecular weight by using organic solvents. The fraction of higher average molecular weight gave higher regioregularity and conductivity. Composites of the P3HT fraction having the highest molecular weight were prepared by use of the following conducting particles as fillers: titanium carbide (TiC), indium tin oxide (ITO), and carbon black (CB). Temperature-conductivity profiles of the composites showed that the resistance change with PTC (positive temperature coefficient) effect was strongly influenced by the content and size of conducting particles and the molecular weight of P3HT. Although no significant PTC effect for P3HT-CB composite and little effect for P3HT-ITO composite system were observed, the P3HT-TiC composite containing TIC of 70-80 wt % showed an obvious PTC effect that brought the conductivity change by about four orders of magnitude near the glass transition temperature of P3HT. However, such a remarkable PTC effect was not observed for the P3HT-TiC composite prepared with the P3HT fraction of low-molecular weight. It was shown that a good PTC effect could be achieved by the composite consisting of the P3HT of high-molecular weight and the conducting particles of relatively large size. (C) 2000 John Wiley & Sons, Inc.

    DOI: 10.1002/1097-4628(20000929)77:14<3069::AID-APP70>3.0.CO;2-B

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  • 金電極土のジヒドロキシボラン誘導体単分子層による糖認識

    大島 賢治, 小林 幸太, 山内 健, 下村 雅人, 宮内 信之助

    日本科学会誌   ( 6 )   405 - 410   2000年

  • Temperature-conductivity charact-eristics of the composites consisting of fractionated poly(3-hexylthiophene) and conducting particles

    Journal of Applied Polymer Science   Vol. 77, pp.3069‐3076   2000年

  • Properties of alpha-chymotrypsin covalently immobilized on poly(acrylic acid)-grafted magnetite particles

    M Shimomura, M Ohta, N Sugiyama, K Oshima, T Yamauchi, S Miyauchi

    POLYMER JOURNAL   31 ( 3 )   274 - 278   1999年

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    記述言語:英語   出版者・発行元:SOC POLYMER SCIENCE JAPAN  

    Enzymatic properties of alpha-chymotrypsin covalently immobilized on magnetic particles rin graft polymerization of acrylic acid were investigated. Graft polymerization was carried out in a redox system consisting of mercapto groups introduced onto the surfaces of magnetite particles and eerie ions, alpha-Chymotrypsin was immobilized on magnetite particles by condensation with the carboxyl groups of the grafted poly(acrylic acid). The amount of alpha-chymotrypsin immobilized on 1 g of magnetic was 13-17mg and the activity of the immobilized alpha-chymotrypsin (at 37 degrees C, pH 8.0) was 70% the maximum activity of the native enzyme. Due to immobilization, optimum pH for alpha-chymotrypsin shifted to a slightly higher value, whereas optimum temperature did not change. A kinetic study of the enzymatic reaction with immobilized alpha-chymotrypsin showed that the immobilization limited accessibility of substrate molecules to the active sites of the enzyme bur caused little decrease of the maximum reaction rate. In water at 37 degrees C, immobilized alpha-chymotrypsin kept 93% of its original activity over a period of 25 days, though the native enzyme was completely deactivated within 5 days by autolytic denaturalization.

    DOI: 10.1295/polymj.31.274

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  • Glucose-sensing characteristics of conducting polymer bound with glucose oxidase

    Synthetic Metals   No. 102, pp.1320   1999年

  • Study of switching characteristic with positive temperature coefficient of poly(3-hexylthiophene)

    Synthetic Metals   No. 101, pp. 451‐452   1999年

  • Glucose-sensing chracteristics of condacting polymer bound with glucose oxidase

    Synthetic Metals   102 ( 1/3 )   1320   1999年

  • Properties of chimotrypsin immobi-lized on poly(acrylic acid) grafted magnetite particles

    Polymer Journal   Vol. 31, No. 3, pp.274‐278   1999年

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  • Study of switching characterisics with positive temperatare coefficient of poly(3-hexylthiophene)

    Synthetic Metals   101 ( 1/3 )   451 - 452   1999年

  • 酸素プラズマ処理により表面修飾した炭素繊維のグルコースセンサへの応用

    電気学会論文誌E   119-E ( 11 )   538   1999年

  • ポリ(3-ヘキシルチオフェン)の導電率-温度特性

    技術教育論文誌   8 ( 1 )   35   1999年

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  • 新規な両親媒性ポルフィリンの合成とLB膜化およびガスセンシングへの応用

    技術教育論文誌   8 ( 2 )   13   1999年

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  • 炭化チタン存在下での3-ヘキシルチオフェンの重合とその複合導電体の導電率-温度特性

    劉 玉文, 日野 慎介, 大島 賢治, 山内 健, 下村 雅人, 宮内 信之助

    (]G0048[)分子論文集   56 ( 7 )   440 - 444   1999年

  • Immobilization of enzymes on poly(acrylic acid)-attached magnetite particles

    M Shimomura, N Sugiyama, T Yamauchi, S Miyauchi

    POLYMER JOURNAL   30 ( 4 )   350 - 351   1998年

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    記述言語:英語   出版者・発行元:SOC POLYMER SCIENCE JAPAN  

    DOI: 10.1295/polymj.30.350

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  • 15. Immobilization of enzymes on poly (acrylic acid)-attached magnetite particles

    Polymer Journal   Vol. 30, No. 4, pp.350‐351   1998年

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  • Covalent immo-bilization of glucose oxidase on poly[1-(2-carboxyl)pyrrole] film for glucose sensing

    Polymer   Vol. 39 No. 11, pp.2079‐2082   1998年

  • Covalent immobilization of glucose oxidase on poly[1-R-carboxyl)pyrrole]film for glucose sensing

    Polymer   39 ( 11 )   2079 - 2082   1998年

  • Pleurotus eryngii菌系体の培養特性

    日本菌学会会報告   39   83   1998年

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  • イオン交換樹脂に共有結合法により固定化したグルコースオキシダーゼの活性評価

    山内 健, 王 楠, 下村 雅人, 宮内 信之助

    高分子論文集   55 ( 7 )   373 - 377   1998年

  • Preparation of polypyrrole covalently attached with glucose oxidase and its application to glucose sensing

    K Kojima, T Unuma, T Yamauchi, M Shimomura, S Miyauchi

    SYNTHETIC METALS   85 ( 1-3 )   1417 - 1418   1997年2月

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    記述言語:英語   出版者・発行元:ELSEVIER SCIENCE SA LAUSANNE  

    Glucose oxidase (GOD) was covalently attached to polypyrrole having carboxyl groups (PPy-COOH), and polypyrrole attached with GOD(PPy-GOD) was applied to glucose sensing. The PPy-COOH was prepared by oxidative polymerization of 1-(2-cyanoethyl)pyrrole followed by hydrolysis of the cyano groups to convert them into carboxyl groups. GOD was bound to the PPy-COOH by condensation reaction between carboxyl groups of the PPy-COOH and amino groups of GOD by use of a carbodiimide reagent. The electrode made of the PPy-GOD thus obtained being used, amperometric response to glucose was monitored. The result shows that the PPy-GOD is a promising material for glucose sensor.

    DOI: 10.1016/S0379-6779(97)80300-1

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  • Positive temperature coefficient characteristics of poly(3-alkylthiophene)s

    T Yamauchi, HM Najib, YW Liu, M Shimomura, S Miyauchi

    SYNTHETIC METALS   84 ( 1-3 )   581 - 582   1997年1月

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    記述言語:英語   出版者・発行元:ELSEVIER SCIENCE SA LAUSANNE  

    Poly(3-alkylthiophene)(P3AT) films were prepared by both electrochemical and chemically oxidative polymerization methods, and their positive temperature coefficient(PTC) characteristics were investigated in the range from 0 to 200 degrees C. The change in the amount of tetrafluoroborate ion(BF4-) or iron(III) perchlorate(FeCl3) which were doped into P3AT film was also estimated by infrared(IR) and ultraviolet(UV) spectrophotometry. It was found that the P3AT films chemically polymerized at a low temperature had PTC characteristics, which was not affected by the dedoping involved in thermal treatment.

    DOI: 10.1016/S0379-6779(97)80866-1

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  • Positive tem-perature coefficient characteristics of poly-(3-alkylthio-phene)s

    Synthetic Metals   No. 84, pp.581‐582   1997年

  • ポリピロール/グルコースオキシダーゼ含有ポリビニルアルコール複合膜の作製とグルコースセンサへの応用

    児島 克典, 那須 肇, 山内 健, 下村 雅人, 宮内 信之助

    (]G0048[)分子論文集   54 ( 2 )   87 - 93   1997年

  • Covalent immobilization of glucose oxidase on magnetite particles via graft polymerization of acrylic acid

    Journal of Macromolecular Science   A33 ( 11 )   1687   1996年

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  • Covalent immo-bilization of glucose oxidase on magnetite particles via graft polymerization of acrylic acid

    Journal of Macromolecular Science, Part A   Vol. 33, No. 11, pp.1687‐1697   1996年

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  • Chemically Oxidative Systhesis and Hydrolysis of Poly [1-(2-cyanoethyl)pyrrole](jointly worked)

    Polymer   37 ( 7 )   1289 - 1291   1996年

  • Chemically oxidative synthesis and hydrolysis of poly[1-(2-cyanoethyl) pyrrole]

    Polymer   Vol. 37, No. 7, pp.1289‐1291   1996年

  • Study of the background current Through polypyrrole/glucose oxidase film for glucose sensing.

    ( 18 )   45   1996年

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  • Electrically controlled separation of maleic acid and fumaric acid through a poly(vinyl alcohol) / poly(acrylic acid) composite membrane

    Polymer Gels and Networks   Vol. 3, No. 4, pp.397‐406   1995年

  • Attaching of poly(acrylic acid) to inorganic surface and its application to enzyme immobolozation.(jointly worked)

    Polymer Journal   27 ( 9 )   974 - 977   1995年

  • Electrically Controlled Separation of Maleic acid and Fumaric acid through a Poly(vinyl alcohol)/Poly(acrlic acid) Composite Membrane(jointly worked)

    Polymer Gels and Networks   3 ( 4 )   397 - 406   1995年

  • Effects of Visible light Irradiation on the Response Characteristics of a Titanium-Containing Plasma-polymerized Organic Thin Film to Organic Vapors

    5,89   1994年

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  • チタン含有プラズマ重合膜の有機ガス応答性に及ぼす可視光照射の効果

    日本化学会誌   5,89   1994年

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  • Synthesis and Properties of Organo-Metal Multiphase Polymer Films Prepared by Plasma Polymerization

    New Functionality Materials   C,163   1993年

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  • Electrically controlled protein permeation through a poly (vinyl alcohol) / poly(acrylic acid) com-posite membrane

    Polymer Gels and Networks   Vol. 1, No. 4, pp.247‐255   1993年

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  • Electrically Controlled Protein Permeation through a Poly(vinyl alcohol)/Poly(acrylic acid) Composite Membrane

    Polymer Gels and Networks   1 ( 4 )   247   1993年

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  • Electrical Conductivity and Gas Response of Plasma-polymerized Titanium Containing Organic Thin Films

    5,547   1992年

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  • チタン含有プラズマ重合膜の導電率と有機ガス応答特性

    日本化学会誌   5,547   1992年

  • PREPARATION, STRUCTURE, AND ELECTRIC PROPERTIES OF PLASMA-POLYMERIZED TITANIUM-CONTAINING ORGANIC THIN-FILMS

    Y KAGAMI, T YAMAUCHI, Y OSADA, YOSHIZAWA, I

    JOURNAL OF APPLIED PHYSICS   68 ( 2 )   610 - 616   1990年7月

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    記述言語:英語   出版者・発行元:AMER INST PHYSICS  

    DOI: 10.1063/1.346787

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産業財産権

  • アミノシラン修飾コロイダルシリカ分散液及びその製造方法

    村上 なつ美, 飛田, 将大。坪川, 紀夫, 山内 健, 前田 智

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    出願番号:特願2017- 517967  出願日:2016年10月

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受賞

  • 学術奨励賞

    2015年10月   合成樹脂工業協会   高分子ネットワーク構造を利用したナノ材料の複合化とスマートテリアル開発

    山内 健

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共同研究・競争的資金等の研究

  • Study on Hybrid Materials and Bio-sensor.

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    資金種別:競争的資金

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  • ハイブリッドマテリアルおよびバイオ素子に関する研究

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    資金種別:競争的資金

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  • 導電性高分子を用いた新規バイオ素子に関する研究

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    資金種別:競争的資金

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担当経験のある授業科目

  • マーケット・インターンシップ

    2021年
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    機関名:新潟大学

  • 創造研究プロジェクトII

    2021年
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    機関名:新潟大学

  • 創造プロジェクトII

    2021年
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    現在
    機関名:新潟大学

  • 創造プロジェクトI

    2021年
    -
    現在
    機関名:新潟大学

  • テクノロジー・インターンシップ

    2021年
    -
    現在
    機関名:新潟大学

  • 創造プロジェクト基礎

    2021年
    -
    現在
    機関名:新潟大学

  • 創造研究プロジェクトI

    2021年
    -
    現在
    機関名:新潟大学

  • 論文輪講I

    2020年
    -
    現在
    機関名:新潟大学

  • 技術英語I

    2020年
    -
    現在
    機関名:新潟大学

  • 論文輪講II

    2020年
    -
    現在
    機関名:新潟大学

  • 特許・経営および製品開発入門

    2020年
    -
    現在
    機関名:新潟大学

  • 技術英語II

    2020年
    -
    現在
    機関名:新潟大学

  • 材料科学PBL

    2020年
    -
    現在
    機関名:新潟大学

  • 水素制御管理特論

    2019年
    機関名:新潟大学

  • 水素エネルギーシステムデザイン演習・実習Ⅲ

    2019年
    機関名:新潟大学

  • 高分子科学

    2018年
    -
    現在
    機関名:新潟大学

  • 材料科学概論

    2017年
    -
    現在
    機関名:新潟大学

  • 総合工学概論

    2017年
    -
    現在
    機関名:新潟大学

  • 工学リテラシー入門(化学材料分野)

    2017年
    -
    現在
    機関名:新潟大学

  • 機能材料化学概論

    2014年
    -
    2016年
    機関名:新潟大学

  • 材料生産システム博士セミナーⅡ

    2013年
    -
    2015年
    機関名:新潟大学

  • 材料生産システム博士特定研究Ⅱ

    2013年
    -
    2015年
    機関名:新潟大学

  • 技術者倫理

    2013年
    機関名:新潟大学

  • Advanced Smart Material

    2013年
    機関名:新潟大学

  • 博士特定研究Ⅲ

    2013年
    機関名:新潟大学

  • 技術英語入門

    2013年
    機関名:新潟大学

  • グローバルミーティング

    2013年
    機関名:新潟大学

  • 機能材料科学演習

    2012年
    -
    2015年
    機関名:新潟大学

  • 外国語論文解説・討論Ⅱ

    2012年
    -
    2015年
    機関名:新潟大学

  • 機能材料科学文献詳読Ⅱ

    2012年
    -
    2015年
    機関名:新潟大学

  • 機能材料科学セミナーⅡ

    2012年
    -
    2015年
    機関名:新潟大学

  • 材料生産システム博士特定研究Ⅲ

    2012年
    -
    2015年
    機関名:新潟大学

  • 材料生産システム特定研究Ⅱ

    2012年
    -
    2015年
    機関名:新潟大学

  • 研究発表演習・発表

    2012年
    -
    2015年
    機関名:新潟大学

  • 中間発表

    2012年
    -
    2015年
    機関名:新潟大学

  • 材料生産システム特定研究Ⅰ

    2012年
    -
    2015年
    機関名:新潟大学

  • 機能材料科学セミナーⅠ

    2012年
    -
    2015年
    機関名:新潟大学

  • 機能材料科学文献詳読Ⅰ

    2012年
    -
    2015年
    機関名:新潟大学

  • 材料生産システム博士特定研究Ⅰ

    2012年
    -
    2014年
    機関名:新潟大学

  • 外国語論文解説・討論Ⅲ

    2012年
    -
    2014年
    機関名:新潟大学

  • 材料生産システム博士セミナーⅢ

    2012年
    -
    2014年
    機関名:新潟大学

  • 外国語論文解説・討論Ⅰ

    2012年
    -
    2014年
    機関名:新潟大学

  • 機能材料科学コース演習

    2012年
    -
    2014年
    機関名:新潟大学

  • 材料生産システム博士セミナーⅠ

    2012年
    -
    2014年
    機関名:新潟大学

  • リサーチキャンプ

    2012年
    -
    2013年
    機関名:新潟大学

  • 最先端技術を支える化学 II

    2012年
    -
    2013年
    機関名:新潟大学

  • 博士セミナーⅢ

    2012年
    -
    2013年
    機関名:新潟大学

  • チームインターンシップ Ⅰ

    2012年
    機関名:新潟大学

  • チームインターンシップ Ⅱ

    2012年
    機関名:新潟大学

  • 自然科学総論Ⅱ

    2011年
    -
    2019年
    機関名:新潟大学

  • 卒業研修

    2009年
    -
    現在
    機関名:新潟大学

  • 工学リテラシー入門(機能材料工学科)

    2009年
    -
    2016年
    機関名:新潟大学

  • 機能材料工学実験III

    2009年
    -
    2010年
    機関名:新潟大学

  • 技術英語

    2007年
    -
    現在
    機関名:新潟大学

  • 複合材料設計

    2007年
    -
    現在
    機関名:新潟大学

  • 卒業研究

    2007年
    -
    現在
    機関名:新潟大学

  • 論文輪講

    2007年
    -
    現在
    機関名:新潟大学

  • 化学実験

    2007年
    -
    現在
    機関名:新潟大学

  • 機能性高分子材料

    2007年
    -
    現在
    機関名:新潟大学

  • 複合材料設計化学

    2007年
    -
    2019年
    機関名:新潟大学

  • 機能材料工学実験IV

    2007年
    -
    2018年
    機関名:新潟大学

  • 基礎高分子化学

    2007年
    -
    2017年
    機関名:新潟大学

  • 材料物性評価演習

    2007年
    -
    2012年
    機関名:新潟大学

  • 卒業基礎研究

    2007年
    機関名:新潟大学

  • 先端高分子材料

    2007年
    機関名:新潟大学

  • インターンシップ

    2007年
    機関名:新潟大学

▶ 全件表示