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Dive into the research topics where Shinsuke Ifuku is active.

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Featured researches published by Shinsuke Ifuku.


Applied Physics Letters | 2006

Fiber-content dependency of the optical transparency and thermal expansion of bacterial nanofiber reinforced composites

Masaya Nogi; Shinsuke Ifuku; Kentaro Abe; Keishin Handa; Antonio Norio Nakagaito; Hiroyuki Yano

We produced transparent nanocomposite reinforced with bacterial cellulose having a wide range of fiber contents, from 7.4to66.1wt%, by the combination of heat drying and organic solvent exchange methods. The addition of only 7.4wt% of bacterial cellulose nanofibers, which deteriorated light transmittance by only 2.4%, was able to reduce the coefficient of thermal expansion of acrylic resin from 86×10−6to38×10−6K−1. As such, the nanofiber network of bacterial cellulose has an extraordinary potential as a reinforcement to obtain optically transparent and low thermal expansion materials.


Applied Physics Letters | 2006

Property enhancement of optically transparent bionanofiber composites by acetylation

Masaya Nogi; Kentaro Abe; Keishin Handa; Fumiaki Nakatsubo; Shinsuke Ifuku; Hiroyuki Yano

The authors studied acetylation of bacterial cellulose (BC) nanofibers to widen the applications of BC nanocomposites in optoelectronic devices. The slight acetylation of BC nanofibers significantly reduces the hygroscopicity of BC nanocomposites, while maintaining their high optical transparency and thermal stability. Furthermore, the degradation in optical transparency at elevated temperature (200°C) was significantly reduced by acetylation treatment. Therefore, the acetylation of bionanofibers has an extraordinary potential as treatment for property enhancement of bionanofiber composites.


Organic and Biomolecular Chemistry | 2004

Preparation of 6-O-(4-alkoxytrityl)celluloses and their properties

Shinsuke Ifuku; Hiroshi Kamitakahara; Toshiyuki Takano; Fumio Tanaka; Fumiaki Nakatsubo

Cellulose was reacted with a series of 4-alkoxytrityl chlorides (C(n)TCl, n: number of carbon atoms in a saturated alkyl chain) under homogeneous reaction conditions in LiCl-N,N-dimethyl acetoamide to give a series of 6-O-(4-alkoxytrityl)celluloses (C(n)TC) with a high degree of substitution (DS), from 0.94 to 0.99, and with high regioselectivity at the 6-O position. Solubility of the C(n)TC in nonpolar solvents depended on the alkyl chain length: as the alkyl chain lengthens, cellulose derivatives become more hydrophobic and are readily soluble in nonpolar solvents, but not in polar solvents. Acetates of the C(4)-C(18)TC (C(4)-C(18)TCAc) showed anisotropic structures over melting temperatures (T(m)) examined under a polarized optical microscope (POM). Over isotropization temperatures (T(i)), flow birefringence were detected for C(12)-C(18)TCAc. The T(m) and T(i) decreased linearly with an increasing number of carbon atoms in the alkyl substituent. Wide-angle X-ray scattering (WAXS) studies of C(n)TC indicated that the fully extended side chains were perpendicular to the polymer backbone and interdigitated. These C(n)TC with the improved solubility may be used as starting materials for further derivatization focused on the secondary hydroxyl groups at the C-2 and C-3 positions.


Journal of Wood Science | 2004

Preparation of novel reagents 4-alkoxytrityl chlorides and their reaction with methyl Α-d-glucoside

Shinsuke Ifuku; Hiroshi Kamitakahara; Fumiaki Nakatsubo

A series of novel 4-O-alkoxytrityl chlorides (1) with different chain lengths was synthesized as a novel reagent for obtaining 6-O-alkylated cellulose with high regioselectivity via trityl groups in one reaction step without the use of any protective groups. These chlorides were reacted with methyl Α-d-glucoside, which was used as a model compound, to examine the reactivities toward the primary hydroxyl groups of cellulose to afford a series of 6-O-alkylated methyl Α-d-glucosides in high yields. The product compounds were found to have interesting solubilities and thermal properties. Thus, newly prepared trityl chloride derivatives were found to be useful regioselective derivatization reagents on the primary hydroxyl group in carbohydrates, especially in cellulose.


Archive | 2013

Chitin Nanofibers, Preparations and Applications

Shinsuke Ifuku; Zameer Shervani; Hiroyuki Saimoto

Chitin nanofibers (CNFs) are mainly extracted from crab and prawn shells [1, 2] and recetly found in small amount in edible species of mushrooms [3]. CNFs are composed of chitin compound. Chitin in powder form is obtained from fish industry wastes which is otherwise thrown as industrial waste. Since CNFs are biodegradable having typical width 10-20 nm and large surface-to-mass ratio thus they are being prepared, studied, and applied more recently world wide along with rapidly growing field nanotechnology dealing with the better proper‐ ties of materials when their sizes are smaller in the range 1-100 nm. Fibrilated chitin in the form of highly viscous gel suspension in water has found scope in pharmaceuticals [4], chiral separation [5], fillers in silsesquioxane [6]. When blended with inorganic metals to prepare advanced hybrid organic-inorganic composites they can have applications in electronics, electrical, optical devices and much needed solar energy production.


Archive | 2006

FIBER-REINFORCED COMPOSITE MATERIAL AND METHOD FOR PRODUCING THE SAME

Masaya Atagi; Shinsuke Ifuku; Fumiaki Nakatsubo; Hiroyuki Yano; 文明 中坪; 伸介 伊福; 浩之 矢野; 雅也 能木


Journal of Polymer Science Part A | 2005

Preparation and characterization of redox cellulose Langmuir–Blodgett films containing a ferrocene derivative

Shinsuke Ifuku; Yoshinobu Tsujii; Hiroshi Kamitakahara; Toshiyuki Takano; Fumiaki Nakatsubo


Archive | 2008

Surface-modified microfibrillated cellulose and composite resin including the same

Shinsuke Ifuku; Hiroyuki Yano; 伸介 伊福; 浩之 矢野


Journal of Chitin and Chitosan Science | 2013

Preparation of Chitin Nanofibers from Dry Chitin Powder by Star Burst System: Dependence on Number of Passes

Ajoy Kumar Dutta; Kiyotaka Yamada; Hironori Izawa; Minoru Morimoto; Hiroyuki Saimoto; Shinsuke Ifuku


Journal of Chitin and Chitosan Science | 2013

A Comparative Study Analysis of -Chitin and -Chitin Nanofibrils by Using an Inflammatory-Bowel Disease Mouse Model

Kazuo Azuma; Tomohiro Osaki; Shinsuke Ifuku; Hiroyuki Saimoto; Takeshi Tsuka; Tomohiro Imagawa; Yoshiharu Okamoto; Saburo Minami

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Hiroyuki Yano

Mitsubishi Chemical Corporation

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