Acetylation of Chitin Nanofibers and their Transparent Nanocomposite Films

被引:96
作者
Ifuku, Shinsuke [1 ]
Morooka, Shin [1 ]
Morimoto, Minoru [2 ]
Saimoto, Hiroyuki [1 ]
机构
[1] Tottori Univ, Dept Chem & Biotechnol, Grad Sch Engn, Tottori 680, Japan
[2] Tottori Univ, Res Ctr Biosci & Technol, Tottori 680, Japan
关键词
BACTERIAL CELLULOSE; ALPHA-CHITIN; COMPOSITES;
D O I
10.1021/bm100109a
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chitin nanofibers were acetylated to modify the fiber surface and were characterized in detail. The acetyl DS could be controlled from 0.99 to 2.96 by changing the reaction time. FT-IR spectra indicate that chitin nanofibers were acetylated completely after 50 min reaction time. X-ray diffraction profiles and TGA curves show that the chitin nanofibers were acetylated heterogeneously from the surface to the core. SEM images show that fiber shape was maintained even in the high-DS sample and that the thickness of the nanofibers increased with the introduction of bulky acetyl groups. Acetylated chitin nanofiber composites were fabricated with acrylic resin with the fiber content of approximately 25 wt %. Due to the size effect, all nanocomposites had high transparency, despite the variety of acetyl DS, and the transparency of the chitin nanofiber composite was less sensitive to acetylation. By only 1 min acetylation, the moisture absorption of the nanocomposite drastically decreased from 4.0 to 2.2%. Although the coefficient of thermal expansion (GTE) of the tricyclodecane dimethanol dimethacrylate (TCDDMA) resin was 6.4 x 10(-5) degrees C(-1), the CTE of the chitin nanofiber/TCDDMA composite decreased to 2.3 x 10(-5) degrees C(-1) by the reinforcement effect of the chitin nanofibers with low thermal expansion.
引用
收藏
页码:1326 / 1330
页数:5
相关论文
共 12 条
[1]   Structure and mechanical properties of crab exoskeletons [J].
Chen, Po-Yu ;
Lin, Albert Yu-Min ;
McKittrick, Joanna ;
Meyers, Marc Andre .
ACTA BIOMATERIALIA, 2008, 4 (03) :587-596
[2]  
Glasser WG, 1999, J APPL POLYM SCI, V73, P1329, DOI 10.1002/(SICI)1097-4628(19990815)73:7<1329::AID-APP26>3.0.CO
[3]  
2-Q
[4]   Surface modification of bacterial cellulose nanofibers for property enhancement of optically transparent composites: Dependence on acetyl-group DS [J].
Ifuku, Shinsuke ;
Nogi, Masaya ;
Abe, Kentaro ;
Handa, Keishin ;
Nakatsubo, Fumiaki ;
Yano, Hiroyuki .
BIOMACROMOLECULES, 2007, 8 (06) :1973-1978
[5]   Preparation of Chitin Nanofibers with a Uniform Width as α-Chitin from Crab Shells [J].
Ifuku, Shinsuke ;
Nogi, Masaya ;
Abe, Kentaro ;
Yoshioka, Masafumi ;
Morimoto, Minoru ;
Saimoto, Hiroyuki ;
Yano, Hiroyuki .
BIOMACROMOLECULES, 2009, 10 (06) :1584-1588
[6]   Surface acetylation of bacterial cellulose [J].
Kim, DY ;
Nishiyama, Y ;
Kuga, S .
CELLULOSE, 2002, 9 (3-4) :361-367
[7]   STRUCTURE OF ALPHA-CHITIN [J].
MINKE, R ;
BLACKWELL, J .
JOURNAL OF MOLECULAR BIOLOGY, 1978, 120 (02) :167-181
[8]   Crab shell chitin whisker reinforced natural rubber nanocomposites. 1. Processing and swelling behavior [J].
Nair, KG ;
Dufresne, A .
BIOMACROMOLECULES, 2003, 4 (03) :657-665
[9]  
NOGI M, 2005, APPL PHYS LETT, V17, P153
[10]   Microstructure and crystallographic texture of the chitin-protein network in the biological composite material of the exoskeleton of the lobster Homarus americanus [J].
Raabe, D ;
Romano, P ;
Sachs, C ;
Fabritius, H ;
Al-Sawalmih, A ;
Yi, S ;
Servos, G ;
Hartwig, HG .
MATERIALS SCIENCE AND ENGINEERING A-STRUCTURAL MATERIALS PROPERTIES MICROSTRUCTURE AND PROCESSING, 2006, 421 (1-2) :143-153