Effective preparation and characterization of montmorillonite/poly(ε-caprolactone)-based polyurethane nanocomposites

被引:23
作者
Jeong, Eun Hwan
Yang, Jie
Lee, Han Sup
Seo, Seung Won
Baik, Du Hyun
Kim, Jeonghan
Youk, Ji Ho [1 ]
机构
[1] Inha Univ, Dept Adv Fiber Engn, Div Nanosyst, Inchon 402751, South Korea
[2] Inha Univ, Intelligent Text Syst Res Ctr, Inchon 402751, South Korea
[3] Hyosung Co, R&D Ctr Fibers & Text, Anyang 431080, South Korea
[4] Chungnam Natl Univ, Dept Text Engn, Taejon 305764, South Korea
[5] Chem Res Inst, Yongin 446797, South Korea
关键词
poly(epsilon-caprolactone) (PCL); polyurethane cationomer; (PUC); montmorillonite (MMT); nanocomposits; exfoliation; hydrolytic degradation;
D O I
10.1002/app.27179
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this study, montmorillonite (MMT)/poly (epsilon-caprolactone)-based polyurethane cationomer (MMT/ PCL-PUC) nanocomposites were prepared and their mechanical properties, thermal stability, and biodegradability were investigated. PCL-PUC has 3 mol % of quaternary ammonium groups in the main chain. The MMT was successfully exfoliated and well dispersed in the PCL-PUC matrix for up to 7 wt % of MMT. The 3 mol % of quaternary ammonium groups facilitated exfoliation of MMT. The I wt % MMT/PCL-PUC nanocomposites showed enhanced tensile properties relative to the pure PCL-PU. As the MMT content increased in the MMT/PCL-PUC nanocomposites, the degree of microphase separation of PCL-PUC decreased because of the strong interactions between the PCL-PUC chains and the exfoliated MMT layers. This resulted in an increase in the Young's modulus and a decrease in the elongation at break and maximum stress of the MMT/PCL-PUC nanocomposites. Biodegradability of the MMT/PCL-PUC nanocomposites was dramatically increased with increasing content of MMT, likely because of the less phase-separated morphology of MMT/PCL-PUC. (C) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:803 / 809
页数:7
相关论文
共 28 条
[1]   Effect of chemical structure on combustion and thermal behaviour of polyurethane elastomer layered silicate nanocomposites [J].
Berta, M ;
Lindsay, C ;
Pans, G ;
Camino, G .
POLYMER DEGRADATION AND STABILITY, 2006, 91 (05) :1179-1191
[2]   Synthesis and characterization of novel segmented polyurethane/clay nanocomposites [J].
Chen, TK ;
Tien, YI ;
Wei, KH .
POLYMER, 2000, 41 (04) :1345-1353
[3]  
Chen TK, 1999, J POLYM SCI POL CHEM, V37, P2225, DOI 10.1002/(SICI)1099-0518(19990701)37:13<2225::AID-POLA37>3.0.CO
[4]  
2-Z
[5]   Biodegradable poly(ether ester urethane)urea elastomers based on poly(ether ester) triblock copolymers and putrescine: synthesis, characterization and cytocompatibility [J].
Guan, JJ ;
Sacks, MS ;
Beckman, EJ ;
Wagner, WR .
BIOMATERIALS, 2004, 25 (01) :85-96
[6]   Phase transitions of lignin-based polycaprolactones and their polyurethane derivatives [J].
Hatakeyama, T ;
Izuta, Y ;
Hirose, S ;
Hatakeyama, H .
POLYMER, 2002, 43 (04) :1177-1182
[7]   Uncatalyzed synthesis, thermal and mechanical properties of polyurethanes based on poly(ε-caprolactone) and 1,4-butane diisocyanate with uniform hard segment [J].
Heijkants, RGJC ;
van Calck, RV ;
van Tienen, TG ;
de Groot, JH ;
Buma, P ;
Pennings, AJ ;
Veth, RPH ;
Schouten, AJ .
BIOMATERIALS, 2005, 26 (20) :4219-4228
[8]   Effective preparation of montmorillonite/polyurethane nanocomposites by introducing cationic groups into the polyurethane main chain [J].
Jeong, Eun Hwan ;
Yang, Jie ;
Hong, Ji Hye ;
Kim, Tae Gon ;
Kim, Jung Hyun ;
Youk, Ji Ho .
EUROPEAN POLYMER JOURNAL, 2007, 43 (06) :2286-2291
[9]  
Lamba NMK., 1998, POLYURETHANES BIOMED
[10]  
LEE JC, 1993, POLYMER, V17, P687