Phase transitions of lignin-based polycaprolactones and their polyurethane derivatives

被引:88
作者
Hatakeyama, T
Izuta, Y
Hirose, S
Hatakeyama, H
机构
[1] Otsuma Womens Univ, Fac Home Econ, Dept Text Sci, Chiyoda Ku, Tokyo 1028357, Japan
[2] Fukui Univ Technol, Grad Sch Engn, Fukui 9108505, Japan
[3] Natl Inst Mat & Chem Res, Tsukuba, Ibaraki 305, Japan
关键词
alcoholysis lignin; kraft lignin; caprolactone;
D O I
10.1016/S0032-3861(01)00714-5
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Alcoholysis and kraft lignin-based polycaprolactones (LigPCL) were synthesized by the polymerization of epsilon -caprolactone which was initiated by the hydroxyl (OH) group in lignin. LigPCL-based polyurethanes were also prepared from LigPCL. The caprolactone (CL)/OH ratio of the CAPCLs was changed from 1 to 25 mol mol(-1). Thermal properties of the LigPCL and LigPCL-based polyurethane (PU) sheets were studied by differential scanning calorimetry (DSC). Glass transition temperature (T-g), heat capacity difference at T-g (DeltaC(p)) cold crystallization temperature (T-cc) and melting temperature (T-m), were determined by DSC. The main chain motion of lignin is observed in the whole CL/OH ratio. When CL/OH ratio exceeds 5 mol mol(-1) in the LigPCL samples and 10 mol mol(-1) in the LigPCL-based PU samples, the crystalline region which is organized by the PCL chain association is observed. It was found that PCL chain association is controlled by both chain length and chemical cross linking. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1177 / 1182
页数:6
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