Thermal degradation behaviour of poly(lactic acid) stereocomplex

被引:156
作者
Fan, YJ
Nishida, H
Shirai, Y
Tokiwa, Y
Endo, T
机构
[1] Kinki Univ, Mol Engn Inst, Iizuka, Fukuoka 8208555, Japan
[2] Kyushu Inst Technol, Grad Sch Life Sci & Syst Engn, Kitakyushu, Fukuoka 8080196, Japan
[3] Natl Inst AIST, Tsukuba, Ibaraki 3058566, Japan
[4] Yamagata Univ, Fac Engn, Yonezawa, Yamagata 9928510, Japan
关键词
polylactide; poly(lactic acid); stereocomplex; thermal degradation; thermal stability; pyrolysis; kinetics;
D O I
10.1016/j.polymdegradstab.2004.03.001
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The thermal degradation of poly(lactic acid) stereocomplex (scPLA) was investigated to clarify the pyrolysis mechanism. Three scPLA samples with different chain end structures were prepared, namely, as-polymerised scPLA-ap, precipitated-with-methanol scPLA-pr, and purified metal-free scPLA-H. From the analyses of thermal degradation kinetics and pyrolysates of the scPLA samples, typical degradation mechanisms of these scPLAs were proposed as follows. The pyrolysis of scPLA-ap proceeds through main unzipping depolymerisation caused by Sn-alkoxide chain ends with apparent E-n = 80-100 U mol(-1), showing zero-order weight loss behaviour. The pyrolysis of scPLA-pr also proceeds via a zero-order weight loss process consisting of main Sn-catalyzed selective lactide elimination with apparent E-n = 100-120 U mol(-1) caused by Sn-carboxylate chain ends. The pyrolysates from scPLA-ap and scPLA-pr were predominantly L,L-/D,D-lactides. In the case of scPLA-H, random degradation is a main process, producing a large amount of meso-lactide and cyclic oligomers. These degradation mechanisms were nearly the same as those of the corresponding PLLAs, except that the scPLA-ap pyrolysis started at higher temperature due to the higher melting point of scPLA. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:197 / 208
页数:12
相关论文
共 52 条
[1]   THE BASIC PROPERTIES OF POLY(LACTIC ACID) PRODUCED BY THE DIRECT CONDENSATION POLYMERIZATION OF LACTIC-ACID [J].
AJIOKA, M ;
ENOMOTO, K ;
SUZUKI, K ;
YAMAGUCHI, A .
JOURNAL OF ENVIRONMENTAL POLYMER DEGRADATION, 1995, 3 (04) :225-234
[2]  
Amass W, 1998, POLYM INT, V47, P89, DOI 10.1002/(SICI)1097-0126(1998100)47:2<89::AID-PI86>3.0.CO
[3]  
2-F
[4]   Biodegradation and biocompatibility of PLA and PLGA microspheres [J].
Anderson, JM ;
Shive, MS .
ADVANCED DRUG DELIVERY REVIEWS, 1997, 28 (01) :5-24
[5]   Thermal degradation of poly[(R)-3-hydroxybutyrate], poly[ε-caprolactone], and poly[(S)-lactide] [J].
Aoyagi, Y ;
Yamashita, K ;
Doi, Y .
POLYMER DEGRADATION AND STABILITY, 2002, 76 (01) :53-59
[6]  
Babanalbandi A, 1999, POLYM INT, V48, P980, DOI 10.1002/(SICI)1097-0126(199910)48:10<980::AID-PI257>3.0.CO
[7]  
2-B
[8]   Influence of residual monomers and metals on poly (L-lactide) thermal stability [J].
Cam, D ;
Marucci, M .
POLYMER, 1997, 38 (08) :1879-1884
[9]  
Doyle C.D., 1961, Journal of Applied Polymer Science, V5, P285, DOI [10.1002/app.1961.070051506, DOI 10.1002/APP.1961.070051506]
[10]  
Doyle CD., 1962, J Appl Polym Sci, V6, P639, DOI [DOI 10.1002/APP.1962.070062406, 10.1002/app.1962.070062406]