Thermal stability of copolymer derived from L-lactic acid and poly(tetramethylene) glycol through direct polycondensation

被引:24
作者
Zeng, Chao [1 ]
Zhang, Nai-Wen [2 ]
Feng, Shu-Qin [1 ]
Ren, Jie [1 ,3 ]
机构
[1] Tongji Univ, Sch Mat Sci & Engn, Inst Nano & Biopolymer Mat, Shanghai 200092, Peoples R China
[2] Shanghai Tong Jie Liang Biomat Co Ltd, Shanghai 200438, Peoples R China
[3] Tongji Univ, Minist Educ, Key Lab Adv Civil Engn Mat, Shanghai 200092, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
Thermal stability; Poly(lactic acid); Direct polycondensation; Triblock copolymers; Thermogravimetry; Activation energy; POLY-L-LACTIDE; POLY(LACTIC ACID); BIODEGRADABLE POLYESTERS; POLY(L-LACTIC ACID); DEGRADATION; POLY(EPSILON-CAPROLACTONE); DECOMPOSITION; ELASTOMERS; BLENDS;
D O I
10.1007/s10973-012-2542-9
中图分类号
O414.1 [热力学];
学科分类号
摘要
The thermogravimetric analysis (TG) of triblock copolymers (PLAG) based on poly(l-lactic acid) (PLLA) and poly(tetramethylene) glycol (PTMEG) segments with different PTMEG content and catalyst concentration was conducted. The thermal degradation behaviors of copolymers were determined by thermogravimetric analysis and the results are also confirmed by hydrogen nuclear magnetic resonance spectrometry (H-1 NMR). The thermal stability of PLA-based copolymer is improved with decreasing use level of Sn catalyst and short-chain molecules with hydroxyl and carboxyl end group also have a significant effect on the thermal degradation of chain-extended products of copolymer (PLAE). PLAE-10 with 0.5 wt% catalyst shows two main decomposition kinetic mechanisms. On the other hand, PLAE-10 with 0.05 wt% catalyst mainly undergoes Sn-catalyzed selective depolymerisation. Moreover, the PTMEG segments in PLAEs seem to increase the mobility of the Sn salt moiety in PLAEs and the activation energy (E (a)) decreases with increasing the PTMEG content in PLAEs.
引用
收藏
页码:633 / 646
页数:14
相关论文
共 39 条
[1]   THERMAL PROPERTIES OF POLYLACTIDES Effect of molecular mass and nature of lactide isomer [J].
Ahmed, J. ;
Zhang, J. -X. ;
Song, Z. ;
Varshney, S. K. .
JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY, 2009, 95 (03) :957-964
[2]   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
[3]   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
[4]   Thermogravimetric study of copolymers derived from p-dioxanone, L-lactide and poly (ethylene glycol) [J].
Bhattarai, N ;
Kim, HY ;
Lee, DR .
POLYMER DEGRADATION AND STABILITY, 2002, 78 (03) :423-433
[5]  
Buchatip S., 2008, J MET MAT MINER, V18, P175
[6]  
Cam D, 1997, POLYMER
[7]   Processing of poly(lactic acid): Characterization of chemical structure, thermal stability and mechanical properties [J].
Carrasco, F. ;
Pages, P. ;
Gamez-Perez, J. ;
Santana, O. O. ;
Maspoch, M. L. .
POLYMER DEGRADATION AND STABILITY, 2010, 95 (02) :116-125
[8]   The phase mixing of moisture cured polyurethane-urea during cure [J].
Chattopadhyay, DK ;
Prasad, PSR ;
Sreedhar, B ;
Raju, KVSN .
PROGRESS IN ORGANIC COATINGS, 2005, 54 (04) :296-304
[9]   Polyurethane elastomers through multi-hydrogen-bonded association of dendritic structures [J].
Chen, CP ;
Dai, SA ;
Chang, HL ;
Su, WC ;
Wu, TM ;
Jeng, RJ .
POLYMER, 2005, 46 (25) :11849-11857
[10]   Thermogravimetric investigation of two classes of block copolymers based on poly(lactic-glycolic acid) and poly(ε-caprolactone) or poly(ethylene glycol) [J].
D'Antone, S ;
Bignotti, F ;
Sartore, L ;
D'Amore, A ;
Spagnoli, G ;
Penco, M .
POLYMER DEGRADATION AND STABILITY, 2001, 74 (01) :119-124