Thermal properties and crystallization behavior of thermoplastic starch/poly(ε-caprolactone) composites

被引:58
作者
Cai, Jie [1 ,2 ,3 ]
Xiong, Zhouyi [1 ]
Zhou, Man [1 ,2 ]
Tan, Jun [1 ]
Zeng, Fanbing [4 ]
MeihuMa [1 ]
Lin, Shun [1 ,2 ]
Xiong, Hanguo [1 ,2 ]
机构
[1] Huazhong Agr Univ, Coll Food Sci & Technol, Wuhan 430070, Peoples R China
[2] Huazhong Agr Univ, Res Inst Comprehens Utilizat Biomat, Wuhan 430070, Peoples R China
[3] Deakin Univ, Inst Frontier Mat, Geelong, Vic 3220, Australia
[4] Huazhong Agr Univ, Coll Sci, Wuhan 430070, Peoples R China
基金
中国国家自然科学基金;
关键词
Thermoplastic starch; Poly(epsilon-caprolactone); Thermal properties; Crystallization behavior; NONISOTHERMAL CRYSTALLIZATION; MECHANICAL-PROPERTIES; POLY(LACTIC ACID); STARCH COMPOSITES; PHASE-CHANGE; KINETICS; BLEND; BIODEGRADATION; MORPHOLOGY; FILMS;
D O I
10.1016/j.carbpol.2013.10.095
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
TPS/PCL composites were prepared by PCL melt blending with modified corn starch. The structure, thermal properties, morphology and crystallization behavior of these composites were investigated by FTIR, TGA, SEM, XRD and DSC. FTIR confirmed the existence of the interaction between PCL and TI'S, whereas TGA showed that the thermal stability was decreased by the addition of TPS. Meanwhile, SEM showed a weak interfacial adhesion with increasing TPS. According to the Avrami theory, TPS functioned as a nucleating agent to improve the crystallinity rate of PCL. However, the XRD analysis revealed that the crystallinity decreased. At the same time, the Delta E-a of the composites was higher than those of neat PCL. These changes in values all indicated that mobility constraints existed in the PCL chains with the increasing of TPS, which leaded to a drop in the crystallization ability of PCL. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:746 / 754
页数:9
相关论文
共 40 条
[1]   Preparation of biodegradable polyester/high-amylose-starch composites by reactive blending and their characterization [J].
Avella, M ;
Errico, ME ;
Rimedio, R ;
Sadocco, P .
JOURNAL OF APPLIED POLYMER SCIENCE, 2002, 83 (07) :1432-1442
[2]   Granulation, Phase Change, and Microstructure - Kinetics of Phase Change. III [J].
Avrami, M .
JOURNAL OF CHEMICAL PHYSICS, 1941, 9 (02) :177-184
[3]   Kinetics of phase change I - General theory [J].
Avrami, M .
JOURNAL OF CHEMICAL PHYSICS, 1939, 7 (12) :1103-1112
[4]  
Avrami M., 1940, J CHEM PHYS, V8, P212, DOI DOI 10.1063/1.1750631
[5]   DSC study of biodegradable poly(lactic acid) and poly(hydroxy ester ether) blends [J].
Cao, X ;
Mohamed, A ;
Gordon, SH ;
Willett, JL ;
Sessa, DJ .
THERMOCHIMICA ACTA, 2003, 406 (1-2) :115-127
[6]   Biodegradation of polycaprolactone and its blends with poly(vinylalcohol) by microorganisms from a compost of house-hold refuse [J].
DeKesel, C ;
VanderWauven, C ;
David, C .
POLYMER DEGRADATION AND STABILITY, 1997, 55 (01) :107-113
[7]   Active packaging by extrusion processing of recyclable and biodegradable polymers [J].
Del Nobile, M. A. ;
Conte, A. ;
Buonocore, G. G. ;
Incoronato, A. L. ;
Massaro, A. ;
Panza, O. .
JOURNAL OF FOOD ENGINEERING, 2009, 93 (01) :1-6
[8]  
Elsenhaber F., 1993, J APPL POLYM SCI, V49, P1491
[9]   Relevance of biofilms for the biodeterioration of surfaces of polymeric materials [J].
Flemming, HC .
POLYMER DEGRADATION AND STABILITY, 1998, 59 (1-3) :309-315
[10]   Isothermal Crystallization Kinetics and Melting Behavior of Poly(ethylene terephthalate)/Barite Nanocomposites [J].
Ge, Chunhua ;
Ding, Peng ;
Sh, Liyi ;
Fu, Jifang .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2009, 47 (07) :655-668