Toughening of poly(propylene carbonate) by hyperbranched poly(ester-amide) via hydrogen bonding interaction

被引:41
作者
Chen, Lijie [1 ,2 ]
Qin, Yusheng [1 ]
Wang, Xianhong [1 ]
Li, Yuesheng [3 ]
Zhao, Xiaojiang [3 ]
Wang, Fosong [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Polymer Ecomat, Changchun 130022, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
[3] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
基金
中国国家自然科学基金;
关键词
poly(propylene carbonate); hyperbranched poly(ester-amide); hydrogen-bonding interaction; biodegradable blends; toughening; MECHANICAL-PROPERTIES; BIODEGRADABLE BLENDS; MOLECULAR-WEIGHT; BINARY BLENDS; MISCIBILITY; COPOLYMERIZATION; COMPLEXES; DIOXIDE; POLY(EPSILON-CAPROLACTONE); EPOXIDES;
D O I
10.1002/pi.3132
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
Poly(propylene carbonate) (PPC) is a biodegradable alternative copolymer of propylene oxide and carbon dioxide. As an amorphous polymer with lower glass transition temperature around 35 degrees C, PPC shows poor mechanical performance in that it becomes brittle below 20 degrees C and its dimensional stability deteriorates above 40 degrees C; thus toughening of PPC is urgently needed. Here we describe a biodegradable hyperbranched poly(ester-amide) (HBP) that is suitable for this purpose. Compared with pure PPC, the PPC/HBP blend with 2.5 wt% HBP loading showed a 51 degrees C increase in thermal decomposition temperature and a 100% increase in elongation at break, whilst the corresponding tensile strength remained as high as 45 MPa and tensile modulus showed no obvious decrease. Crazing as well as cavitation was observed in the scanning electron microscopy images of the blends, which provided good evidence for the toughening mechanism of PPC. The intermolecular hydrogen bonding interaction confirmed by Fourier transform infrared spectral analysis proved to be the reason for the toughening phenomenon. (C) 2011 Society of Chemical Industry
引用
收藏
页码:1697 / 1704
页数:8
相关论文
共 38 条
[1]
Miscibility and intermolecular hydrogen-bonding interactions in poly(3-hydroxybutyrate-co-3-hydroxyhexanoate)/poly(4-vinyl phenol) binary blends [J].
Alata, Hexig ;
Zhu, Bo ;
Inoue, Yoshio .
JOURNAL OF APPLIED POLYMER SCIENCE, 2007, 106 (03) :2025-2030
[2]
Discrete metal-based catalysts for the copolymerization CO2 and epoxides:: Discovery, reactivity, optimization, and mechanism [J].
Coates, GW ;
Moore, DR .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (48) :6618-6639
[3]
COLEMAN MM, 1976, POLYM REV, V16, P197
[4]
Copolymerization of CO2 and epoxides catalyzed by metal salen complexes [J].
Darensbourg, DJ ;
Mackiewicz, RM ;
Phelps, AL ;
Billodeaux, DR .
ACCOUNTS OF CHEMICAL RESEARCH, 2004, 37 (11) :836-844
[5]
THERMAL STABILIZATION OF POLY(ALKYLENE CARBONATE)S [J].
DIXON, DD ;
FORD, ME ;
MANTELL, GJ .
JOURNAL OF POLYMER SCIENCE PART C-POLYMER LETTERS, 1980, 18 (02) :131-134
[6]
FTIR study of poly(propylene carbonate)/bisphenol A blends [J].
Fei, B ;
Chen, C ;
Peng, SW ;
Zhao, XJ ;
Wang, XH ;
Dong, LS .
POLYMER INTERNATIONAL, 2004, 53 (12) :2092-2098
[7]
Comparative study of PHBV/TBP and PHBV/BPA blends [J].
Fei, B ;
Chen, C ;
Wu, H ;
Peng, SW ;
Wang, XY ;
Dong, LS .
POLYMER INTERNATIONAL, 2004, 53 (07) :903-910
[8]
He Y, 2000, J POLYM SCI POL PHYS, V38, P1848, DOI 10.1002/1099-0488(20000715)38:14<1848::AID-POLB30>3.0.CO
[9]
2-F
[10]
Hydrogen-bonding interaction and miscibility between poly(ε-caprolactone) and enzymatically polymerized novel polyphenols [J].
He, Y ;
Li, JC ;
Uyama, H ;
Kobayashi, S ;
Inoue, Y .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2001, 39 (22) :2898-2905