中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Synthesis and characterization of ABBA block copolymer of glycolide and epsilon-caprolactone

文献类型:期刊论文

作者Chen, L; Chen, XS; Deng, MX; Jing, XB
刊名CHEMICAL RESEARCH IN CHINESE UNIVERSITIES
出版日期2005-05-01
卷号21期号:3页码:340-344
关键词Biomaterial Polyglycolide Poly (Epsilon-caprolactone) Ring-opening Polymerization Block Copolymer
ISSN号1005-9040
英文摘要A biodegradable ABBA block copolymer was synthesized via the ring-opening co-polymerization of E-caprolactone (CL, B) and glycolide (A) by means of step polymerization in the presence of ethylene glycol as an initiator and stannous octanoate as a catalyst at 110 degrees C for 48 h. The molecular length of the PCL prepolymer (BB) could be adjusted by controlling the molar ratio of the ethylene glycol initiator to c-caprolactone monomer. The structure and the composition of the block copolymer were determined by the weight ratio of the monomer glycolide (A) to PCL pre-polymer (BB). The block copolymers were characterized by H-1 NMR. GPC, DSC and X-ray. The results confirm the successful synthesis of an ABBA block copolymer.
语种英语
WOS记录号WOS:000229624800020
出版者HIGHER EDUCATION PRESS
源URL[http://ir.iccas.ac.cn/handle/121111/57745]  
专题中国科学院化学研究所
通讯作者Chen, XS
作者单位1.Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
2.NE Normal Univ, Fac Chem, Changchun 130022, Peoples R China
推荐引用方式
GB/T 7714
Chen, L,Chen, XS,Deng, MX,et al. Synthesis and characterization of ABBA block copolymer of glycolide and epsilon-caprolactone[J]. CHEMICAL RESEARCH IN CHINESE UNIVERSITIES,2005,21(3):340-344.
APA Chen, L,Chen, XS,Deng, MX,&Jing, XB.(2005).Synthesis and characterization of ABBA block copolymer of glycolide and epsilon-caprolactone.CHEMICAL RESEARCH IN CHINESE UNIVERSITIES,21(3),340-344.
MLA Chen, L,et al."Synthesis and characterization of ABBA block copolymer of glycolide and epsilon-caprolactone".CHEMICAL RESEARCH IN CHINESE UNIVERSITIES 21.3(2005):340-344.

入库方式: OAI收割

来源:化学研究所

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