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A new approach to prepare high molecular weight poly(p-dioxanone) by chain-extending from dihydroxyl terminated propolymers
被引:21
|作者:
Zeng, Qiang
[1
]
Yang, Ke-Ke
[1
]
Chen, Si-Chong
[1
]
Wang, Xiu-Li
[1
]
Zeng, Jian-Bing
[1
]
Wang, Yu-Zhong
[1
]
机构:
[1] Sichuan Univ, Coll Chem, Ctr Degradable & Flame Retardant Polymer Mat, Chengdu 610064, Peoples R China
基金:
中国国家自然科学基金;
关键词:
poly(p-dioxa none);
hydroxyl-terminated;
chain extending;
toluene-2,4-diisocyanate;
D O I:
10.1016/j.eurpolymj.2007.11.008
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
As poly(p-dioxanone) (PPDO) with a high molecular weight (viscosity-average molecular weight (M-v) > 100,000 g/mol) is not easy to be obtained in a short time, a new approach has been developed to produce high molecular weight poly(p-dioxanone) (HPPDO-T) by chain-extending reaction of hydroxyl-terminated PPDO (HPPDO) prepolymers using toluene-2,4-diisocyanate (TDI) as chain extender. Here HPPDO prepolymers were synthesized via ring-opening polymerization of p-dioxanone (PDO) monomer initiated by 1,4-butanediol (BD) with Stannous octoate (SnOct(2)) as catalyst. The resulting polymers, having a highest Mv of 250,000 g/mol, were characterized by H-1 NMR, TG, DSC and WXRD. HPPDO prepolymers can react with TDI more effectively than the PPDO prepolymers initiated by mono-functional initiators, and the molecular weights of resulting chain-extended products increase several decade times in an hour comparing to the prepolymers. The chain extended products HPPDO-T have better thermal stability, and higher glass transition temperatures and lower crystallization rates than PPDO homopolymer. (c) 2007 Elsevier Ltd. All rights reserved.
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页码:465 / 474
页数:10
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