Hydrolytic degradation of cellulose-graft-poly(L-lactide) copolymers

被引:18
作者
Yan, Chenghu [1 ,2 ]
Wu, Jin [2 ]
Zhang, Jinming [2 ]
He, Jiasong [2 ]
Zhang, Jun [2 ]
机构
[1] Chinese Acad Sci, Inst Proc Engn, Natl Key Lab Biochem Engn, Beijing 100190, Peoples R China
[2] Chinese Acad Sci, BNLMS, KLEP, Inst Chem, Beijing 100190, Peoples R China
基金
美国国家科学基金会;
关键词
Cellulose; Poly(L-lactide); Graft copolymer; Ionic liquids; Hydrolytic degradation; BIODEGRADABLE CELLULOSE DIACETATE-GRAFT-POLY(L-LACTIDE)S; TRIMETHYLSILYL PROTECTION METHOD; RING-OPENING POLYMERIZATION; CYCLIC ESTERS; L-LACTIDE; GRAFT;
D O I
10.1016/j.polymdegradstab.2015.04.019
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A series of cellulose-g-poly(L-lactide) (cellulose-g-PLLA) copolymers with 30.65-85.21 % PLLA weight content and the molar substitution of PLLA (MSPLLA) from 0.99 to 12.73 were synthesized via the homogeneous graft-from reaction in 1-allyl-3-methylimidazolium chloride (AmimCI) with 4-dimethylaminopyridine (DMAP) acting as the catalyst. In common organic solvents, the solubility of obtained graft copolymers was better than cellulose and strongly depended on the MSPLLA. The hydrolytic degradation of cellulose-g-PLLA copolymers was investigated in phosphate buffered solution (PBS, pH 7.4) at 37 degrees C. Interestingly, it was found that, when the MSPLLA was below 8.83, the hydrolytic degradation rate of cellulose-g-PLLA copolymers was obviously faster than that of both pristine cellulose and PLLA. Moreover, as the MSPLLA, decreased, the cellulose-g-PLLA copolymers showed a more rapid weight loss, due to its higher hydrophilicity. Both XPS and H-1 NMR analyses demonstrated the degradation occurred mainly at PLLA segments. The morphological observations indicated that, during the hydrolytic degradation, the graft copolymers firstly experienced a surface erosion process, and then the bulk erosion happened. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:130 / 136
页数:7
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