Preparation and thermo-oxidative degradation of poly(L-lactic acid)/poly(L-lactic acid)-grafted SiO2 nanocomposites

被引:1
作者
Li, Deling [1 ]
Liu, Guangtian [2 ]
Wang, Lihong [1 ]
Shen, Yulong [1 ]
机构
[1] Tangshan Normal Univ, Dept Chem, Tangshan 063000, Peoples R China
[2] Yanshan Univ, Coll Environm & Chem Engn, Qinhuangdao 066004, Peoples R China
关键词
Polymer-matrix composites; Nanocomposites; Thermal properties; Thermogravimetric analysis (TGA); SITU MELT POLYCONDENSATION; WALLED CARBON NANOTUBES; ACIDIC SILICA SOL; L-LACTIC ACID; POLYMERIZATION; COMPOSITES; POLYMERS; CRYSTALLIZATION; BEHAVIORS; FILMS;
D O I
10.1007/s00289-011-0475-2
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(L-lactic acid)/poly(L-lactic acid)-grafted SiO2 nanocomposites were prepared by in situ melt polycondensation, in which "free" poly(L-lactic acid) and poly(L-lactic acid)-grafted SiO2 nanoparticles were formed simultaneously. The maximum values of grafting ratio and grafting efficiency of poly(L-lactic acid) were up to 37.67% and 26.60%, respectively. In the polycondensation system, SiO2 content was a critical parameter of getting nanocomposites with uniformly dispersed SiO2 nanoparticles. At lower SiO2 content, Mn of grafted poly(L-lactic acid) was close to that of "free" poly(L-lactic acid), and poly (L-lactic acid)-grafted SiO2 nanoparticles could be well dispersed in poly(L-lactic acid) matrix. While at higher SiO2 content, Mn of "free" poly(L-lactic acid) and grafted poly(L-lactic acid) decreased seriously, especially GPC curves of "free" poly(L-lactic acid) exhibited two peaks due to the aggregation of SiO2 nanoparticles during the polycondensation process. The grafting ratio and SiO2 content exhibited a clear effect on the thermo-oxidative degradation of nanocomposites. The existence of poly(L-lactic acid)-grafted SiO2 nanoparticles dramatically improved the thermo-oxidative stability of poly(L-lactic acid). Compared with that of pure poly(L-lactic acid), T-g, T-c, and T-m of nanocomposites varied slightly.
引用
收藏
页码:1529 / 1538
页数:10
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