Accelerated Stereocomplex Crystallization of Poly(L-lactide)/Poly(D-lactide) Blends by Long Terminal Linear Alkyl Groups

被引:10
|
作者
Tsuji, Hideto [1 ]
Sugimoto, Shinya [1 ]
机构
[1] Toyohashi Univ Technol, Grad Sch Engn, Dept Environm & Life Sci, Toyohashi, Aichi 4418580, Japan
关键词
blends; crystallization; nucleation; poly(lactic acid); stereocomplex; POLY(L-LACTIC ACID) CRYSTALLIZATION; NONISOTHERMAL CRYSTALLIZATION; POLY(D-LACTIC ACID); MOLECULAR-WEIGHT; THERMAL-PROPERTIES; SPHERULITE GROWTH; POLY(LACTIC ACID); NUCLEATING-AGENT; PHASE-CHANGE; MELT;
D O I
10.1002/mame.201400401
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The accelerating effect of terminal n-alkyl groups (TAGs) on the non-isothermal crystallization of poly(L-lactide)/poly(D-lactide) blends increased with TAG length in the low temperature range below 100 degrees C and that on isothermal stereocomplex crystallization of poly(L-lactide)/poly(D-lactide) blends became maximal at terminal n-hexyl group in the high temperature range above 165 degrees C. However, the decelerating effect on isothermal stereocomplex crystallization was observed for terminal n-docosyl group in the high temperature range above 165 degrees C. The TAG length did not alter the crystallite growth morphology during non-isothermal crystallization, the formed crystalline species (only stereocomplex crystallites) and the crystallite growth mechanism during isothermal crystallization.
引用
收藏
页码:391 / 402
页数:12
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