Simple preparation of multi-branched poly(L-lactic acid) and its role as nucleating agent for poly(lactic acid)

被引:46
作者
Phuphuak, Yupin [1 ]
Chirachanchai, Suwabun [1 ,2 ,3 ]
机构
[1] Chulalongkorn Univ, Petr & Petrochem Coll, Bangkok 10330, Thailand
[2] Chulalongkorn Univ, Ctr Petr & Petrochem & Adv Mat, Bangkok 10330, Thailand
[3] Chulalongkorn Univ, Ctr Innovat Nanotechnol, Bangkok 10330, Thailand
关键词
Multi-branched poly(lactic acid); Nucleating agent; Crystallization; CRYSTALLIZATION BEHAVIOR; MECHANICAL-PROPERTIES; BIODEGRADABLE POLYESTERS; MELTING BEHAVIOR; KINETICS; MORPHOLOGY; BLENDS;
D O I
10.1016/j.polymer.2012.11.070
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The present work proposes a simple preparation of multi-branched poly(L-lactic acid)s (m-PLLAs) and their performance as nucleating agents for PLA. By a simple polycondensation of L-lactic acid (L-LA) on the multi-functional core molecules of succinic acid (SA), malic acid (MA) and citric acid (CA) using stannous octanoate (SnOct(2)) as a catalyst, the m-PLLAs as two, three, and four branched PLLA can be obtained easily. Averagely, about 80% of the L-LA feed contents are successfully polymerized on core molecules. Non-isothermal crystallization studies of the PIA blend which contains 1 wt% m-PLLAs indicate that m-PLLAs induce the crystallization of PIA as evidenced from the decreases in glass transition temperature (T-g) and crystallization temperature (T-c), and the increase in degree of crystallinity (chi(c)) under the alpha-form of perfect crystalline in PTA. Isothermal crystallization studies related to Avrami exponent (n), kinetic constant (k) and crystallization half-time (t(1/2)) indicate that the blend maintains its three-dimensional growth for the film thickness 0.05 mm, whereas the crystallization growth rate increases more than 4 times as observed from polarized optical microscope (POM). Among m-PLLA, the highest number of multi-branches with the shortest chain PLLA, i.e. CA-PLLA1, initiates the blends to increase its tensile strength and elongation at break for as high as 1.5 times and 1.2 times, respectively. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:572 / 582
页数:11
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