Study on the Crystallization Activation Energy of Poly (L-lactic acid) Nucleated with P-tert-butylcalix[8]arene

被引:5
|
作者
Shi, Yaoqi [1 ]
Wen, Liang [1 ]
Xin, Zhong [2 ]
机构
[1] East China Univ Sci & Technol, Coll Chem Engn, Shanghai Key Lab Multiphase Mat Chem Engn, Shanghai 200237, Peoples R China
[2] East China Univ Sci & Technol, Coll Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
来源
POLYMERS & POLYMER COMPOSITES | 2018年 / 26卷 / 02期
关键词
Crystallization activation energy; Nucleation; Poly (L-lactic acid); TEMPERATURE-DEPENDENCE; GROWTH; BEHAVIOR; GLYCOL);
D O I
10.1177/096739111802600205
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The crystallization activation energy (Delta E) of a polymer comprises the nucleation activation energy Delta F and the transport activation energy Delta E-star. In this paper, the Delta E of poly (L-lactic acid) (PLLA) nucleated with nucleating agent p-tert-butylcalix[8]arene (tBC8) was calculated. The results showed that the Delta E of nucleated PLLA was 165.97 kJ/mol, which is higher than that of pure PLLA. The reason why Delta E of PLLA increased when incorporating nucleating agent was studied. The increment of glass transition temperature (Tg) for nucleated PLLA revealed that the polymer chain mobility was restricted by tBC8, which was considered as the reason for the increase of Delta E-star. Further, polyethylene glycol (PEG) was added to improve the chain mobility, thus eliminated the variation of the transport activation energy Delta E-star caused by tBC8. Then the effect of the increment of crystallization temperature range on the increase of Delta F was also taken into consideration. It was concluded that both decreasing the mobility of chain segments and increasing the crystallization temperature range caused an increase of Delta E for PLLA/tBC8.
引用
收藏
页码:169 / 175
页数:7
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