支化(高分子化学)
流变学
粘弹性
材料科学
应变硬化指数
高分子化学
均苯四甲酸二酐
高分子科学
凝胶渗透色谱法
长链
化学工程
化学
复合材料
聚合物
聚酰亚胺
工程类
图层(电子)
作者
Jianye Liu,Lou Li-juan,Wei Yu,Ruogu Liao,Runming Li,Chixing Zhou
出处
期刊:Polymer
[Elsevier]
日期:2010-10-01
卷期号:51 (22): 5186-5197
被引量:177
标识
DOI:10.1016/j.polymer.2010.09.002
摘要
Long chain branching (LCB) of polylactide (PLA) was successfully prepared by the successive reactions of the end hydroxyl groups of PLA with pyromellitic dianhydride (PMDA) and triglycidyl isocyanurate (TGIC) together. The topological structures of the LCB generated from functional group reactions as well as free radical reactions were investigated thoroughly by gel permeation chromatography (GPC) and rheology. Qualitative information about the branching structures could be readily obtained from linear viscoelasticity, non-linear oscillatory shear experiments and strain hardening in elongational experiments. For quantitative information on chain structure, linear viscoelasticity combined with branch-on-branch (BOB) dynamic model was used to predict exact compositions and chain topologies of the products, which were reasonably explained by the suggested mechanism of functional group reactions. It was found out that the tree-like LCB structure generated in these reactions contributed remarkably to the enhancement of strain hardening under elongational flow, which improves the foaming ability substantially.
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