Block copolymer compatibilization of cocontinuous polymer blends

被引:132
|
作者
Galloway, JA
Jeon, HK
Bell, JR
Macosko, CW [1 ]
机构
[1] Univ Minnesota, Dept Mat Sci & Chem Engn, Minneapolis, MN 55455 USA
[2] Sandia Natl Labs, Albuquerque, NM 87185 USA
[3] Dow Chem Co USA, Midland, MI 48674 USA
基金
美国国家科学基金会;
关键词
copolymer; cocontinuous; polystyrene-polyethylene block copolymers;
D O I
10.1016/j.polymer.2004.10.061
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 effect of block copolymers on the cocontinuous morphology of 50/50 (w/w) polystyrene (PS)/high density polyethylene (HDPE) blends was investigated using symmetric polystyrene-polyethylene block copolymers (PS-PE) with molecular weights varying from 6 to 200 kg/mol. The coarsening rate during annealing was compared to the Doi-Ohta theory. An intermediate molecular weight PS-PE, 40 kg/mol, showed remarkable results in reducing the phase size and stabilizing the blend morphology during annealing. Mixing small amounts of 6, 100 or 200 kg/mol PS-PE in the blend did not reduce the phase size significantly, but did decrease the coarsening rate during annealing. In stabilizing the morphology, 6 kg/mol PS-PE was inferior to 100 and 200 kg/mol. The existence of an optimal molecular weight block copolymer is due to a balance between the ability of the block copolymer to reach the interface and its relative stabilization effect at the interface. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:183 / 191
页数:9
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