Phase separation and polymer crystallization in a poly(4-methyl-1-pentene)-dioctylsebacate-dimethylphthalate system via thermally induced phase separation

被引:37
作者
Tao, Haijun
Zhang, Jun [1 ]
Wang, Xiaolin
Gao, Jiali
机构
[1] Nanjing Univ Technol, Coll Mat Sci & Engn, Nanjing 210009, Peoples R China
[2] Tsinghua Univ, Dept Chem Engn, Beijing 100084, Peoples R China
关键词
crystallization; dual-melting-peak behavior; membrane; phase separation; poly(4-methyl-1-pentene); thermally induced phase separation;
D O I
10.1002/polb.20885
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 effects of the polymer concentration and quenching temperature on the phase separation, the membrane morphology and polymer crystallization behavior in a poly(4-methyl-1-pentene) (TPX)-dioctylsebacate (DOS)-dimethylphthalate (DMP) system via thermally induced phase separation were studied with a pseudobinary phase diagram, with the weight ratio of DOS:DMP = 1:1. SEM was used to observe the membrane morphology and structure, whereas the TPX crystallization behavior was studied with DSC and WAXD. Liquid-liquid phase separation occurred, although quenching under the crystallization temperature. As the quenching temperature decreased, the pore size decreased, with better connected pore structure formed. The membranes quenched at 333 and 363 K showed good cellular structures, with an average pore size of about 2.3 mu m, whereas the pores of the membranes quenched at 393 and 423 K were not well formed, with some lamellar crystals on the inner side. The diluent assisted the mobility of the polymer chain, which improved the polymer crystallization. Dual-melting-peak behavior occurred for all the samples studied here. As the quenching temperature increased, the first peak of the melting trace moved to a higher temperature, whereas the second one stayed almost the same. The flexibility of the TPX main chain was restricted by the side groups, which allowed liquid-liquid phase separation to occur first when quenched below the equilibrium crystallization temperature. This allowed primary and secondary crystallization, which was responsible for the dual-melting-peak behavior. (c) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:153 / 161
页数:9
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