Membrane Formation of Poly(vinylidene fluoride)/Poly(methyl methacrylate)/Diluents via Thermally Induced Phase Separation

被引:20
作者
Ma, Wenzhong [1 ]
Chen, Shuangjun [1 ]
Zhang, Jun [1 ]
Wang, Xiaolin [2 ]
Miao, Wenhu [1 ]
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
membrane; thermally induced phase separation (TIPS); crystallization; morphology; POLYMER DILUENT SYSTEMS; DIFFERENTIAL SCANNING CALORIMETRY; ISOTACTIC POLYPROPYLENE MEMBRANES; NUCLEATING-AGENT ADDITION; PVDF-PMMA BLENDS; CRYSTALLIZATION BEHAVIOR; POLY(METHYL METHACRYLATE); NONISOTHERMAL CRYSTALLIZATION; FLUORIDE) PVDF; COOLING RATE;
D O I
10.1002/app.28981
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 role of the single diluents and mixed diluents on the poly (vinylidene fluoride) (PVDF)/poly (methyl methacrylate) (PMMA) blend membranes via thermally induced phase separation (TIPS) process was investigated. The crystallization behaviors of PVDF in the diluted samples were examined by differential scanning calorimetry. The melting and crystallization temperature, of those diluted PVDF blend were decreased with the enhanced interactions between polymer chains and diluent molecules. The crystallinity of PVDF in the diluent was always higher than that obtained in PVDF blend sample. This can be explained by the dilution effects, which increased the average spatial separation distances between crystallizable chains. Thus, the PVDF crystallization was favored. Additionally, solid-liquid (S-L) phase separation Occurred in the quenched samples. fustrated by scanning electron microscopy, inter- and intraspherulitic voids were formed in the ultimate membranes, which related to the polymer/diluent interactions, the kinetics of crystallization and diluent rejection from the growing crystal. The porosity of the PVDF blend membranes obtained from the mixed diluents was higher than those obtained from the single diluent samples. (c) 2008 Wiley Periodicals, Inc. J Appl Polym Sci 111:1235-1245, 2009
引用
收藏
页码:1235 / 1245
页数:11
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