NONEQUILIBRIUM LIQUID LIQUID-PHASE SEPARATION IN CRYSTALLIZABLE POLYMER-SOLUTIONS

被引:73
|
作者
LEE, HK
MYERSON, AS
LEVON, K
机构
[1] POLYTECH INST NEW YORK,DEPT CHEM,333 JAY ST,BROOKLYN,NY 11201
[2] POLYTECH INST NEW YORK,DEPT CHEM ENGN,BROOKLYN,NY 11201
关键词
D O I
10.1021/ma00041a024
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 relation between liquid-liquid phase separation and crystallization was investigated by applying a systematic change in the interaction in isotactic polypropylene (i-PP) solutions with a proper selection of solvents. A series of dialkyl phthalates, with a different number of carbon atoms in the alkyl chain, was used to control the solvent quality. The liquid-liquid phase separation temperature decreased remarkably when the interaction became favorable while the melting point curve remained constant. As the result of this systematic change in polymer-solvent interaction, the liquid-liquid phase separation was observed under nonequilibrium conditions below the equilibrium liquid-solid transition. Liquid-liquid phase separation of the i-PP solutions with strong interaction was probed by using atactic polypropylene (a-PP) in the same solvent systems. The results indicate that although the liquid-liquid phase separation of i-PP solutions with the strong interactions cannot be observed in situ due to the competing crystallization, liquid demixing can occur at a low temperature during rapid quenching. An additional feature oberved under the nonequilibrium conditions was liquid-liquid phase separation induced by crystallization in concentration and temperature regions outside the binodal curve. In polydisperse samples, fractionation during liquid-liquid phase separation resulted in bimodal behavior of the liquid-liquid transition and in deviation of melting points in the biphasic region.
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页码:4002 / 4010
页数:9
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