INTERFACIAL-TENSIONS OF PHASE-SEPARATED POLYMER-SOLUTIONS

被引:36
|
作者
XIA, KQ
FRANCK, C
WIDOM, B
机构
[1] CORNELL UNIV,ATOM & SOLID STATE PHYS LAB,ITHACA,NY 14853
[2] CORNELL UNIV,CTR MAT SCI,ITHACA,NY 14853
来源
JOURNAL OF CHEMICAL PHYSICS | 1992年 / 97卷 / 02期
关键词
D O I
10.1063/1.463220
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Measurements of the capillary length in phase-separated solutions of polymethylmethacrylate in 3-octanone (PMMA/3-OCT) for each of five different molecular weights of PMMA, and in phase-separated solutions of polystyrene in methylcyclohexane (PS/MCH) for a single molecular weight of polymer, are reported. Measurements on PMMA/3-OCT were by the sessile-drop method; those on PS/MCH were by both the sessile-drop and capillary-rise methods. Interfacial tensions are estimated from estimated density differences and the measured capillary lengths. A theoretically predicted scaling law for the dependence of capillary length on polymer molecular weight and temperature is tested and at least semiquantitatively verified. As by-products of the sample preparation, the molecular-weight dependences of the critical composition and critical solution temperature of PMMA/3-OCT were also determined. The volume fraction of polymer at the critical point, phi(c), is found to be proportional to the -0.37+/-0.01 power of the molecular weight, in agreement with values of this exponent found by others for polystyrene solutions.
引用
收藏
页码:1446 / 1454
页数:9
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