Phase separation of polymer casting solution by nonsolvent vapor

Authors
Lee, HJJung, BKang, YSLee, H
Issue Date
2004-12-01
Publisher
ELSEVIER
Citation
JOURNAL OF MEMBRANE SCIENCE, v.245, no.1-2, pp.103 - 112
Abstract
Kinetics of phase separation of polymer solution layers induced by nonsolvent vapor was investigated. Polymer solutions were prepared with polysulfone (PSF) and N-methyl-2-pynolidinone (NMP) as a solvent. The phase separation was induced by exposing the solution layers to controlled water vapor. Using time-resolved small angle light scattering and phase contrast optical microscope, the kinetics of the phase separation was studied for several concentrations of polymer solution films. The phase separation took place as the solution layers absorbed nonsolvent (water) vapor. As the phase separation proceeds, the scattering halo was observed, which implies that the phase separation occurs via spinodal decomposition. Bicontinuous network structure, which is a characteristic morphology of the spinodal decomposition, was confirmed by optical microscopy. The analysis of the early stage of phase separation was based on Cahn-Hilliard theory and mutual diffusion coefficients were evaluated. The late stage of phase separation was analyzed by means of power law (q(m) similar to t(-alpha)). In the late stage of the phase separation, spontaneous pinning of phase domain was observed. Finally, when the phase-separated solution layers were coagulated in the water bath, it was found that the correlation length at pinning regime is proportional to the pore size of the resulting material. (C) 2004 Elsevier B.V. All rights reserved.
Keywords
STAGE SPINODAL DECOMPOSITION; DIFFUSION; MEMBRANES; KINETICS; MIXTURE; GROWTH; NUCLEATION; STAGE SPINODAL DECOMPOSITION; DIFFUSION; MEMBRANES; KINETICS; MIXTURE; GROWTH; NUCLEATION; phase separation; kinetics; nonsolvent; polymer solution; spinodal decomposition
ISSN
0376-7388
URI
https://pubs.kist.re.kr/handle/201004/136926
DOI
10.1016/j.memsci.2004.08.006
Appears in Collections:
KIST Article > 2004
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