聚合物
材料科学
膜
旋节分解
微观结构
玻璃化转变
化学工程
化学物理
旋节
相(物质)
相变
高分子化学
复合材料
化学
热力学
有机化学
生物化学
物理
工程类
作者
Jan Ulric Garcia,Tatsuhiro Iwama,Eva Y. Chan,Douglas R. Tree,Kris T. Delaney,Glenn H. Fredrickson
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2020-10-26
卷期号:9 (11): 1617-1624
被引量:53
标识
DOI:10.1021/acsmacrolett.0c00609
摘要
We report the first simulations of nonsolvent-induced phase separation (NIPS) that predict membrane microstructures with graded asymmetric pore size distribution. In NIPS, a polymer solution film is immersed in a nonsolvent bath, enriching the film in nonsolvent, and leading to phase separation that forms a solid polymer-rich membrane matrix and polymer-poor membrane pores. We demonstrate how mass-transfer-induced spinodal decomposition, thermal fluctuations, and glass-transition dynamics-implemented with mobility contrast between the polymer-rich and polymer-poor phases-are essential to the formation of asymmetric membrane microstructures. Specifically, we show that the competition between the propagation of the phase-separation and glass-transition fronts determines the degree of pore-size asymmetry. We also explore the sensitivity of these microstructures to the initial film composition, and compare their formation in 2D and 3D.
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