Modeling solvent evaporation during thin film formation in phase separating polymer mixtures

被引:48
作者
Cummings, John [1 ]
Lowengrub, John S. [2 ]
Sumpter, Bobby G. [3 ,4 ]
Wise, Steven M. [1 ]
Kumar, Rajeev [1 ,3 ,4 ]
机构
[1] Univ Tennessee, Dept Math, Knoxville, TN 37996 USA
[2] Univ Calif Irvine, Dept Math, Irvine, CA 92697 USA
[3] Oak Ridge Natl Lab, Computat Sci & Engn Div, Oak Ridge, TN 37831 USA
[4] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37831 USA
基金
美国国家科学基金会;
关键词
SPINODAL DECOMPOSITION; CONDENSATION COEFFICIENTS; IRREVERSIBLE-PROCESSES; RECIPROCAL RELATIONS; PATTERN-FORMATION; DROPLETS; BLENDS; DEPOSITION; MORPHOLOGY; EVOLUTION;
D O I
10.1039/c7sm02560b
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
Preparation of thin films by dissolving polymers in a common solvent followed by evaporation of the solvent has become a routine processing procedure. However, modeling of thin film formation in an evaporating solvent has been challenging due to a need to simulate processes at multiple length and time scales. In this work, we present a methodology based on the principles of linear non-equilibrium thermodynamics, which allows systematic study of various effects such as the changes in the solvent properties due to phase transformation from liquid to vapor and polymer thermodynamics resulting from such solvent transformations. The methodology allows for the derivation of evaporative flux and boundary conditions near each surface for simulations of systems close to the equilibrium. We apply it to study thin film microstructural evolution in phase segregating polymer blends dissolved in a common volatile solvent and deposited on a planar substrate. Effects of the evaporation rates, interactions of the polymers with the underlying substrate and concentration dependent mobilities on the kinetics of thin film formation are studied.
引用
收藏
页码:1833 / 1846
页数:14
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