Phase behavior and interfacial properties of diblock copolymer-homopolymer ternary mixtures: Influence of volume fraction of copolymers and interaction energy

被引:4
|
作者
Wang, Jian [1 ,2 ]
Song, Jian-hui [3 ]
Lu, Yu-yuan [1 ]
Ruan, Yong-jin [1 ,2 ]
An, Li-jia [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Qingdao Univ Sci & Technol, Sch Polymer Sci & Engn, Qingdao 266042, Peoples R China
基金
中国国家自然科学基金;
关键词
Ternary mixtures; Phase behavior; Interfacial property; Copolymer compatibilizers; Monte Carlo simulation; POLYMERIC BICONTINUOUS MICROEMULSION; MONTE-CARLO SIMULATIONS; DISSIPATIVE PARTICLE DYNAMICS; SEGMENT DENSITY DISTRIBUTION; 2 MONOMERIC HOMOPOLYMERS; BLOCK-COPOLYMER; MOLECULAR-WEIGHT; ELASTIC PROPERTIES; CHAIN TOPOLOGY; THIN-FILMS;
D O I
10.1007/s10118-017-1915-8
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We use a Monte Carlo method to study the phase and interfacial behaviors of A-b-B diblocks in a blend of homopolymers, A and B, which are confined between two asymmetric hard and impenetrable walls. Our results show that, when the interaction strength is weak, the block copolymers are uniformly distributed in the ternary mixtures under considered concentrations. Under strong interaction strength, distribution region of the block copolymers changes from a single smooth interface to a curved interface or multi-layer interface in the ternary mixtures. Furthermore, our findings show that with increasing volume fraction of A-b-B diblock copolymer (I center dot (C)), copolymer profiles broaden while I center dot (C) >= 0.4, a lamellar phase is formed and by further increasing I center dot(C), more thinner layers are observed. Moreover, the results show that, with the increase of I center dot (C), the phase interface first gradually transforms from plane to a curved surface rather than micelle or lamellar phase while with the increase of the interaction between A and B segments (epsilon (AB)), the copolymer chains not only get stretched in the direction perpendicular to the interface, but also are oriented. The simulations also reveal that the difference between symmetric and asymmetric copolymers is negligible in statistics if the lengths of two blocks are comparable.
引用
收藏
页码:874 / 886
页数:13
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