Self-assembly of ABA triblock copolymers under soft confinement

被引:21
|
作者
Sheng, Yuping [1 ]
An, Jian [1 ]
Zhu, Yutian [2 ]
机构
[1] Jilin Univ, Coll Mat Sci & Engn, Changchun 130022, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
基金
中国国家自然科学基金;
关键词
Self-assembly; Soft confinement; Monte Carlo simulation; MONTE-CARLO-SIMULATION; C-SELECTIVE SOLVENTS; DIBLOCK COPOLYMER; BLOCK-COPOLYMERS; SEPARATION STRUCTURES; DRUG-DELIVERY; PHASE-DIAGRAM; THIN-FILMS; NANOPARTICLES; VESICLES;
D O I
10.1016/j.chemphys.2015.02.019
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
Using Monte Carlo method, the self-assembly of ABA triblock copolymers under soft confinement is investigated in this study. The soft confinement is achieved by a poor solvent environment for the polymer, which makes the polymer aggregate into a droplet. Various effects, including the block length ratio, the solvent quality for the blocks B, and the incompatibility between blocks A and B, on the micellar structures induced by soft confinement are examined. By increasing the solvent quality of B blocks, the micellar structure transforms from stacked lamella to bud-like structure, and then to onion-like structure for A(5)B(8)A(5) triblock copolymers, while the inner micellar structure changes from spherical phase to various cylindrical phase, such as inner single helix, double helixes, stacked rings and cage-like structures, for A(7)B(4)A(7) triblock copolymers. Moreover, the formation pathways of some typical aggregates are examined to illustrate their growth mechanisms. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:46 / 52
页数:7
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