Complex micelles from the self-assembly of amphiphilic triblock copolymers in selective solvents

被引:37
|
作者
He, Pengtao [1 ]
Li, Xuejin [1 ]
Kou, Dazhi [2 ]
Deng, Mingge [1 ]
Liang, Haojun [1 ,3 ]
机构
[1] Univ Sci & Technol China, Dept Polymer Sci & Engn, CAS Key Lab Soft Matter Chem, Hefei 230026, Anhui, Peoples R China
[2] Shanghai Supercomp Ctr, Shanghai 201203, Peoples R China
[3] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China
来源
JOURNAL OF CHEMICAL PHYSICS | 2010年 / 132卷 / 20期
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
aggregation; colloids; crystal microstructure; polymer blends; polymer structure; self-assembly; DISSIPATIVE PARTICLE DYNAMICS; SPONTANEOUS VESICLE FORMATION; BLOCK-COPOLYMER; DIBLOCK COPOLYMER; COMPUTER-SIMULATION; SIZE; MORPHOLOGIES; TRANSITION; ORIGINS;
D O I
10.1063/1.3431203
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
The self-assembled microstructures of amphiphilic block copolymers depend on the selectivity of solvents for each block. By changing the selectivity of solvents, defined in terms of the repulsive interactions between the solvent and the hydrophilic/hydrophobic particles, an extensive simulation study on the spontaneous formation of complex micelles from amphiphilic triblock copolymers in a dilute solution is presented. The dynamic pathways in the formation of these assemblies have been investigated using a particle-based dissipative particle dynamics approach. In addition, the potential mechanism behind the formation of these microstructures has also been studied, which may be helpful in explaining how these aggregates are formed and in understanding the general principle of amphiphilic molecules. (C) 2010 American Institute of Physics. [doi: 10.1063/1.3431203]
引用
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页数:6
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