Dependence of aggregation behavior on concentration in triblock copolymer solutions: The effect of chain architecture

被引:5
作者
Han, Xiang-Gang [1 ]
Zhang, Xue-Feng [1 ]
机构
[1] Inner Mongolia Univ Sci & Technol, Key Lab Integrated Exploitat Bayan Obo Multimet R, Sch Math Phys & Biol Engn, Baotou 014010, Peoples R China
关键词
DISSIPATIVE PARTICLE DYNAMICS; BLOCK-COPOLYMER; DIBLOCK COPOLYMER; MICELLIZATION KINETICS; POLYMER CONCENTRATION; DILUTE-SOLUTION; LIGHT-SCATTERING; AQUEOUS-SOLUTION; DRUG-DELIVERY; MICELLES;
D O I
10.1063/1.4936581
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 the self-consistent field lattice technique, the effects of concentration and hydrophobic middle block length (where the chain length remains constant) on aggregation behavior are studied in amphiphilic symmetric triblock copolymer solutions. The heat capacity peak for the unimer-micelle transition and the distribution peaks for the different degrees of aggregation for micelles and small aggregates (submicelles) are calculated. Analysis of the conducted computer simulations shows that the transition broadness dependence on concentration is determined by the hydrophobic middle block length, and this dependence is distinctly different when the length of the hydrophobic middle block changes. Different size for small aggregates simultaneously appear in the transition region. As temperature decreases, the number of different size small aggregates for the large hydrophobic middle block length first ascends and then descends in aggregation degree order. These results indicate that any transition broadness change with concentration is related to the mechanism of fragmentation and fusion. These results are helpful for interpreting the aggregation process of amphiphilic copolymers at equilibrium. (C) 2015 AIP Publishing LLC.
引用
收藏
页数:7
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