Micelle morphology and chain conformation of triblock copolymers under shear: LA-DPD study

被引:16
|
作者
Prhashanna, Ammu [1 ]
Khan, Saif A. [1 ]
Chen, Shing Bor [1 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 117585, Singapore
关键词
DPD simulations; Lowe-Anderson thermostat; Triblock copolymers; Self-assembly; PARTICLE DYNAMICS SIMULATION; BLOCK-COPOLYMER; PHASE-BEHAVIOR; MESOSCOPIC SIMULATION; MULTIPLE MORPHOLOGIES; DIBLOCK COPOLYMERS; NEUTRON-SCATTERING; AQUEOUS-SOLUTION; THIN-FILMS; ALIGNMENT;
D O I
10.1016/j.colsurfa.2016.07.003
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
We present an investigation on the morphologies of Pluronic (P123 and P84) micelles subject to a simple shear flow via dissipative particle dynamics simulations in conjunction with the Lowe-Anderson thermostat. The most interesting finding is that the polymer chains take a wide variety of conformations, showing a nearly uniform distribution, rather than either a loop or a bridge as speculated previously. The micellar solutions show shear thinning behavior, and the chains are stretched more easily when the concentration is increased at a given shear rate. For the polymer volume fraction phi <= 0.2, weak flows lead to coalescence of spherical micelles, while rodlike micelles are formed in strong flows. At phi = 0.3, the ellipsoidal micelles are disrupted into smaller spherical micelles in weak flow. For P123 at phi = 0.5, a fragile gyroid-type network formed at equilibrium can be easily disrupted into ellipsoidal micelles of very different sizes by a fairly weak shear force. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:457 / 466
页数:10
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