Isotropic-nematic phase separation and demixing in mixtures of spherical nanoparticles with length-polydisperse nanorods

被引:4
作者
Green, Micah J. [1 ]
机构
[1] Texas Tech Univ, Dept Chem Engn, Lubbock, TX 79409 USA
基金
美国国家科学基金会;
关键词
liquid-crystalline polymers (LCP); modeling; theory; MULTIWALL CARBON NANOTUBES; MONTE-CARLO-SIMULATION; HARD SPHEROCYLINDERS; RODLIKE PARTICLES; BINARY-MIXTURES; BEHAVIOR; SPHERES; RODS; TRANSITION; DISPERSIONS;
D O I
10.1002/polb.23126
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
An extension of Onsager theory is developed to simulate isotropicnematic phase separation in a mixture of spheres with length-polydisperse system of rods. This work is motivated by recent experimental data on nanorod liquid crystals. Prior theoretical investigations indicate that both polydispersity and the presence of spheres should increase the biphasicnematic phase transition, that is, the nematic cloud point. Results indicate that the phase diagrams undergo drastic changes depending upon both particle geometry and rod length polydispersity. The key geometric factor is the ratio between the sphere diameter and the rod diameter. In general, length fractionation is enhanced by the addition of spheres, which may be experimentally advantageous for separating short nanorods from a polydisperse population. Simulation results also indicate that the nematic cloud and shadow curves may cross one another because of the scarcity of spheres in the shadow phase. In general, these results do indicate that the nematic cloud point increases as a function of sphere loading; however, in certain areas of phase space, this relationship is nonmonotonic such that the nematic cloud point may actually decrease with the addition of spheres. This work has application to a wide range of nanoparticle systems, including mixtures of spherical nanoparticles with nanorods or nanotubes. Additionally, a number of nonspherical particles and structures may behave as spheres, including crumpled graphene and tightly coiled polymers. (c) 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2012
引用
收藏
页码:1321 / 1327
页数:7
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