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探究具有远程吸引力的胶体-聚合物混合物中相分离的动力学。

Exploring the dynamics of phase separation in colloid-polymer mixtures with long range attraction.

机构信息

Department of Physics, Simon Fraser University, Burnaby, British Columbia V5A 1S6, Canada.

出版信息

Soft Matter. 2016 Jun 28;12(24):5325-33. doi: 10.1039/c6sm00224b. Epub 2016 May 31.

Abstract

We have studied the kinetics of phase separation and gel formation in a low-dispersity colloid - non-adsorbing polymer system with long range attraction using small-angle light scattering. This system exhibits two-phase and three-phase coexistence of gas, liquid and crystal phases when the strength of attraction is between 2 and 4kBT and gel phases when the strength of attraction is increased. For those samples that undergo macroscopic phase separation, whether to gas-crystal, gas-liquid or gas-liquid-crystal coexistence, we observe dynamic scaling of the structure factor and growth of a characteristic length scale that behaves as expected for phase separation in fluids. In samples that gel, the power law associated with the growth of the dominant length scale is not equal to 1/3, but appears to depend mainly on the strength of attraction, decreasing from 1/3 for samples near the coexistence region to 1/27 at 8kBT, over a wide range of colloid and polymer concentrations.

摘要

我们使用小角光散射研究了在具有远程吸引力的低分散胶体-非吸附聚合物系统中相分离和凝胶形成的动力学。当吸引力强度在 2 到 4kBT 之间时,该系统表现出气、液和晶体相的二相和三相共存,当吸引力强度增加时,表现出凝胶相。对于经历宏观相分离的那些样品,无论是气-晶、气-液还是气-液-晶共存,我们观察到结构因子的动态标度和特征长度尺度的增长,这与流体相分离的预期一致。在凝胶化的样品中,与主导长度尺度增长相关的幂律不等于 1/3,而是似乎主要取决于吸引力的强度,从接近共存区域的样品的 1/3 减小到 8kBT 时的 1/27,在广泛的胶体和聚合物浓度范围内。

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