School of Chemistry, Cantock's Close, University of Bristol, Bristol BS8 1TS, United Kingdom.
Centre for Nanoscience and Quantum Information, Bristol BS8 1FD, United Kingdom.
J Chem Phys. 2018 May 14;148(18):184902. doi: 10.1063/1.5023393.
Understanding the phase behaviour of mixtures continues to pose challenges, even for systems that might be considered "simple." Here, we consider a very simple mixture of two colloidal and one non-adsorbing polymer species, which can be simplified even further to a size-asymmetrical binary mixture, in which the effective colloid-colloid interactions depend on the polymer concentration. We show that this basic system exhibits surprisingly rich phase behaviour. In particular, we enquire whether such a system features only a liquid-vapor phase separation (as in one-component colloid-polymer mixtures) or whether, additionally, liquid-liquid demixing of two colloidal phases can occur. Particle-resolved experiments show demixing-like behaviour, but when combined with bespoke Monte Carlo simulations, this proves illusory, and we reveal that only a single liquid-vapor transition occurs. Progressive migration of the small particles to the liquid phase as the polymer concentration increases gives rise to composition inversion-a maximum in the large particle concentration in the liquid phase. Close to criticality, the density fluctuations are found to be dominated by the larger colloids.
即使对于那些被认为“简单”的系统,理解混合物的相行为仍然具有挑战性。在这里,我们考虑了一种非常简单的胶体和一种非吸附聚合物的混合物,甚至可以进一步简化为大小不对称的二元混合物,其中有效胶体-胶体相互作用取决于聚合物浓度。我们表明,这个基本系统表现出惊人的丰富相行为。特别是,我们询问这样的系统是否仅具有液-气相分离(如在单一组分胶体-聚合物混合物中),或者是否还可以发生两个胶体相的液-液分相。颗粒分辨实验显示出类似分相的行为,但与定制的蒙特卡罗模拟相结合时,这被证明是虚幻的,我们揭示出仅发生单一的液-气相转变。随着聚合物浓度的增加,小颗粒逐渐迁移到液相中,导致组成反转-在液相中大颗粒浓度的最大值。在接近临界点时,发现密度涨落主要由较大的胶体主导。