Guevara-Pantoja Francisco Javier, Ruiz-Suárez J C
CINVESTAV-Monterrey, PIIT Autopista Nueva al Aeropuerto Km. 9.5 Apodaca Nuevo León 66600 Mexico
RSC Adv. 2021 Jul 9;11(39):24190-24195. doi: 10.1039/d1ra04252a. eCollection 2021 Jul 6.
Vitrification in a dilute colloidal system needs an asymmetric particle composition (a mixture of nano and micro colloids) to materialize. The volume fraction of the large particles increases (up to ≈0.58) driven by depletion forces produced by the smaller colloids. Such entropic forces are short-ranged and attractive. We found a different type of dynamical arrest in an extremely dilute asymmetric mixture of nanovesicles and polystyrene microparticles, where energy, instead of entropy, is the main protagonist to drive the arrest. Furthermore, when the vesicles go through the gel-fluid phase transition, the mean square displacements of the microparticles suffer a sudden splitting indicating a viscous jump. If the vesicles are doped with negatively charged lipids, particles and vesicles repel each other and the rheology of the mixture becomes athermal and Newtonian. Our findings are important to understand caging phenomena in biological systems, where diverse electrostatic distributions are present.
在稀胶体系统中实现玻璃化需要不对称的颗粒组成(纳米胶体和微米胶体的混合物)。在较小胶体产生的耗尽力作用下,大颗粒的体积分数增加(高达约0.58)。这种熵力作用范围短且具有吸引力。我们在纳米囊泡和聚苯乙烯微粒的极稀不对称混合物中发现了一种不同类型的动力学阻滞,其中能量而非熵是驱动阻滞的主要因素。此外,当囊泡经历凝胶 - 流体相变时,微粒的均方位移会突然分裂,表明存在粘性跳跃。如果囊泡掺杂带负电荷的脂质,颗粒和囊泡会相互排斥,混合物的流变学变为无热和牛顿流体性质。我们的发现对于理解生物系统中存在多种静电分布的笼蔽现象很重要。