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通过流变学测量区分带电胶体系统中的键合和笼。

Differentiating bonding and caging in a charged colloid system through rheological measurements.

机构信息

State Key Laboratory of Polymer Physics and Chemistry, Joint Laboratory of Polymer Science and Materials, Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, CAS, Beijing 100190, China.

出版信息

J Chem Phys. 2013 May 14;138(18):184902. doi: 10.1063/1.4803857.

Abstract

The linear and nonlinear rheological measurements were utilized to study the mechanical response of concentrated mixtures of colloidal particles with opposite charges. The particle volume fraction (Φ) spans the region from low volume fraction (Φ = 0.18) gel to high volume fraction (Φ = 0.53) glass. In the linear viscoelastic region, the storage moduli G' exhibits deferent Φ dependence at low and high Φ's. It follows a power law relationship as G' ~ Φ(6.2±0.2) for Φ < 0.46, and follows an exponential relationship as G' ~ exp[(13.8 ± 0.6)Φ] for Φ ≥ 0.46. The difference can be taken as a distinction between a colloidal gel and an attractive glass (or dense gel) for the present system. The loss moduli G" is almost frequency independent within the whole experimental frequency range (10(-1)-10(2) rad∕s) for colloidal gel, and G" exhibits a weak minimum for attractive glass. In the nonlinear large amplitude rheological measurement, samples with Φ < 0.46 show one-step yielding, and samples with Φ ≥ 0.46 exhibit two-step yielding which is in agreement with numerous experiments in attractive glassy systems. The first yielding is due to the breaking of short range interactions which bond the interconnected clusters or local clusters, while the second yielding is attributed to the breaking of long range interaction, normally the caging forming or glass forming interactions. The qualitative distinction between attractive glass and gel in terms of their yielding behavior is consistent with the linear rheological results. The particle-particle interactions were modulated by salt concentration. It was found that, when the attraction interaction is enhanced, both yielding points in attractive glass shift to higher strain amplitude and the gap between the two yielding points become more separated.

摘要

利用线性和非线性流变测量研究了带相反电荷的胶体颗粒的浓混合物的力学响应。颗粒体积分数 (Φ) 跨越低体积分数 (Φ = 0.18) 凝胶到高体积分数 (Φ = 0.53) 玻璃的区域。在线性粘弹区,储能模量 G' 在低和高 Φ 值下表现出不同的 Φ 依赖性。它遵循幂律关系,即 G'Φ(6.2±0.2),对于 Φ < 0.46,并且遵循指数关系,即 G'exp[(13.8 ± 0.6)Φ],对于 Φ ≥ 0.46。这种差异可以作为本系统中胶体凝胶和吸引力玻璃(或密集凝胶)之间的区别。对于胶体凝胶,损耗模量 G"在整个实验频率范围内(10(-1)-10(2) rad∕s)几乎与频率无关,而吸引力玻璃的 G"表现出微弱的最小值。在非线性大振幅流变测量中,Φ < 0.46 的样品表现出一步屈服,而 Φ ≥ 0.46 的样品表现出两步屈服,这与吸引力玻璃系统中的许多实验一致。第一次屈服是由于打破了将相互连接的团簇或局部团簇结合在一起的短程相互作用,而第二次屈服是由于打破了长程相互作用,通常是笼形成或玻璃形成相互作用。从屈服行为的角度来看,吸引力玻璃和凝胶之间的定性区别与线性流变结果一致。颗粒-颗粒相互作用被盐浓度调节。结果发现,当吸引力相互作用增强时,吸引力玻璃中的两个屈服点都向更高的应变幅度移动,并且两个屈服点之间的间隙变得更加分离。

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