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单价抗衡离子存在下胶体乳胶颗粒的相互作用力和聚集速率

Interaction Forces and Aggregation Rates of Colloidal Latex Particles in the Presence of Monovalent Counterions.

作者信息

Montes Ruiz-Cabello F Javier, Trefalt Gregor, Oncsik Tamas, Szilagyi Istvan, Maroni Plinio, Borkovec Michal

机构信息

Department of Inorganic and Analytical Chemistry, University of Geneva, Quai Ernest-Ansermet 30, 1205 Geneva, Switzerland.

出版信息

J Phys Chem B. 2015 Jun 25;119(25):8184-93. doi: 10.1021/acs.jpcb.5b02556. Epub 2015 Jun 4.

Abstract

Force profiles and aggregation rates involving positively and negatively charged polystyrene latex particles are investigated in monovalent electrolyte solutions, whereby the counterions are varied within the Hofmeister series. The force measurements are carried out with the colloidal probe technique, which is based on the atomic force microscope (AFM), while the aggregation rates are measured with time-resolved multiangle light scattering. The interaction force profiles cannot be described by classical DLVO theory, but an additional attractive short-ranged force must be included. An exponential force profile with a decay length of about 0.5 nm is consistent with the measured forces. Furthermore, the Hamaker constants extracted from the measured force profiles are substantially smaller than the theoretical values calculated from dielectric spectra. The small surface roughness of the latex particles (below 1 nm) is probably responsible for this deviation. Based on the measured force profiles, the aggregation rates can be predicted without adjustable parameters. The measured absolute aggregation rates in the fast regime are somewhat lower than the calculated ones. The critical coagulation concentration (CCC) agrees well with the experiment, including the respective shifts of the CCC within the Hofmeister series. These shifts are particularly pronounced for the positively charged particles. However, the consideration of the additional attractive short-ranged force is essential to quantify these shifts correctly. In the slow regime, the calculated rates are substantially smaller than the experimental ones. This disagreement is probably related to surface charge heterogeneities.

摘要

在单价电解质溶液中研究了涉及带正电和负电的聚苯乙烯乳胶颗粒的力分布和聚集速率,其中抗衡离子在霍夫迈斯特序列内变化。力的测量采用基于原子力显微镜(AFM)的胶体探针技术进行,而聚集速率则通过时间分辨多角度光散射测量。相互作用力分布不能用经典的DLVO理论来描述,而是必须包含一种额外的短程吸引力。衰减长度约为0.5nm的指数力分布与测量的力一致。此外,从测量的力分布中提取的哈梅克常数明显小于从介电谱计算的理论值。乳胶颗粒的小表面粗糙度(低于1nm)可能是造成这种偏差的原因。基于测量的力分布,可以在没有可调参数的情况下预测聚集速率。在快速区域中测量的绝对聚集速率略低于计算值。临界凝聚浓度(CCC)与实验结果吻合良好,包括霍夫迈斯特序列内CCC的相应变化。这些变化对于带正电的颗粒尤为明显。然而,考虑额外的短程吸引力对于正确量化这些变化至关重要。在缓慢区域中,计算的速率明显小于实验值。这种不一致可能与表面电荷不均匀性有关。

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