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Rate of Bubble Coalescence following Quasi-Static Approach: Screening and Neutralization of the Electric Double Layer

机译:准静态方法后气泡合并的速率:双电层的筛选和中和

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摘要

Air-bubble coalescence in aqueous electrolytic solutions, following quasi-static approach, was studied in order to understand its slow rate in purified water and high rate in electrolytic solutions. The former is found to be due to surface charges, originating from the speciation of dissolved CO2, which sustain the electric double layer repulsion. Rapid coalescence in electrolytic solutions is shown to occur via two different mechanisms: (1) neutralization of the carbonaceous, charged species by acids; or (2) screening of the repulsive charge effects by salts and bases. The results do not indicate any ion specificity. They can be explained within the DLVO theory for the van der Waals and electric double layer interactions between particles, in contrast to observations of coalescence following dynamic approach. The present conclusions should serve as a reference point to understanding the dynamic behavior.
机译:为了了解其在纯水中的缓慢速率和在电解溶液中的高速率,按照准静态方法研究了在水溶液中的气泡聚结。发现前者是由于表面电荷所致,该表面电荷源自溶解的CO2的形态,并维持双电层排斥。电解溶液中的快速聚结是通过两种不同的机理发生的:(1)用酸中和含碳的带电物质; (2)筛选盐和碱的排斥电荷效应。结果没有表明任何离子特异性。可以在DLVO理论中解释粒子之间的范德华力和双电层相互作用,这与动态方法后的合并观察相反。本结论应为理解动力学行为提供参考。

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