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在不存在纳米气泡桥接的情况下,溶解气体对疏水表面短程吸引力的影响。

The Effect of Dissolved Gases on the Short-Range Attractive Force between Hydrophobic Surfaces in the Absence of Nanobubble Bridging.

机构信息

School of Chemical Engineering, The University of Queensland, Brisbane, Queensland 4072, Australia.

Sustainable Minerals Institute, The University of Queensland, Brisbane, Queensland 4072, Australia.

出版信息

Langmuir. 2020 Sep 1;36(34):9987-9992. doi: 10.1021/acs.langmuir.0c00117. Epub 2020 Aug 18.

DOI:10.1021/acs.langmuir.0c00117
PMID:32787046
Abstract

The short-range attractive forces between hydrophobic surfaces are key factors in a wide range of areas such as protein folding, lipid self-assembly, and particle-bubble interaction such as in industrial flotation. Little is certain about the effect of dissolved (well-controlled) gases on the interaction forces, in particular in those systems where the formation of surface nanobubble bridges is suppressed. Here, we probe the short-range attractive force between hydrophobized silica surfaces in aqueous solutions with varying but well-controlled isotherms of gas solubility. The first contact approach force measurement method using AFM shows that decreasing gas solubility results in a decrease of the force magnitude as well as shortening of its range. The behavior was found to be consistent across all four aqueous systems and gas solubilities tested. Using numerical computations, we corroborate that attractive force can be adequately explained by a multilayer dispersion force model, which accounts for an interfacial gas enrichment (IGE), that results in the formation of a dense gas layer (DGL) adjacent to the hydrophobic surface. We found that the DGL on the hydrophobic surface is affected only by the concentration of dissolved gases and is independent of the salt type, used to control the gas solubility, which excludes the effect of electrical double-layer interactions on the hydrophobic force.

摘要

短程疏水表面吸引力是蛋白质折叠、脂质自组装和颗粒-气泡相互作用(如工业浮选)等广泛领域的关键因素。对于溶解(良好控制)气体对相互作用力的影响,人们知之甚少,特别是在那些抑制表面纳米气泡桥形成的系统中。在这里,我们在具有不同但良好控制的气体溶解度等温线的水溶液中探测疏水性二氧化硅表面之间的短程吸引力。使用 AFM 的首次接触法接近力测量方法表明,降低气体溶解度会导致力的大小减小,并且其范围缩短。在所有四个测试的水溶液和气体溶解度系统中都发现了这种行为。通过数值计算,我们证实吸引力可以通过多层色散力模型得到充分解释,该模型考虑了界面气体富集(IGE),导致在疏水性表面附近形成致密气体层(DGL)。我们发现,疏水表面上的 DGL 仅受溶解气体浓度的影响,而与用于控制气体溶解度的盐类型无关,这排除了双电层相互作用对疏水力的影响。

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