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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >From Repulsion to Attraction and Back to Repulsion: The Effect of NaCl, KCl, and CsCl on the Force between Silica Surfaces in Aqueous Solution
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From Repulsion to Attraction and Back to Repulsion: The Effect of NaCl, KCl, and CsCl on the Force between Silica Surfaces in Aqueous Solution

机译:从排斥到吸引再到排斥:NaCl,KCl和CsCl对水溶液中硅胶表面之间力的影响

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摘要

The force between silica surfaces in NaCl, KCl and CsCl aqueous solutions is Studied at pH 5.5 using an atomic force microscope (AFM). As ion concentration is increased, more cations adsorb to the negatively charged silica, gradually neutralizing the surface charge, hence, suppressing the electrostatic double layer repulsion and revealing van der Waals attraction. At even higher salt concentrations, repulsion reemerges due to surface charge reversal by excess adsorbed cations. Adsorption grows monotonically with cation radius. At pH 5.5 the smallest ion, Na+, neutralizes the Surface at 0.5-1 M, K+ at 0.2-0.5 M, and Cs+ at similar to 0.1 M. Titration with HCl to pH 4.0 shifts surface neutralization and charge reversal to lower salt concentrations compared with pH 5.5. When attraction dominates, the force curves are practically identical for the three salts, independent of their concentration.
机译:使用原子力显微镜(AFM)在pH 5.5下研究NaCl,KCl和CsCl水溶液中二氧化硅表面之间的力。随着离子浓度的增加,更多的阳离子吸附到带负电荷的二氧化硅上,逐渐中和了表面电荷,因此抑制了静电双层排斥并显示出范德华吸引力。在更高的盐浓度下,由于过量吸附的阳离子使表面电荷逆转,斥力重新出现。吸附随阳离子半径单调增长。在pH 5.5时,最小的离子Na +在0.5-1 M时中和表面,在0.2-0.5 M中的K +中和在0.1 M附近的Cs +。用HCl滴定至pH 4.0可将表面中和和电荷反转转移到较低的盐浓度pH 5.5。当吸引力起主导作用时,三种盐的力曲线实际上是相同的,而与它们的浓度无关。

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