Cation capture and overcharging of a hydrophobized quartz surface in concentrated potassium chloride solutions

被引:9
|
作者
Boinovich, Ludmila B. [1 ]
Sobolev, Vladimir D. [1 ]
Maslakov, Konstantin I. [1 ,2 ]
Domantovsky, Alexandr G. [3 ]
Sergeeva, Inessa P. [1 ]
Emelyanenko, Alexandre M. [1 ]
机构
[1] AN Frumkin Inst Phys Chem & Electrochem, Leninsky Prospect 31 Bldg 4, Moscow 119071, Russia
[2] Lomonosov Moscow State Univ, Moscow 119991, Russia
[3] NRC Kurchatov Inst, Moscow 123182, Russia
基金
俄罗斯科学基金会;
关键词
Electrokinetic potential; Streaming current; Cation complexation; Hydrophobic layer hydrolysis; Hydrophobic layer swelling; SELF-ASSEMBLED MONOLAYERS; ELECTROKINETIC PHENOMENA; POLYMER SURFACES; ALUMINUM-ALLOY; GLASS SURFACES; VIDEO IMAGES; WATER; INTERFACE; CORROSION; CONTACT;
D O I
10.1016/j.colsurfa.2017.10.023
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The paper presents experimental data indicating interesting new phenomena related to overcharging of a hydrophobic surface in concentrated potassium chloride solutions. We attribute these data to cation complexation and capture of the cations by the hydrophobic surface. The analysis of the mechanism of the detected phenomena is based on capillary electrokinetic and wettability studies and confirmed by SEM data and XPS spectra. It was found that cation capture/complexation takes prolonged time, being associated with hydrolysis of Si-O bonds in hydrophobic molecules and affected by salt concentration. In addition, the time necessary for reversal of the sign of zeta-potential when solutions with lower salt concentrations are pumped through the hydrophobic capillary is much longer than that required to simply replace the solution inside the capillary.
引用
收藏
页码:76 / 84
页数:9
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