Hydroxide and hydronium ion adsorption - A survey

被引:214
|
作者
Zimmermann, Ralf [1 ]
Freudenberg, Uwe [1 ]
Schweiss, Ruediger [1 ]
Kuettner, David [1 ]
Werner, Carsten [1 ,2 ]
机构
[1] Max Bergmann Ctr Biomat Dresden, Leibniz Inst Polymer Res Dresden, D-01069 Dresden, Germany
[2] Tech Univ Dresden, Ctr Regenerat Therapies Dresden, D-01307 Dresden, Germany
关键词
SELF-ASSEMBLED MONOLAYERS; STREAMING CURRENT MEASUREMENTS; CHEM.-CHEM.-PHYS; ELECTROKINETIC CHARACTERIZATION; AQUEOUS-SOLUTIONS; WATER-SURFACE; NEAT WATER; ELECTRICAL-PROPERTIES; FORCE SPECTROSCOPY; ZETA-POTENTIALS;
D O I
10.1016/j.cocis.2010.01.002
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 propensity of hydroxide and hydronium ions to accumulate at interfaces is the subject of ongoing scientific debate. Electrokinetic and surface force measurements suggest elevated interfacial concentrations of hydroxide ions across a wide range of pHs. Contrary to this, however, surface-sensitive spectroscopic techniques and molecular dynamic (MD) simulations indicate that hydronium ions have strong surface affinity under similar conditions. Here we review results obtained for gas/water, oil/water and solid/water interfaces. Emphasis is placed on ion adsorption phenomena occurring on polymer films of different hydrophobicity and structure. The results clearly show that asymmetric water ion adsorption is independent of the hydrophobicity of the solid surface. Recently obtained data reveal significant effects of the hydroxide and hydronium ions even on the charging of hydrophobic polymers in the presence of multivalent electrolytes and on the charging of zwitterionic lipid membranes. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:196 / 202
页数:7
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