Tangential flow streaming potential measurements: Hydrodynamic cell characterization and zeta potentials of carboxylated polysulfone membranes

被引:141
|
作者
Mockel, D
Staude, E [1 ]
Dal-Cin, M
Darcovich, K
Guiver, M
机构
[1] Univ Essen Gesamthsch, Inst Chem Tech, D-45141 Essen, Germany
[2] Natl Res Council Canada, Inst Chem Proc & Environm Technol, Ottawa, ON K1A 0R6, Canada
关键词
streaming (zeta) potential measurements; electrochemistry; ultrafiltration; carboxylated polysulfones; computational fluid dynamics simulation;
D O I
10.1016/S0376-7388(98)00077-5
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Computational fluid dynamics calculations were carried out to ensure that a self-made tangential flow mode streaming potential measurement cell meets the hydrodynamic stipulations of laminar, steady and established electrolyte flow necessary for reproducible electrokinetic measurements. The calculations show that the cell design meets all of these conditions. Six carboxylated polysulfones with a range of different degrees of substitution (DS) from 0.26 to 1.74 carboxyl groups per polymer repeat unit were synthesized in a two-stage process of lithiation and carboxylation, Ultrafiltration membranes were made from both the unmodified polysulfone and these hydrophilic materials. The zeta potentials of these membrane surfaces were determined in 0.001 M KCl solution as a function of pH. The curves show the theoretically expected profiles for nonionic and weakly acidic materials. The growing influence of the COOH dissociation on the surface charge formation is indicated by the flattening of the curves at low pH values. The magnitude of the negative zeta potentials plateau values ranged from -52 to -20 mV, While unmodified PSU has a plateau value of -52 mV this value decreases continuously with increasing DS to -20 mV for the PSU-COOH 1.74 material. It is suggested that this arises from a shift of the electrokinetic shear plane into the bulk electrolyte solution due to an extended swelling layer reflecting the enhanced hydrophilicity of these membrane surfaces. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:211 / 222
页数:12
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