Controlling the transport of cations through permselective mesoporous alumina layers by manipulation of electric field and ionic strength

被引:23
作者
Schmuhl, R
Keizer, K
van den Berg, A
ten Elshof, JE [1 ]
Blank, DHA
机构
[1] Univ Twente, Inst Nanotechnol, MESA, POB 217, NL-7500 AE Enschede, Netherlands
[2] Univ Twente, Fac Sci & Technol, NL-7500 AE Enschede, Netherlands
关键词
permselectivity; transport; mesoporous; alumina; membrane; double layer;
D O I
10.1016/j.jcis.2003.10.024
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 electric field-driven transport of ions through supported mesoporous gamma-alumina membranes was investigated. The influence of ion concentration, ion valency, pH, ionic strength, and electrolyte composition on transport behavior was determined. The permselectivity of the membrane was found to be highly dependent on the ionic strength. When the ionic strength was sufficiently low for electrical double-layer overlap to occur inside the pores, the membrane was found to be cation-permselective and the transport rate of cations could be tuned by variation of the potential difference over the membrane. The cation permselectivity is thought to be due to the adsorption of anions onto the pore walls, causing a net negative immobile surface charge density, and consequently, a positively charged mobile double layer. The transport mechanism of cations was interpreted in terms of a combination of Fick diffusion and ion migration. By variation of the potential difference over the membrane the transport of double-charged cations, Cu2+, could be controlled accurately, effectively resulting in on/off tunable transport. In the absence of double-layer overlap at high ionic strength, the membrane was found to be nonselective. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:331 / 338
页数:8
相关论文
共 20 条
[1]  
Atkins P., 2002, Physical Chemistry
[2]  
Bahena JLR, 2002, SEPAR SCI TECHNOL, V37, P1973
[3]  
Benes N, 2000, MEMBR SCI T, V6, P335
[4]  
Biesheuvel PM, 1999, J MEMBRANE SCI, V156, P141
[5]   Surface effects on cation transport across porous alumina membranes [J].
Bluhm, EA ;
Bauer, E ;
Chamberlin, RM ;
Abney, KD ;
Young, JS ;
Jarvinen, GD .
LANGMUIR, 1999, 15 (25) :8668-8672
[6]   PERMPOROMETRY STUDY ON THE SIZE DISTRIBUTION OF ACTIVE PORES IN POROUS CERAMIC MEMBRANES [J].
CAO, GZ ;
MEIJERINK, J ;
BRINKMAN, HW ;
BURGGRAAF, AJ .
JOURNAL OF MEMBRANE SCIENCE, 1993, 83 (02) :221-235
[7]   The role of electrolyte anions (ClO4-, NO3-, and Cl-) in divalent metal (M2+) adsorption on oxide and hydroxide surfaces in salt solutions [J].
Criscenti, LJ ;
Sverjensky, DA .
AMERICAN JOURNAL OF SCIENCE, 1999, 299 (10) :828-899
[8]   Silicon microtechnology and microstructures in separation science [J].
Fintschenko, Y ;
van den Berg, A .
JOURNAL OF CHROMATOGRAPHY A, 1998, 819 (1-2) :3-12
[9]  
HUNTER RJ, 2001, FDN MODERN COLLOID S
[10]   Electric field mediated transport in nanometer diameter channels [J].
Kemery, PJ ;
Steehler, JK ;
Bohn, PW .
LANGMUIR, 1998, 14 (10) :2884-2889