Theoretical and analytical characterization of a flow-through permeation liquid membrane with controlled flux for metal speciation measurements

被引:45
作者
Tomaszewski, L
Buffle, J
Galceran, J
机构
[1] Univ Geneva, CABE, Dept Inorgan Analyt & Appl Chem, CH-1211 Geneva 4, Switzerland
[2] Univ Lleida Udl, ETSEA, Dept Quim, E-25198 Lleida, Catalonia, Spain
关键词
D O I
10.1021/ac020486x
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Speciation measurements with the permeation liquid membrane (PLM) technology require necessarily a good control of the flux of the analyte. In this perspective, a PLM-based multichannel flow-through cell has been designed. The first objective of this study has been to adapt the classical Levich model commonly used for electrochemical flow devices to the characteristic geometry of the PLM cell. In the latter case and contrary to the Levich model, the effects of the channel lateral walls on the flux of active species through the membrane have to be taken into account. The problem was solved by considering the existence of two parabolic Poiseuille profiles perpendicular to each other and developing along the fluid motion. The theoretical results obtained match satisfactorily with experimental data. The analytical study of this PLM system has been performed with copper(II) ions as test species and has shown that the preconcentration factor is (1) linear at least for preconcentration times of less than or equal to 120 min, (2) reproducible on the same membrane as well as on different membranes, and (3) independent of the initial test metal ion concentration in the sample solution. The capabilities of this cell to determine metal speciation by considering lability of complexes and the flux of metal at variable flow rates of the test solution is also discussed by means of Cu(II)/sulfosalicylic complexes.
引用
收藏
页码:893 / 900
页数:8
相关论文
共 29 条
[1]   Hydrodynamic voltammetry with channel microband electrodes: Axial diffusion effects [J].
Alden, JA ;
Compton, RG .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1996, 404 (01) :27-35
[3]  
BARSCH RA, 1996, ACS S SERIES, V642
[4]  
BUFFLE J, 2000, IN SITU MONITORING A, pCH10
[5]   APPLICATION OF SUPPORTED LIQUID MEMBRANES FOR REMOVAL OF URANIUM FROM GROUNDWATER [J].
CHIARIZIA, R ;
HORWITZ, EP ;
RICKERT, PG ;
HODGSON, KM .
SEPARATION SCIENCE AND TECHNOLOGY, 1990, 25 (13-15) :1571-1586
[6]   SEPARATION OF METAL SPECIES BY SUPPORTED LIQUID MEMBRANES [J].
DANESI, PR .
SEPARATION SCIENCE AND TECHNOLOGY, 1984, 19 (11-1) :857-894
[7]   Chromium speciation in natural waters using serially connected supported liquid membranes [J].
Djane, NK ;
Ndung'u, K ;
Johnsson, C ;
Sartz, H ;
Tornstrom, T ;
Mathiasson, L .
TALANTA, 1999, 48 (05) :1121-1132
[8]   Supported liquid membrane coupled on-line to potentiometric stripping analysis at a mercury-coated reticulated vitreous carbon electrode for trace metal determinations in urine [J].
Djane, NK ;
Armalis, S ;
Ndung'u, K ;
Johansson, G ;
Mathiasson, L .
ANALYST, 1998, 123 (02) :393-396
[9]   Finite element simulation of the amperometric response of recessed and protruding microband electrodes in flow channels [J].
Ferrigno, R ;
Brevet, PF ;
Girault, HH .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1997, 430 (1-2) :235-242
[10]   Voltammetric lability of metal complexes at spherical microelectrodes with various radii [J].
Galceran, J ;
Puy, J ;
Salvador, J ;
Cecília, J ;
van Leeuwen, HP .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2001, 505 (1-2) :85-94