Influence of the block geometry on the voltammetric response of partially blocked electrodes:: Application to interfacial liquid-liquid kinetics of aqueous vitamin B12S with random arrays of femtolitre microdroplets of dibromocyclohexane

被引:24
作者
Chevallier, FG
Davies, TJ
Klymenko, OV
Jiang, L
Jones, TGJ
Compton, RG
机构
[1] Univ Oxford, Phys & Theoret Chem Lab, Oxford OX1 3QZ, England
[2] Schlumberger Cambridge Res Ltd, Cambridge CB3 0EL, England
[3] Karkhov Natl Univ Radioelect, Math & Comp Modelling Lab, UA-61166 Kharkov, Ukraine
基金
英国工程与自然科学研究理事会;
关键词
partially blocked electrodes; numerical simulation; cyclic voltammetry; block geometry; hemispheres;
D O I
10.1016/j.jelechem.2005.03.036
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The cyclic voltammetric response of electrodes modified with catalytically reactive blocks is simulated using finite difference methods. The responses of three different models using various block geometries are studied. The results are used to determine kinetic parameters of coupled liquid vertical bar liquid interfacial reactions. First, we examine the liquid-liquid reaction between aqueous vitamin B-12S and pure trans-dibromocyclohexane (DBCH) microdroplets immobilized on a basal plane pyrolytic graphite (bppg) surface, immersed in an aqueous solution of vitamin B-12. Second, cyclic voltammetry on electrodes modified with microdroplets of DBCH diluted in dodecane is employed to determine the apparent bimolecular interfacial rate constant for the initial step in the DBCH(oil)/B-12S(aq) reaction. The results are compared with a previous SECM/ITIES study of a similar reaction. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:265 / 274
页数:10
相关论文
共 16 条
[1]   CHARGE-TRANSFER AT PARTIALLY BLOCKED SURFACES - A MODEL FOR THE CASE OF MICROSCOPIC ACTIVE AND INACTIVE SITES [J].
AMATORE, C ;
SAVEANT, JM ;
TESSIER, D .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1983, 147 (1-2) :39-51
[2]   Liquid-liquid processes and kinetics in acoustically emulsified media [J].
Banks, CE ;
Klymenko, OV ;
Compton, RG .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2003, 5 (08) :1652-1656
[3]   Computational and experimental study of the cyclic voltammetry response of partially blocked electrodes. Part 1. Nonoverlapping, uniformly distributed blocking systems [J].
Brookes, BA ;
Davies, TJ ;
Fisher, AC ;
Evans, RG ;
Wilkins, SJ ;
Yunus, K ;
Wadhawan, JD ;
Compton, RG .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (07) :1616-1627
[4]   Mathematical modelling and numerical simulation of adsorption processes at microdisk electrodes [J].
Chevallier, FG ;
Klymenko, OV ;
Li, J ;
Jones, TGJ ;
Compton, RG .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2005, 574 (02) :217-237
[5]   Surfactant-free emulsion electrosynthesis via power ultrasound:: electrocatalytic formation of carbon-carbon bonds [J].
Davies, TJ ;
Banks, CE ;
Nuthakki, B ;
Rusling, JF ;
France, RR ;
Wadhawana, JD ;
Compton, RG .
GREEN CHEMISTRY, 2002, 4 (06) :570-577
[6]   Cyclic voltammetry at microdroplet modified electrodes.: A comparison of the reaction of vicinal dibromides with vitamin B12s at the liquid/liquid interface with the corresponding homogeneous process:: evidence for polar-solvent effects at the liquid/liquid interface [J].
Davies, TJ ;
Garner, AC ;
Davies, SG ;
Compton, RG .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2004, 570 (02) :171-185
[7]   A computational and experimental study of the cyclic voltammetry response of partially blocked electrodes, part III:: interfacial liquid-liquid kinetics of aqueous vitamin B12s with random arrays of femtolitre microdroplets of dibromocyclohexane [J].
Davies, TJ ;
Brookes, BA ;
Compton, RG .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2004, 566 (01) :193-216
[8]   A computational and experimental study of the cyclic voltammetry response of partially blocked electrodes. Part II: Randomly distributed and overlapping blocking systems [J].
Davies, TJ ;
Brookes, BA ;
Fisher, AC ;
Yunus, K ;
Wilkins, SJ ;
Greene, PR ;
Wadhawan, JD ;
Compton, RG .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (26) :6431-6444
[9]  
Eriksson D., 1996, COMPUTATIONAL DIFFER
[10]   An exponentially expanding mesh ideally suited to the fast and efficient simulation of diffusion processes at microdisc electrodes. 1. Derivation of the mesh [J].
Gavaghan, DJ .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1998, 456 (1-2) :1-12