Studying the kinetics of the ion transfer across the liquid|liquid interface by means of thin film-modified electrodes

被引:39
作者
Mirceski, V
Quentel, F
L'Her, M
Pondaven, A
机构
[1] Univ Arhimedova, Inst Chem, Fac Nat Sci & Math, Dhaka 1000, Bangladesh
[2] Univ Bretagne Occidentale, Chim Analyt Lab, UMR 6521, CNRS, F-29238 Brest, France
关键词
ion transfer kinetics; liquid-liquid interface; thin film-modified electrode; quasireversible maximum; square-wave voltammetry;
D O I
10.1016/j.elecom.2005.08.005
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The kinetics of the ion transfer across the liquid/liquid interface is studied by means of a thin film-modified electrode in combination with square-wave voltammetry. The thin film-modified electrode consists of an edge plane pyrolytic graphite electrode covered with a thin film of a water immiscible electroinactive organic solvent containing a neutral redox probe and a suitable electrolyte. The overall electrochemical process, proceeding as a coupled electron-ion transfer reaction, is controlled either by the electron transfer across the graphite electrodel organic solvent or by the ion transfer across the organic solvent/aqueous electrolyte interface. The theoretical model enabling to distinguish the rate limiting step is developed. The theory is used to measure the kinetics of CIO4-, NO3-, Cl-, SCN-, Na+, K+, (CH3)(4)N+, and (C4H9)(4)N+ across the water/itrobenzene interface utilizing lutetium bis(tetratert-butylphthalocyaninato) as a redox probe. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:1122 / 1128
页数:7
相关论文
共 28 条
[1]   Electrode reactions at sub-micron oil | water | electrode interfaces [J].
Aoki, K ;
Tasakorn, P ;
Chen, JY .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2003, 542 :51-60
[2]   Assessment of a recent thin-layer method for measuring the rates of electron transfer across liquid/liquid interfaces [J].
Barker, AL ;
Unwin, PR .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (10) :2330-2340
[3]   PREDICTION OF SALT EFFECTS ON RATES OF SINGLE-ION CROSSINGS IN ITIES EXPERIMENTS [J].
BUCK, RP ;
BRONNER, WE .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1986, 197 (1-2) :179-188
[4]   Steady-state current at oil|water|electrode interfaces using ion-insoluble polydimethylsiloxane droplets [J].
Chen, JY ;
Sato, M .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2004, 572 (01) :153-159
[5]   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
[6]   Kinetics of electrode reaction coupled to ion transfer across the liquid/liquid interface [J].
Komorsky-Lovric, S ;
Lovric, M .
CENTRAL EUROPEAN JOURNAL OF CHEMISTRY, 2005, 3 (02) :216-229
[7]   KINETIC MEASUREMENTS OF A SURFACE-CONFINED REDOX REACTION [J].
KOMORSKYLOVRIC, S ;
LOVRIC, M .
ANALYTICA CHIMICA ACTA, 1995, 305 (1-3) :248-255
[8]   Determination of rate constants of ion transfer kinetics across immiscible electrolyte solutions [J].
Manzanares, JA ;
Lahtinen, R ;
Quinn, B ;
Kontturi, K ;
Schiffrin, DJ .
ELECTROCHIMICA ACTA, 1998, 44 (01) :59-71
[9]   Enhanced ion transfer rate due to the presence of zwitterionic phospholipid monolayers at the ITIES [J].
Manzanares, JA ;
Allen, RM ;
Kontturi, K .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2000, 483 (1-2) :188-196
[10]   Charge transfer kinetics in thin-film voltammetry. Theoretical study under conditions of square-wave voltammetry [J].
Mirceski, V .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (36) :13719-13725