VOLTAMMETRIC STUDY ON THE OSCILLATION OF THE POTENTIAL DIFFERENCE AT A LIQUID/LIQUID OR LIQUID/MEMBRANE INTERFACE ACCOMPANIED BY ION TRANSFER

被引:2
作者
Kihara, Sorin [1 ]
Maeda, Kohji [2 ]
Suzuki, Mitsuko [1 ]
Yoshida, Yumi [1 ]
Matsui, Masakazu [1 ]
机构
[1] Kyoto Univ, Inst Chem Res, Uji, Kyoto 611, Japan
[2] Kobe Univ, Grad Sch Sci & Technol, Kobe, Hyogo 657, Japan
关键词
oscillation of potential difference; ion transfer; liquid/liquid interface; adsorption of ion-pair; ion transfer voltammetry;
D O I
10.2116/analsci.7.Supple_601
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The oscillations of potential difference at the interface between an aqueous solution (W) containing MgSO4 as a supporting electrolyte (SE) and an organic solution (Org) containing dilute ion i(+) and j(+).Y- as SE were investigated by forcing the transfer of i(+) at the interface through an applied current. The Org employed were Cs+ + tetrapentylammonium tetraphenylborate (TPenA(+).TPliB(-)) in nitrobenzene (NB), tetramethylammonium ion + TPenA(+).TPhB- in NB, H+ + tetraphenylarsonium dipicrylaminate (TPhAs+.DPA(-)) in 1,2-dichloroethane, etc. The necessary conditions for the oscillation were confirmed to be identical to those for the appearance of the maximum in the voltanunogram for the transfer of i(+) at the interface. By referring to the voltammogram and the electrocapillary curve at the interface and taking into account the ion pair (i(+).Y-) formation equilibrium in Org, such characteristics of the oscillation as the amplitude, period, pulse width and range of the applied current available for the oscillation were elucidated, and a mechanism for the oscillation is proposed. The important roles of the adsorption desorption of i(+).Y- at the interface and the dissociation of the desorbed i(+).Y- were emphasized.
引用
收藏
页码:601 / 606
页数:6
相关论文
共 14 条
[1]  
ARAI K, 1990, DENKI KAGAKU, V58, P665
[2]   A NOVEL EXPLANATION FOR THE MECHANISM OF ELECTRICAL OSCILLATION ACROSS A LIQUID MEMBRANE [J].
ARAI, K ;
KUSU, F ;
TAKAMURA, K .
CHEMISTRY LETTERS, 1990, (09) :1517-1520
[3]   THERMODYNAMICS OF A POLARIZED INTERFACE BETWEEN 2 IMMISCIBLE ELECTROLYTE-SOLUTIONS [J].
GIRAULT, HHJ ;
SCHIFFRIN, DJ .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1984, 170 (1-2) :127-141
[4]  
JANISZEWSKA L, 1970, ROCZ CHEM, V44, P1107
[5]   VOLTAMMETRIC MAXIMA OF THE 3RD KIND FROM REACTANT ADSORPTION AT THE HMDE [J].
JOHANSSON, BL ;
WENDSJO, S .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1987, 235 (1-2) :343-355
[6]   FUNDAMENTAL FACTORS IN THE POLAROGRAPHIC MEASUREMENT OF ION TRANSFER AT THE AQUEOUS ORGANIC SOLUTION INTERFACE [J].
KIHARA, S ;
SUZUKI, M ;
MAEDA, K ;
OGURA, K ;
UMETANI, S ;
MATSUI, M ;
YOSHIDA, Z .
ANALYTICAL CHEMISTRY, 1986, 58 (14) :2954-2961
[7]   The dielectric polarization of polar liquids [J].
Kirkwood, JG .
JOURNAL OF CHEMICAL PHYSICS, 1939, 7 (10) :911-919
[8]   VOLTAMMETRIC STUDY ON THE OSCILLATION OF THE POTENTIAL DIFFERENCE AT A LIQUID LIQUID OR LIQUID MEMBRANE INTERFACE ACCOMPANIED BY ION TRANSFER [J].
MAEDA, K ;
KIHARA, S ;
SUZUKI, M ;
MATSUI, M .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1990, 295 (1-2) :183-201
[9]   EXPERIMENTAL AND THEORETICAL-STUDY OF AN INTERFACIAL INSTABILITY AT SOME OIL-WATER INTERFACES INVOLVING A SURFACE-ACTIVE AGENT .1. PHYSICOCHEMICAL DESCRIPTION AND OUTLINES FOR A THEORETICAL APPROACH [J].
NAKACHE, E ;
DUPEYRAT, M ;
VIGNESADLER, M .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1983, 94 (01) :187-200
[10]  
Nalcache E., 1982, BIOELECTROCH BIOENER, V9, P583