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

被引:43
作者
MAEDA, K
KIHARA, S
SUZUKI, M
MATSUI, M
机构
[1] The Institute for Chemical Research, Kyoto University, Uji, Kyoto
来源
JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 1990年 / 295卷 / 1-2期
关键词
D O I
10.1016/0022-0728(90)85015-W
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 containing MgSO4 and an organic solution containing dilute Cs+ or tetramethylammonium ion (TMA+) and fairly concentrated tetrapentylammonium tetraphenylborate (TPenA+· TPhB-) were investigated by forcing the transfer of Cs+ or TMA+ at the interface through an applied current. The organic solvents employed were nitrobenzene, 1,2-dichloroethane and o-nitroanisole. The necessary conditions for the oscillation were confirmed to be identical to those for the appearance of the maximum in the voltammogram for the ion transfer at the interface. By referring to the voltammogram and the drop tune-potential curve and taking into account the ion-pair formation equilibrium in the organic, such characteristics of the oscillation as the amplitude, the pulse width, the period and the range of applied current were elucidated, and a mechanism for the oscillation is proposed. The result at the aqueous/organic interface is connected to the oscillation of the potential at a liquid membrane. © 1990.
引用
收藏
页码:183 / 201
页数:19
相关论文
共 24 条
[1]   CALCULATIONS ON IONIC SOLVATION .5. THE CALCULATION OF PARTITION-COEFFICIENTS OF IONS [J].
ABRAHAM, MH ;
LISZI, J .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1981, 43 (01) :143-151
[2]  
[Anonymous], 2002, MODERN ELECTROCHEMIS, DOI DOI 10.1007/B114168
[3]   APPARENT TRANSFER-COEFFICIENTS FOR ION-TRANSPORT BETWEEN WATER AND NITROBENZENE [J].
BRONNER, WE ;
MELROY, OR ;
BUCK, RP .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1984, 162 (1-2) :263-274
[4]   Properties of electrolytic solutions III The dissociation constant [J].
Fuoss, RM ;
Kraus, CA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1933, 55 :1019-1028
[5]   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
[6]  
JANISZEWSKA L, 1970, ROCZ CHEM, V44, P1107
[7]   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
[8]   THE TRANSFER OF ANIONS AT THE AQUEOUS ORGANIC SOLUTIONS INTERFACE STUDIED BY CURRENT-SCAN POLAROGRAPHY WITH THE ELECTROLYTE DROPPING ELECTRODE [J].
KIHARA, S ;
SUZUKI, M ;
MAEDA, K ;
OGURA, K ;
MATSUI, M .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1986, 210 (01) :147-159
[9]   THE ELECTRON-TRANSFER AT A LIQUID LIQUID INTERFACE STUDIED BY CURRENT-SCAN POLAROGRAPHY AT THE ELECTROLYTE DROPPING ELECTRODE [J].
KIHARA, S ;
SUZUKI, M ;
MAEDA, K ;
OGURA, K ;
MATSUI, M ;
YOSHIDA, Z .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1989, 271 (1-2) :107-125
[10]   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