ELECTRO-OXIDATION OF ACETATE ON PLATINUM AT LOW POTENTIALS

被引:26
作者
KOCH, DFA
WOODS, R
机构
[1] Division of Mineral Chemistry, C.S.I.R.O., Port Melbourne, Vic.
关键词
D O I
10.1016/0013-4686(68)80119-7
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The steady-state electrochemical oxidation of acetate has been observed on smooth and platinized platinum at potentials corresponding, to an oxide-free surface. Carbon dioxide is the only reaction product. It is suggested that the first electron transfer is rate-determining and takes place after a reversible adsorption of acetate. The oxidation rate is pH-dependent, reaching a maximum at pH 6, and these phenomena can be explained in terms of a greater adsorption of acetate ion over the undissociated acid, together with a competitive adsorption of carbonate ion, on the electrode surface. © 1968.
引用
收藏
页码:2101 / &
相关论文
共 35 条
[1]  
BAGOTSKII VS, 1966, FUEL CELLS THEIR ED, P99
[2]  
BAGOTSKII VS, 1964, ELECTROCHIM ACTA, V9, P859
[3]  
Bagotzky V. S., 1966, FUEL CELLS THEIR ELE, P77
[4]  
BINDER H, 1965, ADV CHEM SER, P269
[5]  
BOCKRIS JOM, 1966, MODERN ASPECTS EL ED, P118
[6]  
BOCKRIS JOM, 1964, MODERN ASPECTS EL ED, P371
[7]  
BOCKRIS JOM, 1964, MODERN ASPECTS EL ED, P391
[8]  
BOCKRIS JOM, 1966, MODERN ASPECTS EL ED, P119
[9]  
Bold W., 1961, ELECTROCHIM ACTA, V5, P145
[10]   NEW APPROACHES TO STUDY OF ELECTROCHEMICAL DECARBOXYLATION AND KOLBE REACTION .3. QUANTITATIVE ANALYSIS OF DECAY AND DISCHARGE TRANSIENTS AND ROLE OF ADSORBED INTERMEDIATES [J].
CONWAY, BE ;
DZIECIUCH, M .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1963, 41 (01) :55-&