Evaluation of the electrochemical activity of a Ti-RuO2-TiO2 permanent anode

被引:87
作者
Aromaa, Jari [1 ]
Forsen, Olof [1 ]
机构
[1] Helsinki Univ Technol, Lab Corros & Mat Chem, FI-02015 Helsinki, Finland
关键词
anode composition; ruthenium; electrocatalysis; active area; oxygen evolution;
D O I
10.1016/j.electacta.2005.12.053
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Most of the hydrometallurgical processes use sulphuric acid solutions. The main anodic reaction is oxygen evolution by decomposition of water. Traditional anode materials have been lead alloys that have high overpotential towards oxygen evolution. Oxide type anodes are more active but they are also more expensive. In this work, the activities of binary RuO2-TiO2 anodes were measured using different electrochemical techniques. The activity measurements were based on the measurement of the redox reaction between Ru(III) and Ru(IV) in cyclic voltammetry and on the oxygen evolution reaction in potentiostatic tests and galvanostatic electrochemical impedance spectroscopy. Factors related to intrinsic electrocatalytic properties and electrochemically active surface area could be separated. Above 30 mol% no significant increase in activity towards oxygen evolution is gained by increasing the concentration of active oxide. With low amount of active oxide most of the active sites are inside the pores and cracks. This will cause anode failure by bubble formation inside the anode. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6104 / 6110
页数:7
相关论文
共 12 条
[1]   INNER AND OUTER ACTIVE SURFACE OF RUO2 ELECTRODES [J].
ARDIZZONE, S ;
FREGONARA, G ;
TRASATTI, S .
ELECTROCHIMICA ACTA, 1990, 35 (01) :263-267
[2]   NOTE ON A METHOD TO INTERRELATE INNER AND OUTER ELECTRODE AREAS - REPLY [J].
BARONETTO, D ;
KRSTAJIC, N ;
TRASATTI, S .
ELECTROCHIMICA ACTA, 1994, 39 (16) :2359-2362
[3]  
Beer H. B., 1965, UK Patent, Patent No. [1,147,442, 1147442]
[4]  
BEER HB, 1970, Patent No. 3711385
[5]   OXYGEN-ELECTRODE .8. OXYGEN EVOLUTION AT RUTHENIUM DIOXIDE ANODES [J].
BURKE, LD ;
MURPHY, OJ ;
ONEILL, JF ;
VENKATESAN, S .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1977, 73 :1659-1671
[6]   BEHAVIOR OF THE ABSORBED CL INTERMEDIATE IN ANODIC CL-2 EVOLUTION AT THIN-FILM RUO2 SURFACES [J].
CONWAY, BE ;
GU, P ;
DEBATTISTI, A ;
BARBIERI, A ;
BATTAGLIN, G .
JOURNAL OF MATERIALS CHEMISTRY, 1991, 1 (05) :725-734
[7]   ELECTROCHEMICAL OXIDATION AND REDUCTION OF RUO2-TI ELECTRODE SURFACE [J].
DOBLHOFER, K ;
METIKOS, M ;
OGUMI, Z ;
GERISCHER, H .
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1978, 82 (10) :1046-1050
[8]   APPLICATION OF ION-IMPLANTATION TO THE STUDY OF ELECTROCATALYSIS .1. CHLORINE EVOLUTION AT RU-IMPLANTED TITANIUM ELECTRODES [J].
KELLY, EJ ;
HEATHERLY, DE ;
VALLET, CE ;
WHITE, CW .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1987, 134 (07) :1667-1675
[9]   RUTHENIUM DIOXIDE-BASED FILM ELECTRODES .3. EFFECT OF CHEMICAL COMPOSITION AND SURFACE MORPHOLOGY ON OXYGEN EVOLUTION IN ACID-SOLUTIONS [J].
LODI, G ;
SIVIERI, E ;
DEBATTISTI, A ;
TRASATTI, S .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1978, 8 (02) :135-143
[10]  
SCULTZE JW, 1986, GUNDLAGEN ELEKTRODEN