Electrocatalytic Aspects of the Chlorate Process: A Voltammetric and DEMS Comparison of RuO2 and DSA Anodes

被引:9
作者
Macounova, Katefina Minhova [1 ]
Simic, Nina [2 ]
Ahlberg, Elisabet [3 ]
Krtil, Petr [1 ]
机构
[1] Czech Acad Sci, J Heyrovsky Inst Phys Chem, Prague 18223, Czech Republic
[2] AkzoNobel Pulp & Performance Chem, SE-44580 Bohus, Sweden
[3] Univ Gothenburg, Dept Chem & Mol Biol, SE-41296 Gothenburg, Sweden
关键词
CHLORINE EVOLUTION; HYPOCHLORITE; OXIDATION; OXYGEN; DECOMPOSITION; ELECTRODES; DEPENDENCE; TIO2(110); CHROMATE; TIO2;
D O I
10.1149/2.0241814jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The behavior of RuO2 and DSA anodes in hypochlorite oxidation is compared to outline limitations of the anode performance in the chlorate process. Both electrode materials oxidize hypochlorite via a radical involving mechanism, which produces overstoichiometric amounts of oxygen and hydrogen peroxide. Regardless of the electrode material the hypochlorite oxidation competes with chlorine evolution for the same surface sites. The hypochlorite oxidation prevails at low ionic strengths and in mildly alkaline media. On RuO2 based electrodes the electrochemical hypochlorite oxidation dominates, while on DSA the electrochemical hypochlorite oxidation is complemented by a catalytic decomposition of hypochlorite forming oxygen and hydrochloric acid. The catalytic hypochlorite decomposition observed for DSA represents a serious impediment for the chlorate process outlining the need of further optimization of the industrial grade anode for the chlorate process. (C) The Author(s) 2018. Published by ECS.
引用
收藏
页码:E751 / E758
页数:8
相关论文
共 29 条
[1]   THE SURFACE OXIDATION OF PYRITE IN ALKALINE-SOLUTION [J].
AHLBERG, E ;
FORSSBERG, KSE ;
WANG, X .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1990, 20 (06) :1033-1039
[2]  
Cheng CY, 2007, J APPL ELECTROCHEM, V37, P1203, DOI 10.1007/S10800-007-9364-7
[3]  
Colman J. E., 1981, AICHE S SER, V77, P244
[4]  
Cornell A., ENCY APPL ELECTROCHE, V1, P175
[5]   ON THE THEORY OF ELECTROCHEMICAL CHLORATE FORMATION [J].
DEVALERA, V .
TRANSACTIONS OF THE FARADAY SOCIETY, 1953, 49 (11) :1338-1351
[6]  
Foerster F., 1924, Trans. Am. Electrochem. Soc, V46, P23
[7]   Electronic Origin of the Surface Reactivity of Transition-Metal-Doped TiO2(110) [J].
Garcia-Mota, Monica ;
Vojvodic, Aleksandra ;
Abild-Pedersen, Frank ;
Norskov, Jens K. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2013, 117 (01) :460-465
[8]   Tailoring the Activity for Oxygen Evolution Electrocatalysis on Rutile TiO2(110) by Transition-Metal Substitution [J].
Garcia-Mota, Monica ;
Vojvodic, Aleksandra ;
Metiu, Horia ;
Man, Isabela C. ;
Su, Hai-Yan ;
Rossmeisl, Jan ;
Norskov, Jens K. .
CHEMCATCHEM, 2011, 3 (10) :1607-1611
[9]   THE INFLUENCE OF ELECTROLYTE PARAMETERS ON THE PERCENT OXYGEN EVOLVED FROM A CHLORATE CELL [J].
HARDEE, KL ;
MITCHELL, LK .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1989, 136 (11) :3314-3318
[10]   Spin coated titanium-ruthenium oxide thin films [J].
Hummelgard, Christine ;
Gustavsson, John ;
Cornell, Ann ;
Olin, Hakan ;
Backstrom, Joakim .
THIN SOLID FILMS, 2013, 536 :74-80