X-ray photoelectron spectroscopy study of sodium reactions in carbon cathode blocks of aluminium oxide reduction cells

被引:73
作者
Brisson, P. -Y.
Darmstadt, H.
Fafard, M.
Adnot, A.
Servant, G.
Soucy, G.
机构
[1] Univ Sherbrooke, Dept Genie Chim, Sherbrooke, PQ J1K 2R1, Canada
[2] Alcan Int Ltd, Ctr Rech & Dev Arvida, Jonquiere, PQ G7H 4K8, Canada
[3] Univ Laval, Dept Genie Civil, Quebec City, PQ G1K 7P4, Canada
[4] Univ Laval, Dept Genie Chim, Quebec City, PQ G1K 7P4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
graphite; electrodes; intercalation; X-ray photoelectron spectroscopy; chemical structure;
D O I
10.1016/j.carbon.2005.11.030
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Aluminium oxide reduction was performed in a laboratory electrolysis cell with different industrial carbon cathode blocks (semi-graphitic, graphitic, and graphitized blocks). During electrolysis, sodium species migrate from the bath into the carbon cathode. Consequences of this migration include expansion of the blocks-the so-called sodium swelling-that may lead to failure of the cell. Characterisation of the blocks by XPS indicated that in addition to ionic sodium species (e.g. NaF and NaHCO3) two different types of metallic sodium were present in the cathodes. One type of metallic sodium is associated with a degradation of the graphitic structure, suggesting that this sodium is intercalated between the graphene layers, whereas the other type of metallic sodium was most probably present in micropores. Both types of metallic sodium were detected in semi-graphitic blocks while only the "micropore" sodium was found in graphitic and graphitized blocks. The metallic sodium was remarkably stable in the laboratory atmosphere, probably due to the fact that, after electrolysis, the entire porosity of the carbon cathode is filled with penetrated bath. This limits the access of oxygen and humidity to the metallic sodium. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1438 / 1447
页数:10
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