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Reactivity between carbon cathode materials and electrolyte based on industrial and laboratory data

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dc.contributor.author Chauke, L
dc.contributor.author Garbers-Craig, AM
dc.date.accessioned 2013-10-23T12:05:29Z
dc.date.available 2013-10-23T12:05:29Z
dc.date.issued 2013-07
dc.identifier.citation Chauke, L and Garbers-Craig, A.M. 2013. Reactivity between carbon cathode materials and electrolyte based on industrial and laboratory data. Carbon, vol. 58, pp 40-45 en_US
dc.identifier.issn 0008-6223
dc.identifier.uri http://ac.els-cdn.com/S000862231300153X/1-s2.0-S000862231300153X-main.pdf?_tid=740deea6-2f4d-11e3-ae8f-00000aab0f02&acdnat=1381149725_477ede9c2dc7b67a94cae87e1bca644c
dc.identifier.uri http://hdl.handle.net/10204/6996
dc.description Copyright: 2013 Elsevier. This an ABSTRACT ONLY. The definitive version is published in Carbon, vol. 58, pp 40-45 en_US
dc.description.abstract Interaction between electrolyte and carbon cathodes during the electrolytic production of aluminium decreases cell life. This paper describes the interaction between carbon cathode materials and electrolyte, based on industrial and laboratory data. It also reports on the degree of expansion of semi-graphitic and graphitised materials when exposed to a sodium rich environment. Phase relations in the slow cooled bath electrolyte, spent industrial cathodes and laboratory scale cathode samples were similar: all contained Na(sub3)AlF(sub6), NaF, CaF(sub2) and NaAl(sub11)O(sub17). Al(sub4)C(sub3), AlN and NaCN were only detected in the spent industrial cathodes. The inability to locate Al(sub4)C(sub3) in the laboratory scale samples could be due to very low concentrations of Al4C3 which could not be detected by XRD, or to the limited direct contact between the produced aluminium and carbon material. X-ray diffraction analysis confirmed that sodium intercalation into graphite did not take place. Wear of the examined carbon cathodes proceeded due to penetration of electrolyte and sodium into the cathode, followed by reactions with carbon and N(sub2) whereby AlN and NaCN formed. Once electrolysis started the carbon cathodes expanded rapidly, but slowed down after approximately an hour. Sodium expansion decreased with degree of graphitisation of the carbon cathode material. en_US
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.relation.ispartofseries Workflow;11587
dc.subject Carbon cathode materials en_US
dc.subject Eectrolyte en_US
dc.subject Industrial data en_US
dc.subject Laboratory data en_US
dc.title Reactivity between carbon cathode materials and electrolyte based on industrial and laboratory data en_US
dc.type Article en_US
dc.identifier.apacitation Chauke, L., & Garbers-Craig, A. (2013). Reactivity between carbon cathode materials and electrolyte based on industrial and laboratory data. http://hdl.handle.net/10204/6996 en_ZA
dc.identifier.chicagocitation Chauke, L, and AM Garbers-Craig "Reactivity between carbon cathode materials and electrolyte based on industrial and laboratory data." (2013) http://hdl.handle.net/10204/6996 en_ZA
dc.identifier.vancouvercitation Chauke L, Garbers-Craig A. Reactivity between carbon cathode materials and electrolyte based on industrial and laboratory data. 2013; http://hdl.handle.net/10204/6996. en_ZA
dc.identifier.ris TY - Article AU - Chauke, L AU - Garbers-Craig, AM AB - Interaction between electrolyte and carbon cathodes during the electrolytic production of aluminium decreases cell life. This paper describes the interaction between carbon cathode materials and electrolyte, based on industrial and laboratory data. It also reports on the degree of expansion of semi-graphitic and graphitised materials when exposed to a sodium rich environment. Phase relations in the slow cooled bath electrolyte, spent industrial cathodes and laboratory scale cathode samples were similar: all contained Na(sub3)AlF(sub6), NaF, CaF(sub2) and NaAl(sub11)O(sub17). Al(sub4)C(sub3), AlN and NaCN were only detected in the spent industrial cathodes. The inability to locate Al(sub4)C(sub3) in the laboratory scale samples could be due to very low concentrations of Al4C3 which could not be detected by XRD, or to the limited direct contact between the produced aluminium and carbon material. X-ray diffraction analysis confirmed that sodium intercalation into graphite did not take place. Wear of the examined carbon cathodes proceeded due to penetration of electrolyte and sodium into the cathode, followed by reactions with carbon and N(sub2) whereby AlN and NaCN formed. Once electrolysis started the carbon cathodes expanded rapidly, but slowed down after approximately an hour. Sodium expansion decreased with degree of graphitisation of the carbon cathode material. DA - 2013-07 DB - ResearchSpace DP - CSIR KW - Carbon cathode materials KW - Eectrolyte KW - Industrial data KW - Laboratory data LK - https://researchspace.csir.co.za PY - 2013 SM - 0008-6223 T1 - Reactivity between carbon cathode materials and electrolyte based on industrial and laboratory data TI - Reactivity between carbon cathode materials and electrolyte based on industrial and laboratory data UR - http://hdl.handle.net/10204/6996 ER - en_ZA


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