dc.contributor.author |
Chauke, L
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|
dc.contributor.author |
Garbers-Craig, AM
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dc.date.accessioned |
2013-10-23T12:05:29Z |
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dc.date.available |
2013-10-23T12:05:29Z |
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dc.date.issued |
2013-07 |
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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
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|
dc.identifier.uri |
http://hdl.handle.net/10204/6996
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|
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 -
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en_ZA |