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dc.contributor.authorRowles, Matthew
dc.contributor.authorStyles, M.
dc.contributor.authorMadsen, I.
dc.contributor.authorScarlett, N.
dc.contributor.authorMcGregor, K.
dc.contributor.authorRiley, D.
dc.contributor.authorSnook, G.
dc.contributor.authorUrban, A.
dc.contributor.authorConnolley, T.
dc.contributor.authorReinhard, C.
dc.date.accessioned2017-01-30T12:47:46Z
dc.date.available2017-01-30T12:47:46Z
dc.date.created2015-07-16T06:21:58Z
dc.date.issued2012
dc.identifier.citationRowles, M. and Styles, M. and Madsen, I. and Scarlett, N. and McGregor, K. and Riley, D. and Snook, G. et al. 2012. Quantification of passivation layer growth in inert anodes for molten salt electrochemistry by in situ energy-dispersive diffraction. Journal of Applied Crystallography. 45 (1): pp. 28-37.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/25298
dc.identifier.doi10.1107/S0021889811044104
dc.description.abstract

An in situ energy-dispersive X-ray diffraction experiment was undertaken on operational titanium electrowinning cells to observe the formation of rutile (TiO2) passivation layers on Magnéli-phase (TinO2n-1; n = 4-6) anodes and thus determine the relationship between passivation layer formation and electrolysis time. Quantitative phase analysis of the energy-dispersive data was undertaken using a crystal-structure-based Rietveld refinement. Layer formation was successfully observed and it was found that the rate of increase in layer thickness decreased with time, rather than remaining constant as observed in previous studies. The limiting step in rutile formation is thought to be the rate of solid-state diffusion of oxygen within the anode structure.

dc.publisherIUCr Journals
dc.subjectin situ energy-dispersive diffraction
dc.subjectelectrolysis
dc.subjectRietveld refinement
dc.titleQuantification of passivation layer growth in inert anodes for molten salt electrochemistry by in situ energy-dispersive diffraction
dc.typeJournal Article
dcterms.source.volume45
dcterms.source.number1
dcterms.source.startPage28
dcterms.source.endPage37
dcterms.source.issn0021-8898
dcterms.source.titleJournal of Applied Crystallography
curtin.accessStatusOpen access


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