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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18350
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dc.contributor.authorRosenqvist, Terkel-
dc.contributor.authorHaugom, Jack-
dc.date.accessioned2025-03-12T06:50:49Z-
dc.date.available2025-03-12T06:50:49Z-
dc.date.issued1977-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18350-
dc.description.abstractThe Gibbs energy of formation of SO2 has been measured by an e.m.f. technique with a solid electrolyte, corresponding to the cell: SO2+ S2, Au, Pt |ZrO2+ CaO| Pt, O2., (ptot≃ 1 atm)(po2≃ 1 atm) Gas mixtures with from 0.1 to 10 % S2 were used. For the reaction: S2+ 2O2= 2SO2(1) the following Gibbs energy change in the temperature range 1100–1700 K is obtained: ΔG°1=–724 300 + 150.3 TJ mol–1., This expression is from 2 to 10 kJ more positive than compiled data, and may explain discrepancies that were previously found between calculated and observed equilibria between sulphides and oxides of iron and zinc and between copper and copper sulphide, and the corresponding gas compositions.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1977, 73 (06)en_US
dc.subjectChemistryen_US
dc.subjectGibbs energyen_US
dc.subjectelectrochemicalen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleGibbs energy of formation of SO2. A high temperature electrochemical studyen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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