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dc.contributor.authorWheeler, Brian R.-
dc.contributor.authorGalwey, Andrew K.-
dc.date.accessioned2025-02-17T10:21:40Z-
dc.date.available2025-02-17T10:21:40Z-
dc.date.issued1974-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17815-
dc.description.abstractDecomposition of nickel formate, nickel malonate, nickel maleate and nickel fumarate in oxygen yields nickel oxide and carbon dioxide only. The shape of each fractional reaction-time curve is comparable with that for the vacuum pyrolysis of the salt, there is no evidence that the product oxide provided a progressively increasing barrier to the progress of the oxidation process. The values of the activation energies for the decomposition reactions of all four salts are 150 ± 10 kJ mol–1 and different from those for reactions in vacuum. From the observations we conclude that the geometry of advance of the reactant/product interface, during nucleation and subsequent growth of the product phase, for reactions in oxygen and in vacuum are closely comparable, if not identical. The chemical processes occurring at the metal carboxylate/nickel oxide interface during the reaction in oxygen are discussed. It is suggested that the rate controlling process is largely determined by the surface and defect properties of the nickel oxide product phase.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1974, 70 (1-6)en_US
dc.subjectChemistryen_US
dc.subjectDecomposition Reactionsen_US
dc.subjectNickel Formateen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleDecomposition Reactions of Nickel Formate, Nickel Malonate, Nickel Maleate and Nickel Fumarate in Oxygenen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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