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dc.contributor.authorVasvári, Gábor-
dc.contributor.authorGál, Dezsőa-
dc.date.accessioned2025-03-07T11:19:45Z-
dc.date.available2025-03-07T11:19:45Z-
dc.date.issued1977-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18210-
dc.description.abstractThe decomposition of 1-phenylethyl hydroperoxide has been investigated in the presence of Co(acac)2 and Co(acac)3 in argon and oxygen atmospheres. Co(acac)2 accelerates the decomposition of the hydroperoxide. The decomposition is preceded by the fast formation of a Co(acac)2+ ROOH complex which is unaffected by the presence of oxygen in the temperature range studied. The deactivation of the catalyst by the water formed in the decomposition reaction has been confirmed from kinetic evidence. The rate constants for the formation and decomposition of the catalyst + ROOH complex and the overall activation energy were determined. In the presence of Co(acac)3 the decomposition starts after an induction period being longer in oxygen than in argon. It is assumed that the actual catalyst of this process is also Co(acac)2. The overall activation energy of the decomposition has been determined.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1977, 73 (03)en_US
dc.subjectChemistryen_US
dc.subjectDecompositionen_US
dc.subjectCobalt Acetylacetonatesen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleDecomposition of 1-phenylethyl hydroperoxide in the presence of cobalt acetylacetonatesen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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