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dc.contributor.authorCampbell, I. D.-
dc.date.accessioned2025-03-10T05:54:32Z-
dc.date.available2025-03-10T05:54:32Z-
dc.date.issued1977-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18219-
dc.description.abstractThe thermal decomposition of zinc nitrate hexahydrate in vacuo has been investigated using the technique of electron spin resonance. While the major decomposition of the nitrate ion occurs at 312°C, the presence of nitrogen peroxide can be detected throughout the temperature range 240–550°C, together with a line attributed to the N2O–4 radical. An e.s.r. line at g= 1.96 observed from 240–1000°C indicates the gradual formation of non-stoichiometric zinc oxide with increasing temperature treatment. Photo-effects using light in a spectral band peaking at 490 nm generally enhanced the g= 1.96 line, diminished the NO2 and N2O–4 spectra, but generated two new responses which are attributed to the NO3 radical and a hole associated with a zinc atom vacancy. Evidently the sample is not free of nitrogen oxides until a decomposition temperature of nearly 700°C, and remains as an imperfect zinc oxide lattice even when heated to 1000°C.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.subjectthermal decompositionen_US
dc.subjectzinc nitrate hexahydrateen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleE.s.r. investigation of the thermal decomposition of zinc nitrate hexahydrateen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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