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dc.contributor.authorOwen, Gari P.-
dc.contributor.authorThomas, John M.-
dc.contributor.authorWilliams, John O.-
dc.date.accessioned2025-02-18T11:03:54Z-
dc.date.available2025-02-18T11:03:54Z-
dc.date.issued1974-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17862-
dc.description.abstractD.c. electrical measurements are reported for sulphate-ion-doped and barium-ion-doped ammonium perchlorate. The extension of an impurity-dominated regime in sulphate-ion-doped ammonium perchlorate, and the fact that barium-ion-doped ammonium perchlorate displays no marked difference in electrical behaviour from that of the “pure” salt strongly suggests that the conduction process in ammonium perchlorate is controlled by interstitial ammonium ions. Measurements of surface conduction reveal no evidence for proton conduction at or near the surface where such a process would be expected to dominate via sublimation. The dominant point defect structure deduced from electrical measurements, i.e. interstitial NH+4 ions would seem to favour electron transfer from ClO–4 to NH+4 ions as the first step in the thermal decomposition of the solid, since this mechanism requires the existence of interstitial NH+4 ions.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1974, 70 (11)en_US
dc.subjectChemistryen_US
dc.subjectIonic Conductionen_US
dc.subjectDivalent Ionsen_US
dc.subjectAmmonium Perchlorateen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleIonic Conduction in Ammonium Perchlorate Doped with Divalent Ionsen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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