dc.contributor.author |
Copperthwaite, Richard G. |
|
dc.contributor.author |
Lloyd, John |
|
dc.date.accessioned |
2025-05-09T06:40:12Z |
|
dc.date.available |
2025-05-09T06:40:12Z |
|
dc.date.issued |
1978 |
|
dc.identifier.uri |
http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18895 |
|
dc.description.abstract |
The first-order rate constants for the decomposition of Na[ClO3] and Na[ClO4] when studied by X-p.e.s. are shown to have a linear dependence on the intensity of the ionising radiation used. A simple steady-state model, which emphasises the rôle of molecular excitons in the decomposition process, is constructed to explain this behaviour. Variable temperature studies in the range 293–113 K indicate that the rate of photo-induced decomposition of Na[ClO3] increases as the temperature is lowered, and analysis of the mode of decomposition suggests that the temperature-dependence arises from thermal deactivation of the molecular exciton, [ClO*3]–. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1978, 74 (09-12) |
en_US |
dc.subject |
Chemistry |
en_US |
dc.subject |
X-ray photoelectron spectroscopy |
en_US |
dc.subject |
Journal of the Chemical Society : Faraday Transaction - I |
en_US |
dc.title |
X-ray photoelectron spectroscopic (X-p.e.s.) studies on in situ photoinduced decomposition of inorganic molecular ions. Part 2.—Na[ClOx] system: mechanistic (x= 3, 4) and variable-temperature (x= 3) investigations |
en_US |
dc.type |
Article |
en_US |