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DC Field | Value | Language |
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dc.contributor.author | Buxton, G. V. | - |
dc.contributor.author | Subhani, M. S. | - |
dc.date.accessioned | 2025-02-10T15:17:19Z | - |
dc.date.available | 2025-02-10T15:17:19Z | - |
dc.date.issued | 1972 | - |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17462 | - |
dc.description.abstract | The steady state and flash photolysis of aqueous solutions of chlorite ion has been investigated. The primary photodecomposition reactions are ClO–2[graphic omitted]ClO–+ O (a), ClO–2[graphic omitted]ClO–+ O–(b), ClO–2[graphic omitted](ClO–2)*[graphic omitted]ClO2+ ClO–+ O–(c), with the oxygen atom being formed in the 3P state at 365 nm, and in the 1D state at 313 nm and 253.7 nm. (ClO–2)* may be a long lived triplet state of chlorite ion. The primary quantum yields obtained at pH 10 are the following: (i) at 365 nm, ϕa= 0.23 ± 0.03, ϕb=ϕc= 0.077 ± 0.003., (ii) at 313 nm, ϕa= 0.066 ± 0.002, ϕb=ϕc= 0.065 ± 0.003, (iii) at 253.7 nm, ϕa= 0.11 ± 0.005, ϕb=ϕc= 0.08 ± 0.003. A complete mechanism for the photodecomposition is proposed, and the data are consistent with the reaction of O(3P) with ClO–2 proceeding by two paths O(3P)+ ClO–2→ O2+ Cl–+ O(3P)(d), O(3P)+ ClO–2→ ClO–3(e) with kd/ke= 1.50 ± 0.27. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1972, 68 (5) | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Radiation Chemistry | en_US |
dc.subject | Radiation Chemistry | en_US |
dc.subject | Chlorite Ions | en_US |
dc.subject | Photodecomposition | en_US |
dc.subject | Journal of the Chemical Society : Faraday Transaction - I | en_US |
dc.title | Radiation Chemistry and Photochemistry of Oxychlorine Ions: Part 3.—Photodecomposition of Aqueous Solutions of Chlorite Ions | en_US |
dc.type | Article | en_US |
Appears in Collections: | Journal Articles (before-1995) |
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970-977.pdf Restricted Access | 539.66 kB | Adobe PDF | View/Open Request a copy |
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