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DC Field | Value | Language |
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dc.contributor.author | Johnson, David W. | - |
dc.contributor.author | Salmon, G. Arthur | - |
dc.date.accessioned | 2025-04-09T11:24:47Z | - |
dc.date.available | 2025-04-09T11:24:47Z | - |
dc.date.issued | 1977 | - |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18607 | - |
dc.description.abstract | The rate constant for the reaction of solvated electrons with tetranitromethane (TNM) was measured to be k6=(2.89 ± 0.20)× 1010 dm3 mol–1 s–1 at room temperature. Measurements on nitrous oxide saturated solutions containing TNM indicate that ·CH2OH radicals react rapidly with TNM forming an unstable intermediate C(NO2)4+˙CH2OH [graphic omitted] [X] [graphic omitted] C(NO2)–3+ H++ HCHO + NO2(9), for which k9a=(8.5 ± 0.4)× 109 dm3 mol–1 s–1 and k9b=(2.9 ± 0.1)× 106 s–1. The yields of nitroform anion (NF–) in argon and nitrous oxide saturated solutions of G(NF–)= 5.63 ± 0.05 and 6.45 ± 0.05 are equated to the scavengeable radical yields in these solutions. The difference is ascribed to reactions in spurs between e–s and CH3O˙ radical. The yields obtained are compared with those measured in γ-irradiated systems. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1977, 73 (2) | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Pulse Radiolysis | en_US |
dc.subject | Tetranitromethane | en_US |
dc.subject | Journal of the Chemical Society : Faraday Transaction - I | en_US |
dc.title | Pulse Radiolysis of Methanolic Solutions of Tetranitromethane | en_US |
dc.type | Article | en_US |
Appears in Collections: | Journal Articles (before-1995) |
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