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dc.contributor.authorCathro, W. S.-
dc.contributor.authorMackie, J. C.-
dc.date.accessioned2025-02-07T02:16:13Z-
dc.date.available2025-02-07T02:16:13Z-
dc.date.issued1972-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17299-
dc.description.abstractThe chemical relaxation of shock-heated water vapour in 8–10 % mixtures with argon has been studied over a temperature range of 2000–2400 K. The growth of H atom concentration was followed by introducing LiOH particles into the sample gas and observing the Li concentration profile by atomic absorption spectroscopy. By comparing H concentration profiles with computer simulations, values of the rate constant for H2O + M → H + OH + M were obtained. The results represent an activation energy of 439 ± 42 kJ mol–1(105 ± 10 kcal mol–1) and a pre-exponential factor of (1.8 ± 0.6)× 1016 cm3 mol–1 s–1 for the case M = H2O. The kinetic assumptions of the LiOH method for measuring H concentrations in flames were thereby confirmed experimentally down to relatively short times after thermal excitation. Deviations in the early stages of the experimental profiles were attributed to the reaction LiOH + M → Li + OH + M and the magnitude of the deviations indirectly suggests an activation energy for this reaction of about 377 kJ mol–1(90 kcal mol–1).en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1972, 68 (1)en_US
dc.subjectChemistryen_US
dc.subjectLithium Hydroxideen_US
dc.subjectDissociation Kineticsen_US
dc.subjectWater Vapouren_US
dc.subjectChemical Reactionsen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleLithium Hydroxide and the Dissociation Kinetics of Water Vapouren_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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