The slow gas-phase oxidation of tetrahydrofuran was studied under static conditions at 220ยฐC. The relative amounts of each product, if extrapolated to zero reaction time, show which are the primary reaction products, and the reaction stoichiometry was thus established. Rate constants for hydroperoxi
Gas phase oxidation of nitromethane
โ Scribed by J.C. Tricot; A. Perche; M. Lucquin
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 898 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0010-2180
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โฆ Synopsis
The reaction of nitromethane with oxygen has been studied in the temperature range (700 to 740ยฐK) in a static vessel using both g.p.c, techniques associated with an original sampling procedure [ 11 ] and spectroscopic measurements. The explosion limit, markedly lowered when compared with the case of nitromethane alone, is determined as a function of temperature or of 02 concentration. Accurate atomic balances permit the use of the experimental results to derive a simplified mechanism from a "possible mechanism" comprising 121 steps. The simulation of the "simplified mechanism" gives results that are seen to match the data well not only for the oxidation of CHaNO 2 but also for its pyrolysis and nitration provided that a new way of formation of HCN is introduced. The simulations allow an estimation of the order of magnitude of several rate constants, the values of which are not precisely known. For example, the rate constant of the reaction CH3NO 2 + OH-* CH2NO 2 + H20 may be about 2.4 ร 10 H to3.0 x l0 ll cm 3 tool -I s -l in the temperature range 700 to 740ยฐK.
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