Physics and chemistry of the influence of excited molecules on combustion enhancement
Author(s) -
А. М. Старик,
Boris I. Loukhovitski,
Alexander S. Sharipov,
Н. С. Титова
Publication year - 2015
Publication title -
philosophical transactions of the royal society a mathematical physical and engineering sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.074
H-Index - 169
eISSN - 1471-2962
pISSN - 1364-503X
DOI - 10.1098/rsta.2014.0341
Subject(s) - molecule , singlet oxygen , electric field , excitation , excited state , combustion , oxygen , chemical physics , chemistry , atomic physics , photochemistry , materials science , analytical chemistry (journal) , physics , organic chemistry , quantum mechanics
The paper addresses detailed analysis of kinetic processes in the H(2)-O(2), CO-O(2) and CH(4)-O(2)-reactive systems upon the presence of singlet oxygen molecules O(2)(a(1)Δg) and [Formula: see text] and the influence of the activation of oxygen molecules in electric discharge on the acceleration of ignition in the H(2)-O(2) and CH(4)-O(2) mixtures. The possibility of the intensification of CO oxidation due to excitation of O(2) and N(2) molecule vibrations and generation of singlet oxygen molecules is also considered. It is shown that the effect of accelerating the ignition strongly depends on the reduced electric field and, as a consequence, on the composition of discharge plasma as well as on the features of chain mechanism development in oxy-fuel systems. It is revealed that the most effective approach for the intensification of CO oxidation both in the moist air and in the products of hydrocarbon combustion in air is the generation of O(2)(a(1)Δg) molecules by electric discharge. Computations showed that the presence of 1% O(2)(a(1)Δg) in the total oxygen allowed one to convert CO to CO(2) even at the temperature T=850-900 K in the time of 10(-2) s. The excitation of O(2) and N(2) molecule vibrations is less effective for such a conversion.
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