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Titlebook: Emissions from Continuous Combustion Systems; Proceedings of the S Walter Cornelius,William G. Agnew Conference proceedings 1972 Springer S

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Investigation of No Formation Kinetics in Combustion Processes: the Methane-Oxygen-Nitrogen Reactionh the oxidizer-rich and fuel-rich mixture were consistent with a three-reaction mechanism for nitrogen chemistry,.Reactions 1 and 2 were found to be the principal NO formation reactions, with reaction 3 being of minor importance for the fuel-rich mixture.
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Nitric Oxide Formation and Carbon Monoxide Burnout in a Compact Steam Generatorydrocarbons (HC), CO and NO. The measured emission rates are compared with values calculated assuming that the overall reaction rates are limited by the reaction of CO with OH and N. with O, and that the free radical concentrations are determined by the combination of the reactions.The results are u
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Mathematical Models of Continuous Combustionl, incorporated into a digital-computer program. Morever, since the emission of pollutants is more sensitive to detailed design changes than is the overall heat transfer or power output of the system, the refined insight provided by predictions of concentration distributions is especially valuable n
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Current Kinetic Modeling Techniques for Continuous Flow Combustorsictions of pollutant emissions. Particular emphasis is placed on the kinetic aspects of the models involving liquid fuel droplet evaporation and/or combustion and homogeneous chemical kinetics for hydrocarbon/air combustion. A brief summary of the various flow models is also included. Comparisons wi
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Nitric Oxide Formation in Laminar Diffusion Flamession flame by means of a quartz microprobe have been analyzed for NO as well as for the species CO, CO. N., O. and CH., the fuel employed. In this manner it has been possible to establish detailed radial profiles for each of the above species. Concomitant temperature profiles have been established t
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Investigation of No Formation Kinetics in Combustion Processes: the Methane-Oxygen-Nitrogen Reactiond by argon has been carried out. Concentration histories of NO, OH and CO. were measured during reaction behind reflected shock waves using spectroscopic techniques. Experimental concentration profiles were obtained for an oxidizer-rich and a fuel-rich mixture for initial post-shock temperatures in
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