NOx formed in combustion processes is mainly constituted by nitrogen monoxide (NO) while nitrogen dioxide (NO2) accounts for marginal concentration only However, being NO2 characterized by higher water solubility and equilibrium constant in tie neutralization reaction operated with basic reactants, it is easily removed via dry or wet processes On this basis an innovative process alternative to the conventional DeNO(x) SCR and SNCR can be envisaged, where the oxidation of NO to NO2 makes the successive abatement of the oxidized fraction relatively earlier The scope of the work is the study of the oxidation of NO to NO2, considered as the controlling step of the proposed process, operated with hydrogen peroxide (H2O2) A mathematical model of the oxidation has been developed in the Chemkin v 3 7 environment, describing the gas phase kinetics in the energy recovery section of a generic combustion process through the Miller and 3owman (1989) kinetic mechanism The base model has been improved with the introduction of the oxidation steps induced by the injection of hydrogen pe oxide drawn from the literature The NO oxidation reaction was investigated in a temperature range of 250-700 degrees C, with a 20% excess of oxidizing agent with respect to the NO/oxidizer oxidation reaction stoichiometry The experimental maximum conversion results are less than the calculated one of about 20% The results of the model have been validated through experimental runs conducted in a bench scale pilot plant

Innovative technique for the control of NOx formed in combustion processes / Verdone, Nicola; Scarsella, Marco; Liuzzo, Giuseppe; DE FILIPPIS, Paolo. - STAMPA. - 140:(2010), pp. 11-20. (Intervento presentato al convegno 5th International Conference on Waste Management and the Environment tenutosi a Tallinn, ESTONIA nel JUL, 2010) [10.2495/wm100021].

Innovative technique for the control of NOx formed in combustion processes

VERDONE, Nicola;SCARSELLA, Marco;LIUZZO, Giuseppe;DE FILIPPIS, Paolo
2010

Abstract

NOx formed in combustion processes is mainly constituted by nitrogen monoxide (NO) while nitrogen dioxide (NO2) accounts for marginal concentration only However, being NO2 characterized by higher water solubility and equilibrium constant in tie neutralization reaction operated with basic reactants, it is easily removed via dry or wet processes On this basis an innovative process alternative to the conventional DeNO(x) SCR and SNCR can be envisaged, where the oxidation of NO to NO2 makes the successive abatement of the oxidized fraction relatively earlier The scope of the work is the study of the oxidation of NO to NO2, considered as the controlling step of the proposed process, operated with hydrogen peroxide (H2O2) A mathematical model of the oxidation has been developed in the Chemkin v 3 7 environment, describing the gas phase kinetics in the energy recovery section of a generic combustion process through the Miller and 3owman (1989) kinetic mechanism The base model has been improved with the introduction of the oxidation steps induced by the injection of hydrogen pe oxide drawn from the literature The NO oxidation reaction was investigated in a temperature range of 250-700 degrees C, with a 20% excess of oxidizing agent with respect to the NO/oxidizer oxidation reaction stoichiometry The experimental maximum conversion results are less than the calculated one of about 20% The results of the model have been validated through experimental runs conducted in a bench scale pilot plant
2010
5th International Conference on Waste Management and the Environment
no(x) chemistry; flue gas treatment; nox chemistry; deno(x); denox
04 Pubblicazione in atti di convegno::04b Atto di convegno in volume
Innovative technique for the control of NOx formed in combustion processes / Verdone, Nicola; Scarsella, Marco; Liuzzo, Giuseppe; DE FILIPPIS, Paolo. - STAMPA. - 140:(2010), pp. 11-20. (Intervento presentato al convegno 5th International Conference on Waste Management and the Environment tenutosi a Tallinn, ESTONIA nel JUL, 2010) [10.2495/wm100021].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/210184
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