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    The Role of Carbon Monoxide in NO2 Plume Formation

    Source: Journal of Engineering for Gas Turbines and Power:;2000:;volume( 122 ):;issue: 002::page 287
    Author:
    Alan S. Feitelberg
    ,
    Sanjay M. Correa
    DOI: 10.1115/1.483215
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Through a series of computational studies, carbon monoxide has been identified as an important promoter of NO oxidation to NO2 in combustion turbine exhaust gas at intermediate temperatures (450 to 750°C). NO2 formation is accompanied by enhanced CO burnout at these temperatures. Perfectly stirred reactor and plug flow reactor calculations indicate that concentrations of CO as low as 50 ppmv in exhaust gas containing 25 ppmv NO can result in the conversion of 50 percent of the NO to NO2 in less than 1 s. NO2 concentrations as low as 15 ppmv can result in visible, yellow-brown plumes from large diameter exhaust stacks. If NO2 plumes are to be prevented, then designers of gas turbines and heat recovery steam generators need to be aware of the relationships between time, temperature, and composition which cause NO2 to form in exhaust gas. Reaction path analysis indicates that the mutually promoted oxidation of CO and NO occurs through a self-propagating, three-step chain reaction mechanism. CO is oxidized by OH (CO+OH→CO2+H), while NO is oxidized by HO2:NO+HO2→NO2+OH. In a narrow temperature range, the H-atom produced by the first reaction can react with O2 in a three body reaction to yield the hydroperoxy radical needed in the second reaction: H+O2+M→HO2+M, where M is any third body. The observed net reaction is CO+O2+NO→CO2+NO2, which occurs stoichiometrically at temperatures below about 550°C. As the temperature increases, additional reaction pathways become available for H, HO2, and OH which remove these radicals from the chain and eventually completely decouple the oxidation of CO from NO. An abbreviated set of elementary chemical reactions, including 15 species and 33 reactions, has been developed to model CO-enhanced oxidation of NO to NO2. This reaction set was derived from a larger reaction set with more than 50 species and 230 elementary chemical reactions, and was validated by comparison of PSR and PFR calculations using the two sets. [S0742-4795(00)01402-2]
    keyword(s): Temperature , Plumes (Fluid dynamics) , Carbon , Gas turbines , Exhaust systems , oxidation , Chain , Turbines , Combustion , Mechanisms , Atoms , Flow (Dynamics) AND Heat recovery steam generators ,
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      The Role of Carbon Monoxide in NO2 Plume Formation

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    https://yetl.yabesh.ir/yetl1/handle/yetl/123692
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    contributor authorAlan S. Feitelberg
    contributor authorSanjay M. Correa
    date accessioned2017-05-09T00:02:25Z
    date available2017-05-09T00:02:25Z
    date copyrightApril, 2000
    date issued2000
    identifier issn1528-8919
    identifier otherJETPEZ-26795#287_1.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/123692
    description abstractThrough a series of computational studies, carbon monoxide has been identified as an important promoter of NO oxidation to NO2 in combustion turbine exhaust gas at intermediate temperatures (450 to 750°C). NO2 formation is accompanied by enhanced CO burnout at these temperatures. Perfectly stirred reactor and plug flow reactor calculations indicate that concentrations of CO as low as 50 ppmv in exhaust gas containing 25 ppmv NO can result in the conversion of 50 percent of the NO to NO2 in less than 1 s. NO2 concentrations as low as 15 ppmv can result in visible, yellow-brown plumes from large diameter exhaust stacks. If NO2 plumes are to be prevented, then designers of gas turbines and heat recovery steam generators need to be aware of the relationships between time, temperature, and composition which cause NO2 to form in exhaust gas. Reaction path analysis indicates that the mutually promoted oxidation of CO and NO occurs through a self-propagating, three-step chain reaction mechanism. CO is oxidized by OH (CO+OH→CO2+H), while NO is oxidized by HO2:NO+HO2→NO2+OH. In a narrow temperature range, the H-atom produced by the first reaction can react with O2 in a three body reaction to yield the hydroperoxy radical needed in the second reaction: H+O2+M→HO2+M, where M is any third body. The observed net reaction is CO+O2+NO→CO2+NO2, which occurs stoichiometrically at temperatures below about 550°C. As the temperature increases, additional reaction pathways become available for H, HO2, and OH which remove these radicals from the chain and eventually completely decouple the oxidation of CO from NO. An abbreviated set of elementary chemical reactions, including 15 species and 33 reactions, has been developed to model CO-enhanced oxidation of NO to NO2. This reaction set was derived from a larger reaction set with more than 50 species and 230 elementary chemical reactions, and was validated by comparison of PSR and PFR calculations using the two sets. [S0742-4795(00)01402-2]
    publisherThe American Society of Mechanical Engineers (ASME)
    titleThe Role of Carbon Monoxide in NO2 Plume Formation
    typeJournal Paper
    journal volume122
    journal issue2
    journal titleJournal of Engineering for Gas Turbines and Power
    identifier doi10.1115/1.483215
    journal fristpage287
    journal lastpage292
    identifier eissn0742-4795
    keywordsTemperature
    keywordsPlumes (Fluid dynamics)
    keywordsCarbon
    keywordsGas turbines
    keywordsExhaust systems
    keywordsoxidation
    keywordsChain
    keywordsTurbines
    keywordsCombustion
    keywordsMechanisms
    keywordsAtoms
    keywordsFlow (Dynamics) AND Heat recovery steam generators
    treeJournal of Engineering for Gas Turbines and Power:;2000:;volume( 122 ):;issue: 002
    contenttypeFulltext
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