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    Mechanism Study on Heterogeneous Fenton Catalytic Oxidation of NO Using PrGO as the Carrier

    Source: Journal of Environmental Engineering:;2025:;Volume ( 151 ):;issue: 006::page 04025024-1
    Author:
    Shengqi Li
    ,
    Zhengcheng Wen
    ,
    Zhengyin Yang
    ,
    Heping Li
    DOI: 10.1061/JOEEDU.EEENG-7933
    Publisher: American Society of Civil Engineers
    Abstract: In practical industry, the challenge of removing nitric oxide (NO) from flue gas at temperatures below 200°C persists. The heterogeneous Fenton reaction catalytic oxidation of NO offers an effective approach for achieving denitrification of flue gas at these low temperatures. Utilizing graphene oxide (GO) as the carrier, the Fenton catalyst demonstrates superior catalytic efficiency by effectively facilitating the reduction of Fe(III). Principle analysis shows that reducing GO and using partially reduced graphene oxide (PrGO) as a carrier can further improve catalytic efficiency and stability. Thus, the experimental and theoretical investigation of the mechanism of heterogeneous Fenton catalytic oxidation of NO using PrGO as the carrier is performed in detail in this paper. Experimental studies reveal that the partial reduction of GO significantly enhances catalytic efficiency, leading to an approximate 10% increase in denitrification efficiency at temperatures below 200°C. Furthermore, the catalytic activity of PrGO is observed to rise with increasing reduction degree. Quantum chemical calculations support these findings, showing that the heterogeneous Fenton reaction barrier on PrGO support lacking other oxygen-containing functional groups is significantly lower (34.1  kJ/mol) than that on PrGO support with epoxy, hydroxyl, and carboxy group (75–95  kJ/mol). This confirms the experimental results and underscores the effective enhancement of catalytic activity through GO reduction. Additional investigation employing natural hybrid orbit (NBO) analysis reveals that an increase in oxygen-containing functional groups leads to a decrease in the number of sp2 hybrid carbon atoms in the graphite ring, while the proportion of sp3 hybrid C─ O bonds increases. This disrupts the conjugated structure of the graphite ring, reduces electron mobility, and consequently decreases the conversion rate from ferrous iron to ferric iron, thereby reducing catalytic efficiency. The present study holds significant implications for advancing the development of heterogeneous Fenton reactions for the removal of flue gas pollutants.
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      Mechanism Study on Heterogeneous Fenton Catalytic Oxidation of NO Using PrGO as the Carrier

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    http://yetl.yabesh.ir/yetl1/handle/yetl/4307790
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    contributor authorShengqi Li
    contributor authorZhengcheng Wen
    contributor authorZhengyin Yang
    contributor authorHeping Li
    date accessioned2025-08-17T23:01:18Z
    date available2025-08-17T23:01:18Z
    date copyright6/1/2025 12:00:00 AM
    date issued2025
    identifier otherJOEEDU.EEENG-7933.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4307790
    description abstractIn practical industry, the challenge of removing nitric oxide (NO) from flue gas at temperatures below 200°C persists. The heterogeneous Fenton reaction catalytic oxidation of NO offers an effective approach for achieving denitrification of flue gas at these low temperatures. Utilizing graphene oxide (GO) as the carrier, the Fenton catalyst demonstrates superior catalytic efficiency by effectively facilitating the reduction of Fe(III). Principle analysis shows that reducing GO and using partially reduced graphene oxide (PrGO) as a carrier can further improve catalytic efficiency and stability. Thus, the experimental and theoretical investigation of the mechanism of heterogeneous Fenton catalytic oxidation of NO using PrGO as the carrier is performed in detail in this paper. Experimental studies reveal that the partial reduction of GO significantly enhances catalytic efficiency, leading to an approximate 10% increase in denitrification efficiency at temperatures below 200°C. Furthermore, the catalytic activity of PrGO is observed to rise with increasing reduction degree. Quantum chemical calculations support these findings, showing that the heterogeneous Fenton reaction barrier on PrGO support lacking other oxygen-containing functional groups is significantly lower (34.1  kJ/mol) than that on PrGO support with epoxy, hydroxyl, and carboxy group (75–95  kJ/mol). This confirms the experimental results and underscores the effective enhancement of catalytic activity through GO reduction. Additional investigation employing natural hybrid orbit (NBO) analysis reveals that an increase in oxygen-containing functional groups leads to a decrease in the number of sp2 hybrid carbon atoms in the graphite ring, while the proportion of sp3 hybrid C─ O bonds increases. This disrupts the conjugated structure of the graphite ring, reduces electron mobility, and consequently decreases the conversion rate from ferrous iron to ferric iron, thereby reducing catalytic efficiency. The present study holds significant implications for advancing the development of heterogeneous Fenton reactions for the removal of flue gas pollutants.
    publisherAmerican Society of Civil Engineers
    titleMechanism Study on Heterogeneous Fenton Catalytic Oxidation of NO Using PrGO as the Carrier
    typeJournal Article
    journal volume151
    journal issue6
    journal titleJournal of Environmental Engineering
    identifier doi10.1061/JOEEDU.EEENG-7933
    journal fristpage04025024-1
    journal lastpage04025024-16
    page16
    treeJournal of Environmental Engineering:;2025:;Volume ( 151 ):;issue: 006
    contenttypeFulltext
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    DSpace software copyright © 2002-2015  DuraSpace
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