Effect of catalyst composition and reactor configuration on benzene oxidation with a nonthermal plasma-catalyst combined reactor

研究成果: ジャーナルへの寄稿記事

2 引用 (Scopus)

抄録

Plasma-catalysis system comprising surface discharge reactor (SDR)and catalysts were constructed and tested for benzene decomposition. In benzene oxidation with SDR, benzene conversion and the amount of COx formed monotonically increased with input energy, but the benzene decomposition behavior was not related with ozone formation. The loading of metal oxides, Al2O3, TiO2 and CeO2 in SDR greatly promoted benzene oxidation and CO2 formation. The highest activity was obtained with manganese oxides dispersed on ultrastable zeolite Y (Mn/USY). In the range of low input power, the amount of ozone formed increased with the input power, and ozone can be efficiently consumed in benzene oxidation by loading the Mn/USY catalyst in the latter part of SDR. In the higher power range where the amount of ozone decreased with increasing the power, the loading of Mn/USY catalyst inside the reactor was more effective because not only ozone but also short-lived species formed in SDR were utilized for benzene oxidation. The addition of water vapor to reaction gas did not affect benzene conversion and COx formation with SDR-Mn/USY catalyst system. The preadsorbed benzene on the Mn/USY catalyst can be oxidized to CO2 with high selectivity compared with homogeneous oxidation of benzene in SDR.

元の言語英語
ページ(範囲)144-152
ページ数9
ジャーナルCatalysis Today
DOI
出版物ステータス出版済み - 7 15 2019

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Benzene
Surface discharges
Plasmas
Oxidation
Catalysts
Ozone
Chemical analysis
Decomposition
Zeolites
Manganese oxide
Catalyst selectivity
Steam
Oxides
Water vapor
Catalysis
Gases
Metals

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Chemistry(all)

これを引用

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title = "Effect of catalyst composition and reactor configuration on benzene oxidation with a nonthermal plasma-catalyst combined reactor",
abstract = "Plasma-catalysis system comprising surface discharge reactor (SDR)and catalysts were constructed and tested for benzene decomposition. In benzene oxidation with SDR, benzene conversion and the amount of COx formed monotonically increased with input energy, but the benzene decomposition behavior was not related with ozone formation. The loading of metal oxides, Al2O3, TiO2 and CeO2 in SDR greatly promoted benzene oxidation and CO2 formation. The highest activity was obtained with manganese oxides dispersed on ultrastable zeolite Y (Mn/USY). In the range of low input power, the amount of ozone formed increased with the input power, and ozone can be efficiently consumed in benzene oxidation by loading the Mn/USY catalyst in the latter part of SDR. In the higher power range where the amount of ozone decreased with increasing the power, the loading of Mn/USY catalyst inside the reactor was more effective because not only ozone but also short-lived species formed in SDR were utilized for benzene oxidation. The addition of water vapor to reaction gas did not affect benzene conversion and COx formation with SDR-Mn/USY catalyst system. The preadsorbed benzene on the Mn/USY catalyst can be oxidized to CO2 with high selectivity compared with homogeneous oxidation of benzene in SDR.",
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N2 - Plasma-catalysis system comprising surface discharge reactor (SDR)and catalysts were constructed and tested for benzene decomposition. In benzene oxidation with SDR, benzene conversion and the amount of COx formed monotonically increased with input energy, but the benzene decomposition behavior was not related with ozone formation. The loading of metal oxides, Al2O3, TiO2 and CeO2 in SDR greatly promoted benzene oxidation and CO2 formation. The highest activity was obtained with manganese oxides dispersed on ultrastable zeolite Y (Mn/USY). In the range of low input power, the amount of ozone formed increased with the input power, and ozone can be efficiently consumed in benzene oxidation by loading the Mn/USY catalyst in the latter part of SDR. In the higher power range where the amount of ozone decreased with increasing the power, the loading of Mn/USY catalyst inside the reactor was more effective because not only ozone but also short-lived species formed in SDR were utilized for benzene oxidation. The addition of water vapor to reaction gas did not affect benzene conversion and COx formation with SDR-Mn/USY catalyst system. The preadsorbed benzene on the Mn/USY catalyst can be oxidized to CO2 with high selectivity compared with homogeneous oxidation of benzene in SDR.

AB - Plasma-catalysis system comprising surface discharge reactor (SDR)and catalysts were constructed and tested for benzene decomposition. In benzene oxidation with SDR, benzene conversion and the amount of COx formed monotonically increased with input energy, but the benzene decomposition behavior was not related with ozone formation. The loading of metal oxides, Al2O3, TiO2 and CeO2 in SDR greatly promoted benzene oxidation and CO2 formation. The highest activity was obtained with manganese oxides dispersed on ultrastable zeolite Y (Mn/USY). In the range of low input power, the amount of ozone formed increased with the input power, and ozone can be efficiently consumed in benzene oxidation by loading the Mn/USY catalyst in the latter part of SDR. In the higher power range where the amount of ozone decreased with increasing the power, the loading of Mn/USY catalyst inside the reactor was more effective because not only ozone but also short-lived species formed in SDR were utilized for benzene oxidation. The addition of water vapor to reaction gas did not affect benzene conversion and COx formation with SDR-Mn/USY catalyst system. The preadsorbed benzene on the Mn/USY catalyst can be oxidized to CO2 with high selectivity compared with homogeneous oxidation of benzene in SDR.

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