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Radio-frequency induction heating powered low-temperature catalytic CO2 conversion via bi-reforming of methane

[Display omitted] •All prepared catalysts were activated by RF heating at a low temperature of 400 °C.•About 61 % and 93 % CH4 were converted over the Cu-Co to a syngas ratio of 2.1.•The Cu-Co catalyst preserved its catalytic stability for at least 50 hrs at 500 °C.•The activation mechanisms of all...

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Published in:Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2022-02, Vol.430, p.132934, Article 132934
Main Authors: Nguyen, Hoang M., Phan, Chi M., Liu, Shaomin, Pham-Huu, Cuong, Nguyen-Dinh, Lam
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cited_by cdi_FETCH-LOGICAL-c297t-eadea32cf85d8b17d8631789177e2545d602ba4f1367dcd7902d76df4806f9b23
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container_title Chemical engineering journal (Lausanne, Switzerland : 1996)
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Phan, Chi M.
Liu, Shaomin
Pham-Huu, Cuong
Nguyen-Dinh, Lam
description [Display omitted] •All prepared catalysts were activated by RF heating at a low temperature of 400 °C.•About 61 % and 93 % CH4 were converted over the Cu-Co to a syngas ratio of 2.1.•The Cu-Co catalyst preserved its catalytic stability for at least 50 hrs at 500 °C.•The activation mechanisms of all prepared catalysts were explored.•RF heating powered catalytic CO2 conversion displayed high efficiency. Radio-frequency (RF) induction heating of nanoparticles has unfolded novel routes to heterogeneous catalytic chemical reactions. It offers contactless, direct, time- and energy-saving heating with high-achieved catalytic activity. Herein, the tailored chemical synthesis of mono-metallic Cu, binary Cu-Ni, Cu-Co, and ternary Cu-Ni-Co catalysts was evaluated for CO2 conversion via bi-reforming of methane (combined steam- and dry-reforming processes) under induction heating. All prepared catalysts were activated under RF heating to convert CO2 and co-reactants i.e., H2O (steam) and methane into syngas (H2 and CO) at a relatively low temperature of 400 °C. The Cu-Co sample delivered the highest catalytic performance and stability under all tested conditions. Experimental results elaborated that the concomitant presence of a magnetic element and an electrically conductive component in the catalyst system facilitates highly effective heating occurring via both hysteresis loss and Joule effects mechanisms. On account of Joule heating, the Cu-Co catalyst preserved its excellent stability for at least 50 h over the stream test at a reaction temperature higher than its Curie temperature (TC). The findings provide significant insights into the catalyst development for RF-assisted chemical reactions that are not needed to be heavily dependent on the use of strong magnetic metals or high input current to obtain desired reactant conversions.
doi_str_mv 10.1016/j.cej.2021.132934
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Experimental results elaborated that the concomitant presence of a magnetic element and an electrically conductive component in the catalyst system facilitates highly effective heating occurring via both hysteresis loss and Joule effects mechanisms. On account of Joule heating, the Cu-Co catalyst preserved its excellent stability for at least 50 h over the stream test at a reaction temperature higher than its Curie temperature (TC). 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Radio-frequency (RF) induction heating of nanoparticles has unfolded novel routes to heterogeneous catalytic chemical reactions. It offers contactless, direct, time- and energy-saving heating with high-achieved catalytic activity. Herein, the tailored chemical synthesis of mono-metallic Cu, binary Cu-Ni, Cu-Co, and ternary Cu-Ni-Co catalysts was evaluated for CO2 conversion via bi-reforming of methane (combined steam- and dry-reforming processes) under induction heating. All prepared catalysts were activated under RF heating to convert CO2 and co-reactants i.e., H2O (steam) and methane into syngas (H2 and CO) at a relatively low temperature of 400 °C. The Cu-Co sample delivered the highest catalytic performance and stability under all tested conditions. Experimental results elaborated that the concomitant presence of a magnetic element and an electrically conductive component in the catalyst system facilitates highly effective heating occurring via both hysteresis loss and Joule effects mechanisms. On account of Joule heating, the Cu-Co catalyst preserved its excellent stability for at least 50 h over the stream test at a reaction temperature higher than its Curie temperature (TC). 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Radio-frequency (RF) induction heating of nanoparticles has unfolded novel routes to heterogeneous catalytic chemical reactions. It offers contactless, direct, time- and energy-saving heating with high-achieved catalytic activity. Herein, the tailored chemical synthesis of mono-metallic Cu, binary Cu-Ni, Cu-Co, and ternary Cu-Ni-Co catalysts was evaluated for CO2 conversion via bi-reforming of methane (combined steam- and dry-reforming processes) under induction heating. All prepared catalysts were activated under RF heating to convert CO2 and co-reactants i.e., H2O (steam) and methane into syngas (H2 and CO) at a relatively low temperature of 400 °C. The Cu-Co sample delivered the highest catalytic performance and stability under all tested conditions. Experimental results elaborated that the concomitant presence of a magnetic element and an electrically conductive component in the catalyst system facilitates highly effective heating occurring via both hysteresis loss and Joule effects mechanisms. On account of Joule heating, the Cu-Co catalyst preserved its excellent stability for at least 50 h over the stream test at a reaction temperature higher than its Curie temperature (TC). The findings provide significant insights into the catalyst development for RF-assisted chemical reactions that are not needed to be heavily dependent on the use of strong magnetic metals or high input current to obtain desired reactant conversions.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.cej.2021.132934</doi></addata></record>
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subjects CO2 conversion
Cu-Co catalyst
Induction heating
Methane reforming
RF heating
Ternary catalyst
title Radio-frequency induction heating powered low-temperature catalytic CO2 conversion via bi-reforming of methane
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