4.6 Article

Cold plasma-prepared Ru-based catalysts for boosting plasma-catalytic CO2 methanation

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CHEMICAL ENGINEERING SCIENCE
卷 280, 期 -, 页码 -

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ces.2023.119056

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CO2 methanation; Ru-based catalysts; Cold plasma; CO2 conversion; Plasma preparation

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In this work, Ru-based catalysts supported on γ-Al2O3 were prepared by cold plasma for enhancing plasma-catalytic CO2 methanation without additional heating. The plasma-prepared Ru/γ-Al2O3 showed higher CO2 conversion (76.3%) compared to Ru/γ-Al2O3-C prepared by thermal reduction (52.0%) due to the high dispersion and surface enrichment of Ru induced by plasma. Plasmas-prepared CoRu/γ-Al2O3 and AuRu/γ-Al2O3 exhibited enhanced and similar plasma-catalytic CO2 methanation activity. The CoRu nanoparticles showed smaller size and higher dispersion compared to AuRu nanoparticles, and CoRu showed higher alloying degree and surface enrichment degree. Well alloyed RuCo may reduce the free energy of hydrogen adsorption on the catalysts. Small particle size can improve atom utilization efficiency, and surface enrichment of active species can shorten the heterogeneous reaction from 7 to 5 steps.
In this work, & gamma;-Al2O3 supported Ru-based catalysts were prepared by cold plasma for boosting plasma-catalytic CO2 methanation without additional heating. CO2 conversion over plasma-prepared Ru/& gamma;-Al2O3 (76.3%) was far superior to Ru/& gamma;-Al2O3-C prepared by thermal reduction (52.0%) due to the high dispersion and surface enrichment of Ru induced by plasma. CoRu/& gamma;-Al2O3 and AuRu/& gamma;-Al2O3 prepared by plasma possessed enhanced and similar plasma-catalytic CO2 methantion activity. The sizes of the metal nanoparticles are small, and the CoRu nanoparticles showed smaller size and higher dispersion than those of AuRu. The AuRu and CoRu alloys were formed in AuRu/& gamma;-Al2O3 and CoRu/& gamma;-Al2O3, and the CoRu showed higher alloying degree and surface enrichment degree. Well alloyed RuCo may reduce the free energy of hydrogen adsorption at the catalysts. Small particle size can improve their atom utilization efficiency, and surface enrichment of the active species can shorten the heterogeneous reaction from 7 to 5 steps.

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