Co-promoted Mo-carbide catalytic system for sustainable manufacturing of chemicals via co-processing of CO_(2) with ethane  被引量:1

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作  者:Vera Bikbaeva Nikolay Nesterenko Nuria García-Moncada Valentin Valtchev 

机构地区:[1]Laboratoire Catalyse et Spectrochimie,ENSICAEN,Universitéde Caen,CNRS,6 Boulevard Maréchal Juin,14050 Caen,France [2]Servicios Generales de Investigación,XPS,Centro de Investigación,Tecnología e Innovación de la Universidad de Sevilla(CITIUS),Av.Reina Mercedes 4B,41012,Sevilla,Spain

出  处:《Green Carbon》2023年第1期94-103,共10页绿碳(英文)

基  金:TotalEnergies,the Industrial Chair ANR-TOTAL“NanoClean Energy”[ANR-17-CHIN-0005-01]and project NanoCleanEnergy+(Region Normandy).

摘  要:The study reports progress in developing a molybdenum carbide-based catalyst for co-processing ethane and CO_(2).The cobalt promoting of molybdenum carbide improved the activity and stability of ethane transformation in the presence of CO_(2) substantially without any impact on ethylene selectivity.The Mo-Co supported catalyst also showed interesting performance in catalyzing ethane dry reforming and that application could be a perspective further use for this system.In addition,the comprehensive analysis of mono-and bi-metallic catalysts revealed that Co-promoting prevented rapid Mo-carbide oxidation.Further,tuning operation conditions allowed to control catalyst’s selectivity and maximize CO_(2) utilization or ethylene formation.

关 键 词:CO_(2)utilization Oxidative dehydrogenation CO_(2)negative ethylene production Cobalt-molybdenum synergy Embryonic zeolite 

分 类 号:O64[理学—物理化学]

 

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