Lai Truong-Phuoc , Jean-Mario Nhut , Loïc Vidal , Cuong Duong-Viet , Sécou Sall , Corinne Petit , Christophe Sutter , Mehdi Arab , Alex Jourdan , Cuong Pham-Huu
{"title":"贫铀氧化物负载镍催化剂在非绝热反应器中的自热CO2甲烷化反应","authors":"Lai Truong-Phuoc , Jean-Mario Nhut , Loïc Vidal , Cuong Duong-Viet , Sécou Sall , Corinne Petit , Christophe Sutter , Mehdi Arab , Alex Jourdan , Cuong Pham-Huu","doi":"10.1016/j.jechem.2023.06.035","DOIUrl":null,"url":null,"abstract":"<div><p>Undoped nickel-based catalysts supported on depleted uranium oxide allow one to carry out CO<sub>2</sub> methanation process under extremely low reaction temperature under atmospheric pressure and powered by a contactless induction heating. By adjusting the reaction conditions, the catalyst is able to perform CO<sub>2</sub> methanation reaction under autothermal process operated inside a non-adiabatic reactor, without any external energy supply. Such autothermal process is possible thanks to the high apparent density of the UO<em><sub>x</sub></em> which allows one to confine the reaction heat in a small catalyst volume in order to confine the exothermicity of the reaction inside the catalyst and to operate the reaction at equilibrium heat in-heat out. Such autothermal operation mode allows one to significantly reduce the complexity of the process compared to that operated using adiabatic reactor, where complete insulation is required to prevent heat disequilibrium, in order to reduce as much as possible, the heat exchange with the external medium. The catalyst displays an extremely high stability as a function of time on stream as no apparent deactivation. It is expected that such new catalyst with unprecedented catalytic performance could open new era in the field of heterogeneous catalysis where traditional supports show their limitations to operate catalytic processes under severe reaction conditions.</p></div>","PeriodicalId":14,"journal":{"name":"ACS Combinatorial Science","volume":null,"pages":null},"PeriodicalIF":3.7840,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Depleted uranium oxide supported nickel catalyst for autothermal CO2 methanation in non-adiabatic reactor under induction heating\",\"authors\":\"Lai Truong-Phuoc , Jean-Mario Nhut , Loïc Vidal , Cuong Duong-Viet , Sécou Sall , Corinne Petit , Christophe Sutter , Mehdi Arab , Alex Jourdan , Cuong Pham-Huu\",\"doi\":\"10.1016/j.jechem.2023.06.035\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Undoped nickel-based catalysts supported on depleted uranium oxide allow one to carry out CO<sub>2</sub> methanation process under extremely low reaction temperature under atmospheric pressure and powered by a contactless induction heating. By adjusting the reaction conditions, the catalyst is able to perform CO<sub>2</sub> methanation reaction under autothermal process operated inside a non-adiabatic reactor, without any external energy supply. Such autothermal process is possible thanks to the high apparent density of the UO<em><sub>x</sub></em> which allows one to confine the reaction heat in a small catalyst volume in order to confine the exothermicity of the reaction inside the catalyst and to operate the reaction at equilibrium heat in-heat out. Such autothermal operation mode allows one to significantly reduce the complexity of the process compared to that operated using adiabatic reactor, where complete insulation is required to prevent heat disequilibrium, in order to reduce as much as possible, the heat exchange with the external medium. The catalyst displays an extremely high stability as a function of time on stream as no apparent deactivation. It is expected that such new catalyst with unprecedented catalytic performance could open new era in the field of heterogeneous catalysis where traditional supports show their limitations to operate catalytic processes under severe reaction conditions.</p></div>\",\"PeriodicalId\":14,\"journal\":{\"name\":\"ACS Combinatorial Science\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.7840,\"publicationDate\":\"2023-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Combinatorial Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2095495623003856\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Chemistry\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Combinatorial Science","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2095495623003856","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Chemistry","Score":null,"Total":0}
Depleted uranium oxide supported nickel catalyst for autothermal CO2 methanation in non-adiabatic reactor under induction heating
Undoped nickel-based catalysts supported on depleted uranium oxide allow one to carry out CO2 methanation process under extremely low reaction temperature under atmospheric pressure and powered by a contactless induction heating. By adjusting the reaction conditions, the catalyst is able to perform CO2 methanation reaction under autothermal process operated inside a non-adiabatic reactor, without any external energy supply. Such autothermal process is possible thanks to the high apparent density of the UOx which allows one to confine the reaction heat in a small catalyst volume in order to confine the exothermicity of the reaction inside the catalyst and to operate the reaction at equilibrium heat in-heat out. Such autothermal operation mode allows one to significantly reduce the complexity of the process compared to that operated using adiabatic reactor, where complete insulation is required to prevent heat disequilibrium, in order to reduce as much as possible, the heat exchange with the external medium. The catalyst displays an extremely high stability as a function of time on stream as no apparent deactivation. It is expected that such new catalyst with unprecedented catalytic performance could open new era in the field of heterogeneous catalysis where traditional supports show their limitations to operate catalytic processes under severe reaction conditions.
期刊介绍:
The Journal of Combinatorial Chemistry has been relaunched as ACS Combinatorial Science under the leadership of new Editor-in-Chief M.G. Finn of The Scripps Research Institute. The journal features an expanded scope and will build upon the legacy of the Journal of Combinatorial Chemistry, a highly cited leader in the field.