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{"title":"Catalytic Decomposition of Methane to Hydrogen over Al2O3 Supported Mono- and Bimetallic Catalysts","authors":"G. E. Ergazieva, N. Makayeva, Z. Shaimerden, S. Soloviev, Мoldir Telbayeva, Еrzhan Akkazin, Fariza Ahmetova","doi":"10.9767/bcrec.17.1.12174.1-12","DOIUrl":null,"url":null,"abstract":"This article discusses the decomposition of methane in the temperature range 550–800 °C on low-percentage monometallic (Ni/g-Al2O3, Co/g-Al2O3) and bimetallic (Ni-Co/g-Al2O3) catalysts. It is shown that the bimetallic catalyst is more active in the decomposition of methane to hydrogen than monometallic ones. At a reaction temperature of 600 °C, the highest methane conversion is 81%, and the highest hydrogen yield of 51% is formed on Ni-Co/g-Al2O3. A complex of physicochemical methods (Scanning Electron Microscope (SEM), X-ray Diffraction (XRD), Temperature Programmed Reduction (TPR-H2), etc.) established that the addition of cobalt oxide to the composition of Ni/g-Al2O3 leads to the formation of surface bimetallic Ni-Co alloys, while the dispersion of particles increases and the reducibility of the catalyst is facilitated, which provides an increase in the concentration of metal particles - active centers, which can be the reason for an increase in the catalytic properties of a bimetallic catalyst in comparison with monometallic ones. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).","PeriodicalId":46276,"journal":{"name":"Bulletin of Chemical Reaction Engineering and Catalysis","volume":" ","pages":""},"PeriodicalIF":1.3000,"publicationDate":"2021-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of Chemical Reaction Engineering and Catalysis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9767/bcrec.17.1.12174.1-12","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
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Al2O3负载的单金属和双金属催化剂催化甲烷分解制氢
本文讨论了甲烷在550–800°C的温度范围内在低百分比单金属(Ni/g-Al2O3,Co/g-Al2O3)和双金属(Ni-Co/g-Al2O3)催化剂上的分解。结果表明,双金属催化剂在甲烷分解为氢气方面比单金属催化剂更具活性。在600°C的反应温度下,在Ni-Co/g-Al2O3上形成的甲烷转化率最高为81%,氢气产率最高为51%。复杂的物理化学方法(扫描电子显微镜(SEM)、X射线衍射(XRD)、程序升温还原(TPR-H2)等)证实,在Ni/g-Al2O3的组成中添加氧化钴会导致表面双金属Ni-Co合金的形成,同时颗粒的分散增加,促进了催化剂的还原性,这提供了金属颗粒-活性中心的浓度的增加,这可能是双金属催化剂与单金属催化剂相比催化性能增加的原因。版权所有©2021作者所有,BCREC集团出版。这是CC BY-SA许可证下的开放访问文章(https://creativecommons.org/licenses/by-sa/4.0)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。