Ni/x%Nb2O5/Al2O3 Catalysts Prepared via Coprecipitation-Wet Impregnation Method for Methane Steam Reforming

Juliana F. Gonçalves and Mariana M.V.M. Souza
{"title":"Ni/x%Nb2O5/Al2O3 Catalysts Prepared via Coprecipitation-Wet Impregnation Method for Methane Steam Reforming","authors":"Juliana F. Gonçalves and Mariana M.V.M. Souza","doi":"10.2174/2211544708666190423130340","DOIUrl":null,"url":null,"abstract":"\n\nHydrogen has been considered the energy source of the future and one of the\nprocesses for its production is the methane steam reforming. The catalyst used industrially is Ni/Al2O3\nand the addition of promoter oxides can be an alternative to improve the performance of this catalyst,\nwhich suffers from coke formation and sintering.\n\n\n\nEvaluate the role of niobia on catalytic activity and stability.\n\n\n\nNi/x%Nb2O5/Al2O3 (x = 5, 10 and 20) catalysts were synthesized via coprecipitation-wet impregnation\nmethod and characterized by X-ray fluorescence (XRF), N2 adsorption-desorption, X-ray diffraction\n(XRD), temperature- programmed reduction (TPR), temperature-programmed desorption of\nammonia (TPD-NH3), etc. Finally, the catalysts were tested for methane steam reforming reaction.\n\n\n\n All niobia-doped catalysts presented similar values of methane conversion and when comparing\nwith Ni-Al, the addition of niobia slightly improved the methane conversion. In the stability test at\n800oC, all doped and non-doped catalysts did not deactivate during the 24 h of reaction.\n\n\n\n The addition of 10 and 20 wt.% of niobia had a significant promoter effect over Ni/Al2O3\ncatalyst in terms of activity and stability at 800 oC and the sample with 20 wt.% of niobia presented\nlower coke formation.\n","PeriodicalId":10862,"journal":{"name":"Current Catalysis","volume":"276 1","pages":"80-89"},"PeriodicalIF":0.0000,"publicationDate":"2020-02-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Catalysis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/2211544708666190423130340","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Hydrogen has been considered the energy source of the future and one of the processes for its production is the methane steam reforming. The catalyst used industrially is Ni/Al2O3 and the addition of promoter oxides can be an alternative to improve the performance of this catalyst, which suffers from coke formation and sintering. Evaluate the role of niobia on catalytic activity and stability. Ni/x%Nb2O5/Al2O3 (x = 5, 10 and 20) catalysts were synthesized via coprecipitation-wet impregnation method and characterized by X-ray fluorescence (XRF), N2 adsorption-desorption, X-ray diffraction (XRD), temperature- programmed reduction (TPR), temperature-programmed desorption of ammonia (TPD-NH3), etc. Finally, the catalysts were tested for methane steam reforming reaction. All niobia-doped catalysts presented similar values of methane conversion and when comparing with Ni-Al, the addition of niobia slightly improved the methane conversion. In the stability test at 800oC, all doped and non-doped catalysts did not deactivate during the 24 h of reaction. The addition of 10 and 20 wt.% of niobia had a significant promoter effect over Ni/Al2O3 catalyst in terms of activity and stability at 800 oC and the sample with 20 wt.% of niobia presented lower coke formation.
共沉淀-湿浸渍法制备Ni/x%Nb2O5/Al2O3甲烷蒸汽重整催化剂
氢已被认为是未来的能源,其生产过程之一是甲烷蒸汽重整。工业上使用的催化剂是Ni/ al2o3,添加促进剂氧化物可以作为一种替代方法来改善这种催化剂的性能,这种催化剂容易结焦和烧结。评价铌对催化活性和稳定性的影响。采用共沉淀-湿浸渍法制备了Ni/x%Nb2O5/Al2O3 (x = 5、10和20)催化剂,并通过x射线荧光(XRF)、N2吸附-解吸、x射线衍射(XRD)、程序升温还原(TPR)、程序升温解吸氨(TPD-NH3)等对催化剂进行了表征。最后,对催化剂进行了甲烷蒸汽重整反应试验。所有掺铌催化剂的甲烷转化率相近,且与Ni-Al催化剂相比,掺铌催化剂的甲烷转化率略有提高。在800℃的稳定性测试中,所有掺杂和未掺杂的催化剂在反应的24小时内都没有失活。在800℃时,添加10%和20%的铌对Ni/ al2o3催化剂的活性和稳定性有显著的促进作用,且添加20%铌的样品的结焦量较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信