Influence of Solvent on the Pore Structure and Activity of Pt-Sn/Alumino- Silicate Catalysts

M. Riad, S. Mikhail
{"title":"Influence of Solvent on the Pore Structure and Activity of Pt-Sn/Alumino- Silicate Catalysts","authors":"M. Riad, S. Mikhail","doi":"10.2174/1876214X00902010110","DOIUrl":null,"url":null,"abstract":"Kaolinite supported bimetallic Pt-Sn catalysts were prepared via impregnation technique using different sol- vents, water, ethanol and acetone. The catalysts were characterized by X-ray diffraction pattern and temperature pro- grammed reduction techniques. Surface area and pore size distribution were determined by nitrogen physisorption tech- nique. The activities of the catalysts were measured toward n-pentane isomerization reaction in a pulse micro-catalytic re- actor operated under atmospheric pressure and at reaction temperature ranged from 200-450 o C. The results indicated that the selectivity of the Pt-Sn/kaolinite catalysts toward iso-pentane formation decreased from ethanol to acetone and then to water. Pore size distribution and diffusion coefficient of reactant and products are responsible for the high selectivity of Pt-Sn /kaolinte (ethanol) catalyst towards iso-pentane formation.","PeriodicalId":22755,"journal":{"name":"The Open Catalysis Journal","volume":"32 1","pages":"110-118"},"PeriodicalIF":0.0000,"publicationDate":"2009-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Open Catalysis Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1876214X00902010110","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Kaolinite supported bimetallic Pt-Sn catalysts were prepared via impregnation technique using different sol- vents, water, ethanol and acetone. The catalysts were characterized by X-ray diffraction pattern and temperature pro- grammed reduction techniques. Surface area and pore size distribution were determined by nitrogen physisorption tech- nique. The activities of the catalysts were measured toward n-pentane isomerization reaction in a pulse micro-catalytic re- actor operated under atmospheric pressure and at reaction temperature ranged from 200-450 o C. The results indicated that the selectivity of the Pt-Sn/kaolinite catalysts toward iso-pentane formation decreased from ethanol to acetone and then to water. Pore size distribution and diffusion coefficient of reactant and products are responsible for the high selectivity of Pt-Sn /kaolinte (ethanol) catalyst towards iso-pentane formation.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
溶剂对Pt-Sn/铝硅酸盐催化剂孔隙结构和活性的影响
采用浸渍法制备了高岭石负载型Pt-Sn双金属催化剂,浸渍剂为不同的溶剂孔、水、乙醇和丙酮。用x射线衍射图和程序升温还原技术对催化剂进行了表征。采用氮气物理吸附法测定了其比表面积和孔径分布。在常压下、反应温度200 ~ 450℃的脉冲微催化反应器中测定了催化剂对正戊烷异构化反应的活性。结果表明,Pt-Sn/高岭石催化剂对异戊烷的选择性从乙醇→丙酮→水依次下降。Pt-Sn /高岭石(乙醇)催化剂对异戊烷形成具有高选择性,反应物和生成物的孔径分布和扩散系数是主要原因。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Applied Biocatalysis with an Organic Resistant Partially Purified Lipasefrom P. aeruginosa During FAME Production Porous Ni@Tantalum Silicate as a Tandem Catalyst for Selective Synthesisof C4 Hydrocarbons from Ethanol Hydrodeoxygenation of Phenol Over Hydrotreatment Catalysts in their Reduced and Sulfided States Structure of Co(II) Species Formed on the Surface of γ-Alumina Upon Interfacial Deposition Bioethanol Transformations Over Active Surface Sites Generated on Carbon Nanotubes or Carbon Nanofibers Materials
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1