DEHYDROALKYLATION OF BENZENE WITH PROPANE ON MECHANICAL MIXTURES OF CATALYSTS

F.A. Babayeva F.A. Babayeva
{"title":"DEHYDROALKYLATION OF BENZENE WITH PROPANE ON MECHANICAL \nMIXTURES OF CATALYSTS","authors":"F.A. Babayeva F.A. Babayeva","doi":"10.32010/ajcn05012022-42","DOIUrl":null,"url":null,"abstract":"The conversion of C6H6 : C3H8 mixtures on mixed catalysts (MMC) composed of the metal oxide catalysts M,ReOx/Al2O3 (Pt or Ni -0.5 wt.%, Re-1.0 wt.%) and zeolites Y, МOR, and ZSM-5 in the H form was studied. The products of benzene dehydroalkylation by propane and propane dehydrogenation products are formed at 200–400°C. It has been shown that C3H8 is activated on the metal oxide catalysts and C6H6 interacts with the zeolites yielding the C6H7+ intermediate, which acts as an agent of proton transfer from a zeolite to a metal catalyst, and another intermediate C9H13+ . Cumene, alkylbenzenes, and propene are formed as a result of the conversion . Acomparison of the results of the conversion of these mixtures on the composite catalysts with different zeolites shows that the formation of cumene and propene is thermally controlled and the formation of the other products is kinetically controlled. It has been concluded that the coupling of the redox properties of the metal oxide catalysts with the acid–base properties of the zeolite catalysts facilitates the low–temperature transformations of the C6H6 : C3H8 mixtures.\nKeywords: dehydroalkylation, dehydrogenation, benzene, propane, mechanical mixture of catalysts, zeolite isopropylbenzene, propylene","PeriodicalId":245302,"journal":{"name":"Azerbaijan Journal of Chemical News","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Azerbaijan Journal of Chemical News","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32010/ajcn05012022-42","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

The conversion of C6H6 : C3H8 mixtures on mixed catalysts (MMC) composed of the metal oxide catalysts M,ReOx/Al2O3 (Pt or Ni -0.5 wt.%, Re-1.0 wt.%) and zeolites Y, МOR, and ZSM-5 in the H form was studied. The products of benzene dehydroalkylation by propane and propane dehydrogenation products are formed at 200–400°C. It has been shown that C3H8 is activated on the metal oxide catalysts and C6H6 interacts with the zeolites yielding the C6H7+ intermediate, which acts as an agent of proton transfer from a zeolite to a metal catalyst, and another intermediate C9H13+ . Cumene, alkylbenzenes, and propene are formed as a result of the conversion . Acomparison of the results of the conversion of these mixtures on the composite catalysts with different zeolites shows that the formation of cumene and propene is thermally controlled and the formation of the other products is kinetically controlled. It has been concluded that the coupling of the redox properties of the metal oxide catalysts with the acid–base properties of the zeolite catalysts facilitates the low–temperature transformations of the C6H6 : C3H8 mixtures. Keywords: dehydroalkylation, dehydrogenation, benzene, propane, mechanical mixture of catalysts, zeolite isopropylbenzene, propylene
苯与丙烷在机械混合催化剂上的脱氢烷基化反应
研究了由金属氧化物催化剂M、ReOx/Al2O3 (Pt或Ni -0.5 wt.%, Re-1.0 wt.%)和H型沸石Y、МOR和ZSM-5组成的混合催化剂(MMC)上C6H6: C3H8混合物的转化过程。在200 ~ 400℃的温度下,形成苯丙烷脱氢烷基化产物和丙烷脱氢产物。结果表明,C3H8在金属氧化物催化剂上被活化,C6H6与沸石相互作用生成C6H7+中间体,C6H7+中间体作为质子从沸石向金属催化剂转移的媒介,另一中间体C9H13+。由于这种转化,形成了异丙烯、烷基苯和丙烯。在不同沸石的复合催化剂上对这些混合物的转化结果进行了比较,结果表明,异丙烯和丙烯的生成受热控制,其他产物的生成受动力学控制。综上所述,金属氧化物催化剂的氧化还原性质与沸石催化剂的酸碱性质的耦合作用有利于C6H6: C3H8混合物的低温转化。关键词:脱氢烷基化,脱氢,苯,丙烷,机械混合催化剂,异丙苯,丙烯
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