丁烯在ZnO-SiO2上的异构化

T. Sumiyoshi, K. Tanabe, H. Hattori
{"title":"丁烯在ZnO-SiO2上的异构化","authors":"T. Sumiyoshi, K. Tanabe, H. Hattori","doi":"10.1627/JPI1959.17.65","DOIUrl":null,"url":null,"abstract":"Isomerization of n-butenes was investigated over binary oxides ZnO-SiO2 having different mole ratios and the nature of active sites and the mechanism of the reaction were examined.On mixing of ZnO and SiO2, there appeared acidic sites and basic sites on the surface. The type of the acid sites was of Lewis acid which was determined by IR study of adsorbed pyridine.The isomerization was not retarded by acidic molecule of CO2 but by basic molecules such as pyridine and ammonia. The products formed over the deuterated catalyst contained a small amount of D atoms. The results of co-isomerization indicate that the reaction involves intramolecular hydrogen transfer and that the slow step is C-H bond cleavage. Therefore, it is concluded that the isomerization of butenes takes place on Lewis acid sites and is initiated by the abstraction of hydride ion which is the rate determining step.","PeriodicalId":9596,"journal":{"name":"Bulletin of The Japan Petroleum Institute","volume":"42 1","pages":"65-70"},"PeriodicalIF":0.0000,"publicationDate":"1975-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Isomerization of Butene over ZnO-SiO2\",\"authors\":\"T. Sumiyoshi, K. Tanabe, H. Hattori\",\"doi\":\"10.1627/JPI1959.17.65\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Isomerization of n-butenes was investigated over binary oxides ZnO-SiO2 having different mole ratios and the nature of active sites and the mechanism of the reaction were examined.On mixing of ZnO and SiO2, there appeared acidic sites and basic sites on the surface. The type of the acid sites was of Lewis acid which was determined by IR study of adsorbed pyridine.The isomerization was not retarded by acidic molecule of CO2 but by basic molecules such as pyridine and ammonia. The products formed over the deuterated catalyst contained a small amount of D atoms. The results of co-isomerization indicate that the reaction involves intramolecular hydrogen transfer and that the slow step is C-H bond cleavage. Therefore, it is concluded that the isomerization of butenes takes place on Lewis acid sites and is initiated by the abstraction of hydride ion which is the rate determining step.\",\"PeriodicalId\":9596,\"journal\":{\"name\":\"Bulletin of The Japan Petroleum Institute\",\"volume\":\"42 1\",\"pages\":\"65-70\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1975-04-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bulletin of The Japan Petroleum Institute\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1627/JPI1959.17.65\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of The Japan Petroleum Institute","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1627/JPI1959.17.65","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

摘要

研究了正丁烯在不同摩尔比的ZnO-SiO2二元氧化物上的异构化反应,探讨了活性位点的性质和反应机理。ZnO与SiO2混合后,表面出现酸性位点和碱性位点。通过对吸附吡啶的红外光谱分析,确定其酸位为路易斯酸。酸性的CO2分子对异构化反应没有阻滞作用,而碱性分子如吡啶和氨对异构化反应有阻滞作用。氘化催化剂上形成的产物含有少量的D原子。共异构化结果表明,反应涉及分子内氢转移,反应的慢步是C-H键的裂解。因此,丁烯异构化反应发生在路易斯酸位点,并由氢化物离子的抽离引发,这是反应速率的决定步骤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Isomerization of Butene over ZnO-SiO2
Isomerization of n-butenes was investigated over binary oxides ZnO-SiO2 having different mole ratios and the nature of active sites and the mechanism of the reaction were examined.On mixing of ZnO and SiO2, there appeared acidic sites and basic sites on the surface. The type of the acid sites was of Lewis acid which was determined by IR study of adsorbed pyridine.The isomerization was not retarded by acidic molecule of CO2 but by basic molecules such as pyridine and ammonia. The products formed over the deuterated catalyst contained a small amount of D atoms. The results of co-isomerization indicate that the reaction involves intramolecular hydrogen transfer and that the slow step is C-H bond cleavage. Therefore, it is concluded that the isomerization of butenes takes place on Lewis acid sites and is initiated by the abstraction of hydride ion which is the rate determining step.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Catalytic Cracking of Heavy Oil with Iron Oxide-based Catalysts Using Hydrogen and Oxygen Species from Steam Desulfurization of Heavy Oil with Iron Oxide-based Catalysts Using Steam Improvement of Silica–alumina Supports for Diesel Oxidation Catalysts through Control of Both Composition and Pore Structure Effect of Low-concentration Furfural on Sulfur Amino Acid Biosynthesis in Saccharomyces cerevisiae Development of Highly Active and Durable Platinum Core-shell Catalysts for Polymer Electrolyte Fuel Cells
×
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