Pd/SiO2和Ba-Pd/SiO2催化丁腈气相加氢生产丁胺

Q1 Materials Science Catalysis Structure & Reactivity Pub Date : 2015-07-03 DOI:10.1179/2055075815Y.0000000007
Y. Hao, M. Li, F. Cárdenas-Lizana, M. Keane
{"title":"Pd/SiO2和Ba-Pd/SiO2催化丁腈气相加氢生产丁胺","authors":"Y. Hao, M. Li, F. Cárdenas-Lizana, M. Keane","doi":"10.1179/2055075815Y.0000000007","DOIUrl":null,"url":null,"abstract":"Abstract The gas phase (1 atm, 473-563 K) hydrogenation of butyronitrile has been studied over Pd/SiO2 and Ba-Pd/SiO2. Catalysts characterisation involved TPR, H2/NH3 chemisorption/TPD, XRD and TEM measurements. The incorporation of Ba with Pd resulted in the formation of smaller metal nano-particles (7 nm vs. 28 nm) with a resultant (seven-fold) higher H2 chemisorption and decreased total surface acidity (from NH3 chemisorption/TPD). Temperature related activity maxima were observed for both catalysts and are associated with thermal desorption of the nitrile reactant. Exclusivity to the target butylamine was achieved at T ≥ 543 K where Ba-Pd/SiO2 delivered higher selective hydrogenation rate (91 mol h −1 mol Pd -1 ) than Pd/SiO2 (54 mol h −1 mol Pd −1 ), attributed to greater availability of surface reactive hydrogen. Lower surface acidity served to minimise condensation to higher amines. The rate and selectivity to butylamine exceed those previously reported for gas phase operation.","PeriodicalId":43717,"journal":{"name":"Catalysis Structure & Reactivity","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2015-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1179/2055075815Y.0000000007","citationCount":"4","resultStr":"{\"title\":\"Production of Butylamine in the Gas Phase Hydrogenation of Butyronitrile over Pd/SiO2 and Ba-Pd/SiO2\",\"authors\":\"Y. Hao, M. Li, F. Cárdenas-Lizana, M. Keane\",\"doi\":\"10.1179/2055075815Y.0000000007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract The gas phase (1 atm, 473-563 K) hydrogenation of butyronitrile has been studied over Pd/SiO2 and Ba-Pd/SiO2. Catalysts characterisation involved TPR, H2/NH3 chemisorption/TPD, XRD and TEM measurements. The incorporation of Ba with Pd resulted in the formation of smaller metal nano-particles (7 nm vs. 28 nm) with a resultant (seven-fold) higher H2 chemisorption and decreased total surface acidity (from NH3 chemisorption/TPD). Temperature related activity maxima were observed for both catalysts and are associated with thermal desorption of the nitrile reactant. Exclusivity to the target butylamine was achieved at T ≥ 543 K where Ba-Pd/SiO2 delivered higher selective hydrogenation rate (91 mol h −1 mol Pd -1 ) than Pd/SiO2 (54 mol h −1 mol Pd −1 ), attributed to greater availability of surface reactive hydrogen. Lower surface acidity served to minimise condensation to higher amines. The rate and selectivity to butylamine exceed those previously reported for gas phase operation.\",\"PeriodicalId\":43717,\"journal\":{\"name\":\"Catalysis Structure & Reactivity\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-07-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1179/2055075815Y.0000000007\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Catalysis Structure & Reactivity\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1179/2055075815Y.0000000007\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Materials Science\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Structure & Reactivity","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1179/2055075815Y.0000000007","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Materials Science","Score":null,"Total":0}
引用次数: 4

摘要

研究了Pd/SiO2和Ba-Pd/SiO2上丁腈气相(1atm, 473 ~ 563 K)加氢反应。催化剂的表征包括TPR、H2/NH3化学吸附、TPD、XRD和TEM测试。Ba与Pd的掺入导致形成更小的金属纳米颗粒(7 nm vs 28 nm),由此产生(7倍)更高的H2化学吸附和降低的总表面酸度(来自NH3化学吸附/TPD)。两种催化剂均观察到与温度相关的活性最大值,并且与腈反应物的热脱附有关。当温度≥543 K时,Ba-Pd/SiO2的选择性加氢率(91 mol h−1 mol Pd -1)高于Pd/SiO2 (54 mol h−1 mol Pd -1),这是由于表面活性氢的可用性更高。较低的表面酸度有助于最大限度地减少高胺的缩合。对丁胺的反应速率和选择性超过了以前报道的气相操作。
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
Production of Butylamine in the Gas Phase Hydrogenation of Butyronitrile over Pd/SiO2 and Ba-Pd/SiO2
Abstract The gas phase (1 atm, 473-563 K) hydrogenation of butyronitrile has been studied over Pd/SiO2 and Ba-Pd/SiO2. Catalysts characterisation involved TPR, H2/NH3 chemisorption/TPD, XRD and TEM measurements. The incorporation of Ba with Pd resulted in the formation of smaller metal nano-particles (7 nm vs. 28 nm) with a resultant (seven-fold) higher H2 chemisorption and decreased total surface acidity (from NH3 chemisorption/TPD). Temperature related activity maxima were observed for both catalysts and are associated with thermal desorption of the nitrile reactant. Exclusivity to the target butylamine was achieved at T ≥ 543 K where Ba-Pd/SiO2 delivered higher selective hydrogenation rate (91 mol h −1 mol Pd -1 ) than Pd/SiO2 (54 mol h −1 mol Pd −1 ), attributed to greater availability of surface reactive hydrogen. Lower surface acidity served to minimise condensation to higher amines. The rate and selectivity to butylamine exceed those previously reported for gas phase operation.
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
Catalysis Structure & Reactivity
Catalysis Structure & Reactivity CHEMISTRY, PHYSICAL-
CiteScore
4.80
自引率
0.00%
发文量
0
期刊最新文献
Plasmonic photocatalysis Electrocatalysts Catalysis Catalysis Direct non-oxidative methane conversion in membrane reactor
×
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