Mg/Al and Cu-Mg/Al mixed oxides derived from hydrotalcites as catalysts to produce 1-butanol from ethanol

IF 3.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Molecular Catalysis Pub Date : 2024-09-16 DOI:10.1016/j.mcat.2024.114528
{"title":"Mg/Al and Cu-Mg/Al mixed oxides derived from hydrotalcites as catalysts to produce 1-butanol from ethanol","authors":"","doi":"10.1016/j.mcat.2024.114528","DOIUrl":null,"url":null,"abstract":"<div><p>The interaction between ethanol molecules to produce 1<em>-</em>butanol over surfaces of Mg/Al and Cu-Mg/Al oxides derived from hydrotalcites (HT) was studied experimentally and computationally. For Mg/Al catalyst, the insertion of Al in the MgO lattice generates a selectivity of 11.7 % for 1-butanol and of 5.8 % for diethyl ether at 300 °C, indicating the importance of the presence of acid sites for dehydration. For Cu-Mg/Al catalyst, Cu<sup>2+</sup> cations have been structural substituted, instead of superficial substituted, exhibiting the highest selectivity for 1-butanol at 250 °C (16.5 %). The inclusion of copper increases the number of acid-base pairs, which are important in the dehydrogenation of ethanol molecules, the aldol condensation of acetaldehyde molecules and the subsequent steps to get 1-butanol. According to DFT results, the presence of copper favors the adsorption of ethanol on the surface, weakening the C<sub>α</sub>-H<sub>α</sub> bond of the molecule, contributing to the formation of acetaldehyde.</p></div>","PeriodicalId":393,"journal":{"name":"Molecular Catalysis","volume":null,"pages":null},"PeriodicalIF":3.9000,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2468823124007107/pdfft?md5=fc6a96d8a5fd7a22447b088095b5dc50&pid=1-s2.0-S2468823124007107-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468823124007107","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

The interaction between ethanol molecules to produce 1-butanol over surfaces of Mg/Al and Cu-Mg/Al oxides derived from hydrotalcites (HT) was studied experimentally and computationally. For Mg/Al catalyst, the insertion of Al in the MgO lattice generates a selectivity of 11.7 % for 1-butanol and of 5.8 % for diethyl ether at 300 °C, indicating the importance of the presence of acid sites for dehydration. For Cu-Mg/Al catalyst, Cu2+ cations have been structural substituted, instead of superficial substituted, exhibiting the highest selectivity for 1-butanol at 250 °C (16.5 %). The inclusion of copper increases the number of acid-base pairs, which are important in the dehydrogenation of ethanol molecules, the aldol condensation of acetaldehyde molecules and the subsequent steps to get 1-butanol. According to DFT results, the presence of copper favors the adsorption of ethanol on the surface, weakening the Cα-Hα bond of the molecule, contributing to the formation of acetaldehyde.

Abstract Image

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
以氢化铝酸盐衍生的镁/铝和铜-镁/铝混合氧化物为催化剂,从乙醇生产 1-丁醇
我们通过实验和计算研究了乙醇分子在氢铝酸盐(HT)衍生的 Mg/Al 和 Cu-Mg/Al 氧化物表面上生成 1-丁醇的相互作用。对于镁/铝催化剂,在 300 °C 时,铝插入氧化镁晶格可产生 11.7 % 的 1-丁醇选择性和 5.8 % 的二乙醚选择性,这表明酸性位点的存在对脱水的重要性。在 Cu-Mg/Al 催化剂中,Cu2+ 阳离子被结构取代,而不是表面取代,在 250 °C 时对 1-丁醇的选择性最高(16.5%)。铜的加入增加了酸碱对的数量,而酸碱对在乙醇分子的脱氢、乙醛分子的醛缩合以及随后得到 1-丁醇的步骤中非常重要。根据 DFT 结果,铜的存在有利于乙醇在表面的吸附,削弱了乙醇分子的 Cα-Hα 键,从而促进了乙醛的形成。
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
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
期刊最新文献
F-modified Cu/electrolyte interface boosts CO2 electroreduction into C2H4 and C2H5OH products via an alternative CC coupling mechanism Cu3Pt1 alloys confined by penta-coordinate Al3+ on Al2O3 realize CO oxidation at room temperature Optimizing reverse water gas shift catalysis: Minimizing metal loading and enhancing performance with Pt/ZrO2 catalysts through Rh incorporation Band gap effect of TiO2 on supported Ru single-atom catalysts for CO2 methanation by DFT calculations Molecular complex inspired design of an efficient copper(II)-containing robust porous polymers for electrochemical water oxidation
×
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