Mechanism insight into esterification of levulinic acid with methanol on H-Beta Zeolite: A DFT study

IF 5.2 2区 化学 Q1 CHEMISTRY, APPLIED Catalysis Today Pub Date : 2024-09-13 DOI:10.1016/j.cattod.2024.115047
Gonzalo D. Romero Ojeda , Eduardo Nicolás Esquenazi , Glaucio J. Gomes , Nélida M. Peruchena , María Fernanda Zalazar
{"title":"Mechanism insight into esterification of levulinic acid with methanol on H-Beta Zeolite: A DFT study","authors":"Gonzalo D. Romero Ojeda ,&nbsp;Eduardo Nicolás Esquenazi ,&nbsp;Glaucio J. Gomes ,&nbsp;Nélida M. Peruchena ,&nbsp;María Fernanda Zalazar","doi":"10.1016/j.cattod.2024.115047","DOIUrl":null,"url":null,"abstract":"<div><p>The esterification of levulinic acid (LA) to alkyl levulinate esters from biomass by heterogeneous acid catalysis is a potential chemical route for the sustainable production of high value-added products. Acidic zeolites are promising catalysts for this conversion due to their unique pore structures, high selectivity and strong acidity. In this work, we use Density Functional Calculations (DFT) to study the reaction mechanisms for the esterification of LA with MeOH on H-Beta zeolite. We have studied two mechanisms that we consider relevant to the formation of methyl levulinate in acidic zeolites, one involving an Eley-Rideal type mechanism and the other a Langmuir-Hinshelwood type mechanism. Since the activation energies of the rate-determining steps are quite similar, our results suggest that both mechanisms are favourable for this reaction, depending on how the LA and MeOH molecules are initially adsorbed.</p></div>","PeriodicalId":264,"journal":{"name":"Catalysis Today","volume":"445 ","pages":"Article 115047"},"PeriodicalIF":5.2000,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Today","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0920586124005418","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0

Abstract

The esterification of levulinic acid (LA) to alkyl levulinate esters from biomass by heterogeneous acid catalysis is a potential chemical route for the sustainable production of high value-added products. Acidic zeolites are promising catalysts for this conversion due to their unique pore structures, high selectivity and strong acidity. In this work, we use Density Functional Calculations (DFT) to study the reaction mechanisms for the esterification of LA with MeOH on H-Beta zeolite. We have studied two mechanisms that we consider relevant to the formation of methyl levulinate in acidic zeolites, one involving an Eley-Rideal type mechanism and the other a Langmuir-Hinshelwood type mechanism. Since the activation energies of the rate-determining steps are quite similar, our results suggest that both mechanisms are favourable for this reaction, depending on how the LA and MeOH molecules are initially adsorbed.

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
洞察 H-Beta 沸石上乙酰丙酸与甲醇的酯化机理:DFT 研究
通过异相酸催化将生物质中的乙酰丙酸(LA)酯化为乙酰丙酸烷基酯,是一条可持续生产高附加值产品的潜在化学途径。酸性沸石因其独特的孔隙结构、高选择性和强酸性而成为这种转化的理想催化剂。在这项工作中,我们利用密度泛函计算(DFT)研究了 H-Beta 沸石上 LA 与 MeOH 的酯化反应机理。我们研究了两种我们认为与酸性沸石中乙酰丙酸甲酯的形成有关的机理,一种涉及 Eley-Rideal 型机理,另一种涉及 Langmuir-Hinshelwood 型机理。由于决定速率步骤的活化能非常相似,我们的研究结果表明这两种机理都有利于该反应,具体取决于 LA 和 MeOH 分子最初的吸附方式。
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
Catalysis Today
Catalysis Today 化学-工程:化工
CiteScore
11.50
自引率
3.80%
发文量
573
审稿时长
2.9 months
期刊介绍: Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues. Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.
期刊最新文献
Using waste to treat waste: Catalysts from spent alkaline batteries for glycolysis of PET waste Selective hydrogenation of furfuryl alcohol to 1,2-pentanediol over Pt/Mg2AlO catalysts with different synthesis methods Novel preparation of polyphenylacetylene semiconductor: Potential application in supercapacitors Single atom and sub-nanometer copper clusters deposited on titania for hydrogen evolution reaction: A density functional study Performance of copper-aluminum catalysts impregnated with potassium in NO and N2O reduction by CO
×
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