Iron complex on aminoalcohol modified support PAF-30 as a catalyst for oxidation of sulfur-containing compounds by air

IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Molecular Catalysis Pub Date : 2025-03-15 Epub Date: 2025-02-14 DOI:10.1016/j.mcat.2025.114915
E.A. Eseva, M.O. Lukashov, L.A. Kulikov, A.V. Akopyan
{"title":"Iron complex on aminoalcohol modified support PAF-30 as a catalyst for oxidation of sulfur-containing compounds by air","authors":"E.A. Eseva,&nbsp;M.O. Lukashov,&nbsp;L.A. Kulikov,&nbsp;A.V. Akopyan","doi":"10.1016/j.mcat.2025.114915","DOIUrl":null,"url":null,"abstract":"<div><div>Catalytic aerobic desulfurization is a promising alternative to hydrodesulfurization or additional technology for deep desulfurization of petroleum distillates containing refractory condensed thiophene derivatives. In this study, a catalyst based on a complex of iron on PAF-30 support modified by ethanolamines was developed. The PAF-MEA-Fe catalyst was characterized using various methods: XRD, FTIR, <sup>13</sup>C NMR, low-temperature adsorption-desorption nitrogen, TEM, TGA, UV–vis, XPS and elemental analysis. Compared to a sample prepared by ordinary impregnation of iron salt on a porous support, the chelate complex of iron demonstrated excellent catalytic activity in the oxidation reaction of dibenzothiophene (DBT) by air. The removal rates were achieved at the level of 100, 80 and 75 % for DBT and its mono- and dimethyl-substituted derivatives. The synergistic effect of the PAF-30 mesoporous support, an available complexing ligand and catalytically active iron ions allows you to develop an effective catalyst for aerobic oxidative desulfurization of a sulfur-containing model fuel. High stability of the catalyst during 5 oxidation-regeneration cycles was demonstrated.</div></div>","PeriodicalId":393,"journal":{"name":"Molecular Catalysis","volume":"575 ","pages":"Article 114915"},"PeriodicalIF":4.9000,"publicationDate":"2025-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468823125001014","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/14 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Catalytic aerobic desulfurization is a promising alternative to hydrodesulfurization or additional technology for deep desulfurization of petroleum distillates containing refractory condensed thiophene derivatives. In this study, a catalyst based on a complex of iron on PAF-30 support modified by ethanolamines was developed. The PAF-MEA-Fe catalyst was characterized using various methods: XRD, FTIR, 13C NMR, low-temperature adsorption-desorption nitrogen, TEM, TGA, UV–vis, XPS and elemental analysis. Compared to a sample prepared by ordinary impregnation of iron salt on a porous support, the chelate complex of iron demonstrated excellent catalytic activity in the oxidation reaction of dibenzothiophene (DBT) by air. The removal rates were achieved at the level of 100, 80 and 75 % for DBT and its mono- and dimethyl-substituted derivatives. The synergistic effect of the PAF-30 mesoporous support, an available complexing ligand and catalytically active iron ions allows you to develop an effective catalyst for aerobic oxidative desulfurization of a sulfur-containing model fuel. High stability of the catalyst during 5 oxidation-regeneration cycles was demonstrated.

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
氨基醇改性载体PAF-30上的铁配合物作为含硫化合物空气氧化的催化剂
催化好氧脱硫是一种很有前途的替代加氢脱硫或对含难熔缩合噻吩衍生物的石油馏分进行深度脱硫的附加技术。本研究开发了一种乙醇胺改性PAF-30载体上的铁络合物催化剂。采用XRD、FTIR、13C NMR、低温吸附-解吸氮、TEM、TGA、UV-vis、XPS和元素分析等方法对PAF-MEA-Fe催化剂进行了表征。与多孔载体上普通浸渍铁盐制备的样品相比,铁螯合物在空气氧化二苯并噻吩(DBT)反应中表现出优异的催化活性。DBT及其一甲基和二甲基取代衍生物的去除率分别为100%、80%和75%。PAF-30介孔载体、可用的络合配体和催化活性铁离子的协同作用使您能够开发一种有效的催化剂,用于含硫模型燃料的有氧氧化脱硫。结果表明,该催化剂在5次氧化再生循环中具有较高的稳定性。
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
Redox-active tetra-amino cobalt phthalocyanine electrocatalyst for sustainable electrochemical synthesis of 2-(pyridin-4-yl)-1H-benzo[d]imidazole Multi-strategy metabolic engineering approach to enhance 3´-C-prenylnaringenin production in recombinant Escherichia coli CO2 to sustainable aviation fuel via RWGS and Fischer–Tropsch: A comprehensive review on catalysts, kinetics, and reactor design Identifying descriptors for the rational design of Ni-supported oxide inverse catalysts for dry reforming of methane Cobalt silicate-doped Pt/silicate-1 for enhanced carbonyl selectivity in cinnamaldehyde hydrogenation
×
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:604180095
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