Ni-Fe Nanoparticles Supported on UiO-66-X Catalyst for Hydrogenation of Fatty Acid Esters to Alcohols.

Chem & Bio Engineering Pub Date : 2024-09-16 eCollection Date: 2025-01-23 DOI:10.1021/cbe.4c00108
Pengcheng Li, Tianyu Ma, Youyang Wu, Jianping Wu, Haoran Yu, Lirong Yang, Gang Xu
{"title":"Ni-Fe Nanoparticles Supported on UiO-66-X Catalyst for Hydrogenation of Fatty Acid Esters to Alcohols.","authors":"Pengcheng Li, Tianyu Ma, Youyang Wu, Jianping Wu, Haoran Yu, Lirong Yang, Gang Xu","doi":"10.1021/cbe.4c00108","DOIUrl":null,"url":null,"abstract":"<p><p>Enhancing the performance of non-noble-metal catalysts would facilitate the economic feasibility of the chemical conversion process. Through strategies involving metal nanoparticles (MNPs) size control and support functionalization modification, Ni2Fe6/UiO-66-X-y catalysts (X stands for H, OH, CH<sub>3</sub>, and NH<sub>2</sub>, and y stands for the concentration of NaBH<sub>4</sub> solution) were prepared for the efficiently selective hydrogenation of methyl laurate (ML) to 1-dodecanol. High-concentration NaBH<sub>4</sub> solution facilitated the preparation of smaller-sized MNPs, while support functionalization could alter the chemical microenvironment of the support, thereby promoting electron transfer between appropriately sized MNPs and the support. In particular, the Ni2Fe6/UiO-66-NH<sub>2</sub>-0.4 M catalyst could achieve 99.9% conversion of ML and 98.6% selectivity for 1-dodecanol when it was reacted at 220 °C and 3 MPa H<sub>2</sub> for 8 h. The probable catalytic mechanism based on the η<sup>2</sup>(C, O)-aldehyde conformation was discussed, and reaction kinetics were calculated. Furthermore, the catalyst achieved five stable recycling runs and demonstrated catalytic versatility for other fatty acid methyl esters, including methyl stearate, methyl palmitate, and methyl valerate.</p>","PeriodicalId":100230,"journal":{"name":"Chem & Bio Engineering","volume":"2 1","pages":"23-34"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11835283/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chem & Bio Engineering","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1021/cbe.4c00108","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/23 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Enhancing the performance of non-noble-metal catalysts would facilitate the economic feasibility of the chemical conversion process. Through strategies involving metal nanoparticles (MNPs) size control and support functionalization modification, Ni2Fe6/UiO-66-X-y catalysts (X stands for H, OH, CH3, and NH2, and y stands for the concentration of NaBH4 solution) were prepared for the efficiently selective hydrogenation of methyl laurate (ML) to 1-dodecanol. High-concentration NaBH4 solution facilitated the preparation of smaller-sized MNPs, while support functionalization could alter the chemical microenvironment of the support, thereby promoting electron transfer between appropriately sized MNPs and the support. In particular, the Ni2Fe6/UiO-66-NH2-0.4 M catalyst could achieve 99.9% conversion of ML and 98.6% selectivity for 1-dodecanol when it was reacted at 220 °C and 3 MPa H2 for 8 h. The probable catalytic mechanism based on the η2(C, O)-aldehyde conformation was discussed, and reaction kinetics were calculated. Furthermore, the catalyst achieved five stable recycling runs and demonstrated catalytic versatility for other fatty acid methyl esters, including methyl stearate, methyl palmitate, and methyl valerate.

求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信