Enhancing oxidative desulfurization of polyoxometalate by integrating with a self-reductive framework

IF 6.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Science China Materials Pub Date : 2024-08-06 DOI:10.1007/s40843-023-2873-y
Yonghui Lin  (, ), Xiaojun Zhao  (, ), Shenzhen Chang  (, ), Yixin Zhang  (, ), Letian Gan  (, ), Yuyang Tian  (, ), Qinhe Pan  (, ), Guangshan Zhu  (, )
{"title":"Enhancing oxidative desulfurization of polyoxometalate by integrating with a self-reductive framework","authors":"Yonghui Lin \n (,&nbsp;),&nbsp;Xiaojun Zhao \n (,&nbsp;),&nbsp;Shenzhen Chang \n (,&nbsp;),&nbsp;Yixin Zhang \n (,&nbsp;),&nbsp;Letian Gan \n (,&nbsp;),&nbsp;Yuyang Tian \n (,&nbsp;),&nbsp;Qinhe Pan \n (,&nbsp;),&nbsp;Guangshan Zhu \n (,&nbsp;)","doi":"10.1007/s40843-023-2873-y","DOIUrl":null,"url":null,"abstract":"<div><p>With the strict control of sulfur content in fuels, oxidative desulfurization (ODS), a promising desulphurization technology, needs to be continuously developed. In this study, we integrated multiple approaches (fabricating a porous structure, increasing phosphomolybdic acid (PMo) loading, improving amphiphilicity, and enhancing the intrinsic activity of PMo using a reductive framework) into PAF-54 carriers to improve ODS catalytic ability. The catalytic performance suggested that PAF-54 was not simply used as a carrier for PMo by physical integration. During the binding process, electron transfer between PAF-54 and PMo formed Mo<sup>5+</sup> with superior catalytic activity. Owing to the presence of PAF-54, the catalytic activity of PMo as the active component qualitatively improved to achieve rapid and efficient desulfurization. More importantly, we found that other nitrogen-rich porous organic polymers can also reduce some of Mo<sup>6+</sup> in PMo during loading, and its formation mechanism was investigated. This work provides a feasible strategy for designing highly efficient DOS catalysts.\n</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":773,"journal":{"name":"Science China Materials","volume":"67 9","pages":"2925 - 2933"},"PeriodicalIF":6.8000,"publicationDate":"2024-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science China Materials","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s40843-023-2873-y","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

With the strict control of sulfur content in fuels, oxidative desulfurization (ODS), a promising desulphurization technology, needs to be continuously developed. In this study, we integrated multiple approaches (fabricating a porous structure, increasing phosphomolybdic acid (PMo) loading, improving amphiphilicity, and enhancing the intrinsic activity of PMo using a reductive framework) into PAF-54 carriers to improve ODS catalytic ability. The catalytic performance suggested that PAF-54 was not simply used as a carrier for PMo by physical integration. During the binding process, electron transfer between PAF-54 and PMo formed Mo5+ with superior catalytic activity. Owing to the presence of PAF-54, the catalytic activity of PMo as the active component qualitatively improved to achieve rapid and efficient desulfurization. More importantly, we found that other nitrogen-rich porous organic polymers can also reduce some of Mo6+ in PMo during loading, and its formation mechanism was investigated. This work provides a feasible strategy for designing highly efficient DOS catalysts.

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
通过与自还原框架结合,增强聚氧化金属酸盐的氧化脱硫作用
随着对燃料中硫含量的严格控制,氧化脱硫(ODS)这一前景广阔的脱硫技术需要不断发展。在本研究中,我们将多种方法(制造多孔结构、增加磷钼酸(PMo)负载量、改善两亲性以及利用还原框架增强 PMo 的内在活性)整合到 PAF-54 载体中,以提高 ODS 催化能力。催化性能表明,PAF-54 并非简单地通过物理整合成为 PMo 的载体。在结合过程中,PAF-54 和 PMo 之间的电子转移形成了具有卓越催化活性的 Mo5+。由于 PAF-54 的存在,作为活性成分的 PMo 的催化活性得到了质的提高,从而实现了快速高效的脱硫。更重要的是,我们发现其他富氮多孔有机聚合物在负载过程中也能减少 PMo 中的部分 Mo6+,并对其形成机理进行了研究。这项工作为设计高效 DOS 催化剂提供了一种可行的策略。
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
Science China Materials
Science China Materials Materials Science-General Materials Science
CiteScore
11.40
自引率
7.40%
发文量
949
期刊介绍: Science China Materials (SCM) is a globally peer-reviewed journal that covers all facets of materials science. It is supervised by the Chinese Academy of Sciences and co-sponsored by the Chinese Academy of Sciences and the National Natural Science Foundation of China. The journal is jointly published monthly in both printed and electronic forms by Science China Press and Springer. The aim of SCM is to encourage communication of high-quality, innovative research results at the cutting-edge interface of materials science with chemistry, physics, biology, and engineering. It focuses on breakthroughs from around the world and aims to become a world-leading academic journal for materials science.
期刊最新文献
Reaction-based small-molecule fluorescent probes for endoplasmic reticulum- and mitochondria-targeted biosensing and bioimaging Promising graphdiyne-based nanomaterials for environmental pollutant control Hydrogen embrittlement of retrogression-reaged 7xxx-series aluminum alloys—a comprehensive review Supramolecular glass: a new platform for ultralong phosphorescence Simultaneously achieving high sensitivity, low dark current and low detection limits in anti-perovskites towards X-ray detection
×
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