{"title":"Enhancing oxidative desulfurization of polyoxometalate by integrating with a self-reductive framework","authors":"Yonghui Lin \n (, ), Xiaojun Zhao \n (, ), Shenzhen Chang \n (, ), Yixin Zhang \n (, ), Letian Gan \n (, ), Yuyang Tian \n (, ), Qinhe Pan \n (, ), Guangshan Zhu \n (, )","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.
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.