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MOFs限域多酸团簇的合成及其成型化研究进展

薛丽丽 吴嘉琪 李壮壮 李斯文 王伟 赵建社

化工进展2024,Vol.43Issue(12):6968-6982,15.
化工进展2024,Vol.43Issue(12):6968-6982,15.DOI:10.16085/j.issn.1000-6613.2023-2186

MOFs限域多酸团簇的合成及其成型化研究进展

Research progress in the synthesis and molding of MOFs confined POM

薛丽丽 1吴嘉琪 1李壮壮 1李斯文 1王伟 1赵建社2

作者信息

  • 1. 长安大学水利与环境学院旱区地下水文与生态效应教育部重点实验室,水利部旱区生态水文与水安全重点实验室,陕西 西安 710064
  • 2. 西北大学化学与材料科学学院,陕西 西安 710069
  • 折叠

摘要

Abstract

Polyoxometalate(POM)is a kind of catalyst with excellent properties,but it is usually soluble in organic solvents and has a small specific surface area,which makes recovery and recycling difficult.Meanwhile,metal-organic framework(MOFs)is a porous loading material with a large specific surface area,high porosity,rich pore structure,and adjustable pore size.Starting from porous MOFs materials,this article reviewed how to promote POM to enter the pores of MOFs,constructing a type of MOFs confined POM material(POM@MOF).It clarified that this type of catalytic material could not only exert the efficient catalytic performance of POM,but also effectively utilize the porous properties of MOFs.The current research status in the field of oxidative desulfurization was also summarized.However,even though traditional powder catalysts had superior catalytic performance,their application in practical production was limited by issues such as difficulty in recovery and impact on recycling.Therefore,it was an effective way to shape and treat POM@MOF through methods such as forming fiber fixation and electrospinning.Finally,this article provided an outlook for the application of POM@MOF in the field of oxidative desulfurization,and proposed that the formation of POM@MOF was one of the important directions for future desulfurization applications.

关键词

催化剂/金属有机框架/多金属氧酸盐/氧化/再生

Key words

catalyst/metal-organic framework/polyoxometalates/oxidation/regeneration

分类

资源环境

引用本文复制引用

薛丽丽,吴嘉琪,李壮壮,李斯文,王伟,赵建社..MOFs限域多酸团簇的合成及其成型化研究进展[J].化工进展,2024,43(12):6968-6982,15.

基金项目

长安大学研究生科学创新实践项目(300103723056). (300103723056)

化工进展

OA北大核心CSTPCD

1000-6613

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