Advances in porous adsorbents for perfluorocarbon greenhouse gas sorption and separation

IF 20.3 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Coordination Chemistry Reviews Pub Date : 2024-11-22 DOI:10.1016/j.ccr.2024.216339
Shao-Min Wang, Peigao Duan, Qing-Yuan Yang
{"title":"Advances in porous adsorbents for perfluorocarbon greenhouse gas sorption and separation","authors":"Shao-Min Wang, Peigao Duan, Qing-Yuan Yang","doi":"10.1016/j.ccr.2024.216339","DOIUrl":null,"url":null,"abstract":"Perfluorocarbons (PFCs) such as CF<sub>4</sub>, C<sub>2</sub>F<sub>6,</sub> and C<sub>3</sub>F<sub>8</sub>, are extensively used in the microelectronics and semiconductor industries, yet their global warming potentials—thousands of times greater than that of CO₂—underscore the urgent need for effective mitigation strategies. While converting PFCs into non-PFCs offers a method for their destruction, a more sustainable approach lies in the recovery and recycling of these compounds using advanced adsorbents. This review explores the potential of cutting-edge porous materials, including metal-organic frameworks (MOFs), covalent-organic frameworks (COFs), and porous organic cages (POCs), for the adsorption and separation of PFCs. By precisely tuning pore sizes and chemical environments through modifications of metal ions and ligands, these porous adsorbents can be tailored to exhibit specific adsorption and separation capabilities. The review focuses on the selective separation of PFCs from nitrogen and other fluorinated gases, with particular emphasis on the latest advancements in adsorbents designed to differentiate between PFCs and other fluorinated compounds in the presence of nitrogen.","PeriodicalId":289,"journal":{"name":"Coordination Chemistry Reviews","volume":"198 1","pages":""},"PeriodicalIF":20.3000,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Coordination Chemistry Reviews","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1016/j.ccr.2024.216339","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

Abstract

Perfluorocarbons (PFCs) such as CF4, C2F6, and C3F8, are extensively used in the microelectronics and semiconductor industries, yet their global warming potentials—thousands of times greater than that of CO₂—underscore the urgent need for effective mitigation strategies. While converting PFCs into non-PFCs offers a method for their destruction, a more sustainable approach lies in the recovery and recycling of these compounds using advanced adsorbents. This review explores the potential of cutting-edge porous materials, including metal-organic frameworks (MOFs), covalent-organic frameworks (COFs), and porous organic cages (POCs), for the adsorption and separation of PFCs. By precisely tuning pore sizes and chemical environments through modifications of metal ions and ligands, these porous adsorbents can be tailored to exhibit specific adsorption and separation capabilities. The review focuses on the selective separation of PFCs from nitrogen and other fluorinated gases, with particular emphasis on the latest advancements in adsorbents designed to differentiate between PFCs and other fluorinated compounds in the presence of nitrogen.

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
用于全氟化碳温室气体吸附和分离的多孔吸附剂的研究进展
CF4、C2F6 和 C3F8 等全氟化碳(PFCs)被广泛应用于微电子和半导体行业,但它们的全球升温潜能值是 CO₂ 的数千倍,因此迫切需要有效的减缓战略。将全氟化合物转化为非全氟化合物是一种销毁全氟化合物的方法,而更可持续的方法则是利用先进的吸附剂回收和循环利用这些化合物。本综述探讨了尖端多孔材料(包括金属有机框架 (MOF)、共价有机框架 (COF) 和多孔有机笼 (POC))在吸附和分离 PFCs 方面的潜力。通过对金属离子和配体的改性来精确调整孔隙大小和化学环境,这些多孔吸附剂可以量身定制,从而展现出特定的吸附和分离能力。本综述侧重于从氮气和其他含氟气体中选择性分离全氟化合物,特别强调了吸附剂的最新进展,这些吸附剂旨在区分氮气中的全氟化合物和其他含氟化合物。
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
Coordination Chemistry Reviews
Coordination Chemistry Reviews 化学-无机化学与核化学
CiteScore
34.30
自引率
5.30%
发文量
457
审稿时长
54 days
期刊介绍: Coordination Chemistry Reviews offers rapid publication of review articles on current and significant topics in coordination chemistry, encompassing organometallic, supramolecular, theoretical, and bioinorganic chemistry. It also covers catalysis, materials chemistry, and metal-organic frameworks from a coordination chemistry perspective. Reviews summarize recent developments or discuss specific techniques, welcoming contributions from both established and emerging researchers. The journal releases special issues on timely subjects, including those featuring contributions from specific regions or conferences. Occasional full-length book articles are also featured. Additionally, special volumes cover annual reviews of main group chemistry, transition metal group chemistry, and organometallic chemistry. These comprehensive reviews are vital resources for those engaged in coordination chemistry, further establishing Coordination Chemistry Reviews as a hub for insightful surveys in inorganic and physical inorganic chemistry.
期刊最新文献
Fundamentals of metal-organic framework-based photocatalysts: The role of chemical diversity and structure engineering Coupled binuclear copper sites in biology: An experimentally-calibrated computational perspective Recent advances in Rh(III)-based anticancer complexes Advances in porous adsorbents for perfluorocarbon greenhouse gas sorption and separation Photocatalytic oxidation of various organic substrates using multinuclear Ru(II)-polypyridyl complexes
×
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