Highly Selective Separation of C2H2/CO2 and C2H2/C2H4 in an N-Rich Cage-Based Microporous Metal-Organic Framework

Lingzhi Yang, Wenpeng Xie, Qiuju Fu, Liting Yan, Shuo Zhang, Huimin Jiang, Liangjun Li, X. Gu, Dandan Liu, Pengcheng Dai, Q. Zheng, Xuebo Zhao
{"title":"Highly Selective Separation of C2H2/CO2 and C2H2/C2H4 in an N-Rich Cage-Based Microporous Metal-Organic Framework","authors":"Lingzhi Yang, Wenpeng Xie, Qiuju Fu, Liting Yan, Shuo Zhang, Huimin Jiang, Liangjun Li, X. Gu, Dandan Liu, Pengcheng Dai, Q. Zheng, Xuebo Zhao","doi":"10.1155/2023/4740672","DOIUrl":null,"url":null,"abstract":"The separation of acetylene (C2H2) from carbon dioxide (CO2) and the purification of ethylene (C2H4) from C2H2 are quite essential processes for the chemical industry. However, these processes are challenging due to their similar physical properties, including molecule sizes and boiling points. Herein, we report an N-rich cage-based microporous metal-organic framework (MOF), [Cd5(Tz)9](NO3) (termed as Cd-TZ, TZ stands for tetrazole), and its highly efficient separation of C2H2/CO2 and C2H2/C2H4. Single-component gas adsorption isotherms reveal that Cd-TZ exhibits high C2H2 adsorption capacity (3.10 mmol g-1 at 298 K and 1 bar). The N-rich cages in Cd-TZ can trap C2H2 with a higher isosteric heat of adsorption (40.8 kJ mol-1) than CO2 and C2H4 owing to the robust host-guest interactions between the noncoordinated N atoms and C2H2, which has been verified by molecular modeling studies. Cd-TZ shows a high IAST selectivity for C2H2/CO2 (8.3) and C2H2/C2H4 (13.3). The breakthrough simulations confirm the potential for separating C2H2/CO2 and the purification of C2H4 from C2H2.","PeriodicalId":7279,"journal":{"name":"Adsorption Science & Technology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Adsorption Science & Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2023/4740672","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

The separation of acetylene (C2H2) from carbon dioxide (CO2) and the purification of ethylene (C2H4) from C2H2 are quite essential processes for the chemical industry. However, these processes are challenging due to their similar physical properties, including molecule sizes and boiling points. Herein, we report an N-rich cage-based microporous metal-organic framework (MOF), [Cd5(Tz)9](NO3) (termed as Cd-TZ, TZ stands for tetrazole), and its highly efficient separation of C2H2/CO2 and C2H2/C2H4. Single-component gas adsorption isotherms reveal that Cd-TZ exhibits high C2H2 adsorption capacity (3.10 mmol g-1 at 298 K and 1 bar). The N-rich cages in Cd-TZ can trap C2H2 with a higher isosteric heat of adsorption (40.8 kJ mol-1) than CO2 and C2H4 owing to the robust host-guest interactions between the noncoordinated N atoms and C2H2, which has been verified by molecular modeling studies. Cd-TZ shows a high IAST selectivity for C2H2/CO2 (8.3) and C2H2/C2H4 (13.3). The breakthrough simulations confirm the potential for separating C2H2/CO2 and the purification of C2H4 from C2H2.
富n笼型微孔金属有机骨架中C2H2/CO2和C2H2/C2H4的高选择性分离
从二氧化碳(CO2)中分离乙炔(C2H2)和从C2H2中提纯乙烯(C2H4)是化学工业中非常重要的过程。然而,由于它们相似的物理性质,包括分子大小和沸点,这些过程具有挑战性。本文报道了一种富n笼型微孔金属有机骨架(MOF) [Cd5(Tz)9](NO3)(称为Cd-TZ, Tz代表四氮唑),以及它对C2H2/CO2和C2H2/C2H4的高效分离。单组分气体吸附等温线显示Cd-TZ具有较高的C2H2吸附量(在298 K和1 bar下为3.10 mmol g-1)。由于非配位N原子与C2H2之间存在强大的主客体相互作用,Cd-TZ中的富N笼能以比CO2和C2H4更高的等等吸附热(40.8 kJ mol-1)捕获C2H2,这已被分子模型研究证实。Cd-TZ对C2H2/CO2(8.3)和C2H2/C2H4(13.3)的IAST选择性较高。突破性的模拟证实了分离C2H2/CO2和从C2H2中提纯C2H4的潜力。
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 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