Gate-Opening Effect in a Flexible Metal–Organic Framework for Sieving Acetylene

Xiao-Jing Xie, Qi-Yun Cao, Zhi-Hao Zhang, Min-Yi Zhou, Heng Zeng*, Weigang Lu* and Dan Li*, 
{"title":"Gate-Opening Effect in a Flexible Metal–Organic Framework for Sieving Acetylene","authors":"Xiao-Jing Xie,&nbsp;Qi-Yun Cao,&nbsp;Zhi-Hao Zhang,&nbsp;Min-Yi Zhou,&nbsp;Heng Zeng*,&nbsp;Weigang Lu* and Dan Li*,&nbsp;","doi":"10.1021/cbe.3c00097","DOIUrl":null,"url":null,"abstract":"<p >Adsorptive separation employing porous materials is one of the most promising alternative technologies for C<sub>2</sub>H<sub>2</sub> purification due to its energy-efficient and environmentally friendly advantages. Herein, we present the design and synthesis of a dicopper-paddle-wheel-based metal–organic framework (termed JNU-5-Me) with a carboxylate-azolate organic linker. The use of such a linker results in the axial positions of the dicopper paddle wheels being occupied by azolates, and therefore, a much-improved chemical stability of the framework structure. JNU-5-Me shows negligible adsorption of C<sub>2</sub>H<sub>4</sub>, C<sub>2</sub>H<sub>6</sub>, and CO<sub>2</sub> at 1.0 bar and 298 K, while a gate-opening effect for C<sub>2</sub>H<sub>2</sub> and a large C<sub>2</sub>H<sub>2</sub> adsorption (4.7 mmol g<sup>–1</sup>) at 1.0 bar and 298 K. Dynamic breakthrough studies on JNU-5-Me demonstrate its excellent C<sub>2</sub>H<sub>2</sub> separation performance from C<sub>2</sub>H<sub>2</sub>/CO<sub>2</sub> (50/50, v/v) and C<sub>2</sub>H<sub>2</sub>/CO<sub>2</sub>/C<sub>2</sub>H<sub>4</sub>/C<sub>2</sub>H<sub>6</sub> (70/10/10/10, v/v/v/v) mixtures. Additionally, <i>in-situ</i> infrared spectroscopy and Grand canonical Monte Carlo (GCMC) simulation reveal that the carboxylate oxygens and methyl groups on the framework are involved in the strong binding of C<sub>2</sub>H<sub>2</sub>, which may be attributed to the gate-opening effect of JNU-5-Me.</p>","PeriodicalId":100230,"journal":{"name":"Chem & Bio Engineering","volume":"1 2","pages":"150–156"},"PeriodicalIF":0.0000,"publicationDate":"2024-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/cbe.3c00097","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chem & Bio Engineering","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/cbe.3c00097","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Adsorptive separation employing porous materials is one of the most promising alternative technologies for C2H2 purification due to its energy-efficient and environmentally friendly advantages. Herein, we present the design and synthesis of a dicopper-paddle-wheel-based metal–organic framework (termed JNU-5-Me) with a carboxylate-azolate organic linker. The use of such a linker results in the axial positions of the dicopper paddle wheels being occupied by azolates, and therefore, a much-improved chemical stability of the framework structure. JNU-5-Me shows negligible adsorption of C2H4, C2H6, and CO2 at 1.0 bar and 298 K, while a gate-opening effect for C2H2 and a large C2H2 adsorption (4.7 mmol g–1) at 1.0 bar and 298 K. Dynamic breakthrough studies on JNU-5-Me demonstrate its excellent C2H2 separation performance from C2H2/CO2 (50/50, v/v) and C2H2/CO2/C2H4/C2H6 (70/10/10/10, v/v/v/v) mixtures. Additionally, in-situ infrared spectroscopy and Grand canonical Monte Carlo (GCMC) simulation reveal that the carboxylate oxygens and methyl groups on the framework are involved in the strong binding of C2H2, which may be attributed to the gate-opening effect of JNU-5-Me.

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
用于筛分乙炔的柔性金属有机框架中的开栅极效应
利用多孔材料进行吸附分离具有节能和环保的优势,是最有前途的 C2H2 纯化替代技术之一。在此,我们介绍了一种基于二铜桨轮的金属有机框架(称为 JNU-5-Me)的设计与合成,该框架带有羧基氮杂环有机连接体。使用这种连接剂可使二铜桨轮的轴向位置被偶氮盐占据,从而大大提高框架结构的化学稳定性。在 1.0 巴和 298 K 条件下,JNU-5-Me 对 C2H4、C2H6 和 CO2 的吸附几乎可以忽略不计,但对 C2H2 具有开闸效应,在 1.0 巴和 298 K 条件下,对 C2H2 的吸附量很大(4.7 mmol g-1)。对 JNU-5-Me 的动态突破研究表明,它从 C2H2/CO2(50/50,v/v)和 C2H2/CO2/C2H4/C2H6(70/10/10/10,v/v/v/v)混合物中分离出 C2H2 的性能极佳。此外,原位红外光谱和大规范蒙特卡罗(GCMC)模拟显示,框架上的羧酸氧根和甲基参与了 C2H2 的强结合,这可能归因于 JNU-5-Me 的开闸效应。
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
自引率
0.00%
发文量
0
期刊最新文献
Issue Publication Information Issue Editorial Masthead Advanced Separation Materials and Processes Advanced Separation Materials and Processes. Issue Publication Information
×
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