A Zn-based MOF for efficient C3H6/C2H4 separation with high C2H4 productivity

Wenjiang Zeng, Lei Pei, Yizhen Situ, Zhaoxu Wang, Qingyuan Yang
{"title":"A Zn-based MOF for efficient C3H6/C2H4 separation with high C2H4 productivity","authors":"Wenjiang Zeng, Lei Pei, Yizhen Situ, Zhaoxu Wang, Qingyuan Yang","doi":"10.1016/j.mochem.2025.100007","DOIUrl":null,"url":null,"abstract":"The methanol-to-olefins (MTO) process has emerged as a pivotal technology for ethylene (C 2 H 4 ) production, rendering the development of highly efficient propylene (C 3 H 6 ) adsorbents for the separation of MTO products and the acquisition of polymer-grade C 2 H 4 an urgent research imperative. Despite the reported high C 3 H 6 /C 2 H 4 selectivity or substantial C 3 H 6 adsorption capacity exhibited by certain metal-organic frameworks (MOFs), the inherent trade-off between these two properties often results in a suboptimal yield of high-purity C 2 H 4 . In this study, we have synthesized a novel zinc-based metal-organic framework (Zn-ICA) featuring a cage-like porous architecture through the utilization of a 1H-indazole-5-carboxylic acid ligand. This MOF exhibits an exceptionally high C 3 H 6 adsorption capacity (199.6 ​cm 3 ​g −1 at 100 ​kPa and 298 ​K) coupled with a favorable C 3 H 6 /C 2 H 4 selectivity (8.8), surpassing numerous benchmark MOFs that have been previously documented for C 3 H 6 /C 2 H 4 separation applications. Molecular simulation analyses reveal that the enhanced interaction between C 3 H 6 and the framework is attributable to the presence of π-bonds and accessible N/O sites within the ligand. Notably, breakthrough experiments have unequivocally demonstrated that this MOF is capable of achieving a record-breaking productivity (124.6 ​L ​kg −1 ) of polymer-grade C 2 H 4 (≥99.95 ​%) when employed for the separation of an equimolar C 3 H 6 /C 2 H 4 mixture, thereby positioning it as a highly promising advanced adsorbent for MTO product separation. • The MOF exhibits high C 3 H 6 adsorption capacity and high C 3 H 6 /C 2 H 4 selectivity. • Significant C 2 H 4 productivities can be achieved within a single separation cycle. • The presence of supramolecular binding sites facilitates the interaction between C 3 H 6 and the MOF. • The MOF exhibits favorable adsorption cycling performance along with a relatively low adsorption heat.","PeriodicalId":101529,"journal":{"name":"Molecular Chemistry and Biomolecular Engineering","volume":"1 1","pages":"100007-100007"},"PeriodicalIF":0.0000,"publicationDate":"2025-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Chemistry and Biomolecular Engineering","FirstCategoryId":"0","ListUrlMain":"https://doi.org/10.1016/j.mochem.2025.100007","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

The methanol-to-olefins (MTO) process has emerged as a pivotal technology for ethylene (C 2 H 4 ) production, rendering the development of highly efficient propylene (C 3 H 6 ) adsorbents for the separation of MTO products and the acquisition of polymer-grade C 2 H 4 an urgent research imperative. Despite the reported high C 3 H 6 /C 2 H 4 selectivity or substantial C 3 H 6 adsorption capacity exhibited by certain metal-organic frameworks (MOFs), the inherent trade-off between these two properties often results in a suboptimal yield of high-purity C 2 H 4 . In this study, we have synthesized a novel zinc-based metal-organic framework (Zn-ICA) featuring a cage-like porous architecture through the utilization of a 1H-indazole-5-carboxylic acid ligand. This MOF exhibits an exceptionally high C 3 H 6 adsorption capacity (199.6 ​cm 3 ​g −1 at 100 ​kPa and 298 ​K) coupled with a favorable C 3 H 6 /C 2 H 4 selectivity (8.8), surpassing numerous benchmark MOFs that have been previously documented for C 3 H 6 /C 2 H 4 separation applications. Molecular simulation analyses reveal that the enhanced interaction between C 3 H 6 and the framework is attributable to the presence of π-bonds and accessible N/O sites within the ligand. Notably, breakthrough experiments have unequivocally demonstrated that this MOF is capable of achieving a record-breaking productivity (124.6 ​L ​kg −1 ) of polymer-grade C 2 H 4 (≥99.95 ​%) when employed for the separation of an equimolar C 3 H 6 /C 2 H 4 mixture, thereby positioning it as a highly promising advanced adsorbent for MTO product separation. • The MOF exhibits high C 3 H 6 adsorption capacity and high C 3 H 6 /C 2 H 4 selectivity. • Significant C 2 H 4 productivities can be achieved within a single separation cycle. • The presence of supramolecular binding sites facilitates the interaction between C 3 H 6 and the MOF. • The MOF exhibits favorable adsorption cycling performance along with a relatively low adsorption heat.
一种高效分离C3H6/C2H4的锌基MOF, C2H4产率高
甲醇制烯烃(MTO)工艺已成为乙烯(c2h4)生产的关键技术,因此开发高效的丙烯(c3h6)吸附剂用于分离MTO产品和获得聚合物级c2h4是迫切需要的研究。尽管某些金属有机框架(MOFs)具有较高的c3h6 / c2h4选择性或可观的c3h6吸附能力,但这两种性质之间的内在权衡往往导致高纯度c2h4的产率不理想。在这项研究中,我们通过利用1h -吲哚-5-羧酸配体合成了一种具有笼状多孔结构的新型锌基金属有机骨架(Zn-ICA)。该MOF具有非常高的c3h6吸附容量(在100 kPa和298 K下为199.6 cm 3g−1),以及有利的c3h6 / c2h4选择性(8.8),超过了先前记录的用于c3h6 / c2h4分离应用的许多基准MOF。分子模拟分析表明,c3h6与骨架之间的相互作用增强是由于配体内存在π键和可达的N/O位点。值得注意的是,突破性的实验明确表明,当用于分离等摩尔c3h6 / c2h4混合物时,这种MOF能够达到创纪录的聚合物级c2h4(≥99.95%)的生产率(124.6 L kg−1),从而使其成为一种非常有前途的MTO产品分离的高级吸附剂。•MOF具有较高的c3h6吸附能力和c3h6 / c2h4选择性。•在单个分离周期内可实现显著的c2h4生产率。•超分子结合位点的存在促进了c3h6与MOF之间的相互作用。•MOF具有良好的吸附循环性能和较低的吸附热。
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:604180095
Book学术官方微信
小红书