Nhung T. T. Nguyen, Dr. Hiroyasu Furukawa, Dr. Felipe Gándara, Dr. Hoang T. Nguyen, Kyle E. Cordova, Prof. Omar M. Yaghi
{"title":"疏水恰辉石型沸石咪唑酸骨架在潮湿条件下选择性捕获二氧化碳","authors":"Nhung T. T. Nguyen, Dr. Hiroyasu Furukawa, Dr. Felipe Gándara, Dr. Hoang T. Nguyen, Kyle E. Cordova, Prof. Omar M. Yaghi","doi":"10.1002/anie.201403980","DOIUrl":null,"url":null,"abstract":"<p>Hydrophobic zeolitic imidazolate frameworks (ZIFs) with the chabazite (<b>CHA</b>) topology are synthesized by incorporating two distinct imidazolate links. Zn(2-mIm)<sub>0.86</sub>(bbIm)<sub>1.14</sub> (ZIF-300), Zn(2-mIm)<sub>0.94</sub>(cbIm)<sub>1.06</sub> (ZIF-301), and Zn(2-mIm)<sub>0.67</sub>(mbIm)<sub>1.33</sub> (ZIF-302), where 2-mIm=2-methylimidazolate, bbIm=5(6)-bromobenzimidazolate, cbIm=5(6)-chlorobenzimidazolate, and mbIm=5(6)-methylbenzimidazolate, were prepared by reacting zinc nitrate tetrahydrate and 2-mIm with the respective bIm link in a mixture of <i>N</i>,<i>N</i>-dimethylformamide (DMF) and water. Their structures were determined by single-crystal X-ray diffraction and their permanent porosity shown. All of these structures are hydrophobic as confirmed by water adsorption isotherms. All three ZIFs are equally effective at the dynamic separation of CO<sub>2</sub> from N<sub>2</sub> under both dry and humid conditions without any loss of performance over three cycles and can be regenerated simply by using a N<sub>2</sub> flow at ambient temperature.</p>","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"53 40","pages":"10645-10648"},"PeriodicalIF":16.1000,"publicationDate":"2014-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/anie.201403980","citationCount":"220","resultStr":"{\"title\":\"Selective Capture of Carbon Dioxide under Humid Conditions by Hydrophobic Chabazite-Type Zeolitic Imidazolate Frameworks†\",\"authors\":\"Nhung T. T. Nguyen, Dr. Hiroyasu Furukawa, Dr. Felipe Gándara, Dr. Hoang T. Nguyen, Kyle E. Cordova, Prof. Omar M. Yaghi\",\"doi\":\"10.1002/anie.201403980\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Hydrophobic zeolitic imidazolate frameworks (ZIFs) with the chabazite (<b>CHA</b>) topology are synthesized by incorporating two distinct imidazolate links. Zn(2-mIm)<sub>0.86</sub>(bbIm)<sub>1.14</sub> (ZIF-300), Zn(2-mIm)<sub>0.94</sub>(cbIm)<sub>1.06</sub> (ZIF-301), and Zn(2-mIm)<sub>0.67</sub>(mbIm)<sub>1.33</sub> (ZIF-302), where 2-mIm=2-methylimidazolate, bbIm=5(6)-bromobenzimidazolate, cbIm=5(6)-chlorobenzimidazolate, and mbIm=5(6)-methylbenzimidazolate, were prepared by reacting zinc nitrate tetrahydrate and 2-mIm with the respective bIm link in a mixture of <i>N</i>,<i>N</i>-dimethylformamide (DMF) and water. Their structures were determined by single-crystal X-ray diffraction and their permanent porosity shown. All of these structures are hydrophobic as confirmed by water adsorption isotherms. All three ZIFs are equally effective at the dynamic separation of CO<sub>2</sub> from N<sub>2</sub> under both dry and humid conditions without any loss of performance over three cycles and can be regenerated simply by using a N<sub>2</sub> flow at ambient temperature.</p>\",\"PeriodicalId\":125,\"journal\":{\"name\":\"Angewandte Chemie International Edition\",\"volume\":\"53 40\",\"pages\":\"10645-10648\"},\"PeriodicalIF\":16.1000,\"publicationDate\":\"2014-07-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/anie.201403980\",\"citationCount\":\"220\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Angewandte Chemie International Edition\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/anie.201403980\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/anie.201403980","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Selective Capture of Carbon Dioxide under Humid Conditions by Hydrophobic Chabazite-Type Zeolitic Imidazolate Frameworks†
Hydrophobic zeolitic imidazolate frameworks (ZIFs) with the chabazite (CHA) topology are synthesized by incorporating two distinct imidazolate links. Zn(2-mIm)0.86(bbIm)1.14 (ZIF-300), Zn(2-mIm)0.94(cbIm)1.06 (ZIF-301), and Zn(2-mIm)0.67(mbIm)1.33 (ZIF-302), where 2-mIm=2-methylimidazolate, bbIm=5(6)-bromobenzimidazolate, cbIm=5(6)-chlorobenzimidazolate, and mbIm=5(6)-methylbenzimidazolate, were prepared by reacting zinc nitrate tetrahydrate and 2-mIm with the respective bIm link in a mixture of N,N-dimethylformamide (DMF) and water. Their structures were determined by single-crystal X-ray diffraction and their permanent porosity shown. All of these structures are hydrophobic as confirmed by water adsorption isotherms. All three ZIFs are equally effective at the dynamic separation of CO2 from N2 under both dry and humid conditions without any loss of performance over three cycles and can be regenerated simply by using a N2 flow at ambient temperature.
期刊介绍:
Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.