File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Full metadata record

DC Field Value Language
dc.citation.endPage 30984 -
dc.citation.number 25 -
dc.citation.startPage 30975 -
dc.citation.title ACS APPLIED MATERIALS & INTERFACES -
dc.citation.volume 15 -
dc.contributor.author Cho, Kyung Ho -
dc.contributor.author Yoon, Ji Woong -
dc.contributor.author Lee, Jeong Hyeon -
dc.contributor.author Kim, Jin Chul -
dc.contributor.author Jo, Donghui -
dc.contributor.author Park, Jaedeuk -
dc.contributor.author Lee, Su-Kyung -
dc.contributor.author Kwak, Sang Kyu -
dc.contributor.author Lee, U-Hwang -
dc.date.accessioned 2023-12-21T12:36:58Z -
dc.date.available 2023-12-21T12:36:58Z -
dc.date.created 2023-07-07 -
dc.date.issued 2023-06 -
dc.description.abstract A series of Al-based isomorphs (CAU-10H, MIL-160, KMF-1,and CAU-10pydc)were synthesized using isophthalic acid (ipa), 2,5-furandicarboxylicacid (fdc), 2,5-pyrrole dicarboxylic acid (pyrdc), and 3,5-pyridinedicarboxylicacid (pydc), respectively. These isomorphs were systematically investigatedto identify the best adsorbent for effectively separating C2H6/C2H4. All CAU-10 isomorphs exhibitedpreferential adsorption of C2H6 over that ofC(2)H(4) in mixture. CAU-10pydc exhibited the bestC(2)H(6)/C2H4 selectivity(1.68) and the highest C2H6 uptake (3.97 mmolg(-1)) at 298 K and 1 bar. In the breakthrough experimentusing CAU-10pydc, 1/1 (v/v) and 1/15 (v/v) C2H6/C2H4 gas mixtures were successfully separatedinto high-purity C2H4 (>99.95%), with remarkableproductivities of 14.0 L-STP kg(-1) and32.0 L-STP kg(-1), respectively, at 298K. Molecular simulations revealed that the exceptional separationperformance of CAU-10pydc originated from the increased porosity andreduced electron density of the pyridine ring of pydc, leading toa relatively larger decrease in pi-pi interactionswith C2H4 than in the C-H center dot center dot center dot pi interactions with C2H6. This study demonstratesthat the pore size and geometry of the CAU-10 platform are modulatedby the inclusion of heteroatom-containing benzene dicarboxylate orheterocyclic rings of dicarboxylate-based organic linkers, therebyfine-tuning the C2H6/C2H4 separation ability. CAU-10pydc was determined to be an optimum adsorbentfor this challenging separation. -
dc.identifier.bibliographicCitation ACS APPLIED MATERIALS & INTERFACES, v.15, no.25, pp.30975 - 30984 -
dc.identifier.doi 10.1021/acsami.3c03971 -
dc.identifier.issn 1944-8244 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/64781 -
dc.identifier.wosid 001008513700001 -
dc.language 영어 -
dc.publisher AMER CHEMICAL SOC -
dc.title Design of Pore Properties of an Al-Based Metal-Organic Framework for the Separation of an Ethane/Ethylene Gas Mixture via Ethane-Selective Adsorption -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Nanoscience & Nanotechnology; Materials Science, Multidisciplinary -
dc.relation.journalResearchArea Science & Technology - Other Topics; Materials Science -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor Al-metal-organic framework -
dc.subject.keywordAuthor CAU-10 isomorphs -
dc.subject.keywordAuthor ethane -
dc.subject.keywordAuthor ethylene gas separation -
dc.subject.keywordAuthor ethane-selective adsorption -
dc.subject.keywordAuthor high-purity ethylene production -
dc.subject.keywordPlus OLEFIN-PARAFFIN SEPARATION -
dc.subject.keywordPlus PI-COMPLEXATION -
dc.subject.keywordPlus HIGH-CAPACITY -
dc.subject.keywordPlus ETHYLENE -
dc.subject.keywordPlus HYDROCARBONS -
dc.subject.keywordPlus ADSORBENTS -
dc.subject.keywordPlus CRACKING -
dc.subject.keywordPlus IRMOF-8 -
dc.subject.keywordPlus SITES -
dc.subject.keywordPlus ZIF-7 -

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.