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dc.contributor.authorRieth, Adam Joseph
dc.contributor.authorDinca, Mircea
dc.date.accessioned2018-08-27T15:37:05Z
dc.date.available2018-08-27T15:37:05Z
dc.date.issued2018-06
dc.date.submitted2018-06
dc.identifier.issn2374-7943
dc.identifier.issn2374-7951
dc.identifier.urihttp://hdl.handle.net/1721.1/117543
dc.description.abstractAmmonia serves as an essential feedstock in several large industries, including fertilizer and explosives manufacturing, and as a key coolant in large-scale applications such as ice rinks, making it one of the most important industrial gases.(1) It is also extremely corrosive and toxic, which makes its adsorption in applications such as air remediation, gas masks, and adsorption heat pumps very challenging. The current commercial adsorbent, activated carbon, suffers from low affinity for ammonia and relatively low capacity of only 11 mmol g⁻¹.(2) Although recent developments in porous materials including metal–organic frameworks (MOFs) and covalent organic frameworks (COFs) have produced remarkable advances in the state-of-the-art sorbents for a variety of gases and even water vapor, most of these materials have been surprisingly ineffective at storing NH₃. Now, reporting in ACS Central Science, Yang et al. demonstrate systematically designed COFs that meet this challenge.(3) Through a series of programmed modifications to the pore surface (Figure 1), the authors successfully install metal ions with open coordination sites which confer exceptional affinity for ammonia.en_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/acscentsci.8b00337en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceACSen_US
dc.titleProgramming Framework Materials for Ammonia Captureen_US
dc.typeArticleen_US
dc.identifier.citationRieth, Adam J., and Mircea Dincă. “Programming Framework Materials for Ammonia Capture.” ACS Central Science 4, 6 (June 2018): 666–667 © 2018 American Chemical Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorRieth, Adam Joseph
dc.contributor.mitauthorDinca, Mircea
dc.relation.journalACS Central Scienceen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-08-24T11:49:34Z
dspace.orderedauthorsRieth, Adam J.; Dincă, Mirceaen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-9890-1346
dc.identifier.orcidhttps://orcid.org/0000-0002-1262-1264
mit.licensePUBLISHER_POLICYen_US


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