Show simple item record

dc.contributor.authorArnold, Tim
dc.contributor.authorHarth, C. M.
dc.contributor.authorMuhle, Jens
dc.contributor.authorManning, Alistair J.
dc.contributor.authorSalameh, Peter K.
dc.contributor.authorKim, Jooil
dc.contributor.authorSteele, L. Paul
dc.contributor.authorPetrenko, Vasilii V.
dc.contributor.authorSeveringhaus, Jeffrey P.
dc.contributor.authorBaggenstos, Daniel
dc.contributor.authorWeiss, Ray F.
dc.contributor.authorIvy, Diane J
dc.date.accessioned2013-08-08T17:40:13Z
dc.date.available2013-08-08T17:40:13Z
dc.date.issued2013-01
dc.date.submitted2012-08
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/79808
dc.description.abstractNitrogen trifluoride (NF[subscript 3]) has potential to make a growing contribution to the Earth’s radiative budget; however, our understanding of its atmospheric burden and emission rates has been limited. Based on a revision of our previous calibration and using an expanded set of atmospheric measurements together with an atmospheric model and inverse method, we estimate that the global emissions of NF[subscript 3 ] in 2011 were 1.18 ± 0.21 Gg⋅y[superscript −1], or ∼20 Tg CO[subscript 2]-eq⋅y[superscript−1] (carbon dioxide equivalent emissions based on a 100-y global warming potential of 16,600 for NF[subscript 3]). The 2011 global mean tropospheric dry air mole fraction was 0.86 ± 0.04 parts per trillion, resulting from an average emissions growth rate of 0.09 Gg⋅y[superscript −2] over the prior decade. In terms of CO[subscript 2] equivalents, current NF[subscript 3] emissions represent between 17% and 36% of the emissions of other long-lived fluorinated compounds from electronics manufacture. We also estimate that the emissions benefit of using NF[subscript 3] over hexafluoroethane (C[subscript 2]F[subscript 6]) in electronics manufacture is significant—emissions of between 53 and 220 Tg CO[subscript 2]-eq⋅y[superscript −1] were avoided during 2011. Despite these savings, total NF[subscript 3] emissions, currently ~10% of production, are still significantly larger than expected assuming global implementation of ideal industrial practices. As such, there is a continuing need for improvements in NF[subscript 3] emissions reduction strategies to keep pace with its increasing use and to slow its rising contribution to anthropogenic climate forcing.en_US
dc.description.sponsorshipNASA Upper Atmospheric Research Programen_US
dc.language.isoen_US
dc.publisherNational Academy of Sciences (U.S.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/pnas.1212346110en_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.sourcePNASen_US
dc.titleNitrogen trifluoride global emissions estimated from updated atmospheric measurementsen_US
dc.typeArticleen_US
dc.identifier.citationArnold, T., C. M. Harth, J. Muhle, A. J. Manning, P. K. Salameh, J. Kim, D. J. Ivy, et al. “Nitrogen trifluoride global emissions estimated from updated atmospheric measurements.” Proceedings of the National Academy of Sciences 110, no. 6 (February 5, 2013): 2029-2034.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciencesen_US
dc.contributor.mitauthorIvy, Diane J.en_US
dc.relation.journalProceedings of the National Academy of Sciences of the United States of Americaen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsArnold, T.; Harth, C. M.; Muhle, J.; Manning, A. J.; Salameh, P. K.; Kim, J.; Ivy, D. J.; Steele, L. P.; Petrenko, V. V.; Severinghaus, J. P.; Baggenstos, D.; Weiss, R. F.en_US
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record