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dc.contributor.authorKumar, Amit
dc.contributor.authorPhillips, Katherine Reece
dc.contributor.authorThiel, Gregory P.
dc.contributor.authorSchröder, Uwe
dc.contributor.authorLienhard, John H
dc.date.accessioned2019-08-15T16:31:23Z
dc.date.available2019-08-15T16:31:23Z
dc.date.issued2019-02
dc.date.submitted2017-10
dc.identifier.issn2520-1158
dc.identifier.urihttps://hdl.handle.net/1721.1/121991
dc.description.abstractSeawater is an abundant resource across the world, and its purification and by-product recovery methods are crucial for economical, environmentally safe and sustainable utilization. Desalinating seawater generally produces brine as a by-product that cannot be purified economically with current technologies and which is instead released to the environment. In this Perspective, we discuss direct electrosynthesis of sodium hydroxide (NaOH) and hydrochloric acid (HCl) from sea-water desalination brine as an emerging alternative solution. In this direct electrosynthesis (DE) process, the water splitting reaction is used to produce H⁺ and OH⁻ , which combine with the brine stream to produce NaOH and HCl. After introducing the scope of the process, we describe developments in earth-abundant catalysts for water splitting and the competing chlorine evolution reaction (CER), as well as challenges in inefficiency and productivity associated with these processes. Finally, we discuss the economic impact and feasibility of direct electrosynthesis.en_US
dc.language.isoen
dc.publisherSpringer Natureen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/s41929-018-0218-yen_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceProf. Lienharden_US
dc.titleDirect electrosynthesis of sodium hydroxide and hydrochloric acid from brine streamsen_US
dc.typeArticleen_US
dc.identifier.citationKumar, Amit et al. "Direct electrosynthesis of sodium hydroxide and hydrochloric acid from brine streams." Nature Catalysis 2, 2 (February 2019): 106–113 © 2019 Springer Nature Limiteden_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.relation.journalNature Catalysisen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-05-08T14:06:11Z
dspace.date.submission2019-05-08T14:06:12Z
mit.journal.volume2en_US
mit.journal.issue2en_US


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