dc.contributor.author | Moore, Jason Stuart | |
dc.contributor.author | Smith, Christopher D | |
dc.contributor.author | Jensen, Klavs F | |
dc.date.accessioned | 2017-07-07T15:55:25Z | |
dc.date.available | 2017-07-07T15:55:25Z | |
dc.date.issued | 2016-02 | |
dc.date.submitted | 2016-01 | |
dc.identifier.issn | 2058-9883 | |
dc.identifier.uri | http://hdl.handle.net/1721.1/110538 | |
dc.description.abstract | Temperature, pressure, gas stoichiometry, and residence time were varied to control the yield and product distribution of the palladium-catalyzed aminocarbonylation of aromatic bromides in both a silicon microreactor and a packed-bed tubular reactor. Automation of the system set points and product sampling enabled facile and repeatable reaction analysis with minimal operator supervision. It was observed that the reaction was divided into two temperature regimes. An automated system was used to screen steady-state conditions for offline analysis by gas chromatography to fit a reaction rate model. Additionally, a transient temperature ramp method utilizing online infrared analysis was used, leading to more rapid determination of the reaction activation energy of the lower temperature regimes. The entire reaction spanning both regimes was modeled in good agreement with the experimental data. | en_US |
dc.language.iso | en_US | |
dc.publisher | Royal Society of Chemistry, The | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1039/c6re00007j | en_US |
dc.rights | Creative Commons Attribution 3.0 Unported licence | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/ | en_US |
dc.source | Royal Society of Chemistry | en_US |
dc.title | Kinetics analysis and automated online screening of aminocarbonylation of aryl halides in flow | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Moore, Jason S.; Smith, Christopher D. and Jensen, Klavs F. “Kinetics Analysis and Automated Online Screening of Aminocarbonylation of Aryl Halides in Flow.” Reaction Chemistry & Engineering 1, 3 (2016): 272–279 © 2016 The Royal Society of Chemistry | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Chemical Engineering | en_US |
dc.contributor.mitauthor | Moore, Jason Stuart | |
dc.contributor.mitauthor | Smith, Christopher D | |
dc.contributor.mitauthor | Jensen, Klavs F | |
dc.relation.journal | Reaction Chemistry & Engineering | en_US |
dc.eprint.version | Final published version | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dspace.orderedauthors | Moore, Jason S.; Smith, Christopher D.; Jensen, Klavs F. | en_US |
dspace.embargo.terms | N | en_US |
dc.identifier.orcid | https://orcid.org/0000-0001-7192-580X | |
mit.license | PUBLISHER_CC | en_US |