Please use this identifier to cite or link to this item: https://doi.org/10.1021/ie100523u
DC FieldValue
dc.titleImproving the stability of cobalt Fischer-Tropsch catalysts by boron promotion
dc.contributor.authorSaeys, M.
dc.contributor.authorTan, K.F.
dc.contributor.authorChang, J.
dc.contributor.authorBorgna, A.
dc.date.accessioned2014-06-19T06:14:33Z
dc.date.available2014-06-19T06:14:33Z
dc.date.issued2010-11-03
dc.identifier.citationSaeys, M., Tan, K.F., Chang, J., Borgna, A. (2010-11-03). Improving the stability of cobalt Fischer-Tropsch catalysts by boron promotion. Industrial and Engineering Chemistry Research 49 (21) : 11098-11100. ScholarBank@NUS Repository. https://doi.org/10.1021/ie100523u
dc.identifier.issn08885885
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/74626
dc.description.abstractSupported Co catalysts exhibit favorable activity and selectivity for Fischer-Tropsch synthesis (FTS) but deactivate slowly. To explore deactivation by carbon deposition, the stability of various forms of deposited carbon was evaluated using density functional theory (DFT). A surface carbide and graphene islands were calculated to be thermodynamically stable. Two forms of deposited carbon are also distinguished experimentally after 200 h of FTS. On the basis of this mechanistic insight, boron was proposed as a promoter to enhance the stability of Co catalysts. DFT calculations indicate that boron and carbon display similar binding preferences, and boron could selectively block the deposition of resilient carbon deposits. To evaluate the theoretical predictions, supported 20 wt % Co catalysts were promoted with 0.5 wt % boron and tested under realistic FTS conditions. Boron promotion was found to reduce the deactivation rate 6-fold, without affecting selectivity and activity. © 2010 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ie100523u
dc.sourceScopus
dc.typeConference Paper
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1021/ie100523u
dc.description.sourcetitleIndustrial and Engineering Chemistry Research
dc.description.volume49
dc.description.issue21
dc.description.page11098-11100
dc.description.codenIECRE
dc.identifier.isiut000283463600104
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