Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.jcat.2008.11.007
DC FieldValue
dc.titleEffect of boron on the stability of Ni catalysts during steam methane reforming
dc.contributor.authorXu, J.
dc.contributor.authorChen, L.
dc.contributor.authorTan, K.F.
dc.contributor.authorBorgna, A.
dc.contributor.authorSaeys, M.
dc.date.accessioned2014-10-09T06:46:18Z
dc.date.available2014-10-09T06:46:18Z
dc.date.issued2009-01-25
dc.identifier.citationXu, J., Chen, L., Tan, K.F., Borgna, A., Saeys, M. (2009-01-25). Effect of boron on the stability of Ni catalysts during steam methane reforming. Journal of Catalysis 261 (2) : 158-165. ScholarBank@NUS Repository. https://doi.org/10.1016/j.jcat.2008.11.007
dc.identifier.issn00219517
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/88787
dc.description.abstractNi catalysts promoted with 0.5 and 1.0 wt% boron were synthesized, characterized and tested during steam methane reforming, to evaluate the effect of boron on the deactivation behavior. Boron adsorbs on the γ-Al2O3 support and on the Ni particles and 1.0 wt% boron is found to enhance the stability without compromising the activity. Catalytic studies at 800 °C, 1 atm, a stoichiometric methane to steam ratio, and space velocities of 330,000 cm3/(h gcat) show that promotion with 1.0 wt% boron reduces the rate of deactivation by a factor of 3 and increases the initial methane conversion from 56% for the unpromoted catalyst to 61%. Temperature-programmed oxidation (TPO) and scanning electron microscopy (SEM) studies confirm the formation of carbonaceous deposits and illustrate that 1.0 wt% boron reduces the amount of deposited carbon by 80%. © 2008 Elsevier Inc. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.jcat.2008.11.007
dc.sourceScopus
dc.subjectBoron
dc.subjectCarbon deposition
dc.subjectCatalyst deactivation
dc.subjectNi catalyst
dc.subjectSteam reforming
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1016/j.jcat.2008.11.007
dc.description.sourcetitleJournal of Catalysis
dc.description.volume261
dc.description.issue2
dc.description.page158-165
dc.identifier.isiut000263564900004
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