Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.ijhydene.2006.08.002
DC FieldValue
dc.titleHydrogen or synthesis gas production via the partial oxidation of methane over supported nickel-cobalt catalysts
dc.contributor.authorKoh, A.C.W.
dc.contributor.authorChen, L.
dc.contributor.authorKee Leong, W.
dc.contributor.authorJohnson, B.F.G.
dc.contributor.authorKhimyak, T.
dc.contributor.authorLin, J.
dc.date.accessioned2014-10-16T08:30:46Z
dc.date.available2014-10-16T08:30:46Z
dc.date.issued2007-05
dc.identifier.citationKoh, A.C.W., Chen, L., Kee Leong, W., Johnson, B.F.G., Khimyak, T., Lin, J. (2007-05). Hydrogen or synthesis gas production via the partial oxidation of methane over supported nickel-cobalt catalysts. International Journal of Hydrogen Energy 32 (6) : 725-730. ScholarBank@NUS Repository. https://doi.org/10.1016/j.ijhydene.2006.08.002
dc.identifier.issn03603199
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93986
dc.description.abstractActivity, selectivity, and coking-resistance of a series of Nix Coy (where x, y are the respective metal loadings of 0, 1, 2 or 3 wt.%; x + y = 3) bimetallic catalysts supported on CaAl2 O4 / Al2 O3 have been studied for hydrogen/synthesis gas production via the catalytic partial oxidation (CPO) of methane. Catalysts were characterized by temperature programmed reduction (TPR), transmission electron microscopy (TEM) and X-ray fluorescence multi-element analysis (XRF). Their activity for the partial oxidation of methane to hydrogen and carbon monoxide (at 1 bar, gas hourly space velocity (GHSV) of 144, 000 cm3 g- 1 h- 1 and CH4/O2 molar ratio of 2) was investigated, and coke deposited on the spent catalysts was studied by scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX) and thermogravimetric analysis (TGA). The activity was found to decrease in the order of Ni2 Co > Ni3 > NiCo2 ≫ Co3, while CO and H2 selectivities were found to be in the order ofNi2 Co > Ni3 ≈ NiCo2 > Co3 . Ni2Co is also shown to be more resistant to coking as compared to Ni3, which is a current catalyst of choice. Results show that not only does Ni2Co have the highest activity and selectivity among all the catalysts tested, it is also relatively resistant to coking. This finding would be helpful for catalyst design to achieve high coking resistivity catalysts for hydrogen production from CPO of methane. © 2006 International Association for Hydrogen Energy.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.ijhydene.2006.08.002
dc.sourceScopus
dc.subjectCobalt
dc.subjectHydrogen production
dc.subjectNickel
dc.subjectPartial oxidation of methane
dc.subjectSynthesis gas
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/j.ijhydene.2006.08.002
dc.description.sourcetitleInternational Journal of Hydrogen Energy
dc.description.volume32
dc.description.issue6
dc.description.page725-730
dc.description.codenIJHED
dc.identifier.isiut000246092500010
Appears in Collections:Staff Publications

Show simple item record
Files in This Item:
There are no files associated with this item.

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.