Please use this identifier to cite or link to this item: https://doi.org/10.1039/c2ra20359f
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dc.titleNovel Cu-Fe bimetal catalyst for the formation of dimethyl carbonate from carbon dioxide and methanol
dc.contributor.authorZhou, Y.
dc.contributor.authorWang, S.
dc.contributor.authorXiao, M.
dc.contributor.authorHan, D.
dc.contributor.authorLu, Y.
dc.contributor.authorMeng, Y.
dc.date.accessioned2014-10-16T08:35:19Z
dc.date.available2014-10-16T08:35:19Z
dc.date.issued2012
dc.identifier.citationZhou, Y., Wang, S., Xiao, M., Han, D., Lu, Y., Meng, Y. (2012). Novel Cu-Fe bimetal catalyst for the formation of dimethyl carbonate from carbon dioxide and methanol. RSC Advances 2 (17) : 6831-6837. ScholarBank@NUS Repository. https://doi.org/10.1039/c2ra20359f
dc.identifier.issn20462069
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/94375
dc.description.abstractA novel Cu-Fe bimetal supported catalytic system was prepared and applied to the direct dimethyl carbonate (DMC) formation from methanol and CO 2. The prepared catalysts were characterized by means of temperature-programmed reduction (TPR), X-ray powder diffraction (XRD), laser Raman spectra (LRS), X-ray photoelectron spectroscopy (XPS) and temperature programmed desorption (TPD). Metallic Cu, Fe and oxygen deficient Fe 2O3-x (0 < x < 3) were formed during the reduction and activation step. The supported Cu-Fe bimetal catalysts exhibited good catalytic activity and high stability for the direct DMC formation. Under the reaction conditions at 120 °C and 1.2 MPa with space velocity of 360 h -1, the highest methanol conversion of 5.37% with DMC selectivity of 85.9% could be achieved. The high catalytic performance of the Cu-Fe bimetal catalysts in the DMC formation could be attributed to the interaction of base sites functioned by metallic Cu and Fe with acid sites provided by oxygen deficient Fe2O3-x (0 < x < 3) in the activation of methanol and CO2. The moderate concentration balance of acid and base sites was in favor of DMC formation. © 2012 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c2ra20359f
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c2ra20359f
dc.description.sourcetitleRSC Advances
dc.description.volume2
dc.description.issue17
dc.description.page6831-6837
dc.identifier.isiut000306669300021
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