Please use this identifier to cite or link to this item:
https://doi.org/10.1039/c2ra20359f
DC Field | Value | |
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dc.title | Novel Cu-Fe bimetal catalyst for the formation of dimethyl carbonate from carbon dioxide and methanol | |
dc.contributor.author | Zhou, Y. | |
dc.contributor.author | Wang, S. | |
dc.contributor.author | Xiao, M. | |
dc.contributor.author | Han, D. | |
dc.contributor.author | Lu, Y. | |
dc.contributor.author | Meng, Y. | |
dc.date.accessioned | 2014-10-16T08:35:19Z | |
dc.date.available | 2014-10-16T08:35:19Z | |
dc.date.issued | 2012 | |
dc.identifier.citation | Zhou, 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.issn | 20462069 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/94375 | |
dc.description.abstract | A 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.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c2ra20359f | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1039/c2ra20359f | |
dc.description.sourcetitle | RSC Advances | |
dc.description.volume | 2 | |
dc.description.issue | 17 | |
dc.description.page | 6831-6837 | |
dc.identifier.isiut | 000306669300021 | |
Appears in Collections: | Staff Publications |
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