Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.cclet.2013.02.001
DC FieldValue
dc.titleEffects of Mo promoters on the Cu-Fe bimetal catalysts for the DMC formation from CO2 and methanol
dc.contributor.authorZhou, Y.-J.
dc.contributor.authorXiao, M.
dc.contributor.authorWang, S.-J.
dc.contributor.authorHan, D.-M.
dc.contributor.authorLu, Y.-X.
dc.contributor.authorMeng, Y.-Z.
dc.date.accessioned2014-10-16T08:26:57Z
dc.date.available2014-10-16T08:26:57Z
dc.date.issued2013-04
dc.identifier.citationZhou, Y.-J., Xiao, M., Wang, S.-J., Han, D.-M., Lu, Y.-X., Meng, Y.-Z. (2013-04). Effects of Mo promoters on the Cu-Fe bimetal catalysts for the DMC formation from CO2 and methanol. Chinese Chemical Letters 24 (4) : 307-310. ScholarBank@NUS Repository. https://doi.org/10.1016/j.cclet.2013.02.001
dc.identifier.issn10018417
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93666
dc.description.abstractThe Mo-promoted Cu-Fe bimetal catalysts were prepared and used for the formation of dimethyl carbonate (DMC) from CO2 and methanol. The catalysts were characterized by X-ray diffraction (XRD), temperature programmed reduction (TPR), laser Raman spectra (LRS), energy dispersive spectroscopy (EDS) and temperature programmed desorption (TPD) techniques. The experimental results demonstrated that the Mo promoters can decrease the reducibility and increase the dispersion of Cu-Fe clusters. The concentration balance of base-acid sites can be readily adjusted by changing the Mo content. The moderate concentration balance of acid and base sites was in favor of the DMC formation. Under optimal experimental conditions, the highest methanol conversion of 6.99% with a DMC selectivity of 87.7% can be obtained when 2.5 wt% of Mo was loaded. © 2013 Min Xiao.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.cclet.2013.02.001
dc.sourceScopus
dc.subjectBimetal catalyst
dc.subjectCarbon dioxide
dc.subjectCatalysis
dc.subjectDimethyl carbonate
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/j.cclet.2013.02.001
dc.description.sourcetitleChinese Chemical Letters
dc.description.volume24
dc.description.issue4
dc.description.page307-310
dc.description.codenCCLEE
dc.identifier.isiut000319307900011
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