Please use this identifier to cite or link to this item: https://doi.org/10.3390/catal8080302
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dc.titleEffect of alkali-doping on the performance of diatomite supported cu-ni bimetal catalysts for direct synthesis of dimethyl carbonate
dc.contributor.authorHan, D
dc.contributor.authorChen, Y
dc.contributor.authorWang, S
dc.contributor.authorXiao, M
dc.contributor.authorLu, Y
dc.contributor.authorMeng, Y
dc.date.accessioned2020-10-20T03:32:29Z
dc.date.available2020-10-20T03:32:29Z
dc.date.issued2018
dc.identifier.citationHan, D, Chen, Y, Wang, S, Xiao, M, Lu, Y, Meng, Y (2018). Effect of alkali-doping on the performance of diatomite supported cu-ni bimetal catalysts for direct synthesis of dimethyl carbonate. Catalysts 8 (8) : 302. ScholarBank@NUS Repository. https://doi.org/10.3390/catal8080302
dc.identifier.issn20734344
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/177846
dc.description.abstractAlkali-adopted Cu-Ni/diatomite catalysts were designed and used for the direct synthesis of dimethyl carbonate (DMC) from carbon dioxide and methanol. Alkali additives were introduced into Cu-Ni/diatomite catalyst as a promoter because of its lower work function (Ni > Cu > Li > Na > K > Cs) and stronger electron-donating ability. A series of alkali-promoted Cu-Ni/diatomite catalysts were prepared by wetness impregnation method with different kind and different loading of alkali. The synthesized catalysts were fully characterized by means of X-ray diffraction (XRD), scanning electron microscope (SEM), temperature-programmed reduction (TPR), and NH3/CO2-TPD. The experimental results demonstrated that alkali adoption can significantly promote the catalytic activity of Cu–Ni bimetallic catalysts. Under the catalytic reaction conditions of 120?C and 1.0 MPa; the highest CH3OH conversion of 9.22% with DMC selectivity of 85.9% has been achieved when using 15%(2Cu-Ni) 2%Cs2O/diatomite catalyst (CuO + NiO = 15 wt. %, atomic ratio of Cu/Ni = 2/1, Cs2O = 2 wt. %). © 2018 by the authors. Licensee MDPI, Basel, Switzerland.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.3390/catal8080302
dc.description.sourcetitleCatalysts
dc.description.volume8
dc.description.issue8
dc.description.page302
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