Novel Cu-Fe bimetal catalyst for the formation of dimethyl carbonate from carbon dioxide and methanol

被引:59
|
作者
Zhou, Yingjie [1 ]
Wang, Shuanjin [1 ]
Xiao, Min [1 ]
Han, Dongmei [1 ]
Lu, Yixin [2 ,3 ]
Meng, Yuezhong [1 ]
机构
[1] Sun Yat Sen Univ, Key Lab Low Carbon Chem & Energy Conservat Guangd, State Key Lab Optoelect Mat & Technol, Guangzhou 510275, Guangdong, Peoples R China
[2] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
[3] Natl Univ Singapore, Med Chem Program, Off Life Sci, Singapore 117543, Singapore
关键词
SELECTIVE SYNTHESIS; XPS SPECTRA; COPPER; IRON; CO2; DMC; HYDROGENATION; ACID;
D O I
10.1039/c2ra20359f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel Cu-Fe bimetal supported catalytic system was prepared and applied to the direct dimethyl carbonate (DMC) formation from methanol and CO2. 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 Fe2O3-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 degrees 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.
引用
收藏
页码:6831 / 6837
页数:7
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