Junsong Wang

Epoxidation of Propylene by Molecular Oxygen over Modified Ag–MoO3 Catalyst

Epoxidation of propylene to propylene oxide by molecular oxygen was studied over a modified Ag-MoO3 catalyst. The results show that MoO3 plays an important role in improving the efficiency of the catalyst, and a suitable content of MoO3 is 40-50 wt%. XPS reveals that some of the silver and molybdenum in the catalyst exist as Ag+ and Mo(6 - δ)+, respectively. The promotion effect of NaCl, Ce(NO3)3, BaCl2 and CsNO3 on the Ag-MoO3 catalyst was studied. As a modifier of the Ag-MoO3 catalyst, NaCl or Ce(NO3)3 are more suitable than BaCl2 or CsNO3 and the optimal loading of NaCl or Ce(NO3) is about 2 wt%. Using a feedstock gas of 15.6% C3H6, 12.2% O2 and balance N2 without any addition of NO, EtCl or CO2 at a space velocity of 4500 h-1, 6.8% O2 conversion and 53.1% selectivity to propylene oxide were achieved over the Ag-MoO3-2.0% NaCl catalyst at 400 °C. At 450 °C the O2 conversion and selectivity to propylene oxide were 11.4 and 43.6%, respectively.

Modification of Ag-MoO3/ZrO2Catalyst with Metallic Chloride for Propylene Epoxidation by Molecular Oxygen

The modification of the Ag-MoO3/ZrO2catalyst with metallic chloride was studied for a gas-phase epoxidation of propylene by molecular oxygen. As a modifier, the presence of NaCl, CsCl or CaCl2can effectively regulate an electronic property of the Ag-MoO3/ZrO2catalyst and improve obviously its catalytic epoxidation performance. When NaCl (1000 ppm), CsCl (1500 ppm) or CaCl2(1000 ppm) was used to modify the 20%Ag-4%MoO3/ZrO2catalyst, the selectivity to propylene oxide (PO) increased to 63. 5%, 66. 7% and 62. 9%, from 47. 9%, respectively, and the corresponding O2conversion was 7. 3%, 7. 7% and 8. 1%, respectively. The studies of XPS indicates that the electron-interaction between the active component of catalyst and metallic chloride has occurred obviously, and the presence of chloride can enhance the electron-deficient property of Ag to improve the electrophilic property of adsorbed oxygen and inhibit an isomerization and deep oxidation of PO to improve the selectivity to PO.