| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 62529 | Journal of Catalysis | 2008 | 10 Pages |
A series of CrOx–Y2O3 catalysts were prepared by a deposition–precipitation method and tested for the fluorination of 2-chloro-1,1,1-trifluoroethane (CF3CH2Cl) to synthesize 1,1,1,2-tetrafluoroethane (CF3CH2F). The highest activity was obtained on a pre-fluorinated catalyst calcined at 400 °C, with 19% of CF3CH2Cl conversion at 320 °C. The effect of the calcination temperature on the CrOx species was investigated. X-ray diffraction and Raman results indicated that the CrOx species (Cr(VI)) were well dispersed on the catalyst surface when the catalyst was calcined at 400 °C. With increasing calcination temperature, most of the CrOx species changed from high oxidation state Cr(VI) to low oxidation state Cr(V) or Cr(III) species, which resulted in difficulty in pre-fluorination of the catalyst. It was also found that the CrFx, CrOxFy or Cr(OH)xFy phases originated from high oxidation state Cr(VI) species were the active sites for the fluorination reaction.
