| Autor: |
Lazareva S; a Department of Heterogeneous Catalysis, Boreskov Institute of Catalysis SB RAS , Novosibirsk , Russia., Ismagilov Z; a Department of Heterogeneous Catalysis, Boreskov Institute of Catalysis SB RAS , Novosibirsk , Russia.; b Laboratory of Catalysis in Coal Chemistry, Institute of Coal Chemistry and Material Science of Federal Research Center of Coal and Coal Chemistry SB RAS , Kemerovo , Russia., Kuznetsov V; a Department of Heterogeneous Catalysis, Boreskov Institute of Catalysis SB RAS , Novosibirsk , Russia., Shikina N; a Department of Heterogeneous Catalysis, Boreskov Institute of Catalysis SB RAS , Novosibirsk , Russia., Kerzhentsev M; a Department of Heterogeneous Catalysis, Boreskov Institute of Catalysis SB RAS , Novosibirsk , Russia. |
| Abstrakt: |
Huge amounts of nuclear waste, including depleted uranium, significantly contribute to the adverse environmental situation throughout the world. An approach to the effective use of uranium oxides in catalysts for the deep oxidation of chlorine-containing hydrocarbons is suggested. Investigation of the catalytic activity of the synthesized supported uranium oxide catalysts doped with Cr, Mn and Co transition metals in the chlorobenzene oxidation showed that these catalysts are comparable with conventional commercial ones. Physicochemical properties of the catalysts were studied by X-ray diffraction, temperature-programmed reduction with hydrogen (H 2 -TPR), and Fourier transform infrared spectroscopy. The higher activity of Mn- and Co-containing uranium oxide catalysts in the H 2 -TPR and oxidation of chlorobenzene in comparison with non-uranium catalysts may be related to the formation of a new disperse phase represented by uranates. The study of chlorobenzene adsorption revealed that the surface oxygen is involved in the catalytic process. |
