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EN
Two step modification of Norit CNR115 active carbon led to formation of mesoporous turbostratic carbon structure. Ni-Pd catalysts were prepared by incipient wetness impregnation of turbostratic active carbon with an aqueous solution of nickel and palladium chloride salts and were investigated by the Temperature-Programmed Reduction (TPR), Scanning Electron Microscopy (SEM), High Resolution Transmission Electron Microscopy (HRTEM), X-Ray Diffraction (XRD) and Temperature- Programmed Hydrogenation (TPH). The aqueous-phase hydrodechlorination of 1,1,2-trichloroethene (TCE) were carried out in a batch reactor at room temperature. Addition of palladium to nickel catalysts resulted in increasing of TCE conversion from 85% for Ni100 to more than 90% for Ni95Pd05 after 150 minutes of reaction. Aqueous-phase hydrodechlorination of TCE led to the formation of hydrocarbons (ethane and ethene) as the main products. Temperature-programmed hydrogenation of the catalysts after kinetic run have shown that during reactions with TCE only a small amount of carbon species were deposited on the catalysts surface and that chloride species were not observed.
EN
The search for the most suitable hydrodechlorination catalysts should consider both the C-Cl bond strength in a molecule subjected to reaction and the metal-chlorine bond, which should be neither too strong nor too weak. An improvement of Pd- and Pt-based catalysts can be achieved by alloying with metals which bind chlorine even less strongly, e.g. with gold. Addition of platinum to palladium would also be beneficial because of metal-chloride bond energy considerations. Analogous effects occur in the hydrodechlorination of dichlorodifluoromethane and 1,2-dichloroethane, the molecules characterized by stronger carbon-chlorine bonds.
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