Comparison of different precious metals in activated carbon-supported catalysts for the gas-phase hydrodechlorination of chloromethanes
Four precious metals supported on activated carbon are compared as catalysts in the gas-phase hydrodechlorination (HDC) of chloromethanes. The intrinsic activity or turnover frequency (TOF) of the catalysts follows the order Pd/C > Rh/C > Pt/C > Ru/C in the HDC of dichloromethane (DCM) whil...
| Autores: | , , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2013 |
| País: | España |
| Institución: | Universidad Autónoma de Madrid |
| Repositorio: | Biblos-e Archivo. Repositorio Institucional de la UAM |
| Idioma: | inglés |
| OAI Identifier: | oai:repositorio.uam.es:10486/709445 |
| Acceso en línea: | http://hdl.handle.net/10486/709445 https://dx.doi.org/10.1016/j.apcatb.2012.11.041 |
| Access Level: | acceso abierto |
| Palabra clave: | hydrodechlorination residual gases chloromethanes carbon-supported metallic catalysts reaction scheme Física Química |
| Sumario: | Four precious metals supported on activated carbon are compared as catalysts in the gas-phase hydrodechlorination (HDC) of chloromethanes. The intrinsic activity or turnover frequency (TOF) of the catalysts follows the order Pd/C > Rh/C > Pt/C > Ru/C in the HDC of dichloromethane (DCM) while the sequence Pd/C > Pt/C > Rh/C > Ru/C was found for the HDC of chloroform (TCM). High selectivities to non-chlorinated products were obtained in all cases except for the HDC of TCM with Rh/C and Ru/C where the selectivity to DCM greatly depends on the operating conditions. A wider diversity of non-chlorinated hydrocarbons was obtained as reaction products with these two catalysts, especially in the HDC of TCM, favoring the formation of carbonaceous deposits which provoked a marked deactivation of the catalysts. In contrast, CH4 was the only non-chlorinated product obtained with the Pt/C catalysts which showed by far the highest stability. Different reaction pathways were found depending on the catalyst and the starting chloromethane. The different reactivity of the metals is explained in terms of their different electronic structure and the physicochemical properties of the catalysts |
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