Affiliation: | a Inst. de Recherches sur la Catalyse, CNRS-Lyon, 2 Avenue Albert Einstein, 69626, Villeurbanne Cedex, France b SINTEF Materials Technology, P.O. Box 124 Blindern, N-0314, Oslo, Norway c Due Miljø AS, P.O.Box 138 Lilleaker, N-0216, Oslo, Norway |
Abstract: | A wet air oxidation reaction was carried out in a gas/liquid catalytic membrane reactor of the contactor type. The oxidation of formic acid was used as a model reaction. The mesoporous top-layer of a ceramic tubular membrane was used as catalyst (Pt) support, and was placed at the interface of the gas (air) and liquid (HCOOH solution) phases. A similar reaction was carried out in a conventional batch reactor, using a steering rate high enough to avoid gas-diffusion limitations, and exactly identical conditions than for the CMR (amount of catalyst, pressure, etc.). At room temperature, the CMR showed an initial activity three to six times higher than the conventional reactor. This activity increase was attributed to an easier oxygen access to the catalytic sites. Nevertheless, the catalytic membrane gradually deactivated after a few hours of operation. Different deactivation mechanisms are presented. |