Abstract

The destructive oxidation of malodorous compounds known to occur in process emissions was investigated using commercial catalysts containing platinum, supported on alumina, carried by a ceramic honeycomb (“platinum-honeycomb” catalysts). Initially parameters relevant to catalyst evaluation were examined: temperature, space-velocity (SV), honeycomb cell size and odorant inlet concentration in the range 10–100 vpm. The catalytic oxidation of single odorant compounds (100 vpm in air), viz. acrolein, n- butanal , n- propylamine , toluene, n- butyric acid, 1,1,1-trichloroethane and dimethyl sulphide, was measured in terms of removal and total oxidation to CO 2 as a function of temperature. The performance of Pt-honeycomb catalysts for destructive oxidation was compared with published data for Co 3O 4 granular catalysts measured under identical reaction conditions. When single sulphur compounds (100 vpm dimethyl sulphide, methyl mercaptan, carbonyl sulphide or hydrogen sulphide in air) were oxidised over Pt-honeycomb catalysts (SV ~ 25,000h −1), sulphur dioxide formation exhibited complex behaviour, and separate observations of SO 2 oxidation were also made. In mixtures of odorants, n- butanal oxidation was inhibited by the presence of 100 vpm methyl mercaptan, H 2S or COS, (the temperature for 80% butanal oxidation was increased by 50–100° C) whereas SO 2 had little effect. The inhibiting effect of H 2S in the range 0–140 vpm was determined.

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