In this study we have examined the adsorption of hydrogen sulfide and methanethiol over platinum catalysts and examined the effect of these poisons on the steam reforming of ethane. Adsorption of hydrogen sulfide was measured at 293 and 873 K. At 873 K the adsorbed state of hydrogen sulfide in the presence of hydrogen was SH rather than S, even though the Pt:S ratio was unity. The effect of 11.2 ppm hydrogen sulfide or methanethiol on the steam reforming of ethane was studied at 873 K and 20 barg. Both poisons deactivated the catalyst over a number of hours, but methanethiol was found to be more deleterious, reducing the conversion by almost an order of magnitude, possibly due to the co-deposition of sulfur and carbon. Changes in the selectivity revealed that the effect of sulfur was not uniform on the reactions occurring, with the production of methane reduced proportionally more than the other products, due to the surface sensitivity of the hydrogenolysis and methanation reactions. The water-gas shift reaction was affected to a lesser extent. No regeneration was observed when hydrogen sulfide was removed from the feedstream in agreement with adsorption studies. A slight regeneration was observed when methanethiol was removed from the feed, but this was believed to be due to the removal of carbon rather than sulfur. The overall effect of sulfur poisoning was to reduce activity and enhance hydrogen selectivity.
In this study, we have examined the adsorption of hydrogen sulphide and carbon monoxide over rhodium/ silica and rhodium/alumina catalysts. Adsorption of hydrogen sulphide was measured at 293 and 873 K and at 873 K in a 1:1 ratio with hydrogen. At 293 K, over Rh/ silica, hydrogen sulphide adsorption capacity was similar to that of carbon monoxide; however, over Rh/alumina, the carbon monoxide adsorption capacity was higher, probably due to the formation of Rh I (CO) 2 . Over Rh/silica, the primary adsorbed state was HS(ads), in contrast to Rh/alumina, where the H 2 :S ratio was 1:1 indicating that the adsorbed state was S(ads). Competitive adsorption between CO and H 2 S over Rh/silica and Rh/alumina revealed adsorption sites on the metal that only adsorbed carbon monoxide, only adsorbed hydrogen sulphide or could adsorb both species. At 873 K, hydrogen sulphide adsorption produced the bulk sulphide Rh 2 S 3 ; however, when a 1:1 H 2 :H 2 S mixture was used formation of the bulk sulphide was inhibited and a reduced amount of hydrogen sulphide was adsorbed.
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