The isotopic exchange has been studied between catalyst radiosulfur and H 2 S, formed in thiophene hydrodesulfurization (HDS) (named S-displace) on alumina supported molybdena, on CoMoO x , PdMoO x , PtMoO x and on silica-alumina supported NiWO x . S-displace was compared with radiosulfur exchange data between catalyst radiosulfur and gas phase H 2 S (S exc ) determined previously. The extent of S exc was higher than that of the S-displace for Mo, CoMo in and NiW, whereas the extent of S-displace from PdMoO and PtMoO was significantly higher, than that of S exc . Thiophene HDS product distribution data are discussed in terms of increased C@C hydrogenation and C-C hydrogenolysis activity, explained by increasing H 2 S production with longer circulation time of the thiophene/H 2 mixture, The C 1 =C 3 <1 ratios among C 4 -hydrogenolysis products indicate some coke formation. The decrease of thiophene HDS activity is presumably a consequence of increasing site-blocking with the formation of more H 2 S and coke with longer duration of thiophene treatment.