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Title: Deuterodesulfurization of thiophene: an investigation of the reaction mechanism

Journal Article · · J. Catal.; (United States)

The deuterodesulfurization of thiophene was investigated using selected MoS/sub 2/ and reduced molybdenum sulfide (Chevrel phase) catalysts. The extent of deuterium incorporation into thiophene and into specific desulfurization products (hydrogen sulfide, butadiene, and butenes) was determined at 400/sup 0/C for thiophene conversions near 4%. Unpromoted MoS/sub 2/ introduced up to 10 times more deuterium into thiophene than did the promoted catalysts (including the Chevrel phase materials). For all catalysts, H/sub 2/S was formed almost exclusively (typically 90+%), with only small amounts of HDS and D/sub 2/S being detected. Except for the unpromoted MoS/sub 2/ catalyst, the deuterium distributions determined for the cis- and trans-2-butene products were nearly identical; the deuterium distribution found for 1-butene was distinct. A mechanism of thiophene hydrodesulfurization can be proposed in which butadiene is the initial desulfurized reaction product. The hydrogen available for hydrogen sulfide formation is derived via hydrogen exchange with thiophene. 23 references.

Research Organization:
Iowa State Univ., Ames
OSTI ID:
5667343
Journal Information:
J. Catal.; (United States), Vol. 103:2
Country of Publication:
United States
Language:
English