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Methane suppression in the Fischer-Tropsch synthesis: Final report

Technical Report ·
OSTI ID:5200659
The objective of the project was to investigate the possiblity of modifying methane formation during the F-T synthesis independent from other hyfrocarbons by systematically changing catalyst characteristics. It would seem that the best way to decrease methane selectivity is still via the use of catalyst modifiers. Inorder to ''tailor-make'' catalyst surfaces which minimize ''extraneous'' methane synthesis without disrupting F-T synthesis, it is necessary for us to fully understand the mechanism(s) by which such modifiers operate. An investigation of Fischer-Tropsch synthesis on K- and Cl-modified Ru Catalysts was carried out. The steady-steady reaction results illustrate how chlorine enhances the selectivity of methane formation while potassium decreases it. In order to better understand methane slectivity changes, a detailed study of Cl-modification of Ru catalysts was made. Amonnia synthesis and methanation reaction results on the same series of catalysts (obtained by using the steady-state isotopic transient technique) in addition to the deactivation results for F-T suggest that structural rearrangements induced by the presence of chlorine, rather than selective site blocking or electronic interactions, may be the primary mechanism of chlorine modification of supported ruthenium catalysts. The results of this study indicate that catalyst modifiers may act to change the catalytic properties by inducing certain metal surface structures. This is a mechanism of modification which has, yet, not been addressed in detail. 49 refs., 16 figs., 7 tabs.
Research Organization:
Pittsburgh Univ., PA (USA). Dept. of Chemical and Petroleum Engineering
DOE Contract Number:
AC22-84PC70020
OSTI ID:
5200659
Report Number(s):
DOE/PC/70020-T1; ON: DE88006658
Country of Publication:
United States
Language:
English