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Title: Selective methane oxidation over promoted oxide catalysts. Quarterly report, March--May 1994

Technical Report ·
DOI:https://doi.org/10.2172/10175607· OSTI ID:10175607

Experimental work aiming at developing active catalysts for selective oxidation of methane to methanol was started in this quarter. Some of the experiments used a double catalyst bed design and with H{sub 2}O as cofeed. The first catalyst bed, which serves as CH{sub 3} radical generator, was chosen to be 1 wt % SO{sub 4}{sup 2{minus}}/Sr/La{sub 2}O{sub 3}, as this catalyst exhibits remarkable activity and selectivity at lower temperature (500{degrees}C--550{degrees}C). A few transition metal oxides were used as the second catalyst bed to react with CH{sub 3} to form CH{sub 3}O{sup {minus}}M{sup +} species, which was then hydrolyzed to form CH{sub 3}OH. It was found that unsupported metal oxides ZrO{sub 2}, Y{sub 2}O{sub 3}, SrO; Fe{sub 2}O{sub 3},MnO{sub 2}, Cr{sub 2}O{sub 3}, CaO, and MgO did not produce CH{sub 3}OH between 430{degrees}C and 600{degrees}C when used as the only catalysts, while MoO{sub 3} supported on silica produced CH{sub 3}0H in the temperature range of 430{degrees}C--480{degrees}C under the current single-bed reactor configuration. However, when the double-bed configuration was used with the 1 wt % SO{sub 4}{sup 2{minus}}/Sr/La{sub 2}O{sub 3} as the first methyl radical generating catalyst bed, CH{sub 3}0H was observed when ZrO{sub 2}and Y{sub 2}O{sub 3} were used as the second bed catalysts. Preliminary quantitative analysis showed that the ability of producing CH{sub 3}OH was in the order of unsupported Y{sub 2}O{sub 3} > unsupported ZrO{sub 2} > MoO{sub 3} on silica. For all of these cases, the CH{sub 3}OH space time yield was within a dozen grams per kilogram catalyst per hour.

Research Organization:
Lehigh Univ., Bethlehem, PA (United States). Zettlemoyer Center for Surface Studies
Sponsoring Organization:
USDOE, Washington, DC (United States)
DOE Contract Number:
FG21-92MC29228
OSTI ID:
10175607
Report Number(s):
DOE/MC/29228-3837; ON: DE94012270; BR: AB0530150/AB0550000
Resource Relation:
Other Information: PBD: Jun 1994
Country of Publication:
United States
Language:
English