TY - JOUR
T1 - Methane to methanol in supercritical water
AU - Savage, Phillip E.
AU - Li, Ruokang
AU - Santini, John T.
N1 - Funding Information:
ACKNOWLEDGMENTS Leonard Buccellato and Scott Schneider helped to develop the experimental procedures. Eric Brock assisted with the modeling work. We acknowledge helpful discussions with Professor John Barker about mechanistic modeling, and we thank Professor Jeff Tester for providing thermodynamics and kinetics data for the elementary reactions. This research was supported in part by the Office of the Vice-President for Research at the University of Michigan and by an REU Supplement to grant CTS-9015738 from the National Science Foundation.
PY - 1994/6
Y1 - 1994/6
N2 - We examined the feasibility of producing methanol from the partial oxidation of methane in near-critical and supercritical water. Oxygen was always the limiting reactant. The parameter space investigated experimentally included temperatures between 349 and 481 °C, batch holding times between 1 and 9 min, water densities between 0.15 and 0.35 g mL-1, initial methane to water molar ratios between 0.05 and 0.27, and initial methane to oxygen molar ratios between 10 and 26. Experiments within this parameter space led to methane conversions up to 6%, and oxygen conversions up to 100%. Methanol, carbon monoxide, and carbon dioxide were the major products. The methanol selectivities ranged from 0.04 to 0.75, with the highest selectivities occurring at the lower conversions. The highest methanol yield was 0.7%. Reactions performed in glass-lined reactors proceeded to higher conversions than did reactions in stainless-steel reactors under otherwise identical conditions. A detailed chemical kinetics model showed that the methanol selectivity increased with temperature and with the methane to oxygen molar ratio, but decreased with increasing oxygen conversion. The methanol yield showed the same trends with temperature and the methane to oxygen ratio, but the yield increased with oxygen conversion.
AB - We examined the feasibility of producing methanol from the partial oxidation of methane in near-critical and supercritical water. Oxygen was always the limiting reactant. The parameter space investigated experimentally included temperatures between 349 and 481 °C, batch holding times between 1 and 9 min, water densities between 0.15 and 0.35 g mL-1, initial methane to water molar ratios between 0.05 and 0.27, and initial methane to oxygen molar ratios between 10 and 26. Experiments within this parameter space led to methane conversions up to 6%, and oxygen conversions up to 100%. Methanol, carbon monoxide, and carbon dioxide were the major products. The methanol selectivities ranged from 0.04 to 0.75, with the highest selectivities occurring at the lower conversions. The highest methanol yield was 0.7%. Reactions performed in glass-lined reactors proceeded to higher conversions than did reactions in stainless-steel reactors under otherwise identical conditions. A detailed chemical kinetics model showed that the methanol selectivity increased with temperature and with the methane to oxygen molar ratio, but decreased with increasing oxygen conversion. The methanol yield showed the same trends with temperature and the methane to oxygen ratio, but the yield increased with oxygen conversion.
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U2 - 10.1016/0896-8446(94)90050-7
DO - 10.1016/0896-8446(94)90050-7
M3 - Article
AN - SCOPUS:0001664065
SN - 0896-8446
VL - 7
SP - 135
EP - 144
JO - Journal of Supercritical Fluids
JF - Journal of Supercritical Fluids
IS - 2
ER -