METHANE TO METHANOL IN SUPERCRITICAL WATER

被引:47
作者
SAVAGE, PE
LI, RK
SANTINI, JT
机构
[1] University of Michigan, Department of Chemical Engineering, Ann Arbor
基金
美国国家科学基金会;
关键词
SUPERCRITICAL WATER; METHANE; PARTIAL OXIDATION; MECHANISM; MODELING;
D O I
10.1016/0896-8446(94)90050-7
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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 degrees 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.
引用
收藏
页码:135 / 144
页数:10
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