Carbon Dioxide → Methyl formate

HRID 1588214ノート

反応式

HRID 1588214 の反応式
[C:1](=[O:3])=[O:2].[Cr]([O-])([O-])(=O)=O.[Cs+].[Cs+].[CH3:11][OH:12]>[Cu].[Cr]([O-])([O-])=O.O>[C:1](=[O:3])=[O:2].[CH:11]([O:2][CH3:1])=[O:12].[CH3:11][O:3][CH3:1]

参加物

8

実験手順

Synthesis gas having an inlet composition of 66.6% H2, 33.3% CO and 0.1% CO2 was fed to a 300 cc. stainless steel autoclave charged with 3 gms. copper-chromite (containing 31.1% copper and 29% chromium), 1.36 gms. of cesium chromate and 150 cc. methanol, reduced in situ using a stream of pure H2 flowing at 25 cc/min. for 16 hours at 170° C. Both catalysts were added separately in the powder form. The reactor was pressurized to 910 psig. and the temperature was adjusted to 150° C. Synthesis gas at a flow rate of 105 cc/min. (measured under standard conditions) was made to react under isothermal conditions. After an initial transient period, the process reached a steady state with respect to the amount of synthesis gas converted. A methanol production rate based on H2 consumption of 11.44 gmoles/h/kg catalyst was obtained with 50% synthesis gas conversion and 95% selectivity towards methanol. An exit gas composition of 63.55% H2, 33.75% CO, 0.45% CO2, 1.1% methanol, 1.0% methyl formate, 0.125% H2O and 0.004% dimethyl ether was obtained. A liquid composition of 95 6% methanol, 4% methyl formate, 0 3% water and traces of dimethyl ether and dissolved gases was obtained.

後処理

  1. customSynthesis gas
  2. customfor 16 hours
  3. customat 170° C
  4. additionBoth catalysts were added separately in the powder form
  5. customwas adjusted to 150° C
  6. customSynthesis gas at a flow rate of 105 cc/min. (measured under standard conditions)
  7. customto react under isothermal conditions
  8. customto the amount of synthesis gas
  9. customA methanol production rate based on H2 consumption of 11.44 gmoles/h/kg catalyst
  10. customwas obtained with 50% synthesis gas conversion and 95% selectivity towards methanol

出典と根拠

ORDレコード
ord-990917c13fc64be58a5cdaeb32a3d52b
出典データセット
uspto-grants-1993_06
特許番号
US05221652

反応ノート

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