Carbon Dioxide → Methyl formate

HRID 1770246Notes

Reaction equation

HRID 1770246 reaction equation
[C:1](=[O:3])=[O:2].[C:4]([O-:7])([O-])=[O:5].[K+].[K+].[CH3:10][OH:11]>[Cr]([O-])([O-])=O.[Cu+2].O>[C:1](=[O:3])=[O:2].[CH:10]([O:5][CH3:4])=[O:11].[CH3:1][O:7][CH3:4]

Participants

8

Procedure

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 gm of activated copper chromite (containing 31.1% copper and 29% chromium) impregnated with 10% K2CO3 and 150 cc methanol and then reduced in situ using a stream of pure H2 flowing at 25 cc/min. for 16 hours at 170° C. The catalyst was added as a powder. 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 an H2 consumption of 12.5 gmols/h/kg. cat was obtained with 42% synthesis gas conversion and 95% selectivity towards methanol. An exit gas composition of 65.5% H2, 32.7% CO, 0.3% CO2, 0.7% methanol, 0.6% methyl formate, 0.2% H2O and 0.07% dimethyl ether was obtained. A liquid composition of 95.6% methanol, 4% methyl formate, 0.3% H2O and traces of dimethyl ether and dissolved gases was obtained. No higher alcohols were detected.

Workup

  1. customSynthesis gas
  2. customfor 16 hours
  3. customat 170° C
  4. additionThe catalyst was added as a powder
  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 an H2 consumption of 12.5 gmols/h/kg
  10. customcat was obtained with 42% synthesis gas conversion and 95% selectivity towards methanol

Sources & evidence

ORD record
ord-1820b7dff6034a3d8250d7bba829e605
Source dataset
uspto-grants-1995_01
Patent number
US05385949

Reaction notes

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