Carbon Dioxide → Carbon Dioxide

HRID 1588208Notes

Reaction equation

HRID 1588208 reaction equation
[C:1](=[O:3])=[O:2].[O-2].[Ba+2].[CH3:6]O>[Cu].[Cr]([O-])([O-])=O.O>[C:1](=[O:3])=[O:2].[CH:1]([O:3][CH3:6])=[O:2].[CH3:6][O:3][CH3:1]

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 gms. copper-chromite (containing 31.1% copper and 29% chromium), 2.185 gms. barium oxide and 150 cc. methanol, reduced in situ using a stream of pure H2 flowing at 25 cc/min. for 16 hrs. 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 2.3 gmoles/h/kg catalyst was obtained with 9% synthesis gas conversion and 95% selectivity towards methanol. An exit gas composition of 65.7% H2, 32% CO, 0.8% CO2, 1 0% methanol, 0.3% methyl formate, 0.1% H2O and 0.02% dimethyl ether was obtained. A liquid composition of 95.6% methanol, 4.0% methyl formate, 0.3% water and traces of dimethyl ether and dissolved gases was obtained at the end of the run.

Workup

  1. customSynthesis gas
  2. customfor 16 hrs
  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 2.3 gmoles/h/kg catalyst
  10. customwas obtained with 9% synthesis gas conversion and 95% selectivity towards methanol

Sources & evidence

ORD record
ord-ffa191fe224442f785f46d48d5fd1cb8
Source dataset
uspto-grants-1993_06
Patent number
US05221652

Reaction notes

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