Carbon Dioxide → Carbon Dioxide
Reaktionsgleichung
[C:1](=[O:3])=[O:2].[CH:4]([O-:6])=[O:5].[K+].[CH3:8][OH:9]>[Cu].[Cr]([O-])([O-])=O.O>[C:1](=[O:3])=[O:2].[CH:8]([O:5][CH3:4])=[O:9].[CH3:1][O:6][CH3:4]Komponenten
Edukt 3
Produkt 3
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
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), 1.2 gm. potassium formate 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 17.16 gmoles/h/kg catalyst was obtained with 60% synthesis gas conversion and 95% selectivity towards methanol. An exit gas composition of 62% H2, 36% CO, 0.7% CO2, 0.6% methanol, 0.4% methyl formate, 0.1% H2O and 0.07% dimethyl ether was obtained. A liquid composition of 95.4% methanol, 4% methyl formate, 0.3% water and traces of dimethyl ether and dissolved gases was obtained.
Aufarbeitung
- customSynthesis gas
- customfor 16 hours
- customat 170° C
- additionBoth catalysts were added separately in the powder form
- customwas adjusted to 150° C
- customSynthesis gas at a flow rate of 105 cc/min. (measured under standard conditions)
- customto react under isothermal conditions
- customto the amount of synthesis gas
- customA methanol production rate based on H2 consumption of 17.16 gmoles/h/kg catalyst
- customwas obtained with 60% synthesis gas conversion and 95% selectivity towards methanol
Quellen und Nachweise
- ORD-Eintrag
- ord-779f3146765f43efbc5263d20094e66d
- Quelldatensatz
- uspto-grants-1993_06
- Patentnummer
- US05221652
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