Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Formate | HCID 2735122 | — |
| Catalyst | HCID 178505379 | HCID 178505379 | — |
| Solvent | Water | HCID 962 | — |
| Product | Carbon Dioxide | HCID 280 | 0.7% |
| Product | Methyl formate | HCID 7865 | 0.4% |
| Product | Dimethyl Ether | HCID 8254 | 0.07% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05384335 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-334bc8ebb98b4eacbba6a011937c9d6f |
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| Source note | uspto-grants-1995_01 |
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