Method for low temperature preparation of isopropanol
An isopropanol, low-temperature technology, applied in the field of isopropanol preparation, can solve the problems of long reaction time, high requirements on equipment under operating conditions, poor selectivity, etc., achieve simple and easy preparation and production methods, and reduce the burden of product separation , the effect of preventing surface oxidation
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Embodiment 1
[0028] Weigh 0.15g of ammonium perrhenate and 0.18g of anhydrous ruthenium chloride and dissolve them in 200ml of glycerol, add 3.15g of PVA, stir until completely dissolved, raise the temperature to 250°C under the protection of argon, and keep the temperature down to At room temperature, add 200ml of ethanol and 2g of ascorbic acid to adjust the pH=2, add 6g of carbon nanotubes, keep stirring for 3h, filter and wash, and vacuum dry at 80°C for 12h. After drying, raise the temperature at 3°C / min to 400°C under the atmosphere of hydrogen gas, keep the temperature for 2 hours and then cool down to room temperature, and the flow rate of hydrogen gas is 80ml / min, then the Ru-Re / C catalyst is prepared, in which the loadings of Ru and Re are respectively Between 0.1% and 1.6%.
[0029] Put liquid acetone in a batch-type autoclave, put in the above-mentioned catalyst, pass through hydrogenation gas, and hydrogenate acetone under the action of the catalyst to react for 6 minutes to p...
Embodiment 2
[0031] The catalyst and its preparation method are the same as those in Example 1. The prepared catalyst is pretreated before feeding. Specifically, the nitrogen-oxygen mixture containing 20% oxygen is passed through the catalyst bed at a flow rate of 100 ml / min. The catalyst bed is kept at 50°C. The processing time is 2h.
[0032] Put liquid acetone in a batch-type autoclave, put in the above-mentioned pretreated catalyst, pass through hydrogenation gas, hydrogenate acetone and react for 6 minutes under the action of the catalyst to prepare isopropanol. The catalyst dosage / substrate is 0.005g / ml, the operating temperature is 28°C, the reaction time is 6min, the hydrogen pressure is 5.3MPa, and the stirring speed is 500 rpm. The conversion rate of hydrogenation of acetone was measured to be 100%, and the selectivity of isopropanol was 100%.
Embodiment 3
[0034] Weigh 0.1g of ammonium perrhenate and 0.1g of chloroauric acid and dissolve in 150ml of propylene glycol, add 2.96g of PVP, stir until completely dissolved, raise the temperature to 100°C under the protection of argon, keep the temperature down to room temperature after 3 hours, add 250ml Ethanol and 1.35g ascorbic acid, adjust pH=1.5, add 6g carbon black, keep stirring for 8h, filter and wash, and vacuum dry at 70°C for 14h. After drying, the temperature was raised to 300°C at 3°C / min in a hydrogen atmosphere, and then lowered to room temperature after a constant temperature of 2h. The gas flow rate was 60ml / min, and the Au-Re / C catalyst was prepared. The loadings of Au and Re were respectively at Between 0.1% and 1.6%.
[0035] The prepared catalyst was pretreated. Specifically, nitrogen-oxygen mixture containing 20% oxygen was passed through the catalyst bed at a flow rate of 80ml / min. The catalyst bed was kept at a room temperature of 28° C., and the pretreatment ...
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