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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

Inactive Publication Date: 2015-04-01
XIAMEN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Japanese patent Ping-41038, Soviet patent SU1118632A introduced acetone hydrogenation method using Cu-Cr catalyst, Russian patent RU2047590 used catalysts containing NiO, CuO and other components, but the conversion rate of these catalysts was not high and the selectivity was poor , the use of Cr2O3 as an additive will cause environmental pollution at the same time, which does not meet the requirements of green chemical industry
CN103030525A has reported a kind of method that acetone liquid phase hydrogenation prepares isopropanol, but reaction temperature is higher, at 100~200 ℃, reaction time is longer (4 hours), and the conversion rate of acetone is more than 96%, and isopropanol The selectivity is greater than 95%
The performance of the catalysts used in the above acetone hydrogenation process is not ideal, the temperature required for the reaction process is high, the reaction time is long, the operating conditions of the pressure have high requirements on the equipment, and the conversion rate of acetone and the selectivity of isopropanol cannot be simultaneously high. standard, resulting in high production cost, heavy burden on the later separation link, high energy consumption and low efficiency, making it difficult to meet the requirements of green chemical industry

Method used

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Examples

Experimental program
Comparison scheme
Effect test

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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PUM

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Abstract

The invention discloses a method for low temperature preparation of isopropanol; acetone is added with hydrogen and subjected to a reaction under the action of a catalyst to generate isopropanol, and the specific steps include that a carbon-based material is used as a carrier to prepare the double-metal supported catalyst represented by M1-M2 / C, wherein M1 is selected from one of Mo, Au and Ru, and M2 is selected from one of Re, Ag and Mn; liquid acetone is placed in a batch autoclave, the prepared catalyst is added, hydrogen is introduced, the reaction is carried out for a period of time, and thus isopropanol is obtained. The operation temperature for preparing isopropanol is low, the reaction is quick, the conversion rate is high, and the product has high selectivity.

Description

technical field [0001] The invention relates to isopropanol preparation technology, in particular to a method for preparing isopropanol at low temperature. Background technique [0002] The demand for phenol in my country is relatively large, and domestic phenol manufacturers mostly adopt the cumene peroxidation method and realize the co-production with acetone. The increase in phenol production has brought about the excess production of acetone, and there has been an imbalance between supply and demand. Considering the market space of isopropanol, hydrogenation of acetone to produce isopropanol is an economically feasible route. The process of hydrogenation of acetone to isopropanol is easy to produce by-products such as ethers. The purity of the product in the reaction process determines the cost of the later separation, and also determines the quality of the final product to a certain extent. Patent CN1083415C uses the CuO-ZnO mixture formed by pressing as a catalyst, an...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07C31/10C07C29/145B01J23/656B01J23/68B01J23/50B01J23/36
CPCB01J23/36B01J23/50B01J23/6562B01J23/6567B01J23/68C07C29/145C07C31/10
Inventor 陈秉辉郑进保杨昭张诺伟
Owner XIAMEN UNIV
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