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Catalyst for preparing 3-pentanol by hydrogenation of 3-pentanone and preparation method thereof

A catalyst, pentanone technology, applied in chemical instruments and methods, preparation of hydroxyl compounds, metal/metal oxide/metal hydroxide catalysts, etc., can solve the problems of long reaction time, non-compliance with green chemical industry, environmental pollution, etc. To achieve the effect of simple and easy preparation and production methods, reducing the burden of product separation, and reducing production costs

Inactive Publication Date: 2016-08-17
XIAMEN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

3-Pentanol can be produced by hydrogenation of 3-Pentanone, and there are no patents related to catalytic technology. There have been patent documents reporting catalysts and processes for hydrogenation of ketones to alcohols
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 temperature of ketone hydrogenation reported in the patent is relatively high, or the reaction time is long, or the operating conditions of pressure have high requirements on the equipment, or the conversion rate and product selectivity cannot reach high standards at the same time, if a Highly active and highly selective catalysts for short-term low-temperature reactions will greatly reduce the cost of the production process and reduce the burden on the later stage of separation. The overall low energy consumption and high-efficiency production meet the requirements of green chemical industry

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0024] Weigh 0.008g of cerium nitrate hexahydrate, put it into 50ml of deionized water, add 0.6g of activated carbon, adjust pH=10 with ammonia water after stirring for 3h, keep stirring for 3h, filter and wash. Dry in vacuum at 60°C for 12h. In nitrogen, the temperature was raised to 400°C at 5°C / min, and the temperature was kept constant for 3h to cool down to room temperature. Ce / C is produced.

[0025] Weigh 0.024g of ruthenium chloride hydrate and 0.024g of copper chloride hydrate into 50ml of ethylene glycol, and stir for 30min. Put the Ce / C prepared in the previous step into the above solution, adjust the pH to 10 with sodium hydroxide, stir and raise the temperature to 230° C. for 2 hours. Cool down to room temperature, filter and wash, and dry under vacuum at 60°C for 12h. In nitrogen, the temperature was raised to 400°C at 6°C / min, and the temperature was kept at room temperature for 2 hours to prepare a Ru-Cu-Ce / C catalyst, in which the loading amount of Ru was 0...

Embodiment 2

[0027] Weigh 0.008g of lanthanum nitrate hexahydrate, put it into 50ml of deionized water, add 0.6g of carbon black, stir for 3h, adjust pH=12 with sodium hydroxide, keep stirring for 2h, filter and wash. Vacuum dry at 40°C for 14h. In nitrogen, the temperature was raised to 500°C at 5°C / min, and the temperature was kept constant for 3h to cool down to room temperature. La / C was prepared.

[0028] Weigh 0.015g of ruthenium chloride hydrate and 0.015g of chloroauric acid, put them into 50ml of deionized water, and stir for 30min. Put the La / C prepared in the previous step into the above solution, adjust the pH to 3 with hydrochloric acid, and stir at room temperature for 12 h. Infrared lamp rapid drying, vacuum drying at 60 ℃ for 10h. In hydrogen, the temperature was raised to 230°C at 3°C / min, and then the temperature was lowered to room temperature after 8h to prepare the Ru-Au-La / C catalyst, in which the loading amount of Ru was 0.1%-1.7%, and the loading amount of Au was...

Embodiment 3

[0030]Weigh 0.008g of yttrium nitrate hexahydrate, put it into 50ml of deionized water, add 0.6g of carbon nanotubes, stir for 3 hours, adjust the pH to 12 with sodium hydroxide, keep stirring for 5 hours, filter and wash, and vacuum dry at 80°C for 12 hours . In nitrogen, the temperature was raised to 500°C at 5°C / min, and the temperature was kept constant for 3h to cool down to room temperature. Y / C was prepared.

[0031] Weigh 0.01g of chloroiridic acid hydrate and 0.01g of silver nitrate, put them into 50ml of deionized water, and stir for 30min. Put the Y / C prepared in the previous step into the above solution, adjust the pH to 2 with 10% hydrochloric acid, and stir at room temperature for 8 hours. Infrared lamp rapid drying, 60 ℃ vacuum drying for 12h. In hydrogen, the temperature was raised to 200°C at 2°C / min, and the temperature was kept at room temperature for 6 hours to prepare the Ag-Ir-Y / C catalyst, in which the loading of Ag was 0.1%-1.7%, and the loading of I...

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PUM

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Abstract

The invention discloses a catalyst for preparing 3-pentanol through 3-pentanone hydrogenation. The catalyst comprises a carbon-based carrier and a multi-metal component recorded as M1-M2-M3 / C, wherein M1 is selected from one of Ru, Mn and Ag; M2 is selected from one of Ir, Au and Cu; and M3 is selected from one of La, Ce and Y. The catalyst is applied to the liquid phase 3-pentanone hydrogenation process. The conversion rate of 3-pentanone can be 100 percent within a short time, and the selectivity of the 3-pentanol is 100 percent. The invention also provides a method for preparing the catalyst, and the industrial preparation is easily realized.

Description

technical field [0001] The invention relates to a catalyst, in particular to a catalyst for preparing 3-pentanol by hydrogenating 3-pentanone and a preparation method thereof. Background technique [0002] 3-Pentanol is an important chemical raw material. In addition to being used in organic synthesis, it is also used as a flotation agent and solvent. It belongs to a pharmaceutical intermediate, a material intermediate, and a fine chemical. 3-pentanol can be produced by hydrogenation of 3-pentanone, and there are no patents related to catalytic technology. There have been patent documents reporting catalysts and processes for hydrogenation of ketones to alcohols. Patents CN1152744C, CN1114490C and CN1347758A report the method for preparing 2-octyl alcohol by hydrogenation of 2-octanone, using its self-made catalyst system (copper-containing catalyst, nickel-containing catalyst), using a fixed-bed liquid-phase hydrogenation process to achieve, the reaction temperature 100-25...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J23/89B01J23/66B01J23/63B01J23/889B01J23/656C07C31/125C07C29/145
Inventor 陈秉辉郑进保杨昭张诺伟
Owner XIAMEN UNIV
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