Method for combined production of ethyl methyl ketone and ethanol

A technology for methyl ethyl ketone and ethanol, applied in the field of co-production of methyl ethyl ketone and ethanol, can solve problems such as potential safety hazards, waste of hydrogen resources, etc., and achieve the effects of high production income, cost reduction, and good technical effect

Inactive Publication Date: 2015-12-09
SHANGHAI HUAYI GRP CO
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Hydrogen will be produced by dehydration of sec-butanol to produce methyl ethyl ketone. In this method, hydrogen is mainly vented or used as fuel, which not only wastes hydrogen resources, but also has potential safety hazards.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Example Embodiment

[0018] [Example 1]

[0019] Preparation of CuO-ZnO-ZrO by Co-precipitation 2 Hydrogenation industrial catalyst (cylindrical, Φ5*5mm), with CuO content 65wt%, ZnO content 25wt%, ZrO 2 Content 10wt%. The CuO-ZnO-MgO dehydrogenation industrial catalyst (cylindrical, Φ5*5mm) was prepared by co-precipitation method, wherein the CuO content was 60wt%, the ZnO content was 25wt%, and the MgO content was 15wt%. The hydrogenation reactor and the dehydrogenation reactor are both 316 stainless steel tubes, with an inner diameter of 38mm, the hydrogenation catalyst loading amount is 9Kg, and the dehydrogenation reactor catalyst loading amount is 0.4Kg. The sec-butyl acetate enters the hydrogenation reactor, and the hydrogenation reaction product is separated by a rectifying tower; after separation, the sec-butanol enters the dehydrogenation reactor, and the hydrogen produced by the dehydrogenation reactor is pressurized by a supercharger, and then mixed with the hydrogenation raw materials.

Example Embodiment

[0023] [Example 2]

[0024] According to the conditions and steps described in Example 1, the hydrogenation catalyst prepared by the co-precipitation method is CuO-CaO-SiO 2 (cylindrical, Φ5*5mm), with CuO content 60wt%, CaO content 10wt%, SiO 2 Content 30wt%. Preparation of CuO-K by Co-precipitation 2 O-SiO 2 Dehydrogenation industrial catalyst (cylindrical, Φ5*5mm), of which CuO content is 55wt%, SiO 2 Content 40wt%, K 2 The O content was 5 wt%. The hydrogenation catalyst loading amount is 4Kg, and the dehydrogenation reactor catalyst loading amount is 1.8Kg.

[0025] Hydrogenation reaction conditions: the molar ratio of sec-butyl acetate raw material and hydrogen is 20; the liquid hourly space velocity of sec-butyl acetate raw material mass is 2.0h -1 ; The reaction temperature is 220°C; the reaction pressure is 2.0MPaG.

[0026] Dehydrogenation reaction conditions: sec-butanol mass liquid hourly space velocity of 3.0h -1 ; The reaction temperature is 200°C; the reactio

Example Embodiment

[0028] [Example 3]

[0029] According to the conditions and steps described in Example 1, the hydrogenation catalyst prepared by the co-precipitation method is CuO-ZnO-Al 2 O 3 -MnO 2 (cylindrical, Φ5*5mm), with CuO content 60wt%, ZnO content 15wt%, MnO 2 3wt%, Al 2 O 3 22wt%. Preparation of CuO-La by Impregnation Method 2 O 3 -CaO-Al 2 O 3 Dehydrogenation industrial catalyst (spherical, Φ5mm), in which CuO content is 15wt%, La 2 O 3 Content 2wt%, Al 2 O 3 Content 80wt%, CaO3wt%. The hydrogenation catalyst loading amount is 4Kg, and the dehydrogenation reactor catalyst loading amount is 1.2Kg.

[0030] Hydrogenation reaction conditions: the molar ratio of sec-butyl acetate raw material and hydrogen is 30; the mass liquid hourly space velocity of sec-butyl acetate raw material is 4.5h -1 ; The reaction temperature is 240°C; the reaction pressure is 8.0MPaG.

[0031] Dehydrogenation reaction conditions: sec-butanol mass liquid hourly space velocity of 10.0h -1 ; Th

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PUM

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Abstract

The invention relates to a method for combined production of ethyl methyl ketone and ethanol. The method solves the problem that the prior art cannot recycle hydrogen. The method comprises 1, feeding a sec-butyl acetate raw material and a hydrogen raw material into a hydrogenation unit, feeding a material flow from a hydrogenation unit outlet into a first separation unit, carrying out separation to obtain an unreacted sec-butyl acetate flow, a sec-butyl alcohol flow, an ethanol flow and a by-product flow, and returning the unreacted sec-butyl acetate flow to the hydrogenation unit, 2, feeding the sec-butyl alcohol flow into a dehydrogenation reaction unit to obtain an ethyl methyl ketone flow and a hydrogen flow, feeding the ethyl methyl ketone flow and unreacted sec-butyl alcohol in the dehydrogenation reaction unit into a second separation unit, carrying out separation to obtain an ethyl methyl ketone flow and an unreacted sec-butyl alcohol flow, and returning the hydrogen flow into the hydrogenation unit. The method successfully solves the above problem and can be used for ethyl methyl ketone and ethanol production.

Description

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Claims

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Application Information

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Owner SHANGHAI HUAYI GRP CO
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