Method for preparing copper-zinc-based catalyst used in synthesis of methanol through CO2 hydrogenation

Patent metadata

Field	Value
Publication number	US-10010875-B2
Application number	US-201514928345-A
Country	US
Kind code	B2
Filing date	Oct 30, 2015
Priority date	Oct 30, 2014
Publication date	Jul 3, 2018
Grant date	Jul 3, 2018

Abstract

Disclosed is a method for preparing a copper-zinc-based catalyst used in synthesis of methanol through CO 2 hydrogenation, and ultrasonic waves are used for control over crystalline phase's composition of a catalyst precursor. Further related to is a catalyst prepared by such a method. An amount of aurichalcite in an active catalyst precursor can be improved through the method, and the specific surface area of the metal copper in a reduced state catalyst is high. The catalyst presents high activity and hydrothermal stability, and promotes high space time yield of methanol in the synthesis of methanol through CO 2 hydrogenation.

First claim

The invention claimed is:

1. A method for preparing a copper-zinc-based catalyst used in synthesis of methanol through CO 2 hydrogenation, comprising the following steps:
step S1: preparing an aqueous solution containing a copper salt, a zinc salt, and a metal salt promoter, and blending said aqueous solution and an aqueous solution of a precipitator, to produce a first feed liquid, imposing radiation of ultrasonic waves on the first feed liquid thereby generating a first reaction product, aging, solid-liquid separating, and washing the first reaction product to produce a parent body;
step S2: preparing a solution of a carrier precursor, which is blended with the aqueous solution of a precipitator, to produce a second feed liquid, imposing radiation of ultrasonic waves on the second feed liquid thereby generating a second product, stirring, solid-liquid separating, and washing the second product to produce a carrier material; and
step S3: blending and then stirring the parent body and the carrier material, to generate a third product, solid-liquid separating, washing, and drying to produce a catalyst precursor, followed by roasting of the catalyst precursor to obtain the catalyst,
wherein said aging of the first reaction product is hydrothermal aging performed for 4 to 24 hours under airtight conditions at a temperature in the range from 60 to 80° C.

2. The method according to claim 1 , wherein the ultrasonic waves have a frequency in the range from 20 to 40 kHz, and a power in the range from 50 to 500 W.

3. The method according to claim 1 , wherein said blending and/or reaction in steps S1 and S2 are performed each time at a temperature in the range from 40 to 75° C.

4. The method according to claim 1 , wherein said blending in steps S1 and S2 is performed each time in a blender having a passage diameter in the range from 50 to 2000 μm, and a residence time of the first and second feed liquids in the blender ranges from 5 to 1,000 ms; and/or
wherein said reaction is performed each time in a reaction tube having an inner diameter in the range from 0.5 to 8 mm, and a residence time of the first and second feed liquids in the reaction tube ranges from 5 to 40 min.

5. The method according to claim 1 , wherein main crystalline phase's composition of the catalyst precursor comprises rosasite crystalline phase, aurichalcite crystalline phase, and malachite crystalline phase, wherein:
the ratio of X-ray diffraction peak intensity of the malachite crystalline phase to the sum of X-ray diffraction peak intensity of the rosasite crystalline phase and X-ray diffraction peak intensity of the aurichalcite crystalline phase is in the range from 0.05:1 to 0.12:1; and
the ratio of the X-ray diffraction peak intensity of the aurichalcite crystalline phase to the X-ray diffraction peak intensity of the rosasite crystalline phase is in the range from 0.25:1 to 0.45:1.

6. The method according to claim 1 , wherein: the aqueous solution containing a copper salt, a zinc salt, and a metal salt promoter is an aqueous solution of copper-nitrate, zinc-nitrate, and a metal nitrate promoter; or
the metal nitrate salt promoter comprises at least one selected from the group consisting of alkaline earth metal salts and rare earth element salts; or
the carrier precursor is at least one selected from the group consisting of aluminum nitrate, zirconium nitrate, and tetrabutyl titanate.

7. The method according to claim 1 , wherein:
the zinc salt is used at such an amount that the molar ratio of copper to zinc in the catalyst is in the range from 3:7 to 7:3; or
the metal nitrate salt promoter is used at such an amount that the molar ratio of the promoter in total to the element of copper in the catalyst is (0.05-0.1):1; or
the carrier precursor is used at such an amount that the molar ratio of the carrier in total to the element of copper in the catalyst is (0.1-1):1.

8. The method according to claim 1 , wherein the precipitator comprises at least one selected from the group consisting of sodium carbonate, sodium bicarbonate, potassium carbonate, and potassium bicarbonate; or a mixture of at least one selected from the group consisting of sodium carbonate, sodium bicarbonate, potassium carbonate, and potassium bicarbonate, and at least one selected from the group consisting of sodium hydroxide and potassium hydroxide, wherein when the precipitator comprises a mixture of at least one selected from the group consisting of sodium carbonate, sodium bicarbonate, potassium carbonate, and potassium bicarbonate, and at least one selected from the group consisting of sodium hydroxide and potassium hydroxide, the molar ratio of the at least one selected from the group consisting of sodium carbonate, sodium bicarbonate, potassium carbonate, and potassium bicarbonate to the at least one selected from the group consisting of sodium hydroxide and potassium hydroxide is not lower than 1:3; or
wherein the aqueous solution of a precipitator has a concentration of the precipitator in the range from 0.05 to 1 mol/L.

9. A method for preparing a copper-zinc-based catalyst used in synthesis of methanol through CO 2 hydrogenation, comprising: preparing a solution containing a copper salt, a zinc salt, a metal salt promoter, and a carrier precursor, and blending said solution and an aqueous solution of a precipitator, to produce a third feed liquid, imposing radiation of ultrasonic waves on the third feed liquid, thereby generating a third product, stirring, aging, solid-liquid separating, washing, and drying the third product to produce a catalyst precursor, followed by roasting the catalyst precursor to obtain the catalyst,
wherein said aging of the third product is hydrothermal aging performed for 4 to 24 hours under airtight conditions at a temperature in a range from 60 to 80° C.

10. The method according to claim 9 , wherein the ultrasonic waves have a frequency in the range from 20 to 40 kHz, and a power in the range from 50 to 500 W.

11. The method according to claim 9 , wherein said blending and/or reaction are performed at a temperature in the range from 40 to 75° C.

12. The method according to claim 9 , wherein said blending is performed in a blender having a passage diameter in the range from 50 to 2,000 μm, and a residence time of the third feed liquid in the blender ranges from 5 to 1,000 ms; and/or
wherein said reaction is performed in a reaction tube having an inner diameter in the range from 0.5 to 8 mm, and a residence time of the third feed liquid in the reaction tube ranges from 5 to 40 min.

13. The method according to claim 9 , wherein main crystalline phase's composition of the catalyst precursor comprises rosasite crystalline phase, aurichalcite crystalline phase, and malachite crystalline phase, or alternatively comprises rosasite crystalline phase, aurichalcite crystalline phase, and hydrotalcite crystalline phase, wherein:
the ratio of X-ray diffraction peak intensity of the malachite crystalline phase or X-ray diffraction peak intensity of the hydrotalcite crystalline phase to the sum of X-ray diffraction peak intensity of the rosasite crystalline phase and X-ray diffraction peak intensity of the aurichalcite crystalline phase is in the range from 0.05:1 to 0.12:1; and
the ratio of the X-ray diffraction peak intensity of the aurichalcite crystalline phase to the X-ray diffraction peak intensity of the rosasite crystalline phase is in the range from 0.25:1 to 0.45:1.

14. The method according to claim 9 , wherein: the solution containing a copper salt, a zinc salt, and a metal salt promoter is a solution of copper-nitrate, zinc-nitrate, and a metal nitrate pro

Assignees

• China Petroleum & Chem Corp
• Res Institute Of Nanjing Chemical Industry Gr
• Res Inst Nanjing Chemical Ind Group

Inventors

• Yu Yang
• Hao Aixiang
• Chen Haibo
• Wei Shixin
• Yin Yusheng
• Xie Tianming
• He Jian
• Mao Chunpeng
• Tan Jiedong

Classifications

• B01J23/83

  with rare earths or actinides · CPC title

• B01J2523/25

  Barium · CPC title

• B01J2523/48

  Zirconium · CPC title

• B01J37/03

  Precipitation; Co-precipitation · CPC title

• C07C29/154

  containing copper, silver, gold, or compounds thereof · CPC title