Preparation method for olefin epoxidation catalyst and applications thereof

Patent metadata

Field	Value
Publication number	US-11213811-B2
Application number	US-201816484574-A
Country	US
Kind code	B2
Filing date	May 24, 2018
Priority date	May 25, 2017
Publication date	Jan 4, 2022
Grant date	Jan 4, 2022

Abstract

Disclosed in the present invention are a preparation method for an olefin epoxidation catalyst and applications thereof. The method comprises: loading an auxiliary metal salt onto a silica gel carrier, and carrying out a drying treatment to the silica gel carrier; loading a titanium salt (preferably TiCl 4 ) onto the silica gel carrier by a chemical vapor deposition method; calcining to obtain a silica gel on which the auxiliary metal oxide and Ti species are loaded; obtaining an catalyst precursor (Ti-MeO—SiO 2 composite oxide) by water vapor washing; loading alkyl silicate (preferably tetraethyl orthosilicate) onto the surface of the catalyst precursor by a chemical vapor deposition method and calcining the catalyst precursor to obtain a Ti-MeO—SiO 2 composite oxide with the surface coated with a SiO 2 layer; and carrying out a silylanization treatment to obtain the catalyst. The catalyst can be applied to a chemical process of propylene epoxidation to prepare propylene oxide, and has an average selectivity to PO up to 96.7%, the method of the present invention and the applications thereof have industrial application prospects.

First claim

The invention claimed is:

1. A preparation method for an olefin epoxidation catalyst, which comprises the following steps: (1) loading an auxiliary metal salt onto a silica gel carrier to obtain an auxiliary metal salt modified silica gel carrier A; (2) carrying out a drying treatment for the A obtained in step (1); (3) carrying out a chemical vapor deposition for the dried A using a titanium salt vapor to obtain a silica gel B on which the auxiliary metal salt and the titanium salt, are loaded; (4) calcining the B obtained in step (3) to obtain a silica gel C on which the auxiliary metal salt and Ti species are loaded; (5) carrying out a water vapor washing for the C obtained in step (4) to obtain a Ti-MeO—SiO 2 composite oxide; (6) carrying out a vapor deposition for the Ti-MeO—SiO 2 composite oxide using an alkyl silicate vapor to obtain the Ti-MeO—SiO 2 composite oxide D having a silicon-containing compound loaded on the surface of the composite oxide (7) calcining the D obtained in step (6) to obtain a Ti-MeO—SiO 2 composite oxide having a SiO2 layer coated on the surface of the composite oxide, which is referred to as SiO2—Ti-MeO—SiO2; (8) carrying out a silylanization treatment for the SiO2—Ti-MeO—SiO2 obtained in step (7), wherein the auxiliary metal salt in the step (1) is selected from the group consisting of Ce(NO3) 3 , Pr(NO 3 ) 3 , Tb(NO 3 ) 3 , La(NO 3 ) 3 , and combinations thereof.

2. The method according to claim 1 , wherein in step (1) the auxiliary metal salt is added in an amount ranging from 0.6-2.4 wt % based on the mass of the silica gel carrier.

3. The method according to claim 1 , wherein the silica gel carrier used in step (1) is a C-type silica gel.

4. The method according to claim 3 , wherein the silica gel carrier used in step (1) has a spherical shape or is a block C-type silica gel.

5. The method according to claim 3 , wherein the silica gel carrier used in step (1) is an irregular blocky C-type silica gel.

6. The method according to claim 3 , wherein the silica gel carrier used in step (1) has a specific surface area of 100-350 m2/g, an average pore diameter of 8-11 nm, a pore volume of 0.7-1.2 ml/g, a Na2O impurity content of <100 ppm, a Fe2O3 impurity content of <500 ppm and a size of a spherical equivalent diameter of 0.5-2 mm.

7. The method according to claim 1 , wherein in step (2), the drying temperature is 150-240° C. and drying time is 120 min-240 min.

8. The method according to claim 1 , wherein based on the weight of the silica gel carrier used in step (1), in step (3), Ti is loaded on the silica gel carrier in an amount ranges from 0.1-5.0 wt %.

9. The method according to claim 8 , wherein Ti is loaded on the silica gel carrier in an amount from 2.5-4.5 wt %.

10. The method according to claim 8 , wherein the chemical vapor deposition of step (3) is carried out in a reaction tube, the dried A is charged in the reaction tube, an inert gas is used to introduce the titanium salt vapor into the reaction tube, the inert gas has a flow rate of 0.05-2.0 cm/s, the chemical vapor deposition temperature of the reaction is 150-300° C., and the chemical vapor deposition time is 120-240 min.

11. The method according to claim 1 , wherein the calcination in step (4) is carried out in a N 2 atmosphere, at a temperature ranging from 450-700° C. a time ranging from 30-240 min, and the flow rate of N 2 is 0.05-2.0 cm/s.

12. The method according to claim 1 , wherein the water vapor used for water vapor washing in step (5) has a temperature of 100-200° C.; based on the amount of the Ti element in the titanium salt vapor used in step (3), the molar ratio of the water vapor to Ti is 20-150:1, the water vapor washing time is 180-240 min.

13. The method according to claim 12 , wherein the water vapor used for water vapor washing in step (5) has a temperature of 120-180° C., and based on the amount of the Ti element in the titanium salt vapor used in step (3), the molar ratio of the water vapor to Ti is 50-100:1.

14. The method according to claim 12 , wherein the water vapor washing of step (5) is carried out in a reaction tube, water vapor is introduced into the reaction tube using an inert gas at a flow rate of 1-2.5 cm/s.

15. The method according to claim 1 , wherein the alkyl silicate vapor used in step (6) is heated to a temperature of 166-200° C.; the vapor deposition of step (6) is carried out in a reaction tube, and the alkyl silicate vapor is introduced into the reaction tube using an inert gas; the flow rate of the inert gas in the reaction tube is 0.05-2.0 cm/s, the reaction temperature is 166-200° C., the deposition time is 120-180 min, and the weight ratio of alkyl silicate to the silica gel carrier used in step (1) is 0.5-1:1.

16. The method according to claim 1 , wherein the calcination in step (7) is carried out in air atmosphere at a temperature of 500-700° C., with a calcination time of 30-120 min, and the flow rate of air is 0.5-1 cm/s.

17. The method according to claim 1 , wherein the silylanization reagent used for the silylanization treatment in step (8) is hexamethyl disilylamine, based on the weight of the silica gel carrier used in step (1), hexamethyl disilylamine is used in an amount of 5 wt %-15 wt %; the temperature of hexamethyl disilylamine used in step (8) is 126-150° C.; the silylanization treatment is carried out in a reaction tube, the silylanization reagent is introduced into the reaction tube using an inert gas, the flow rate of the inert gas in the reaction tube is 0.5-1 cm/s, the silylanization temperature is 200-300° C., and the silylanization time is 60-180 min.

18. A method for catalyzing propylene epoxidation to prepare propylene oxide, comprising contacting a feed with the catalyst prepared by the method according to claim 1 and recovering the propylene oxide.

19. The method according to claim 18 , wherein the contacting conditions for catalyzing propylene epoxidation to prepare propylene oxide are as follows: a reaction temperature of 40-120° C., a gauge pressure of 2-4.5 MPa, a molar ratio of propylene to ethylbenzene hydroperoxide of 3-10:1 and a mass space velocity of 1-5 h −1 .

20. The method according to claim 1 , wherein the titanium salt vapor is TiCl 4 vapor.

Assignees

• Wanhua Chemical Group Co Ltd

Inventors

• Wang Lei
• Wang Tongji
• Ye Fei
• Yang Lichao
• Yi Guangquan
• Cui Jiaoying
• Chu Naibo
• Li Yuan
• Hua Weiqi

Classifications

• B01J37/0201 Primary

  Impregnation · CPC title

• C07D301/19

  with organic hydroperoxides · CPC title

• C07D303/04

  containing only hydrogen and carbon atoms in addition to the ring oxygen atoms · CPC title

• B01J2231/72

  Epoxidation · CPC title

• B01J37/0238

  via the gaseous phase-sublimation · CPC title