Method for preparing a nickel- and copper-based bimetallic catalyst for hydrogenating aromatic compounds

Patent metadata

Field	Value
Publication number	US-11364490-B2
Application number	US-201917048223-A
Country	US
Kind code	B2
Filing date	Apr 5, 2019
Priority date	Apr 18, 2018
Publication date	Jun 21, 2022
Grant date	Jun 21, 2022

Abstract

Method for preparing a catalyst comprising a bimetallic active phase made of nickel and copper, and a support comprising a refractory oxide, comprising the following steps:a step of bringing the support into contact with a solution containing a nickel precursor is carried out;a step of bringing the support into contact with a solution containing a copper precursor is carried out;a step of drying the catalyst precursor at a temperature lower than 250° C. is carried out;the catalyst precursor obtained is supplied to a hydrogenation reactor, and a step of reduction by bringing said precursor into contact with a reducing gas at a temperature lower than 200° C. for a period greater than or equal to 5 minutes and less than 2 hours is carried out.

First claim

The invention claimed is:

1. A method for preparing a catalyst for the hydrogenation of aromatic or polyaromatic compounds comprising a bimetallic active phase based on a first nickel metal element, in a proportion of 10 to 50% by weight of nickel element relative to the total weight of the catalyst, and a second copper metal element, in a proportion of 0.5 to 15% by weight of copper element relative to the total weight of the catalyst, the molar ratio between the copper and the nickel being less than 1, and a support comprising at least one refractory oxide chosen from silica, alumina and silica-alumina, said method comprising the following steps:
a) at least one step of bringing the support into contact with at least one solution containing at least one nickel precursor is carried out;
b) a step of bringing the support into contact with at least one solution containing at least one copper precursor is carried out;
the steps a) and b) being carried out separately in either order;
c) at least one step of drying the catalyst precursor at the end of step a) and b), orb) and a), at a temperature lower than 250° C. is carried out;
d) the catalyst precursor obtained at the end of step c) is supplied to a reactor for the hydrogenation of aromatic compounds, and a step of reduction by bringing said precursor into contact with a reducing gas at a temperature lower than 200° C. for a period greater than or equal to 5 minutes and less than 2 hours is carried out;
e) a step of passivation of the catalyst obtained in step d) with a sulfur compound is carried out.

2. The method as claimed in claim 1 , wherein step b) is carried out before step a).

3. The method as claimed in claim 1 , wherein step d) is carried out at a temperature of between 130 and 190° C.

4. The method as claimed in claim 1 , wherein step d) is carried out for between 10 minutes and 110 minutes.

5. The method as claimed in claim 1 , wherein step e) is carried out at a temperature of between 20 and 350° C. for 10 to 240 minutes.

6. The method as claimed in claim 1 ,
wherein, in step e), the sulfur compound is chosen from thiophene, thiophane, dimethyl sulfide, diethyl sulfide, dipropyl sulfide, propylmethyl sulfide and dithiodiethanol.

7. The method as claimed in claim 1 , wherein a step of drying the catalyst precursor is carried out between step a) and step b), at a temperature less than 250° C.

8. The method as claimed in claim 1 , wherein the copper content is between 0.5 and 12% by weight of copper element relative to the total weight of the catalyst.

9. The method as claimed in claim 1 , wherein the copper precursor is chosen from copper acetate, copper acetylacetonate, copper nitrate, copper sulfate, copper chloride, copper bromide, copper iodide or copper fluoride.

10. The method as claimed in claim 9 , wherein the copper precursor is copper nitrate.

11. The method as claimed in claim 1 , wherein the reducing gas of step d) is hydrogen.

12. The method as claimed in claim 11 , wherein the hydrogen flow rate, expressed in 1/hour/gram of catalyst precursor is between 0.01 and 100 1/hour/gram of catalyst precursor.

13. The method as claimed in claim 1 , wherein a step of heat treatment of the dried catalyst precursor obtained in step c) is carried out, before step d), at a temperature of between 250 and 1000° C.

14. The method as claimed in claim 1 , wherein the support is an alumina.

15. A method for the hydrogenation of at least one aromatic or polyaromatic compound present in a hydrocarbon feedstock having a final boiling point of less than or equal to 650° C., said method being carried out in the gas phase or in the liquid phase, at a temperature of between 30 and 350° C., at a pressure of between 0.1 and 20 MPa, at a hydrogen/(aromatic compounds to be hydrogenated) molar ratio between 0.1 and 10 and at an hourly space velocity HSV of between 0.05 and 50 h −1 , in the presence of a catalyst obtained as claimed in claim 1 .

Assignees

• Ifp Energies Now

Inventors

• Boualleg Malika
• Quoineaud Anne-Agathe

Classifications

• B01J21/04

  Alumina · CPC title

• B01J37/024

  Multiple impregnation or coating · CPC title

• C10G45/48

  containing nickel or cobalt metal, or compounds thereof · CPC title

• B01J23/755 Primary

  Nickel · CPC title

• B01J23/72

  Copper · CPC title