Method for rejuvenating a catalyst of a hydroprocessing and/or hydrocracking process

Patent metadata

Field	Value
Publication number	US-11779908-B2
Application number	US-201917414209-A
Country	US
Kind code	B2
Filing date	Dec 10, 2019
Priority date	Dec 18, 2018
Publication date	Oct 10, 2023
Grant date	Oct 10, 2023

Abstract

The invention concerns a method for rejuvenating an at least partially used catalyst originating from a hydroprocessing and/or hydrocracking process, the at least partially used catalyst being derived from a fresh catalyst comprising at least one group VIII metal (in particular, Co), at least one group VIB metal (in particular, Mo), an oxide support, and optionally phosphorus, the method comprising the steps: ⋅a) regenerating the at least partially used catalyst in a gas stream containing oxygen at a temperature between 300° C. and 550° C. so as to obtain a regenerated catalyst, ⋅b) then placing the regenerated catalyst in contact with phosphoric acid and an organic acid, each having acidity constant pKa greater than 1.5, ⋅c) performing a drying step at a temperature less than 200° C. without subsequently calcining it, so as to obtain a rejuvenated catalyst.

First claim

The invention claimed is:

1. A process for the rejuvenation of an at least partially spent catalyst resulting from a hydrotreating and/or hydrocracking process, said at least partially spent catalyst resulting from a fresh catalyst comprising at least one metal from group VIII, at least one metal from group VIb, an oxide support, and optionally phosphorus, said process comprising
a) regenerating the at least partially spent catalyst in an oxygen-containing gas stream at a temperature of between 300° C. and 550° C., so as to obtain a regenerated catalyst,
b) bringing said regenerated catalyst into contact with an aqueous impregnation solution, which contains only water, phosphoric acid and an organic acid, wherein phosphoric acid and the organic acid each have an acidity constant pKa greater than 1.5,
c) then drying said regenerated catalyst in a drying stage at a temperature of less than 200° C., without subsequently calcining said regenerated catalyst, so as to obtain a rejuvenated catalyst.

2. The process as claimed in claim 1 , wherein the organic acid is chosen from acetic acid, maleic acid, malic acid, malonic acid, gluconic acid, tartaric acid, citric acid, γ-ketovaleric acid, lactic acid, pyruvic acid, ascorbic acid, and succinic acid.

3. The process as claimed in claim 1 , wherein the organic acid is an organic acid having each an acidity constant pKa greater than 3.5.

4. The process as claimed in claim 1 , wherein the organic acid added per metal/metals from group VIb present in the regenerated catalyst molar ratio is between 0.01 and 5 mol/mol.

5. The process as claimed in claim 1 , wherein in b) the phosphorus added per metal from group VIb already present in the regenerated catalyst molar ratio is between 0.01 and 5 mol/mol.

6. The process as claimed in claim 1 , wherein the fresh catalyst has a content of metal from group VIb of between 1% and 40% by weight of oxide of said metal from group VIb, with respect to the weight of the catalyst, and a total content of metal from group VIII of between 1% and 10% by weight of oxide of said metal from group VIII, with respect to the weight of the catalyst.

7. The process as claimed in claim 1 , wherein the fresh catalyst contains phosphorus, the total content of phosphorus being between 0.1% and 20% by weight, expressed as P 205 , with respect to the total weight of the catalyst.

8. The process as claimed in claim 1 , wherein the oxide support of the rejuvenated catalyst is chosen from aluminas, silica, silica-aluminas or titanium or magnesium oxides, used alone or as a mixture with alumina or silica-alumina.

9. The process as claimed in claim 1 , wherein a) is preceded by a deoiling stage which comprises bringing an at least partially spent catalyst resulting from a hydrotreating and/or hydrocracking process into contact with a stream of inert gas at a temperature of between 300° C. and 400° C.

10. The process as claimed in claim 1 , in which the rejuvenated catalyst is subjected to a sulfidation stage after c).

11. A process for hydrotreating and/or hydrocracking of hydrocarbon cuts, comprising subjecting said hydrocarbon cuts to hydrotreating and/or hydrocracking in the presence of a catalyst obtained according to the process of claim 1 .

12. The process as claimed in claim 1 , wherein the fresh catalyst has a content of metal from group VIb of between 1% and 35% by weight of oxide of said metal from group VIb, with respect to the weight of the catalyst, and a total content of metal from group VIII of between 1.5% and 9% by weight of oxide of said metal from group VIII, with respect to the weight of the catalyst.

13. The as claimed in claim 1 , wherein the fresh catalyst a molar ratio of the metal from group VIII to metal from group VIb of between 0.1 and 0.8.

14. The process as claimed in claim 1 , wherein the regenerated catalyst has a specific surface of between 5 and 400 m 2 /g, and a pore volume of between 0.1 cm3/g and 1.5 cm3/g.

15. The process as claimed in claim 1 , wherein c) is carried out at a temperature of between 50° C. and 180° C.

16. The process as claimed in claim 1 , wherein c) is carried out for a duration of between 5 minutes and 4 hours.

17. The process as claimed in claim 1 , wherein the total content of phosphorus in the rejuvenated catalyst is generally between 0.3% and 25% by weight of P 2 O 5 , with respect to the total weight of catalyst.

Assignees

• Ifp Energies Now

Inventors

• Devers Elodie

Classifications

• B01J27/285 Primary

  of catalysts comprising compounds of phosphorus · CPC title

• B01J21/04

  Alumina · CPC title

• B01J27/19

  Molybdenum · CPC title

• B01J38/02

  Heat treatment · CPC title

• B01J38/12

  Treating with free oxygen-containing gas · CPC title