Catalyst to attain low sulfur gasoline

Patent metadata

Field	Value
Publication number	US-10252247-B2
Application number	US-201715434896-A
Country	US
Kind code	B2
Filing date	Feb 16, 2017
Priority date	Feb 21, 2008
Publication date	Apr 9, 2019
Grant date	Apr 9, 2019

Abstract

This invention relates to a hydrodesulfurization catalyst, a method for preparing the catalyst, and a method for the preparation of low sulfur gasoline fuel with minimal loss of RON. The catalyst particles include a group VIB metal and a support material having relatively high surface area, and optionally includes one or more group VIIIB metal. The method for preparing the catalyst allows for greater loading of the active metal species on the surface of the support material under aqueous reaction conditions.

First claim

We claim:

1. A method for preparing a hydrodesulfurization catalyst comprising:
placing an activated carbon catalyst support that is not acidic under vacuum;
heating the activated carbon catalyst support under vacuum to a temperature of up to 100° C., the vacuum at a pressure of 1 torr or less;
preparing an aqueous solution comprising a first metal salt, a second metal salt, and water;
introducing, after placing the activated carbon catalyst support under vacuum, the aqueous solution to the activated carbon catalyst support, such that the aqueous solution and activated carbon catalyst support are under vacuum;
removing the water from the solution under vacuum and collecting the catalyst particles;
calcinating the catalyst particles by heating the catalyst particles to a temperature of greater than 200° C.; and
partially sulfiding the catalyst particles by contacting the calcined catalyst particles with a liquid hydrocarbon comprising dimethyldisulfide at a temperature of 320° C.

2. The method of claim 1 , wherein the first metal salt comprises molybdenum.

3. The method of claim 1 , wherein the second metal salt comprises a metal selected from the group consisting of iron, ruthenium, osmium, cobalt, rhenium, iridium, nickel, palladium, and platinum.

4. The method of claim 1 , wherein the first metal salt comprises molybdenum and the second metal salt comprises cobalt, wherein the calcinated catalyst particles comprise 25% by weight molybdenum oxide and 6.2% by weight cobalt oxide.

5. The method of claim 1 , wherein the step of calcinating the solid catalyst particles comprises heating the particle in the presence of oxygen to a temperature greater than 300° C.

6. The method of claim 1 wherein the molar concentration of the first metal and the second metal in solution is between about 0.001 and 1.5 M.

7. The method of claim 1 wherein the molar ratio of the first metal to the second metal is between 1.5:1 and 5:1.

8. The method of claim 1 wherein the activated carbon support has a surface area of greater than 1000 m 2 /g.

9. The method of claim 1 wherein the weight ratio of the oxide form of the first metal to the activated carbon catalyst support is greater than about 15% by weight.

10. The method of claim 1 wherein the weight ratio of the oxide form of the second metal to the activated carbon catalyst support is between about 4% and 10% by weight.

11. A method of preparing a desulfurization catalyst comprising:
placing an activated carbon catalyst support that is not acidic under vacuum;
heating the activated carbon catalyst support under vacuum to a temperature of up to 100° C., the vacuum at a pressure of 1 torr or less;
preparing a first mixture comprising a first metal salt and water;
introducing, after placing the activated carbon catalyst support under vacuum, the first mixture to the activated carbon catalyst support, such that the aqueous solution and activated carbon catalyst support are under vacuum;
removing the water under vacuum from the first mixture to produce a solid catalyst precursor;
preparing a second mixture comprising a second metal salt, water, and the solid catalyst precursor;
removing the water under vacuum from the second mixture to produce catalyst particles;
calcinating the catalyst particles by heating the particles in an oxygen containing atmosphere to a temperature of 320° C. at a rate of 2° C. per minute; and
sulfiding the calcinated catalyst particles to a sulfur content of 2.5% by weight.

12. The method of claim 11 wherein the surface area of the activated carbon catalyst support that is not acidic is about 250 m2/g to about 500 m2/g.

13. The method of claim 11 , wherein the first metal salt comprises molybdenum.

14. The method of claim 11 , wherein the second metal salt comprises a metal selected from the group consisting of iron, ruthenium, osmium, cobalt, rhenium, iridium, nickel, palladium, and platinum.

15. The method of claim 11 , wherein the first metal salt comprises molybdenum and the second metal salt comprises cobalt, wherein the calcinated catalyst particles comprise 25% by weight molybdenum oxide and 6.2% by weight cobalt oxide.

Assignees

• Saudi Arabian Oil Co

Inventors

• Choi Ki-Hyouk
• Al-Ghamdi Sameer Ali
• Al-Shareef Ali H
• Al-Hamadah Ali H

Classifications

• B01J37/0236

  Drying, e.g. preparing a suspension, adding a soluble salt and drying · CPC title

• B01J23/652

  Chromium, molybdenum or tungsten · CPC title

• B01J23/883

  and nickel · CPC title

• B01J23/28

  Molybdenum · CPC title

• C10G45/04

  characterised by the catalyst used · CPC title