Hydroprocessing catalysts and their production

Patent metadata

Field	Value
Publication number	US-10022712-B2
Application number	US-201414269497-A
Country	US
Kind code	B2
Filing date	May 5, 2014
Priority date	Jun 1, 2010
Publication date	Jul 17, 2018
Grant date	Jul 17, 2018

Abstract

The precursor of a hydroprocessing catalyst is made by impregnating a metal oxide component comprising at least one metal from Group 6 of the Periodic Table and at least one metal from Groups 8-10 of the Periodic Table with an amide formed from a first organic compound containing at least one amine group, and a second organic compound containing at least one carboxylic acid group. Following impregnation heat treatment follows to form in situ generated unsaturation additional to that in the two organic compounds. The catalyst precursor is sulfided to form an active, sulfide hydroprocessing catalyst.

First claim

The invention claimed is:

1. An amide-containing catalyst precursor comprising an oxide from of at least one metal from Group 6, an oxide from of at least one metal from Groups 8-10 impregnated with a pre-formed amide, wherein the amide-containing catalyst precursor is made according to a process comprising:
(a) impregnating a catalyst precursor composition comprising a metal oxide from of (i) at least one metal from Group 6 of the Periodic Table of the Elements and (ii) at least one metal from Groups 8-10 of the Periodic Table of the Elements with a pre-formed amide made from a first organic compound containing at least one amine group and a second organic compound containing at least one carboxylic acid group, to form an organically treated catalyst precursor; and
(b) heating the organically treated catalyst precursor at a temperature from about 190° C. to about 275° C. for a time sufficient to form additional in situ unsaturated carbon atoms not present in the first or second organic compounds, or both, but not for so long that the amide substantially decomposes;
wherein the catalyst precursor composition exhibits a ratio of chemical functionalities, as measured according to peak area ratios using transmission infrared spectroscopic techniques of a deconvoluted peak centered from about 1700 cm −1 to about 1730 cm −1 , compared to a deconvoluted peak centered from about 1380 cm −1 to about 1450 cm −1 , of at least 0.9.

2. The amide-containing catalyst precursor of claim 1 in which the first organic compound comprises 10 to 30 carbon atoms, the second organic compound comprises 10 to 30 carbon atoms, the Group 6 metal is nickel and the Group 8 metal is tungsten.

3. The amide-containing catalyst precursor of claim 2 in which the pre-formed amide is made using a ratio of the first organic compound to the second organic compound of nominally 1:1.

4. The amide-containing catalyst precursor of claim 2 in which the pre-formed amide is made using a molar excess of the first organic compound to the second organic compound.

5. A sulfided hydroprocessing catalyst composition made by performing steps (a) and (b) of claim 1 to form an amide-containing catalyst precursor, and then sulfiding the amide-containing catalyst precursor.

6. A catalyst precursor composition comprising a metal oxide from of (i) at least one metal from Group 6 of the Periodic Table of the Elements and at least one metal from Groups 8-10 of the Periodic Table of the Elements, and an impregnated, pre-formed amide formed from (i) a first organic compound containing at least one amine group, and (ii) a second organic compound separate from said first organic compound and containing at least one carboxylic acid group; wherein the catalyst precursor composition exhibits a ratio of chemical functionalities, as measured according to peak area ratios using transmission infrared spectroscopic techniques of a deconvoluted peak centered from about 1700 cm −1 to about 1730 cm −1 , compared to a deconvoluted peak centered from about 1380 cm −1 to about 1450 cm −1 , of at least 0.9.

7. A catalyst precursor composition according to claim 6 which contains in situ formed unsaturated carbon atoms.

8. A catalyst precursor composition according to claim 6 which exhibits a ratio of chemical functionalities, as measured according to peak area ratios using transmission infrared spectroscopic techniques of a deconvoluted peak centered from about 1700 cm −1 to about 1730 cm −1 , compared to a deconvoluted peak centered from about 1380 cm −1 to about 1450 cm −1 , from 0.9 to 15.

9. The catalyst precursor composition of claim 6 in which the metal oxide from Group 6 is an oxide of Mo, W, or a combination thereof, and the metal oxide from Groups 8-10 is an oxide of Co, Ni, or a combination thereof.

10. The catalyst precursor composition of claim 6 in which the first organic compound comprises at least 10 carbon atoms and/or the second organic compound comprises at least 10 carbon atoms.

11. The catalyst precursor composition of claim 10 in which the first organic compound comprises a primary monoamine having from 10 to 30 carbon atoms, and/or the second organic compound comprises only one carboxylic acid group and has from 10 to 30 carbon atoms.

12. A sulfided hydroprocessing catalyst, comprising a sulfide from of (i) at least one metal from Group 6 of the Periodic Table of the Elements and (ii) at least one metal of a metal from Groups 8-10 of the Periodic Table of the Elements, and an impregnated, heat treated organic prepared by sulfiding the amide-containing catalyst precursor composition catalyst precursor composition of claim 6 .

13. A sulfided hydroprocessing catalyst composition according to claim 12 which exhibits a layered structure comprising a plurality of stacked YS 2 layers, where Y is the Group 6 metal(s), such that the average number of stacks from about 1.1 to about 3.5.

14. A sulfided hydroprocessing catalyst composition according to claim 13 in which the number of stacks is less than that obtained with an equivalent sulfided mixed metal (oxide) containing precursor composition produced without the amide and the heat treatment.

Assignees

• Exxonmobil Res & Eng Co

Inventors

• Soled Stuart L
• Miseo Sabato
• Baumgartner Joseph E
• Nistor Iulian
• Nandi Partha
• Guzman Javier
• Levin Doron
• Wilson Keith
• Bergweff Jacob Arie
• Huiberts Ronald Jan
• Van Loevezijn Arnold

Classifications

• B01J2531/64

  Molybdenum · CPC title

• C11B3/02

  by chemical reaction {(C11B3/003 takes precedence)} · CPC title

• B01J37/08

  Heat treatment {(B01J37/0009, B01J37/0018 take precedence)} · CPC title

• B01J23/883

  and nickel · CPC title

• B01J23/882

  and cobalt · CPC title