Multi-metallic bulk hydroprocessing catalysts

Patent metadata

Field	Value
Publication number	US-2022401931-A1
Application number	US-202217736169-A
Country	US
Kind code	A1
Filing date	May 4, 2022
Priority date	Jun 22, 2021
Publication date	Dec 22, 2022
Grant date	—

Abstract

Multi-metallic bulk catalysts and methods for synthesizing the same are provided. The multi-metallic bulk catalysts contain nickel, molybdenum tungsten, yttrium, and optionally, copper, titanium and/or niobium. The catalysts are useful for hydroprocessing, particularly hydrodesulfurization and hydrodenitrogenation, of hydrocarbon feedstocks.

First claim

1 . A bulk catalyst precursor comprising:
(a) 1 to 60 wt. % of Ni, on a metal oxide basis; (b) 1 to 40 wt. % of Mo, on a metal oxide basis; (c) 5 to 80 wt. % of W, on a metal oxide basis; (d) 0.01 to 30 wt. % of Y, on a metal oxide basis; (e) 0 to 20 wt. % of Cu, on a metal oxide basis; (f) 0 to 45 wt. % of Ti, on a metal oxide basis; and (g) 0 to 20 wt. % of Nb, on a metal oxide basis.

2 . The bulk catalyst precursor of claim 1 , further comprising an organic compound-based component.

3 . The bulk catalyst precursor of claim 2 , wherein the organic compound-based component is selected from the group of an organic acid or salt thereof, a sugar, a sugar alcohol, or a combination thereof.

4 . The bulk catalyst precursor of claim 2 , wherein the organic compound-based component is selected from the group of glyoxylic acid, pyruvic acid, lactic acid, malonic acid, oxaloacetic acid, malic acid, fumaric acid, maleic acid, tartaric acid, gluconic acid, citric acid, oxamic acid, serine, aspartic acid, glutamic acid, iminodiacetic acid, ethylenediaminetetraacetic acid, fructose, glucose, galactose, mannose, sucrose, lactose, maltose, erythritol, xylitol, mannitol, sorbitol, or a combination thereof.

5 . The bulk catalyst precursor of claim 2 , wherein a molar ratio of Ni to the organic compound-based component is in a range of 3:1 to 20:1.

6 . The bulk catalyst precursor of claim 1 , wherein a molar ratio of Y/(Ni+Mo+W+Cu+Ti+Nb) is in a range of from 10:1 to 1:100.

7 . The bulk catalyst precursor of claim 1 , wherein a molar ratio of Ni/W is in a range of 10:1 to 1:10.

8 . The bulk catalyst precursor of claim 1 , wherein a molar ratio of W/Mo is in a range of 100:1 to 1:100.

9 . The bulk catalyst precursor of claim 1 , wherein the bulk catalyst precursor is of formula:
A v [Ni 1-a-b-c Y a Cu b Nb c (OH) x (L)P y ] z [Mo m W 1-m O 4 ][Ti(OH) n O 2-n/2 ] w
wherein:
(i) A is an alkali metal cation, a rare earth metal cation, an ammonium cation, an organic ammonium cation, phosphonium cation, or a combination thereof;
(ii) L is an organic compound-based component; and
(iii) 0<a<1; 0≤b<1; 0≤c<1; a+b+c<1; 0<y≤2/p; 0<x<2; 0≤v<2; 0<z; 0<m<1; 0<n<4; 0≤w/(z+1)<10.

10 . The bulk catalyst precursor of claim 1 , further comprising 1 to 15 wt. % of a binder.

11 . The bulk catalyst precursor of claim 1 , having one or more of the following properties: a BET specific surface area of from 50 to 250 m 2 /g; a pore volume of from 0.02 to 0.80 cm 3 /g; and particle density of 1.00 to 3.00 cm 3 /g.

12 . A sulfided bulk catalyst characterized in that it is a bulk catalyst precursor according to claim 1 that has been sulfided.

13 . A method for preparing the bulk catalyst precursor of claim 1 , the method comprising:
(a) combining in a reaction mixture:
(i) a Ni-containing precursor;
(ii) a Mo-containing precursor;
(iii) a W-containing precursor;
(iv) a Y-containing precursor;
(v) optionally, a Cu-containing precursor, a Ti-containing precursor and/or a Nb-containing precursor;
(vi) optionally, an organic compound-based component; and
(vii) a protic liquid; and
(b) reacting the mixture under conditions sufficient to cause precipitation of the bulk catalyst precursor; wherein the steps to prepare the bulk catalyst precursor are carried out at a temperature of no more than 200° C.

14 . The method of claim 13 , wherein the reaction mixture is prepared by:
preparing a first mixture comprising a Ni-containing precursor, a Y-containing precursor, an optional Cu-containing precursor, an optional Nb-containing precursor, a protic liquid, and an optional organic compound-based component; preparing a second mixture comprising a Mo-containing precursor, a W-containing precursor, and a protic liquid; optionally, adding a Ti-containing precursor to the first mixture, the second mixture, or a combination thereof; heating both the first and second mixtures to a temperature of from 60° C. to 150° C.; combining the first and second mixtures together.

15 . The method of claim 14 , wherein the Ti-containing precursor is selected from TiO 2 nanoparticles, colloidal TiO 2 , fumed TiO 2 , titanium hydroxide, organotitanium compounds, titanium halides, organotitanium halides, water-soluble titanium salts, or a combination thereof.

16 . A method for preparing the bulk catalyst precursor of claim 1 , the method comprising:
(a) combining in a reaction mixture:
(i) a Ni-containing precursor;
(ii) a Mo-containing precursor;
(iii) a W-containing precursor;
(iv) a Y-containing precursor;
(v) optionally, a Cu-containing precursor and/or a Nb-containing precursor;
(vi) optionally, an organic compound-based component; and
(vii) a protic liquid; and
(b) reacting the mixture under conditions sufficient to cause precipitation of an intermediate bulk catalyst precursor; and (c) compositing the intermediate bulk catalyst precursor with a Ti-containing precursor to form the bulk catalyst precursor; wherein the steps to prepare the bulk catalyst precursor are carried out at a temperature of no more than 200° C.

17 . The method of claim 16 , wherein the reaction mixture is prepared by:
preparing a first mixture comprising a Ni-containing precursor, a Y-containing precursor, an optional Cu-containing precursor, an optional Nb-containing precursor, a protic liquid, and an optional organic compound-based component; preparing a second mixture comprising a Mo-containing precursor, a W-containing precursor, and a protic liquid; heating both the first and second mixtures to a temperature of from 60° C. to 150° C.; and combining the first and second mixtures together.

18 . The method of claim 16 , wherein the Ti-containing precursor is selected from TiO 2 nanoparticles, fumed TiO 2 , or a combination thereof.

19 . The method of claim 16 , wherein the intermediate bulk catalyst precursor is a Ni—Mo—W—Y, Ni—Mo—W—Y—Cu, Ni—Mo—W—Y—Nb, or Ni—Mo—W—Y—Cu—Nb bulk catalyst precursor.

20 . The method of claim 13 or claim 16 , wherein the reacting is carried out at one or more temperatures either (a) in a range of 60° C. to 100° C. under atmospheric pressure or (b) above 100° C. under autogenous pressure.

21 . The method of claim 13 or claim 16 , wherein the organic compound-based component is selected from an organic acid or salt thereof, a sugar, a sugar alcohol, or a combination thereof.

22 . The method of claim 21 , wherein the organic compound-based component is selected from glyoxylic acid, pyruvic acid, lactic acid, malonic acid, oxaloacetic acid, malic acid, fumaric acid, maleic acid, tartaric acid, gluconic acid, citric acid, oxamic acid, serine, aspartic acid, glutamic acid, iminodiacetic acid, ethylenediaminetetraacetic acid, fructose, glucose, galactose, mannose, sucrose, lactose, maltose, erythritol, xylitol, mannitol, sorbitol, or a combination thereof.

23 . The method of claim 13 or claim 16 , further comprising one or more of the following steps:
compositing the bulk catalyst precursor with 0 to 40 wt. % with a material selected from the group of binder materials, conventional hydroprocessing catalysts, cracking compounds, or mixtures thereof;
spray-drying, (flash) drying, milling, kneading, slurry-mixing, dry or wet mixing, or combinations thereof;
shaping,
drying and/or thermally treating at a temperature of no more than 200° C.; or
sulfiding.

24 . A process for hydroprocessing a hyd

Assignees

• Chevron Usa Inc

Inventors

• Ouyang Xiaoying
• Kuperman Alexander E

Classifications

• B01J37/20

  Sulfiding · CPC title

• B01J37/0205

  in several steps · CPC title

• B01J23/8871

  Rare earth metals or actinides · CPC title

• B01J37/0203

  the impregnation liquid containing organic compounds · CPC title

• B01J23/8885 Primary

  containing also molybdenum · CPC title