Mesoporous composite of molecular sieves for hydrocracking of heavy crude oils and residues

Patent metadata

Field	Value
Publication number	US-10030202-B2
Application number	US-201815878626-A
Country	US
Kind code	B2
Filing date	Jan 24, 2018
Priority date	Nov 6, 2012
Publication date	Jul 24, 2018
Grant date	Jul 24, 2018

Abstract

A hydrocracking catalyst having a support of a composite of mesoporous materials, molecular sieves and alumina, is used in the last bed of a multi-bed system for treating heavy crude oils and residues and is designed to increase the production of intermediate distillates having boiling points in a temperature range of 204° C. to 538° C., decrease the production of the heavy fraction (>538° C.), and increase the production of gasoline fraction (<204° C.). The feedstock to be processed in the last bed contains low amounts of metals and is lighter than the feedstock that is fed to the first catalytic bed.

First claim

What is claimed is:

1. A method for treating heavy crude oils and residues comprising the steps of;
feeding the heavy crude oil feedstock containing residues to a hydrocracking reaction zone of a reactor in the presence of a catalyst support obtained from boehmite, zeolite Y, and SBA-15 in a molar ratio of 60-85:5-15:10-35, respectively, and where said catalyst has a cylindrical shape and includes 3-15 wt % of a Group VIB metal comprising molybdenum as molybdenum oxide or molybdenum sulfide and 1-5 wt % of a Group VIII metal comprising nickel as nickel oxide or nickel sulfide, said catalyst having a specific surface area of 150-300 m 2 /g, an average pore diameter of 6.0 to 15.0 nm, a pore volume of 0.2 to 0.7 cm 3 /g, and a pore distribution of 20% of pores having a diameter of up to 5 nm, 70 to 85% of pores having a diameter of 5 to 50 nm, and less than 5% of pores having a diameter greater than 50 nm, and a total acidity at 100° C. equivalent to 180 to 360 micromoles of pyridine per gram of catalyst; and
hydrocracking the heavy crude oil feedstock in the presence of said catalyst to obtain a reaction product.

2. The method of claim 1 , wherein said reaction product has an increased API gravity with respect to said heavy crude oil feedstock.

3. The method of claim 1 , wherein said catalyst has a cylindrical shape with a diameter of 1.59 mm and a length of 2-7 mm.

4. The method of claim 1 , further comprising subjecting said heavy crude oil feedstock to a demetallization step, desulfurization step, denitrogenation step and combinations thereof prior to feeding to said hydrocracking reaction zone.

5. The method of claim 1 , wherein the support is prepared by mechanical blending of a boehmite, zeolite and SBA-15, which is peptized with nitric acid, extruded, and calcined.

6. The method of claim 5 , wherein the support is impregnated with a solution of ammonium heptamolybdate and nickel nitrate to obtain a Mo and Ni impregnated catalyst.

7. The method of claim 1 , wherein said Mo and said Ni are present in a molar ratio of Mo/Ni+Mo=0.3.

8. The method of claim 1 , wherein said catalyst has 74-85% of the pores with a diameter in the range of 5-50 nm.

9. The method of claim 1 , wherein said catalyst has a pore diameter of 6-12 nm.

10. The method of claim 1 , wherein said catalyst comprised 9-12 wt % molybdenum and 2.8-4.4 wt % nickel.

11. The method of claim 1 , wherein said catalyst has surface area of 220-235 m 2 /g.

12. The method of claim 11 , wherein said catalyst has a pore volume of 0.3-0.6 cm3/g, and average pore diameter of 6.6-9.2 nm, and a pore distribution of <5 nm in an amount of 13.6-23.3 vol %, 5-50 nm in an amount of 75.6-84.8 vol %, and >50 nm in an amount of 1.3-3.0 vol %.

13. The method of claim 1 , wherein said catalyst has a molybdenum concentration of 10 wt % and a nickel concentration of 2.6 wt %.

14. The method of claim 1 , wherein said catalyst comprised 74-85% of pores in a range of 5-50 nm.

15. The method of claim 1 , wherein said reactor is a multizone reactor, wherein the feedstock is subjected to hydrodemetallization and/or hydrodemetallization/hydrodesulfurization in a first zone and then to said hydrocracking in a second zone.

16. The method of claim 15 , wherein the second zone is operated at a temperature between 360 and 380° C. and the catalyst has hydrogenating ability and low to moderate acidity to perform the cracking of molecules with high molecular weight in the feed to the second zone.

17. The method of claim 16 , wherein the second zone is operated at a temperature ≥to 400° C. to increase the production of intermediate distillates.

18. The method of claim 16 , wherein the temperature is increased from 360 to 410° C.

19. A method for hydrocracking heavy crude oils and residues to increase production of intermediate distillates and increase an API gravity relative to a heavy crude oil feed, comprising the steps of:
feeding the heavy crude oil feed to a hydrocracking zone of a reactor and reacting the heavy crude oil feed in the presence of a catalyst comprising a catalyst support and obtaining a reaction produce, wherein the catalyst is obtained from boehmite, zeolite Y, and SBA-15 in a molar ratio of 60-85:5-15; 10-35, Mo and Ni, and is prepared by a method of
preparing a support by combining boehmite, zeolite Y, and SBA-15 in amounts of 60-85 wt %, 5-15 wt % and 10-35 wt %, respectively, peptizing the resulting mixture, drying the mixture and calcining to obtain the support, and
impregnating said support with a solution of ammonium heptamolybdate and nickel nitrate, drying the impregnated support, and calcining to obtain said catalyst containing Mo and Ni, wherein said catalyst comprises 3-15 wt % of molybdenum as molybdenum oxide or molybdenum sulfide and 1-5 wt % of nickel as nickel oxide or nickel sulfide, said catalyst having a specific surface area of 150-300 m 2 /g, an average pore diameter of 6.0 to 15.0 nm and a pore volume of 0.2 to 0.7 cm 3 /g, and a pore distribution of 20% of a pore volume of pores of 0 to 5 nm, 70 to 85% of its pore volume of pores of 5 to 50 nm and less than 5% of said pore volume in pores with diameter greater than 50 nm, and a total acidity at 100° C., equivalent to 180 to 360 micromoles of pyridine per gram of catalyst.

20. The method of claim 19 , further comprising subjecting said heavy crude oil feedstock to a demetallization step, desulfurization step, denitrogenation step and combinations thereof prior to feeding to said hydrocracking reaction zone.

Assignees

• Mexicano Inst Petrol

Inventors

• Rayo Mayoral Patricia
• Ancheyta Juarez Jorge
• Marroquin Sanchez Gustavo Jesus
• Centeno Nolasco Guillermo
• Ramirez Solis Jorge Fernando

Classifications

• B01J29/084

  Y-type faujasite · CPC title

• B01J37/08

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

• C10G45/10

  containing platinum group metals or compounds thereof · CPC title

• C10G47/18

  the catalyst containing platinum group metals or compounds thereof · CPC title

• C10G45/12

  containing crystalline alumino-silicates, e.g. molecular sieves · CPC title