Catalysts, processes for obtaining and processes for steam reforming

Patent metadata

Field	Value
Publication number	US-12017915-B2
Application number	US-202117399448-A
Country	US
Kind code	B2
Filing date	Aug 11, 2021
Priority date	Aug 20, 2020
Publication date	Jun 25, 2024
Grant date	Jun 25, 2024

Abstract

The present invention refers to processes for obtaining steam reforming catalysts containing nickel, cerium, lanthanum and copper oxides, free from potassium or alkali metals, preferably with the oxide layer being located externally with a thickness of less than 0.5 mm on the support particle, preferably the support being based on alumina, magnesium aluminate, hexaaluminates or mixtures thereof. The catalysts according to present invention show high activity, resistance to thermal deactivation and resistance to coke accumulation in the steam reforming reaction of hydrocarbons.

First claim

The invention claimed is:

1. A steam reforming catalyst comprising:
a) an inorganic oxide support selected from theta-alumina, magnesium aluminate, hexaaluminates, or a mixture thereof, having a surface area above 15 m 2 /g; and
b) a mixture of nickel, copper, lanthanum, and cerium oxides, with the total nickel content, expressed as nickel oxide (NiO) between 5 and 25% w/w; the copper content expressed as copper oxide (CuO) between 0.5 to 5% w/w, a Ni/(La+Ce) atomic ratio between 3 to 5 and a Ce/AI atomic ratio between 1 to 4;
wherein the inorganic oxide support comprises cylindrical or sphere-shaped particles.

2. The steam reforming catalyst according to claim 1 , wherein the inorganic oxide support has a surface area above 60 m 2 /g.

3. A process for obtaining the steam reforming catalyst of claim 1 , comprising the following steps:
a) preparing a solution in a polar solvent, of a nickel salt, in the form of nickel nitrate, acetate or carbonate together with copper, lanthanum, and cerium salts in the form of nitrates;
b) impregnating the solution containing the nickel, copper, cerium, and lanthanum salts in an inorganic oxide support selected from theta-alumina, magnesium aluminate, hexaaluminates, or a mixture thereof, by means of the wet spot technique or by placing the support of inorganic oxide in an excess of solution to form an impregnated material; and
c) drying the impregnated material in air, at a temperature ranging between 50° C. and 150° C., and for a time interval in a range of values between 1 and 24 hours, and then calcining the impregnated material in air at a temperature ranging between 250° C. and 650° C., and for a time interval in a range of values between 1 and 4 hours.

4. The process for obtaining the steam reforming catalyst according to claim 3 , wherein the polar solvent is water.

5. The process for obtaining the steam reforming catalyst according to claim 3 , wherein the final calcination step is replaced with a direct reduction comprising the following steps:
a) contacting the steam reforming catalyst with a flow of a reducing agent, selected from hydrogen, formaldehyde, methanol, or natural gas in the presence of water vapor at a temperature ranging from 300° C. to 800° C. and for a time interval in a range of values between 1 to 5 hours; and
b) cooling in a flow of N 2 and subjecting the reduced catalyst to an air flow at a temperature in a range of values between 20° C. to 100° C., and for a time interval in a range of values between 1 to 5 hours.

6. A process for obtaining the steam reforming catalyst of claim 1 , comprising the following steps:
a) preparing a solution in a polar solvent, of a nickel inorganic salt, in the form of nickel nitrate, acetate, or carbonate together with lanthanum and cerium salts in the form of nitrates;
b) impregnating the solution containing the nickel, cerium, and lanthanum salts in an inorganic oxide support selected from theta-alumina, magnesium aluminate, or hexaaluminates, by means of the wet spot technique or by placing the support of inorganic oxide in an excess of solution to form an impregnated material;
c) drying the impregnated material in air, at a temperature ranging between 50° C. and 150° C., and for a time interval in a range of values between 1 and 24 hours, and then calcining the impregnated material in air at a temperature ranging between 250° C. and 650° C., and for a time interval in a range of values between 1 and 4 hours;
d) preparing a solution in a polar solvent, of an inorganic copper salt, in the form of nitrate;
e) impregnating the material consisting of the inorganic oxide support and nickel, cerium, and lanthanum oxides with the solution containing the copper salt by means of the wet spot technique or by placing the inorganic oxide support in an excess of solution; and
f) drying the impregnated material in air, at a temperature ranging between 50° C. and 150° C., and for a time interval in a range of values between 1 and 24 hours, and then calcining the impregnated material in air at a temperature ranging between 250° C. and 650° C., and for a time interval in a range of values between 1 and 4 hours.

7. The process for obtaining the steam reforming catalyst according to claim 6 , wherein the polar solvent is water.

8. The process for obtaining the steam reforming catalyst according to claim 6 , wherein the final calcination step is replaced with a direct reduction comprising the following steps:
a) contacting the steam reforming catalyst with a flow of a reducing agent, selected from hydrogen, formaldehyde, methanol, or natural gas in the presence of water vapor at a temperature ranging from 300° C. to 800° C. and for a time interval in a range of values between 1 to 5 hours; and
b) cooling in a flow of N 2 and subjecting the reduced catalyst to an air flow at a temperature in a range of values between 20° C. to 100° C., and for a time interval in a range of values between 1 to 5 hours.

9. A process of steam reforming of hydrocarbon streams comprising conducting the hydrocarbon stream with the steam reforming catalyst of claim 1 , carried out in the presence of water vapor and hydrogen, temperatures ranging between 450° C. to 950° C., pressures between 10 kgf/cm 2 to 50 kgf/cm 2 and water vapor/carbon ratio between 1 to 5 mol/mol.

10. The process of steam reforming of hydrocarbon streams according to claim 9 , wherein the temperature ranges between 550° C. to 930° C., pressures between 20 kgf/cm 2 to 40 kgf/cm 2 and water vapor/carbon ratio between 2.5 to 3.5 mol/mol.

11. The process of steam reforming of hydrocarbon streams according to claim 9 , wherein the hydrocarbon stream comprises natural gas, liquefied petroleum gas, naphtha, or gases containing olefins.

12. A steam reforming catalyst comprising:
a) an inorganic oxide support selected from theta-alumina, magnesium aluminate, hexaaluminates, or a mixture thereof, having a surface area above 15 m 2 /g; and
b) a mixture of nickel, copper, lanthanum, and cerium oxides, with the total nickel content, expressed as nickel oxide (NiO) deposited on the outside of the support particles at a depth equal to or less than 1 mm, with the content nickel oxide in this layer ranging between 5 and 25% w/w; the copper content expressed as copper oxide (CuO) between 0.5 to 5% w/w, a Ni/(La+Ce) atomic ratio ranging between 3 to 5 and a Ce/AI atomic ratio ranging between 1 to 4;
wherein the inorganic oxide support comprises cylindrical or sphere-shaped particles.

13. The steam reforming catalyst according to claim 12 , wherein the inorganic oxide support has a surface area above 60 m 2 /g.

14. The steam reforming catalyst according to claim 12 , wherein the mixture of nickel, copper, lanthanum, and cerium oxides is deposited on the outside of the support particles at a depth equal to or less than 0.5 mm.

15. A process for obtaining the steam reforming catalyst of claim 12 , comprising the following steps:
a) impregnating the inorganic oxide support, selected from theta-alumina, magnesium aluminate, or hexaaluminates with a glycerine and water solution;
b) drying the inorganic support at a temperature ranging between 50° C. and 150° C. to remove the water;
c) impregnating the support with the pores partially occupied by glycerin with an aqueous solution of soluble salts of nickel, copper, lanthanum, and cerium using the wet spot technique; and
d) drying the inorganic oxide support at 50° C. to 150° C. for 1 to 4 hours and then calcining in air at 350° C. to 650° C. for 1 to 4 hours to obtain a layer of nickel, copper, lanthanum, and cerium oxides, located on the ou

Assignees

• Petroleo Brasileiro S A —Petrobras

Inventors

• Pontes Bittencourt Roberto Carlos

Classifications

• B01J35/40 Primary

  characterised by dimensions, e.g. grain size (in a colloidal state B01J35/23; crystallite size B01J35/77) · CPC title

• B01J35/613

  10-100 m2/g · CPC title

• B01J35/612

  less than 10 m2/g · CPC title

• B01J23/755

  Nickel · CPC title

• C01B2203/1058

  Nickel catalysts · CPC title