Mesoporous and macroporous nickel-based catalyst having a median macropore diameter of greater than 200 nm and its use with regard to hydrogenation

Patent metadata

Field	Value
Publication number	US-10618033-B2
Application number	US-201515318615-A
Country	US
Kind code	B2
Filing date	Jun 9, 2015
Priority date	Jun 13, 2014
Publication date	Apr 14, 2020
Grant date	Apr 14, 2020

Abstract

The invention relates to a supported catalyst that comprises an oxide substrate that is for the most part calcined aluminum and an active phase that comprises nickel, with the nickel content being between 5 and 65% by weight of said element in relation to the total mass of the catalyst, with said active phase not comprising a metal from group VIB, the nickel particles having a diameter that is less than or equal to 20 nm, said catalyst having a median mesopore diameter of between 8 nm and 25 nm, a median macropore diameter of greater than 200 nm, a mesopore volume that is measured by mercury porosimetry that is greater than or equal to 0.30 mL/g, and a total pore volume that is measured by mercury porosimetry that is greater than or equal to 0.34 mL/g. The invention also relates to the method for preparation of said catalyst and its use in a hydrogenation method.

First claim

The invention claimed is:

1. Supported catalyst that comprises an oxide substrate that is 90% or more by weight of calcined aluminum with respect to the total weight of the matrix and an active phase that comprises nickel, with the nickel content being between 5 and 65% by weight of said element in relation to the total mass of the catalyst, with said active phase not comprising a metal from group VIB, the nickel particles having a diameter that is less than or equal to 20 nm, said catalyst having a median mesopore diameter of between 8 nm and 25 nm, a median macropore diameter that is greater than 200 nm, a mesopore volume that is measured by mercury porosimetry that is greater than or equal to 0.30 mL/g, and a total pore volume that is measured by mercury porosimetry that is greater than or equal to 0.34 mL/g,
wherein the catalyst has a macropore volume in the range 20% to 35% of the total pore volume, and
wherein the catalyst includes NiO crystallites with diameters of 15.6 nm to 16.2 nm.

2. Catalyst according to claim 1 , in which the nickel content is between 10 and 34% by weight of said element in relation to the total mass of the catalyst.

3. Catalyst according to claim 1 , in which the mesopore volume of the catalyst is between 0.35 mL/g and 0.8 mL/g.

4. Catalyst according to claim 1 , which does not contain micropores.

5. Method for preparation of a catalyst according to claim 1 , comprising the following steps:
a) A step for solublization of an acid precursor of aluminum that is selected from among aluminum sulfate, aluminum chloride, and aluminum nitrate in water, at a temperature of between 20 and 90° C., at a pH of between 0.5 and 5, for a period of between 2 and 60 minutes,
b) A step for adjustment of the pH by adding into the suspension that is obtained in step a) at least one basic precursor that is selected from among sodium aluminate, potassium aluminate, ammonia, sodium hydroxide, and potassium hydroxide, at a temperature of between 20 and 90° C., and at a pH of between 7 and 10, for a period of between 5 and 30 minutes,
c) A step for co-precipitation of the suspension that is obtained at the end of step b) by adding into the suspension at least one basic precursor that is selected from among sodium aluminate, potassium aluminate, ammonia, sodium hydroxide, and potassium hydroxide, and at least one acid precursor that is selected from among aluminum sulfate, aluminum chloride, aluminum nitrate, sulfuric acid, hydrochloric acid, and nitric acid, at least one of the basic or acid precursors comprising aluminum, with the relative flow rate of the acid and basic precursors being selected in such a way as to obtain a pH of the reaction medium of between 7 and 10, and the flow rate of the acid and basic precursor(s) containing aluminum being regulated in such a way as to obtain a final alumina concentration in the suspension of between 10 and 38 g/L,
d) A step for filtering the suspension that is obtained at the end of step c) of co-precipitation for obtaining an alumina gel,
e) A step for drying said alumina gel that is obtained in step d) for obtaining a powder,
f) A shaping step,
g) A step of heat treatment that is carried out between steps e) and f) or after step f) at a temperature of between 500 and 1000° C., with or without the presence of an air stream containing up to 60% by volume of water for obtaining a calcined aluminum porous oxide substrate,
h) A step for impregnating said substrate with a solution that comprises the salt(s) of the precursor(s) of the nickel-based active phase,
i) A step for drying the impregnated substrate at a temperature of between 15 and less than 250° C., in such a way as to obtain a dried catalyst,
j) Optionally a heat treatment of said dried catalyst at a temperature of between 250 and 1000° C. with or without the presence of water.

6. Method according to claim 5 , in which at least one step k) of reducing treatment is carried out in the presence of a reducing gas after steps i) or j) in such a way as to obtain a catalyst that comprises nickel at least partially in metallic form.

7. Method according to claim 6 , in which a step 1) of passivation is carried out by a sulfur-containing compound or an oxidized compound or by CO 2 before or after step k) of reducing treatment.

8. Method according to claim 5 , in which the concentration of alumina of the alumina gel suspension obtained in step c) is between 13 and 35 g/L.

9. Method according to claim 5 , in which the acid precursor of steps a) and c) is selected from among aluminum sulfate, aluminum chloride, and aluminum nitrate, and in which the basic precursor of steps a) and c) is selected from among sodium aluminate and potassium aluminate.

10. Hydrogenation method in which a catalyst prepared according to claim 5 is brought into contact in the presence of hydrogen with a hydrocarbon feedstock that contains polyunsaturated molecules and/or aromatic compounds in such a way as to obtain an at least partially hydrogenated effluent.

11. Hydrogenation method according to claim 10 , in which a selective hydrogenation is carried out at a temperature of between 0 and 500° C., at a pressure of between 0.1 and 20 MPa, at a hydrogen/(polyunsaturated compounds to be hydrogenated) molar ratio of between 0.1 and 10, and at an hourly volumetric flow rate of between 0.1 and 200 h −1 for a liquid feedstock, between 100 and 15000 h −1 for a gaseous feedstock of a hydrocarbon feedstock that contains polyunsaturated compounds that contain at least 2 carbon atoms per molecule and that have a final boiling point that is less than or equal to 250° C.

12. Hydrogenation method according to claim 10 , in which hydrogenation of the aromatic compounds is carried out at a temperature of between 30 and 350° C., at a pressure of between 0.1 and 20 MPa, at a hydrogen/(aromatic compounds to be hydrogenated) molar ratio of between 0.1 and 10, and at an hourly volumetric flow rate of between 0.05 and 50 h −1 of a hydrocarbon feedstock that contains aromatic compounds and that has a final boiling point that is less than or equal to 650° C.

Assignees

• Ifp Energies Now

Inventors

• Boualleg Malika
• Dubreuil Anne-Claire
• Maille Emily
• Thomazeau Cecile

Classifications

• B01J23/835

  with germanium, tin or lead · CPC title

• C07C5/10

  of aromatic six-membered rings · CPC title

• C10G45/48

  containing nickel or cobalt metal, or compounds thereof · CPC title

• C07C5/03

  of non-aromatic carbon-to-carbon double bonds · CPC title

• B01J37/031

  Precipitation · CPC title