Catalyst comprising a support based on silico-aluminic matrix and on zeolite, preparation thereof and process for hydrocracking hydrocarbon feedstocks

Patent metadata

Field	Value
Publication number	US-2025058305-A1
Application number	US-202218722379-A
Country	US
Kind code	A1
Filing date	Dec 9, 2022
Priority date	Dec 21, 2021
Publication date	Feb 20, 2025
Grant date	—

Abstract

The invention describes a catalyst comprising at least one hydro/dehydrogenating element chosen from the group formed by the elements from group VIB and from group VIII of the periodic table, alone or as a mixture, and a support comprising at least one zeolite and one amorphous silica-alumina, wherein the zeolite has an acid site distribution index (ASDI) of greater than 0.15 and a density of acid sites (determined by H/D exchange) of between 0.05 and 1 mmol/g, and wherein the support has a pore volume, measured by nitrogen porosimetry, developed within the pores with a diameter of between 6 nm and 11 nm, of less than 0.5 ml/g, a grain density, measured by mercury displacement under a pressure of 0.003 MPa, of greater than 0.93 g/ml, and a tapped packing density (TPD) of greater than 0.5 g/ml and less than 0.65 g/ml. A further subject of the present invention relates to the process for preparing said catalyst, comprising at least one step of preparing a silica-alumina gel by mixing a silica precursor with a specific alumina precursor, and to a process for hydrocracking a hydrocarbon feedstock in the presence of said catalyst.

First claim

1 . Catalyst comprising at least one hydro/dehydrogenating element chosen from the group formed by the elements from group VIB and from group VIII of the periodic table, alone or as a mixture, and a support comprising at least one zeolite and one amorphous silica-alumina, wherein the support has:
a pore volume, measured by nitrogen porosimetry, developed within the pores with a diameter of between 6 nm and 11 nm, of less than 0.5 ml/g, a grain density, measured by mercury displacement under a pressure of 0.003 MPa, of greater than 0.93 g/ml, a tapped packing density (TPD) of greater than 0.5 g/ml and less than 0.65 g/ml.

2 . Catalyst according to claim 1 , wherein the content in the catalyst of element from group VIII is between 0.03% and 15% by weight of oxide relative to the total weight of said catalyst, preferably between 0.5% and 10% by weight of oxide and very preferably between 1.0% and 8% by weight of oxide, and the content in the catalyst of element from group VIB is between 1% and 50% by weight of oxide relative to the total weight of said catalyst, preferably between 5% and 40% by weight of oxide, and more preferably still between 10% and 35% by weight of oxide.

3 . Catalyst according to claim 1 , wherein the element from group VIII is nickel and the element from group VIB is tungsten.

4 . Catalyst according to claim 1 , wherein the zeolite is chosen from Y, USY, VUSY, SDUSY, mordenite, beta, EU-1, EU-2, EU-11, Nu-87, ZSM-48 or ZBM-30 zeolites.

5 . Catalyst according to claim 4 , wherein the zeolite is chosen from Y, ultrastable Y(USY), very ultrastable Y(VUSY) or dealuminated ultrastable Y(SDUSY) zeolites.

6 . Catalyst according to claim 1 , wherein the zeolite has an acid site distribution index (ASDI) determined by H/D exchange of greater than 0.15.

7 . Catalyst according to claim 1 , wherein the zeolite has a volume developed within the pores with a diameter of greater than 50 nm, and measured by nitrogen physisorption, which represents less than 15% and preferably less than 10% of the total pore volume.

8 . Catalyst according to claim 1 , wherein the support has a pore volume, measured by nitrogen physisorption, contained within the pores with a diameter of greater than 6 nm and less than 11 nm, of between 0.05 and 0.45 ml/g and preferably of between 0.1 and 0.35 ml/g.

9 . Catalyst according to claim 1 , wherein the support also comprises a binder consisting of at least one refractory oxide chosen from the group formed by alumina, silica-alumina, clay, titanium oxide, boron oxide and zirconia, taken alone or as a mixture; and preferably the binder is alumina.

10 . Catalyst according to claim 1 , wherein the content by weight of silica-alumina in the catalyst is generally between 1% and 99% relative to the total weight of said catalyst, advantageously between 10% and 85% by weight, and preferably between 40% and 75% by weight.

11 . Catalyst according to claim 1 , wherein the content by weight of zeolite in the catalyst is generally between 0.1% and 30% relative to the total weight of said catalyst, advantageously between 0.2% and 20% by weight, preferably between 0.5% and 10% by weight, more preferably between 1% and 9% by weight and more preferably still between 1.5% and 8% by weight.

12 . Process for preparing the catalyst according to claim 1 , comprising at least the following steps:
a) a step of preparing a silica-alumina gel by mixing a silica precursor with an alumina precursor, said alumina precursor having:
a dispersibility index of between 15% and 70%,
a sodium content of between 0.003% and 2% by weight, relative to the total mass of the alumina precursor,
a sulfur content of between 0.005% and 2% by weight, relative to the total mass of the alumina precursor,
b) a step of mixing at least one zeolite with the silica-alumina gel resulting from step a), said zeolite having an acid site distribution index (ASDI) measured by H/D exchange of greater than 0.15, c) a step of shaping, optionally in the presence of an aluminic binder, of the mixture obtained, d) at least one step of drying the shaped material, e) at least one step of heat and/or hydrothermal treatment of the dried material to obtain the support, f) a step of introducing onto the support at least one hydro/dehydrogenating element chosen from the group formed by the elements from group VIB of the periodic table and the non-noble elements from group VIII of the periodic table, g) at least one step of drying the impregnated support, e) and optionally at least one step of heat and/or hydrothermal treatment of the impregnated and dried support to obtain said catalyst.

13 . Process for hydrocracking at least one hydrocarbon feedstock, preferably in liquid form, of which at least 50% by weight of the compounds have a boiling point greater than 300° C. and less than 650° C., at a temperature of between 200° C. and 480° C., at a total pressure of between 1 MPa and 25 MPa, with a ratio of volume of hydrogen per volume of hydrocarbon feedstock of between 80 and 5000 litres per litre and at an hourly space velocity (HSV) defined by the ratio of the volume flow rate of hydrocarbon feedstock, which is preferably liquid, per the volume of catalyst charged into the reactor of between 0.1 and 50 h −1 , in the presence of the catalyst according to claim 1 .

Assignees

• Ifp Energies Now

Inventors

• Dubreuil Anne-Claire
• Lambert Arnold
• Rivallan Mickael
• Pirngruber Gerhard

Classifications

• B01J2235/00

  Indexing scheme associated with group B01J35/00, related to the analysis techniques used to determine the catalysts form or properties · CPC title

• B01J2235/10

  Infrared [IR] · CPC title

• B01J2235/15

  X-ray diffraction · CPC title

• B01J35/80

  characterised by their amorphous structures · CPC title

• B01J35/30

  characterised by their physical properties · CPC title