Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J38/00—Regeneration or reactivation of catalysts, in general
  • B01J38/04—Gas or vapour treating; Treating by using liquids vaporisable upon contacting spent catalyst
  • B01J38/12—Treating with free oxygen-containing gas
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
  • B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
  • B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
  • B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
  • B01J23/85—Chromium, molybdenum or tungsten
  • B01J23/88—Molybdenum
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
  • B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
  • B01J21/04—Alumina
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
  • B01J23/90—Regeneration or reactivation
  • B01J23/94—Regeneration or reactivation of catalysts comprising metals, oxides or hydroxides of the iron group metals or copper
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
  • B01J27/02—Sulfur, selenium or tellurium; Compounds thereof
  • B01J27/04—Sulfides
  • B01J27/047—Sulfides with chromium, molybdenum, tungsten or polonium
  • B01J27/051—Molybdenum
  • B01J27/0515—Molybdenum with iron group metals or platinum group metals
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
  • B01J27/14—Phosphorus; Compounds thereof
  • B01J27/185—Phosphorus; Compounds thereof with iron group metals or platinum group metals
  • B01J27/1853—Phosphorus; Compounds thereof with iron group metals or platinum group metals with iron, cobalt or nickel
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
  • B01J27/14—Phosphorus; Compounds thereof
  • B01J27/186—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
  • B01J27/188—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium with chromium, molybdenum, tungsten or polonium
  • B01J27/19—Molybdenum
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
  • B01J27/28—Regeneration or reactivation
  • B01J27/285—Regeneration or reactivation of catalysts comprising compounds of phosphorus
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
  • B01J37/12—Oxidising
  • B01J37/14—Oxidising with gases containing free oxygen
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
  • B01J37/20—Sulfiding
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J38/00—Regeneration or reactivation of catalysts, in general
  • B01J38/02—Heat treatment
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J38/00—Regeneration or reactivation of catalysts, in general
  • B01J38/48—Liquid treating or treating in liquid phase, e.g. dissolved or suspended
  • B01J38/60—Liquid treating or treating in liquid phase, e.g. dissolved or suspended using acids
  • B01J38/62—Liquid treating or treating in liquid phase, e.g. dissolved or suspended using acids organic
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
  • C07C5/02—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation
  • C07C5/10—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation of aromatic six-membered rings
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
  • C10G45/02—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing
  • C10G45/04—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used
  • C10G45/06—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used containing nickel or cobalt metal, or compounds thereof
  • C10G45/08—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used containing nickel or cobalt metal, or compounds thereof in combination with chromium, molybdenum, or tungsten metals, or compounds thereof
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G47/00—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
  • C10G47/02—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions characterised by the catalyst used
  • C10G47/10—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions characterised by the catalyst used with catalysts deposited on a carrier
  • C10G47/12—Inorganic carriers
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
  • C07C2523/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
  • C07C2523/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups C07C2523/02 - C07C2523/36
  • C07C2523/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups C07C2523/02 - C07C2523/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
  • C07C2523/85—Chromium, molybdenum or tungsten
  • C07C2523/88—Molybdenum
  • C07C2523/883—Molybdenum and nickel

Definitions

• the invention relates to a process for rejuvenating a hydrotreating and/or hydrocracking catalyst and the use of the rejuvenated catalyst in the field of hydrotreating and/or hydrocracking.
• a hydrotreatment catalyst for hydrocarbon cuts aims to eliminate the sulfur or nitrogen compounds contained therein in order to bring, for example, a petroleum product to the required specifications (sulfur content, aromatic content, etc.) for a given application (automobile fuel, gasoline or diesel, domestic fuel oil, jet fuel).
• Conventional hydrotreatment catalysts generally include an oxide support and an active phase based on Group VI B and VIII metals in their oxide forms as well as phosphorus.
• the preparation of these catalysts generally includes a step of impregnation of metals and phosphorus on the support, followed by drying and calcination to obtain the active phase in their oxide forms.
• these catalysts are generally subjected to sulfurization in order to form the active species.
• the catalyst is deactivated by accumulation of coke and/or sulfur compounds or compounds containing other heteroelements on the surface of the catalyst. After a certain period, replacement is therefore necessary.
• the rejuvenation process consists of re-impregnating the regenerated catalyst with a solution containing metal precursors in the presence or absence of organic or inorganic additives. These so-called rejuvenation processes are well known to those skilled in the art in the field of middle distillates.
• Patent US 7,956,000 in particular describes a rejuvenation process bringing into contact a catalyst comprising a metal oxide from group VI B and a metal oxide from group VIII with an acid and an organic additive whose boiling point is between 80 and 500°C and a solubility in water of at least 5 grams per liter (20°C, atmospheric pressure), possibly followed by drying under conditions such that at least 50% of the additive is maintained in the catalyst.
• the hydrotreating catalyst may be a fresh hydrotreating catalyst or a spent hydrotreating catalyst that has been regenerated.
• the objective of the present invention is to propose an improvement of the rejuvenation process described in FR 3 089 826 by carrying out controlled regeneration in a precise temperature range.
• the invention relates to a process for rejuvenating an at least partially spent catalyst resulting from a hydrotreatment and/or hydrocracking process, said at least partially spent catalyst coming from a fresh catalyst comprising at least one metal of the group VIII, at least one metal from group VIB, an oxide support not comprising zeolite, and optionally phosphorus, said process comprises the following steps: a) the at least partially spent catalyst is regenerated in a gas flow containing oxygen at a temperature between 360°C and less than 420°C so as to obtain a regenerated catalyst comprising a carbon content of between 0.1 and 0.5% by weight, a sulfur content of between 0, 3 and 0.8% by weight and a proportion of crystalline phase originating from at least one metal from group VIII and from at least one metal from group VIB determined by X-ray diffraction and characterized by a ratio between the surface of the peak of diffraction of the crystal at 26.6°, 20 and the surface of the characteristic peak of alumina at 45.7°, 20 less than 0.6, b)
• regeneration is carried out to remove coke and/or sulfur compounds and/or other heteroelements which have accumulated in the catalyst during its use.
• the disappearance of coke and other impurities by regeneration makes it possible to unclog the pores of the catalyst and thus make the active phase accessible to the charge again.
• regeneration at too high a temperature causes a crystalline phase to appear resulting from at least one metal from group VIII and at least one metal from group VIB (for example nickel molybdate NiMoCL and/or cobalt molybdate CoMoCU) which is form by sintering the oxide precursors of the active phase composed of group VIII metals and/or group VIB metals.
• group VIB for example nickel molybdate NiMoCL and/or cobalt molybdate CoMoCU
• the choice of regeneration temperature is therefore antagonistic. On the one hand the temperature must be high enough to remove the coke and/or other impurities in order to release access to the active phase, and on the other hand the temperature must not be too high finally to avoid the formation of the crystalline phase.
• the regeneration temperature conditions must therefore be chosen in order to obtain a regenerated catalyst which contains between 0.1 and 0.5% by weight of carbon, between 0.3 and 0.8% by weight of sulfur, and a proportion of phase crystalline originating from at least one metal from group VIII and from at least one metal from group VIB determined by X-ray diffraction and characterized by a ratio between the surface of the diffraction peak of the crystal at 26.6° 20 and the surface of the characteristic peak of alumina at 45.7° 20 less than 0.6.
• the regeneration temperature conditions which make it possible to obtain such a solid are between 360°C and less than 420°C.
• Such rejuvenation thus seems to allow good dissolution of the crystalline phase and dispersion of the metallic phases in order to recover a dispersion close to the fresh catalyst and therefore an activity close to the fresh catalyst, and this without it being necessary to add metals of the active phase.
• the increase in catalytic performance can be observed on catalysts based on cobalt or nickel, but particularly on catalysts based on nickel.
• the temperature necessary to reach a desired sulfur or nitrogen content is close to that of the fresh catalyst.
• the temperature of step a) is between 380 and 410°C.
• the proportion of crystalline phase originating from at least one metal from group VIII and from at least one metal from group VI B determined by X-ray diffraction and characterized by a ratio between the surface of the diffraction peak of the crystal at 26.6° 20 and the characteristic peak area of alumina at 45.7° 20 in step a) is less than 0.50.
• the organic acid used in step b) is chosen from acetic acid, maleic acid, malic acid, malonic acid, gluconic acid, tartaric acid, citric acid, y-ketovaleric acid, lactic acid, pyruvic acid, ascorbic acid or succinic acid.
• the organic acid used in step b) is an organic acid having each acidity constant pKa greater than 3.5.
• the organic acid used in step b) is chosen from gluconic acid, y-ketovaleric acid, lactic acid, pyruvic acid, ascorbic acid or succinic acid.
• the molar ratio of organic acid added per metal/group VI B metals present in the regenerated catalyst is between 0.01 to 5 mol/mol.
• the fresh catalyst has a Group VI B metal content of between 1 and 40% by weight of oxide of said Group VI B metal relative to the weight of the catalyst and a total Group VIII metal content of between 1 and 10% by weight of oxide of said Group VIII metal relative to the weight of the catalyst.
• the fresh catalyst contains phosphorus, the total phosphorus content being between 0.1 and 20% by weight expressed as P2O5 relative to the total weight of the catalyst.
• the oxide support not comprising zeolite is chosen from aluminas, silica, silica-alumina or even titanium or magnesium oxides used alone or in mixture with alumina or silica-alumina.
• the rejuvenated catalyst resulting from step c) contains a proportion of crystalline phase originating from at least one metal from group VIII and from at least one metal from group VIB determined by X-ray diffraction and characterized by a ratio between the peak area of diffraction of the crystal at 26.6°, 20 and the surface of the characteristic peak of alumina at 45.7°, 20 less than 0.4.
• the regeneration step a) is preceded by a de-oiling step which comprises bringing an at least partially spent catalyst resulting from a hydrotreatment and/or hydrocracking process into contact with a current. of inert gas at a temperature between 300°C and 400°C.
• the rejuvenated catalyst is subjected to a sulfurization step after step c).
• the invention also relates to the use of the rejuvenated catalyst prepared according to the process of the invention in a process for hydrotreating and/or hydrocracking hydrocarbon cuts.
• the expressions "between ... and " and “between .... and " are equivalent and mean that the limit values of the interval are included in the range of values described . If this were not the case and the limit values were not included in the range described, such precision will be provided by the present invention.
• the different parameter ranges for a given step such as the pressure ranges and the temperature ranges can be used alone or in combination.
• a range of preferred pressure values can be combined with a range of more preferred temperature values.
• group VIII (or VIIIB) according to the CAS classification corresponds to the metals of columns 8, 9 and 10 according to the new IIIPAC classification.
• the pressures are absolute pressures, also denoted abs., and are given in absolute MPa (or abs. MPa), unless otherwise indicated.
• the metal content is measured by X-ray fluorescence.
• hydrotreatment is meant reactions including in particular hydrodesulfurization (HDS), hydrodenitrogenation (HDN) and hydrogenation of aromatics (HDA).
• HDS hydrodesulfurization
• HDN hydrodenitrogenation
• HDA hydrogenation of aromatics
• the rejuvenated catalyst obtained by the process according to the invention comes from an at least partially spent catalyst, itself from a fresh catalyst, used in a process of hydrotreatment and/or hydrocracking of hydrocarbon cuts for a period of time. certain period of time and which presents an activity significantly lower than the fresh catalyst which requires its replacement.
• the fresh catalyst used in a hydrotreatment and/or hydrocracking process of hydrocarbon cuts is known to those skilled in the art. It comprises at least one metal from Group VIII, at least one metal from Group VIB, an oxide support not comprising zeolite, and optionally phosphorus and/or an organic compound as described below.
• the group VI B metal present in the active phase of the fresh catalyst is preferably chosen from molybdenum and tungsten.
• the Group VIII metal present in the active phase of the fresh catalyst is preferably chosen from cobalt, nickel and the mixture of these two elements.
• the active phase of the fresh catalyst is preferably chosen from the group formed by the combination of the elements nickel-molybdenum, cobalt-molybdenum, nickel-tungsten, nickel-molybdenum-tungsten and nickel-cobalt-molybdenum, and very preferably the phase active consists of cobalt and molybdenum, nickel and molybdenum, nickel and tungsten or a nickel-molybdenum-tungsten combination.
• the active phase consists of nickel and molybdenum.
• the Group VIII metal content is between 1 and 10% by weight, preferably between 1.5 and 9% by weight, and more preferably between 2 and 8% by weight expressed as Group VIII metal oxide relative to the weight. total fresh catalyst.
• the metal content of group VIB is between 1 and 40% by weight, preferably between 1 and 35% by weight, and more preferably between 2 and 30% by weight expressed as metal oxide of group VIB relative to the total weight of the fresh catalyst.
• the phosphorus/(group VIB metal) molar ratio is generally between 0.08 and 1, preferably between 0.1 and 0.9, and very preferably between 0.15 and 0.8 .
• the oxide support not comprising zeolite of the fresh catalyst is usually a porous solid chosen from the group consisting of: aluminas, silica, alumina silicas or even titanium or magnesium oxides used alone or in mixture with the alumina or silica alumina.
• the oxide support not comprising zeolite is a support based on alumina or silica or silica-alumina.
• the oxide support not comprising zeolite is based on alumina, it contains more than 50% by weight of alumina relative to the total weight of the support and, generally speaking, it contains only alumina or silica-alumina as defined below.
• the oxide support not comprising zeolite comprises alumina, and preferably extruded alumina.
• the alumina is gamma alumina.
• the alumina support advantageously has a total pore volume of between 0.1 and 1.5 cm 3 . g'1 , preferably between 0.4 and 1.1 cm 3 . g'1 .
• the total pore volume is measured by mercury porosimetry according to the ASTM D4284 standard with a wetting angle of 140°, as described in the work Rouquerol F.; Rouquerol J.; Singh K. “Adsorption by Powders & Porous Solids: Principle, methodology and applications”, Academic Press, 1999, for example using an Autopore IIITM model device from the MicromeriticsTM brand.
• the specific surface area of the alumina support is advantageously between 5 and 400 m 2 .g' 1 , preferably between 10 and 350 m 2 .g' 1 , more preferably between 40 and 350 m 2 .g' 1 .
• the specific surface area is determined in the present invention by the BET method according to standard ASTM D3663, method described in the same work cited above.
• the oxide support is a silica-alumina containing at least 50% by weight of alumina relative to the total weight of the support.
• the silica content in the support is at most 50% by weight relative to the total weight of the support, most often less than or equal to 45% by weight, preferably less than or equal to 40%.
• the sources of silicon are well known to those skilled in the art. Examples include silicic acid, silica in powder form or in colloidal form (silica sol), tetraethylorthosilicate Si(OEt) 4 .
• the support of said catalyst is based on silica, it contains more than 50% by weight of silica relative to the total weight of the support and, generally, it contains only silica.
• the oxide support consists of alumina, silica or silica-alumina.
• the support is advantageously in the form of balls, extrudates, pellets or irregular and non-spherical agglomerates whose specific shape can result from a crushing step.
• the fresh catalyst may also further comprise at least one organic compound containing oxygen and/or nitrogen and/or sulfur before sulfurization.
• organic compound is chosen from a compound comprising one or more chemical functions chosen from a carboxylic function, alcohol, thiol, thioether, sulfone, sulfoxide, ether, aldehyde, ketone, ester, carbonate, amine, nitrile, imide, oxime, urea and amide or even compounds including a furan cycle or even sugars.
• the organic compound containing oxygen may be one or more chosen from compounds comprising one or more chemical functions chosen from a carboxylic function, alcohol, ether, aldehyde, ketone, ester or carbonate or even compounds including a furanic cycle or even sugars.
• the organic compound containing oxygen may be one or more chosen from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, a polyethylene glycol (with a molecular weight between 200 and 1500 g /mol), propylene glycol, 2-butoxyethanol, 2-(2-butoxyethoxy)ethanol, 2-(2-methoxyethoxy)ethanol, triethylene glycol dimethyl ether, glycerol, acetophenone, 2,4-pentanedione, pentanone, acetic acid, maleic acid, malic acid, malonic acid, oxalic acid, gluconic acid, tartaric acid, citric acid, y-ketovaleric acid, a succinate of dialkyl 01-04, and more particularly dimethyl succinate, methyl acetoacetate, ethyl acetoacetate, 2-methoxyethyl 3-oxobutanoate, 2-methacryloyloxyethyl 3-oxobutano
• the organic compound containing nitrogen may be one or more chosen from compounds comprising one or more chemical functions chosen from an amine or nitrile function.
• the organic compound containing nitrogen may be one or more chosen from the group consisting of ethylenediamine, diethylenetriamine, hexamethylenediamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, acetonitrile , octylamine, guanidine or a carbazole.
• the organic compound containing oxygen and nitrogen may be one or more chosen from compounds comprising one or more chemical functions chosen from a carboxylic acid, alcohol, ether, aldehyde, ketone, ester, carbonate, amine function. , nitrile, imide, amide, urea or oxime.
• the organic compound containing oxygen and nitrogen may be one or more chosen from the group consisting of 1,2-cyclohexanediaminetetraacetic acid, monoethanolamine (MEA), 1- methyl-2-pyrrolidinone, dimethylformamide, ethylenediaminetetraacetic acid (EDTA), alanine, glycine, nitrilotriacetic acid (NTA), N-(2-hydroxyethyl)ethylenediamine-N,N',N acid '-triacetic acid (HEDTA), diethylene-triaminepentaacetic acid (DTPA), tetramethylurea, glutamic acid, dimethylglyoxime, bicine, tricine, 2-methoxyethyl cyanoacetate, 1-ethyl-2-pyrrolidinone, 1-vinyl-2-pyrrolidinone, 1,3-dimethyl-2-imidazolidinone, 1-(2-hydroxyethyl)-2-pyrrolidinone, 1-(2-hydroxye
• the organic compound containing sulfur may be one or more chosen from compounds comprising one or more chemical functions chosen from a thiol, thioether, sulfone or sulfoxide function.
• the organic compound containing sulfur may be one or more chosen from the group consisting of thioglycolic acid, 2,2'-thiodiethanol, 2-hydroxy-4-methylthiobutanoic acid, a sulfonated derivative of a benzothiophene or a sulfoxidized derivative of a benzothiophene, methyl 3-(methylthio)propanoate and ethyl 3-(methylthio)propanoate.
• the organic compound contains oxygen, and more preferably, it contains only oxygen as a heteroatom.
• it is chosen from y-valerolactone, 2-acetylbutyrolactone, triethylene glycol, diethylene glycol, ethylene glycol, ethylenediaminetetraacetic acid (EDTA), maleic acid, malonic acid, citric acid, gluconic acid, dimethyl succinate, glucose, fructose, sucrose, sorbitol, xylitol, y-ketovaleric acid, dimethylformamide, 1-methyl-2-pyrrolidinone, propylene carbonate, 2-methoxyethyl 3-oxobutanoate, bicine , tricine, 2-furaldehyde (also known as furfural), 5-hydroxymethylfurfural (also known as 5-(hydroxymethyl)-2-furaldehyde or 5-HMF), 2-acetylfuran, 5- methyl-2-furaldehyde, ascorbic acid, butyl
• the content of organic compound(s) containing oxygen and/or nitrogen and/or sulfur on the fresh catalyst is between 1 and 30% by weight, preferably between 1.5 and 25%. weight, and more preferably between 2 and 20% by weight relative to the total weight of the fresh catalyst.
• the preparation of the fresh catalyst is known and generally comprises a step of impregnation of metals from group VIII and group VIB and optionally phosphorus and/or the organic compound on the oxide support not comprising zeolite, followed by a drying, then an optional calcination to obtain the active phase in their oxide forms.
• the fresh catalyst is generally subjected to sulfurization in order to form the active species as described below.
• the impregnation step of the preparation of the fresh catalyst can be carried out either by impregnation in slurry, or by excess impregnation, or by dry impregnation, or by any other means known to those skilled in the art.
• the sources of molybdenum can use oxides and hydroxides, molybdic acids and their salts, in particular ammonium salts such as ammonium molybdate, ammonium heptamolybdate, phosphomolybdic acid (H3PM012O40), and their salts, and optionally silicomolybdic acid (H4SiMoi204o) and its salts.
• the sources of molybdenum can also be any heteropolycompound of the Keggin type, lacunar Keggin, substituted Keggin, Dawson, Anderson, Strandberg, for example.
• Molybdenum trioxide and heteropolycompounds of the Keggin, lacunar Keggin, substituted Keggin and Strandberg type are preferably used.
• the tungsten precursors which can be used are also well known to those skilled in the art.
• tungstic acids and their salts can be used, in particular ammonium salts such as ammonium tungstate, ammonium metatungstate, phosphotungstic acid and their salts. salts, and possibly silicotungstic acid (H 4 SiWi 2 04o) and its salts.
• the sources of tungsten can also be any heteropolycompound of the Keggin type, lacunar Keggin, substituted Keggin, Dawson, for example.
• Ammonium oxides and salts are preferably used, such as ammonium metatungstate or heteropolyanions of the Keggin, lacunar Keggin or substituted Keggin type.
• cobalt precursors which can be used are advantageously chosen from oxides, hydroxides, hydroxycarbonates, carbonates and nitrates, for example. Cobalt hydroxide and cobalt carbonate are preferably used.
• the nickel precursors which can be used are advantageously chosen from oxides, hydroxides, hydroxycarbonates, carbonates and nitrates, for example. Nickel hydroxide and nickel hydroxycarbonate are preferably used.
• the preferred phosphorus precursor is orthophosphoric acid H3PO4, but its salts and esters such as ammonium phosphates are also suitable. Phosphorus can also be introduced at the same time as the element(s) of group VI B in the form of Keggin, lacunar Keggin, substituted Keggin or Strandberg type heteropolyanions.
• the impregnation step includes several implementation modes. They are distinguished in particular by the moment of the introduction of the organic compound when it is present and which can be carried out either at the same time as the impregnation of the compound comprising a metal of group VIB (co-impregnation), or after (post -impregnation), or before (pre-impregnation). In addition, the implementation methods can be combined.
• the impregnated support is allowed to mature.
• Any maturation step is advantageously carried out at atmospheric pressure, in an atmosphere saturated with water and at a temperature between 17°C and 50°C, and preferably at room temperature. Generally, a maturation period of between ten minutes and forty-eight hours and preferably between thirty minutes and six hours is sufficient.
• the impregnation solution may comprise any polar solvent known to those skilled in the art. Said polar solvent used is advantageously chosen from the group formed by methanol, ethanol, water, phenol, cyclohexanol, taken alone or as a mixture.
• Said polar solvent can also be advantageously chosen from the group formed by propylene carbonate, DMSO (dimethylsulfoxide), N-methylpyrrolidone (NMP) or sulfolane, taken alone or as a mixture.
• a polar protic solvent is used.
• the solvent used is water or ethanol, and particularly preferably, the solvent is water. In one possible embodiment, the solvent may be absent in the impregnation solution.
• the catalyst is subjected to a drying step at a temperature below 200°C, advantageously between 50°C and 180°C, preferably between 70°C and 150°C, very preferably between 75°C and 130°C, without subsequent calcination step.
• the drying step is preferably carried out under an inert atmosphere or under an atmosphere containing oxygen.
• the fresh catalyst has not undergone calcination during its preparation, that is to say the impregnated catalytic precursor has not been subjected in a heat treatment step at a temperature above 200°C under an inert atmosphere or under an atmosphere containing oxygen, in the presence of water or not.
• the fresh catalyst underwent a calcination step during its preparation, that is to say the impregnated catalytic precursor was subjected to a heat treatment step at a temperature between 200 and 1000°C and preferably between 250 and 750°C, for a period typically between 15 minutes and 10 hours, under an inert atmosphere or under an atmosphere containing oxygen, in the presence of water or not.
• the at least partially spent catalyst is composed of the oxide support not comprising zeolite and the active phase formed of at least one metal from group VI B and at least one metal from group VIII and optionally the phosphorus of the catalyst fresh, as well as carbon, sulfur and optionally other contaminants from the charge such as silicon, arsenic and metals.
• the contents of Group VI B metal, Group VIII metal and phosphorus in the fresh, at least partially spent, regenerated or rejuvenated catalyst are expressed in oxides after correction for the loss on ignition of the catalyst sample at 550° C for two hours in a muffle oven. Loss on ignition is due to the loss of moisture, carbon, sulfur and/or other contaminants. It is determined according to ASTM D7348.
• the contents of group VIB metal, group VIII metal and optionally phosphorus in the at least partially spent catalyst are substantially identical to the contents of the fresh catalyst from which it comes.
• substantially identical we mean that each of the metallic elements mentioned is present in the same proportions as in the initial fresh catalyst to within 5% relative.
• coal or "carbon” in the present application designates a hydrocarbon-based substance deposited on the surface of the hydrotreatment catalyst at least partially spent during its use, strongly cyclized and condensed and having an appearance similar to graphite.
• the at least partially spent catalyst contains in particular carbon at a content generally greater than or equal to 2% by weight, preferably between 2% and 25% by weight, and even more preferably between 4 and 16% by weight relative to the weight. total catalyst at least partially worn.
• the at least partially spent catalyst contains in particular sulfur at a content generally greater than or equal to 2% by weight, preferably between 2% and 25% by weight, and even more preferably between 4 and 16% by weight relative to the weight. total catalyst at least partially worn.
• the rejuvenation process according to the invention of the at least partially spent catalyst comprises a step of eliminating coke and sulfur (regeneration step).
• the at least partially spent catalyst is regenerated in a gas flow containing oxygen at a temperature between 360°C and less than 420°C so as to obtain a catalyst regenerated comprising a carbon content of between 0.1 and 0.5% by weight, a sulfur content of between 0.3 and 0.8% by weight and a proportion of crystalline phase derived from at least one metal from group VIII and of at least one metal from group VI B determined by ° 20 less than 0.6.
• the regeneration is preferably not carried out by retaining the catalyst loaded in the hydrotreatment reactor (in-situ regeneration).
• the at least partially spent catalyst is therefore extracted from the reactor and sent to a regeneration installation in order to carry out regeneration in said installation (ex-situ regeneration).
• Regeneration step a) is preferably preceded by a de-oiling step.
• the de-oiling step generally comprises bringing the at least partially spent catalyst into contact with a stream of inert gas (that is to say essentially free of oxygen), for example in an atmosphere of nitrogen or the like, at a temperature between 300°C and 400°C, preferably between 300°C and 350°C.
• the flow rate of inert gas in terms of flow rate per unit volume of the catalyst is 5 to 150 NL.L'1.h'1 for 3 to 7 hours.
• the de-oiling step can be carried out using light hydrocarbons, by steam treatment or any other similar process.
• the de-oiling step eliminates soluble hydrocarbons which could prove dangerous in the regeneration step, because they present risks of flammability in an oxidizing atmosphere.
• Regeneration step a) is generally carried out in a gas flow containing oxygen, generally air.
• the water content is generally between 0 and 50% by weight.
• the gas flow rate in terms of flow rate per unit volume of the at least partially spent catalyst is preferably 20 to 2000 NL.L -1.h'1 , more preferably 30 to 1000 NL.L- 1.h'1 , and particularly preferably from 40 to 500 NL.L -1.h'1 .
• the duration of the regeneration is preferably 2 hours or more, more preferably 2.5 hours or more, and particularly preferably 3 hours or more.
• the regeneration of the at least partially spent catalyst is generally carried out at a temperature between 360°C and less than 420°C, preferably between 360 and 415°C, preferably between 360 and 410°C or even between 380 and 410°C.
• Regeneration step a) can be carried out for example in a crossed bed, in a licked bed or in a static atmosphere.
• the oven used can be a rotating rotary kiln or a vertical kiln with radially crossed layers or even a belt kiln.
• the temperature is high enough to remove the coke and/or other impurities in order to free access to the active phase, and at the same time it must not be too high to avoid the formation of the crystalline phase.
• the regenerated catalyst is composed of the oxide support not comprising a zeolite and the active phase formed of at least one metal from group VIB and at least one metal from group VIII and optionally phosphorus from the fresh catalyst.
• the hydrogenating function comprising the metals of group VIB and group VIII of the regenerated catalyst is in an oxide form.
• the contents of group VIB metal, group VIII metal and optionally phosphorus in the regenerated catalyst are substantially identical to the contents of the at least partially spent catalyst and to the contents of the fresh catalyst from which it comes.
• substantially identical we mean that each of the metallic elements mentioned is present in the same proportions as in the initial fresh catalyst to within 5% relative.
• the regenerated catalyst is characterized by a specific surface area of between 5 and 400 m 2 /g, preferably between 10 and 350 m 2 /g, preferably between 40 and 350 m 2 /g, very preferably between 150 and 340 m 2 /g.
• the pore volume of the regenerated catalyst is generally between 0.1 cm 3 /g and 1.5 cm 3 /g, preferably between 0.3 cm 3 /g and 1.1 cm 3 /g.
• the regenerated catalyst obtained in regeneration step a) contains residual carbon at a content of between 0.1 and 0.5% by weight relative to the total weight of the regenerated catalyst, preferably between 0.1 and 0.49 % by weight relative to the total weight of the regenerated catalyst, preferably between 0.1 and 0.45% by weight and particularly preferably between 0.1 and 0.4% by weight.
• residual carbon in the present application means carbon (coke) remaining in the regenerated catalyst after regeneration of the spent hydrotreatment catalyst. This residual carbon content in the regenerated hydrotreatment catalyst is measured by elemental analysis according to the ASTMD 5373 standard.
• the regenerated catalyst may contain residual sulfur at a content of between 0.3 and 0.8% by weight relative to the total weight of the regenerated catalyst, preferably between 0.3 and 0.75% by weight relative to the total weight of the regenerated catalyst, preferably between 0.4 and 0.75% by weight and particularly preferably between 0.4 and 0.7% by weight.
• This residual sulfur content in the regenerated hydrotreatment catalyst is measured by elemental analysis according to ASTM D5373.
• part of the active phase can form a crystalline phase resulting from at least one metal from group VIII and at least one metal from group VIB.
• the crystalline phase can be a single crystalline compound or a mixture of different crystalline compounds.
• different crystalline compounds can be formed, for example nickel molybdate NiMoCL, cobalt molybdate CoMoO4, nickel tungstate NiWCL or cobalt tungstate COWO4, mixtures of these or mixed metal crystals can also be trained.
• the proportion of crystalline phase originating from at least one metal from group VIII and from at least one metal from group VIB is characterized by a ratio between the surface of the diffraction peak of the crystal at 26.6°, 20 and the surface of the characteristic peak of alumina at 45.7°, less than 0.6, preferably less than 0.55, preferably less than 0.5.
• the regenerated catalyst may also not contain a crystalline phase.
• the crystalline phase content is measured by X-ray diffraction (XRD).
• XRD X-ray diffraction
• the absolute error A(20) is ⁇ 0, 5°.
• the relative area A rei assigned to each value of dhki is measured by integration of the corresponding diffraction peak after subtracting the baseline.
• Software for integrating and subtracting the baseline is known and conventionally used by those skilled in the art.
• the proportion of the crystalline phase is evaluated relative to the alumina signal from the X-ray diffractogram by evaluating the ratio between the diffraction peak area of the crystal, for example nickel molybdate (26.6° 20) or cobalt molybdate (also 26.6° 20), and the area of a characteristic peak of alumina (for example that at 45.7° 20 for y-alumina), the areas having been calculated after subtraction of the line basis of the diffractogram.
• the regenerated catalyst may also have a low content of contaminants from the charge treated by the fresh catalyst from which it originates, such as silicon, arsenic and metals such as nickel, vanadium, iron.
• the silicon content (apart from that possibly present on the fresh catalyst) is less than 2% by weight and very preferably less than 1% by weight relative to the total weight of the regenerated catalyst.
• the arsenic content is less than 2000 ppm by weight and very preferably less than 1000 ppm by weight relative to the total weight of the regenerated catalyst.
• the content for each metal, nickel, vanadium, iron is less than 1% by weight and very preferably less than 5000 ppm by weight relative to the total weight of the regenerated catalyst.
• the rejuvenation process according to the invention comprises, after step a) of regeneration, a step b) according to which said regenerated catalyst is brought into contact with an aqueous solution consisting of water, phosphoric acid and an organic acid having each acidity constant pKa greater than 1.5, preferably greater than 3.5.
• the organic acid may contain one or more carboxylic functions, each acidity constant being greater than 1.5 and preferably greater than 3.0, and particularly preferably greater than 3.5.
• the acidity constant is measured at 25°C in water.
• the organic acid may contain, in addition to the carboxylic function(s), other chemical functions such as alcohol, ether, aldehyde, ketone or ester.
• the organic acid is preferably chosen from acetic acid, maleic acid, malic acid, malonic acid, gluconic acid, tartaric acid, citric acid, y-ketovaleric acid. , lactic acid, pyruvic acid, ascorbic acid or even acid succinic, and preferably, the organic acid is chosen from citric acid, acetic acid, gluconic acid, y-ketovaleric acid, lactic acid, ascorbic acid and succinic acid .
• the acid is an organic acid having each acidity constant pKa greater than 3.5.
• the organic acid is chosen from gluconic acid, y-ketovaleric acid, lactic acid, ascorbic acid or succinic acid.
• a molar ratio of organic acid added per metal/group VIII metals present in the regenerated catalyst of between 0.02 to 17 mol/mol, preferably between 0.1 to 10 mol/mol, preferably between 0 .15 and 5 mol/mol and very preferably, between 0.2 and 3.5 mol/mol.
• the different molar ratios apply for each of the organic acids present.
• the phosphoric acid this is advantageously introduced into the aqueous impregnation solution in a quantity corresponding to a molar ratio of phosphorus added per metal of group VI B already present in the regenerated catalyst of between 0.01 to 5 mol /mol, preferably between 0.05 and 3 mol/mol, preferably between 0.05 and 2 mol/mol and very preferably, between 0.1 and 1.5 mol/mol.
• Step b) of bringing said contacting can be carried out either by impregnation in slurry, or by excess impregnation, or by dry impregnation, or by any other means known to those skilled in the art.
• Impregnation at equilibrium consists of immersing the support or the catalyst in a volume of solution (often significantly) greater than the porous volume of the support or catalyst while maintaining the system under agitation to improve the exchanges between the solution and the support or catalyst. An equilibrium is finally reached after diffusion of the different species in the pores of the support or catalyst. Control of the quantity of elements deposited is ensured by the prior measurement of an adsorption isotherm which links the concentration of the elements to be deposited contained in the solution to the quantity of elements deposited on the solid in equilibrium with this solution.
• Dry impregnation consists of introducing a volume of impregnation solution equal to the pore volume of the support or catalyst. Dry impregnation allows all of the components contained in the impregnation solution to be deposited on a given support or catalyst.
• Step b) can advantageously be carried out by one or more impregnations in excess of solution or preferably by one or more dry impregnations and very preferably by a single dry impregnation of said catalyst at least partially spent and previously regenerated in the step a), using the impregnation solution.
• the phosphoric acid and the organic acid can be introduced together in a single impregnation step (co-impregnation) or independently in several impregnation steps, and this in any order.
• the impregnated regenerated catalyst is allowed to mature. Maturation allows the impregnation solution to disperse homogeneously within the regenerated catalyst.
• Any maturation step is advantageously carried out at atmospheric pressure, in an atmosphere saturated with water and at a temperature between 17°C and 50°C, and preferably at room temperature.
• a maturation period of between ten minutes and forty-eight hours, preferably between thirty minutes and fifteen hours and particularly preferably between thirty minutes and six hours, is sufficient.
• each impregnation step is preferably followed by an intermediate drying step at a temperature below 200°C, advantageously between 50°C and 180°C, preferably between 70°C. °C and 150°C, very preferably between 75°C and 130°C and optionally a maturation period was observed between the impregnation step and the intermediate drying step.
• the catalyst is subjected to a drying step at a temperature below 200°C, advantageously between 50°C and 180°C, preferably between 70°C and 150°C, in a very preferred between 75°C and 130°C, without subsequent calcination step.
• the drying step is preferably carried out under an inert atmosphere or under an atmosphere containing oxygen.
• the drying step can be carried out by any technique known to those skilled in the art. It is advantageously carried out at atmospheric pressure or at reduced pressure. Preferably, this step is carried out at atmospheric pressure. It is advantageously carried out in a crossed bed using air or any other hot gas. Preferably, when the drying is carried out in a fixed bed, the gas used is either air or an inert gas such as argon or nitrogen. Very preferably, drying is carried out in a crossed bed in the presence of nitrogen and/or air. Preferably, the drying step has a duration of between 5 minutes and 4 hours, preferably between 30 minutes and 4 hours and very preferably between 1 hour and 3 hours.
• the drying is carried out so as to preferably preserve at least 30% by weight of the organic acid introduced during an impregnation step, preferably this quantity is greater than 50% by weight and even more preferably, greater than 70%. % weight, calculated based on the carbon remaining on the rejuvenated catalyst.
• calcination means a treatment thermal under a gas containing air or oxygen at a temperature greater than or equal to 200°C.
• a rejuvenated catalyst is then obtained, which will preferably be subjected to an optional activation step (sulfurization) for its subsequent implementation in a hydrotreatment and/or hydrocracking process.
• the rejuvenated catalyst is composed of the oxide support not comprising zeolite and the active phase formed of at least one metal from group VI B and at least one metal from group VIII, phosphorus and organic acid and contains a proportion of crystalline phase originating from at least one metal from group VIII and from at least one metal from group VIB determined by X-ray diffraction and characterized by a ratio between the surface of the diffraction peak of the crystal at 26, 6°, 20 and the characteristic peak area of alumina at 45.7°, 20 less than 0.4.
• the total content of Group VIII metal is between 1 and 15% by weight of oxide of the Group VIII metal relative to the total weight of the rejuvenated catalyst, preferably between 1.5 and 12% by weight, preferably between 2 and 10%, weight of Group VIII metal oxide relative to the total weight of the rejuvenated catalyst.
• the total content of Group VIB metal is between 5 and 45% by weight of oxide of the Group VIB metal relative to the total weight of the rejuvenated catalyst, preferably between 8 and 40% by weight, very preferably between 10 and 30% by weight of Group VIB metal oxide relative to the total weight of the rejuvenated catalyst.
• the molar ratio of Group VIII metal to Group VIB metal of the rejuvenated catalyst is generally between 0.1 and 0.8, preferably between 0.2 and 0.6.
• the proportion of crystalline phase originating from at least one metal from group VIII and from at least one metal from group VIB determined by X-ray diffraction and characterized by a ratio between the surface of the diffraction peak of the crystal at 26.6° , 20 and the area of the characteristic peak of alumina at 45.7°, 20 is less than 0.4, preferably less than 0.35, preferably less than 0.3 and even more preferably less than 0.25.
• the rejuvenated catalyst may also not contain a crystalline phase.
• the content of organic acid(s) on the rejuvenated catalyst is between 1 and 45% by weight, preferably between 2 and 30% by weight, and more preferably between 3 and 25% by weight relative to the total weight of the rejuvenated catalyst.
• the total phosphorus content (introduced by the phosphoric acid during step b) and possibly already present in the regenerated catalyst) in the rejuvenated catalyst is generally between 0.3 and 25% by weight of P 2 Os relative to the total weight of catalyst, preferably between 0.5 and 20% by weight of P 2 Os relative to the total weight of catalyst, very preferably between 1 and 15% by weight of P 2 Os relative to the total weight of catalyst.
• the rejuvenated catalyst obtained according to the process according to the invention Before its use for the hydrotreatment and/or hydrocracking reaction, it is advantageous to transform the rejuvenated catalyst obtained according to the process according to the invention into a sulfide catalyst in order to form its active species.
• This activation or sulfidation step is carried out by methods well known to those skilled in the art, and advantageously under a sulfo-reducing atmosphere in the presence of hydrogen and hydrogen sulfide.
• step c) of the rejuvenation process according to the invention said rejuvenated catalyst is therefore advantageously subjected to a sulfurization step, without an intermediate calcination step.
• Said rejuvenated catalyst is advantageously sulfurized ex situ or in situ.
• the sulfurizing agents are H 2 S gas, elemental sulfur, CS 2 , mercaptans, sulphides and/or polysulphides, hydrocarbon cuts with a boiling point below 400°C containing sulfur compounds or any other compound containing sulfur used for the activation of the hydrocarbon charges with a view to sulphurizing the catalyst.
• Said sulfur-containing compounds are advantageously chosen from alkyl disulfides such as for example dimethyl disulfide (DMDS), alkyl sulfides, such as for example dimethyl sulfide, thiols such as for example n- butyl mercaptan (or 1-butanethiol) and polysulphide compounds of the tertiononyl polysulphide type.
• the catalyst can also be sulfurized by the sulfur contained in the feed to be desulfurized.
• the catalyst is sulfurized in situ in the presence of a sulfurizing agent and a hydrocarbon filler.
• the catalyst is sulphurized in situ in the presence of a hydrocarbon feed additive with dimethyl disulphide.
• Another object of the invention is the use of the rejuvenated catalyst according to the invention in hydrotreatment and/or hydrocracking processes of hydrocarbon cuts.
• the hydrotreatment and/or hydrocracking process for hydrocarbon cuts can be carried out in one or more series reactors of the fixed bed type or the bubbling bed type.
• the hydrotreatment and/or hydrocracking process of hydrocarbon cuts is carried out in the presence of a rejuvenated catalyst. It can also be carried out in the presence of a mixture of a rejuvenated catalyst and a fresh catalyst or a regenerated catalyst.
• the fresh or regenerated catalyst when it is present, it comprises at least one metal from group VIII, at least one metal from group VIB and an oxide support, and optionally phosphorus and/or an organic compound as described above .
• the active phase and the support of the fresh or regenerated catalyst may or may not be identical to the active phase and the support of the rejuvenated catalyst.
• the active phase and the support of the fresh catalyst may or may not be identical to the active phase and the support of the regenerated catalyst.
• hydrotreatment and/or hydrocracking process of hydrocarbon cuts is carried out in the presence of a rejuvenated catalyst and a fresh or regenerated catalyst, it can be carried out in a fixed bed type reactor containing several catalytic beds.
• a catalytic bed containing the fresh or regenerated catalyst can precede a catalytic bed containing the rejuvenated catalyst in the direction of circulation of the charge.
• a catalytic bed containing the rejuvenated catalyst can precede a catalytic bed containing the fresh or regenerated catalyst in the direction of circulation of the charge.
• a catalytic bed may contain a mixture of a rejuvenated catalyst and a fresh catalyst and/or a rejuvenated catalyst.
• the operating conditions are those described above. They are generally identical in the different catalytic beds with the exception of the temperature which generally increases in a catalytic bed following the exotherm of hydrodesulfurization reactions.
• a reactor can include a rejuvenated catalyst while another reactor may include a fresh catalyst or regenerated, or a mixture of a rejuvenated catalyst and a fresh and/or regenerated catalyst, and this in any order.
• a device can be provided for eliminating H 2 S from the effluent from the first hydrodesulfurization reactor before treating said effluent in the second hydrodesulfurization reactor. In these cases, the operating conditions are those described above and may or may not be identical in the different reactors.
• the rejuvenated catalyst and having preferably previously undergone a sulfurization step is advantageously used for hydrotreatment and/or hydrocracking reactions of hydrocarbon feeds such as petroleum cuts, cuts from coal or hydrocarbons produced from gas natural, possibly in mixtures or even from a hydrocarbon cut from biomass and more particularly for the reactions of hydrogenation, hydrodenitrogenation, hydrodearomatization, hydrodesulfurization, hydrodeoxygenation, hydrodemetallation or hydroconversion of hydrocarbon feedstocks.
• the rejuvenated catalyst and having preferably previously undergone a sulfurization step has improved activity compared to the catalysts of the prior art.
• This catalyst can also advantageously be used during the pretreatment of catalytic cracking or hydrocracking feeds, or the hydrodesulfurization of residues or the extensive hydrodesulfurization of gas oils (IILSD Ultra Low Sulfur Diesel according to Anglo-Saxon terminology).
• the feeds used in the hydrotreatment process are for example gasolines, gas oils, vacuum gas oils, atmospheric residues, vacuum residues, atmospheric distillates, vacuum distillates, heavy fuel oils, oils, waxes and paraffins, used oils, residues or deasphalted crudes, feeds from thermal or catalytic conversion processes, lignocellulosic feeds or more generally feeds from biomass, taken alone or in a mixture.
• the fillers that are processed, and in particular those mentioned above, generally contain heteroatoms such as sulfur, oxygen and nitrogen and, for heavy fillers, they most often also contain metals.
• the operating conditions used in the processes implementing the hydrotreatment reactions of hydrocarbon feeds described above are generally as follows: the temperature is advantageously between 180 and 450°C, and preferably between 250 and 440°C, the pressure is advantageously between 0.5 and 30 MPa, and preferably between 1 and 18 MPa, the hourly volume velocity is advantageously between 0.1 and 20 h' 1 and preferably between 0.2 and 5 h' 1 , and the hydrogen/charge ratio expressed in volume of hydrogen, measured under normal conditions of temperature and pressure, per volume of liquid charge is advantageously between 50 l/l to 5000 l/l and preferably 80 to 2000 l/l.
• said hydrotreatment process is a hydrotreatment process, and in particular hydrodesulfurization (HDS) of a gas oil cut carried out in the presence of at least one rejuvenated catalyst according to the invention.
• Said hydrotreatment process aims to eliminate the sulfur compounds present in said diesel cut so as to achieve the environmental standards in force, namely an authorized sulfur content of up to 10 ppm. It also makes it possible to reduce the aromatic and nitrogen contents of the diesel cut to be hydrotreated.
• Said diesel cut to be hydrotreated contains from 0.02 to 5.0% by weight of sulfur. It advantageously comes from direct distillation (or straight run gas oil according to Anglo-Saxon terminology), from a coking unit (coking according to Anglo-Saxon terminology), from a visbreaking unit (visbreaking according to Anglo-Saxon terminology). Saxon), a steam cracking unit (steam cracking according to Anglo-Saxon terminology), a hydrotreatment unit and/or hydrocracking of heavier feeds and/or a catalytic cracking unit (Fluid Catalytic Cracking according to Anglo-Saxon terminology). Said diesel cut preferably presents at least 90% of the compounds whose boiling temperature is between 250°C and 400°C at atmospheric pressure.
• the process for hydrotreating said gas oil cut is implemented under the following operating conditions: a temperature between 200 and 400°C, preferably between 300 and 380°C, a total pressure between 2 MPa and 10 MPa and more preferably between 3 MPa and 8 MPa with a ratio volume of hydrogen per volume of hydrocarbon feedstock, expressed in volume of hydrogen, measured under normal conditions of temperature and pressure, per volume of liquid feedstock, of between 100 and 600 liters per liter and more preferably between 200 and 400 liters per liter and an hourly volume velocity (WH) of between 1 and 10 h'1 , preferably between 2 and 8 h'1 .
• WH hourly volume velocity
• the WH corresponds to the reciprocal of the contact time expressed in hours and is defined by the ratio of the volume flow rate of liquid hydrocarbon feed to the volume of catalyst loaded into the reaction unit implementing the hydrotreatment process according to the invention .
• the reaction unit implementing the hydrotreatment process of said gas oil cut is preferably operated in a fixed bed, in a moving bed or in a bubbling bed, preferably in a fixed bed.
• said hydrotreatment and/or hydrocracking process is a hydrotreatment process (in particular hydrodesulfurization, hydrodeazoation, Tl hydrogenation of aromatics) and/or hydrocracking of a cut of distillate under vacuum carried out in the presence of at least one rejuvenated catalyst according to the invention.
• Said hydrotreatment and/or hydrocracking process otherwise called hydrocracking or hydrocracking pretreatment process, aims, depending on the case, to eliminate the sulfur, nitrogen or aromatic compounds present in said distillate cut so as to carry out a pretreatment before conversion in catalytic cracking or hydroconversion processes, or to hydrocrack the distillate cut which may have been pretreated previously if necessary.
• feedstocks can be treated by the vacuum distillate hydrotreating and/or hydrocracking processes described above. Generally they contain at least 20% volume and often at least 80% volume of compounds boiling above 340°C at atmospheric pressure.
• the feed may be, for example, vacuum distillates as well as feeds coming from units for extracting aromatics from lubricating oil bases or from solvent dewaxing of lubricating oil bases, and/or deasphalted oils.
• the filler can be a deasphalted oil or paraffins from the Fischer-Tropsch process or any mixture of the previously mentioned fillers.
• the fillers have a boiling point T5 greater than 340°C at atmospheric pressure, and better still greater than 370°C at atmospheric pressure, that is to say that 95% of the compounds present in the filler have a boiling point boiling point greater than 340°C, and better still greater than 370°C.
• the nitrogen content of the feeds treated in the processes according to the invention is usually greater than 200 ppm by weight, preferably between 500 and 10,000 ppm by weight.
• the sulfur content of the feeds treated in the processes according to the invention is usually between 0.01 and 5.0% by weight.
• the filler may optionally contain metals (e.g. nickel and vanadium).
• the asphaltene content is generally less than 3,000 ppm by weight.
• the rejuvenated catalyst is generally brought into contact, in the presence of hydrogen, with the charges described above, at a temperature above 200°C, often between 250°C and 480°C, advantageously between 320°C and 450°C. C, preferably between 330°C and 435°C, under a pressure greater than 1 MPa, often between 2 and 25 MPa, preferably between 3 and 20 MPa, the volume velocity being between 0.1 and 20, 0 h -1 and preferably 0.1-6.0 h -1 , preferably 0.2-3.0 h -1 , and the quantity of hydrogen introduced is such that the volume ratio liter of hydrogen/ liter of hydrocarbon, expressed in volume of hydrogen, measured under normal conditions of temperature and pressure, per volume of liquid charge, i.e.
• the hydrotreatment and/or hydrocracking processes for distillates under vacuum using the rejuvenated catalysts according to the invention cover the pressure and conversion areas ranging from mild hydrocracking to high pressure hydrocracking.
• Mild hydrocracking means hydrocracking leading to moderate conversions, generally less than 40%, and operating at low pressure, generally between 2 MPa and 6 MPa.
• the rejuvenated catalyst according to the invention can be used alone, in a single or several catalytic beds in a fixed bed, in one or more reactors, in a so-called one-step hydrocracking scheme, with or without liquid recycling of the unconverted fraction. , or even in a so-called two-stage hydrocracking scheme, possibly in association with a hydrorefining catalyst located upstream of the rejuvenated catalyst.
• said hydrotreatment and/or hydrocracking process is advantageously implemented as pretreatment in a fluidized bed catalytic cracking process (or FCC process for Fluid Catalytic Cracking according to Anglo-Saxon terminology) .
• the operating conditions of the pretreatment in terms of temperature range, pressure, hydrogen recycling rate, hourly volume velocity are generally identical to those described above for the hydrotreatment and/or hydrocracking processes of vacuum distillates.
• the FCC process can be carried out in a conventional manner known to those skilled in the art under suitable cracking conditions in order to produce hydrocarbon products of lower molecular weight.
• a summary description of catalytic cracking can be found in ULLMANS ENCYCLOPEDIA OF INDUSTRIAL CHEMISTRY VOLUME A 18, 1991, pages 61 to 64.
• said hydrotreatment and/or hydrocracking process according to the invention is a hydrotreatment process (in particular hydrodesulfurization) of a gasoline cut in the presence of at least one rejuvenated catalyst according to the invention.
• the hydrotreatment (in particular hydrodesulfurization) of gasolines must make it possible to respond to a double antagonistic constraint: ensuring deep hydrodesulfurization of gasolines and limiting the hydrogenation of the unsaturated compounds present in order to limit the loss of octane number.
• the feed is generally a hydrocarbon cut having a distillation range of between 30 and 260°C.
• this hydrocarbon cut is a gasoline type cut.
• the gasoline cut is an olefinic gasoline cut coming for example from a catalytic cracking unit (Fluid Catalytic Cracking according to Anglo-Saxon terminology).
• the hydrotreatment process consists of bringing the hydrocarbon cut into contact with the rejuvenated catalyst and hydrogen under the following conditions: at a temperature between 200 and 400°C, preferably between 230 and 330°C, at a total pressure of between 1 and 3 MPa, preferably between 1.5 and 2.5 MPa, at an Hourly Volume Velocity (WH), defined as being the volume flow rate of charge relative to the volume of catalyst, of between 1 and 10 h -1 , preferably between 2 and 6 h -1 and at a hydrogen/petrol charge volume ratio of between 100 and 600 Nl/I, preferably between 200 and 400 Nl/I.
• WH Hourly Volume Velocity
• the gasoline hydrotreatment process can be carried out in one or more series reactors of the fixed bed type or the bubbling bed type. If the process is implemented using at least two reactors in series, it is possible to provide a device for eliminating H 2 S from the effluent from the first hydrodesulfurization reactor before treating said effluent in the second hydrodesulfurization reactor.
• Example 1 Obtaining the regenerated catalyst A1
• a hydrotreatment catalyst was used in a refinery for 2 years on a gas oil hydrotreatment unit.
• the spent catalyst contains 10% by weight of carbon and 9% of sulfur.
• the catalyst undergoes regeneration under an oxidizing atmosphere at 480°C.
• the regenerated catalyst A1 is obtained which contains nickel, molybdenum, phosphorus whose oxide equivalent contents are 4.5% NiO, 20.3% MoO3 and 4.4% P2O5, supported on a gamma alumina.
• the water retention volume of catalyst A1 is 0.4 cc/g.
• This catalyst has carbon and sulfur contents of 0.03% by weight and 0.2% by weight respectively. Its ratio of NiMoO4 (26.6° 20) / y-ALOa (45.7° 20) diffraction peak areas is 0.85. 2: Obtaining grades A2, A3, A4, A5, A6
• the same spent and deoiled catalyst from Example 1 undergoes regeneration under an oxidizing atmosphere at different temperatures: 450°C, 400°C, 380°C, 360°C and 340°C to obtain respectively the regenerated catalysts A2, A3, A4, A5 and A6 which have a water retention volume of 0.4 cc/g.
• Catalyst A2 has carbon and sulfur contents of 0.05% by weight and 0.3% by weight respectively. Its ratio of NiMoO4 (26.6° 20) / y-ALOa (45.7° 20) diffraction peak areas is 0.78.
• Catalyst A3 has carbon and sulfur contents of 0.1% by weight and 0.6% by weight respectively. Its ratio of NiMoO4 (26.6° 20) / y-AhOa (45.7° 20) diffraction peak areas is 0.47.
• Catalyst A4 has carbon and sulfur contents of 0.3% by weight and 0.7% by weight respectively. Its ratio of NiMoCL (26.6° 20) / y-AI 2 C>3 (45.7° 20) diffraction peak areas is 0.23.
• Catalyst A5 has carbon and sulfur contents of 0.5% by weight and 0.8% by weight respectively. Its NiMoCL/Alumina area ratio is 0.11.
• Example 3 Obtaining catalysts B1 and B2 not in accordance with the invention
• Catalyst B1 is prepared from regenerated catalyst A1 onto which a solution containing phosphoric acid and gluconic acid is dry impregnated so as to obtain on the rejuvenated catalyst the P/Mo molar ratios of 0.8 and acid gluconic/Mo of 0.8. After maturing for 3 hours, the catalyst is dried at 120°C for 2 hours. Its ratio of NiMoO4 (26.6° 20) / y-ALOa (45.7° 20) diffraction peak areas is 0.57. Catalyst B2 is obtained with the same steps but from the regenerated catalyst A2. Its ratio of NiMoCU (26.6° 20) / y-AI 2 C>3 (45.7° 20) diffraction peak areas is 0.45.
• Example 4 Obtaining catalysts B3, B4 and B5 in accordance with the invention
• Catalyst B3 is prepared from regenerated catalyst A3 onto which a solution containing phosphoric acid and gluconic acid is dry impregnated so as to obtain on the rejuvenated catalyst the P/Mo molar ratios of 0.8 and acid gluconic/Mo of 0.8. After maturing for 3 hours, the catalyst is dried at 120°C for 2 hours. Its ratio of NiMoO4 (26.6° 20) / y-A Os (45.7° 20) diffraction peak areas is 0.20. Catalysts B4 and B5 are obtained with the same steps but respectively from the regenerated catalysts A4 and A5. Their NiMoO4 (26.6° 20) / y-ALCh (45.7° 20) diffraction peak area ratios are 0.13 and 0.06, respectively.
• Example 5 Obtaining catalyst B6 not in accordance with the invention
• Catalyst B6 is prepared from regenerated catalyst A6 on which a solution containing phosphoric acid and gluconic acid is dry impregnated so as to obtain on the rejuvenated catalyst the P/Mo molar ratios of 0.8 and acid gluconic/Mo of 0.8. After maturing for 3 hours, the catalyst is dried at 120°C for 2 hours. Its ratio of NiMo ⁇ 4 (26.6° 20) / y-ALOa (45.7° 20) diffraction peak areas is 0.05.
• Catalysts B1, B2 and B6 (not in accordance with the invention) and B3, B4 and B5 (in accordance with the invention) were tested in diesel HDA.
• the regenerated catalyst B1 serves as a reference.
• the feed is a mixture of 30% volume of gas oil from atmospheric distillation (also called straight-run according to Anglo-Saxon terminology) and 70% volume of light gas oil from a catalytic cracking unit (also called LCO for light cycle oil). according to Anglo-Saxon terminology).
• test is carried out in an isothermal pilot reactor with a crossed fixed bed, the fluids circulating from bottom to top.
• the aromatic hydrogenation tests were carried out under the following operating conditions: a total pressure of 8 MPa, a catalyst volume of 4 cm 3 , a temperature of 330°C, with a hydrogen flow rate of 3.0 L /h and with a load flow of 4.5 cm 3 /h.
• the characteristics of the effluents are analyzed: density at 15°C (NF EN ISO 12185), refractive index at 20°C (ASTM D1218-12), simulated distillation (ASTM D2887), sulfur content and nitrogen content.
• the residual aromatic carbon contents are calculated by the ndM method (ASTM D3238).
• the aromatic hydrogenation rate is calculated as the ratio of the aromatic carbon content of the effluent to that of the test load.
• the catalytic performances of the catalysts tested are given in Table 1. They are expressed in relative volume activity (RVA) relative to the catalyst B1 chosen as reference, assuming an order of 1.7 for the reaction concerned.
• Catalysts B3, B4 and B5 in accordance with the invention have the best activities beyond RVA 110 because they were prepared on regenerated catalysts having both carbon and sulfur contents of respectively between 0.1 and 0. .5% by weight and 0.3 and 0.8% by weight S and a ratio of the areas of the diffraction peaks NiMoCL (26.6° 20) / y-AI 2 C>3 (45.7° 20) less than 0 .6 thanks to controlled regeneration.
• the rejuvenation step then makes it possible to partially dissolve the NiMoCL crystalline phase in order to redisperse the species based on molybdenum and nickel and thus obtain rejuvenated catalysts according to the invention having a ratio of the surfaces of the NiMoCL diffraction peaks (26, 6° 20) / y-AhCh (45.7° 20) less than 0.4.

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