Hydrodesulphurization catalyst selective of gasolines from FCC

Abstract

The present invention relates to a hydrotreating catalyst comprising at least one group VIB metal, at least one group VIII metal and an alumina support having a gamma alumina content greater than 50% by weight and less than 100% by weight with respect to the weight of the support, said support having a specific surface area comprised between 25 and 150 m.sup.2/g.

Claims

1. A hydrotreating catalyst comprising 3 to 35% by weight as oxide with respect to total weight of support of at least one group VIB metal, 0.1 to 10% by weight as oxide with respect to total weight of the catalyst of at least one group VIII metal and an alumina support comprising gamma alumina and delta, theta and/or alpha alumina, said alumina support having a gamma alumina content of 60% to 95% by weight with respect to the weight of the support, said support having a specific surface area of 60 to 100 m.sup.2/g, said catalyst having a specific surface area of 50 to 90 m.sup.2/g.

2. The catalyst according to claim 1, in which the molar ratio (group VIII metal)/(group VIB metal) is 0.1 to 0.8.

3. The catalyst according to claim 1, further comprising 0.3 to 10% by weight phosphorus, expressed as P.sub.2O.sub.5 with respect to the total weight of the catalyst″ the catalyst having a molar ratio of phosphorus/(group VIB metal) of 0.1 to 0.7.

4. The catalyst according to claim 1, having a density of group VIB metal, expressed as the number of atoms of group VIB metal per unit of area of the catalyst of 3 to 30 atoms of group VIB metal per nm.sup.2 of catalyst.

5. The catalyst according to claim 1, in which the group VIB metal is tungsten or molybdenum and the group VIII metal is nickel or cobalt.

6. The catalyst according to claim 1, in which the alumina support is obtained by heat treatment at a temperature less than or equal to 770° C. from a precursor of alumina.

7. The catalyst according to claim 1, also comprising at least one organic compound containing oxygen and/or nitrogen.

8. The catalyst according to claim 7, in which the organic compound is a carboxylic acid, an alcohol, an aldehyde, an ester, an amine, an amino carboxylic acid, an amino alcohol, a nitrile or an amide.

9. The catalyst according to claim 8, in which the organic compound is γ-valerolactone, 2-acetylbutyrolactone, triethylene glycol, diethylene glycol, ethylene glycol, ethylenediaminetetraacetic acid (EDTA), maleic acid, malonic acid, citric acid, γ-ketovaleric acid, dimethylformamide, N-methylpyrrolidone, propylene carbonate, 2-methoxyethyl 3-oxobutanoate, 2-(methacryloyloxy)ethyl 3-oxobutanoate, bicine, or tricine.

10. The catalyst according to claim 1, that is sulphurized.

11. A process for preparing the hydrotreating catalyst according to claim 1 comprising the following stages: a) carrying out a heat treatment at a temperature less than or equal to 770° C. of a precursor of alumina so as to obtain a support having a gamma alumina content 60-95% by weight with respect to the weight of the support, said support having a specific surface area of 60-100 m.sup.2/g, b) bringing at least one component of a group VIB metal, at least one component of a group VIII metal and optionally phosphorus into contact with said support, so as to obtain a catalyst precursor having 3-35% by weight of oxide of said group VIB metal with respect to total weight of the catalyst and 0.1-10% by weight of oxide of said group VIII metal with respect to the total weight of the catalyst, c) drying said catalyst precursor originating from stage b) at a temperature less than 200° C.

12. The process according to claim 11, in which the stage a) of heat treatment is carried out from a precursor of alumina containing at least 50% by weight of boehmite AlOOH with respect to the total weight of the precursor of alumina.

13. The process for preparing a catalyst according to claim 11, also comprising a stage of calcination d) at a temperature of 200° C. to 600° C. carried out after stage c).

14. The process for preparing a catalyst according to claim 11, also comprising a stage of sulphurization carried out after stage c) or d).

15. A process for the hydrodesulphurization of a gasoline cut comprising contacting said gasoline cut, hydrogen and a catalyst according to claim 1, said catalyst being sulphurized contacting being carried out at: a temperature of 200° C. to 400° C.; a total pressure of 1 to 3 M pa; an hourly space velocity, defined as being the volume flow rate of feedstock with respect to the volume of catalyst, of 1 to 10 h.sup.−1; a ratio by volume of hydrogen/gasoline feedstock of 100 to 600 NI/I.

16. The process according to claim 15, in which the gasoline cut is a gasoline originating from a catalytic cracking unit.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The diagram of the delta alumina is distinguished from that of the gamma alumina by a general narrowing of the beams, relative changes in intensity and above all by a splitting of the two beams 400 and 440 (FIG. 1). The relative proportion of γ and δ alumina is then established using the correlation in FIG. 2, which associates the asymmetry of the beam 440 with the proportion of δ alumina.

PREPARATION PROCESS

(2) The catalyst according to the invention may be prepared by any preparation mode known to a person skilled in the art.

(3) According to a second aspect of the invention, the invention relates to a process for preparing a catalyst according to the invention utilizing a stage of heat treatment of a precursor of alumina so as to obtain an alumina support having a gamma alumina content greater than 50% by weight and less than 100% by weight with respect to the weight of the support, said support having a specific surface area comprised between 25 and 150 m.sup.2/g.

(4) More particularly, the invention also relates to a process for preparing the hydrotreating catalyst according to the invention comprising the following stages: a) carrying out a heat treatment at a temperature less than or equal to 770° C. of a precursor of alumina so as to obtain a support having a gamma alumina content greater than 50% by weight and less than 100% by weight with respect to the weight of the support, said support having a specific surface area comprised between 25 and 150 m.sup.2/g. b) bringing at least one component of a group VIB metal, at least one component of a group VIII metal and optionally phosphorus into contact with said support, so as to obtain a catalyst precursor; c) drying said catalyst precursor originating from stage b) at a temperature less than 200° C.

(5) The precursor of alumina used in the stage a) of preparing the catalyst can be obtained according to different embodiments.

(6) According to an embodiment, the precursor of alumina used in the stage a) of preparing the catalyst can be obtained from aluminium salts such as aluminium chloride, aluminium nitrate, aluminium sulphate or sodium aluminate. Preparing the precursor of alumina thus involves a precipitation reaction between one or more aluminium salts and optionally one or more acids (for example nitric acid, sulphuric acid, hydrochloric acid, etc.) or one or more bases (for example, soda, potassium hydroxide, ammonia, etc.). According to one of the embodiments, the suspension obtained at the precipitation stage is subjected directly to a heat treatment in liquid phase, with a temperature comprised between 80° C. and 300° C. and a duration comprised between 30 minutes and 2 weeks. Optionally, one or more acids and one or more bases can be added to the suspension before the heat treatment. According to another embodiment, the suspension obtained at the precipitation stage is subjected to a stage of solid-liquid separation and optionally to washing. The solid fraction is then re-suspended in a solvent and subjected to a heat treatment in liquid phase, with a temperature comprised between 80° C. and 300° C. and a duration comprised between 30 minutes and 2 weeks. Optionally, one or more acids and one or more bases can be added to the re-suspended solid fraction before the heat treatment. At the end of the stage of heat treatment, one or more stages of solid-liquid separation and/or drying (for example by spray-drying) and/or forming (for example by granulation, mixing-extrusion, oil-drop, pelletization, etc.) make it possible to obtain the precursor of alumina. Examples of preparing the precursor of alumina according to this preferred embodiment can be found in T. HE et al. Materials Let. 62 (2008) 17-17, 2939-2942 or in D. Yida et al. Ceramics Inter. 36 (2010) 1773-1777.

(7) According to another particular embodiment of the invention, the precursor of alumina used according to the present invention can be obtained from aluminium alcoholates such as Al(O-Et).sub.3, Al(O-iPr).sub.3, Al(O-secBu).sub.3, Al(O-nBu).sub.3, Al(O—R).sub.3 with R being a linear alkyl chain containing between 6 and 18 carbon atoms. Preparation of the precursor of alumina thus involves a hydrolysis reaction of one or more aluminium alcoholates. According to one of the embodiments of the invention, the medium obtained at the hydrolysis stage is subjected directly to a heat treatment in liquid phase, with a temperature comprised between 80° C. and 300° C. and a duration comprised between 30 minutes and 2 weeks. Optionally, one or more acids and one or more bases can be added to the medium obtained at the hydrolysis stage before the heat treatment. According to another embodiment of the invention, the medium obtained at the hydrolysis stage is subjected to a stage of solid-liquid separation (and optionally washing) then the solid fraction is re-suspended and subjected to a heat treatment in liquid phase, with a temperature comprised between 80° C. and 300° C. and a duration comprised between 30 minutes and 2 weeks. Optionally, one or more acids and one or more bases can be added to the re-suspended solid fraction before the heat treatment. According to another embodiment, the medium obtained at the hydrolysis stage is subjected to a stage of separation of an organic liquid phase and an aqueous suspension, then the aqueous suspension is subjected to a heat treatment in liquid phase, with a temperature comprised between 80° C. and 300° C. and a duration comprised between 30 minutes and 2 weeks. Optionally, one or more acids and one or more bases can be added to the aqueous suspension before the heat treatment. According to another embodiment, the medium obtained at the hydrolysis stage is subjected to a stage of evaporation of the organic solvent, then the aqueous fraction is subjected to a heat treatment in liquid phase, with a temperature comprised between 80° C. and 300° C. and a duration comprised between 30 minutes and 2 weeks. Optionally, one or more acids and one or more bases can be added to the aqueous fraction before the heat treatment. At the end of the stage of heat treatment, one or more stages of solid-liquid separation and/or drying (for example by spray-drying) and/or forming (for example by granulation, mixing-extrusion, oil-drop, pelletization, etc.) make it possible to obtain the precursor of alumina. Examples of preparing the precursor of alumina according to this preferred embodiment can be found in A. Meyer et al. U.S. Pat. No. 5,055,019 or in K. Noweck et al. U.S. Pat. No. 8,414,854.

(8) According to another particular embodiment of the invention, the precursor of alumina can be obtained from a powder composed of boehmite, gibbsite, bayerite, diaspore, chi alumina, kappa alumina, eta alumina, gamma alumina, delta alumina or a mixture of these different oxides. The preparation of the precursor of alumina thus involves the re-suspension in water of this powder, then a stage of heat treatment at a temperature comprised between 80° C. and 300° C. and for a duration comprised between 30 minutes and 2 weeks. Optionally, one or more acids and one or more bases can be added to the aqueous suspension before the heat treatment. At the end of the stage of heat treatment, one or more stages of solid-liquid separation and/or drying (for example by spray-drying) and/or forming (for example by granulation, mixing-extrusion, oil-drop, pelletization, etc.) make it possible to obtain the precursor of alumina. Examples of preparing the precursor of alumina according to this preferred embodiment can be found in J.-C. Li et al. App. Surface Sc. 253 (2006) 766-770 or in L. Guangci et al. App. Catal. A 437-438 (2012) 79-80.

(9) According to another particular embodiment of the invention, the precursor of alumina can be obtained from objects of millimetric size (defined as objects having at least one dimension greater than 0.5 mm) in the form of beads, extrudates or pellets. These solids can be boehmite, gibbsite, bayerite, diaspore, chi alumina, kappa alumina, eta alumina, gamma alumina, delta alumina compounds or a mixture of these different oxides. The preparation of the precursor of alumina thus involves a stage of autoclaving the objects of millimetric size at a temperature comprised between 80° C. and 300° C. and a duration comprised between 30 minutes and 2 weeks. The term autoclaving here denotes treatment under saturation vapour pressure or under a partial water vapour pressure at least equal to 70% of the saturation vapour pressure corresponding to the treatment temperature. Optionally, the objects of millimetric size can be impregnated with water or acid or base aqueous solutions before the stage of autoclaving. This impregnation, before the stage of autoclaving, can be carried out dry or by immersing the objects of millimetric size in an acid or base aqueous solution. By dry impregnation, is meant bringing the objects of millimetric size into contact with a volume of solution less than or equal to the water uptake volume thereof. Preferably, impregnation is carried out dry. Examples of preparing the precursor of alumina according to this preferred embodiment can be found in A. A. Lamberov et al. Russ. J. Appl. Chem. 87 (2014) 6, 676-683 or A. Stanislaus et al. J. Mol. Catal. A 181 (2002) 33-39 or J. L. Le Loarer et al. FR2823193.

(10) In general, and for all of the embodiments described above, the stages of heat treatment or autoclaving are generally carried out at a temperature comprised between 80° C. and 300° C., preferably comprised between 120 and 250° C. The stages of heat treatment or autoclaving are generally carried out for a duration comprised between 30 minutes and 2 weeks, preferably comprised between 1 hour and 48 hours.

(11) Preferably, the acids added before the stage of heat treatment or impregnated on the support before the stage of autoclaving are selected from nitric, hydrochloric, sulphuric, perchloric, phosphoric, formic or acetic acid.

(12) Preferably, the bases added before the stage of heat treatment or impregnated on the support before the stage of autoclaving are selected from soda, potassium hydroxide, ammonia, tetraethylammonium hydroxide and triethylamine.

(13) According to a preferred embodiment, the precursor of alumina obtained comprises a precursor of the aluminium oxy(hydroxide) (AIO(OH)) type—also denoted boehmite. Preferably, the precursor of alumina contains at least 50% by weight of boehmite AlOOH with respect to the total weight of the precursor of alumina. Particularly preferably, the precursor of alumina consists of boehmite.

(14) Stage a) of Heat Treatment

(15) The precursor of alumina is optionally dried before undergoing the heat treatment. For example, drying is carried out at a temperature comprised between 100 and 200° C.

(16) The dried precursor of alumina then undergoes a stage of heat treatment at a temperature less than or equal to 770° C. which makes it possible to give it physical properties corresponding to the envisaged application. More particularly, the precursor of alumina thus obtained is then subjected to a heat treatment at a temperature less than or equal to 770° C., preferably comprised between 500° C. and 770° C., and particularly preferably comprised between 550° C. and 750° C., so as to obtain a support having a gamma alumina content greater than 50% by weight and less than 100% by weight with respect to the total weight of the support, said support having a specific surface area comprised between 25 and 150 m.sup.2/g.

(17) Preferably, the support is prepared by heat treatment at a temperature less than or equal to 770° C., and preferably comprised between 500° C. and 770° C., and particularly preferably comprised between 550° C. and 750° C. of a precursor of alumina containing at least 50% by weight of boehmite AlOOH with respect to the total weight of the precursor of alumina.

(18) Preferably, the heat treatment is carried out for a duration comprised between 1 and 8 hours under air. Optionally, the air can contain a water content generally comprised between 0 and 50% by weight.

(19) At the end of the heat treatment stage a) of the process of preparation of the catalyst according to the invention, an alumina support is obtained having a gamma alumina content greater than 50% by weight and less than 100% by weight with respect to the weight of the support, said support having a specific surface area comprised between 25 and 150 m.sup.2/g.

(20) Stage b) Introduction of the Active Phase

(21) According to stage b) of the process of preparing the catalyst according to the invention, at least one group VIB metal component, at least one group VIII metal component, and optionally phosphorus are brought into contact with the support, so as to obtain a catalyst precursor.

(22) The stage b) of bringing the support into contact comprises several embodiments. According to a first embodiment of stage b) of the process for the preparation of the catalyst, said group VIB, group VIII metal components and optionally phosphorus are deposited on said support, by one or more stages of co-impregnation, i.e. said components of the group VIB metals, of the group VIII metals and optionally phosphorus are introduced simultaneously into said support. The stage or stages of co-impregnation is (are) preferably carried out by dry impregnation or by impregnation with excess of solution. When this first embodiment comprises the utilization of several co-impregnation stages, each stage of co-impregnation is preferably followed by an intermediate drying stage generally at a temperature less than 200° C., advantageously comprised between 50 and 180° C., preferably between 60 and 150° C., very preferably between 75 and 140° C.

(23) According to a preferred embodiment by co-impregnation, the impregnation solution is preferably an aqueous solution. Preferably, the aqueous impregnation solution when it contains cobalt, molybdenum and phosphorus is prepared under pH conditions promoting the formation of heteropolyanions in solution. For example, the pH of one such aqueous solution is comprised between 1 and 5.

(24) According to a second embodiment of stage b) of the process for preparing the catalyst, the catalyst precursor is prepared by proceeding to the successive depositions in any order of a group VIB metal component, a group VIII metal component and optionally phosphorus on said support. The depositions can be carried out by dry impregnation, by impregnation in excess or also by deposition-precipitation according to methods that are well known to a person skilled in the art. In this second embodiment, the deposition of the components of the group VIB and VIII metals and optionally phosphorus can be carried out by means of several impregnations with an intermediate drying stage between two successive impregnations, generally at a temperature less than 200° C., advantageously comprised between 50 and 180° C., preferably between 60 and 150° C., very preferably between 75 and 140° C.

(25) Regardless of the mode of deposition of the metals and of the optional phosphorus utilized, the solvent forming part of the composition of the impregnation solutions is selected so as to solubilize the metal precursors of the active phase, such as water or an organic solvent (for example an alcohol).

(26) By way of example, among the sources of molybdenum, the oxides and hydroxides, the molybdic acids and salts thereof can be used, in particular the ammonium salts such as ammonium molybdate, ammonium heptamolybdate, phosphomolybdic acid (H.sub.3PMo.sub.12O.sub.40) and salts thereof, and optionally silicomolybdic acid (H.sub.4SiMo.sub.12O.sub.40) and salts thereof. The sources of molybdenum may also be any heteropoly compound of the Keggin, lacunar Keggin, substituted Keggin, Dawson, Anderson, or Strandberg type, for example. Molybdenum trioxide and the heteropoly compounds of the Keggin, lacunar Keggin, substituted Keggin and Strandberg type are preferably used.

(27) The tungsten precursors that may be used are also well known to a person skilled in the art. For example, among the sources of tungsten, the oxides and hydroxides, the tungstic acids and salts thereof can be used, in particular the ammonium salts such as ammonium tungstate, ammonium metatungstate, phosphotungstic acid and salts thereof, and optionally silicotungstic acid (H.sub.4SiW.sub.12O.sub.40) and salts thereof. The sources of tungsten may also be any heteropoly compound of the Keggin, lacunar Keggin, substituted Keggin, or Dawson type, for example. The oxides and the ammonium salts such as ammonium metatungstate or the heteropolyanions of the Keggin, lacunar Keggin or substituted Keggin type are preferably used.

(28) The precursors of cobalt that can be used are advantageously selected from the oxides, hydroxides, hydroxycarbonates, carbonates and nitrates, for example. Cobalt hydroxide and cobalt carbonate are preferably used.

(29) The precursors of nickel that can be used are advantageously selected from the oxides, hydroxides, hydroxycarbonates, carbonates and nitrates, for example. Nickel hydroxide and nickel hydroxycarbonate are preferably used.

(30) When phosphorus is present, the phosphorus can advantageously be introduced into the catalyst at various stages of its preparation and in various ways. The phosphorus can be introduced during the forming of said alumina support, or preferably after this forming. It may for example be introduced just before or just after peptization of the matrix selected, such as for example and preferably the precursor of alumina aluminium oxyhydroxide (boehmite). It may also advantageously be introduced alone or in a mixture with at least one of the group VIB and group VIII metals. The phosphorus is preferably introduced in a mixture with the precursors of the group VIB and group VIII metals, wholly or partly on the formed alumina support by dry impregnation of said alumina support using a solution containing the precursors of the metals and the precursor of phosphorus. The preferred source of phosphorus is orthophosphoric acid H.sub.3PO.sub.4, but salts and esters thereof such as the ammonium phosphates or mixtures thereof are also suitable. The phosphorus may also be introduced at the same time as the group VIB element(s) in the form, for example, of heteropolyanions of the Keggin, lacunar Keggin, substituted Keggin or Strandberg type.

(31) Stage c) Drying

(32) At the end of the stage or stages of impregnation of the group VIII, group VIB metals and optionally phosphorus, the catalyst precursor is subjected to a stage c) of drying carried out by any technique known to a person skilled in the art. It is advantageously carried out at atmospheric pressure or at reduced pressure. Preferably, this stage is carried out at atmospheric pressure. This stage c) is carried out at a temperature less than 200° C., preferably comprised between 50 and 180° C., preferably comprised between 60° C. and 150° C. and very preferably comprised between 75° C. and 140° C. Stage c) is advantageously carried out in a transverse bed using air or any other hot gas. Preferably, when drying is carried out in a transverse bed, the gas used is either air, or an inert gas such as argon or nitrogen. Very preferably, drying is carried out in a transverse bed in the presence of air.

(33) Preferably, the duration of this drying stage is comprised between 30 minutes and 4 hours and very preferably comprised between 1 hour and 3 hours.

(34) At the end of stage c) of the process according to the invention, a dried catalyst is obtained which can be used as a hydrotreating catalyst after an activation phase (stage of sulphurization).

(35) According to a variant, the dried catalyst can be subjected to a subsequent calcination stage d), for example under air, at a temperature greater than or equal to 200° C. The calcination is generally carried out at a temperature less than or equal to 600° C., and preferably comprised between 200° C. and 600° C., and particularly preferably comprised between 250° C. and 500° C. The duration is generally comprised between 0.5 and 16 hours, preferably between 1 hour and 5 hours. It is generally carried out under air. Calcination makes it possible to convert the precursors of the group VIB and group VIII metals to oxides.

(36) Before the use thereof as a hydrotreating catalyst, it is advantageous to subject the dried or optionally calcined catalyst to a stage of sulphurization (activation phase). This activation phase is carried out by the methods well known to a person skilled in the art, and advantageously under a sulpho-reducing atmosphere in the presence of hydrogen and hydrogen sulphide. The sulphurized hydrogen can be used directly or generated by a sulphide agent (such as dimethyl disulphide).

(37) According to another aspect of the invention, the hydrotreating catalyst as described above also comprises one or more organic compounds containing oxygen and/or nitrogen known for the additive role thereof. Such a catalyst is denoted by the term “additive-containing catalyst” in the remainder of the description. The organic compound present in the catalyst contains more than 2 carbon atoms and at least one oxygen and/or nitrogen atom.

(38) The organic compound containing oxygen may be one or more selected from the compounds containing one or more chemical functions selected from a carboxyl, alcohol, ether, aldehyde, ketone, ester or carbonate function. By way of example, the organic compound containing oxygen may be one or more selected from the group constituted by ethylene glycol, diethylene glycol, triethylene glycol, a polyethylene glycol (with a molecular weight comprised between 200 and 1500 g/mol), propylene glycol, 2-butoxyethanol, 2-(2-butoxyethoxy)ethanol, 2-(2-methoxyethoxy)ethanol, triethyleneglycol dimethyl ether, glycerol, acetophenone, 2,4-pentanedione, pentanone, acetic acid, maleic acid, malic acid, malonic acid, oxalic acid, gluconic acid, tartaric acid, citric acid, γ-ketovaleric acid, a C.sub.1-C.sub.4 dialkyl succinate, methyl acetoacetate, ethyl acetoacetate, 2-methoxyethyl 3-oxobutanoate, 2-(methacryloyloxy)ethyl 3-oxobutanoate, dibenzofuran, a crown ether, orthophthalic acid, glucose, γ-valerolactone, 2-acetylbutyrolactone and propylene carbonate.

(39) The organic compound containing nitrogen may be one or more selected from the compounds containing one or more chemical functions selected from an amine or nitrile function. By way of example, the organic compound containing nitrogen may be one or more selected from the group constituted by ethylenediamine, diethylenetriamine, hexamethylenediamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, acetonitrile, octylamine, guanidine or a carbazole.

(40) The organic compound containing oxygen and nitrogen may be one or more selected from the compounds comprising one or more chemical functions selected from a carboxylic acid, alcohol, ether, aldehyde, ketone, ester, carbonate, amine, nitrile, imide, amide, urea or oxime function. By way of example, the organic compound containing oxygen and nitrogen may be one or more selected from the group constituted by 1,2-cyclohexanediaminetetraacetic acid, monoethanolamine (MEA), N-methylpyrrolidone, dimethylformamide, ethylenediaminetetraacetic acid (EDTA), alanine, glycine, nitrilotriacetic acid (NTA), N-(2-hydroxyethyl)ethylenediamine-N,N′,N′-triacetic acid (HEDTA), diethylenetriaminepentaacetic acid (DTPA), tetramethylurea, glutamic acid, dimethylglyoxime, bicine, tricine, or also a lactam.

(41) Preferably, the organic compound contains oxygen; preferably it is selected from γ-valerolactone, a C.sub.1-C.sub.4 dialkyl succinate, 2-acetylbutyrolactone, triethylene glycol, diethylene glycol, ethylene glycol, ethylenediaminetetraacetic acid (EDTA), maleic acid, malonic acid, citric acid, γ-ketovaleric acid, dimethylformamide, N-methylpyrrolidone, propylene carbonate, 2-methoxyethyl 3-oxobutanoate, 2-(methacryloyloxy)ethyl 3-oxobutanoate, bicine, or tricine.

(42) The molar ratio in play, of organic compound(s) containing oxygen and/or nitrogen to group VIB element(s) on the additive-containing catalyst precursor, is generally comprised between 0.05 and 9 mol/mol, preferably comprised between 0.1 and 8 mol/mol, preferably comprised between 0.2 and 7 mol/mol before the drying stage ii).

(43) The organic compound containing oxygen and/or nitrogen can be introduced according to several embodiments during the preparation process.

(44) According to a first embodiment, said group VIB and group VIII metal components, the organic compound and optionally phosphorus are introduced simultaneously into said support. This first embodiment comprises the utilization of one or more stages of co-impregnation, each stage of co-impregnation is preferably followed by an intermediate drying stage, generally at a temperature less than 200° C., advantageously comprised between 50 and 180° C., preferably comprised between 60 and 150° C., very preferably comprised between 75 and 140° C.

(45) According to a second embodiment of the process for preparing the additive-containing catalyst, at least one organic compound containing oxygen and/or nitrogen is brought into contact with at least one component containing at least one group VIII metal, at least one component comprising a group VIB metal, optionally phosphorus and the support. This second embodiment is a preparation by so-called “post-impregnation of the organic compound”. Preparation of the catalytic precursor comprising at least one group VIII metal, at least one group VIB metal, optionally phosphorus, and the support is carried out according to the stages b) of introducing the active phase and the stage c) of drying and optionally the stage d) of calcination described above. Said organic compound(s) can then advantageously be deposited in one or more stages either by impregnation in excess, or by dry impregnation, or by any other means known to a person skilled in the art. Preferably, introduction of the organic compound is carried out by means of a single stage of impregnation, and particularly preferably by means of a single stage of dry impregnation.

(46) After introduction of the organic compound, the additive-containing catalyst precursor, optionally after a stage of maturation, is subjected to a drying stage at a temperature less than 200° C. The drying stage is carried out as described above.

(47) When the catalyst comprises an organic compound, it is preferably not subjected to a stage of calcination at a temperature greater than or equal to 200° C. after introduction of the organic compound.

(48) According to another alternative embodiment, the process of preparing the additive-containing catalyst can combine the co-impregnation of an organic compound and the post-impregnation of an organic compound which can be identical or different to that used for the co-impregnation. In this case, an organic compound is introduced containing oxygen and/or nitrogen by co-impregnation with the group VIB and VIII metal components and optionally phosphorus on the support, it is dried at a temperature less than 200° C., the or another organic compound containing oxygen and/or nitrogen is introduced on the dried catalyst precursor, and it is dried for a second time at a temperature less than 200° C. The operating conditions described above are of course applicable in the context of this embodiment.

(49) Before its use, it is advantageous to activate the additive-containing catalyst. This activation phase corresponds to a sulphurization which is carried out by the methods well known to a person skilled in the art, and advantageously under a sulpho-reducing atmosphere in the presence of hydrogen and hydrogen sulphide.

(50) The additive-containing catalyst obtained is therefore advantageously subjected to a stage of sulphurization, without an intermediate stage of calcination. Said additive-containing catalyst is advantageously sulphurized ex situ or in situ. The same sulfurizing agents as those described for the non additive-containing catalyst according to the invention can be used.

(51) Hydrotreating Process

(52) The invention also relates to a hydrotreating process for a hydrocarbon cut. In particular, the process is a hydrodesulphurization of a hydrocarbon cut having a distillation range comprised between 30 and 260° C. Preferably, this hydrocarbon cut is a cut of the gasoline type. Very preferably, the gasoline cut is an olefinic gasoline cut originating for example from a catalytic cracking unit (Fluid Catalytic Cracking).

(53) The hydrodesulphurization process according to the invention makes it possible to convert the organo-sulphur compounds of the hydrocarbon feedstock into hydrogen sulphide (H.sub.2S) while as far as possible limiting the hydrogenation of the olefins present in said feedstock.

(54) The hydrotreating process consists of bringing the hydrocarbon cut into contact with the catalyst according to the invention and hydrogen under the following conditions: a temperature comprised between 200 and 400° C., preferably comprised between 230 and 330° C.; at a total pressure comprised between 1 and 3 MPa, preferably comprised between 1.5 and 2.5 MPa; an hourly space velocity (HSV), defined as being the volume flow rate of feedstock with respect to the volume of catalyst, comprised between 1 and 10 h.sup.−1, preferably comprised between 2 and 6 h.sup.−1; a ratio by volume of hydrogen/gasoline feedstock comprised between 100 and 600 Nl/l, preferably comprised between 200 and 400 Nl/l.

(55) The process for catalytic hydrodesulphurization may be carried out in one or more reactors in series of the fixed bed type or of the ebullating bed type. If the process is carried out by means of at least two reactors in series, it is possible to provide a device for removing H.sub.2S from the effluent originating from the first hydrodesulphurization reactor before treating said effluent in the second hydrodesulphurization reactor.

(56) Without further elaboration, it is believed that one skilled in the art can, using the preceding description, utilize the present invention to its fullest extent. The preceding preferred specific embodiments are, therefore, to be construed as merely illustrative, and not limitative of the remainder of the disclosure in any way whatsoever.

(57) In the foregoing and in the examples, all temperatures are set forth uncorrected in degrees Celsius and, all parts and percentages are by weight, unless otherwise indicated.

(58) The entire disclosures of all applications, patents and publications, cited herein and of corresponding application No. FR 1762158, filed Dec. 14, 2017 are incorporated by reference herein.

EXAMPLES

Example 1 (Comparative): Preparation of High Temperature Alumina S1 Having a BET Specific Surface Area Less than 100 m.SUP.2./g

(59) An alumina support is prepared by direct calcination of a precursor of alumina (boehmite) at high temperature (1000° C.). The BET surface area of the support S1 is determined with nitrogen according to the standard ASTM D3663-03. Identification of the phases and of the asymmetry of beam [440] is carried out by XRD according to the method described previously.

(60) TABLE-US-00002 Support S1 Phases detected by XRD Delta, Theta and Alpha Asymmetry of beam [440] 2.3 S.sub.BET (m.sup.2/g) 79 Gamma alumina content (% by weight) 0

(61) Traces of alpha alumina are observed (of the order of less than one percent by weight of α alumina).

(62) By using the method as described in the description of the invention, the quantity of 8 alumina is estimated from a pure sample of θ alumina available from the XRD laboratory and by choosing the isolated beams of θ alumina at angles (30-35°, 51°, 73° and 108°). The relative content of theta alumina in this sample is 50% by weight.

(63) The asymmetry of the beam [440] indicates the absence of gamma alumina. The support is therefore composed of 50% by weight of theta alumina and 50% by weight of delta alumina.

Example 2 (Comparative): Preparation of Low Temperature Alumina S2 Having a BET Specific Surface Area Greater than 100 m.SUP.2./g

(64) An alumina support is prepared by direct calcination of a precursor of alumina (boehmite) at low temperature (540° C.). The BET surface area of the support S2 is determined with nitrogen according to the standard ASTM D3663-03. XRD analysis does not show θ and α phases. The asymmetry of the beam [440] is 1.25. This sample is therefore composed of 82% by weight of γ alumina.

(65) TABLE-US-00003 Support S2 S.sub.BET (m.sup.2/g) 264 Gamma alumina content (% by 82 weight)

Example 3 (According to the Invention): Preparation of Low Temperature Alumina S3 Having a BET Specific Surface Area Less than 100 m.SUP.2./g

(66) An alumina support is prepared by dry impregnation of extrudates of gamma alumina with 1% of acetic acid, followed by autoclaving at 180° C. for 8 hours, then a low temperature calcination (700° C.). The BET surface area of the support S3 is determined with nitrogen according to the standard ASTM D3663-03. XRD analysis does not show θ and α phases. The asymmetry of the beam [440] is 1.36. This sample is therefore composed of 74% by weight of γ alumina.

(67) TABLE-US-00004 Support S3 S.sub.BET (m.sup.2/g) 79 Gamma alumina content (% by weight) 74

Example 4 (According to the Invention): Preparation of Low Temperature Alumina S4 Having a BET Specific Surface Area at 120 m.SUP.2./g

(68) An alumina support is prepared by heat treatment at 225° C. for 6 hours of a boehmite powder at 10% by weight in suspension in water. The solid is then separated by filtration then subjected to a low temperature calcination (600° C.). The BET surface area of the support S4 is determined with nitrogen according to the standard ASTM D3663-03. XRD analysis does not show θ and α phases. The asymmetry of the beam [440] is 1.20. This sample is therefore composed of 87% of γ alumina.

(69) TABLE-US-00005 Support S4 S.sub.BET (m.sup.2/g) 120 Gamma alumina content (% by 87 weight)

Example 5 (According to the Invention): Preparation of Low Temperature Alumina S5 Having a BET Specific Surface Area Less than 100 m.SUP.2./g

(70) A solution of aluminium tri-n-hexanolate is hydrolyzed at 90° C. by the addition of water. The hexanol is then removed by azeotropic distillation. The residue is heated at 110° C. for 24 hours in a reactor. The solid is then separated by filtration then subjected to a low temperature calcination (700° C.).

(71) The BET surface area of the support S5 is determined with nitrogen according to the standard ASTM D3663-03. XRD analysis does not show θ and α phases. The asymmetry of the beam [440] is 1.26. This sample is therefore composed of 82% by weight of γ alumina.

(72) TABLE-US-00006 Support S5 S.sub.BET (m.sup.2/g) 95 Gamma alumina content (% by 82 weight)

Example 6 (According to the Invention): Preparation of Low Temperature Alumina S6 Having a BET Specific Surface Area Less than 100 m.SUP.2./g

(73) A soda solution is added to an aluminium chloride solution in water. The reaction medium is heated at 200° C. for 24 h. The solid is then separated by filtration then subjected to a low temperature calcination (560° C.).

(74) The BET surface area of the support S6 is determined with nitrogen according to the standard ASTM D3663-03. XRD analysis does not show θ and α phases. The asymmetry of the beam [440] is 1.10. This sample is therefore composed of 95% by weight of γ alumina.

(75) TABLE-US-00007 Support S6 S.sub.BET (m.sup.2/g) 97 Gamma alumina content (% by 95 weight)

Example 7 (Comparative): Synthesis of a CoMo/Alumina A1 Catalyst with a Low Surface Density of Molybdenum

(76) The catalyst A1 is obtained by dry impregnation of an aqueous solution prepared from molybdenum oxide, cobalt hydroxide, phosphoric acid and citric acid, the volume of said solution containing the precursors of cobalt, molybdenum and phosphorus and the citric acid organic additive being strictly equal to the pore volume of the solid alumina support S1. The concentrations of precursors and of organic additive in the aqueous solution are adjusted so as to deposit on the alumina support the weight contents of Co, Mo and P in order to obtain a fixed surface density of molybdenum of 4.5 atoms of molybdenum per nm.sup.2 of catalyst, Co/Mo and P/Mo atomic ratios equal to 0.4 and 0.55 respectively and an additive/Mo molar ratio equal to 1. After a stage of maturation for 12 hours, the solid is dried for 12 hours at 120° C.

(77) TABLE-US-00008 Catalyst A1 Support S1 S.sub.BET (m.sup.2/g-catalyst) 70 Asymmetry of the beam 440 2.35 CoO (% by weight) 1.6 MoO.sub.3 (% by weight) 7.7 P.sub.2O.sub.5 (% by weight) 2.1

Example 8 (Comparative): Synthesis of a CoMo/Alumina A2 Catalyst with a High Surface Density of Molybdenum

(78) The catalyst A2 is obtained by dry impregnation of an aqueous solution prepared from molybdenum oxide, cobalt hydroxide, phosphoric acid and citric acid, the volume of said solution containing the precursors of cobalt, molybdenum and phosphorus and the citric acid organic additive being strictly equal to the pore volume of the solid alumina support S2. The concentrations of precursors and of organic additive in the aqueous solution are adjusted so as to deposit on the alumina support the weight contents of Co, Mo and P in order to obtain a surface density of molybdenum fixed at 5.2 atoms of molybdenum per nm.sup.2 of catalyst, Co/Mo and P/Mo atomic ratios equal to 0.4 and 0.55 respectively and an additive/Mo molar ratio equal to 1. After a stage of maturation for 12 hours, the solid is dried for 12 hours at 120° C.

(79) TABLE-US-00009 Catalyst A2 Support S2 S.sub.BET (m.sup.2/g-catalyst) 178 Asymmetry of the beam 440 1.29 CoO (% by weight) 4.5 MoO.sub.3 (% by weight) 22.0 P.sub.2O.sub.5 (% by weight) 6.0

Example 9: Synthesis of the CoMo/Alumina A3 Catalyst (According to the Invention)

(80) The catalyst A3 is obtained by dry impregnation of an aqueous solution prepared from molybdenum oxide, cobalt hydroxide, phosphoric acid and citric acid, the volume of said solution containing the precursors of cobalt, molybdenum and phosphorus and the citric acid organic additive being strictly equal to the pore volume of the solid alumina support S3. The concentrations of precursors and of organic additive in the aqueous solution are adjusted so as to deposit on the alumina support the weight content of Co, Mo and P in order to obtain a fixed surface density of molybdenum of 7 atoms of molybdenum per nm.sup.2 of catalyst, Co/Mo and P/Mo atomic ratios equal to 0.4 and 0.55 respectively and an additive/Mo molar ratio equal to 1. After a stage of maturation for 12 hours, the solid is dried for 12 hours at 120° C.

(81) TABLE-US-00010 Catalyst A3 Support S3 S.sub.BET (m.sup.2/g-catalyst) 66 Asymmetry of the beam 440 1.40 CoO (% by weight) 2.3 MoO.sub.3 (% by weight) 11.1 P.sub.2O.sub.5 (% by weight) 3.0

Example 10: Synthesis of the CoMo/Alumina A4 Catalyst without Additive (According to the Invention)

(82) Catalyst A4 is obtained by dry impregnation of an aqueous solution prepared from molybdenum oxide, cobalt hydroxide and phosphoric acid, the volume of said solution containing the precursors of cobalt, molybdenum and phosphorus being strictly equal to the pore volume of the solid alumina support S5. The concentrations of precursors in the solution are adjusted so as to deposit on the alumina support the weight contents of Co, Mo and P in order to obtain a fixed surface density of molybdenum of 4.5 atoms of molybdenum per nm.sup.2 of catalyst, Co/Mo and P/Mo atomic ratios equal to 0.4 and 0.32 respectively. After a stage of maturation for 12 hours, the solid is dried for 12 hours at 120° C. then calcined for 4 h at 450° C.

(83) TABLE-US-00011 Catalyst A4 Support S5 S.sub.BET (m.sup.2/g-catalyst) 83 Asymmetry of the beam 440 1.26 CoO (% by weight) 1.9 MoO.sub.3 (% by weight) 9.0 P.sub.2O.sub.5 (% by weight) 1.4

Example 11: Assessment of Catalysts A1, A2, A3 and A4

(84) A model feedstock representative of a catalytic cracking (FCC) gasoline containing 10% by weight of 2,3-dimethylbut-2-ene and 0.33% by weight of 3-methylthiophene (i.e. 1000 ppm by weight of sulphur in the feedstock) is used for the assessment of the catalytic performances of the different catalysts. The solvent used is heptane.

(85) The hydrodesulphurization reaction (HDS) is carried out in a traverse fixed-bed reactor under a total pressure of 1.5 MPa, 210° C., HSV=6 h.sup.−1 (HSV=volume flow rate of feedstock/volume of catalyst) in the presence of 4 mL of catalyst. Prior to the HDS reaction, the catalyst is sulphurized in-situ at 450° C. for 2 hours under a flow of H.sub.2 containing 15% mol of H.sub.2S at atmospheric pressure.

(86) Each of the catalysts are successively placed in said reactor. Samples are taken at different time intervals and are analysed by gas phase chromatography so as to observe the disappearance of the reagents and the formation of the products.

(87) The catalytic performances of the catalysts are assessed from the catalytic activity and the selectivity.

(88) The HDS activity is expressed from the velocity constant for the HDS reaction of 3-methylthiophene (kHDS), normalized by volume of catalyst introduced, assuming a kinetic of order 1 with respect to the sulphurized compound.

(89) The HydO activity is expressed from the velocity constant for the hydrogenation reaction of the olefin (HydO), namely in the present case for the hydrogenation reaction of 2,3-dimethylbut-2-ene, normalized by volume of catalyst introduced, assuming a kinetic of order 1 with respect to the olefin.

(90) The selectivity of the catalyst is expressed as the normalized ratio of the velocity constants kHDS/kHydO. The more selective the catalyst, the higher will be the kHDS/kHydO ratio, meaning a limited hydrogenation of 2,3-dimethylbut-2-ene. An increase in the kHDS/kHydO ratio is therefore favourable for the quality of the gasoline obtained at the end of the hydrodesulphurization reaction, given that as the hydrogenation of the olefins was limited, the drop in octane number of the resultant gasoline is greatly minimized.

(91) The HDS activity and the selectivity of the catalysts are given in the following table. The values are normalized by taking catalyst A1 as reference, i.e. the HDS activity and the selectivity of catalysts A2, A3 and A4 are compared relative to those of catalyst A1 for which the HDS activity and the selectivity are set at 100. It is observed that the catalysts according to the invention show an increase in selectivity while maintaining the activity.

(92) Relative selectivity and activity of catalysts A1, A2 and A3.

(93) TABLE-US-00012 Catalysts A1 A2 A3 A4 (comp) (comp) (inv) (inv) S.sub.BET (m.sup.2/g of catalyst) 70 178 66 83 Asymmetry of beam 440 2.35 1.29 1.40 1.26 Gamma alumina content (% by 0 82 74 82 weight) Relative HDS activity 100 230 100 103 Relative selectivity 100 78 142 114

(94) The preceding examples can be repeated with similar success by substituting the generically or specifically described reactants and/or operating conditions of this invention for those used in the preceding examples.

(95) From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention and, without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions.