CATALYST AND MACROPOROUS CATALYST WITH COMALATED ACTIVE PHASE, PROCESS FOR THE PREPARATION THEREOF A

专利摘要:
The invention relates to a mesoporous and macroporous hydroconversion catalyst comprising: a predominantly aluminized calcined oxide matrix; a hydro-dehydrogenating active phase comprising at least one Group VI B metal of the periodic table of elements, optionally at least one metal of group VIII of the periodic table of the elements, optionally phosphorus, said active phase being at least partly comalaxée within said calcined predominantly aluminum oxide matrix, said catalyst having a surface area Sbet greater than 100 m 2 / g, a mesoporous median diameter by volume between 12 nm and 25 nm, limits included, a median macroporous volume diameter between 50 and 250 nm, inclusive, a mesoporous volume as measured by mercury porosimeter intrusion greater than or equal to 0.65 ml / g and a total pore volume measured by mercury porosimetry greater than or equal to 0.75 ml / boy Wut. The invention also relates to a catalyst preparation process suitable for the hydroconversion / hydrotreatment of residues by comalaxing the active phase with a particular alumina. The invention finally relates to the use of the catalyst in hydrotreating processes, in particular the hydrotreatment of heavy feedstocks.
公开号:FR3022156A1
申请号:FR1455413
申请日:2014-06-13
公开日:2015-12-18
发明作者:Malika Boualleg；Bertrand Guichard
申请人:IFP Energies Nouvelles IFPEN；
IPC主号:

专利说明:

[0001] TECHNICAL FIELD OF THE INVENTION The invention relates to hydrotreatment catalysts, especially residues catalysts, and relates to the preparation of comalaxed active phase hydrotreatment catalysts having a texture and a formulation that is favorable for the hydrotreatment of residues, in particular for hydrodemetallation. The preparation process according to the invention also makes it possible to avoid the impregnation step usually carried out on a previously shaped support. The invention consists of the use of active phase catalysts comalaxed in an aluminum oxide matrix comprising at least one element of group VIB, optionally at least one group VIII element, and optionally the phosphorus element. The introduction of this type of active phase before the shaping step by comalaxing with a particular alumina, itself originating from the calcination of a specific gel, allows, unexpectedly, in hydrotreatment processes, in particular residues, in fixed bed, but also in a bubbling bed process, to significantly improve the activity in hydrodesulphurization, but also in hydrodemetallization of the catalyst, compared to catalysts comalaxed on boehmite, while reducing the cost of significantly, compared to impregnated catalysts of the prior art.
[0002] PRIOR ART It is known to a person skilled in the art that catalytic hydrotreating makes it possible, by bringing a hydrocarbon feedstock into contact with a catalyst whose properties, in terms of metals of the active phase and of porosity, are previously well adjusted, significantly reduce its content of asphaltenes, metals, sulfur and other impurities while improving the ratio hydrogen on carbon (H / C) and while transforming it more or less partially into lighter cuts. The fixed bed residue hydrotreating processes (commonly called "Residual Desulfurization" unit or RDS) lead to high refining performance: typically they can produce a boiling temperature cut above 370 ° C. containing less than 0 ° C. , 5% by weight of sulfur and less than 20 ppm of metals from fillers containing up to 5% by weight of sulfur and up to 250 ppm of metals (Ni + V). The different effluents thus obtained can be used as a basis for the production of good quality heavy fuel oils and / or pretreated feedstocks for other units such as "Fluid Catalytic Cracking". On the other hand, the hydroconversion of the residue in slices lighter than the atmospheric residue (gas oil and petrol in particular) is generally low, typically of the order of 10 to 20% by weight. In such a process, the feed, premixed with hydrogen, circulates through a plurality of fixed bed reactors arranged in series and filled with catalysts. The total pressure is typically between 100 and 200 bar (10 and 20 MPa) and the temperatures between 340 and 420 ° C. The effluents withdrawn from the last reactor are sent to a fractionation section. Conventionally, the fixed bed hydrotreating process consists of at least two steps (or sections). The first so-called hydrodemetallation (HDM) stage is mainly aimed at eliminating the majority of metals from the feedstock by using one or more hydrodemetallization catalysts. This stage mainly includes vanadium and nickel removal operations and, to a lesser extent, iron. The second step, or so-called hydrodesulfurization (HDS) section, consists in passing the product of the first step over one or more hydrodesulfurization catalysts, which are more active in terms of hydrodesulphurization and hydrogenation of the feedstock, but less tolerant to metals.
[0003] When the metal content in the feed is too high (above 250 ppm) and / or when a large conversion (conversion of the heavy fraction 540 ° C + (or 370 ° C +) to a lighter fraction 540 ° C- (or 370 ° C) is preferred, ebullated hydrotreating processes are preferred, and in this type of process (see MS Rana et al., Fuel 86 (2007), p1216), the purification performance is lower than that of RDS processes, but the hydroconversion of the residue fraction is high (around 45 to 85% volume) The high temperatures involved, between 415 and 440 ° C, contribute to this high hydroconversion. Thermal cracking is favored because the catalyst does not generally have a specific hydroconversion function, and the effluents formed by this type of conversion may have stability problems (sediment formation). Due to this, the development of versatile, efficient and stable catalysts is essential.
[0004] For bubbling bed processes, the patent application WO 2010/002699 teaches in particular that it is advantageous to use a catalyst whose support has a median pore diameter of between 10 and 14 nm and whose distribution is narrow. It specifies that less than 5% of the pore volume must be developed in pores larger than 21 nm and in the same way, less than 10% (3% of the volume must be observed in small pores of sizes less than 9 nm US Patent 5,968,348 confirms that it is preferable to use a support whose mesoporosity remains close to 11 to 13 nm, possibly with the presence of macropores and a high BET surface, here at least 175 m 2 / g .
[0005] For fixed bed processes, US Pat. No. 6,780,817 teaches that it is necessary to use a catalyst support that has at least 0.32 ml / g macroporous volume for stable fixed bed operation. Such a catalyst further has a median diameter, in the mesopores, of 8 to 13 nm and a high specific surface area of at least 180 m 2 / g.
[0006] US Pat. No. 6,919,294 also describes the use of so-called bimodal, therefore mesoporous and macroporous carriers, with the use of high macroporous volumes, but with a mesoporous volume limited to not more than 0.4 ml / g. US Pat. Nos. 4,976,848 and 5,089,463 disclose a heavy charge hydrodemetallation and hydrodesulphurisation catalyst comprising a hydrogenating active phase based on Group VI and VIII metals and an inorganic refractory oxide support, the catalyst having precisely between 5 and 11% of its porous volume as macropores and mesopores with a median diameter greater than 16.5 nm.
[0007] US Pat. No. 7,169,294 discloses a heavy charge hydroconversion catalyst comprising between 7 and 20% of Group VI metal and between 0.5 and 6 weight percent of Group VIII metal on an aluminum support. The catalyst has a specific surface area of between 100 and 180 m 2 / g, a total pore volume greater than or equal to 0.55 ml / g, and at least 50% of the total pore volume is included in pores larger than 20 nm, at least 5% of the total pore volume is contained in pores larger than 100 nm, at least 85% (3% of the total pore volume being included in pores between 10 and 120 nm in size, less than 2 (3/0 of the total pore volume being contained in pores with a diameter greater than 400 nm, and less than 1 (3/0 of the total pore volume being contained in pores with a diameter greater than 1000 nm.
[0008] Numerous developments include the optimization of the porous distribution of the catalyst or catalyst mixtures by optimizing the catalyst support.
[0009] Thus, US Pat. No. 6,589,908 describes, for example, a process for the preparation of an alumina characterized by the absence of macropores, less than 5% of the total pore volume constituted by pores with a diameter greater than 35 nm, a high volume. porous greater than 0.8 ml / g, and a bimodal mesopore distribution in which the two modes are separated by 1 to 20 nm and the primary porous mode is greater than the median pore diameter. describes two stages of precipitation of alumina precursors under well-controlled conditions of temperature, pH and flow rates The first stage operates at a temperature of between 25 and 60 ° C., a pH of between 3 and 10. The suspension is then heated to a temperature between 50 and 90 ° C. Reagents are again added to the suspension, which is then washed, dried, shaped and calcined to form a catalyst support. said support is then impregnated with an active phase solution to obtain a hydrotreatment catalyst; a catalyst for hydrotreating residues on a mesoporous monomodal support of porous median diameter around 20 nm is described.
[0010] US Pat. No. 7,790,652 discloses hydroconversion catalysts obtainable by coprecipitation of an alumina gel, then introduction of the metals onto the support obtained by any method known to those skilled in the art, in particular by impregnation. The resulting catalyst has a mesoporous monomodal distribution with a mesoporous median diameter of between 11 and 12.6 nm and a porous distribution width of less than 3.3 nm. Alternative approaches to the conventional introduction of metals onto aluminum supports have also been developed, such as the incorporation of catalyst fines into the support. Thus, patent application WO2012 / 021386 discloses hydrotreatment catalysts comprising a porous refractory oxide support shaped from alumina powder and from 5% to 45% by weight of catalyst fines. The support comprising the fines is then dried, calcined. The support obtained has a specific surface area of between 50 m 2 / g and 450 m 2 / g, a mean pore diameter of between 50 and 200 A (5 to 20 nm), and a total pore volume exceeding 0.55 cm 3 / g. The support thus comprises metal incorporated thanks to the metals contained in the catalyst fines. The resulting support can be treated with a chelating agent. The pore volume may be partially filled by means of a polar additive, and may be impregnated with a metal impregnating solution.
[0011] In view of the prior art, it seems very difficult to obtain in a simple manner a catalyst having both a bimodal porosity, with a high mesoporous volume coupled to a macroporous volume, a very high mesopore median diameter, and a hydro-dehydrogenating active phase. Moreover, the increase in porosity is often at the expense of the specific surface area, and the mechanical strength. Surprisingly, the Applicant has discovered that a catalyst prepared from an alumina resulting from the calcination of a specific alumina gel having a low dispersibility, by comalaxing a hydro-dehydrogenating active phase with the alumina calcined had a porous structure particularly interesting for the hydrotreatment of heavy loads, while having a suitable active phase content. The invention relates to a hydroconversion / hydrotreating residue catalyst having an optimized porous distribution and an active phase comalaxed in a calcined aluminic matrix. The invention also relates to a catalyst preparation process suitable for the hydroconversion / hydrotreatment of residues by comalaxing the active phase with a particular alumina. The invention finally relates to the use of the catalyst in hydrotreating processes, in particular the hydrotreatment of heavy feedstocks.
[0012] SUMMARY OF THE INVENTION The invention relates to a process for the preparation of a comalaxed active phase catalyst, comprising at least one metal of group VI B of the periodic table of elements, optionally at least one metal of group VIII of the periodic table. elements, optionally phosphorus and a predominantly aluminum oxide matrix, comprising the following steps: a) a first step of precipitation, in an aqueous reaction medium, of at least one basic precursor chosen from sodium aluminate, sodium aluminate and potassium, ammonia, sodium hydroxide and potassium hydroxide and at least one acid precursor selected from aluminum sulphate, aluminum chloride, aluminum nitrate, sulfuric acid, hydrochloric acid and nitric acid, wherein at least one of the basic or acidic precursors comprises aluminum, the relative flow rate of the acidic and basic precursors is chosen so to obtain a pH of the reaction medium of between 8.5 and 10.5 and the flow rate of the aluminum-containing acidic and basic precursor (s) is adjusted so as to obtain a degree of progression of the first step of between 5 and 13%, the advancement rate being defined as being the proportion of alumina formed in A1203 equivalent during said first precipitation step relative to the total amount of alumina formed in A1203 equivalent at the end of step c ) the preparation process, said step operating at a temperature between 20 and 90 ° C and for a period of between 2 minutes and 30 minutes; b) a step of heating the suspension at a temperature between 40 and 90 ° C for a period of between 7 minutes and 45 minutes; c) a second step of precipitating the suspension obtained at the end of the heating step b) by adding to the suspension at least one basic precursor chosen from sodium aluminate, potassium aluminate, ammonia, sodium hydroxide and potassium hydroxide and at least one acidic precursor selected from aluminum sulphate, aluminum chloride, aluminum nitrate, sulfuric acid, acid hydrochloric acid and nitric acid, wherein at least one of the basic or acidic precursors comprises aluminum, the relative flow rate of the acidic and basic precursors is chosen so as to obtain a pH of the reaction medium of between 8.5 and 10, 5 and the flow rate of the aluminum-containing acidic and basic precursor (s) is adjusted so as to obtain a progress rate of the second stage of between 87 and 95 ° A, the rate of progress being defined as the proportion of alumina formed in equivalent A1203 during the said second precipitation step relative to the total amount of alumina formed in equivalent A1203 at the end of step c) of the preparation process, said step operating at a temperature between 40 and 90 ° C and for a period of time between 2 minutes and 50 minutes; d) a filtration step of the suspension obtained at the end of the second precipitation step c) to obtain an alumina gel; e) a step of drying said alumina gel obtained in step d) to obtain a powder; f) a step of heat treatment of the powder obtained at the end of step e) between 500 and 1000 ° C, for a period of between 2 and 10 h, in the presence or absence of a flow of air containing up to 60% water volume to obtain a calcined aluminous porous oxide; g) a step of kneading the calcined aluminous porous oxide obtained with a solution of at least one metal precursor of the active phase to obtain a paste; h) a step of forming the paste obtained; i) a step of drying the shaped dough at a temperature of less than or equal to 200 ° C to obtain a dried catalyst; j) a possible step of heat treatment of the dried catalyst at a temperature between 200 and 1000 ° C, in the presence or absence of water. The rate of advance of the first precipitation step a) is advantageously between 6 and 12%.
[0013] The rate of advance of the first precipitation step a) is very preferably between 7 and 11%. The acidic precursor is advantageously chosen from aluminum sulphate, aluminum chloride and aluminum nitrate, preferably aluminum sulphate.
[0014] The basic precursor is advantageously chosen from sodium aluminate and potassium aluminate, preferably sodium aluminate. Preferably, in steps a), b), c) the aqueous reaction medium is water and said steps operate with stirring, in the absence of organic additive. The invention also relates to a mesoporous and macroporous hydroconversion catalyst comprising: a predominantly aluminized calcined oxide matrix; a hydro-dehydrogenating active phase comprising at least one Group VIB metal of the periodic table of the elements, optionally at least one metal of group VIII of the periodic table of the elements, optionally phosphorus, said active phase being at least partially comalaxed; within said calcined alumina-predominantly aluminum oxide matrix, said catalyst having an SBET surface area of greater than 100 m 2 / g, a mesoporous median volume diameter of between 12 nm and 25 nm, limits included, a median macroporous volume diameter between 50 and 250 nm, inclusive, a mesoporous volume as measured by mercury porosimeter intrusion greater than or equal to 0.65 ml / g and a total pore volume measured by mercury porosimetry greater than or equal to 0.75 ml / boy Wut. Preferably, said catalyst has a mesoporous median diameter in volume determined by mercury porosimeter intrusion of between 13 and 17 nm, limits included. Preferably, said catalyst has a macroporous volume of between 15 and 35% of the total pore volume.
[0015] Preferably, the mesoporous volume is between 0.65 and 0.75 ml / g. Preferably, the catalyst does not have micropores. Preferably, the group VI B metal content is between 2 and 10% by weight of trioxide of at least Group VI B metal relative to the total mass of the catalyst, the Group VIII metal content is between 0.0 and 3.6% by weight of the oxide of at least Group VIII metal relative to the total mass of the catalyst, the content of phosphorus element is between 0 and 5% by weight of phosphorus pentoxide relative to the total mass of the catalyst.
[0016] The hydro-dehydrogenating active phase may be composed of molybdenum (Mo), or nickel and molybdenum (NiMo), or cobalt and molybdenum (CoMo). The hydrodehydrogenating active phase preferably also comprises phosphorus.
[0017] Advantageously, the hydro-dehydrogenating active phase is fully comalaxed. In one embodiment, a portion of the hydro-dehydrogenating active phase may be impregnated onto the predominantly aluminum oxide matrix. The invention also relates to a process for the hydrotreatment of a heavy hydrocarbon feedstock chosen from atmospheric residues, vacuum residues resulting from direct distillation, deasphalted oils, residues resulting from conversion processes such as, for example, those originating from coking, hydroconversion fixed bed, bubbling bed or moving bed, taken alone or in mixture, said hydrotreatment process comprising contacting said feedstock with hydrogen and a catalyst capable of being prepared according to the invention or a catalyst as described above.
[0018] The process may be carried out partly in a bubbling bed at a temperature of between 320 ° and 450 ° C., under a hydrogen partial pressure of between 3 MPa and 30 MPa, at a space velocity advantageously between 0.1 and 10 vol. charge per volume of catalyst per hour, and with a hydrogen gas ratio on a hydrocarbon liquid charge advantageously between 100 and 3000 normal cubic meters per cubic meter. The process may be carried out at least in part in a fixed bed at a temperature of between 320 ° C. and 450 ° C., at a hydrogen partial pressure of between 3 MPa and 30 MPa, at a space velocity of between 0.05 and 5. volume of charge per volume of catalyst per hour, and with a hydrogen gas ratio on a hydrocarbon liquid charge of between 200 and 5000 normal cubic meters per cubic meter. Said process may be a heavy bed hydrocarbon feedstock hydrotreatment process comprising at least: a) a hydrodemetallation step b) a hydrodesulfurization step and said catalyst is used in at least one of said steps a) and B).
[0019] DETAILED DESCRIPTION OF THE INVENTION The applicant has discovered that the comalaxing of an alumina obtained from a particular gel prepared according to a preparation method described below with a metal formulation containing at least one element of group VIB, optionally at least one Group VIII element and optionally the phosphorus element makes it possible to obtain a catalyst which simultaneously has a high total pore volume (greater than or equal to 0.75 ml / g), a mesoporous volume (greater than or equal to 0.65 ml / g) raised a median mesopore diameter high (between 12 and 25 nm), a macroporous median diameter between 50 and 250 nm, but also active phase characteristics favorable to hydrotreatment. Furthermore, in addition to reducing the number of steps and therefore the cost of manufacture, the advantage of a comparison compared to an impregnation is that it avoids any risk of partial blockage of the porosity of the support during the deposit of the active phase and therefore the appearance of problems of limitations. In addition to being able to be synthesized at a lower cost, such a catalyst has a significant gain in hydrodemetallation compared to other comalaxed catalysts of the prior art, and therefore requires a lower operating temperature than these to reach the same level of conversion of metallated compounds. By implementing in particular the said catalyst according to the invention at the beginning of complete chaining to a fixed bed, ie a hydrodemetallation section (HDM), then a hydrodesulfurization section (HDS), the overall performance of the sequence is improved. .
[0020] Terminology and characterization techniques Throughout the rest of the text, dispersibility is defined as the weight of solid or gel of peptised alumina that can not be dispersed by centrifugation in a 3600G polypropylene tube for 3 min. The catalyst of the present invention has a specific porous distribution, where the macroporous and mesoporous volumes are measured by mercury intrusion and the microporous volume is measured by nitrogen adsorption. "Macropores" means pores whose opening is greater than 50 nm. By "mesopores" is meant pores whose opening is between 2 nm and 50 nm, limits included.
[0021] By "micropores" is meant pores whose opening is less than 2 nm. In the following description of the invention, the term "specific surface" means the specific surface B.E.T. determined by nitrogen adsorption according to ASTM D 3663-78 established from the BRUNAUER-EMMETT-TELLER method described in the journal "The Journal of the American Society", 60, 309, (1938). In the following description of the invention, the term "total pore volume of the alumina or the predominantly aluminum matrix or catalyst" means the volume measured by mercury porosimeter intrusion according to ASTM D4284-83 at a pressure of maximum of 4000 bar (400 MPa), using a surface tension of 484 dyne / cm and a contact angle of 140 °. The angle of anchorage was taken equal to 140 ° following the recommendations of the book "Techniques of the engineer, treated analysis and characterization", p.1050-5, written by Jean Charpin and Bernard Rasneur.
[0022] In order to obtain a better precision, the value of the total pore volume in ml / g given in the following text corresponds to the value of the total mercury volume (total pore volume measured by mercury porosimeter intrusion) in ml / g measured on the sample minus the mercury volume value in ml / g measured on the same sample for a pressure corresponding to 30 psi (approximately 0.2 MPa). The volume of macropores and mesopores is measured by mercury intrusion porosimetry according to ASTM D4284-83 at a maximum pressure of 4000 bar (400 MPa), using a surface tension of 484 dyne / cm and a contact angle of 140 °.
[0023] The value at which mercury fills all the intergranular voids is fixed at 0.2 MPa, and it is considered that beyond this mercury enters the pores of the sample.
[0024] The macroporous volume of the catalyst is defined as the cumulative volume of mercury introduced at a pressure of between 0.2 MPa and 30 MPa, corresponding to the volume contained in the pores with an apparent diameter greater than 50 nm.
[0025] The mesoporous volume of the catalyst is defined as the cumulative volume of mercury introduced at a pressure of between 30 MPa and 400 MPa, corresponding to the volume contained in the pores with an apparent diameter of between 2 and 50 nm. The micropore volume is measured by nitrogen porosimetry. The quantitative analysis of the microporosity is carried out using the "t" method (Lippens-De Boer method, 1965) which corresponds to a transformation of the starting adsorption isotherm as described in the book "Adsorption by powders and porous solids. Principles, methodology and applications "written by F. Rouquérol, J. Rouquérol and K. Sing, Academic Press, 1999.
[0026] The mesoporous median diameter is also defined as a diameter such that all pores less than this diameter constitute 50% of the total mesoporous volume determined by mercury porosimeter intrusion. Macroporous median diameter is also defined as a diameter such that all pores smaller than this diameter constitute 50% of the total macroporous volume determined by mercury porosimeter intrusion. In the following, groups of chemical elements are given according to the CAS classification (CRC Handbook of Chemistry and Physics, publisher CRC Press, editor in chief D.R. Lide, 81st edition, 2000-2001). For example, group VIII according to the CAS classification corresponds to the metals of columns 8, 9 and 10 according to the new IUPAC classification. General description of the catalyst. The invention relates to a comalaxed active phase hydroconversion catalyst comprising at least one Group VI B metal of the Periodic Table of Elements, optionally at least one Group VIII metal of the Periodic Table of Elements, optionally phosphorus and a predominantly calcined aluminum oxide matrix, its method of preparation and its use in a hydrotreatment process for heavy hydrocarbon feedstocks such as petroleum residues (atmospheric or vacuum). The catalyst according to the invention is in the form of a matrix comprising for the most part a calcined porous refractory oxide in which the metals of the active phase are distributed. The invention also relates to the process for preparing the catalyst which is carried out by comalaxing a particular alumina with a metal solution of formulation adapted to the target metal target for the final catalyst. The characteristics of the gel which has led to the obtaining of alumina, as well as the textural and active phase properties obtained, give the catalyst according to the invention its specific properties.
[0027] The Group VI B metals are advantageously selected from molybdenum and tungsten, and preferably said Group VI B metal is molybdenum. Group VIII metals are preferably selected from iron, nickel or cobalt and nickel or cobalt, or a combination of both, is preferred. The respective quantities of group VI B metal and of group VIII metal are advantageously such that the atomic ratio metal (aux) of group VIII to group VI B (VIII: VI B) metal (s) is between 0.0 : 1 and 0.7: 1, preferably between 0.1: 1 and 0.6: 1 and more preferably between 0.2: 1 and 0.5: 1. This ratio can in particular be adjusted according to the type of load and the process used. The respective amounts of Group VI B metal and phosphorus are such that the atomic phosphorus to metal (A) group VI (P / VI B) atomic ratio is between 0.2: 1 and 1.0: 1, preferably between 0.4: 1 and 0.9: 1 and even more preferably between 0.5: 1.0 and 0.85: 1.
[0028] The metal content of group VI B is advantageously between 2 and 10% by weight of trioxide of at least Group VI B metal relative to the total mass of the catalyst, preferably between 3 and 8%, and still more preferably more preferred between 4 and 7% weight.
[0029] The metal content of group VIII is advantageously between 0.0 and 3.6% by weight of the oxide of at least one group VIII metal relative to the total mass of the catalyst, preferably between 0.4 and 2.5% and even more preferably between 0.7 and 1.8% by weight. The content of phosphorus element is advantageously between 0.0 and 5% by weight of phosphorus pentoxide relative to the total mass of the catalyst, preferably between 0.6 and 3.5% by weight and even more preferably between 1 and 5% by weight. , 0 and 3.0% weight. The predominantly calcined aluminum matrix of said catalyst according to the invention comprises an alumina content greater than or equal to 90% and a silica content of at most 10% by weight of SiO 2 equivalent relative to the mass of the matrix, preferably a content of The silica may be introduced, by any technique known to those skilled in the art, during the synthesis of the alumina gel or to a silica content of less than 5% by weight. at the time of the comalaxing.
[0030] Even more preferably, the aluminic matrix contains nothing other than alumina. The said co-axial phase active catalyst according to the invention is generally presented in all the forms known to those skilled in the art. Preferably, it consists of extrudates of diameter generally between 0.5 and 10 mm, preferably between 0.8 and 3.2 mm and very preferably between 1.0 and 2.5 mm. This may advantageously be in the form of extruded cylindrical, trilobed or quadrilobed. Preferably, its shape will be trilobed or quadrilobed. The shape of the lobes can be adjusted according to all known methods of the prior art. The comalaxed catalyst according to the invention has particular textural properties.
[0031] The catalyst according to the invention has a total pore volume (VPT) of at least 0.75 ml / g and preferably at least 0.80 ml / g. In a preferred embodiment, the catalyst has a total pore volume of between 0.80 and 1.05 ml / g.
[0032] The catalyst used according to the invention advantageously has a macroporous volume, Vmacro or V5onm defined as the pore volume with a diameter greater than 50 nm, between 15 and 35% of the total pore volume, and preferably between 15 and 30% of the volume. total porous. In a very preferred embodiment, the macroporous volume represents between 20 and 30% of the total pore volume.
[0033] The mesoporous volume (Vmeso) of the catalyst is at least 0.65 ml / g, preferably between 0.65 and 0.80 ml / g. In a preferred embodiment, the mesoporous volume of the catalyst is between 0.65 ml / g and 0.75 ml / g.
[0034] The mesoporous median diameter (DpméS0) is between 12 nm and 25 nm, limits included, and preferably between 12 and 18 nm, limits included. Very preferably, the median mesoporous diameter is between 13 and 17 nm, inclusive. The catalyst advantageously has a macroporous median diameter (DpmaCrO) of between 50 and 250 nm, preferably between 80 and 200 nm, even more preferably between 80 and 150 nm. Very preferably, the macroporous median diameter is between 90 and 130 nm. The catalyst according to the present invention has a BET specific surface area (SBET) of at least 100 m 2 / g, preferably at least 120 m 2 / g and even more preferably between 150 and 250 m 2 / g. Preferably, the catalyst has a low microporosity, very preferably no microporosity is detectable in nitrogen porosimetry.
[0035] If necessary, it is possible to increase the metal content by introducing a second part of the active phase by impregnation on the catalyst already comalaxed with a first part of the active phase.
[0036] It is important to emphasize that the catalyst according to the invention differs structurally from a catalyst obtained by simply impregnating a metal precursor on an alumina support in which the alumina forms the support and the active phase is introduced into the pores of this support. Without wishing to be bound by any theory, it appears that the process for preparing the catalyst according to the invention by comalaxing a particular aluminous porous oxide with one or more precursors of metals makes it possible to obtain a composite in which the metals and the The alumina is intimately mixed thereby forming the catalyst structure with porosity and active phase content at the desired reactions.
[0037] Process for the Preparation of the Catalyst According to the Invention Main Steps The catalyst according to the invention is prepared by co-mixing a calcined porous aluminum oxide obtained from a specific alumina gel and the precursor (s) of metals. The process for preparing the catalyst according to the invention comprises the following steps: a) to e): Synthesis of the precursor gel of the porous oxide f) Heat treatment of the powder obtained at the end of step e) g) Comalaxing of the porous oxide obtained with at least one precursor of the active phase h) Shaping of the paste obtained by kneading, for example by extrusion i) Drying of the shaped dough obtained j) Possible heat treatment (preferably in dry air) The solid obtained at the end of steps a) to f) undergoes a step g) of comalaxing. It is then shaped in a step h), then can then simply be dried at a temperature of less than or equal to 200 ° C (step i) or dried, and then subjected to a new calcination heat treatment in a step j) optional.
[0038] Prior to its use in a hydrotreatment process, the catalyst is usually subjected to a final sulfurization step. This step consists in activating the catalyst by transforming, at least in part, the oxide phase in a sulpho-reducing medium. This activation treatment by sulphurisation is well known to those skilled in the art and can be performed by any previously known method already described in the literature. A conventional sulphurization method well known to those skilled in the art consists in heating the mixture of solids under a stream of a mixture of hydrogen and hydrogen sulphide or under a stream of a mixture of hydrogen and of hydrocarbons containing sulfur-containing molecules at a temperature of temperature between 150 and 800 ° C, preferably between 250 and 600 ° C, generally in a crossed-bed reaction zone. DETAILED DESCRIPTION OF THE PROCESS OF PREPARATION The comalaxed active phase catalyst according to the invention is prepared from a specific alumina gel, which is dried and calcined, before comalaxing with the active phase, and then shaped. The steps for preparing the alumina gel used during the preparation of the catalyst according to the invention are detailed below.
[0039] According to the invention, said method for preparing the alumina gel comprises a first step a) of precipitation, a step b) of heating, a step c) of second precipitation, a step d) of filtration, a step e) drying.
[0040] The rate of progress for each of the precipitation steps is defined as the proportion of alumina formed in A1203 equivalent during said first or second precipitation step relative to the total amount of alumina formed in equivalent A1203 at the end of of the two precipitation stages and more generally after the steps of preparation of the alumina gel and in particular at the end of step c) of the preparation process according to the invention. Step a): first precipitation This step consists in bringing into contact, in an aqueous reaction medium, at least one basic precursor chosen from sodium aluminate, potassium aluminate, ammonia and sodium hydroxide. and potassium hydroxide and at least one acidic precursor selected from aluminum sulphate, aluminum chloride, aluminum nitrate, sulfuric acid, hydrochloric acid, and nitric acid, in which at least one of the basic or acidic precursors comprises aluminum, the relative flow rate of the acidic and basic precursors is chosen so as to obtain a pH of the reaction medium of between 8.5 and 10.5 and the flow rate of the or aluminum-containing acidic and basic precursors are set so as to obtain a first step progress rate of between 5 and 13%, the feed rate being defined as the proportion of alumina formed in equivalent A1203 during said step a) of cipitation with respect to the total quantity of alumina formed in equivalent A1203 at the end of step c), said step operating at a temperature of between 20 and 90 ° C., and for a duration of between 2 minutes and 30 minutes .
[0041] The mixture in the aqueous reaction medium of at least one basic precursor and at least one acidic precursor requires that at least one of the acidic or basic precursors comprises aluminum. It is also possible that at least two of the basic and acidic precursors comprise aluminum.
[0042] Basic precursors comprising aluminum are sodium aluminate and potassium aluminate. The preferred basic precursor is sodium aluminate. Acidic precursors comprising aluminum are aluminum sulphate, aluminum chloride and aluminum nitrate. The preferred acidic precursor is aluminum sulphate.
[0043] Preferably, the aqueous reaction medium is water. Preferably, said step a) operates with stirring.
[0044] Preferably, said step a) is carried out in the absence of organic additive. The acidic and basic precursors, whether they contain aluminum or not, are mixed, preferably in solution, in the aqueous reaction medium, in such proportions that the pH of the resulting suspension is between 8.5 and 10. 5.
[0045] According to the invention, the alumina acid precursors and the basic alumina precursors can be used alone or as a mixture in the precipitation step.
[0046] According to the invention, the relative flow rate of the acidic and basic precursors they contain aluminum or not, is chosen so as to obtain a pH of the reaction medium of between 8.5 and 10.5.
[0047] In the preferred case where the basic and acidic precursors are respectively sodium aluminate and aluminum sulphate, the mass ratio of said basic precursor to said acidic precursor is advantageously between 1.60 and 2.05. For the other basic and acidic precursors, whether they contain aluminum or not, the base / acid mass ratios are established by a curve of neutralization of the base by the acid. Such a curve is easily obtained by those skilled in the art. Preferably, said precipitation step a) is carried out at a pH of between 8.5 and 10.0 and very preferably between 8.7 and 9.9.
[0048] According to the invention, the first precipitation step a) is carried out at a temperature of between 20 and 90 ° C, preferably between 20 and 70 ° C and more preferably between 30 and 50 ° C.
[0049] According to the invention, the first step a) of precipitation is carried out for a duration of between 2 and 30 minutes, preferably between 5 and 20 minutes, and very preferably between 5 and 15 minutes. According to the invention, the advancement rate of said first precipitation step a) is between 5 and 13%, preferably between 6 and 12 (3/0 and very preferably between 7 and 11%. and alkaline containing aluminum are therefore introduced in amounts to obtain a suspension containing the desired amount of alumina, depending on the final concentration of alumina to achieve.In particular, said step a) allows obtaining 5 to 13 (3/0 weight of alumina relative to the total amount of alumina formed in equivalent A1203 at the end of step c) of the preparation process. Step b): Heating According to the invention, said preparation method comprises a step b) of heating the suspension obtained at the end of the first step a) of precipitation.
[0050] According to the invention, before the second precipitation step is carried out, a heating step of the suspension obtained at the end of the precipitation step a) is carried out between the two precipitation stages.
[0051] Said step of heating the suspension obtained at the end of step a), carried out between said first precipitation step a) and the second precipitation step c) operates at a temperature of between 40 and 90 ° C. preferably between 40 and 80 ° C, very preferably between 40 and 70 ° C and even more preferably between 40 and 65 ° C.
[0052] Said heating step is carried out for a period of between 7 and 45 minutes and preferably between 7 and 35 minutes. Said heating step is advantageously carried out according to all the heating methods known to those skilled in the art. Step c): Second Precipitation According to the invention, said preparation method comprises a second step of precipitation of the heated suspension obtained at the end of the heating step b), said second step operating by adding in said suspension of at least one basic precursor selected from sodium aluminate, potassium aluminate, ammonia, sodium hydroxide and potassium hydroxide and at least one acidic precursor selected from aluminum sulphate, aluminum chloride, aluminum nitrate, sulfuric acid, hydrochloric acid, and nitric acid, wherein at least one of the basic or acidic precursors comprises aluminum, the relative acidic and basic precursors is chosen in such a way as to obtain a pH of the reaction medium of between 8.5 and 10.5 and the flow rate of the acidic and basic precursor (s) containing aluminum is adjusted so as to obtain a degree of progress. of the second a step of between 87 and 95%, the degree of progress being defined as the proportion of alumina formed in Al 2 O 3 equivalent during said second precipitation step relative to the total amount of alumina formed in Al 2 O 3 equivalent at the end of step c) of the preparation process, said step operating at a temperature between 40 and 90 ° C, and for a period of between 2 minutes and 50 minutes.
[0053] The basic precursor (s) and acid (s) are added in the said second co-precipitation step in aqueous solution. As in the first precipitation step a), the addition to the heated suspension of at least one basic precursor and at least one acidic precursor requires that at least one of the basic or acid precursors comprises aluminum. It is also possible that at least two of the basic and acidic precursors comprise aluminum.
[0054] Basic precursors comprising aluminum are sodium aluminate and potassium aluminate. The preferred basic precursor is sodium aluminate. Acidic precursors comprising aluminum are aluminum sulphate, aluminum chloride and aluminum nitrate. The preferred acidic precursor is aluminum sulphate.
[0055] Preferably, said second precipitation step operates with stirring. Preferably, said second step is carried out in the absence of organic additive.
[0056] The acidic and basic precursors, whether they contain aluminum or not, are mixed, preferably in solution, in the suspension, in such proportions that the pH of the resulting suspension is between 8.5 and 10.5. . As in step a) of precipitation, the relative flow rate of the acidic and basic precursors, whether they contain aluminum or not, is chosen so as to obtain a pH of the reaction medium of between 8.5 and 10. , 5, preferably between 8.5 and 10, even more preferably between 8.7 and 9.9.
[0057] In the preferred case where the basic and acidic precursors are respectively sodium aluminate and aluminum sulphate, the mass ratio of said basic precursor to said acidic precursor is advantageously between 1.60 and 2.05.
[0058] For the other basic and acidic precursors, whether they contain aluminum or not, the base / acid mass ratio is established by a curve of neutralization of the base by the acid. Such a curve is easily obtained by those skilled in the art. The aluminum precursors are also mixed in amounts to obtain a suspension containing the desired amount of alumina, depending on the final concentration of alumina to be achieved. In particular, said second precipitation step makes it possible to obtain 87 to 95% by weight of alumina with respect to the total amount of alumina formed in A1203 equivalent at the end of the two precipitation stages.
[0059] As in step a) of precipitation, it is the flow rate of the acidic and basic precursor (s) containing aluminum which is adjusted so as to obtain a progress rate of the second stage between 87 and 95 %, preferably between 88 and 94 (3/0, very preferably between 89 and 93 (3/0, the feed rate being defined as the proportion of alumina formed in equivalent A1203 during said second step of precipitation with respect to the total amount of alumina formed in equivalent Al 2 O 3 at the end of stage c) of the preparation process Thus, as a function of the concentration of alumina targeted at the end of the precipitation steps, preferably between 20 and 100 g / l, the quantities of aluminum to be provided by the acid and / or basic precursors are calculated and the flow rate of the precursors is adjusted as a function of the concentration of said added aluminum precursors, the amount of water added to the reaction medium and the rate of progress required for each of the precipitation steps.
[0060] As in step a) of precipitation, the flow rates of the acid-containing precursor (s) and / or base (s) containing aluminum depend on the size of the reactor used and thus on the amount of water added to the reaction medium.
[0061] For example, if one works in a 3 1 reactor and that 1 1 alumina suspension Al20A final concentration of 50 g / I is targeted, with a targeted advancement rate of 10% for the first precipitation step, 10% of the total alumina must be provided during step a) of precipitation. The alumina precursors are sodium aluminate at a concentration of 155 g / l in Al 2 O 3 and aluminum sulphate at a concentration of 102 g / l in Al 2 O 3. The precipitation pH of the first stage is set at 9, And the pH of the second step at 9. The amount of water added to the reactor is 620 ml. For the first step a) of precipitation operating at 30 ° C and for 8 minutes, the flow rate of aluminum sulphate must be 2.1 ml / min and the flow rate of sodium aluminate is 2.6 ml / min . The mass ratio of sodium aluminate to aluminum sulfate is therefore 1.91. For the second precipitation stage, operating at 70 ° C., for 30 minutes, the aluminum sulfate flow rate should be 5.2 ml / min and the sodium aluminate flow rate is 6.3 ml / min. The mass ratio of sodium aluminate to aluminum sulfate is therefore 1.84. Preferably, the second precipitation step is carried out at a temperature between 40 and 80 ° C, preferably between 45 and 70 ° C and very preferably between 50 and 70 ° C. Preferably, the second precipitation step is carried out for a period of between 5 and 45 minutes, and preferably of 7 to 40 minutes.
[0062] The second precipitation step generally makes it possible to obtain an alumina suspension having an Al 2 O 3 concentration of between 20 and 100 g / l, preferably between 20 and 80 g / l, preferably between 20 and 50 g / l. Step d) Filtration The alumina preparation process according to the invention also comprises a filtration step of the suspension obtained at the end of the second precipitation step c). Said filtration step is carried out according to the methods known to those skilled in the art.
[0063] The filterability of the suspension obtained at the end of the two precipitation steps is improved by the low dispersibility of the alumina gel obtained, which makes it possible to improve the productivity of the process according to the invention as well as to allow extrapolation of the process. at the industrial level. Said filtration step is advantageously followed by at least one washing step, preferably with water and preferably from one to three washing steps, with a quantity of water equal to the amount of filtered precipitate.
[0064] The sequence of the first precipitation a), the heating b) and the second precipitation c) stages and the filtration stage d) makes it possible to obtain a specific alumina gel having a dispersibility ratio of less than 15%, preferably between 5 and 15% and preferably between 6 and 14%, very preferably between 7 and 13%, and even more preferably between 7 and 10% and a crystallite size between 1 and 35 nm and preferably between 2 to 35 nm. The alumina gel obtained also advantageously has a sulfur content, measured by the X-ray fluorescence method, of between 0.001% and 2% by weight and preferably between 0.01% and 0.2% by weight and a sodium content, measured. by ICP-MS or inductively coupled plasma spectrometry between 0.001 and 2 (3/0 weight, and preferably between 0.01 and 0.1 (3/0 weight, the weight percentages being expressed relative to the total mass of alumina gel.
[0065] In particular, the alumina gel or the boehmite in powder form according to the invention is composed of crystallites whose size, obtained by the Scherrer formula in X-ray diffraction according to the crystallographic directions [020] and [120] are respectively between 2 and 20 nm and between 2 and 35 nm.
[0066] Preferably, the alumina gel according to the invention has a crystallite size in the crystallographic direction [020] of between 1 to 15 nm and a crystallite size in the crystallographic direction [120] of between 1 to 35 nm.
[0067] X-ray diffraction on alumina or boehmite gels was performed using the conventional powder method using a diffractometer. Scherrer's formula is a formula used in X-ray diffraction on powders or polycrystalline samples which connects the width at half height of the diffraction peaks to the size of the crystallites. It is described in detail in the reference: Appl. Cryst. (1978). 11, 102-113 "Scherrer after sixty years: A survey and some new results in the determination of crystallite size", J. I. Langford and A. J. C. Wilson.
[0068] The low dispersibility rate of the gel thus prepared makes it possible to facilitate the step of shaping said gel according to all the methods known to those skilled in the art and in particular by extrusion kneading, by granulation and by the technique known as drop (draining) according to the English terminology. Step e): Drying of the Alumina Gel According to the invention, the alumina gel obtained at the end of the second precipitation step c), followed by a filtration step d), is dried in a drying step e) for obtaining a powder, said drying step being carried out by drying, for example by drying at a temperature of between 20 and 200 ° C. and for a period of between 8 h and 15 h, or by spraying or by any other drying technique known to those skilled in the art. In the case where said drying step e) is carried out by atomization, the cake obtained at the end of the second precipitation step, followed by a filtration step, is resuspended. Said suspension is then sprayed in fine droplets, in a vertical cylindrical chamber in contact with a stream of hot air to evaporate the water according to the principle well known to those skilled in the art. The powder obtained is driven by the heat flow to a cyclone or a bag filter that will separate the air from the powder.
[0069] Preferably, in the case where said drying step e) is carried out by atomization, the atomization is carried out according to the operating protocol described in the publication Asep Bayu Dani Nandiyanto, Kikuo Okuyama, Advanced Powder Technology, 22, 1-19 , 2011.35 Step f): Heat treatment of the powder obtained at the end of step e) According to the invention, the powder obtained at the end of step e) of drying is subjected to a step f) heat treatment at a temperature between 500 and 1000 ° C, for a period of between 2 and 10 h, in the presence or absence of a flow of air containing up to 60% water volume. Preferably, said heat treatment step f) operates at a temperature of between 540 ° C. and 850 ° C. Preferably, said heat treatment step f) operates for a duration of between 2 h and 10 h.
[0070] Said f) heat treatment step allows the transition of the boehmite to the final alumina. The heat treatment step may be preceded by drying at a temperature between 50 ° C and 120 ° C, according to any technique known to those skilled in the art.
[0071] According to the invention, the powder obtained after drying step e), after heat treatment in a step f), is comalaxed with the metal precursor (s) of the active phase, in a step g) comalaxing allowing the contact or solutions containing the active phase to come into contact with the powder, and then shaping the resulting material to obtain the catalyst in a step h). Step q): Comalaxaqe Step In this step, the calcined aluminous porous oxide from step f) is kneaded in the presence of the active phase in the form of a solution of the precursors of the metal or metals chosen from group VIB elements, possibly group VIII elements and possibly phosphorus.
[0072] The active phase is provided by one or more solutions containing at least one Group VIB metal, optionally at least one Group VIII metal and optionally the phosphorus element. The said solution (s) may be aqueous, consisting of an organic solvent or a mixture of water and at least one organic solvent ( for example ethanol or toluene). Preferably, the solution is aquo-organic and even more preferably aqueous-alcoholic. The pH of this solution may be modified by the possible addition of an acid. Among the compounds which can be introduced into the solution as sources of group VIII elements, advantageously are: citrates, oxalates, carbonates, hydroxycarbonates, hydroxides, phosphates, sulphates, aluminates, molybdates, tungstates, oxides, nitrates, halides for example, chlorides, fluorides, bromides, acetates, or any mixture of the compounds set forth herein.
[0073] As regards the sources of the group VIB element which are well known to those skilled in the art, there are advantageously, for example, for molybdenum and tungsten: oxides, hydroxides, molybdic and tungstic acids and their salts, in particular sodium salts. ammonium, ammonium heptamolybdate, ammonium tungstate, phosphomolybdic acid, phosphotungstic acid and their salts. Oxides or ammonium salts such as ammonium molybdate, ammonium heptamolybdate or ammonium tungstate are preferably used. The preferred phosphorus source is orthophosphoric acid, but its salts and esters such as alkaline phosphates, ammonium phosphate, gallium phosphate or alkyl phosphates are also suitable. Phosphorous acids, for example hypophosphorous acid, phosphomolybdic acid and its salts, phosphotungstic acid and its salts can be advantageously used. An additive, for example a chelating agent of organic nature, may advantageously be introduced into the solution if the person skilled in the art deems it necessary. Any other element, for example silica in the form of a solution or emulsion of silicic precursor, can be introduced into the mixing tank at the time of this step.
[0074] Comalaxing is advantageously carried out in a kneader, for example a "Brabender" kneader, well known to those skilled in the art. The aluminous porous oxide in the form of calcined powder obtained in step f) and one or more additives or other possible elements are placed in the tank of the kneader. Then the solution of metal precursors, for example nickel and molybdenum, and optionally deionized water are added to the syringe or any other means for a period of a few minutes, typically about 2 minutes at a given kneading speed. After obtaining a paste, the kneading can be maintained for a few minutes, for example about 15 minutes at 50 rpm.
[0075] Step h): Shaping The paste obtained after the comalaxing step g) is then shaped according to any technique known to those skilled in the art, for example extrusion shaping methods, by pelleting, by the method of the drop of oil, or by granulation at the turntable. Preferably, said support used according to the invention is shaped by extrusion in the form of extrudates of diameter generally between 0.5 and 10 mm and preferably 0.8 and 3.2 mm. In a preferred embodiment, it will be composed of trilobed or quadrilobed extrudates of size between 1.0 and 2.5 mm in diameter. Very preferably, said comalling step g) and said shaping step h) are combined in a single kneading-extruding step. In this case, the paste obtained after the mixing can be introduced into a piston extruder through a die having the desired diameter, typically between 0.5 and 10 mm. Step i): drying of the shaped dough According to the invention, the catalyst obtained after the galting and shaping step h) h) undergoes drying i) at a temperature less than or equal to at 200 ° C, preferably below 150 ° C according to any technique known to those skilled in the art, for a period of typically between 2 and 12 hours.
[0076] Step i): heat treatment or hydrothermal The catalyst thus dried can then undergo a complementary heat treatment or hydrothermal step j) at a temperature between 200 and 1000 ° C, preferably between 300 and 800 ° C and even more preferably between 350 and 550 ° C, for a duration typically between 2 and 10 h, in the presence or absence of a flow of air containing up to 60% by volume of water. Several combined cycles of thermal or hydrothermal treatments can be carried out.
[0077] In the case where the catalyst does not undergo a complementary step of heat treatment or hydrothermal, the catalyst is only advantageously dried in step i). In the case where water is added, the contact with the steam can take place at atmospheric pressure (steaming) or autogenous pressure (autoclaving). In case of steaming, the water content is preferably between 150 and 900 grams per kilogram of dry air, and even more preferably between 250 and 650 grams per kilogram of dry air. According to the invention, it is possible to envisage introducing all or part of the metals mentioned during the comalaxing of the metal solution (s) with the calcined aluminous porous oxide. In one embodiment, in order to increase the overall active phase content on the comalaxed catalyst, a part of the metals may be introduced by impregnation of said catalyst from step i) or j), according to any known method of the A person skilled in the art, the most common being that of dry impregnation. In another embodiment, all of the metal phase is introduced during the preparation by comalaxing the porous aluminum oxide and no additional impregnation step will therefore be necessary. Preferably, the active phase of the catalyst is fully comalaxed within the calcined porous aluminum oxide.
[0078] Description of the Process for Using the Catalyst According to the Invention The catalyst according to the invention can be used in hydrotreatment processes making it possible to convert heavy hydrocarbon feeds containing sulfur impurities and metallic impurities. One objective sought by the use of the catalysts of the present invention relates to an improvement of the performances, in particular in hydrodemetallation and hydrodesulphurization, while improving the ease of preparation with respect to the catalysts known from the prior art. The catalyst according to the invention makes it possible to improve the performances in hydrodemetallation and in hydrodesulphalate with respect to conventional catalysts, while having a high stability over time. In general, the hydrotreatment processes for converting heavy hydrocarbon feeds, containing sulfur impurities and metal impurities, operate at a temperature of between 320 and 450 ° C. under a hydrogen partial pressure of between 3 MPa and 30 MPa, at a space velocity advantageously between 0.05 and 10 volumes of filler per volume of catalyst and per hour, and with a hydrogen gas ratio on a hydrocarbon liquid feed advantageously between 100 and 5000 normal cubic meters per cubic meter .
[0079] Charges The feedstocks treated in the process according to the invention are advantageously chosen from atmospheric residues, vacuum residues resulting from the direct distillation, deasphalted oils, residues resulting from conversion processes such as, for example, those resulting from coking, hydroconversion in fixed bed, bubbling bed, or moving bed, taken alone or in mixture. These fillers can advantageously be used as they are or else diluted by a hydrocarbon fraction or a mixture of hydrocarbon fractions which may be chosen from the products of the FCC process, a light cutting oil (LCO according to the initials of the English name of Light Cycle Oil), a heavy cutting oil (HCO according to the initials of the English name of Heavy Cycle Oil), a decanted oil (OD according to the initials of the English name of Decanted Oil), a slurry, or From the distillation, gas oil fractions including those obtained by vacuum distillation called according to the English terminology VGO (Vacuum Gas Oil). The heavy charges can thus advantageously comprise cuts resulting from the process of liquefying coal, aromatic extracts, or any other hydrocarbon cut. Said heavy charges generally have more than 1% by weight of molecules having a boiling point greater than 500 ° C., a Ni + V metals content of greater than 1 ppm by weight, preferably greater than 20 ppm by weight, and very preferably greater than 50 ppm by weight, an asphaltene content, precipitated in heptane, greater than 0.05% by weight, preferably greater than 1% by weight, very preferably greater than 2%.
[0080] The heavy fillers can advantageously also be mixed with coal in the form of powder, this mixture being generally called slurry. These fillers can advantageously be by-products from the conversion of the coal and mixed again with fresh coal. The coal content in the heavy load is generally and preferably a ratio 1/4 (Oil / Coal) and may advantageously vary widely between 0.1 and 1.
[0081] The coal may contain lignite, be a sub-bituminous coal (according to the English terminology), or bituminous. Any other type of coal is suitable for the use of the invention, both in fixed bed reactors and in bubbling bed reactors.
[0082] Use of the Catalyst According to the Invention According to the invention, the comalaxed active phase catalyst is preferably used in the first catalytic beds of a process comprising successively at least one hydrodemetallation step and at least one hydrodesulfurization step . The process according to the invention is advantageously carried out in one to ten successive reactors, the catalyst (s) according to the invention can advantageously be loaded into one or more reactors and / or in all or some of the reactors. . In a preferred embodiment, reactive reactors, ie reactors operating alternately, in which hydrodemetallation catalysts according to the invention can preferably be used, can be used upstream of the unit. . In this preferred embodiment, the reactive reactors are then followed by series reactors, in which hydrodesulfurization catalysts are used which can be prepared according to any method known to those skilled in the art. In a very preferred embodiment, two permutable reactors are used upstream of the unit, preferably for the hydrodemetallation and containing one or more catalysts according to the invention. They are advantageously monitored by one to four reactors in series, advantageously used for hydrodesulfurization. The process according to the invention may advantageously be carried out in a fixed bed with the objective of eliminating metals and sulfur and lowering the average boiling point of the hydrocarbons. In the case where the process according to the invention is carried out in fixed bed, the operating temperature is advantageously between 320 ° C. and 450 ° C., preferably 350 ° C. to 410 ° C., under a partial pressure. in hydrogen advantageously between 3 MPa and 30 MPa, preferably between 10 and 20 MPa, at a space velocity advantageously between 0.05 and 5 volume of charge per volume of catalyst per hour, and with a gaseous hydrogen gas on charge ratio hydrocarbon liquid advantageously between 200 and 5000 normal cubic meters per cubic meter, preferably 500 to 1500 normal cubic meters per cubic meter.
[0083] The process according to the invention can also advantageously be implemented partly in bubbling bed on the same charges. In the case where the process according to the invention is carried out in an ebullated bed, the catalyst is advantageously used at a temperature of between 320 and 450 ° C. under a hydrogen partial pressure advantageously between 3 MPa and 30 ° C. MPa, preferably between 10 and 20 MPa, at a space velocity advantageously between 0.1 and 10 volumes of filler per volume of catalyst and per hour, preferably between 0.5 and 2 volumes of filler by volume of catalyst and by hour, and with a gaseous hydrogen gas on hydrocarbon liquid charge advantageously between 100 and 3000 normal cubic meters per cubic meter, preferably between 200 to 1200 normal cubic meters per cubic meter.
[0084] According to a preferred embodiment, the method according to the invention is implemented in a fixed bed.
[0085] Before they are used in the process according to the invention, the catalysts of the present invention are preferably subjected to a sulphurization treatment making it possible, at least in part, to convert the metallic species into sulphide before they come into contact with the charge. treat. This activation treatment by sulphurisation is well known to those skilled in the art and can be performed by any previously known method already described in the literature. A conventional sulphurization method well known to those skilled in the art consists in heating the mixture of solids under a stream of a mixture of hydrogen and hydrogen sulphide or under a stream of a mixture of hydrogen and of hydrocarbons containing sulfur-containing molecules at a temperature of temperature between 150 and 800 ° C, preferably between 250 and 600 ° C, generally in a crossed-bed reaction zone. The sulfurization treatment can be carried out ex situ (before the introduction of the catalyst into the hydrotreatment / hydroconversion reactor) or in situ by means of an organosulfur precursor agent of H2S, for example DMDS (dimethyl disulphide).
[0086] The following examples illustrate the invention without limiting its scope.
[0087] EXAMPLES Example 1 Preparation of the Metal Solutions A, B Solutions A and B used for the preparation of the catalysts Al, Bi, A2, A3 were prepared by dissolving in water the precursors of the following phases MoO 3, Ni (OH) 2 , H3PO4. All these precursors come from Sigma-Aldrich®. The concentration of elements of the various solutions is indicated in the following table. Table: Molar concentration of prepared aqueous solutions (expressed in mol / I) Ni / Mo P / Mo Catalyst Mo Ni P mol / mol mol / mol A 0.49 0.23 0.27 0.47 0.55 B 0, 68 0.31 0.36 0.45 0.53 EXAMPLE 2 Preparation of the Comalaxed Catalysts A1, B1 According to the Invention The synthesis of an Al (A1) alumina according to the invention is carried out in a 5L reactor in 3 steps. The concentration of the precursors is as follows: aluminum sulphate Al2 (SO4) 3 at 102 g / l in Al2O3 and sodium aluminate Naa100 at 155 g / l in Al2O3 Alumina Al (Al) used according to the invention is manufactured according to following steps: a) A first co-precipitation of aluminum sulphate Al2 (SO4) 3 and sodium aluminate NaA100 at 30 ° C and pH = 9.1 in 8 min: the rate of progress is 10 %. The rate of progress corresponds to the proportion of alumina formed during the first stage, ie a final alumina concentration of 45 g / l. If one works in a reactor of 5 1 and 4 l of alumina suspension A1203 final concentration of 45 g / I, with a target rate of 10 ° / 0 for the first precipitation step 10% of the total alumina must be added during the precipitation stage a). The precipitation pH of the first step is set at 9.1 and the precipitation pH of the second step is 9.1. The amount of water initially present in the reactor is 1330 ml.
[0088] For the first step a) of precipitation operating at 30 ° C and for 8 minutes, the flow rate of aluminum sulfate should be 7.6 ml / min, the flow rate of sodium aluminate is 9.1 ml / min and the water flow rate of 24.6 ml / min. The mass ratio of sodium aluminate to aluminum sulfate is therefore 1.91. b) A rise in temperature of 30 to 70 ° C in 20 to 30 min; b) A rise in temperature of 30 to 70 ° C in 20 to 30 min; c) A second co-precipitation of aluminum sulphate Al2 (SO4) 3 and sodium aluminate NaA100 at 70 ° C and pH = 9.1 in 30 min, with a degree of progress of 90%; for the second precipitation stage operating at 70 ° C for 30 minutes, the flow rate of aluminum sulphate should be 18.5 ml / min, the flow of sodium aluminate is 29 ml / min and the flow rate of water of 33.8 ml / min. The mass ratio of sodium aluminate to aluminum sulfate is therefore 1.84. d) Filtration by displacement on a Buchner tool type sintered P4 and washing 3 times with 5L of distilled water at 70 ° C; e) drying overnight at 120 ° C; f) Calcination of the powder at 750 ° C. The synthesis of an Al (B1) alumina according to the invention is carried out in a reactor in 51 in 3 steps. The concentration of the precursors is as follows: aluminum sulphate Al2 (SO4) 3 at 102 g / l in Al2O3 and sodium aluminate Naa100 at 155 g / l in Al2O3 Alumina Al (B1) according to the invention is manufactured according to the steps following: a) A first co-precipitation of aluminum sulphate Al2 (SO4) 3 and sodium aluminate NaA100 at 30 ° C and pH = 9.1 in 8 min: the rate of progress is 8 %. The rate of progress corresponds to the proportion of alumina formed during the first step, ie a final concentration of alumina at 45 g / l. If one works in a reactor of 51 and that one targets 30 4 1 of suspension of alumina with a final concentration of Al 2 O 3 of 45 g / l, with a targeted advancement rate of 8 (3/0 for the first precipitation stage, 8 (3/0 of the total alumina must be provided during the first Precipitation step a) The precipitation pH of the first step is set at 9.1 and the precipitation pH of the second step is 9.1 The amount of water initially present in the reactor is 1330 ml.
[0089] For the first step a) of precipitation operating at 30 ° C and for 8 minutes, the flow rate of aluminum sulphate should be 6.1 ml / min, the flow rate of sodium aluminate is 7.6 ml / min and the water flow rate of 69.7 mL / min. The mass ratio of sodium aluminate to aluminum sulfate is therefore 1.91. b) A rise in temperature of 30 to 70 ° C in 20 to 30 min; c) A second co-precipitation of aluminum sulphate Al2 (SO4) 3 and sodium aluminate NaA100 at 70 ° C and pH = 9.1 in 30 min, with a percentage of progress of 92%; For the second precipitation stage, operating at 70 ° C., for 30 minutes, the flow rate of aluminum sulphate must be 19 ml / min, the sodium aluminate flow rate is 23 ml / min and the flow rate of water of 24.7 mL / min. The mass ratio of sodium aluminate to aluminum sulfate is therefore 1.84. d) Filtration by displacement on a Buchner tool type sintered P4 and washing 3 times with 5 l of distilled water; e) drying overnight at 120 ° C; f) Calcination of the powder at 750 ° C. The impregnation solutions A and B were respectively kneaded in the presence of Al (A1) and Al (B1) aluminas prepared above to prepare the Al and Bi catalysts.
[0090] The comalaxing takes place in a "Brabender" mixer with a tank of 80 cm3 and a kneading speed of 30 rpm. The alumina powder is placed in the bowl of the kneader. Then the MoNi solution (P) is added to the syringe for about 2 minutes at 15 rpm. The kneading is maintained 15 minutes after obtaining a paste at 50 rpm. The paste thus obtained is introduced into the capillary rheometer MIS through a 2.1 mm die at 10 mm / min. the extrudates thus obtained are then dried overnight in an oven at 80 ° C. and then calcined for 2 hours in air (1 L / h / g) in a tubular oven at 400 ° C. The catalysts thus obtained Al and B1 have the characteristics reported in Table 2 below. Table 2: Properties of the comalaxed catalysts E, Al, Bi, A2, A3 Catalyst E Al B1 A2 A3 Objective of the comparative preparation according to US Pat. Comparative Comparative Invention calcined calcined aluminic precursor state Calcined calcined calcined Mode of introduction of metals Dry impregnation - ^ - comalaxing Textural properties by mercury pycnometry (except BET) Vtotal (ml / g) 0.77 0.93 0, 87 1.08 0.71 VmSo (mL / g) 0.54 0.69 0.66 0.50 0.36 Dpmreso (nm) 14.7 14.0 13.8 7.7 7.4 Vmacro (mL) / g) 0.23 0.24 0.21 0.58 (54%) 0.35 (`) / 0 of the total volume) (30%) (26%) (24%) (49%) Dpmacro (nm) ) 574 120 145 1672 1053 SBET (m2 / g) 157 215 204 227 311 Analyzes of metal contents (by X-ray fluorescence)% w Mo03 impregnated 6.05 6.01 8.24 5.94 5.89% wt NiO impregnated 1.44 1.46 1.89 1.45 1.47% by weight impregnated P205 1.68 1.63 2.27 1.58 1.59 Example 3 (comparative): Prep. Catalyst E is a catalyst prepared by boehmite extrusion-mixing, followed in the order of calcination and hydrothermal treatment before dry impregnation of the support. S (E) with an aqueous solution so that the content of metals is the same as that introduced by comalaxing on the catalyst Ai. Catalyst E is prepared by dry impregnation of an aluminum support S (E) prepared as hereinafter.
[0091] The synthesis of an alumina is carried out in a reactor at 51 in 3 steps. The concentration of the precursors is as follows: aluminum sulphate Al2 (SO4) 3 at 102g / L in Al2O3 and sodium aluminate NaA100 at 155g / L in Al2O3 Alumina is manufactured according to the following steps: a) A first co-product precipitation of aluminum sulphate Al2 (SO4) 3 and sodium aluminate NaA100 at 30 ° C and pH = 9.1 in 8 min: the rate of progress is 20%. The rate of progress corresponds to the proportion of alumina formed during the first stage, ie a final alumina concentration of 45 g / l. If one works in a reactor of 51 and that one aims 4 1 of alumina suspension of final concentration of A1203 of 45 g / I, with a targeted progress rate of 20% for the first precipitation step, % of the total alumina must be provided during step a) of precipitation The precipitation pH of the first step is set at 9.1. The amount of water initially present in the reactor is 1330 ml.
[0092] For the first step a) of precipitation operating at 30 ° C and for 8 minutes, the flow rate of aluminum sulfate should be 15.2 ml / min, the flow of sodium aluminate is 19 ml / min and the water flow rate is 49.2 mL / min. The mass ratio of sodium aluminate to aluminum sulfate is therefore 1.91. b) A rise in temperature of 30 to 70 ° C in 20 to 30 min; c) A second co-precipitation of aluminum sulphate Al2 (504) 3 and sodium aluminate NaA100 at 70 ° C. and pH = 9.1 in 30 min, with a degree of progress of 80%; For the second precipitation stage, operating at 70 ° C., for 30 minutes, the flow rate of aluminum sulphate must be 16.5 ml / min, the sodium aluminate flow rate is 20 ml / min and the flow rate of water is 30.1 mL / min The mass ratio of sodium aluminate on aluminum sulfate is therefore 1.84. d) Filtration by displacement on a Buchner type Sintered P4 tool and washing 3 times with 5L of distilled water; e) drying overnight at 120 ° C; The cake is dried (step e) in an oven for at least one night at 120 ° C. The powder is obtained which must be shaped. The shaping is carried out on a Brabender kneader with an acid level (total, expressed relative to dry alumina) of 1%, a neutralization rate of 20% and acid and basic fire losses respectively of 62 and 64%. The extrusion is carried out on a piston extruder through a trilobal die with a diameter of 2.1 mm.
[0093] After extrusion, the rods are dried overnight at 80 ° C. and calcined for 2 hours at 800 ° C. under a moist air stream in a tubular furnace (VVH = 1 l / h / g with 30% water). Extruded support S (E) is obtained.
[0094] The support S (E) is then impregnated with a NiMoP metal phase by the so-called dry method using the same precursors as in Example 1, ie MoO 3, Ni (OH) 2, H 3 PO 4. The concentration of the metals in solution fixed the content, which was chosen to be compared with that of the Al and Bi catalysts. After impregnation, the catalyst undergoes a maturing stage of 24 hours in a saturated water atmosphere, before being dried for 12 hours at 120 ° C. in air and then calcined under air at 400 ° C. for 2 hours. Catalyst E is obtained. The metal contents have been checked and are reported in Table 2 above. EXAMPLE 4 (COMPARATIVE) Preparation of a Non-Conforming Catalytic Catalyst A2 Catalyst A2 is prepared by co-ordinating the active phase with a calcined alumina Al (A2) obtained from a non-compliant alumina gel (rate non-compliant first stage progress). The synthesis of Al (A2) alumina is carried out by following the steps of Example 2 (Al (A1) alumina). The operating conditions are strictly identical, with the exception of the following two points: in step a) of first precipitation, the rate of progress is 20%. In step c) of second precipitation, the rate of progress is 80%. The synthesis of an alumina used according to the invention is carried out in a reactor in 51 in 3 steps. The concentration of the precursors is as follows: aluminum sulphate Al2 (SO4) 3 at 102 g / l in Al2O3 and sodium aluminate Naa100 at 155 g / l in Al2O3 Alumina Al (A2) is manufactured according to the following steps: ) A first co-precipitation of Al2 (SO4) 3 aluminum sulphate and NaA100 sodium aluminate at 30 ° C and pH = 9.1 in 8 min: the rate of advance is 20%. The rate of progress corresponds to the proportion of alumina formed during the first stage, ie a final alumina concentration of 45 g / l. If one works in a reactor of 51 and that one aims 4 1 of alumina suspension of final concentration of A1203 of 45 g / I, with a targeted progress rate of 20% for the first precipitation step, % of the total alumina must be provided during step a) of precipitation The precipitation pH of the first step is set at 9.1. The amount of water initially present in the reactor is 1330 ml.
[0095] For the first step a) of precipitation operating at 30 ° C and for 8 minutes, the flow rate of aluminum sulfate should be 15.2 ml / min, the flow of sodium aluminate is 19 ml / min and the water flow rate is 49.2 mL / min. The mass ratio of sodium aluminate to aluminum sulfate is therefore 1.91. b) A rise in temperature of 30 to 70 ° C in 20 to 30 min; c) A second co-precipitation of aluminum sulphate Al2 (SO4) 3 and sodium aluminate NaA100 at 70 ° C. and pH = 9.1 in 30 min, with a progress rate of 80%; For the second precipitation stage, operating at 70 ° C., for 30 minutes, the flow rate of aluminum sulphate must be 16.5 ml / min, the sodium aluminate flow rate is 20 ml / min and the flow rate of water is 30.1 mL / min. The mass ratio of sodium aluminate to aluminum sulfate is therefore 1.84. d) Filtration by displacement on a Buchner type Sintered P4 tool and washing 3 times with 51 of distilled water; e) drying overnight at 120 ° C; f) Calcination of the powder at 750 ° C. The comalaxing takes place in a "Brabender" mixer with a tank of 80 cm3 and a kneading speed of 30 rpm. The alumina powder is placed in the bowl of the kneader.
[0096] Then MoNi solution A (P) is added to the syringe for about 2 minutes at 15 rpm. The kneading is maintained 15 minutes after obtaining a paste at 50 rpm. The paste thus obtained is introduced into the capillary rheometer MIS through a 2.1 mm die at 10 mm / min. the extrudates thus obtained are then dried overnight in an oven at 80 ° C. and then calcined for 2 hours in air (1 L / h / g) in a tubular oven at 400 ° C.
[0097] The catalyst A2 is obtained. The catalyst A2 has the characteristics reported in Table 2. It has in particular an excessively high macroporous volume, to the detriment of the mesoporous volume which remains low and the median mesoporous diameter (Dpmeso) which remains low (less than 8 nm).
[0098] Example 5 (Comparative): Preparation of non-compliant comalaxed catalyst A3 The non-compliant catalyst A3 is prepared by co-ordinating the active phase with non-calcined boehmite powder B (A3). The synthesis of a boehmite is carried out in a 5L reactor in 3 steps. The concentration of the precursors is as follows: aluminum sulphate Al2 (SO4) 3 at 102g / l in Al2O3 and sodium aluminate Naa100 at 155g / l in Al2O3 Boehmite B (A3) is manufactured according to steps a) to e) following, under the same conditions as in Example 1, but without step f) calcination: a) A first co-precipitation of aluminum sulphate Al2 (SO4) 3 and sodium aluminate NaA100 at 30 ° C and pH = 9.1 in 8 min: the rate of progress is 10%. The rate of progress corresponds to the proportion of alumina formed during the first stage, ie a final alumina concentration of 45 g / l. b) A rise in temperature of 30 to 70 ° C in 20 to 30 min; c) A second co-precipitation of Al2 (SO4) 3 aluminum sulphate and NaA100 sodium aluminate at 70 ° C and pH = 9.1 in 30 min, with a 90% feed rate; d) Filtration by displacement on a Buchner tool type sintered P4 and washing 3 times with 5L of distilled water at 70 ° C; e) Drying overnight at 120 ° C to obtain a boehmite powder. No calcination of the powder occurs at this stage. Solution A is kneaded in the presence of the alumina precursor powder B (A3) (in the form A100H) obtained in step e), without subjecting it to any additional heat treatment. It is therefore a boehmite powder. To do this, the mixing conditions used are strictly the same as those described above. The comalaxing takes place in a "Brabender" mixer with a tank of 80 cm3 and a kneading speed of 30 rpm. The powder is placed in the bowl of the mixer. Then the MoNi solution (P) is added to the syringe for about 2 minutes at 15 rpm. The kneading is maintained 15 minutes after obtaining a paste at 30 rpm. The paste thus obtained is introduced into the capillary rheometer MIS through a 2.1 mm die at 10 mm / min. The extrudates thus obtained are then dried overnight in an oven at 80 ° C. and then calcined for 2 hours in air (1 L / h / g) in a tubular oven at 400 ° C. The catalyst A3 obtained has the characteristics reported in Table 2. Compared to the catalyst A2, the macroporous volume is lower, but it remains too high. Furthermore, the mesoporous volume is very low and the median mesoporous diameter (Dpméso) unchanged with respect to the catalyst A2, therefore less than 8 nm. Example 6 Test Evaluation Model Molecules of Catalysts A1, Bi, A2, A3 and E In applications such as hydrotreatment in particular, vacuum distillates and residues, the hydro-dehydrogenating function plays a critical role in view of the high content of aromatic compounds of these fillers. The hydrogenation test of toluene was therefore used to know the interest of catalysts for applications such as those targeted here, in particular the hydrotreatment of residues. The catalysts previously described in Examples 2 to 5 are in-situ sulfide-dynamic in the fixed-bed tubular reactor passed through a Microcat-type pilot unit (manufacturer: Vinci Company), the fluids flowing from top to bottom. The measurements of hydrogenating activity are carried out immediately after sulphurization under pressure and without re-airing with the hydrocarbon feedstock which was used to sulphurize the catalysts. The sulfurization and test load is composed of 5.8% dimethyldisulphide (DMDS), 20% toluene and 74.2% cyclohexane (by weight). ambient temperature up to 350 ° C, with a temperature ramp of 2 ° C / min, a VVH = 411-1 and H2 / HC = 450 NI / 1. The catalytic test is carried out at 350 ° C at VVH = 2 11-1 and H2 / HC equivalent to that of sulfurization, with minimum sampling of 4 recipes that are analyzed by gas chromatography.
[0099] The stabilized catalytic activities of equal volumes of catalysts are thus measured in the hydrogenation reaction of toluene.
[0100] The detailed conditions for measuring activity are as follows: Total pressure: 6.0 MPa Toluene pressure: 0.37 MPa Cyclohexane pressure: 1.42 MPa Methane pressure 0.22 MPa Hydrogen pressure: 3.68 MPa H2S pressure: 0.22 MPa Catalyst volume: 4 cm3 (extruded length between 2 and 4 mm) Hourly space velocity: 2 h -1 Sulfurization and test temperature: 350 ° C Samples from the liquid effluent are analyzed by gas chromatography. The determination of the unconverted toluene (T) molar concentrations and the concentrations of its hydrogenation products (methylcyclohexane (MCC6), ethylcyclopentane (EtCC5) and dimethylcyclopentanes (DM005)) make it possible to calculate a hydrogenation rate of toluene. XHyD defined by: MCC6 + EtCC5 + DMCC5 X HyD (%) = 100x T + MCC6 + EtCC5 + DMCC5 The hydrogenation reaction of toluene being of order 1 under the test conditions used and the reactor behaving like an ideal piston reactor, the hydrogenating activity AHyD of the catalysts is calculated by applying the formula: A. - In (100 100 - X HyD) The table below makes it possible to compare the relative hydrogenating activities of the catalysts. Table 3: Comparison of the performances in hydrogenation toluene catalysts according to the invention (Ai, B1) and comparison with non-compliant catalysts A2, A3 and E Catalyst precursor state alumina Compliant % Mo03 comalaxed AHyD relative to E (`) / 0) Al calcined yes 6% yes 83 B1 calcined yes 8% yes 104 A2 calcined no 6% yes 45 A3 dried no 6% yes 18 E calcined no 6% no 100 These catalytic results show the particular effect of the comalaxing of a metal solution with a particular alumina as described in the invention. It is clearly shown that by performing the comalaxing according to the invention, in addition to reducing the cost of manufacture of the catalyst, performance is almost as good as for catalysts prepared by dry impregnation (catalyst E), and much better than for catalysts comalaxed from calcined alumina from non-conformally prepared alumina gels (Catalyst A2) or from Boehmite (Catalyst A3). EXAMPLE 7 Batch Evaluation of Catalysts A1, Bi, A2, A3 and E The catalysts A1, B1 prepared according to the invention, but also the comparative catalysts A2, A3 and E, were subjected to a batch reactor catalytic test perfectly. stirred on an RSV Arabian Light charge (see characteristics in Table 4).
[0101] Table 4: Characteristics of the load used (RSV Arabian Light) Arabian Light Density 15/4 0.9712 Viscosity at 100 ° C mm2 / s 45 Sulfur (3/0 wt) 3.38 Nitrogen ppm 2257 Nickel ppm 10.6 Vanadium ppm 41.0 Aromatic carbon (3/0 24.8 Conradson carbon% wt 10.2 C7 asphaltenes (3/0 wt 3.2 SARA Saturated% wt 28.1 Aromatic (3/0 wt 46.9% Resins wt 20, 1 Asphaltenes% wt 3,5 Simulated distillation PI ° C 219 5% ° C 299 10% ° C 342 20% ° C 409 30% ° C 463 40% ° C 520 50% 576 DS: PF ° C ° C 614 DS To this end, after an ex-situ sulphurization step by circulating an H2S / H2 gas mixture for 2 hours at 350 ° C., 15 ml of catalyst is charged in the absence of air. The operating conditions applied are then as follows: Table 5: Operating conditions used in a batch reactor Total pressure 9.5 MPa Test temperature 370 ° C. Duration of the test 3 hours At the end of the test, the reactor is cooled and after triple stripping the atmosphere under nitrogen (10 minutes at 1 MPa), the effluent is collected and analyzed by X-ray fluorescence (sulfur and metals). The HDS ratio is defined as follows: HDS (`) / 0) = pds S1, load- (° A wt S) recipe) / (% wt S) load x 100 Similarly, the rate of HDM is defined as follows: recipe, HDM (° / 0) = ((ppm wt Ni + V) load (ppm wt Ni + V) 1 / (bbm wt Ni + V) load X 100 - Performance Catalysts are summarized in Table 6. It is clearly shown that by performing the comalaxing according to the invention, in addition to reducing the cost of manufacture of the catalyst, performance is observed at least as good as for catalysts prepared by impregnation with and much better than for catalysts comalaxed from calcined alumina from non-compliant alumina gels or from boehmite.
[0102] Table 6: HDS, HDM performance of the catalysts according to the invention (Ai, B1) and comparison with non-compliant catalysts (A2, A3 and E) HDS (c) / 0) HDM (c) / 0) Al catalysts (according to the invention) 51.2 75.2 B1 (according to the invention) 52.0 75.0 A2 (comparative) 35.6 68.3 A3 (comparative) 28.4 63.2 E (comparative) 50.3 76.1 EXAMPLE 7 Evaluation in fixed bed hydrotreatment of the catalysts Al and B1 according to the invention and comparison with the catalytic performances of the catalyst E. The catalysts Al and B1 prepared according to the invention were compared in a hydrotreatment test of oil residues in comparison with the performance of the catalyst E. The charge consists of a mixture between an atmospheric residue (RA) of Middle East origin (Arabian medium) and a vacuum residue (RSV) of Middle Eastern origin (Arabian Light). The feedstock is characterized by high contents of Conradson carbon (14.4% by weight) and asphaltenes (6.1% by weight) and a high amount of nickel (25 ppm by weight), vanadium ( 79 ppm by weight) and sulfur (3.90 (3/0 by weight).) The full characteristics of this load are reported in Table 7.30 Table 7: Characteristics of the RA AM / RSV AL loads used for Mix RA AM / RSV AL Density 15/4 0.9920 Sulfur (3/0 wt) 3.90 Nitrogen ppm 2995 Nickel ppm 25 Vanadium ppm 79 Conradson carbon (3/0 wt 14.4 C7 Asphalenes (3/0 wt) 6.1 Simulated distillation PI ° C 265 5% ° C 366 10% ° C 408 20% ° C 458 30% ° C 502 40% ° C 542 50% ° C 576 60% ° C 609 70% ° C 80% ° C 90% ° C DS: After a sulphurization step by circulation in the reactor of a gas oil fraction supplemented with DMDS at a final temperature of 350.degree. C., the unit is operated with the petroleum residue described in FIGS. below in the operating conditions Table 8: Operating conditions used in a fixed-bed reactor Total pressure 15 MPa Test temperature 370 ° C Hourly space velocity of the residue 0.811-1 Hydrogen flow rate 1200 std1H2 / 1-charge The mixture is injected RA AM / RSV AL charges then rise to the test temperature. After a stabilization period of 300 hours, the hydrodesulfurization (HDS) and hydrodemetallation (HDM) performances are recorded. The performances obtained (Table 9) confirm the results of Example 8, that is to say the good performance of the catalysts comalaxés according to the invention relative to the reference catalyst, prepared by dry impregnation. The loss of activity compared to the reference is negligible. It therefore appears that the catalysts according to the invention, with a lower manufacturing cost, make it possible to obtain a satisfactory activity, which is almost equivalent to that obtained with a catalyst prepared by dry impregnation. This confirms the interest of the preparation route according to the invention, the latter being easier to implement and much less expensive therefore for the catalyst manufacturer.
[0103] Table 9: HDS, HDM performance of the catalysts A1 and 131 relative to the comparative catalyst E Catalyst H DS (`) / 0) HDM (`) / 0) Al (according to the invention) -1.2% -1.2% B1 (according to the invention) the invention) -0.5% -1.7% E (comparative) Base Base15

权利要求:
Claims (20)
[0001]
REVENDICATIONS1. Process for the preparation of a comalaxed active phase catalyst comprising at least one Group VI B metal from the Periodic Table of Elements, optionally at least one Group VIII metal of the Periodic Table of Elements, optionally phosphorus and an oxide matrix predominantly calcined aluminum, comprising the following steps: a) a first step of precipitation, in an aqueous reaction medium, of at least one basic precursor chosen from sodium aluminate, potassium aluminate, ammonia, hydroxide of sodium and potassium hydroxide and of at least one acidic precursor selected from aluminum sulphate, aluminum chloride, aluminum nitrate, sulfuric acid, hydrochloric acid and nitric acid wherein at least one of the basic or acidic precursors comprises aluminum, the relative flow rate of the acidic and basic precursors is selected so as to obtain a pH of the reaction medium. l between 8.5 and 10.5 and the flow rate of the aluminum-containing acidic and basic precursor (s) is adjusted so as to obtain a degree of progress of the first step of between 5 and 13%, the rate of advancement being defined as being the proportion of alumina formed in equivalent A1203 during said first precipitation step relative to the total amount of alumina formed at the end of step c) of the preparation process, said step operating at a temperature between 20 and 90 ° C and for a period of between 2 minutes and 30 minutes; b) a step of heating the suspension at a temperature between 40 and 90 ° C for a period of between 7 minutes and 45 minutes, c) a second precipitation step of the suspension obtained at the end of the step of heating b) by adding to the suspension at least one basic precursor selected from sodium aluminate, potassium aluminate, ammonia, sodium hydroxide and potassium hydroxide and at least one acid precursor selected from aluminum sulphate, aluminum chloride, aluminum nitrate, sulfuric acid, hydrochloric acid and nitric acid, wherein at least one of the basic or acidic precursors comprises aluminum, the relative flow rate of the acidic and basic precursors is chosen so as to obtain a pH of the reaction medium of between 8.5 and 10.5 and the flow rate of the aluminum-containing acidic and basic precursor (s) is adjusted in such a way as to to get a rate of advancement of the second between 87 and 95%, the degree of progress being defined as being the proportion of alumina formed in A1203 equivalent during said second precipitation step relative to the total amount of alumina formed at the end of the step c) of the preparation process, said step operating at a temperature of between 40 and 90 ° C and for a time of between 2 minutes and 50 minutes; d) a filtration step of the suspension obtained at the end of the second precipitation step c) to obtain an alumina gel; e) a step of drying said alumina gel obtained in step d) to obtain a powder; f) a step of heat treatment of the powder obtained at the end of step e) between 500 and 1000 ° C, for a period of between 2 and 10 h, in the presence or absence of a flow of air containing up to 60% water volume to obtain a calcined aluminous porous oxide; g) a step of kneading the calcined aluminous porous oxide obtained with a solution of at least one metal precursor of the active phase to obtain a paste; h) a step of forming the paste obtained; i) a step of drying the shaped dough at a temperature of less than or equal to 200 ° C to obtain a dried catalyst; j) a possible step of heat treatment of the dried catalyst at a temperature between 200 and 1000 ° C, in the presence or absence of water.
[0002]
2. The method of claim 1 wherein the rate of advance of the first precipitation step a) is between 6 and 12%.
[0003]
3. Method according to one of claims 1 or 2 wherein the rate of advance of the first precipitation step a) is between 7 and 11%.
[0004]
4. Method according to one of claims 1 to 3 wherein the acidic precursor is selected from aluminum sulfate, aluminum chloride and aluminum nitrate, preferably aluminum sulfate.
[0005]
5. Method according to one of claims 1 to 4 wherein the basic precursor is selected from sodium aluminate and potassium aluminate, preferably sodium aluminate.
[0006]
6. Method according to one of claims 1 to 5 wherein in steps a), b), c) the aqueous reaction medium is water and said steps operate with stirring, in the absence of organic additive.
[0007]
7. A mesoporous and macroporous hydroconversion catalyst comprising: a predominantly aluminized calcined oxide matrix; a hydro-dehydrogenating active phase comprising at least one Group VI B metal of the periodic table of elements, optionally at least one metal of group VIII of the periodic table of the elements, optionally phosphorus, said active phase being at least partly comalaxée within said oxide matrix, mostly calcined alumina, said catalyst having a surface area Sbet greater than 100 m 2 / g, a mesoporous median diameter by volume between 12 nm and 25 nm, limits included, a median macroporous diameter by volume included between 50 and 250 nm, inclusive, a mesoporous volume as measured by mercury porosimeter intrusion greater than or equal to 0.65 ml / g and a total pore volume measured by mercury porosimetry greater than or equal to 0.75 ml /boy Wut.
[0008]
8. Hydroconversion catalyst according to claim 7 having a median mesoporous volume diameter determined by mercury porosimeter intrusion between 13 and 17 nm, limits included.
[0009]
9. Hydroconversion catalyst according to one of claims 7 to 8 having a macroporous volume of between 15 and 35 (3/0 of the total pore volume.
[0010]
10. The hydroconversion catalyst according to one of claims 7 to 9 wherein the mesoporous volume is between 0.65 and 0.75 ml / g.
[0011]
11. Hydroconversion catalyst according to one of claims 7 to 10 not having micropores.
[0012]
12. A hydroconversion catalyst according to one of claims 7 to 11 wherein the group VI B metal content is between 2 and 10% by weight of Group VI B metal trioxide relative to the total mass of the catalyst, the group VIII metal content is between 0.0 and 3.6% by weight of the Group VIII metal oxide relative to the total weight of the catalyst, the phosphorus element content is between 0 and 5% by weight; phosphorus pentoxide weight relative to the total mass of the catalyst.
[0013]
13. A hydroconversion catalyst according to one of the preceding claims wherein the hydro-dehydrogenating active phase is composed of molybdenum, or nickel and molybdenum, or cobalt and molybdenum.
[0014]
The hydroconversion catalyst of claim 13 wherein the hydrodehydrogenating active phase also comprises phosphorus.
[0015]
15. The hydroconversion catalyst according to one of claims 7 to 14 wherein the hydro-dehydrogenating active phase is fully comalaxed.
[0016]
16. A hydroconversion catalyst according to one of claims 7 to 14 wherein a portion of the hydro-dehydrogenating active phase is impregnated on the oxide matrix predominantly calcined aluminum.
[0017]
17. Process for hydrotreatment of a heavy hydrocarbon feedstock selected from atmospheric residues, vacuum residues from direct distillation, deasphalted oils, residues resulting from conversion processes such as, for example, those originating from coking, from hydroconversion in a fixed bed, in an ebullated bed or in a moving bed, taken alone or as a mixture comprising contacting said feedstock with hydrogen and a catalyst which can be prepared according to one of claims 1 to 6 or a catalyst according to one of claims 7 to 16.
[0018]
18. The hydrotreatment process according to claim 17, partially carried out in a bubbling bed at a temperature of between 320 and 450 ° C., under a hydrogen partial pressure of between 3 MPa and 30 MPa, at a space velocity advantageously between 0.degree. , 1 and 10 volumes of filler per volume of catalyst and per hour, and with a gaseous hydrogen gas to liquid hydrocarbon feed advantageously between 100 and 3000 normal cubic meters per cubic meter.
[0019]
19. hydrotreatment process according to claim 17 or 18 made at least partly in fixed bed at a temperature between 320 ° C and 450 ° C, at a hydrogen partial pressure of between 3 MPa and 30 MPa, at a speed of space between 0.05 and 5 volumes of filler per volume of catalyst per hour, and with a hydrogen gas ratio on a hydrocarbon liquid charge of between 200 and 5000 normal cubic meters per cubic meter.
[0020]
20. Process for the hydrotreatment of heavy hydrocarbon feedstock of the fixed bed residue type according to claim 19, comprising at least: a) a hydrodemetallation step b) a hydrodesulfurization step in which said catalyst is used in at least one of said stages a) and b).

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公开号 | 公开日 | 专利标题

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EP3154681B1|2019-12-25|Mesoporous and macroporous catalyst for hydrotreating petroleum residue and preparation method thereof

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EP3154682B1|2019-12-25|Mesoporous catalyst for hydrotreating petroleum residue and preparation method thereof

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EP3154683A1|2017-04-19|Mesoporous and macroporous catalyst with an active phase obtained by comulling, method for preparing same and use thereof for the hydrotreatment of residuum

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FR3023184A1|2016-01-08|HYDROPROCESSING CATALYST WITH HIGH MOLYBDENES DENSITY AND METHOD OF PREPARATION.

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JP2018086656A|2018-06-07|Self-activating hydroprocessing catalyst and process for treating heavy hydrocarbon feedstocks

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EP3155073B1|2018-10-10|Method for the hydrotreatment of distillate cuts using a catalyst made from an amorphous mesoporous alumina having high connectivity

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JP6400677B2|2018-10-03|Activation of hydroprocessing catalyst using steam.

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FR2999454A1|2014-06-20|New catalyst comprising at least one element of group VIB, optionally at least one element of group VIII, phosphorous and at least one aluminosilicate oxide support, useful for hydrotreating heavy hydrocarbon feedstocks

同族专利:

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公开号 | 公开日

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EP3154683A1|2017-04-19|

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RU2686697C2|2019-04-30|

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US20170137725A1|2017-05-18|

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FR3022156B1|2018-02-23|

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WO2015189197A1|2015-12-17|

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RU2017100947A|2018-07-16|

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CN106660019B|2019-06-04|

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RU2017100947A3|2018-10-18|

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CN106660019A|2017-05-10|

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法律状态:
2015-06-02| PLFP| Fee payment|Year of fee payment: 2 |

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2015-12-18| PLSC| Publication of the preliminary search report|Effective date: 20151218 |

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2016-06-07| PLFP| Fee payment|Year of fee payment: 3 |

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2017-06-22| PLFP| Fee payment|Year of fee payment: 4 |

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2018-06-27| PLFP| Fee payment|Year of fee payment: 5 |

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2019-06-25| PLFP| Fee payment|Year of fee payment: 6 |

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2021-03-12| ST| Notification of lapse|Effective date: 20210205 |

优先权:

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申请号 | 申请日 | 专利标题

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FR1455413A|FR3022156B1|2014-06-13|2014-06-13|CATALYST AND MACROPOROUS CATALYST WITH COMALATED ACTIVE PHASE, PROCESS FOR THE PREPARATION THEREOF AND USE THEREOF IN HYDROTREATMENT OF RESIDUES|FR1455413A| FR3022156B1|2014-06-13|2014-06-13|CATALYST AND MACROPOROUS CATALYST WITH COMALATED ACTIVE PHASE, PROCESS FOR THE PREPARATION THEREOF AND USE THEREOF IN HYDROTREATMENT OF RESIDUES|

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EP15738845.5A| EP3154683A1|2014-06-13|2015-06-09|Mesoporous and macroporous catalyst with an active phase obtained by comulling, method for preparing same and use thereof for the hydrotreatment of residuum|

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US15/318,617| US20170137725A1|2014-06-13|2015-06-09|Mesoporous and macroporous catalyst with a co-mixed active phase, the preparation process thereof and the use thereof in hydrotreating of residues|

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RU2017100947A| RU2686697C2|2014-06-13|2015-06-09|Mesoporous and macroporous catalyst with active phase obtained by comulling, method for preparing same and use thereof for hydrotreatment of residuum|

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CN201580042698.6A| CN106660019B|2014-06-13|2015-06-09|By the mesoporous and macroporous catalyst, preparation method and its purposes of the hydrotreating for residual oil that grind the active phase of acquisition altogether|

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PCT/EP2015/062823| WO2015189197A1|2014-06-13|2015-06-09|Mesoporous and macroporous catalyst with an active phase obtained by comulling, method for preparing same and use thereof for the hydrotreatment of residuum|