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    • 专利摘要:
    The invention relates to a supported catalyst comprising a calcined, predominantly aluminum oxide support and an active phase comprising nickel, the nickel content being between 5 and 65% by weight of said element relative to the total mass of the catalyst, said active phase not comprising no Group VIB metal, the nickel particles having a diameter of less than or equal to 20 nm, said catalyst having a mesoporous median diameter between 8 nm and 25 nm, a macroporous median diameter greater than 200 nm, a mesoporous volume measured by mercury porosimetry greater than or equal to 0.30 mL / g and a total pore volume measured by mercury porosimetry greater than or equal to 0.34 mL / g. The invention also relates to the process for preparing said catalyst and its use in a hydrogenation process.
    公开号:FR3022163A1
    申请号:FR1455434
    申请日:2014-06-13
    公开日:2015-12-18
    发明作者:Malika Boualleg；Anne-Claire Dubreuil；Emily Maille；Cecile Thomazeau
    申请人:IFP Energies Nouvelles IFPEN；
    IPC主号:
    专利说明:

    [0001] FIELD OF THE INVENTION The invention relates to a catalyst supported on a nickel-phase calcined predominantly aluminic oxide support having a texture and a formulation which are favorable to hydrogenation reactions, in particular to the selective hydrogenation reactions of polyunsaturated compounds or of hydrogenation of aromatics. The invention also relates to the process for preparing said catalyst as well as its use in hydrogenation reactions. The catalysts for selective hydrogenation or hydrogenation of aromatics are generally based on metals of group VIII of the periodic table of elements such as nickel. The metal is in the form of nanometric metal particles deposited on a support which may be a refractory oxide. The metal content of group VIII, the possible presence of a second metallic element, the size of the metal particles and the distribution of the active phase in the support as well as the nature and porous distribution of the support are parameters that are important. on the performance of the catalysts. The speed of the hydrogenation reaction is governed by several criteria, such as the diffusion of the reagents on the surface of the catalyst (external diffusional limitations), the diffusion of the reagents in the porosity of the support towards the active sites (internal diffusion limitations) and the intrinsic properties of the active phase such as the size of the metal particles and the distribution of the active phase within the support. As regards the size of the metal particles, it is generally accepted that the catalyst is all the more active as the size of the metal particles is small. In addition, it is important to obtain a particle size distribution centered on the optimum value as well as a narrow distribution around this value. With regard to the internal diffusion limitations, it is important that the porous distribution of the macropores and mesopores is adapted to the desired reaction in order to ensure the diffusion of the reagents in the porosity of the support towards the active sites as well as the diffusion of the formed products. outwards. The importance of a suitable porous distribution and in particular the presence of macropores in a selective hydrogenation reaction of a pyrolysis gasoline in the case of a palladium-based catalyst has for example been described by Z.Zhou, T. Zeng, Z. Cheng, W. Yuan, in AICHE Journal, 2011, Vol. 57, No. 8, pages 2198-2206. Numerous developments thus relate to optimizing the porous distribution of the catalyst by optimizing the support of the catalyst. WO2011 / 080515 discloses an alumina-supported nickel hydrogenation catalyst having a nickel content of greater than 35% by weight, said catalyst having a high dispersion of nickel (O) on the surface of a highly porous alumina open and with a high specific surface. The porous distribution of the support is bimodal: at least 30% of the total pore volume is constituted by pores having a diameter of between 5 and 20 nm, and at least 20% of the total pore volume consists of pores with a diameter of between 100 and 700 nm with a total pore volume of the carrier of at least 1.0 mL / g. The nickel surface must be greater than or equal to 110 m2 per gram of nickel.
    [0002] In this context, one of the objectives of the present invention is to provide a nickel-phase supported supported catalyst with hydrogenation performance in terms of activity at least as good as the known catalysts of the state of the art. More particularly, the invention relates to a supported catalyst comprising a calcined, predominantly aluminum oxide support and an active phase comprising nickel, the nickel content being between 5 and 65% by weight of said element relative to the total mass of the catalyst, said phase active compound not comprising a group VIB metal, the nickel particles having a diameter of less than or equal to 20 nm, said catalyst having a mesoporous median diameter between 8 nm and 25 nm, a macroporous median diameter greater than 200 nm, a volume mesoporous measured by mercury porosimetry greater than or equal to 0.30 ml / g and a total pore volume measured by mercury porosimetry greater than or equal to 0.34 ml / g. The Applicant has discovered that a catalyst prepared by impregnation of the active phase on an alumina resulting from the calcination of a particular alumina gel prepared according to the preparation method described below, makes it possible to obtain a catalyst which has a porous distribution as well as a size of nickel particles particularly adapted to hydrogenation reactions, in particular to the selective hydrogenation reactions of polyunsaturated molecules such as diolefins, acetylenics or alkenylaromates, or to the hydrogenation reactions of aromatics . In fact, the resulting porous distribution of the calcined aluminized oxide support preparation process resulting from a specific alumina gel makes it possible to provide a porosity that is particularly adapted to promoting the diffusion of the reagents in the porous medium and then their reaction with the active phase. . Without being bound by any theory, it seems that the particular textural properties of the catalyst according to the invention, in particular a bimodal porosity with the presence of macropores and mesopores of controlled size makes it possible to obtain a catalyst having hydrogenation performance in terms of activity at least as good as the known catalysts of the state of the art. The catalyst according to the invention is distinguished by a high mesoporous volume coupled to a macroporous volume, but not too high with a relatively high median macropore diameter. Indeed, it is well known that although the presence of a macroporous volume can reduce the internal diffusion limitations, it also weakens the mechanical strength of the catalyst. It is therefore important to control the percentage of the macroporous volume with respect to the total pore volume in order to obtain a catalyst having the desired catalytic performance and sufficient mechanical strength. In addition, the presence of a high total pore volume of the catalyst according to the invention makes it possible to impregnate a high content of active phase in a single pass. According to a variant, the support, before introduction of the active phase, has a pore volume contained in the pores with a diameter of between 100 and 700 nm less than 20% of the total pore volume of the support, preferably less than 15% of the volume. total porous support. According to one variant, the nickel content is between 10 and 34% by weight of said element relative to the total mass of the catalyst.
    [0003] According to one variant, the macroporous volume of the catalyst is between 10 and 40% of the total pore volume. According to one variant, the mesoporous volume of the catalyst is between 0.35 ml / g and 0.8 ml / g.
    [0004] According to one variant, the catalyst does not contain micropores. The invention also relates to the process for preparing said catalyst. The invention also relates to the use of the catalyst in a hydrogenation process in which the catalyst according to the invention or capable of being prepared according to the preparation method according to the invention is brought into contact in the presence of hydrogen with a hydrocarbon feed containing polyunsaturated and / or aromatic molecules so as to obtain an effluent that is at least partially hydrogenated. Detailed Description The Catalyst According to the Invention The catalyst according to the invention is in the form of a supported catalyst comprising a calcined, predominantly aluminum oxide support and an active phase comprising nickel. The characteristics of the alumina gel having led to the production of the alumina mainly contained in said support, as well as the textural properties obtained with the active phase, confer on the catalyst according to the invention its specific properties. More particularly, the invention relates to a supported catalyst comprising a calcined, predominantly aluminum oxide support and an active phase comprising nickel, the nickel content being between 5 and 65% by weight of said element relative to the total mass of the catalyst, said phase active compound not comprising a group VIB metal, the nickel particles having a diameter of less than or equal to 20 nm, said catalyst having a mesoporous median diameter between 8 nm and 25 nm, a macroporous median diameter greater than 200 nm, a volume mesoporous measured by mercury porosimetry greater than or equal to 0.30 ml / g and a total pore volume measured by mercury porosimetry greater than or equal to 0.34 ml / g.
    [0005] The catalyst according to the invention and the support used for the preparation of the catalyst according to the invention have particular textural properties, in particular 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 and less than 7000 nm. By "mesopores" is meant pores whose opening is between 2 nm and 50 nm, limits included.
    [0006] By "micropores" is meant pores whose opening is less than 2 nm. The total pore volume of the catalyst or support used for the preparation of the catalyst according to the invention is understood to mean the volume measured by mercury porosimeter intrusion 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 °. The anchoring angle was taken equal to 140 ° according to the recommendations of the book "Techniques of the engineer, treated analysis and characterization", pages 1050-1055, written by Jean Charpin and Bernard Rasneur. In order to obtain a better accuracy, the value of the total pore volume corresponds to the value of the total pore volume measured by mercury porosimeter intrusion measured on the sample minus the value of the total pore volume measured by mercury porosimeter intrusion measured on the same sample for a pressure corresponding to 30 psi (about 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 °. 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. The macroporous volume of the catalyst or support used for the preparation of the catalyst according to the invention 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 of diameter apparent greater than 50 nm. The mesoporous volume of the catalyst or support used for the preparation of the catalyst according to the invention 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 of apparent diameter included 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. Rouquerol, J. Rouquerol and K. Sing, Academic Press, 1999. The median mesoporous diameter is also defined as the diameter such that all the pores, among all the pores constituting the mesoporous volume, smaller than this diameter constitute 50% of the total mesoporous volume determined by mercury porosimeter intrusion. The macroporous median diameter is also defined as the diameter such that all the pores, among all the pores constituting the macroporous volume, of size less than this diameter constitute 50% of the total macroporous volume determined by intrusion into the mercury porosimeter. By the specific surface of the catalyst or of the support used for the preparation of the catalyst according to the invention, 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, 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 classification I U PAC.
    [0007] Characteristics of the support according to the invention The support of the catalyst according to the invention mainly comprises a calcined aluminous porous oxide. Said support has a calcined alumina content greater than or equal to 90% by weight relative to the total weight of said matrix, optionally supplemented with silica and / or phosphorus to a total content of at most 10% by weight of SiO 2 equivalent and or P205, preferably less than 5% by weight, and very preferably less than 2% by weight relative to the total weight of said matrix. Silica and / or phosphorus can be introduced by any technique known to those skilled in the art, during the synthesis of the alumina gel or by impregnation of the support used for the preparation of the catalyst according to the invention. Even more preferably, the predominantly calcined aluminum porous oxide support is made of alumina. Preferably, the alumina present in said support is a transition alumina such as a gamma, delta, theta, chi, rho or eta alumina, alone or as a mixture. More preferably, the alumina is a gamma, delta or theta transition alumina, alone or as a mixture. The following characteristics of the support correspond to the characteristics of the support used for the preparation of the catalyst according to the invention before impregnation of the active phase. The support used for the preparation of the catalyst according to the invention has a total pore volume of at least 0.33 ml / g, preferably between 0.36 and 1.3 ml / g, and particularly preferably between 0.40 and 1.2 mL / g. The support used for the preparation of the catalyst according to the invention advantageously has a macroporous volume of between 10 and 40% of the total pore volume of the support, preferably between 15 and 38% of the total pore volume of the support, and even more preferred between 20 and 35% of the total pore volume of the support.
    [0008] The mesoporous volume of the support used for the preparation of the catalyst according to the invention is at least 0.30 ml / g, preferably between 0.35 and 1.0 ml / g, and particularly preferably between 0 , 35 and 0.9 mL / g. The support used for the preparation of the catalyst according to the invention advantageously has a pore volume of pores having a pore diameter of between 100 and 700 nm less than 20% of the total pore volume of the support, preferably less than 18% of the pore volume. total support and particularly preferably less than 15% of the total pore volume of the support. The median mesoporous diameter of the support used for the preparation of the catalyst according to the invention is between 8 nm and 25 nm, and preferably between 9 and 22 nm. The support used for the preparation of the catalyst according to the invention has a macroporous median diameter greater than 200 nm, preferably between 250 and 1500 nm, preferably between 270 and 1000 nm, even more preferably between 300 and 800 nm. nm. The support used for the preparation of the catalyst according to the invention has a specific surface B.E.T. at least 40 m 2 / g, preferably at least 50 m 2 / g, and even more preferably between 60 and 400 m 2 / g. When it is desired to use the catalyst according to the invention in a reaction for the selective hydrogenation of polyunsaturated molecules such as diolefins, acetylenics or alkenylaromates, the support used for the preparation of the catalyst according to the invention advantageously has a specific surface area. BET between 60 and 230 m2 / g. When it is desired to use the catalyst according to the invention in an aromatic hydrogenation reaction, the support used for the preparation of the catalyst according to the invention advantageously has a B.E.T. between 130 and 400 m2 / g.
    [0009] Preferably, the support used for the preparation of the catalyst according to the invention has a low microporosity, very preferably it has no microporosity.
    [0010] Characteristics of the Catalyst The finished catalyst, that is to say with the active phase deposited on the support by any method known to those skilled in the art, as described below, therefore has the textural properties to follow. The catalyst according to the invention has a total pore volume of at least 0.34 ml / g, preferably at least 0.37 ml / g, and particularly preferably between 0.40 and 0.9 ml. / g. The catalyst according to the invention advantageously has a macroporous volume of between 10 and 40% of the total pore volume of the catalyst, preferably between 15 and 38% of the total pore volume of the catalyst, and even more preferably between 20 and 35%. % of the total pore volume of the catalyst. The mesoporous volume of the catalyst is at least 0.30 ml / g, preferably at least 0.35 ml / g, and particularly preferably between 0.35 ml / g and 0.8 ml / g. . The mesoporous median diameter of the catalyst is between 8 nm and 25 nm, and preferably between 9 and 22 nm. The catalyst has a macroporous median diameter greater than 200 nm, preferably between 250 and 1500 nm, preferably between 270 and 1000 nm, even more preferably between 300 and 800 nm. The catalyst according to the present invention has a specific surface B.E.T. at least 40 m 2 / g, preferably at least 50 m 2 / g, and even more preferably between 55 and 250 m 2 / g. When it is desired to use the catalyst according to the invention in a selective hydrogenation reaction of polyunsaturated molecules such as diolefins, acetylenics or alkenylaromates, the catalyst according to the invention advantageously has a B.E.T. between 55 and 170 m2 / g. When it is desired to use the catalyst according to the invention in a reaction for the hydrogenation of aromatics, the catalyst according to the invention advantageously has a B.E.T. between 90 and 250 m2 / g. Preferably, the catalyst has a low microporosity, very preferably it has the nickel content is between 5 and 65% by weight of said element relative to the total mass of the catalyst, preferably between 8 and 55% by weight, more preferably still between 10 and 40% by weight, and particularly preferably between 10 and 34% by weight. The Ni content is measured by X-ray fluorescence. When it is desired to use the catalyst according to the invention in a selective hydrogenation reaction of polyunsaturated molecules such as diolefins, acetylenes or alkenyl aromatics, the nickel content is advantageously included. between 5 and 25% by weight, preferably between 8 and 25% by weight, and more preferably between 10 and 23% by weight of said element relative to the total mass of the catalyst. When it is desired to use the catalyst according to the invention in a reaction for the hydrogenation of aromatics, the nickel content is advantageously between 15 and 65% by weight, preferably between 18 and 55% by weight, and more preferably between between 19 and 34% by weight of said element relative to the total mass of the catalyst. The size of the nickel particles in the catalyst according to the invention is less than 20 nm, preferably between 1.5 and 18 nm. The term "size of the nickel particles" is understood to mean the diameter of the crystallites of nickel in oxide form. The diameter of nickel crystallites in oxide form is determined by X-ray diffraction from the width of the diffraction line at the angle 2theta = 43 ° (i.e. in the crystallographic direction [200] ]) using Scherrer's relationship. This method, used in X-ray diffraction on powders or polycrystalline samples which connects the half-height width of the diffraction peaks to the particle size, 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. The active phase of the catalyst may further comprise at least one additional metal selected from Group VIII metals, Group IB metals and / or tin. Preferably, the additional metal of group VIII is chosen from platinum, ruthenium and rhodium, as well as palladium. Advantageously, the additional metal of group IB is chosen from copper, gold and silver. The additional metal (s) of the group VIII and / or of the group IB is (are) preferably present at a content representing from 0.01 to 20% by weight of the mass of the catalyst, preferably from 0.05 to 10% by weight of the catalyst mass and even more preferably from 0.05 to 5% by weight of the mass of said catalyst.
    [0011] The tin is preferably present at a content representing from 0.02 to 15% by weight of the catalyst mass, such that the Sn / Ni molar ratio is between 0.01 and 0.2, preferably between 0.025 and 0.055, and even more preferably between 0.03 to 0.05. The active phase of the catalyst does not include a Group VIB metal. It does not include molybdenum or tungsten. Said catalyst according to the invention is generally presented in all the forms known to those skilled in the art, for example in the form of beads (generally having a diameter of between 1 and 6 mm), extrudates, tablets, hollow cylinders . 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 cylindrical, multilobed, trilobed or quadrilobed extrudates. 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.
    [0012] The present invention also relates to a process for preparing said catalyst according to the invention. The catalyst according to the invention is prepared from a specific alumina gel. The particular porous distribution observed in the catalyst is in particular due to the process of preparation from the specific alumina gel. The preparation of said alumina gel comprises the successive steps: a step of dissolving an aluminum acid precursor, a step of adjusting the pH of the suspension by means of a basic precursor, and a coprecipitation step at least one acidic precursor and at least one basic precursor, at least one of which contains aluminum and a filtration step. The gel is then subjected to a drying step to obtain a powder. The powder is then either shaped and then subjected to a heat treatment, or first subjected to a heat treatment and then shaped in order to obtain in both cases a calcined aluminum porous oxide support. The calcined aluminous porous oxide support is then impregnated with a solution comprising the salt (s) of the precursor (s) of the active phase, and then dried to obtain a dried catalyst. Then the dried catalyst is optionally subjected to heat treatment, then generally reduced and subjected to a passivation treatment.
    [0013] More particularly, the process for preparing the catalyst according to the invention comprises the following steps: a) a step of dissolving an aluminum acid precursor chosen from aluminum sulphate, aluminum chloride and nitrate of aluminum in water, at a temperature between 20 and 90 ° C, at a pH between 0.5 and 5, for a period of between 2 and 60 minutes, b) a step of adjusting the pH by adding to the suspension obtained in step a) at least one basic precursor selected from sodium aluminate, potassium aluminate, ammonia, sodium hydroxide and potassium hydroxide, at a temperature between 20 and 90 ° C, and at a pH between 7 and 10, for a period of between 5 and 30 minutes, C) a step of coprecipitation of the suspension obtained at the end of step b) by adding to the suspension at least one basic precursor chosen from sodium aluminate, pot aluminate assium, 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, at least one of the basic or acidic precursors comprising aluminum, the relative flow rate of the acidic and basic precursors being chosen so as to obtain a pH of the reaction medium of between 7 and 10 and the the flow rate of the aluminum-containing acidic and basic precursor (s) being adjusted so as to obtain a final alumina concentration in the suspension of between 10 and 38 g / l; (d) a filtration stage of the suspension obtained at the end of step c) of coprecipitation to obtain an alumina gel, e) a step of drying said alumina gel obtained in step d) to obtain a powder, f) a shaping step, g) a heat treatment step performed between steps e) and f) or after step f) at a temperature between 500 and 1000 ° C, with or without a flow of air containing up to 60% by volume of water to obtain a calcined aluminum porous oxide support, h ) a step of impregnating said support with a solution comprising the salt (s) of the precursor (s) of the nickel-based active phase, i) a step of drying the impregnated support at a temperature between and less than 250 ° C, so as to obtain a dried catalyst, j) optionally a heat treatment of said dried catalyst at a temperature between 250 and 1000 ° C in the presence or absence of water. Step a) of dissolving Step a) is a step of dissolving an aluminum acid precursor chosen from aluminum sulphate, aluminum chloride and aluminum nitrate in the water, at a temperature between 20 and 90 ° C, at a pH between 0.5 and 5, for a period of between 2 and 60 minutes. Step a) is carried out at a temperature between 20 and 90 ° C, preferably between 20 and 75 ° C, and more preferably between 30 and 70 ° C. The pH of the suspension obtained is between 0.5 and 5, preferably between 1 and 4, preferably between 1.5 and 3.5. This step advantageously contributes to an amount of alumina introduced relative to the final alumina of between 0.5 and 4%, preferably between 1 and 3%, very preferably between 1.5 and 2.5%. The suspension is left stirring for a period of between 2 and 60 minutes, and preferably 5 to 30 minutes. Step b) Adjusting the pH The pH adjustment step b) consists in adding to the suspension obtained in step a) at least one basic precursor chosen from sodium aluminate, potassium aluminate, ammonia, sodium hydroxide and potassium hydroxide. Preferably, the basic precursor is chosen from sodium aluminate and potassium aluminate. Very preferably, the basic precursor is sodium aluminate. Step b) is carried out at a temperature between 20 and 90 ° C, preferably between 20 and 80 ° C and more preferably between 30 and 70 ° C and at a pH between 7 and 10, preferably between 8 and 10, preferably between 8.5 and 10 and very preferably between 8.7 and 9.9. The duration of step b) of pH adjustment is between 5 and 30 minutes, preferably between 8 and 25 minutes, and very preferably between 10 and 20 minutes. Step c) of coprecipitation Step c) is a step of coprecipitating the suspension obtained at the end of step b) by adding to this suspension an aqueous solution of 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, nitrate d aluminum, sulfuric acid, hydrochloric acid and nitric acid, at least one of the basic precursors or acid comprising aluminum, said precursors being selected identical or not to the precursors introduced in steps a) and b). The relative flow rate of the acidic and basic precursors being chosen so as to obtain a pH of the reaction medium of between 7 and 10 and the flow rate of the acidic and basic precursor (s) containing aluminum being adjusted so as to obtain a final alumina concentration. in the suspension of between 10 and 38 g / l, preferably between 13 and 35 g / l and more preferably between 15 and 33 g / l. Preferably, the coprecipitation step is conducted at a temperature between 20 and 90 ° C, and more preferably between 30 and 70 ° C.
    [0014] Step c) of coprecipitation is carried out at a pH of between 7 and 10, preferably between 8 and 10, preferably between 8.5 and 10, and very preferably between 8.7 and 9.9. Step c) of coprecipitation is carried out for a period of between 1 and 60 minutes, and preferably between 5 and 45 minutes.
    [0015] Preferably, said steps a), b) and c) are carried out in the absence of organic additive. Preferably, steps a), b) and c) are carried out with stirring. Filtration step d) The process for preparing the alumina according to the invention also comprises a step d) of filtering the suspension obtained at the end of step c) so as to obtain an alumina gel. Said filtration step is carried out according to the methods known to those skilled in the art. Said filtration step is advantageously followed by at least one washing step, with an aqueous solution, preferably with water and preferably from one to three washing steps, with a quantity of water equal to the amount of precipitate filtered. Step e) of drying the alumina gel According to the invention, the alumina gel obtained at the end of the precipitation step c), followed by a filtration step d), is dried in a step e) drying to obtain a powder. Said drying step is generally carried out at a temperature greater than or equal to 120 ° C. or by atomization or by any other drying technique known to a person skilled in the art. In the case where said drying step e) is carried out by drying at a temperature greater than or equal to 120 ° C., said drying step d) may advantageously be carried out in a closed and ventilated oven. Preferably said drying step is carried out at a temperature between 120 and 300 ° C, very preferably at a temperature between 150 and 250 ° C. 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.
    [0016] 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. Step f) Shaping In accordance with the invention, a shaping step f) is then carried out. According to a first, preferred variant, the powder obtained at the end of step e) of the drying of the alumina gel is shaped according to step f), and then the powder shaped at the end of the step f) is subjected to a heat treatment according to step g) described below to obtain a calcined aluminous porous oxide support.
    [0017] According to a second variant, the powder obtained at the end of step e) of drying the alumina gel is first subjected to a heat treatment according to step g) described below, and then subsequently shaped. according to step f) to obtain a calcined aluminous porous oxide support.
    [0018] Preferably, said shaping step f) is carried out according to any technique known to those skilled in the art, for example extrusion forming methods, pelletizing, by the method of the drop of oil (dewatering) or by granulation at the turntable.
    [0019] In a very preferred manner, said shaping step f) is carried out by extrusion. A piston extruder can be used through a die having the desired diameter, typically between 0.5 and 10 mm. The extrudates generally have a diameter of between 0.5 and 10 mm, preferably 0.8 and 3.2 mm, and very preferably between 1.0 and 2.5 mm. The extrudates may advantageously be in the form of cylindrical, multilobed, trilobed or quadrilobed extrudates. Preferably the shape will be trilobed or quadrilobed. Any other element, for example silica in the form of a solution or a silicic precursor emulsion, may be introduced during the shaping. Step c1) Heat Treatment According to the invention, a heat treatment step is carried out between steps e) and f) or after step f) at a temperature of between 500 and 1000 ° C., in the presence or absence of a flow of air containing up to 60% by volume of water to obtain a calcined aluminous porous oxide. According to the first, preferred variant, the heat treatment step is carried out after the shaping step f). In this case, the heat treatment step may be preceded by drying at a temperature between 50 ° C and 200 ° C, according to any technique known to those skilled in the art. According to a second variant, the heat treatment step is carried out between the drying step e) of the alumina gel and the shaping step f).
    [0020] Preferably, said heat treatment step g) operates at a temperature of between 540 and 850 ° C. Preferably, said heat treatment step f) operates for a duration of between 2 and 10 hours.
    [0021] The term "heat treatment" means the temperature treatment respectively without presence or in the presence of water. In the latter case, the contact with the water vapor can take place at atmospheric pressure ("steaming") or autogenous pressure (autoclaving). Several combined cycles without presence or with presence of water can be realized. In the presence of water, 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. Said heat treatment step g) allows the transition of the alumina gel, also called boehmite, to the calcined aluminized porous oxide support having the textural characteristics as described above. The alumina has a crystallographic structure of the type transition alumina gamma, delta, theta, chi, rho or eta, alone or in mixture. More preferably, the alumina is a gamma, delta or theta transition alumina, alone or as a mixture. The existence of the different crystallographic structures is related to the conditions of implementation of step g) of heat treatment. Step h) Impregnation of the active phase According to step h) of the process according to the invention, the aluminized porous aluminum oxide support is impregnated with a solution comprising the salt (s) of the precursor (s) of the phase active nickel based. The active phase is provided by one or more solutions containing at least nickel. The said solution (s) may be aqueous or consist of an organic solvent or a mixture of water and at least one organic solvent ( for example ethanol or toluene). Preferably, the solution is aqueous. The pH of this solution may be modified by the possible addition of an acid. According to another preferred variant, the aqueous solution may contain ammonia or ammonium ions NH4. Preferably, said nickel precursor is introduced in aqueous solution, for example in the form of nitrate, carbonate, acetate, chloride, hydroxide, hydroxycarbonate, oxalate, complexes formed by a polyacid or an acid-alcohol and its salts, complexes formed with acetylacetonates, or any other soluble inorganic derivative in aqueous solution, which is brought into contact with said calcined aluminous porous oxide. Preferably, nickel precursor nickel nitrate, nickel chloride, nickel acetate or nickel hydroxycarbonate is advantageously used. Very preferably, the nickel precursor is nickel nitrate or nickel hydroxycarbonate. According to another preferred variant, said nickel precursor is introduced into an ammoniacal solution by introducing a nickel salt, for example nickel hydroxide or nickel carbonate, into an ammoniacal solution or into an ammonium carbonate or ammonium carbonate solution. ammonium hydrogen carbonate. The quantities of the nickel precursor (s) introduced into the solution are chosen such that the total nickel content is between 5 and 65% by weight, preferably between 8 and 55% by weight, preferably between 10 and 40% by weight. weight, and particularly preferably between 10 and 34% by weight of said element relative to the total mass of the catalyst. The nickel contents are generally adapted to the intended hydrogenation reaction as described above in the section of the catalyst description. Any other additional element may be introduced at the time of this step: When it is desired to introduce phosphorus, a solution of phosphoric acid may be introduced into the impregnating solution. When it is desired to introduce an additional metal chosen from Group VIII metals, Group IB metals and / or tin, a salt chosen from nitrate, sulphate, chloride or any other precursor is advantageously used as precursor. conventional. 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. The impregnation of the active phase can be carried out according to all the methods known to those skilled in the art, in particular by dry impregnation. Preferably, the nickel and optionally at least one additional element such as an additional metal selected from Group VIII metals, Group IB metals and / or tin, phosphorus or an additive such as an agent chelants of organic nature are deposited by dry impregnation of their associated precursors on the oxide support according to the invention. The deposition can be done via a single step of dry impregnation of the oxide support according to the invention via the use of a solution containing simultaneously at least one nickel compound, and optionally at least one additional element. The deposit can also be advantageously achieved via at least two cycles of dry impregnation. The different elements can thus be advantageously impregnated successively or one of the elements can also be impregnated into several sequences. One of the impregnations which is carried out can in particular make it possible to introduce an organic compound in addition to the active phase of the catalyst. In these cases, each impregnation is advantageously followed by drying and optionally heat treatment. The drying can be carried out at a temperature between 15 and 250 ° C, preferably between 80 and 200 ° C, generally for a period of between 10 minutes and 24 hours. The heat treatment can be carried out at a temperature of between 200 and 1000 ° C., preferably between 250 and 750 ° C., generally for a period of between 15 minutes and 10 hours. Step i) Drying of the impregnated support According to the invention, the impregnated support obtained at the end of step h) of impregnation of the active phase undergoes a drying step i) at a temperature of between 15 and less than 250 ° C, preferably between 80 and 200 ° C, according to any technique known to those skilled in the art, for a period of typically between 10 minutes and 24 hours. A dried catalyst is obtained. Step i) Heat Treatment of the Dried Catalyst The catalyst thus dried can then undergo a further thermal treatment step j) at a temperature of between 250 and 1000 ° C and preferably between 250 and 750 ° C for a period of time typically between minutes and 10 hours, with or without water. The term "heat treatment" means the temperature treatment respectively without presence or with the presence of water. In the latter case, the contact with the water vapor can take place at atmospheric pressure ("steaming") or autogenous pressure (autoclaving). Several combined cycles of thermal or hydrothermal treatments can be carried out. After this or these treatment (s), the catalyst precursor comprises nickel in oxide form, that is to say in NiO form.
    [0022] In case of hydrothermal treatment, 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. Step k) Reduction by a reducing agent Prior to the use of the catalyst in the catalytic reactor and the implementation of a hydrogenation process, at least one reducing treatment step k) is advantageously carried out in the presence of a gas. reducing agent after steps i) or j) so as to obtain a catalyst comprising nickel at least partially in metallic form. This treatment makes it possible to activate the said catalyst and to form metal particles, in particular nickel in the zero state. Said reducing treatment can be carried out in situ or ex situ, that is to say after or before the catalyst is loaded into the hydrogenation reactor. Said step k) of reducing treatment can be carried out on the catalyst which has or has not been subjected to the passivation step I), described below.
    [0023] The reducing gas is preferably hydrogen. The hydrogen can be used pure or as a mixture (for example a hydrogen / nitrogen mixture, hydrogen / argon, hydrogen / methane). In the case where the hydrogen is used as a mixture, all proportions are possible.
    [0024] Said reducing treatment is carried out at a temperature between 120 and 500 ° C, preferably between 150 and 450 ° C. When the catalyst is not passivated, or undergoes a reducing treatment before passivation, the reducing treatment is carried out at a temperature between 350 and 500 ° C, preferably between 350 and 450 ° C. When the catalyst has been previously passivated, the reducing treatment is generally carried out at a temperature of between 120 and 350 ° C, preferably between 150 and 350 ° C. The duration of the reducing treatment is generally between 2 and 40 hours, preferably between 3 and 30 hours. The rise in temperature to the desired reduction temperature is generally slow, for example set between 0.1 and 10 ° C / min, preferably between 0.3 and 7 ° C / min. The flow rate of hydrogen, expressed in L / hour / g of catalyst is between 0.1 and 100 L / hour / g of catalyst, preferably between 0.5 and 10 L / hour / g of catalyst, still more preferred between 0.7 and 5 L / hour / gram of catalyst. Step I) Passivation Prior to its implementation in the catalytic reactor, the catalyst according to the invention may optionally undergo a passivation step (step I) with a sulfur or oxygen compound or with CO2 before or after the treatment step reducer k). This passivation step may be performed ex situ or in situ. The passivation step is performed by the implementation of methods known to those skilled in the art. The sulfur passivation step makes it possible to improve the selectivity of the catalysts and to avoid thermal runaways during start-up of new catalysts (<< run away »in the English terminology). Passivation generally consists in irreversibly poisoning with the sulfur compound the most virulent active sites of the nickel which exist on the new catalyst and thus in attenuating the activity of the catalyst in favor of its selectivity. The passivation step is carried out by the implementation of methods known to those skilled in the art and, for example, by the use of one of the methods described in patent documents EP0466567, US5153163, FR2676184, WO2004 / 098774, EP0707890. The sulfur compound is for example chosen from the following compounds: thiophene, thiophane, alkylmonosulfides such as dimethylsulfide, diethylsulfide, dipropylsulfide and propylmethylsulphide or an organic disulfide of formula HO-R1-SS-R2-OH such as di-thio-di -ethanol of formula HO-C2H4-SS-C2H4-OH (often called DEODS) .The sulfur content is generally between 0.1 and 2% by weight of said element relative to the mass of the catalyst. The passivation step with an oxygenated compound or with CO 2 is generally carried out after a preliminary reducing treatment at elevated temperature, generally between 350 and 500 ° C., and makes it possible to preserve the metallic phase of the catalyst in the presence of air. A second reducing treatment at a lower temperature, generally between 120 and 350 ° C., is then generally carried out. The oxygenated compound is generally air or any other stream containing oxygen.
    [0025] The present invention also relates to the use of the catalyst according to the invention in a hydrogenation process and in particular in a process for the selective hydrogenation of polyunsaturated molecules such as diolefins, acetylenics or alkenylaromatiques, also called styrenics.
    [0026] Monounsaturated organic compounds such as, for example, ethylene and propylene, are at the source of the manufacture of polymers, plastics and other value-added chemicals. These compounds are obtained from natural gas, naphtha or gas oil which have been treated by steam cracking or catalytic cracking processes. These processes are operated at high temperature and produce, in addition to the desired monounsaturated compounds, polyunsaturated organic compounds such as acetylene, propadiene and methylacetylene (or propyne), 1-2-butadiene and 1-3 -butadiene, vinylacetylene and ethylacetylene, and other polyunsaturated compounds whose boiling point corresponds to the C5 + gasoline fraction (gasolines containing hydrocarbon compounds having 5 or more carbon atoms), in particular diolefinic or styrenic compounds or indene. These polyunsaturated compounds are very reactive and lead to spurious reactions in the polymerization units. It is therefore necessary to eliminate them before valuing these cuts. Selective hydrogenation is the main treatment developed to specifically remove undesired polyunsaturated compounds from these hydrocarbon feeds. It allows the conversion of the polyunsaturated compounds to the corresponding alkenes or aromatics, avoiding their total saturation and thus the formation of the corresponding alkanes or naphthenes. In the case of steam cracking gasolines used as filler, the selective hydrogenation also makes it possible to selectively hydrogenate the alkenyl aromatics to aromatics by avoiding the hydrogenation of the aromatic rings. The hydrocarbon feedstock treated in the selective hydrogenation process has a final boiling point of less than or equal to 250 ° C and contains at least 2 carbon atoms per molecule and comprises at least one polyunsaturated compound. The term "polyunsaturated compounds" means compounds comprising at least one acetylenic function and / or at least one diene function and / or at least one alkenylaromatic function. More particularly, the filler is selected from the group consisting of a steam cracking section C2, a steam cracking section C3, a steam cracking section C4, a steam cracking section C5 and a steam cracking gasoline also known as pyrolysis gasoline. The steam-cracking gasoline or pyrolysis gasoline corresponds to a hydrocarbon fraction whose boiling point is generally between 0 and 250 ° C., preferably between 10 and 220 ° C. The polyunsaturated hydrocarbons to be hydrogenated present in said steam cracking gasoline are, in particular, diolefinic compounds (butadiene, isoprene, cyclopentadiene, etc.), styrene compounds (styrene, alpha-methylstyrene, etc.) and indene compounds (indene). .). Steam cracking gasoline generally comprises the C5-C12 cut with traces of C3, C4, C13, C14, C15 (for example between 0.1 and 3% by weight for each of these cuts). For example, a charge of pyrolysis gasoline generally has the following composition: 5 to 25 wt% paraffins, 40 to 70 wt% aromatics, 5 to 20 wt% monoolefins, 5 to 40 wt% of diolefins, 1 to 10% by weight of alkenylaromatic compounds and from 20 to 300 ppm by weight of sulfur, all the compounds forming 100%. Preferably, the polyunsaturated hydrocarbon feedstock treated according to the selective hydrogenation process according to the invention is a steam-cracking gasoline.
    [0027] The selective hydrogenation process according to the invention aims at eliminating said polyunsaturated hydrocarbons present in said feedstock to be hydrogenated without hydrogenating the monounsaturated hydrocarbons. For example, when said feed is a C2 cut, the selective hydrogenation process aims to selectively hydrogenate acetylene. When said feedstock is a C3 cut, the selective hydrogenation process aims to selectively hydrogenate propadiene and methylacetylene. In the case of a C4 cut, it is intended to remove butadiene, vinylacetylene (VAC) and butyne, in the case of a C5 cut, it is intended to eliminate pentadienes. When said feed is a steam cracking gasoline, the selective hydrogenation process aims to selectively hydrogenate said polyunsaturated hydrocarbons present in said feed to be treated so that the diolefinic compounds are partially hydrogenated to mono-olefins and that the styrenic and indene compounds are partially hydrogenated to corresponding aromatic compounds by avoiding the hydrogenation of aromatic rings. The technological implementation of the selective hydrogenation process is for example carried out by injection, in ascending or descending current, of the polyunsaturated hydrocarbon feedstock and hydrogen in at least one fixed bed reactor. Said reactor may be of the isothermal or adiabatic type. An adiabatic reactor is preferred. The polyunsaturated hydrocarbon feedstock may advantageously be diluted by one or more re-injection (s) of the effluent, from said reactor where the selective hydrogenation reaction occurs, at various points of the reactor, located between the inlet and the outlet. the reactor outlet to limit the temperature gradient in the reactor. The technological implementation of the selective hydrogenation process according to the invention may also be advantageously carried out by implanting at least one of said supported catalyst in a reactive distillation column or in reactor-exchangers. The flow of hydrogen can be introduced at the same time as the feedstock to be hydrogenated and / or at one or more different points of the reactor. The selective hydrogenation of the C2, C3, C4, C5 and C5 + cuts can be carried out in the gas phase or in the liquid phase, preferably in the liquid phase for the C3, C4, C5 and C5 + cuts. Indeed, a reaction in the liquid phase makes it possible to lower the energy cost and to increase the cycle time of the catalyst. In general, the selective hydrogenation is carried out at a temperature of between 0 and 500 ° C., at a pressure of between 0.1 and 20 MPa, at a molar ratio of hydrogen / (polyunsaturated compounds to be hydrogenated) between 0 and 500 ° C. , 1 and 10 and at an hourly volume velocity VVH (defined as the ratio of the volume flow rate of charge to the volume of the catalyst) between 0.1 and 200 h-1 for a liquid charge, between 100 and 15 000 h-1 for a gaseous charge of a hydrocarbon charge containing polyunsaturated compounds containing at least 2 carbon atoms per molecule and having a final boiling point of less than or equal to 250 ° C. Preferably, a selective hydrogenation process is carried out in which the feedstock is a steam cracking gasoline containing polyunsaturated compounds, the molar ratio (hydrogen) / (polyunsaturated compounds to be hydrogenated) is generally between 1 and 2, the temperature is generally between 40 and 200 ° C, preferably between 50 and 180 ° C, the hourly volume velocity (VVH) is generally between 0.5 and 50 h-1, preferably between 1 and 20 h-1 and the pressure is generally between 0.3 and 6.5 MPa, preferably between 2.0 and 3.5 MPa. The hydrogen flow rate is adjusted in order to dispose of it in sufficient quantity to theoretically hydrogenate all of the polyunsaturated compounds and to maintain an excess of hydrogen at the outlet of the reactor. The present invention also relates to the use of the catalyst according to the invention in a hydrogenation process and in particular in a process for the hydrogenation of aromatics for converting aromatic compounds of petroleum or petrochemical cuts by conversion. aromatic rings to naphthenic rings. The hydrocarbon feedstock treated in the aromatic hydrogenation process has a final boiling point less than or equal to 650 ° C, generally between 20 and 650 ° C, and preferably between 20 and 450 ° C, and contains at least less an aromatic or polyaromatic compound. Examples of petroleum or petrochemical cuts containing aromatic compounds include, for example, kerosene, light gas oil, heavy gas oil and cracking distillates, such as FCC recycle oil, coker unit gas oil, distillates and the like. hydrocracking, and the reformate of catalytic reforming. The content of aromatic hydrocarbons in a feed treated in the hydrogenation process is generally between 0.1 and 80% by weight, preferably between 1 and 50% by weight, and particularly preferably between 2 and 35% by weight, the percentage by weight. weight being based on the total weight of the hydrocarbon feed.
    [0028] The aromatics present are, for example, benzene or alkylaromatics such as toluene, ethylbenzene, o-xylene, m-xylene, or p-xylene, or aromatics having a plurality of aromatic (polyaromatic) rings, such as naphthalene. The sulfur or chlorine content of the feedstock is generally less than 5000 ppm by weight of sulfur or chlorine respectively, preferably less than 100 ppm by weight, and particularly preferably less than 10 ppm. The technological implementation of the aromatic hydrogenation process can be carried out as described in the selective hydrogenation part. The hydrogenation of the aromatics can be carried out in the gas phase or in the liquid phase, preferably in the liquid phase. In general, the hydrogenation of the aromatics is carried out at a temperature of between 30 and 350 ° C., preferably between 50 and 325 ° C., at a pressure of between 0.1 and 20 MPa, preferably between 0 and 20 ° C. , 5 and 10 MPa, at a molar ratio of hydrogen / (aromatic compounds to be hydrogenated) between 0.1 and 10 and at an hourly volume velocity VVH between 0.05 and 50 h -1, preferably between 0.1 and 10 h -1 of a hydrocarbon feedstock containing aromatic compounds and having a final boiling point of less than or equal to 650 ° C. The hydrogen flow rate is adjusted in order to dispose of it in sufficient quantity to theoretically hydrogenate all of the polyunsaturated compounds and to maintain an excess of hydrogen at the outlet of the reactor.
    [0029] The conversion of the aromatic or polyaromatic compounds is generally greater than 20 mol%, preferably greater than 40 mol%, more preferably greater than 80 mol%, and particularly preferably greater than 90 mol% of the aromatic compounds. or polyaromatic content contained in the hydrocarbon feedstock. The conversion is calculated by dividing the difference between the total moles of the aromatic or polyaromatic compounds in the hydrocarbon feedstock and the product by the total moles of the aromatic or polyaromatic compounds in the hydrocarbon feedstock. According to one particular variant, the catalyst according to the invention is used in a process for the hydrogenation of a benzene-containing hydrocarbon feedstock such as, for example, reformate from a catalytic reforming unit. The benzene content is generally between 0.1 and 40% by weight, preferably between 0.5 and 35% by weight, and particularly preferably between 2 and 30% by weight, the percentage by weight being based on the total weight of the hydrocarbon load. The sulfur or chlorine content of the feedstock is generally less than 10 ppm by weight of sulfur or chlorine respectively, and preferably less than 2 ppm by weight. The hydrogenation of the feed containing benzene can be carried out in the gas phase or in the liquid phase, preferably in the liquid phase. When carried out in the liquid phase, a solvent may be present. In general, the hydrogenation of benzene is carried out at a temperature of between 30 and 250 ° C., preferably between 50 and 200 ° C., and more preferably between 80 and 180 ° C., at a pressure comprised between between 0.1 and 10 MPa, preferably between 0.5 and 4 MPa, at a hydrogen / (benzene) molar ratio of between 0.1 and 10 and at an hourly volume velocity VVH between 0.05 and 50 h -1, preferably between 0.5 and 10 h -1.
    [0030] The conversion of benzene is generally greater than 50 mol%, preferably greater than 80 mol%, more preferably greater than 90 mol% and particularly preferably greater than 98 mol%. The invention is illustrated by the following examples.
    [0031] EXAMPLES Example 1 Preparation of an aqueous solution of Ni precursors The aqueous solution of Ni precursors (solution S) used for the preparation of catalysts A, A ', B and C is prepared by dissolving 46.1 g of nitrate of nickel (NiNO 3, supplier Strem Chemicals) in a volume of 13 mL of distilled water. Solution S is obtained whose NiO concentration is 20.1% by weight (relative to the mass of the solution).
    [0032] EXAMPLE 2 Preparation of Catalysts A and A 'According to the Invention Catalysts A and A' according to the invention are prepared by dry impregnation of solution S of Ni precursors on alumina A1 and alumina A2. The aim is a content of 20% by weight of nickel relative to the total mass of catalyst A or A '. The alumina Al synthesis according to the invention is carried out in a laboratory reactor with a capacity of about 7000 ml. The synthesis proceeds at 70 ° C with stirring in seven steps, named a) to g) below. It is sought to prepare 5 L of solution at a concentration fixed at 27 g / L of alumina in the final suspension (obtained at the end of step c) and with a contribution rate of the first step (a) to 2 , 1% of the total alumina. a) Dissolving: 70 ml of Al 2 (504) 3 aluminum sulphate are introduced in one go into the reactor containing a 1679 ml foot of water. The evolution of the pH, which remains between 2.5 and 3, is followed for 10 minutes. This step contributes to the introduction of 2.1% of alumina relative to the total mass of alumina formed at the end of the synthesis of the gel. The solution is stirred for a period of 10 minutes. b) Adjustment of the pH: About 70 ml of sodium aluminate NaA100 are gradually added. The goal is to reach a pH between 7 and 10 in a period of 5 to 15 minutes. c) Coprecipitation: In the suspension obtained after step b) is added in 30 minutes, - 1020 ml of aluminum sulfate Al2 (SO4) 3, a flow rate of 34 ml / min, - 1020 ml sodium aluminate NaA100, a flow rate of 34 mL / min, 1150 mL of distilled water, a flow rate of 38.3 mL / min. The pH is between 8.7 and 9.9. d) Filtration: The suspension obtained at the end of step c) is filtered by displacement on a sintered Buchner tool P4 and washed several times with distilled water. An alumina gel is obtained. e) Drying: The alumina gel obtained at the end of step d) is dried in an oven overnight at 200 ° C. f) Heat Treatment: The dried alumina gel obtained at the end of step e) is then calcined at 750 ° C. under an air flow of 1 L / h / g of alumina at 750 ° C. for 2 minutes. hours (ramp up temperature 5 ° C / min). g) Shaping: Shaping is carried out using a "Brabender" type kneader with an acid content of 1% (total acid level, expressed relative to dry alumina). a neutralization rate of 20% and acid and basic fire losses of 62% and 64 ° A, respectively). Then the extrusion is carried out on a piston extruder through a trilobe die diameter 2.1 mm. After extrusion, the extrudates are dried overnight at 80 ° C. Alumina Al is then obtained. The characteristics of alumina Al thus obtained are reported in Table 1 below. Catalyst A is then prepared by dry impregnation of solution S of Ni precursors, described in Example 1, on alumina Al according to the three stages, named below h) to i): h) Impregnation dry alumina Al by adding dropwise a volume of 11.5 ml of solution S on a mass of 10.5 g of alumina Al, for a period of 10 minutes. i) A drying of the catalytic precursor obtained at the end of step h) in an oven at 120 ° C. overnight. j) A thermal treatment by calcination of the dried catalyst under a flow of air of 1 L / h / g of catalyst, at 450 ° C for 2 hours (ramp temperature rise of 5 ° C / min). The calcined catalyst A is then obtained. The characteristics of the calcined catalyst A thus obtained are given in Table 2 below. The synthesis of alumina A2 is carried out by following steps a) to e) of the synthesis of alumina Al. The operating conditions are strictly identical for these steps. After the drying of step e), a shaping is carried out first and then a heat treatment as follows: f) Shaping: The dried alumina gel from step e) is shaped using a "Brabender" type mixer with an acid level of 1% (total acid level, expressed relative to dry alumina), a neutralization rate of 20% and acid and basic fire losses of 62% and 64 ° A respectively, then the extrusion is carried out on a piston extruder through a trilobe die with a diameter of 2.1 mm. After extrusion, the extrudates are dried overnight at 80 ° C. g) Heat treatment: The extrudates obtained at the end of step f) are then calcined at 750 ° C. under a flow of air of 1 L / h / g of alumina at 750 ° C. for 2 hours (ramp of temperature rise 5 ° C / min). Alumina A2 is then obtained. The characteristics of the alumina A2 thus obtained are reported in Table 1 below. The catalyst A 'is then prepared by dry impregnation of the solution S of precursors of Ni, described in Example 1, on the alumina A2 according to the three steps h), i) and j) described for the above. the synthesis of catalyst A, the operating conditions being strictly identical.
    [0033] The characteristics of the calcined catalyst A 'thus obtained are reported in Table 2 below. Table 1: Properties of alumina Al and A2 (according to the invention), and B1 and Cl (comparative) ALUMINES Al A2 B1 Cl According to Comparative Comparative the invention the invention Surface B.E.T. (m2 / g) 225 175 180 298 Total pore volume (mL / g) 0.94 0.97 0.82 0.57 Mesoporous volume (mL / g) 0.67 0.75 0.63 0.55 Median diameter mesoporous (nm) 12.5 17 13.0 17 Macroporous volume (mL / g) 0.27 0.22 0.19 0 Macroporous volume (° / 0 of total pore volume) 29 23 23 0 Macroporous medial diameter (nm) 644 353 143 No macroporosity Pore volume of pores with a pore diameter of 100 to 700 nm (mL / g and% of total pore volume) 0.07 0.01 0.12 0 8% 5% 14.5 Microporous Volume (mL / g) Table 2: Properties of Catalysts A and A '(According to the Invention), and B and C (Comparative) CATALYSTS AA' BC According to According Comparative Comparative to Invention Invention Ni (% wt) 20.7 20.6 19.4 21.0 BET surface (m2 / g) 156 121 119 206 Total pore volume (mL / g) 0.66 0.67 0.62 0.47 Mesoporous volume (mL / g) 0.47 0.53 0.48 0.47 Median diameter mesoporous (nm) 11.5 15.6 10.5 10.5 Macroporous volume (mL / g and% of total pore volume) 0.19 0.14 0.14 0 29% 21% 23% 0% Median diameter macroporous (nm) 638 346 132 No macroporosity Microporous volume (mL / g) 0 0 0 0 Size of NiO crystallites (nm) 15.6 16.2 14.1 11.0 Example 3: Preparation of catalyst B having a different porous distribution (comparative) The catalyst B is prepared by dry impregnation of the solution S of precursors of Ni aiming a content of 20% by weight of nickel relative to the total mass of the catalyst on a B1 alumina having a different porous distribution that of alumina A1 described in Example 2 above. The characteristics of this B1 alumina are reported in Table 1. In particular, this B1 alumina has a macroporous volume lower than that of alumina Al and a macroporous median diameter much smaller than that of alumina Al. Catalyst B is then prepared by dry impregnation of solution S of precursors of Ni, described in Example 1, on alumina B1 according to the three steps, steps h) to i), of Example 2 described herein. -above. The operating conditions are strictly identical. Calcined catalyst B is then obtained. The characteristics of the calcined catalyst B thus obtained are reported in Table 2. It has a macroporous volume lower than that of catalyst A and a macroporous median diameter much smaller than that of catalyst A. In addition, it has NiO crystallites slightly smaller than those of catalyst A. Example 4: Preparation of catalyst C with a different porous distribution (comparative) Catalyst C is prepared by dry impregnation of solution S of Ni precursors with a view to a a content of 20% by weight of nickel relative to the total mass of the catalyst on a Cl alumina having a porous distribution still different from that of the Al alumina described in Example 2 above. The characteristics of this Cl alumina are shown in Table 1. In particular, this Cl alumina does not exhibit macroporosity.
    [0034] Catalyst C is then prepared by dry impregnation of solution S of precursors of Ni, described in Example 1, on alumina Ci. On this alumina of small pore volume, two successive impregnations were necessary to reach a carbon content. in Ni of about 20% by weight; the sequence of the three steps h) to i) of Example 2 described above, was then repeated twice (according to the sequence h, i, j, h, i, j). The first impregnation stage makes it possible to obtain a content of 13% by weight of nickel, the second impregnation stage makes it possible to reach a content of 21% by weight of nickel relative to the total mass of the catalyst. For each step, the operating conditions are strictly identical to those described in Example 2 above. The calcined catalyst C is then obtained.
    [0035] The characteristics of the calcined catalyst C thus obtained are reported in Table 2. This catalyst does not exhibit macroporosity. In addition, it has NiO crystallites smaller than those of catalyst A.
    [0036] EXAMPLE 5 Evaluation of the Catalytic Properties of Catalysts A, A ', B and C in Selective Hydrogenation of a Mixture Containing Styrene and Isoprene The catalysts A, A', B and C described in the examples above are tested against the selective hydrogenation reaction of a mixture containing styrene and isoprene. The composition of the filler to be selectively hydrogenated is as follows: 8% by weight styrene (supplier Sigma Aldrich®, purity 99%), 8% by weight isoprene (supplier Sigma Aldrich®, purity 99%), 84% by weight n-heptane (solvent ) (VWRO supplier, purity> 99% chromanorm HPLC). This feed also contains very low sulfur compounds: 10 ppm wt of sulfur introduced in the form of pentanethiol (supplier Fluka0, purity> 97%) and 100 ppm wt of sulfur introduced in the form of thiophene (Merck® supplier, purity 99% ). This composition corresponds to the initial composition of the reaction mixture. This mixture of model molecules is representative of a pyrolysis species.
    [0037] The selective hydrogenation reaction is carried out in a 500 ml autoclave made of stainless steel, equipped with magnetic stirring mechanical stirring and capable of operating at a maximum pressure of 100 bar (10 MPa) and temperatures of between 5 ° C. and 5 ° C. 200 ° C. Prior to its introduction into the autoclave, a quantity of 3 mL of catalyst is reduced ex situ under a flow of hydrogen of 1 L / h / g of catalyst, at 400 ° C. for 16 hours (temperature rise ramp of 1 ° C / min), then it is transferred to the autoclave, protected from the air. After addition of 214 ml of n-heptane (supplier VWRO, purity> 99% chromanorm HPLC), the autoclave is closed, purged, then pressurized under 35 bar (3.5 MPa) of hydrogen, and brought to the temperature of test equal to 30 ° C. At time t = 0, about 30 g of a mixture containing styrene, isoprene, n-heptane, pentanethiol and thiophene are introduced into the autoclave. The reaction mixture then has the composition described above and stirring is started at 1600 rpm. The pressure is kept constant at 35 bar (3.5 MPa) in the autoclave using a reservoir bottle located upstream of the reactor. The progress of the reaction is monitored by taking samples of the reaction medium at regular time intervals: the styrene is hydrogenated to ethylbenzene, without hydrogenation of the aromatic ring, and the isoprene is hydrogenated to methyl-butenes. If the reaction is prolonged longer than necessary, the methyl-butenes are in turn hydrogenated to isopentane. Hydrogen consumption is also monitored over time by the pressure decrease in a reservoir bottle located upstream of the reactor. The catalytic activity is expressed in moles of H2 consumed per minute and per gram of Ni. The catalytic activities measured for catalysts A, A ', B and C are reported in Table 3 below. They are related to the catalytic activity measured for catalyst A (AHypi). Table 3: Comparison of the performances in selective hydrogenation of a mixture containing styrene and isoprene (AHypi) and hydrogenation of toluene (AHyD2) - Catalyst Conform Size of AHYD1 AHYD2 crystallites of (° / 0) (° / 0) NiO (nm) A Yes 15.6 100 100 A 'Yes 16.2 89 81 B No 14.1 49 55 C No 11.0 63 42 This shows well the improved performance of catalysts A and A 'prepared according to the invention and in particular the impact of their specific textural properties. Indeed, catalysts B and C, although they have NiO crystallites smaller than those of catalysts A and A ', have poorer catalytic performance. The presence of macropores and mesopores of controlled size is therefore necessary to obtain the improved performances of the catalysts A and A '.
    [0038] EXAMPLE 6 Evaluation of the Catalytic Properties of Catalysts A, A ', B and C in Hydrogenation of Toluene Catalysts A, A', B and C described in the examples above are also tested against the reaction of hydrogenation of toluene. The selective hydrogenation reaction is carried out in the same autoclave as that described in Example 5. Prior to its introduction into the autoclave, a quantity of 2 ml of catalyst is reduced ex situ under a flow of hydrogen of 1 L / h / g of catalyst at 400 ° C for 16 hours (ramp temperature rise of 1 ° C / min), then it is transferred into the autoclave, protected from air. After addition of 216 ml of n-heptane (supplier VWRO, purity> 99% chromanorm HPLC), the autoclave is closed, purged, then pressurized under 35 bar (3.5 MPa) of hydrogen, and brought to the temperature of test equal to 80 ° C. At time t = 0, about 26 g of toluene (supplier SDSO, purity> 99.8%) are introduced into the autoclave (the initial composition of the reaction mixture is then toluene 6% w / n-heptane 94% wt) and the agitation is started at 1600 rpm. The pressure is kept constant at 35 bar (3.5 MPa) in the autoclave using a reservoir bottle located upstream of the reactor. The progress of the reaction is monitored by taking samples of the reaction medium at regular time intervals: toluene is completely hydrogenated to methylcyclohexane. Hydrogen consumption is also monitored over time by the pressure decrease in a reservoir bottle located upstream of the reactor. The catalytic activity is expressed in moles of H2 consumed per minute and per gram of Ni. The catalytic activities measured for the catalysts A, A ', B and C are reported in Table 3. They are related to the catalytic activity measured for the catalyst A (AHyD2). The improved performances of catalysts A and A 'prepared according to the invention are found.
    权利要求:
    Claims (10)
    [0001]
    REVENDICATIONS1. Supported catalyst comprising a calcined, predominantly aluminum oxide support and an active phase comprising nickel, the nickel content being between 5 and 65% by weight of said element relative to the total mass of the catalyst, said active phase not comprising any metal of the group VIB, nickel particles having a diameter less than or equal to 20 nm, said catalyst having a mesoporous median diameter of between 8 nm and 25 nm, a macroporous median diameter greater than 200 nm, a mesoporous volume measured by high mercury porosimetry or equal to 0.30 mL / g and a total pore volume measured by mercury porosimetry greater than or equal to 0.34 mL / g.
    [0002]
    2. Catalyst according to claim 1, wherein the support has a pore volume contained in pores with a diameter of between 100 and 700 nm less than 20% of the total pore volume of the support.
    [0003]
    3. Catalyst according to claim 2, wherein the support has a pore volume contained in pores with a diameter of between 100 and 700 nm less than 15% of the total pore volume of the support.
    [0004]
    4. Catalyst according to claims 1 to 3, wherein the nickel content is between 10 and 34% by weight of said element relative to the total mass of the catalyst.
    [0005]
    5. Catalyst according to claims 1 to 4, wherein the macroporous volume of the catalyst is between 10 and 40% of the total pore volume.
    [0006]
    The catalyst of claims 1 to 5, wherein the mesoporous volume of the catalyst is from 0.35 mL / g to 0.8 mL / g.
    [0007]
    7. Catalyst according to claims 1 to 6, which does not contain micropores.
    [0008]
    8. Process for the preparation of a catalyst according to claims 1 to 7, comprising the following steps: a) a step of dissolving an aluminum acid precursor chosen from aluminum sulphate, sodium chloride; aluminum and aluminum nitrate in water, at a temperature between 20 and 90 ° C, at a pH between 0.5 and 5, for a period of between 2 and 60 minutes, b) a step of adjusting the pH by adding to the suspension obtained in step a) at least one basic precursor chosen from sodium aluminate, potassium aluminate, ammonia, sodium hydroxide and sodium hydroxide. potassium, at a temperature between 20 and 90 ° C, and at a pH between 7 and 10, for a period of between 5 and 30 minutes, c) a step of coprecipitation of the suspension obtained at the end of the step b) by adding to the suspension at least one basic precursor chosen from sodium aluminate, potassium aluminate ium, 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, at least one of the basic or acidic precursors comprising aluminum, the relative flow rate of the acidic and basic precursors being chosen so as to obtain a pH of the reaction medium of between 7 and 10 and the the flow rate of the aluminum-containing acidic and basic precursor (s) being adjusted so as to obtain a final alumina concentration in the suspension of between 10 and 38 g / l; (d) a filtration stage of the suspension obtained at the end of step c) of coprecipitation to obtain an alumina gel, e) a step of drying said alumina gel obtained in step d) to obtain a powder, f) a shaping step, g) a heat treatment step performed between steps e) and f) or after step f) at a temperature between 500 and 1000 ° C, with or without a flow of air containing up to 60% by volume of water to obtain a calcined aluminous porous oxide support, h) a step of impregnating said support with a solution comprising the salt (s) of the precursor (s) of the nickel-based active phase, i) a step of drying the impregnated support at a temperature of between 15 and below 250 ° C, so as to obtain a dried catalyst, j) optionally a heat treatment of said dried catalyst at a temperature between 250 and 1000 ° C in the presence or absence of water.
    [0009]
    9. Process according to claim 8, wherein at least one reducing treatment step k) is carried out in the presence of a reducing gas after steps i) or j) so as to obtain a catalyst comprising nickel at least partially in the form of metallic.
    [0010]
    10. The method of claim 9 wherein, a passivation step I) is carried out with a sulfur or oxygen compound or with CO2 before or after the reducing treatment step k). Process according to one of Claims 8 to 10, in which the alumina concentration of the alumina gel suspension obtained in stage c) is between 13 and 35 g / l. Process according to one of Claims 8 to 11, in which the acidic precursor of steps a) and c) is chosen from aluminum sulphate, aluminum chloride and aluminum nitrate and in which the basic precursor of the Steps a) and c) are selected from sodium aluminate and potassium aluminate. Hydrogenation process in which the catalyst according to one of Claims 1 to 7 or capable of being prepared according to one of Claims 8 to 12 is brought into contact in the presence of hydrogen with a hydrocarbon feed containing molecules. polyunsaturated and / or aromatic so as to obtain an effluent that is at least partially hydrogenated. Hydrogenation process according to Claim 13, in which a selective hydrogenation is carried out at a temperature of between 0 and 500 ° C., at a pressure of between 0.1 and 20 MPa, at a molar ratio of hydrogen / (polyunsaturated compounds to be hydrogenated). ) between 0.1 and 10 and at an hourly space velocity of between 0.1 and 200 h-1 for a liquid charge, between 100 and 15000 h-1 for a gaseous charge of a hydrocarbon charge containing compounds polyunsaturates containing at least 2 carbon atoms per molecule and having a final boiling point of less than or equal to 250 ° C. 15. The hydrogenation process as claimed in claim 13, wherein the aromatics are hydrogenated at a temperature of between 30 and 350 ° C. 12. 13. 14. At a pressure of between 0.1 and 20 MPa, at a molar ratio of hydrogen / (aromatic compounds to be hydrogenated) between 0.1 and 10 and at an hourly space velocity of between 0.05 and 50 hours. -1 a hydrocarbon feed containing aromatic compounds and having a final boiling point less than or equal to 650 ° C.
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    同族专利:
    公开号 | 公开日
    WO2015189189A1|2015-12-17|
    EP3154684A1|2017-04-19|
    DK3154684T3|2020-03-16|
    EP3154684B1|2019-12-25|
    US10618033B2|2020-04-14|
    US20170128912A1|2017-05-11|
    FR3022163B1|2021-05-07|
    引用文献:
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    US5478791A|1993-04-03|1995-12-26|Huels Aktiengesellschaft|Nickel/aluminum oxide catalyst, preparation thereof, use thereof and hydrogenation of aromatic hydrocarbons with the aid of the catalyst|
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    US6589908B1|2000-11-28|2003-07-08|Shell Oil Company|Method of making alumina having bimodal pore structure, and catalysts made therefrom|
    WO2005028106A1|2003-09-17|2005-03-31|Shell Internationale Research Maatschappij B.V.|Process and catalyst for the hydroconversion of a heavy hydrocarbon feedstock|
    US4301037A|1980-04-01|1981-11-17|W. R. Grace & Co.|Extruded alumina catalyst support having controlled distribution of pore sizes|
    US4920089A|1987-05-08|1990-04-24|Unilever Patent Holdings B.V.|Hydrogenation catalyst|US11104575B2|2016-05-12|2021-08-31|Fujian Institute Of Research On The Structure Of Matter, Chinese Academy Of Science|Nanocatalysts, preparation methods and applications for reforming carbon dioxide and methane to syngas|
    FR3061195B1|2016-12-22|2019-06-28|IFP Energies Nouvelles|SELECTIVE HYDROGENATION PROCESS USING A PREPARED NICKEL CATALYST USING AN ADDITIVE COMPRISING AMINO ACID, AMIDE FUNCTION OR AN AMINO ACID|
    US20190233741A1|2017-02-12|2019-08-01|Mag&#275;m&#257; Technology, LLC|Multi-Stage Process and Device for Reducing Environmental Contaminates in Heavy Marine Fuel Oil|
    US10604709B2|2017-02-12|2020-03-31|Magēmā Technology LLC|Multi-stage device and process for production of a low sulfur heavy marine fuel oil from distressed heavy fuel oil materials|
    FR3068983B1|2017-07-13|2019-07-12|IFP Energies Nouvelles|SELECTIVE HYDROGENATION PROCESS USING A CATALYST OBTAINED BY IMPREGNATION COMPRISING A SPECIFIC SUPPORT|
    法律状态:
    2015-06-02| PLFP| Fee payment|Year of fee payment: 2 |
    2015-12-18| PLSC| Publication of the preliminary search report|Effective date: 20151218 |
    2016-06-07| PLFP| Fee payment|Year of fee payment: 3 |
    2017-06-22| PLFP| Fee payment|Year of fee payment: 4 |
    2018-06-27| PLFP| Fee payment|Year of fee payment: 5 |
    2020-06-26| PLFP| Fee payment|Year of fee payment: 7 |
    2021-06-25| PLFP| Fee payment|Year of fee payment: 8 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1455434A|FR3022163B1|2014-06-13|2014-06-13|MESOPOREOUS AND MACROPOROUS NICKEL BASED CATALYST WITH A MEDIAN MACROPOROUS DIAMETER GREATER THAN 200 NM AND ITS USE IN HYDROGENATION|FR1455434A| FR3022163B1|2014-06-13|2014-06-13|MESOPOREOUS AND MACROPOROUS NICKEL BASED CATALYST WITH A MEDIAN MACROPOROUS DIAMETER GREATER THAN 200 NM AND ITS USE IN HYDROGENATION|
    EP15726214.8A| EP3154684B1|2014-06-13|2015-06-09|Mesoporous and macroporous nickel-based catalyst having a median diameter of macropores greater than 200 nm and use thereof for hydrocarbon hydrogenation|
    PCT/EP2015/062815| WO2015189189A1|2014-06-13|2015-06-09|Catalyst made from mesoporous and macroporous nickel having a macroporous median diameter greater than 200 nm and use of same in hydrocarbon hydrogenation|
    US15/318,615| US10618033B2|2014-06-13|2015-06-09|Mesoporous and macroporous nickel-based catalyst having a median macropore diameter of greater than 200 nm and its use with regard to hydrogenation|
    DK15726214.8T| DK3154684T3|2014-06-13|2015-06-09|MESOPOROUS AND MACROPOROUS NICKEL-BASED CATALYST WITH AN AVERAGE MACROPORIAMETER OF MORE THAN 200 NM AND ITS APPLICATION FOR HYDROGENATION OF CARBON HYDROIDS|
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