Classifications

• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G25/00—Refining of hydrocarbon oils in the absence of hydrogen, with solid sorbents
  • C10G25/003—Specific sorbent material, not covered by C10G25/02 or C10G25/03
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
  • B01J20/0203—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of metals not provided for in B01J20/04
  • B01J20/0225—Compounds of Fe, Ru, Os, Co, Rh, Ir, Ni, Pd, Pt
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
  • B01J20/06—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
  • B01J20/06—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04
  • B01J20/08—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04 comprising aluminium oxide or hydroxide; comprising bauxite
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/28—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
  • B01J20/28054—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their surface properties or porosity
  • B01J20/28057—Surface area, e.g. B.E.T specific surface area
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/28—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
  • B01J20/28054—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their surface properties or porosity
  • B01J20/28057—Surface area, e.g. B.E.T specific surface area
  • B01J20/28061—Surface area, e.g. B.E.T specific surface area being in the range 100-500 m2/g
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/28—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
  • B01J20/28054—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their surface properties or porosity
  • B01J20/28069—Pore volume, e.g. total pore volume, mesopore volume, micropore volume
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/28—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
  • B01J20/28054—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their surface properties or porosity
  • B01J20/28069—Pore volume, e.g. total pore volume, mesopore volume, micropore volume
  • B01J20/28073—Pore volume, e.g. total pore volume, mesopore volume, micropore volume being in the range 0.5-1.0 ml/g
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/28—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
  • B01J20/28054—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their surface properties or porosity
  • B01J20/28088—Pore-size distribution
  • B01J20/28092—Bimodal, polymodal, different types of pores or different pore size distributions in different parts of the sorbent
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/30—Processes for preparing, regenerating, or reactivating
  • B01J20/3078—Thermal treatment, e.g. calcining or pyrolizing
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/30—Processes for preparing, regenerating, or reactivating
  • B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
  • B01J20/3202—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the carrier, support or substrate used for impregnation or coating
  • B01J20/3204—Inorganic carriers, supports or substrates
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/30—Processes for preparing, regenerating, or reactivating
  • B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
  • B01J20/3231—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the coating or impregnating layer
  • B01J20/3234—Inorganic material layers
  • B01J20/3236—Inorganic material layers containing metal, other than zeolites, e.g. oxides, hydroxides, sulphides or salts
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/30—Processes for preparing, regenerating, or reactivating
  • B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
  • B01J20/3291—Characterised by the shape of the carrier, the coating or the obtained coated product
  • B01J20/3293—Coatings on a core, the core being particle or fiber shaped, e.g. encapsulated particles, coated fibers
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
  • C10G2300/20—Characteristics of the feedstock or the products
  • C10G2300/201—Impurities
  • C10G2300/202—Heteroatoms content, i.e. S, N, O, P
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
  • C10G2300/20—Characteristics of the feedstock or the products
  • C10G2300/201—Impurities
  • C10G2300/205—Metal content
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
  • C10G2400/02—Gasoline

Definitions

• the present invention relates to a process for capturing organometallic impurities contained in a gasoline-type hydrocarbon charge containing sulfur compounds and olefins using a nickel-based capture mass.
• the specifications for automotive fuels provide for a sharp reduction in the sulfur content in these fuels, and in particular in gasolines. This reduction is intended to limit, in particular, the sulfur and nitrogen oxide content in automobile exhaust gases.
• the specifications currently in force in Europe since 2009 for gasoline fuels set a maximum sulfur content of 10 ppm by weight (parts per million). Such specifications are also in force in other countries such as the United States and China, for example, where the same maximum sulfur content has been required since January 2017. To achieve these specifications, it is necessary to treat gasoline with desulfurization processes.
• the main sources of sulfur in gasoline bases are so-called cracked gasolines, and mainly the gasoline fraction resulting from a catalytic cracking process of a residue from the atmospheric or vacuum distillation of a crude oil.
• the fraction of gasoline resulting from catalytic cracking which represents on average 40% of the gasoline bases, in fact contributes for more than 90% to the contribution of sulfur in gasolines. Consequently, the production of low-sulphur gasolines requires a stage of desulphurization of catalytic cracking gasolines.
• the elimination of sulfur in gasoline cuts consists in specifically treating these sulfur-rich gasolines by desulphurization processes in the presence of hydrogen. This is referred to as hydrodesulphurization (HDS) processes.
• HDS hydrodesulphurization
• these gasoline cuts and more particularly the gasolines from the FCC contain a significant proportion of unsaturated compounds in the form of mono-olefins (approximately 20 to 50% by weight) which contribute to a good octane number, diolefins (0.5 at 5% by weight) and aromatics.
• unsaturated compounds are unstable and react during the hydrodesulfurization treatment.
• Diolefins form gums by polymerization during hydrodesulfurization treatments. This formation of gums leads to progressive deactivation of the hydrodesulphurization catalysts or progressive clogging of the reactor. Consequently, the diolefins must be eliminated by hydrogenation before any treatment of these gasolines.
• the hydrodesulfurization processes are operated continuously over periods of at least 3 to 5 years.
• the catalysts used to carry out the hydrodesulfurization of sulfur-containing gasolines must therefore have good activity, good selectivity and good stability over time in order to be operated continuously for several years.
• heavy metals such as mercury or arsenic, or of contaminants such as phosphorus and silicon in the form of organometallics in the hydrocarbon feedstocks to be desulphurized leads to rapid deactivation of the hydrotreating catalysts. It is therefore necessary to remove these contaminants from the charge before bringing it into contact with these hydrodesulphurization catalysts.
• a capture mass is placed either in a reactor located upstream of the hydrodesulphurization unit or in the hydrodesulphurization reactor, upstream of the catalytic bed containing the hydrodesulphurization catalyst.
• adsorbent is described in documents FR2794381 and W02006/037884. These adsorbents are used in the presence of hydrogen, which presents a drawback when the gasolines to be treated comprise unsaturated compounds. This results in a decrease in octane number and a drop in the quality of the gasoline considered from the stage of adsorption of the impurities.
• adsorbents also have the drawback of being catalytically inactive for hydrodesulphurization reactions. Furthermore, they occupy a non-negligible volume in the reactor, reducing the volume available for the beds of hydrodesulphurization catalysts and therefore lead to an overall loss in the performance of the process. It is therefore necessary to seek solutions which make it possible to eliminate these impurities such as arsenic, with the aim of limiting the hydrogenation reactions responsible for a reduction in the octane number of the gasolines concerned. These solutions must also make it possible to increase the hydrodesulphurization performance and without loss of selectivity of the hydrodesulphurization reaction with respect to the hydrogenation of olefins.
• porous distribution of the support can have a beneficial impact on the catalytic performance.
• Document US6,589,908 discloses a method for preparing a catalyst support, which does not contain macroporosity and has a bimodal porous structure in the mesoporosity such that the two modes of porosity are separated by 1 to 20 nm.
• the support can be used in numerous catalytic applications, and in particular in hydrotreating, in particular in hydrodenitrogenation.
• US 5,266,300 discloses a method for preparing a porous alumina support for use as a hydrodesulphurization or hydrodemetallization catalyst support, said support comprising a total pore volume between 0.65 to 1.30 cm 3 / g, said porous support comprising two populations of macropores, of which approximately 2 to 20% by volume relative to the total pore volume is in the form of macropores having a diameter of between 10,000 Angstroms and 100,000 Angstroms (1000 and 10000 nm), about 5-30% by volume of the total pore volume is in the form of macropores having a diameter between 1,000 Angstroms and 10,000 Angstroms (100 and 1000 nm), and about 50-93% by volume relative to the total pore volume is in the form of mesopores having a pore diameter between 30 Angstroms and 1000 Angstroms (3-100 nm).
• US7,790,130 discloses an alumina for the capture of halides comprising a tri-modal porosity of which 40 to 49% by volume relative to the total pore volume of the support is in the form of pores having a diameter between 15 and 50 nm .
• one of the objectives of the present invention is to propose a process for capturing organometallic impurities in a gasoline-type hydrocarbon charge containing sulfur compounds and olefins, in which the capture mass comprises an active phase comprising at least nickel, on a mesoporous and macroporous support, presenting both a bimodal mesoporous porosity, with a high mesoporous volume coupled with a determined macroporous volume.
• this capture mass makes it possible to effectively capture organometallic impurities, and in particular the arsenic contained in a gasoline containing olefins and sulfur, while limiting the rate of hydrogenation of the olefins at values generally below 30%, preferably below 20%, and even more preferably below 10%.
• the use of such a capture mass improves the phenomena of internal diffusion of reagents and products by the presence of populations of different sizes of mesopores.
• the combined presence of macroporosity is particularly judicious when the feed to be treated contains a significant quantity of reactive olefins (unsaturated compounds), in particular diolefins, which is the case of gasolines, which can give rise to the formation of gums and thus blocking the porosity of the capture mass without the presence of macroporosity.
• the subject of the present invention is a process for capturing organometallic impurities in a gasoline-type hydrocarbon charge containing sulfur compounds and olefins, in which a capture mass is brought into contact with the charge to be treated and a flow of hydrogen at a temperature of between 200 and 400° C., a pressure of between 0.2 and 5 MPa and a ratio of the flow rate of hydrogen to the flow rate of hydrocarbon feed of between 50 and 800 Nm 3 /m 3 , said capture mass comprising an active phase based on nickel, and a mesoporous and macroporous alumina support comprising a bimodal distribution of mesopores and in which:
• the volume of mesopores with a diameter greater than or equal to 2 nm and less than 18 nm corresponds between 10 and 30% by volume of the total pore volume of said support;
• the volume of mesopores with a diameter greater than or equal to 18 nm and less than 50 nm corresponds between 30 and 50% by volume of the total pore volume of said support;
• the volume of macropores with a diameter greater than or equal to 50 nm and less than 8000 nm corresponds between 30 and 50% by volume of the total pore volume of said support.
• said support comprises a specific surface of between 50 and 210 m 2 /g.
• said support comprises a total pore volume of between 0.7 and 1.3 mL/g.
• the volume of mesopores with a diameter greater than or equal to 2 nm and less than 18 nm corresponds between 15 and 25% by volume of the total pore volume of said support.
• the volume of mesopores with a diameter greater than or equal to 18 nm and less than 50 nm corresponds between 35 and 45% by volume of the total pore volume of said support.
• the volume of the macropores with a diameter greater than or equal to 50 nm and less than 8000 nm corresponds between 35 to 50% by volume of the total porous volume of said support.
• the nickel content, expressed in NiO form is between 5 and 65% by weight relative to the total weight of said capture mass.
• the active phase consists solely of nickel.
• the active phase of said capture mass further comprises cobalt, molybdenum and phosphorus.
• the nickel content, expressed in NiO oxide form is between 5 and 65% by weight relative to the total weight of said capture mass
• the cobalt content, expressed in CoO form is between between 0.5 and 10% by weight relative to the total weight of said capture mass
• the molybdenum content, expressed as MOO3 is between 2 and 20% by weight relative to the total weight of said capture mass
• the content phosphorus, expressed as P2O5 is between 0.2 and 10% by weight relative to the total weight of said capture mass.
• the porous distribution of the mesopores with a diameter greater than or equal to 2 nm and less than 18 nm is centered on a range of values comprised between 10.5 and 14.5 nm.
• the porous distribution of the mesopores with a diameter greater than or equal to 18 nm and less than 50 nm is centered on a range of values comprised between 22 and 28 nm.
• said support comprises a specific surface of between 70 and 180 m 2 /g.
• said support is in the form of balls with a diameter of between 2 and 4 mm.
• said support when said support is in the form of beads, said support is obtained according to the following steps: s1) dehydration of an aluminum hydroxide or an aluminum oxyhydroxide at a temperature between 400°C and 1200°C, preferably between 600°C and 900°C, for a time of between 0.1 second and 5 seconds, preferably between 0.1 second and 4 seconds, to obtain an alumina powder ; s2) shaping of said alumina powder obtained in step s1) in the form of balls; s3) heat treatment of the alumina balls obtained in step s2) at a temperature greater than or equal to 200° C.; s4) hydrothermal treatment of the alumina balls obtained at the end of step s3) by impregnation with water or an aqueous solution, then residence in an autoclave at a temperature between 100° C. and 300° C.; s5) calcining the alumina balls obtained at the end of step s4) at a temperature between 500°C and 820°C.
• the hydrocarbon feed is a catalytic cracking gasoline containing between 5% and 60% by weight of mono-olefins, between 50 and 6000 ppm by weight of sulfur compounds and between 10 and 1000 ppb of arsenic with respect to to the total weight of said load.
• the organometallic impurities are chosen from organometallic impurities of heavy metals, silicon, phosphorus and arsenic.
• the organometallic impurity is an organometallic arsenic impurity.
• group VIII according to the CAS classification corresponds to the metals of columns 8, 9 and 10 according to the new IUPAC classification.
• the BET specific surface is measured by physisorption with nitrogen according to standard ASTM D3663-03, method described in the work Rouquerol F.; Rouquerol J.; Singh K. “Adsorption by Powders & Porous Solids: Principle, methodology and applications”, Academy Press, 1999.
• micropores are understood to mean pores whose diameter is less than 2 nm, that is to say 0.002 ⁇ m; by mesopores pores whose diameter is greater than 2 nm, ie 0.002 pm and less than 50 nm, ie 0.05 pm and by macropores pores whose diameter is greater than or equal to 50 nm , i.e. 0.05 ⁇ m.
• total pore volume of the alumina or of the capture mass is understood to mean the volume measured by intrusion with a mercury porosimeter according to the ASTM D4284-83 standard at a maximum pressure of 4000 bar (400 MPa), using a surface tension of 484 dyne/cm and a contact angle of 140°.
• the wetting angle was taken as equal to 140° by following the recommendations of the book “Engineering techniques, analysis and characterization treatise”, p.1050-5, written by Jean Charpin and Bernard Rasneur.
• 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 intrusion with a mercury porosimeter) 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°.
• the value from which the mercury fills all the intergranular voids is fixed at 0.2 MPa, and it is considered that beyond that the mercury penetrates into the pores of the sample.
• the macropore volume of the catalyst is defined as being 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.
• the mesoporous volume of the catalyst is defined as being 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 pore modes correspond to the inflection points of the function represented.
• the metallic element (group VIII metal, group VI B metal) and phosphorus contents are measured by X-ray fluorescence.
• the present invention relates to a method for capturing organometallic impurities such as heavy metals, silicon or phosphorus, and more particularly arsenic, contained in a hydrocarbon charge implementing a capture mass as defined below. , wherein said capture mass is brought into contact with the hydrocarbon feedstock in the presence of hydrogen.
• the capture process according to the invention is a process for at least partial capture of arsenic and optionally of silicon from the hydrocarbon feedstock in the presence of hydrogen to produce an effluent with a heavy metal content. and especially reduced arsenic, with limited loss of octane rating.
• the hydrocarbon feedstock to be treated is advantageously a catalytic cracking gasoline from catalytic cracking, thermal cracking or steam cracking units.
• the method can also be applied to the treatment of mixtures straight run gasolines which may contain heavy metals from the crude with cracked gasolines comprising mono-olefins and diolefins.
• the hydrocarbon feedstock to be treated is a catalytic cracking gasoline comprising between 5% and 60% by weight of mono-olefins, between 50 ppm and 6000 ppm by weight of sulfur compounds and between 10 and 1000 ppb by weight of arsenic.
• the sulfur compounds contained in the hydrocarbon feedstock to be treated can be organic sulfur compounds such as, for example, mercaptans, thiophenic, benzothiophenic compounds and other aromatic sulfur compounds, disulphide compounds, etc.
• the arsenic compounds contained in the hydrocarbon feedstock to be treated can be organic arsenic compounds such as, for example, trimethylarsine or triethylarsine.
• Mono-olefins designate hydrocarbon molecules having a single carbon-carbon double bond and diolefins are hydrocarbon molecules comprising at least two carbon-carbon double bonds.
• Mono-olefins and diolefins can be linear, branched and/or cyclic hydrocarbon molecules.
• the capture mass according to the invention is advantageously implemented under operating conditions such that the rate of capture of arsenic is maximized, while limiting the rate of hydrogenation of the olefins.
• the contacting is generally carried out at a temperature between 200 and 400° C., at a pressure between 0.2 and 5 MPa and with a ratio of the hydrogen flow rate to the hydrocarbon feed flow rate of between 50 and 800 Nm 3 /m 3 .
• the hydrogen used can come from any source of hydrogen.
• fresh hydrogen from the refinery and/or hydrogen recycled from a hydrodesulfurization unit, preferably from the hydrodesulfurization unit of the hydrocarbon cut to be purified, is used.
• reactor technologies can be envisaged for carrying out the capture of arsenic from a hydrocarbon charge in the presence of the capture mass according to the invention, the most conventional and most widespread technology being the fixed-bed technology.
• a reactor is charged with the capture mass according to the invention and a hydrodesulphurization catalyst, operating in adsorption of arsenic and in hydrodesulphurization, in principle until the appearance of arsenic in the effluent output (phenomenon known to those skilled in the art as drilling).
• the total amount of poisoned catchment mass can be replaced by an equivalent amount of fresh catchment mass.
• the choice of a technology for replacing the capture mass according to the invention is not considered within the scope of the present invention as a limiting element.
• the capture mass can be implemented in a moving bed reactor, i.e. the used capture mass is continuously withdrawn and replaced by fresh capture mass.
• This type of technology makes it possible to maintain the capture of arsenic by the capture mass and to avoid the penetration of the latter in the effluents produced.
• expanded bed reactors which also allows continuous withdrawal and make-up of the capture mass in order to maintain the hydrodesulphurization activity of the capture mass.
• the capture process according to the invention is preferably coupled with at least one additional catalytic hydrodesulphurization or selective hydrogenation stage which is carried out on the effluent resulting from the contact with the capture mass according to the invention.
• the stage of treatment of the hydrocarbon charge by the capture mass is considered as a pre-treatment which makes it possible in particular to preserve the catalytic activity of the catalyst used in the subsequent hydrodesulphurization or selective hydrogenation stage.
• the capture process according to the invention comprises one or more other complementary stages of hydrodesulphurization or selective hydrogenation in which the effluent resulting from the contacting of the charge hydrocarbon with the capture mass according to the invention, with at least one other catalyst for hydrodesulphurization or selective hydrogenation of the diolefins present in the feed.
• Said complementary hydrodesulfurization step(s) makes it possible to eliminate the residual sulfur compounds contained in the effluent depleted in arsenic and with a lower sulfur content. Some of these residual sulfur compounds may result from the addition of HS to the olefins present in the charge. The HS can form during the contacting of the hydrocarbon feed with the capture mass, that is to say, during the capture of the arsenic.
• Said complementary hydrodesulphurization stage(s) is (are) implemented when the effluent resulting from the contacting of the hydrocarbon charge with the capture mass generally has a sulfur content greater than 10 ppm and that it is necessary to produce gasolines with low sulfur content meeting the current specifications which are in many countries lower than 10 ppm.
• the effluent freed from arsenic and part of the sulfur compounds is then treated in at least one of said complementary stages of selective hydrodesulphurization.
• said effluent is brought into contact with at least one other hydrodesulphurization catalyst under operating conditions which may be identical to or different from those for bringing the hydrocarbon feedstock into contact with the mass. of capture.
• the catalyst(s) used in the said additional hydrodesulphurization stage(s) is (are) protected from deactivation by the arsenic present in the charge thanks to the capture mass according to the invention.
• catalysts very selective hydrodesulphurization processes which are sensitive to the presence of arsenic can be implemented in said complementary hydrodesulphurization step(s).
• Any hydrodesulphurization catalyst can be used in said complementary hydrodesulphurization step(s).
• catalysts are used which exhibit a high selectivity with respect to hydrodesulfurization reactions relative to the hydrogenation reactions of olefins.
• Such catalysts comprise at least one amorphous and porous mineral support, a metal from group VI B, a metal from group VIII.
• the group VI B metal is preferably molybdenum or tungsten and the group VIII metal is preferably nickel or cobalt.
• the support is generally selected from the group consisting of aluminas, silica, silica-aluminas, silicon carbide, titanium oxides alone or mixed with alumina or silica alumina, magnesium oxides alone or as a mixture with alumina or silica alumina.
• the support is selected from the group consisting of aluminas, silica and silica-aluminas.
• the hydrodesulphurization catalyst used in the additional hydrodesulphurization stage or stages has the following characteristics:
• group VIII elements the content of group VIII elements is between 0.1 and 20% by weight of oxides of group VIII elements
• the molar ratio (elements of group VIII/elements of group VI B) is between 0.1 and 0.8.
• a very preferred hydrodesulfurization catalyst comprises cobalt and molybdenum and has the characteristics mentioned above.
• the hydrodesulphurization catalyst may comprise phosphorus.
• the phosphorus content is preferably between 0.1 and 10% by weight of P 2 O 5 relative to the total weight of catalyst and the phosphorus to group VI B elements molar ratio is greater than or equal to 0, 25, preferably greater than or equal to 0.27.
• the arsenic-depleted effluent resulting from the contacting of the hydrocarbon charge with the capture mass according to the invention is brought into contact with at least one other selective hydrodesulfurization catalyst under the following operating conditions:
• - a temperature between approximately 210° C. and approximately 410° C., preferably between 240 and 360° C.;
• - a total pressure between 0.2 and 5 MPa and more preferably between 0.5 and 3 MPa; - a volume ratio of hydrogen per volume of hydrocarbon charge of between 50 and 800 Nm 3 /m 3 and more preferably between 60 and 600 Nm 3 /m 3 .
• the operating conditions for bringing the hydrocarbon feedstock into contact with the capture mass according to the invention are identical to those implemented in the said step(s). ) additional hydrodesulfurization(s).
• the step of hydrotreating the effluent from the capture step by means of the capture mass according to the invention is a selective hydrogenation which allows the hydrogenation of the diolefins into olefins and optionally unsaturated sulfur compounds but also the transformation (heaviness) of light sulfur compounds (i.e. having a temperature lower than that of thiophene) into sulfur compounds whose temperature is higher than that of thiophene, for example by adding mercaptans to olefins.
• This hydrogenation step is carried out in the presence of hydrogen and a catalyst containing at least one metal from group VI B and at least one non-noble metal from group VIII deposited on a porous support.
• a catalyst is used of which:
• the content by weight of oxide of the element of group VIII is between 4 and 12% relative to the weight of the catalyst;
• the specific surface of the catalyst is between 200 and 270 m 2 /g;
• the density of the element of group VI B expressed as being the ratio between the said content by weight of oxide of the element of group VI B and the specific surface of the catalyst, is between 4 and 6.10 4 g/m 2 ;
• the molar ratio between the group VIII metal and the group VIB metal is between 0.6 and 3 mol/mol.
• the group VIB metal is preferably chosen from molybdenum and tungsten, very preferably the group VIB metal is molybdenum.
• the Group VIII metal is preferably nickel and/or cobalt, very preferably nickel.
• the hydrogen is generally introduced in slight excess, up to 5 moles per mole, relative to the stoichiometry necessary to hydrogenate the diolefins (one mole of hydrogen per mole of diolefin).
• This reactor is separate and is placed upstream of the reactor(s) containing the catalyst(s) used in said complementary hydrodesulphurization step(s) and / or selective hydrogenation.
• the volume ratio of the capture mass according to the invention relative to the volume of (of ) catalyst(s) used in said additional hydrodesulphurization and/or selective hydrogenation step(s) is advantageously between 4 and 50%, preferably between 5 and 40 %, more preferably between 5 and 35%.
• the capture mass used in the context of the process according to the invention comprises an active phase comprising nickel, optionally at least one additional element from group VIII, optionally at least one element from group VIB, and optionally phosphorus.
• the nickel content expressed in NiO form, is advantageously between 5 and 65% by weight relative to the total weight of the capture mass, preferably between 10 and 30% by weight.
• the content of additional group VIII element, when it is present and expressed in oxide form, is advantageously between 0.5 and 10% by weight relative to the total weight of the capture mass.
• the content of group VIB element, when present and expressed in oxide form, is advantageously between 2 and 20% by weight relative to the total weight of the capture mass.
• the phosphorus content when present and expressed in oxide form, is between 0.2 and 10% by weight relative to the total weight of the capture mass.
• the active phase consists solely of nickel.
• the nickel content, expressed in NiO form is advantageously between 5 and 65% by weight relative to the total weight of the capture mass, preferably between 10 and 30% by weight.
• the active phase comprises nickel, cobalt, molybdenum and phosphorus.
• the nickel content expressed in NiO oxide form is advantageously between 5 and 65% by weight relative to the total weight of the capture mass, preferably between 10 and 30% by weight.
• the cobalt content expressed in CoO form is advantageously between 0.5 and 10% by weight relative to the total weight of the capture mass, preferably between 0.5 and 5% by weight.
• the molybdenum content expressed in MOO3 form is advantageously between 2 and 20% by weight relative to the total weight of the capture mass, preferably between 3 and 15% by weight.
• the phosphorus content expressed in P2O5 form is advantageously between 0.2 and 10% by weight relative to the total weight of the capture mass, preferably between 0.5 and 5% by weight.
• the capture mass generally comprises a specific surface comprised between 50 and 200 m 2 /g, preferably comprised between 60 and 170 m 2 /g and preferably comprised between 70 and 130 m 2 /g.
• the pore volume of the capture mass is generally between 0.5 mL/g and 1.3 mL/g, preferably between 0.6 mL/g and 1.1 mL/g.
• the alumina support of the capture mass used in the context of the process according to the invention is a macroporous and mesoporous alumina support comprising a bimodal distribution of mesopores in which:
• the volume of mesopores with a diameter greater than or equal to 2 nm and less than 18 nm corresponds between 10 and 30% by volume of the total pore volume of said support;
• the volume of mesopores with a diameter greater than or equal to 18 nm and less than 50 nm corresponds between 30 and 50% by volume of the total pore volume of said support;
• the volume of macropores with a diameter greater than or equal to 50 nm and less than 8000 nm corresponds between 30 and 50% by volume of the total pore volume of said support.
• the volume of the mesopores of the support with a diameter greater than or equal to 2 nm and less than 18 nm corresponds to between 15 and 25% by volume of the total porous volume of said support.
• the volume of the mesopores of the support with a diameter greater than or equal to 18 nm and less than 50 nm corresponds to between 35 and 45% by volume of the total porous volume of said support.
• the volume of the macropores of the support with a diameter greater than or equal to 50 nm and less than 8000 nm corresponds between 35 to 50% by volume of the total porous volume of said support.
• the porous distribution of the mesopores with a diameter greater than or equal to 2 nm and less than 18 nm is centered on a range of values comprised between 10.5 and 14.5 nm, preferably between 12 and 13 nm.
• the porous distribution of the mesopores with a diameter greater than or equal to 18 nm and less than 50 nm is centered on a range of values comprised between 22 and 28 nm, preferably between 23 and 27 nm.
• the support generally comprises a specific surface of between 50 and 210 m 2 /g, preferably between 70 and 180 m 2 /g, and even more preferably between 70 and 160 m 2 /g.
• the porous volume of the support is generally between 0.7 mL/g and 1.3 mL/g, preferably between 0.8 mL/g and 1.2 mL/g.
• the support is in the form of balls with a diameter of between 0.8 and 10 mm, preferentially between 1 and 5 mm, and more preferentially between 2 and 4 mm.
• alumina support of the capture mass used in the context of the process according to the invention can be synthesized by any method known to those skilled in the art.
• the alumina support used according to the invention is in the form of beads.
• the preparation of the support comprises the following steps: s1) dehydration of an aluminum hydroxide or an aluminum oxyhydroxide at a temperature between 400° C. and 1200° C., preferably between 600° C.
• step s2) shaping of said alumina powder obtained in step s1) in the form of balls; s3) heat treatment of the alumina balls obtained in step s2) at a temperature greater than or equal to 200° C.; s4) hydrothermal treatment of the alumina balls obtained at the end of step s3) by impregnation with water or a preferentially acidic aqueous solution, then residence in an autoclave at a temperature between 100° C. and 300° C, preferably between 150°C and 250°C; s5) calcining the alumina balls obtained at the end of step s4) at a temperature between 500°C and 820°C.
• Steps s1) to s5) are described in detail below. Step s1)
• step s1) dehydration of an aluminum hydroxide or an aluminum oxyhydroxide is carried out at a temperature between 400° C. and 1200° C., preferably between 600° C. and 900° C., for a period of between 0.1 second and 5 seconds, preferably between 0.1 second and 4 seconds, to obtain an alumina powder.
• the aluminum hydroxide can be chosen from hydrargillite, gibbsite or bayerite.
• the aluminum oxyhydroxide can be chosen from boehmite or diaspore.
• step s1) is carried out using hydrargillite.
• step s1) is carried out in the presence of a current of hot gas, such as dry air or humid air, allowing the evaporated water to be eliminated and carried away quickly.
• a current of hot gas such as dry air or humid air
• the active alumina powder obtained after the dehydration of the aluminum hydroxide or oxyhydroxide is ground to a particle size of between 10 to 200 ⁇ m.
• the active alumina powder obtained after the dehydration of aluminum hydroxide or oxyhydroxide is washed with water or an acidic aqueous solution.
• any mineral or organic acid may be used, preferably nitric acid, hydrochloric acid, perchloric or sulfuric acid for mineral acids, and a carboxylic acid (formic, acetic or malonic acid), a sulphonic acid (para-toluene sulphonic acid) or a sulfuric ester (lauryl sulphate) for organic acids.
• step s2) the said alumina powder obtained at the end of step s1) is shaped.
• the shaping of said alumina powder is carried out so as to obtain balls, called granulation, is generally carried out by means of rotating technology such as a rotating bezel or a rotating drum.
• This type of process makes it possible to obtain balls of controlled diameter and pore distributions, these dimensions and these distributions being, in general, created during the agglomeration step.
• the porosity can be created by various means, such as the choice of the particle size of the alumina powder or the agglomeration of several alumina powders of different particle sizes. Another method consists in mixing with the alumina powder, before or during the agglomeration step, one or more compounds, called porogens, which disappear on heating and thus create porosity in the balls.
• pore-forming compounds used mention may be made, by way of example, of wood flour, charcoal, activated carbon, black carbon, sulfur, tars, plastics or emulsions of plastics such as polyvinyl chloride, polyvinyl alcohols, naphthalene or the like.
• the amount of pore-forming compounds added is determined by the volume desired to obtain beads with a raw filling density of between 500 and 1100 kg/m 3 , preferably between 700 and 950 kg/m 3 , and with a diameter of between 0.8 and 10 mm, preferably between 1 and 5 mm, and ink more preferably between 2 and 4 mm.
• a selection by sieving of the balls obtained can be carried out according to the desired particle size.
• a heat treatment is carried out on the alumina powder shaped in the form of beads obtained at the end of step s2) at a temperature greater than or equal to 200° C., preferably between between 200°C and 1200°C, preferably between 300°C and 900°C, very preferably between 400°C and 750°C, for a period generally between 1 and 24 hours, preferably between 1 and 6 hours .
• the beads obtained at this intermediate step comprise a specific surface between 50 and 420 m 2 /g, preferably between 60 and 350 m 2 /g, and even more preferably between 80 and 300 m 2 /g.
• step s4) the alumina balls obtained at the end of step s3) undergo a hydrothermal treatment by impregnation with water or a preferably acidic aqueous solution, then stay in an autoclave at a temperature between between 100°C and 300°C, preferably between 150°C and 250°C.
• the hydrothermal treatment is generally carried out at a temperature of 100° C. to 300° C., preferentially from 150° C. to 250° C., for a duration greater than 45 minutes, preferentially from 1 to 24 hours, very preferentially from 1.5 to 12 hours.
• the hydrothermal treatment is generally carried out using an aqueous acid solution comprising one or more mineral and/or organic acids, preferably nitric acid, hydrochloric acid, perchloric acid, sulfuric acid, weak whose solution has a pH lower than 4 such as acetic acid or formic acid.
• said acidic aqueous solution also comprises one or more compounds capable of releasing anions capable of combining with aluminum ions, preferably compounds comprising a nitrate ion (such as aluminum nitrate), chloride, sulphate, perchlorate, chloroacetate, trichloroacetate, bromoacetate, dibromoacetate, and anions of general formula: R-COO such as formates and acetates.
• a nitrate ion such as aluminum nitrate
• chloride sulphate, perchlorate, chloroacetate, trichloroacetate, bromoacetate, dibromoacetate, and anions of general formula: R-COO such as formates and acetates.
• the alumina balls obtained at the end of step s4) undergo calcination at a temperature of between 500° C. and 820° C., preferably between 550° C. and 750° C., and for a period generally between 1 hour and 24 hours, preferably between 1 hour and 6 hours.
• the alumina balls obtained comprise a specific surface between 50 and 210 m 2 /g, preferably between 70 and 180 m 2 /g, and even more preferably between 70 and 160 m 2 /g .
• the metals of the active phase of the capture mass can be deposited on the support according to techniques well known to those skilled in the art, for example by impregnation from a solution of metal precursors.
• the impregnation can for example be carried out according to the known method of dry impregnation in which the desired quantity of elements is introduced in the form of salts soluble in the chosen solvent, for example demineralized water, so as to also fill exactly as possible the porosity of the support.
• the support thus filled with the solution is preferably dried.
• the metals can be deposited in co-impregnation or by successive addition. Phosphorus can be added to the impregnation solution(s).
• nickel nitrate, nickel hydroxide or nickel carbonate are used as precursor of the active phase of nickel.
• the active phase comprises cobalt as an additional group VIII element
• cobalt nitrate, cobalt hydroxide or cobalt carbonate is advantageously used as precursor.
• the active phase comprises molybdenum as a group VIB metal
• ammonium heptamolybdate or molybdenum oxide MOO3 is advantageously used as precursor.
• phosphoric acid is advantageously used as precursor. Any other salt known to those skilled in the art having sufficient solubility in aqueous solution and decomposable during a drying step or any type of oxidizing treatment can also be used.
• the capture mass is preferably subjected to a calcining treatment.
• the purpose of this treatment is to transform the molecular precursors of the metals into the oxide phase. In this case, it is an oxidizing treatment but a simple drying of the mass of capture can also be performed.
• the capture mass is subjected to a calcination treatment, prior to its implementation in the process according to the invention. Said calcination treatment is advantageously carried out in air or in dilute oxygen, at a temperature of between 200°C and 550°C, preferably between 300°C and 500°C.
• the metals deposited on the support are in the form of oxide.
• the calcined capture mass is also subjected to a sulfurization treatment before its implementation in the process according to the invention.
• Sulphidation is carried out in a sulphur-reducing medium, ie in the presence of h ⁇ S and hydrogen, in order to transform the metal oxides into sulphides of transition metals such as M0S2, N1 3 S2 and CogSs.
• Sulfurization is carried out by injecting onto the capture mass a stream containing hkS and hydrogen, or else a sulfur compound capable of decomposing into H2S in the presence of the capture mass and hydrogen.
• Polysulphides such as dimethyldisulphide are precursors of h ⁇ S commonly used to sulphide catalysts.
• the temperature is adjusted so that the hkS reacts with the metal oxides to form metal sulphides.
• This sulfurization can be carried out in-situ or ex-situ (inside or outside the hydrodesulfurization reactor) at temperatures between 200 and 600°C and more preferably between 250°C and 500°C.
• the metals should preferably be substantially sulfurized.
• the degree of sulfurization of the metals constituting the active phase of the capture mass is advantageously at least equal to 60%, preferably at least equal to 80%.
• the sulfur content in the sulphide material is measured by elemental analysis according to ASTM D5373.
• a metal is considered sulphurized when the overall sulphidation rate defined by the molar ratio between the sulfur (S) present on the capture mass and said metal is at least equal to 60% of the theoretical molar ratio corresponding to the total sulphidation of ( of the metal(s) considered.
• the overall sulfurization rate is defined by the following equation:
• the capture mass is ready to be used in the process according to the invention.
• the support S1 of the mass for capturing arsenic A is prepared by dehydration of hydrargillite ( EMPLURA® , Merck) in order to obtain an alumina powder.
• the temperature is set at 800° C. and the contact time of the material to be dehydrated with a flow of dry air is 1 second.
• the alumina powder obtained is ground to a particle size between 10 and 200 ⁇ m and then washed three times with a volume of distilled water equal to twice the volume of the powder used.
• Said alumina powder is shaped in the presence of carbon black (N990 Thermax ® ) with a plate granulator (GRELBEX P30) equipped with a conical cylindrical bowl at an angle of 30° and a rotation speed of 40 revolutions per minute so as to obtain balls with a diameter mostly comprised between 2 and 4 mm after sieving the solid.
• the quantity of carbon black is adjusted to obtain a raw filling density of the objects of 800 kg/m 3 .
• Said balls undergo a heat treatment in air at 720° C. so as to give them a specific surface area of 200 m 2 /g.
• a hydrothermal treatment is applied to said balls by impregnation of the porous volume with an aqueous solution of nitric acid (0.1 N, MerckTM).
• the hydrothermal treatment is carried out at a temperature of 200° C. for 6.5 hours, in a rotating basket autoclave.
• the balls thus obtained undergo a final calcination treatment in air at 650° C. for 2 hours.
• the support S1 has a specific surface of 141 m 2 /g, a total pore volume of 0.97 mL/g as well as the following pore distribution given by mercury porosimetry:
• - a volume of mesopores with a diameter greater than or equal to 2 nm and less than 18 nm, whose pore distribution is centered on 13 nm, of 0.15 mL/g corresponding to 15% of the total pore volume; - a volume of mesopores with a diameter greater than or equal to 18 nm and less than 50 nm, whose pore distribution is centered on 26 nm, of 0.43 mL/g corresponding to 44% of the total pore volume;
• - a volume of macropores with a diameter greater than or equal to 50 nm and less than 8000 nm of 0.39 mL/g, corresponding to 40% of the total pore volume.
• the arsenic A capture mass is obtained by double dry impregnation of the alumina support via an aqueous solution of nickel nitrate.
• Support S1 has a water uptake volume of 0.95 mL/g.
• the impregnation solution is prepared by diluting 18.24 grams of nickel nitrate (Ni(NC> 3 ) 2 .6H 2 O, 99.5%, MerckTM) in 37.2 mL of distilled water. After dry impregnation of 40 grams of support and a maturation step for 12 hours in an atmosphere saturated with humidity, the solid is dried for 12 hours at 120° C. to obtain a catalyst precursor.
• a second impregnation step is carried out with a solution prepared by diluting 19.35 grams of nickel nitrate (Ni(NC> 3 ) 2 .6H 2 O, 99.5%, MerckTM) in 33.7 mL of 'distilled water. After dry impregnation of the catalyst precursor and a maturation step for 12 hours in an atmosphere saturated with humidity, the solid is dried for 12 hours at 120°C. The solid is then calcined in air at 450° C. for 2 hours. The arsenic A capture mass obtained contains 20% by weight of NiO relative to the total weight of the capture mass. The capture mass of arsenic A has a total pore volume of 0.87 mL/g and a specific surface of 112 m 2 /g.
• Example 2 Non-compliant capture mass B (monomodal macroporous and large mesoporous capture mass)
• the support S2 of the capture mass B is prepared by dehydration of hydrargillite (EM PLU RA ® , MerckTM) in order to obtain an active alumina powder.
• the temperature is set at 800° C. and the contact time of the material to be dehydrated with a flow of dry air is 1 second.
• the active alumina powder obtained is ground to a particle size of between 10 and 200 ⁇ m and then washed three times with a volume of distilled water equal to twice the volume of the powder used.
• Said active alumina powder is shaped with a plate granulator (GRELBEXTM P30) equipped with a conical cylindrical bowl at an angle of 30° and a rotation speed of 40 revolutions per minute so as to obtain balls with a diameter mostly between 2 and 4 mm (after sieving the solid) and a raw filling density of the objects of 780 kg/m 3 .
• Said balls undergo a heat treatment in air at 700° C. so as to give them a specific surface area of 250 m 2 /g.
• a hydrothermal treatment is applied to said balls by impregnation of the porous volume with an aqueous solution of nitric acid (0.1 N, MerckTM). The treatment hydrothermal test is carried out at a temperature of 200° C.
• the support S2 has a specific surface of 71 m 2 /g, a total porous volume of 0.56 mL/g as well as the following porous distribution given by mercury porosimetry:
• the arsenic B capture mass is obtained by double dry impregnation of the alumina support via an aqueous solution of nickel nitrate.
• Support S2 has a water uptake volume of 0.54 mL/g.
• the impregnation solution is prepared by dissolving 18.24 grams of nickel nitrate hexahydrate (Sigma-AldrichTM, purity 3 98.5%) in 20.8 mL of distilled water. After dry impregnation of 40 grams of support and a maturation step for 12 hours in an atmosphere saturated with humidity, the solid is dried for 12 hours at 120° C. to obtain a catalyst precursor.
• a second impregnation step is carried out with a solution prepared by diluting 19.35 grams of nickel nitrate (Ni(NC>3)2, 6H2O, 99.5%, MerckTM) in 17.5 mL of water distilled.
• the arsenic B capture mass obtained contains 20% by weight of NiO relative to the total weight of the capture mass.
• the arsenic B capture mass has a total pore volume of 0.48 mL/g and a specific surface of 66 m 2 /g.
• Example 3 Evaluation of the performance of the capture masses with respect to the capture of arsenic.
• capture masses A and B Prior to their introduction into the reactor for the arsenic capture test, capture masses A and B are sulfurized ex-situ under a flow of a 15% vol. H2/H2S mixture. of H2S and at a temperature of 350°C for 2 hours, then cooled under pure hydrogen with a plateau of 2 hours at 200°C.
• the arsenic uptake performance test consists of monitoring the rate of disappearance of an arsenic compound dissolved in a model load.
• the reaction carried out in static mode in a stirred and closed autoclave reactor, at a temperature of 210° C., in the presence of hydrogen and under a total pressure of 35 bar (3.5 MPa).
• the model load is composed of a volume of 250 cm 3 of toluene, i.e. 217 g, and of triphenyl-arsine (AsPhb), at a content of 500 ppm weight in "As" equivalent, i.e. approximately 1.45 mmol of As.
• the mass of solid used is adjusted so as to obtain an initial Ni/As molar ratio of 5.
• FCC Fluid Catalytic Cracking according to the English terminology

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