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
  • C10G61/00—Treatment of naphtha by at least one reforming process and at least one process of refining in the absence of hydrogen
  • C10G61/02—Treatment of naphtha by at least one reforming process and at least one process of refining in the absence of hydrogen plural serial stages only
  • C10G61/04—Treatment of naphtha by at least one reforming process and at least one process of refining in the absence of hydrogen plural serial stages only the refining step being an extraction
• • 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
  • C10G61/00—Treatment of naphtha by at least one reforming process and at least one process of refining in the absence of hydrogen
  • C10G61/02—Treatment of naphtha by at least one reforming process and at least one process of refining in the absence of hydrogen plural serial stages only
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
  • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
  • B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
  • B01J23/42—Platinum
• • 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
  • C10G35/00—Reforming naphtha
  • C10G35/04—Catalytic reforming
  • C10G35/06—Catalytic reforming characterised by the catalyst used
  • C10G35/085—Catalytic reforming characterised by the catalyst used containing platinum group metals or compounds thereof
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G49/00—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00
  • C10G49/02—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00 characterised by the catalyst used
• • 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
  • C10G49/00—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00
  • C10G49/02—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00 characterised by the catalyst used
  • C10G49/06—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00 characterised by the catalyst used containing platinum group metals or compounds thereof
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
  • C10G49/00—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00
  • C10G49/02—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00 characterised by the catalyst used
  • C10G49/08—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00 characterised by the catalyst used containing crystalline alumino-silicates, e.g. molecular sieves
• • 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
  • C10G2300/10—Feedstock materials
  • C10G2300/1096—Aromatics or polyaromatics
• • 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
  • C10G2300/40—Characteristics of the process deviating from typical ways of processing
  • C10G2300/4006—Temperature
• • 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
  • C10G2300/40—Characteristics of the process deviating from typical ways of processing
  • C10G2300/4012—Pressure
• • 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
  • C10G2300/40—Characteristics of the process deviating from typical ways of processing
  • C10G2300/4081—Recycling aspects
• • 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
  • C10G2400/30—Aromatics

Definitions

• the present invention relates to the field of processes for the production of aromatic compounds, and more particularly to aromatic compounds of the benzene, toluene and xylene type by catalytic reforming of a hydrocarbon feedstock of the naphtha type.
• the objective of a catalytic reforming unit is to convert the naphthenic and paraffinic compounds (n-pa raffines and iso-paraffins) into aromatic compounds.
• the main reactions involved are dehydrogenation of naphthenes and dehydrocyclization of paraffins to aromatics, isomerization of paraffins and naphthenes.
• Other so-called "parasite” reactions can also occur such as the hydrocracking and hydrogenolysis of paraffins and naphthenes, the hydro-dealkylation of the alkyl-aromatics giving rise to lighter compounds and lighter aromatics, as well as the formation of coke on the surface of the catalysts.
• Charges typically sent to a catalytic reforming unit are rich in paraffinic and naphthenic compounds and relatively low in aromatic compounds. These are generally naphthas from the distillation of crude oil or condensates of natural gas. Other fillers may also be available, containing varying amounts of aromatics, namely heavy naphthas catalytic cracking, coking, hydrocracking, or steam crackers.
• Aromatic compounds are generally treated in an aromatic complex to maximize the production of one or more products, most often xylenes and benzene. Toluene and heavier aromatics can be valorized for the constitution of gasoline bases or by the production of xylenes mixture.
• the production of C6-C7 aromatic compounds makes it possible, in particular, to improve the octane number of the gasoline, and / or to increase the supply of benzene, toluene and xylenes.
• the presence of a catalytic system In order to maximize the production of C6-C7 aromatic compounds by catalytic reforming, the presence of a catalytic system
• SUBSTITUTE SHEET (RULE 26) Specifically comprising a catalytically active metal (generally platinum) and a non-acidic zeolite is used.
• a catalytically active metal generally platinum
• a non-acidic zeolite is used.
• patent application US2012 / 0277505 discloses a process for improving the production of benzene and toluene from a naphtha feed comprising the following steps:
• a naphtha stream is sent to a fractionation unit, generating a first stream comprising C7 and lighter hydrocarbons, and a second stream comprising heavier hydrocarbons;
• the first stream is sent to a first reforming unit generating a first effluent
• the second stream is sent to a second reforming unit at a temperature higher than the temperature applied in the first reforming unit, generating a second effluent
• the first effluent and the second effluent are sent to a reformate separation column, thus creating a head flow and a bottom flow;
• the head stream is sent to a purification unit for aromatic compounds, thus creating a purified aromatic stream comprising aromatic compounds C6 and C7, and a raffinate stream,
• the raffinate stream is recycled to the first reforming unit.
• Such a process allows increased production of aromatic hydrocarbons, and in particular benzene and toluene, from a naphtha feed stream. More particularly, the raffinate recycling step and the repositioning of the aromatics extraction unit with respect to the two catalytic reforming units in parallel results in a 25% increase in benzene yields and an increase in benzene yields. about 10% of the toluene yields.
• Catalysts commonly used for the catalytic reforming of C7 and lighter hydrocarbon cuts generally comprise an active phase based on a zeolite supported Group VIII metal.
• catalysts are very sensitive and can be rapidly deactivated by the formation of carbonaceous deposits (or "coke") during the reforming reaction.
• the "coke” is indeed responsible for the deactivation of the zeolites, in particular by deactivating the active centers (Bronsted acid sites) of in different ways: by adsorbing it more strongly than reagent molecules, by reacting with them, or by sterically blocking their access.
• An object of the invention is to provide a process for the production of aromatic compounds, in particular benzene and toluene, by catalytic reforming of a naphtha-type filler, while limiting the deactivation of the zeolitic catalytic reforming catalysts.
• the Applicant has surprisingly discovered that it is possible to limit the deactivation of catalytic reforming catalysts supported on zeolite in a process for extracting aromatic compounds, in particular benzene and toluene, by a judicious sequence of process steps. to reduce the aromatic content at the inlet of the catalytic reforming.
• the initial concentration of aromatic compounds may be higher or lower, especially in heavy naphthas catalytic cracking, coking, hydrocracking, or steam cracking gasolines, which may cause "spurious" reactions during the catalytic reforming step, including reactions generating coke formation.
• the subject of the present invention is a process for producing C6-C7 aromatic compounds from a hydrocarbon feedstock of the naphtha type comprising the following steps: a) sending said feedstock into a first fractionation unit in order to obtain a higher flow comprising predominantly C6 and C7 hydrocarbon compounds and a lower stream comprising predominantly C8 to C10 hydrocarbon compounds; b) the upper stream and a stream comprising predominantly C6-C7 aromatic compounds obtained at the end of step e) are sent to an aromatics extraction unit to obtain an aromatic base and a liquid effluent;
• step b) sending said first reformate effluent into a reformate separation section to obtain a first stream comprising predominantly C5- hydrocarbon compounds and a second stream comprising predominantly C6 and C7 aromatic compounds; e) at least partly recycling the second stream comprising predominantly aromatic compounds C6 and C7 in step b).
• a first catalytic reforming unit means that there is no other reforming unit that would be upstream of it in the process of the invention: there is no catalytic reforming unit, in particular, upstream of the fractionation unit of step a) or upstream of the aromatics extraction unit of step b), comprising "upstream And "downstream” as referring to the general direction of displacement of the load in the process and the installation that implements it.
• the invention thus operates an extraction of aromatics before any catalytic reforming operation.
• the term "predominantly" throughout the present text means that the flow in question comprises, by weight, at least 50% of the components in question, in particular at least 80%, in particular at least 90% or 95% by weight. % by weight of said components. It can also be all the components considered, with the usual impurities.
• step e it is possible to recycle at least part of the second stream, and in particular the entire second stream.
• the step of catalytic reforming of the liquid effluent in the first catalytic reforming unit is carried out at a temperature of between 400 and 600 ° C., a pressure of between 0.1 and 3 MPa, the molar ratio between hydrogen and the hydrocarbons of the liquid effluent is between 0.8 and 8 mole / mole, the mass flow rate of flux to be treated per unit mass of catalyst and per hour is between 1 and 10 h 1 .
• the lower stream comprising mainly C8 to C10 hydrocarbon compounds is sent to a second catalytic reforming unit to obtain a second reformate effluent.
• the step of catalytic reforming of the lower stream in the second catalytic reforming unit is carried out at a temperature of between 400 and 600 ° C., a pressure of between 0.1 and 3 MPa, and the molar ratio of hydrogen. and the hydrocarbons of the lower stream is between 0.8 and 8 moles / mole, the mass flow rate of flux to be treated per unit mass of catalyst and per hour is between 1 and 10 h 1 .
• said second reformate effluent is sent into said reformate separation section together with said first reformate effluent.
• a hydrodesulfurization step of the upper flow is carried out in a hydrotreatment unit.
• a step of hydrodesulphurization of the lower stream is carried out in a hydrotreatment unit located upstream of the second catalytic reforming reactor.
• the first catalytic reforming unit comprises a catalyst comprising an active phase comprising at least one metal chosen from platinum, zinc or molybdenum, taken alone or as a mixture, a support comprising a zeolite chosen from a zeolite L, a zeolite X, a zeolite Y, a zeolite ZSM-5, and optionally a binder selected from aluminosilicate, alumina, silica, clays, silicon carbides.
• the catalyst comprises an active phase comprising platinum.
• the zeolite is an L zeolite.
• the binder is silica.
• the catalyst further comprises at least one doping metal chosen from the group formed by gallium, gold, nickel, rhenium, barium, silver, iron, bismuth, indium, yttrium, cerium, dysprosium, ytterbium, taken alone or as a mixture.
• doping metal chosen from the group formed by gallium, gold, nickel, rhenium, barium, silver, iron, bismuth, indium, yttrium, cerium, dysprosium, ytterbium, taken alone or as a mixture.
• the catalyst further comprises at least one halogen selected from chlorine or fluorine.
• the second catalytic reforming unit comprises a catalyst comprising an active phase comprising at least one metal chosen from nickel, ruthenium, rhodium, palladium, iridium or platinum, at least one promoter chosen from rhenium , tin, germanium, cobalt, nickel, iridium, rhodium or ruthenium, and a support based on alumina, silica-alumina or silica.
• Figure 1 is a schematic representation of a first embodiment of the method according to the invention.
• Figure 2 is a schematic representation of a second embodiment of the method according to the invention.
• FIG. 3 is a schematic representation of the method according to the prior art. Detailed description of the invention
• the aromatics extraction unit designates a combination of different fractionation units whether by adsorption, distillation, extractive distillation, liquid-liquid extraction, or crystallization, and / or conversion units, whether of aromatic rearrangement such as processes for transalkylation or disproportionation, selective or not, the units of de-alkylation or alkylation of aromatics, or the isomerization units of xylenes with or without de-alkylation of ethylbenzene.
• aromatic bases such as benzene, paraxylene, ortho-xylene, metha-xylene, xylenes, ethylbenzene, styrene monomers, cumene or the linear alkylbenzenes, or the ingredients for constituting the gasoline bases such as toluene, or a heavy aromatics cut.
• aromatic bases such as benzene, paraxylene, ortho-xylene, metha-xylene, xylenes, ethylbenzene, styrene monomers, cumene or the linear alkylbenzenes, or the ingredients for constituting the gasoline bases such as toluene, or a heavy aromatics cut.
• the feedstock entering the aromatic complex may be hydrotreated.
• hydrocarbon fraction C n is meant a section comprising hydrocarbons with n carbon atoms.
• C n + cut means a cut comprising hydrocarbons having at least n carbon atoms.
• C n- By cutting C n- is meant a cut comprising hydrocarbons having at most n carbon atoms.
• group IB according to the CAS classification corresponds to the metals of column 1 1 according to the new IUPAC classification.
• the present invention relates to a process for the production of aromatic compounds, and in particular benzene and toluene, from a naphtha cut comprising predominantly C6 to C10 hydrocarbons.
• the method comprises the following steps.
• step e) said charge is sent to a first fractionation unit in order to obtain a higher flow mainly comprising C6 and C7 hydrocarbon compounds and a lower stream comprising predominantly C8 to C10 hydrocarbon compounds; b) the upper stream and a stream comprising predominantly C6-C7 aromatic compounds obtained at the end of step e) are sent to an aromatics extraction unit to obtain an aromatic base and a liquid effluent;
• the reformate effluent is fed into a reformate separation section to obtain a first stream comprising predominantly C5- hydrocarbon compounds and a second stream comprising predominantly C6 and C7 aromatic compounds;
• the catalytic reforming step in the first reforming unit is carried out under operating conditions adjusted to promote dehydrocyclization reactions and to limit parasitic reactions.
• the pressure used is generally between 0.1 and 3 MPa
• the hydrogen / hydrocarbon molar ratio of the liquid effluent (H 2 / HC) is generally between 1: 1 to 10: 1, preferably between 2: 1 and 6: 1.
• the temperature is generally between 400 and 600 ° C, preferably between 470 and 570 ° C.
• the mass flow rate of the stream to be treated per unit mass of catalyst per hour (PPH) is generally between 0.1 and 10 h 1 , preferably between 0.5 and 6 h 1 .
• the catalytic reforming step c) is carried out in the presence of a catalyst comprising an active phase comprising at least one metal chosen from platinum, zinc or molybdenum, taken alone or as a mixture, and a support comprising a zeolite and optionally a binder. More preferably, the metal is platinum.
• the catalyst contains a quantity of metal of between 0.02 and 2% by weight, preferably between 0.05 and 1.5% by weight, even more preferably between 0.1 and 0.8% by weight relative to to the total weight of the catalyst.
• the zeolite is chosen from a zeolite L, a zeolite X, a zeolite Y, a zeolite ZSM-5. More preferentially, the zeolite is an L zeolite.
• the binder is chosen from aluminosilicate, alumina, silica, clays, silicon carbides, taken alone or in combination. More preferably, the binder is selected from silica.
• the catalyst may also comprise at least one doping metal selected from the group consisting of gallium, gold, nickel, rhenium, barium, silver, iron, bismuth, indium, yttrium, lanthanides (cerium, dysprosium, ytterbium), taken alone or as a mixture.
• the content of each doping metal is in relation to the total weight of the catalyst between 0 at 2% by weight, preferably from 0.01 to 1% by weight, preferably from 0.01 to 0.7% by weight relative to the total weight of the catalyst.
• the catalyst may also comprise at least one halogen used to acidify the alumina support.
• the halogen content may represent between 0.1 to 15% by weight relative to the total weight of the catalyst, preferably 0.2 to 5% relative to the total weight of the catalyst.
• the chlorine content is between 0.5 and 2% by weight relative to the total weight of the catalyst.
• the catalyst may also comprise an alkali metal in proportions of the order of 0.1 to 3% by weight relative to the total weight of the catalyst.
• the alkali metal is potassium.
• a catalytic reforming stage of the lower stream predominantly comprising C8 to C10 hydrocarbon compounds is carried out in a second dedicated catalytic reforming unit
• said reforming step is carried out in the presence of a catalyst comprising a catalyst.
• active phase comprising at least one metal chosen from nickel, ruthenium, rhodium, palladium, iridium or platinum, and at least one promoter chosen from rhenium, tin, germanium, cobalt and nickel , iridium, rhodium or ruthenium.
• the catalyst comprises an active phase comprising platinum and tin.
• the amount of metal is between 0.02 and 2% by weight, preferably between 0.05 and 1.5% by weight, more preferably between 0.1 and 0.8% by weight relative to the total weight of the product.
• the catalyst comprises a support selected from alumina, silica-alumina or silica.
• the support is based on alumina.
• the alumina (s) of the porous support used in the catalyst are of type c, h, g or d.
• they are of type g or d. Even more preferably, they are of type y.
• the catalytic reforming step is carried out at a pressure generally of between 0.1 and 3 MPa, preferably between 0.3 and 2.5 MPa, a hydrogen / H 2 / H 2 hydrocarbon molar ratio generally between 0.8 and 8. mol / mole, a temperature generally of between 400 and 600 ° C., preferably between 470 and 570 ° C., and a mass flow rate of flux to be treated per unit mass of catalyst and per hour of between 0.1 and 10 h 1 preferably between 0.5 and 6 h 1 .
• FIGS. 1 and 2 showing particularly advantageous embodiments. Although these embodiments are provided to illustrate the present invention, they are not intended to limit its scope.
• a naphtha-type feedstock 1 comprising C 6 to C 10 hydrocarbons is sent to a separation column 2 to obtain a flow.
• higher 3 comprising predominantly C6 and C7 hydrocarbon compounds and a lower stream 4 comprising predominantly C8 to C10 compounds.
• the lower stream 4 comprises less than 10% by volume of C7- compounds.
• the upper stream 3 is optionally sent to a hydrodesulfurization unit (hydrotreatment) 13 and then the upper stream, optionally hydrodesulphurized, is sent to an aromatics extraction unit 5 to form a stream of purified aromatic compounds 6 and a liquid effluent 7 which is fed to a catalytic reforming unit 8, comprising a catalyst comprising a platinum-based active phase and a zeolite-type support.
• the operating conditions in the reforming unit 8 are as follows: the temperature is between 400 and 600 ° C., the pressure is between 0.5 and 2.5 MPa, the molar ratio between hydrogen and the effluent treated liquid is between 0.8 and 8 mole / mole, the mass flow rate of the flow to be treated per unit mass of catalyst per hour (PPH) is between 1 and 10 h 1 .
• the reformate effluent 9 is sent to a reformate separation section 10 in order to obtain a first stream 11 comprising mainly C5- hydrocarbon compounds and a second stream 12 comprising mainly C6 and C7 aromatic compounds.
• the stream 12 comprising mainly aromatic compounds C6 and C7 is then recycled upstream of the aromatics extraction unit 5 via line 15.
• a purge 14 may be provided to prevent the accumulation of said compounds in the process .
• a naphtha-type feedstock 1 comprising C 6 to C 10 hydrocarbons is sent to a separation column 2 to obtain a flow.
• higher 3 comprising predominantly C6 and C7 hydrocarbon compounds and a lower stream 4 comprising predominantly C8 to C10 compounds.
• the lower stream 4 comprises less than 10% by volume of C7- compounds.
• the upper stream 3 is optionally sent to a hydrodesulfurization unit (hydrotreatment) 13 and then the upper stream, optionally hydrodesulphurized, is sent to an aromatics extraction unit 5 to form a stream of purified aromatic compounds 6 and a liquid effluent 7 which is fed to a catalytic reforming unit 8, comprising a catalyst comprising a platinum-based active phase and a zeolite-type support.
• the operating conditions in the reforming unit 8 are as follows: the temperature is between 400 and 600 ° C., the pressure is between 0.3 and 2.5 MPa, the molar ratio between hydrogen and the hydrocarbons of the liquid effluent is between 0.8 and 8 mole / mole, the mass flow rate of flux to be treated per unit mass of catalyst per hour (PPH) is between 1 and 10 h 1 .
• the lower stream 4 is optionally sent to a hydrodesulfurization unit (not shown in FIG. 2) and then the lower stream, possibly hydrodesulfurized, is sent to a second catalytic reforming unit 16, comprising a bifunctional catalyst comprising an active phase.
• the operating conditions in the second reforming unit 16 are as follows: the temperature is between 400 and 600 ° C., the pressure is between 0.5 and 2.5 MPa, the molar ratio between hydrogen and the hydrocarbons of the lower flow (optionally desulphurized) is between 0.8 and 8 mol / mol, the mass flow rate of the flow to be treated per unit mass of catalyst per hour (PPH) is between 1 and 10 h 1 .
• the first reformate 9 from the first reforming unit 8 and the second reformate 17 from the second reforming unit 16 are then combined with each other to form a reformate stream 18 which is then sent to a separation section 10 (not detailed in the figure) in order to obtain a first stream 11 comprising mainly C5- hydrocarbon compounds, a second stream 12 comprising predominantly C6 and C7 aromatic compounds, and a third stream 19 comprising predominantly C8 + hydrocarbon compounds.
• the second stream 12 comprising mainly aromatic compounds C6 and C7 is then recycled upstream of the aromatics extraction unit 5 via line 15.
• a purge 14 may be provided to prevent the accumulation of said compounds in the process.
• the 1-naphtha feedstock comprising C 6 to C 10 hydrocarbons is sent to a separation column 20 to obtain a higher stream comprising predominantly C 6 and C 7 hydrocarbon compounds and a lower stream comprising predominantly C8 to C10 compounds.
• the lower stream 40 comprises less than 10% by volume of C7- compounds.
• the upper stream 30 is fed to a catalytic reforming unit 50 comprising five reactors in series, comprising a catalyst comprising a platinum-based active phase and an L-zeolite carrier.
• the operating conditions below represent the operating conditions used in a pilot unit for the first reforming unit 50:
• the catalyst used in the first catalytic reforming unit is a platinum-based catalyst (0.3% by weight of Pt relative to the total weight of the catalyst) supported on an L zeolite.
• the reformate 60 derived from the first reforming unit 50 is sent to a reformate separation column 70 in order to obtain a top stream 80 comprising mainly C 5 -C 5 hydrocarbon compounds and a bottom stream 90 mainly comprising aromatic compounds in the form of carbon dioxide. C6 and C7.
• the background stream 90 is then sent to a unit extraction of aromatics 100 to form a stream of purified aromatic compounds 110 and a liquid effluent 120, a portion of which is recycled to the catalytic reforming unit 50 via line 140.
• the other part of stream 120 is removed from the process via line 130.
• the aromatics extraction unit 100 is situated downstream of the catalytic reforming unit 50 (in the direction of the circulation of the fluids) and not upstream of the catalytic reforming unit as is the case in the context of the method according to the invention.
• the operating conditions below represent the operating conditions used in pilot unit for the first reforming unit 5, comprising five series reforming reactors:
• the catalyst used in the first catalytic reforming unit is a platinum-based catalyst (0.3% by weight of Pt relative to the total weight of the catalyst) supported on an L zeolite.
• Example 1 In the context of Example 1 not in accordance with the invention and Example 2 according to the invention, it is simulated in an accelerated manner on a pilot unit in isothermal condition the formation of coke obtained on the catalyst used in the invention.
• first catalytic reforming unit compared to a process carried out on an industrial scale. The test is performed in a limited time (in this example a duration of 15 days). This test simulates accelerated aging of the catalyst.
• the test was carried out by operating at a temperature of 470 ° C., a pressure of 0.39 MPa, a mass flow rate of flow to be treated in the first reforming unit of 1 h 1 during a duration of 15 days.
• the coke rate measured on the catalyst after 15 days of test is shown in Table 1 below.
• Coke is indeed responsible for the deactivation of zeolites, in particular by deactivating the active centers (Bronsted acid sites) in different ways: by adsorbing them more strongly than the reagent molecules, by reacting with them, or again. by sterically blocking their access.

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• 2017
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