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WO2018057125A2 - Utilisation de sous-produits légèrement gazeux pour la production de paraxylène par méthylation de toluène et/ou de benzène - Google Patents

Utilisation de sous-produits légèrement gazeux pour la production de paraxylène par méthylation de toluène et/ou de benzène Download PDF

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Publication number
WO2018057125A2
WO2018057125A2 PCT/US2017/045097 US2017045097W WO2018057125A2 WO 2018057125 A2 WO2018057125 A2 WO 2018057125A2 US 2017045097 W US2017045097 W US 2017045097W WO 2018057125 A2 WO2018057125 A2 WO 2018057125A2
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Prior art keywords
alkylation
methanol
light gas
zsm
catalyst
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WO2018057125A3 (fr
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Todd E. DETJEN
Robert G. TINGER
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ExxonMobil Chemical Patents Inc
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ExxonMobil Chemical Patents Inc
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Priority to CN201780068337.8A priority Critical patent/CN109906213B/zh
Priority to US16/335,581 priority patent/US10961168B2/en
Publication of WO2018057125A2 publication Critical patent/WO2018057125A2/fr
Publication of WO2018057125A3 publication Critical patent/WO2018057125A3/fr
Anticipated expiration legal-status Critical
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/86—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon
    • C07C2/862—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon the non-hydrocarbon contains only oxygen as hetero-atoms
    • C07C2/864—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon the non-hydrocarbon contains only oxygen as hetero-atoms the non-hydrocarbon is an alcohol
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/86—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon
    • C07C2/862—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon the non-hydrocarbon contains only oxygen as hetero-atoms
    • C07C2/865—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon the non-hydrocarbon contains only oxygen as hetero-atoms the non-hydrocarbon is an ether
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00—Purification; Separation; Use of additives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2529/00—Catalysts comprising molecular sieves
    • C07C2529/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites, pillared clays
    • C07C2529/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • C07C2529/40—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11

Definitions

  • This disclosure relates to a process for utilizing off-gas produced in the production of paraxylene by the alkylation of benzene and/or toluene with methanol.
  • paraxylene is of particular value since it is useful in the manufacture of terephthalic acid, which is an intermediate in the manufacture of synthetic fibers and resins.
  • paraxylene is commercially produced by hydrotreating of naphtha (catalytic reforming), steam cracking of naphtha or gas oil, and toluene disproportionation.
  • paraxylene selectivity means that PX is produced in amounts greater than is present in a mixture of xylene isomers at thermodynamic equilibrium, which at ordinary processing temperatures is about 24 mol%.
  • PX selectivity is highly sought after because of the economic importance of PX relative to MX and OX. Although each of the xylene isomers have important and well- known end uses, PX is currently the most economically valuable.
  • toluene and/or benzene are alkylated with methanol, in the presence of a suitable catalyst, to form xylenes in a reactor in a system illustrated schematically in Figure 1, wherein a feed comprising reactants enter fluid bed reactor 11 via conduit 1 and effluent comprising product exits through conduit 5, and the catalyst circulates between fluid bed reactor 11, apparatus 12, which strips fluid from the catalyst, and catalyst regenerator 13, via conduits 2, 3, and 4, respectively.
  • Water is typically co-fed with toluene and methanol to minimize toluene coking in the feed lines and methanol self-decomposition.
  • Other side reactions include the formation of light olefins, light paraffins, as reactions that convert PX to other xylene isomers or heavier aromatics.
  • Embodiments disclosed herein provide a process for producing PX by the catalytic alkylation of benzene and/or toluene with methanol.
  • the alkylation process produces a PX-rich mixture of xylene isomers, together with water and some light organic by-products, particularly dimethyl ether and C 4- olefins.
  • the off-gas stream, containing the C 4- olefins may be recycled back to the reaction to be co-injected with methanol to reduce the methanol self-decomposition and the reaction of methanol to olefins or to fluidize catalyst particles recovered by the reactor cyclone.
  • recycled off-gas rather than water or steam, the deleterious effects of water and/or steam on the catalyst aging and activity rates and the size of downstream equipment necessary to recover olefin by-products may be reduced.
  • the process for the alkylation of toluene and/or benzene to produce PX comprises contact of toluene and/or benzene with an alkylating agent selected from methanol, dimethyl ether, and mixtures thereof, in the presence of an alkylation catalyst in a fluidized bed alkylation reactor under conditions effective to produce an alkylation effluent comprising PX and light gas by-products including olefins.
  • an alkylating agent selected from methanol, dimethyl ether, and mixtures thereof
  • the alkylation effluent is separated into a stream comprising PX and a light gas stream, and at least a portion of the light gas stream including olefins is recycled to the alkylation reactor for injection with alkylating agent, fluidizing particles of the alkylation catalyst recovered from the alkylation effluent, or both.
  • FIG. 1 Other embodiments are directed to a process for producing PX in which toluene and/or benzene are contacted with methanol in the presence of an alkylation catalyst in an alkylation reactor under conditions effective to produce an alkylation effluent comprising PX and a light gas by-products including olefins.
  • the alkylation effluent is separated into a product stream containing PX and a light gas stream containing the light gas by-products.
  • PX is recovered from the product stream, and at least a portion of the light gas stream including olefins are recycled to the alkylation reactor for at least one of: injection with the methanol, fluidizing particles of the alkylation catalyst recovered from the alkylation effluent, or both.
  • Fig 1 is a schematic of a reactor system including reactor and regenerator and some associated auxiliary devices and transfer piping per se known in the art.
  • Described herein is a process for producing PX by the catalytic alkylation of benzene and/or toluene with methanol.
  • the alkylation process produces a PX-rich mixture of xylene isomers, together with water and some light organic by-products, particularly dimethyl ether and C 4- olefins.
  • the off-gas stream, containing the C 4- olefins may be recycled back to the reaction to be co-injected with methanol to reduce the methanol self- decomposition and the reaction of methanol to olefins or to fluidize catalyst particles recovered by the intemal reactor cyclone.
  • recycled off-gas rather than water or steam, the deleterious effects of water and/or steam on the catalyst aging and activity rates and the size of downstream equipment necessary to recover olefin by-products may be reduced.
  • the alkylation process employed herein can employ any aromatic feedstock comprising benzene and/or toluene, although in general it is preferred that the aromatic feed contains at least 90 wt%, especially at least 99 wt%, of toluene.
  • the composition of the methanol-containing feed is not critical, it is generally desirable to employ feeds containing at least 90 wt%, especially at least 99 wt%, of methanol.
  • the catalyst employed in the alkylation process is generally a porous crystalline material and, in one preferred embodiment, is a porous crystalline material having a Diffusion Parameter for 2,2 dimethylbutane of about 0.1-15 sec "1 when measured at a temperature of 120°C and a 2,2 dimethylbutane pressure of 60 torr (8 kPa).
  • the Diffusion Parameter of a particular porous crystalline material is defined as D/r 2 x 10 6 , wherein D is the diffusion coefficient (cm 2 /sec) and r is the crystal radius (cm).
  • the diffusion parameter can be derived from sorption measurements provided the assumption is made that the plane sheet model describes the diffusion process.
  • Q/Qeq where Qeq is the equilibrium sorbate loading
  • t is the time (sec) required to reach the sorbate loading Q.
  • the porous crystalline material is preferably a medium-pore size aluminosilicate zeolite.
  • Medium pore zeolites are generally defined as those having a pore size of about 5 to about 7 Angstroms, such that the zeolite freely sorbs molecules such as n-hexane, 3-methylpentane, benzene, and PX.
  • Another common definition for medium pore zeolites involves the Constraint Index test which is described in U.S. Patent No. 4,016,218, which is incorporated herein by reference.
  • medium pore zeolites have a Constraint Index of about 1-12, as measured on the zeolite alone without the introduction of oxide modifiers and prior to any steaming to adjust the diffusivity of the catalyst.
  • SAPOs silicoaluminophosphates
  • suitable medium pore zeolites include ZSM-5, ZSM-11, ZSM-12, ZSM-22, ZSM-23, ZSM-35, and ZSM-48, with ZSM-5 and ZSM-11 being particularly preferred.
  • the zeolite employed in the processes disclosed herein is ZSM-5 having a silica to alumina molar ratio of at least 250, as measured prior to any treatment of the zeolite to adjust its diffusivity.
  • Zeolite ZSM-5 and the conventional preparation thereof are described in U.S. Patent No. 3,702,886.
  • Zeolite ZSM-11 and the conventional preparation thereof are described in U.S. Patent No. 3,709,979.
  • Zeolite ZSM-12 and the conventional preparation thereof are described in U.S. Patent No. 3,832,449.
  • Zeolite ZSM-23 and the conventional preparation thereof are described in U.S. Patent No. 4,076,842.
  • Zeolite ZSM-35 and the conventional preparation thereof are described in U.S. Patent No. 4,016,245.
  • the medium pore zeolites described above are preferred for the present process since the size and shape of their pores favor the production of PX over the other xylene isomers.
  • conventional forms of these zeolites have Diffusion Parameter values in excess of the 0.1-15 sec -1 range desired for the present process.
  • the required diffusivity can be achieved by severely steaming the zeolite so as to effect a controlled reduction in the micropore volume of the catalyst to not less than 50%, and preferably 50- 90%, of that of the unsteamed catalyst. Reduction in micropore volume is monitored by measuring the n-hexane adsorption capacity of the zeolite, before and after steaming, at 90°C and 75 torr n-hexane pressure.
  • Steaming to achieve the desired reduction in the micropore volume of the porous crystalline material can be effected by heating the material in the presence of steam at a temperature of at least about 950°C, preferably about 950 to about 1075°C, and most preferably about 1000 to about 1050°C for about 10 minutes to about 10 hours, preferably from 30 minutes to 5 hours.
  • the porous crystalline material prior to steaming, with at least one oxide modifier, preferably selected from oxides of the elements of Groups IIA, IIIA, IIIB, IV A, VA, VB and VIA of the Periodic Table (IUPAC version).
  • said at least one oxide modifier is selected from oxides of boron, magnesium, calcium, lanthanum and preferably phosphorus.
  • the total amount of oxide modifier present in the catalyst may be between about 0.05 and about 20 wt%, such as between about 0.1 and about 10 wt%, based on the weight of the final catalyst.
  • modifier includes phosphorus
  • incorporation of modifier in the alkylation catalyst is conveniently achieved by the methods described in U.S. Patent Nos. 4,356,338; 5,110,776; 5,231,064 and 5,348,643, the entire disclosures of which are incorporated herein by reference.
  • Treatment with phosphorus-containing compounds can readily be accomplished by contacting the porous crystalline material, either alone or in combination with a binder or matrix material, with a solution of an appropriate phosphorus compound, followed by drying and calcining to convert the phosphorus to its oxide form.
  • Contact with the phosphorus -containing compound is generally conducted at a temperature of about 25°C and about 125°C for a time between about 15 minutes and about 20 hours.
  • the concentration of the phosphorus in the contact mixture may be between about 0.01 and about 30 wt%.
  • R is an alkyl or aryl, such as phenyl radical
  • X is hydrogen, R, or halide
  • These compounds include primary, RPH2, secondary, R2PH, and tertiary, R 3 P, phosphines such as butyl phosphine, the tertiary phosphine oxides, R 3 PO, such as tributyl phosphine oxide, the tertiary phosphine sulfides, R 3 PS, the primary, RP(0)(OX)2, and secondary, R2P(0)OX, phosphonic acids such as benzene phosphonic acid, the corresponding sulfur derivatives such as RP(S)(SX)2 and R2P(S)SX, the esters of the phosphonic acids such as dialkyl phosphonate, (RO)2P(0)H, dialkyl alkyl phosphonates, (RO)2P(0)R, and alkyl dialkylphosphinates, (RO)P(0)R2; phosphinous acids, R2POX, such as diethylphosphinous acid, primary, (RO)
  • Corresponding sulfur derivatives may also be employed including (RS) 2 P(S)H, (RS) 2 P(S)R, (RS)P(S)R 2 , R2PSX, (RS)P(SX) 2 , (RS) 2 PSX, (RS) 3 P, (RS)PR 2 , and (RS)2PR.
  • phosphite esters include trimethylphosphite, triethylphosphite, diisopropylphosphite, butylphosphite, and pyrophosphites such as tetraethylpyrophosphite.
  • the alkyl groups in the mentioned compounds preferably contain one to four carbon atoms.
  • Suitable phosphorus-containing compounds include ammonium hydrogen phosphate, the phosphorus halides such as phosphorus trichloride, bromide, and iodide, alkyl phosphorodichloridites, (RO)PCl 2 , dialkylphosphoro-chloridites, (RO) 2 PCl, dialkylphosphinochloroidites, R ⁇ PCl, alkyl alkylphosphonochloridates, (RO)(R)P(0)Cl, dialkyl phosphinochloridates, R 2 P(0)C1, and RP(0)C1 2 .
  • the phosphorus halides such as phosphorus trichloride, bromide, and iodide
  • alkyl phosphorodichloridites such as phosphorus trichloride, bromide, and iodide
  • alkyl phosphorodichloridites such as phosphorus trichloride, bromide, and iodide
  • Applicable corresponding sulfur derivatives include (RS)PC1 2 , (RS) 2 PC1, (RS)(R)P(S)C1, and P ⁇ P ⁇ Cl.
  • Particular phosphorus-containing compounds include ammonium phosphate, ammonium dihydrogen phosphate, diammonium hydrogen phosphate, diphenyl phosphine chloride, trimethylphosphite, phosphorus trichloride, phosphoric acid, phenyl phosphine oxychloride, trimethylphosphate, diphenyl phosphinous acid, diphenyl phosphinic acid, diethylchlorothiophosphate, methyl acid phosphate, and other alcohol-P 2 0 5 reaction products.
  • Representative boron-containing compounds which may be used to incorporate a boron oxide modifier into the catalysts disclosed herein, include boric acid, trimethylborate, boron oxide, boron sulfide, boron hydride, butylboron dimethoxide, butylboric acid, dimethylboric anhydride, hexamethylborazine, phenyl boric acid, triethylborane, diborane, and triphenyl boron.
  • Representative magnesium-containing compounds include magnesium acetate, magnesium nitrate, magnesium benzoate, magnesium propionate, magnesium 2-ethylhexoate, magnesium carbonate, magnesium formate, magnesium oxylate, magnesium bromide, magnesium hydride, magnesium lactate, magnesium laurate, magnesium oleate, magnesium palmitate, magnesium salicylate, magnesium stearate, and magnesium sulfide.
  • Representative calcium-containing compounds include calcium acetate, calcium acetylacetonate, calcium carbonate, calcium chloride, calcium methoxide, calcium naphthenate, calcium nitrate, calcium phosphate, calcium stearate, and calcium sulfate.
  • Representative lanthanum-containing compounds include lanthanum acetate, lanthanum acetylacetonate, lanthanum carbonate, lanthanum chloride, lanthanum hydroxide, lanthanum nitrate, lanthanum phosphate, and lanthanum sulfate.
  • the porous crystalline material employed in the embodiments disclosed herein may be combined with a variety of binder or matrix materials resistant to the temperatures and other conditions employed in the process.
  • binder or matrix materials resistant to the temperatures and other conditions employed in the process.
  • Such materials include active and inactive materials such as clays, silica and/or metal oxides such as alumina. The latter may be either naturally occurring or in the form of gelatinous precipitates or gels including mixtures of silica and metal oxides.
  • Inactive materials suitably serve as diluents to control the amount of conversion in a given process so that products can be obtained economically and orderly without employing other means for controlling the rate of reaction.
  • These materials may be incorporated into naturally occurring clays, e.g., bentonite and kaolin, to improve the crush strength of the catalyst under commercial operating conditions.
  • Said materials i.e., clays, oxides, etc., function as binders for the catalyst. It is desirable to provide a catalyst having good crush strength because in commercial use it is desirable to prevent the catalyst from breaking down into powder-like materials.
  • These clay and/or oxide binders have been employed normally only for the purpose of improving the crush strength of the catalyst.
  • Naturally occurring clays which can be composited with the porous crystalline material include the montmorillonite and kaolin family, which families include the subbentonites, and the kaolins commonly known as Dixie, McNamee, Georgia, and Florida clays or others in which the main mineral constituent is halloysite, kaolinite, dickite, nacrite, or anauxite.
  • Such clays can be used in the raw state as originally mined or initially subjected to calcination, acid treatment, or chemical modification.
  • the porous crystalline material can be composited with a porous matrix material such as silica-alumina, silica-magnesia, silica- zirconia, silica-thoria, silica-beryllia, silica-titania, as well as ternary compositions such as silica-alumina-thoria, silica-alumina-zirconia, silica-alumina-magnesia, and silica-magnesia- zirconia.
  • a porous matrix material such as silica-alumina, silica-magnesia, silica- zirconia, silica-thoria, silica-beryllia, silica-titania, as well as ternary compositions such as silica-alumina-thoria, silica-alumina-zirconia, silica-alumina-magnesia, and silica-magnesia- zirconia.
  • porous crystalline material and inorganic oxide matrix vary widely, with the content of the former ranging from about 1 to about 90% by weight and more usually, particularly when the composite is prepared in the form of beads, in the range of about 2 to about 80 wt% of the composite.
  • the conditions employed in the alkylation stage of the present process are not narrowly constrained but, in the case of the methylation of toluene, generally include the following ranges: (a) temperature between about 500 and about 700°C, such as between about 500 and about 600°C; (b) pressure of between about 1 atmosphere and about 1000 psig (between about 100 and about 7000 kPa), such as between about 10 psig and about 200 psig (between about 170 and about 1480 kPa); (c) moles toluene/moles methanol (in the reactor charge) of at least about 0.2, such as from about 0.2 to about 20; and (d) a weight hourly space velocity ("WHSV") for total hydrocarbon feed to the reactor(s) of about 0.2 to about 1000, such as about 0.5 to about 500 for the aromatic reactant, and about 0.01 to about 100 for the combined methanol reagent stage flows, based on total catalyst in the reactor(s).
  • WHSV weight hourly space velocity
  • the alkylation process can be conducted in any known reaction vessel but generally the methanol and aromatic feeds are contacted with the catalyst described above with the catalyst particles being disposed in one or more fluidized or fixed beds.
  • Each of the methanol and aromatic feeds can be injected into the fluidized or fixed beds in a single stage.
  • the methanol feed is injected in stages into the fluidized or fixed beds at one or more locations downstream from the location of the injection of the aromatic reactant into the fluidized or fixed beds.
  • a fluidized bed reactor may be used, and the aromatic feed can be injected into a lower portion of a single vertical fluidized bed of catalyst, with the methanol being injected into the bed at a plurality of vertically spaced intermediate portions of the bed and the product being removed from the top of the bed.
  • the catalyst can be disposed in a plurality of vertically spaced catalyst beds, with the aromatic feed being injected into a lower portion of the first fluidized bed and part of the methanol being injected into an intermediate portion of the first bed and part of the methanol being injected into or between adjacent downstream catalyst beds.
  • water is co-injected with the methanol feed to reduce the methanol partial pressure and minimize side reactions of methanol to olefin by-products.
  • Methanol injected without a diluent, such as water generally leads to a higher amount of light gas byproducts. Diluting the methanol decreases the amount available for the side reactions upon introduction into the reactor.
  • some embodiments may employ one or more cyclones that are disposed (at least partially) inside and/or outside of the reaction vessel.
  • the product of the reaction between the methanol and toluene and/or benzene is an alkylation effluent comprising PX and other xylene isomers, water vapor, unreacted toluene and/or benzene, unreacted methanol, phenolic impurities, and a variety of light gas by-products, such as C 4- hydrocarbons, including paraffins, olefins, and contaminants such as nitrogen, nitrogen oxides, carbon monoxide, carbon dioxide, and oxygenates such as ethanal and dimethyl ether.
  • the alkylation effluent will also generally contain some C9+ aromatic byproducts.
  • the alkylation effluent is fed through a series of separation steps where the alkylation effluent is first separated into a C6+ hydrocarbon stream containing xylenes and a C5- hydrocarbon stream containing the light gas by-products.
  • the C6+ hydrocarbon stream may then be separated to recover the unreacted benzene and/or toluene and produce a Cs+ hydrocarbon stream, from which the heavy (C9+) by-products may be separated to produce a C8 hydrocarbon stream.
  • PX is recovered from the Cs hydrocarbon stream, typically by fractional crystallization or selective adsorption and the remaining Cs hydrocarbons may be isomerized to produce more PX.
  • the C5- hydrocarbon stream containing the light gas by-products may be treated by a series of treatment steps, such as that disclosed in U.S. Patent Publication Nos. 2014/0100402 and 2016/0060187.
  • the C5- hydrocarbon light gas stream goes through a series of wash steps, such as a methanol wash to remove oxygenates, a water wash to remove methanol, and a caustic wash to remove carbon dioxide.
  • the light gas stream may then be dried to remove water, such as with a molecular sieve drier or by washing with methanol, which itself has preferably been dried to remove water, such as with a molecular sieve drier.
  • the dried light gas stream may then be sent to a fractionation tower primarily to remove dimethyl ether from the light olefins, so as to minimize the impact of dimethyl ether on olefins recovery equipment.
  • Dimethyl ether can also be deleterious to a later-recovered propylene product by negatively impacting propylene in downstream processes such as polymerization.
  • the fractionation tower acts to fractionate the light gas stream into an overhead stream, containing at least some, and preferably most, of the C3- hydrocarbons, and almost all of the dimethyl ether and C4+ hydrocarbons as a liquid bottoms stream.
  • ethylene and at least about 80 wt%, preferably at least about 90 wt%, of the propylene, and about 67 wt% of the propane from the fractionation column are recovered in the overhead stream, while nearly 100 wt% of the dimethyl ether and nearly 100 wt% of C4+ hydrocarbons are removed in the liquid bottoms stream.
  • the overhead vapor stream from the fractionation tower which generally comprises less than about 100 ppm dimethyl ether, preferably 20 ppm or less by weight, more preferably 1 ppm or less by weight is sent to a contaminant removal system, and the recovered dimethyl ether may be recycled to the methylation reaction.
  • the overhead stream from the fractionation tower may be treated to remove the contaminants from the light gas stream as described in U.S. Patent Publication No. 2016/0060187.
  • the contaminant-free light gas stream may be sent to olefins recovery to recover at least the valuable olefinic component of the stream, but in one embodiment, the light gas stream, including olefins, is recycled to the methylation reaction to decrease the amount of water and/or steam necessary.
  • the light gas stream may be recycled to the reactor with any combination of the above treatment steps, or without being subjected to any of the above-mentioned treatment steps.
  • the Cs- hydrocarbon stream containing the light gas by-products separated from the alkylation effluent may be recycled to the reactor without removing oxygenates, methanol, carbon dioxide, water, or dimethyl ether, or after removing any one of the contaminants, or after removing any combination of the contaminants.
  • light gas preferably recycled light gas from the alkylation effluent, including olefins
  • Another benefit of co-injecting an olefin-rich light gas with the methanol is the higher utilization of the methanol in the aromatic alkylation reaction rather than the methanol reacting to form olefin by-products.
  • the molar ratio of light gas to methanol is maintained in the range of 0.01 : 1 to 20: 1.
  • the methanol/light gas mixture may be injected into a single stage or into multiple stages axially along the reactor.
  • the total rate of methanol/light gas mixture and the methanol/light gas mixture molar ratio injected into each stage may be held constant or varied in each stage to optimize reactor yields.
  • water and light gas may be co-injected with the methanol.
  • light gas preferably recycled light gas from the alkylation effluent
  • compositions, an element or a group of components are preceded with the transitional phrase “comprising,” it is understood that we also contemplate the same composition or group of components with transitional phrases “consisting essentially of,” “consisting of,” “selected from the group of consisting of,” or “is” preceding the recitation of the composition, component, or components, and vice versa.

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Abstract

L'invention concerne un procédé de production de paraxylène par l'alkylation catalytique de benzène et/ou de toluène avec du méthanol, qui produit un mélange riche en p- d'isomères de xylène, conjointement avec de l'eau et certains sous-produits organiques légers, particulièrement un diméthyléther et des oléfines en C4. Le flux de dégagement gazeux, contenant les oléfines en C4, peut être recyclé vers la réaction à co-injecter avec du méthanol pour réduire l'auto-décomposition de méthanol et la réaction du méthanol en oléfines ou pour fluidiser des particules de catalyseur récupérées par un cyclone de réacteur. L'utilisation de gaz de dégagement recyclé plutôt que d'eau ou de vapeur permet de réduire les effets délétères de l'eau et/ou de la vapeur sur les vitesses de vieillissement et d'activité de catalyseur ainsi que la taille de l'équipement aval nécessaire pour récupérer des sous-produits d'oléfine.
PCT/US2017/045097 2016-09-22 2017-08-02 Utilisation de sous-produits légèrement gazeux pour la production de paraxylène par méthylation de toluène et/ou de benzène Ceased WO2018057125A2 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CN201780068337.8A CN109906213B (zh) 2016-09-22 2017-08-02 轻质气体副产物在通过甲苯和/或苯的甲基化制备对二甲苯中的用途
US16/335,581 US10961168B2 (en) 2016-09-22 2017-08-02 Use of light gas by-products in the production of paraxylene by the methylation of toluene and or benzene

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US201662398252P 2016-09-22 2016-09-22
US62/398,252 2016-09-22
EP16197276 2016-11-04
EP16197276.5 2016-11-04

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020005781A1 (fr) * 2018-06-27 2020-01-02 Uop Llc Procédés et appareils pour la méthylation de toluène et de benzène dans un complexe de composés aromatiques
WO2020197888A1 (fr) * 2019-03-28 2020-10-01 Exxonmobil Chemical Patents Inc. Procédés et systèmes de conversion de benzène et/ou de toluène par méthylation
CN112121850A (zh) * 2019-06-24 2020-12-25 中国石油化工股份有限公司 流化床催化剂和二甲苯的生产方法

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WO2020005781A1 (fr) * 2018-06-27 2020-01-02 Uop Llc Procédés et appareils pour la méthylation de toluène et de benzène dans un complexe de composés aromatiques
US11192833B2 (en) 2018-06-27 2021-12-07 Uop Llc Processes and apparatuses for toluene and benzene methylation in an aromatics complex
WO2020197888A1 (fr) * 2019-03-28 2020-10-01 Exxonmobil Chemical Patents Inc. Procédés et systèmes de conversion de benzène et/ou de toluène par méthylation
CN113574037A (zh) * 2019-03-28 2021-10-29 埃克森美孚化学专利公司 用于经由甲基化转化苯和/或甲苯的方法和系统
CN112121850A (zh) * 2019-06-24 2020-12-25 中国石油化工股份有限公司 流化床催化剂和二甲苯的生产方法
CN112121850B (zh) * 2019-06-24 2023-05-02 中国石油化工股份有限公司 流化床催化剂和二甲苯的生产方法

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