Indian Patents. 216734:"A PROCESS FOR THE ISOMERIZATION OF A NON-EQUILIBRIUM FEED MIXTURE OF XYLENES AND ETHYLBENZENE"

Title of Invention	"A PROCESS FOR THE ISOMERIZATION OF A NON-EQUILIBRIUM FEED MIXTURE OF XYLENES AND ETHYLBENZENE"
Abstract	This invention is drawn to a process for isomerizing a non-equilibrium mixture of xylenes and ethylbenzene using a catalyst comprising a zeolite, a platinum-group metal and an aluminophosphate binder or silica, resulting in a greater yield of para-xylene at favorable conditions compared to processes of the known art.

Full Text	This invention relates to a process for the isomerization of a non equiliblem feed mixtures of xylenes and ethylbenzen BACKGROUND The xylenes, para-xylene, meta-xylene and ortho-xylene, are important intermediates which find wide and varied application in chemical syntheses. Para-xylene upon oxidation yields terephthalic acid which is used in the manufacture of synthetic textile fibers and resins. Meta-xylene is used in the manufacture of plasticizers, azo dyes, wood preservers, etc. Ortho-xylene is feedstock for phthalic anhydride production. Xylene isomers from catalytic reforming or other sources generally do not match demand proportions as chemical intermediates, and further comprise ethylbenzene which is difficult to separate or to convert. Para-xylene in particular is a major chemical intermediate with rapidly growing demand, but amounts to only 20-25% of a typical Cs-aromatics stream. Adjustment of isomer ratio to demand can be effected by combining xylene-isomer recovery, such as adsorption for para-xylene recovery, with isomerization to yield an additional quantity of the desired isomer. Isomerization converts a non-equilibrium mixture of the xylene isomers which is lean in the desired xylene isomer to a mixture which approaches equilibrium concentrations. Various catalysts and processes have been developed to effect xylene isomerization. In selecting appropriate technology, it is desirable to run the isomerization process as close to equilibrium as practical in order to maximize the para-xylene yield; however, associated with this is a greater cyclic C& loss due to side reactions. The approach to equilibrium that is used is an optimized compromise between high C8 cyclic loss at high conversion (i.e. very close approach to equilibrium) and high utility costs due to the large recycle rate of unconverted Cs aromatics. Catalysts for isomerization of C8 aromatics ordinarily are classified by the manner of processing ethylbenzene associated with the xylene isomers. Ethylbenzene is not easily isomerized to xylenes, but it normally is converted in the isomerization unit because separation from the xylenes by superfractionation or adsorption is very expensive. One approach is to react the ethylbenzene to form a xylene mixture via conversion to and reconversion from naphthenes in the presence of a solid acid catalyst with a hydrogenation-dehydrogenation function. An alternative widely used approach is to dealkylate ethylbenzene to form principally benzene while isomerizing xylenes to a near-equilibrium mixture. The former approach enhances xylene yield by forming xylenes from ethylbenzene, while the latter approach commonly results in higher ethylbenzene conversion, thus lowering the quantity of recycle to the para-xylene recovery unit and concomitant processing costs. In the past twenty years or so, crystalline aluminosilicate zeolite-containing catalysts have become prominent for xylene isomerization. US-A-3,856,872,)for example, teaches xylene isomerization and ethylbenzene conversion with a catalyst containing ZSM-5, -12, or -21 zeolite/ US-A-4,626,609 discloses conversion of xylene isomers using a catalyst comprising a composite which has been steamed at 200° to 500°C US-A-4,899,012 teaches the use of a catalyst containing lead, a Group VIII metal, a pentasil zeolite and an inorganic-oxide binder to isomerize xylenes and dealkylate ethylbenzene. Development efforts continue toward realizing economically attractive isomerization catalysts with a superior combination of activity, selectivity and stability. SUMMARY A principal object of the present invention is to provide a novel isomerization process for alkylaromatic hydrocarbons. More specifically, this invention is directed to the processing of C8 aromatics to increase the concentration of a desired xylene isomer. This invention is based on the discovery that improved conversion of Cs aromatics and selectivity for xylene isomerization can be obtained using a zeolitic catalyst component in a finished catalyst composition that has a certain low water capacity and includes an inert silica or aluminum phosphate binder in the finished composition. Accordingly, a broad embodiment of the invention is directed toward an alkylaromatics-isomerization process using a catalyst comprising a zeolitic aluminosilicate having a pore diameter of from about 5 to 8Å, a platinum-group metal component and with an inert silica binder or with an aluminum phosphate binder when in the form of an oil dropped spherical catalyst. The process comprises isomerization preferably of a feedstock comprising a non-equilibrium mixture of xylenes and ethylbenzene at isomerization conditions to obtain a product having an increased para-xylene content relative to that of the feedstock. Relevant isomerization conditions comprise a temperature of from about 300° to 600°C, a pressure of from about 100 kPa to 5 MPa, a mass hourly space velocity of from about 0.5 to 100 hr"1. Operation at a temperature of between 350° to 500°C at a mass hourly space velocity of from about 10 to 50 hr"1 is especially favored. MFI-type zeolite is the favored zeolitic aluminosilicate. The catalyst has a low 4.6 torr water capacity of less than about 7 mass-%, and preferably between about 3 and about 5 mass-%. The platinum-group metal preferably comprises platinum in a low concentration of between 100 and 2000 mass-ppm, and optimally between about 200 and 800 mass-ppm, of the catalyst. These, as well as other objects and embodiments, will become evident from the following detailed description of the invention. According to the present invention there is provided a process for the isomerization of a non-equilibrium feed mixture of xylenes and ethylbenzene comprising contacting the feed mixture in the presence of hydrogen with a catalyst comprising a zeolitic aluminosilicate comprising a zeolite selected from the group consisting of MFI,MEL,EUO,FER,MFS,MTT,MTW,TON,MOR,FAU and combinations thereof , having a pore diameter of from 5 to 8 Angstroms said finished catalyst having a 4.6 torr water capacity of less than 7 mass-%, a platinum-group metal component and an aluminum phosphate or a silica binder in an isomerization zone at isomerization conditions comprising a temperature of from 300° to 600°C, a pressure of from 100 kPa to 5 MPa, a mass hourly space velocity of from 0.5 to 100 hr" to obtain an isomerized product comprising a higher proportion of one xylene isomer selected from the group consisting of para-xylene,meta-xylene, ortho-xylene and combinations thereof than in the feed mixture. BRIEF DESCRIPTION OF THE ACCOMPANYING DRAWINGS Figure 1 shows relative activity and selectivity, in terms of process xylenes losses, of catalysts of the invention and the known art. Figure 2 shows process xylenes losses as a function of catalyst water capacity. DETAILED DESCRIPTION OF THE INVENTION The feedstock to aromatics isomerization comprises isomerizable alkylaromatic hydrocarbons of the general formula C6H(6-n)Rn, where n is an integer from 1 to 5 and R is CH3 C2H5, C3H7, or C4H9, in any combination and including all the isomers thereof to obtain more valuable isomers of the alkylaromatic. Suitable alkylaromatic hydrocarbons include, for example but without so limiting the invention, ortho-xylene, meta-xylene, para-xylene, ethylbenzene, ethyltoluenes, trimethylbenzenes, propylbenzenes, ethyldimethyl-benzenes, diethylbenzenes, methylpropylbenzenes, ethylpropylbenzenes, triethylbenzenes, di-isopropylbenzenes, and mixtures thereof. Isomerization of a C8-aromatic mixture containing ethylbenzene and xylenes is a particularly preferred application of the invention. Generally such a mixture will have an ethylbenzene content in the approximate range of 5 to 50 mass-%, an ortho-xylene content in the approximate range of 0 to 35 mass-%, a meta-xylene content in the approximate range of 20 to 95 mass-% and a para-xylene content in the approximate range of 0 to 15 mass-%. It is preferred that the feed C8 aromatics comprise a non-equilibrium mixture, i.e., at least one C9-aromatic isomer is present in a concentration that differs substantially from the equilibrium concentration at isomerization conditions. Usually the non-equilibrium mixture is prepared by removal of para- and/or ortho-xylene from a fresh C8-aromatics feed obtained from processes, such as catalytic reforming and/or extraction, for the production and recovery of aromatics from other hydrocarbons. The alkylaromatic hydrocarbons may be utilized in the present invention as found in appropriate fractions from various refinery petroleum streams, e.g., as individual components or as certain boiling-range fractions obtained by the selective fractionation and distillation of catalytically cracked or reformed hydrocarbons. The isomerizable aromatic hydrocarbons need not be concentrated; the process of this invention allows the isomerization of alkylaromatic-containing streams such as catalytic reformate with or without subsequent aromatics extraction to produce specified xylene isomers and particularly to produce para-xylene. A C8-aromatics feed to the present process may contain nonaromatic hydrocarbons, i.e., naphthenes and paraffins, in an amount up to 30 mass-%. Preferably the isomerizable hydrocarbons consist essentially of aromatics, however, to ensure pure products from downstream recovery processes. According to the process of the present invention, an alkylaromatic hydrocarbon feed mixture, preferably in admixture with hydrogen, is contacted with a catalyst of the type hereinafter described in an alkylaromatic hydrocarbon isomerization zone. Contacting may be effected using the catalyst in a fixed-bed system, a moving-bed system, a fluidized-bed system, or in a batch-type operation. In view of the danger of attrition loss of the valuable catalyst and of the simpler operation, it is preferred to use a fixed-bed system. In this system, a hydrogen-rich gas and the feed mixture are preheated by suitable heating means to the desired reaction temperature and then passed into an isomerization zone containing a fixed bed of catalyst. The conversion zone may be one or more separate reactors with suitable means therebetween to ensure that the desired isomerization temperature is maintained at the entrance to each zone. The reactants may be contacted with the catalyst bed in either upward-, downward-, or radial-flow fashion, and the reactants may be in the liquid phase, a mixed liquid-vapor phase, or a vapor phase when contacted with the catalyst. The alkylaromatic feed mixture, preferably a non-equilibrium mixture of C& aromatics, is contacted with the isomerization catalyst at suitable alkylaromatic-isomerization conditions. Such conditions comprise a temperature ranging from about 100° to 600°C or more, and preferably is in the range of from about 350° to 500°C. The pressure generally is from about 100 kPa to 10 MPa, and more usually no more than about 5 MPa. Sufficient catalyst is contained in the isomerization zone to provide a mass hourly space velocity with respect to the hydrocarbon feed mixture of from about 0.5 to 100 hr"1, and preferably 2 to 50 hr"1; favorable results have been obtained at mass hourly space velocities of at least about 10 hr"1 and higher. The hydrocarbon feed mixture optimally is reacted in admixture with hydrogen at a hydrogen/hydrocarbon mole ratio of about 0.5:1 to about 10:1 or more; other inert diluents such as nitrogen, argon and light hydrocarbons may be present. The particular scheme employed to recover an isomerized product from the effluent of the reactors of the isomerization zone is not deemed to be critical to the instant invention, and any effective recovery scheme known in the art may be used. In a separation/isomerization process combination relating to the processing of an ethylbenzene/xylene mixture, a fresh C8-aromatics feed is combined with isomerized product comprising C8 aromatics and naphthenes from the isomerization reaction zone and fed to a para-xylene separation zone from which pure para-xylene is recovered. The para-xylene-depleted stream from the separation zone, comprising a non-equilibrium mixture of C8 aromatics, comprising xylenes and ethylbenzene, is fed to the isomerization reaction zone, where the C8-aromatic isomers are isomerized to near-equilibrium levels to obtain the isomerized product. In this process scheme non-recovered C8-aromatic isomers preferably are recycled to extinction until they are either converted to para-xylene or lost due to side-reactions. Ortho-xylene separation, preferably by fractionation, also may be effected on the fresh C8-aromatic feed or isomerized product, or both in combination, preferably prior to para-xylene separation. The isomerization catalyst of the present invention comprises a molecular sieve and a refractory inorganic oxide. The preferred molecular sieves are zeolitic alumino-silicates selected from those which have a Si:AI2 ratio greater than about 10, preferably greater than 20, and a pore diameter of about 5 to 8 Angstroms (A). Specific examples of suitable zeolites are the MFI, MEL, EDO, PER, MFS, MTT, MTW, TON, MOR and FAU types of zeolites. Pentasil zeolites MFI, MEL, MTW and TON are preferred, and MFI-type zeolites, often designated ZSM-5, are especially preferred. The relative proportion of zeolite in the catalyst may range from about 10 to about 99 mass-%, with about 20 to about 90 mass-% being preferred. There is a tradeoff between the zeolite content of the catalyst composite and the pressure, temperature and space velocity of an isomerization operation in maintaining low xylene losses. A refractory binder or matrix is utilized to facilitate fabrication of the isomerization catalyst. The binder should be uniform in composition and relatively refractory to the conditions used in the process. Suitable binders include inorganic oxides such as one or more of alumina, magnesia, zirconia, chromia, titania, boria and silica. A first preferred binder is an amorphous silica. The preferred amorphous silica is a synthetic, white, amorphous silica (silicon dioxide) powder which is classed as wet-process, hydrated silica. This type of silica is produced by a chemical reaction in a water solution, from which it is precipitated as ultra-fine, spherical particles. It is preferred that the BET surface area of the silica is in the range from about 50 to 800 m2/g, especially 120 to 160 m2/g. A low content of sulfate salts is desired, preferably less than 0.3 wt.%. It is especially preferred that the amorphous silica binder be nonacidic, e.g., that the pH of a 5% water suspension be neutral or basic (pH about 7 or above). A second preferred binder is an amorphous aluminum phosphate. The zeolite and aluminum phosphate binder maybe formed into particles by means well known in the art. A preferred method of preparing the zeolite/aluminum phosphate support involves adding the zeolite either to an alumina sol or a phosphorus compound, forming a mixture of the alumina sol/zeolite/phosphorus compound into particles by employing the oil-drop method described hereinbelow, and calcining the spherical particles. The preferred oil-drop method-of-preparing the aluminum phosphate bound catalyst is described ia,US-A-4,629,717 Which is incorporated by reference. The technique described in the 717 patent involves the gellation of a hydrosol of alumina which contains a phosphorus compound using the well-known oil-drop method. Generally this technique involves preparing a hydrosol by digesting aluminum in aqueous hydrochloric acid at reflux temperatures of about 80° to 105°C. The ratio of aluminum to chloride in the sol ranges from about 0.7:1 to 1.5:1 mass ratio. A phosphorus compound is now added to the sol. Preferred phosphorus compounds are phosphoric acid, phosphorous acid and ammonium phosphate. The relative amount of phosphorus and aluminum expressed in molar ratios ranges from about 10:1 to 1:100, respectively, on an elemental basis. The zeolite is added to the aluminum phosphate hydrosol and the mixture is gelled. One method of gelling this mixture involves combining a gelling agent with the mixture and then dispersing the resultant combined mixture into an oil bath or tower which has been heated to elevated temperatures such that gellation occurs with the formation of spheroidal particles. The gelling agents which may be used in this process are hexamethylene tetraamine, urea or mixtures thereof. The gelling agents release ammonia at the elevated temperatures which sets or converts the hydrosol spheres into hydrogel spheres. The spheres are then continuously withdrawn from the oil bath and typically subjected to specific aging and drying treatments in oil and in ammoniacal solution to further improve their physical characteristics. The resulting aged and gelled particles are then washed and dried at a relatively low temperature of about 100° to 150°C and subjected to a calcination procedure at a temperature of about 450° to 700°C for a period of about 1 to 20 hours. The amount of phosphorus-containing alumina component present (as the oxide) in the catalyst can range from about 10 to 70 mass percent and preferably from about 20 to 50 mass percent. The combined mixture preferably is dispersed into the oil bath in the form of droplets from a nozzle, orifice or rotating disk. Alternatively, the particles may be formed by spray-drying of the mixture at a temperature of from about 425° to 760°C. In any event, conditions and equipment should be selected to obtain small spherical particles; the particles preferably should have an average diameter of less than about 1.0 mm, more preferably from about 0.2 to 0.8 mm, and optimally from about 0.3 to 0.8 mm. The degree of crystallinity of the aluminum phosphate binder can be controlled by varying the proportion of the phosphorus component. Material that is not in an amorphous phase generally is present as gamma-alumina; as the phosphorus content is decreased, the degree of crystallinity, therefore, is increased. The apparent bulk density of the spheres also varies with the phosphorus content, as a higher proportion of phosphorus decreases the average bulk density. Surface area also is controlled by phosphorus content: gamma-alumina oil-dropped spherical particles typically have surface areas up to about 250 m2/g, while spheroidal particles of aluminum phosphate may have surface areas of up to about 450 m2/g. AI/P atomic ratios of the binder/matrix generally range from about 1/10 to 100/1, and more typically from about 1/5 to 20/1. An alternative shape for the catalyst composite is an extrudate. Extrusion is preferred with a silica binder. The well-known extrusion method initially involves mixing of the molecular sieve, either before or after adding metallic components, with the binder and a suitable peptizing agent to form a homogeneous dough or thick paste having the correct moisture content to allow for the formation of extrudates with acceptable integrity to withstand direct calcination. Extrudability is determined from an analysis of the moisture content of the dough, with a moisture content in the range of from 30 to 50 wt. % being preferred. A multitude of different extrudate shapes are possible, including, but not limited to, cylinders, cloverleaf, dumbbell and symmetrical and asymmetrical polylobates. The catalyst of the present invention may contain a halogen component. The halogen component may be either fluorine, chlorine, bromine or iodine or mixtures thereof, with chlorine being preferred. The halogen component is generally present in a combined state with the inorganic-oxide support. The optional halogen component is preferably well dispersed throughout the catalyst and may comprise from more than 0.2 to about 15 wt.%, calculated on an elemental basis, of the final catalyst. Preferably, however, the catalyst contains no added halogen other than that associated with other catalyst components. The formed catalyst composite is dried at a temperature of from about 100° to about 320°C for a period of from about 2 to about 24 or more hours and, usually, calcined at a temperature of from 400° to about 650°C in an air atmosphere for a period of from about 0.1 to about 10 hours until the metallic compounds present are converted substantially to the oxide form. The catalytic composite optimally is subjected to steaming to tailor its acid activity. The steaming may be effected at any stage of the zeolite treatment, but usually is carried out on the composite of zeolite and binder prior to incorporation of the platinum-group metal. Steaming conditions comprise a water concentration of about 5 to 100 volume-%, pressure of from about 100 kPa to 2 MPa, and temperature of from about 600° to about 1200°C; the steaming temperature preferably is at least about 650°C, more preferably at least about 750°C and optionally may be about 775°C or higher. In some cases, temperatures of about 800° to 850°C or more may be employed. The steaming should be carried out for a period of at least one hour, and periods of 6 to 48 hours are preferred. Alternatively or in addition to the steaming, the composite may be washed with one or more of a solution of ammonium nitrate, a mineral acid, and/or water. Considering the first alternative, the catalyst may be washed with a solution of about 5 to 30 mass-% ammonium nitrate. When acid washing is employed, a mineral acid such as HCI or HNO3 is preferred; sufficient acid is added to maintain a pH of from more than 1 to about 6, preferably from about 1.5 to 4. The catalyst is maintained in a bed over which the solution and/or water is circulated for a period of from about 0.5 to 48 hours, and preferably from about 1 to 24 hours. The washing may be effected at any stage of the preparation, and two or more stages of washing may be employed. Prior to addition of the platinum-group metal component, the composite preferably is ion-exchanged with a salt solution containing at least one hydrogen-forming cation such as NH4 or quaternary ammonium. The hydrogen-forming cation replaces principally alkali-metal cations to provide, after calcination, the hydrogen form of the zeolite component. A platinum-group metal, including one or more of platinum, palladium, rhodium, ruthenium, osmium, and iridium, is an essential component of the present catalyst. The preferred platinum-group metals are platinum and palladium, with platinum being especially preferred. The platinum-group metal component may exist within the final catalyst composite as a compound such as an oxide, sulfide, halide, oxysulfide, etc., or as an elemental metal or in combination with one or more other ingredients of the catalyst composite. It is believed that the best results are obtained when substantially all of the platinum-group metal component exists in a reduced state. The platinum-group metal component generally comprises from about 100 to about 5000 mass-ppm (parts per million) of the final catalyst composite, calculated on an elemental basis, with a level of about 100 to about 2000 mass-ppm being particularly suitable. When using a platinum component, very low levels of about 200 to 800 mass-ppm of platinum on the catalyst, on an elemental basis, are favored; levels of less than about 600 mass-ppm are especially favored and levels of about 300 to about 500 mass-ppm show excellent results. When using a palladium component, levels of about 400 to 2000 mass-ppm of palladium on the catalyst, on an elemental basis, are favored and levels of from about 500 to about 1200 mass-ppm are especially favored. The platinum-group metal component may be incorporated into the catalyst composite in any suitable manner. One method of preparing the catalyst involves the utilization of a water-soluble, decomposable compound of a platinum-group metal to impregnate the calcined sieve/binder composite. Alternatively, a platinum-group metal compound may be added at the time of compositing the sieve component and binder. Yet another method of effecting a suitable metal distribution is by compositing the metal component with the binder prior to co-extruding the sieve and binder. Complexes of platinum-group metals which may be employed according to the above or other known methods include chloroplatinic acid, chloropalladic acid, ammonium chloroplatinate, bromoplatinic acid, platinum trichloride, platinum tetrachloride hydrate, platinum dichlorocarbonyl dichloride, tetraamineplatinum chloride, dinitrodiaminoplatinum, sodium tetranitroplatinate (II), palladium chloride, palladium nitrate, palladium sulfate, diaminepalladium (II) hydroxide, tetraaminepalladium (II) chloride, and the like. It is within the scope of the present invention that the catalyst may contain other metal components known to modify the effect of the platinum-group metal component. After addition of the metal component, the resultant catalytic composite usually is dried at a temperature of about 100° to about 320°C for a period of from about 1 to about 24 or more hours. The dried composite then is calcined at a temperature of from about 400° to about 600°C in an air atmosphere for a period of from about 0.1 to 10 hours to convert the metallic components substantially to the oxide form. The calcined composite optimally is subjected to a substantially water-free reduction step to insure a uniform and finely divided dispersion of the optional metallic components. The reduction optionally may be effected on the catalyst as loaded in the isomerization-process reactor of the present invention prior to the startup of the isomerization process. Substantially pure and dry hydrogen (i.e., less than 20 vol. ppm H2O) preferably is used as the reducing agent in this step. The reducing agent contacts the catalyst at conditions, including a temperature of from about 200° to about 650°C and for a period of from about 0.5 to about 10 hours, effective to reduce substantially all of the Group VIII metal component to the metallic state. In some cases the resulting reduced catalyst composite may also be beneficially subjected to presulfiding by a method known in the art to incorporate in the catalyst composite from about 0.01 to about 0.5 mass-% sulfur, on an elemental basis, into the catalyst. The finished catalyst has a McBain water capacity at 4.6 torr of between about 2 and 7 mass-%, preferably between about 3.0 and about 5.0 mass-%, and with the usual optimum being between about 3.5 and 4.5 mass-%. Water capacity may be measured by the following procedure: Activation step: Empty pails readings (W1) are taken, then the catalyst is activated in vacuum for about 16 hours overnight at 375° to 400°C; the vacuum of the system should be less than 1 millitorr. The catalyst is cooled to room temperature and the McBain tubes containing the activated catalyst are closed off; a room-temperature reading (W2) of the activated catalyst then is taken. An ice bath then is assembled around the water reservoir so that the water is maintained at 0°C during the adsorption step Adsorption step: The manifold is purged of water vapor by opening the water reservoir; the mercury U-type manometer should read a pressure of 4.6 torr. The tubes are opened and the adsorption starting time recorded. The catalyst is allowed to equilibrate for at least 1.5 hours, the final time is recorded, and the reading (W3) is taken of the catalyst equilibrated with water vapor. The water capacity is calculated as: Capacity, mass-% = [(W2-W3)/(W1-W2)]*100 The gradual accumulation of coke and other deactivating carbonaceous deposits on the catalyst during the operation of the isomerization process will eventually reduce the activity and selectivity of the process to a level such that regeneration is desirable. When the performance of the catalyst has decayed to the point where it is desired to regenerate the catalyst, the introduction of the hydrocarbon charge stock into the conversion zone containing the catalyst is stopped and the conversion zone purged with a suitable gas stream. Regeneration may be performed to restore catalyst activity and selectivity, either in situ or by unloading and regenerating the catalyst in an off-line facility. EXAMPLES Example I An aluminum-phosphate-bound MFI catalyst was prepared to illustrate the transalkylation process of the invention. A first solution was prepared by adding phosphoric acid to an aqueous solution of hexamethylenetetraamine (HMT) in an amount to yield a phosphorus content of the finished catalyst equal to about 11 mass-%. A second solution was prepared by adding an ammonia-exchanged MFI-type zeolite having an Si/AI2 ratio of about 39 to enough alumina sol, prepared by digesting metallic aluminum in hydrochloric acid, to yield a zeolite content in the finished catalyst equal to about 67 mass-%. These two solutions were commingled to achieve a homogeneous admixture of HMT, phosphorus, alumina sol, and zeolite. This admixture was dispersed as droplets into an oil bath maintained at about 93°C. The droplets remained in the oil bath until they set and formed hydrogel spheres having a diameter of about 1.6 mm. The spheres were removed from the oil bath, water washed, air dried, and calcined at a temperature of about 550°C. The calcined spheres then were subjected to steaming at a temperature of about 660°C in an atmosphere of 40% steam in air for 12 hours. The steamed spheres then were metal-impregnated using a solution of tetraamine platinum chloride. Upon completion of the impregnation, the catalyst was dried, oxidized, and reduced to yield a catalyst containing about 460 mass parts per million (ppm) platinum. This isomerization catalyst, utilized to illustrate the process of the invention, was designated as Catalyst A. Example II A silica-bound MFI catalyst was prepared to illustrate the transalkylation process of the invention. Ammonia-exchanged MFI-type zeolite having an Si/AI2 ratio of about 38 was blended with Methocel in a muller. Hydrated amorphous silica powder, Ludox AS-40, was added in proportion to effect a final catalyst MFI content of about 67 mass-%. The mixture and sufficient deionized water to effect an extrudable dough having a moisture content of about 40 mass-% was blended thoroughly in the muller. The dough then was extruded through a cylindrical die to form cylindrical extrudates having a diameter of about 1.6 mm. The extrudates then were water washed, air dried, and calcined at a temperature of about 550°C and then subjected to steaming at a temperature of about 660°C in an atmosphere of 40% steam in air for 12 hours. The steamed extrudates then were column-washed with ammonium nitrate at 88°C for 5 hours, then washed with deionized water and dried at 510°C for about 9 hours. The dried extrudates were metal-impregnated by rolling in a solution of chloroplatinic acid at temperatures of 60-100°C for 6-7 hours. Upon completion of the impregnation, the composite was dried, oxidized, and reduced to yield a catalyst containing about 460 mass parts per million (ppm) platinum. This isomerization catalyst, utilized to illustrate the process of the invention, was designated as Catalyst A'. Example III An alumina-bound catalyst was prepared as a control for comparison of isomerization results with Catalyst A. A first solution of aluminum nitrate was prepared to which was added a second solution of NH4OH. The second solution was added slowly maintaining the pH of the first solution at 8 until gellation of the aluminum occurred. The hydrogel of alumina was slurried with water and filtered to obtain a filter cake having a moisture content of approximately 90 wt.%. A portion of this filter cake was dried at 150°C to a moisture content of about 60 wt. %. This dried material was then ground to produce powdered alumina. An extrudable dough was prepared by combining and mixing about 67 mass-% MFI zeolite with hydrogel alumina and powdered alumina. The dough then was extruded to form cylindrical extrudates. The extrudates were directly subjected to calcination in flowing air at a temperature of about 600°C. The calcined extrudates were then subjected to an impregnation procedure using a solution of tetraamine platinum chloride. The catalyst then was dried, oxidized, and reduced to yield a catalyst containing about 400 mass-ppm platinum. This reference catalyst is designated Catalyst X. Example IV A second control catalyst was prepared for comparison with the catalyst of the invention. This catalyst consisted essentially of approximately 11 mass-% hydrogen-form ZSM-5 zeolite and 0.29 mass-% platinum, with the remainder being alumina binder. MFI zeolite was added to an alumina sol solution, prepared by digesting metallic aluminum in hydrochloric acid, in an amount sufficient to yield a zeolite content in the finished catalyst of about 11 mass-%. A second solution of hexamethylenetetramine (HMT) was prepared and added to the zeolite/alumina sol mixture to give homogeneous admixture. This admixture was then dispersed as droplets into an oil bath maintained at about 93°C. The droplets remained in the oil bath at 150°C until they set and formed hydrogel spheres. These spheres were removed from the oil bath, water washed with a 0.5% ammonia/water solution, air dried, and calcined at a temperature of about 650°C. These calcined spheres were then coimpregnated with a solution of chloroplatinic acid, lead as Pb(N03)2 and hydrochloric acid to yield about 0.2 mass-% platinum and 0.8 mass-% lead on the finished catalyst. The impregnated spheres were oxidized, subjected to a reducing environment of H2 at 565°C, and sulfided with H2S. This catalyst of the known art was designated Catalyst Y. Example V The comparative isomerization performance of the catalyst of the invention and the control catalysts were evaluated using a pilot plant processing non-equilibrium Ca-aromatic feed having the following composition in mol-%: ethylbenzene 7.3-7.4% para-xylene 0.1% meta-xylene 70.8-71.3% ortho-xylene 21.3-21.8% This feed was isomerized at a pressure of 1.3 MPa, a mass hourly space velocity of 10 hr"1, and a hydrogen/hydrocarbon mole ratio of 4. Reactor temperature was adjusted to effect a range of conversion levels, expressed as the disappearance per pass of ethylbenzene. Ethylbenzene, plus the small amount of xylene loss, is converted primarily to benzene and toluene with smaller amounts of light gases. Results of the tests, comparing the loss of valuable xylenes, may be summarized as follows at 65% ethylbenzene conversion: Catalyst: A_ A X Y Temperature, °C 391 364 372 391 Product para-xylene/xylenes, % 23.9 23.7 23.8 24.0 Xylenes loss, % 1.3 2.6 7.4 2.6 Catalyst A of the invention showed substantially lower xylene losses at consistent isomerization conditions than the catalysts of the known art. Catalyst A' of the invention demonstrated exceptional activity as evidenced by the low temperature required to achieve 65% ethylbenzene conversion, along with low xylene losses in comparison to catalysts of the prior art. The relative performance of the catalysts A, X and Y, indicating xylene losses and activity as a function of conversion, is shown in Figure 1. Example VI A series of catalysts of the invention were prepared to compare the effect of the concentration of platinum-group metal on performance in an isomerization process. Calcined spheres having a zeolite content of about 67 mass-% were prepared and steamed according to the procedure described in Example I. The spheres then were impregnated using a solution of tetraamine platinum chloride, dried, oxidized and reduced. The spheres were designated and had platinum contents as follows in mass parts per million: Catalyst Platinum A 460 ppm B 200 ppm C 390 ppm D 540 ppm E 740 ppm Example VII The comparative isomerization performance of the catalysts of the invention having varying platinum contents was evaluated using a pilot plant processing non-equilibrium C8-aromatic feed having the following composition in mol-%: ethylbenzene 7.3% para-xylene 0.1% meta-xylene 71.3% ortho-xylene 21.3% This feed was isomerized at a pressure of a pressure of 1.3 MPa, a mass hourly space velocity of 10 hr-1, and a hydrogen/hydrocarbon mole ratio of 4. The ratios of para-xylene/xylenes was established at about 23.9%. Reactor temperature was adjusted as shown to effect a range of conversion levels, expressed as the disappearance per pass of ethylbenzene. Results of the tests with respect to loss of valuable xylenes may be summarized as follows at 65% ethylbenzene conversion: Catalyst: Temperature. °C Xylene Loss A 392 1.5% B 408 1.4% C 382 1.7% D 392 3.8% E 388 4.7% Xylene loss was minimized at catalyst platinum contents of about 400 mass-ppm and less. Catalyst activity was more favorable at catalyst platinum contents of about 400 mass-ppm and above. Example VIII The effect of steaming temperature on catalyst properties and performance was studied by preparing and testing a series of catalysts. Calcined spheres having a zeolite content of about 67 mass-% were prepared and steamed according to the procedure described in Example I. Steaming was effected either by ramping to the temperature indicated ("ramp") or by immediately subjecting the catalyst to the temperature ("flat"). The spheres then were impregnated to effect a platinum content of the catalyst of 350-460 mass-ppm, dried, oxidized and reduced. The finished catalysts had 4.6 torr water capacities in mass-%, as measured by the previously described McBain water-capacity test, as indicated below: Catalyst Steaming Temp.. °C Water Capacity A 660 ramp 5.02 F 705 ramp 6.01 G 732 ramp 5.44 H 760 ramp 5.26 J 788 ramp 5.36 K 788 flat 4.29 Example IX The comparative isomerization performance of the catalysts of Example VII was evaluated using a pilot plant processing non-equilibrium C8-aromatic feed as described in Example IV. This feed was isomerized at a pressure of a pressure of 1.3 MPa, a mass hourly space velocity of 10 hr-1, a hydrogen/hydrocarbon mole ratio of 4 and a temperature as indicated below. Results of the tests may be summarized as follows at 65% ethylbenzene conversion: Catalyst Temperature. °C Xvlene Loss A 392 1.5% F 357 2.7% G 363 2.5% H 363 2.0% J 357 3.3% K 382 1.4% Reduced water capacity is a concomitant of catalyst activity, and xylene loss is low when this is achieved with high-temperature steaming without ramping. The results are shown graphically in Figure 2. Example X A further series of catalysts was prepared employing high steaming temperatures according to the invention, and performance was studied according to previously described testing procedures. Calcined spheres having a zeolite content of about 67 mass-% were prepared and steamed according to the procedure described in Example I. Steaming was effected in successive zones at temperatures of about 725° and 850°C respectively. Catalysts O and Q were ammonium-exchanged. The spheres then were impregnated to effect a platinum content of the catalyst of 350-460 mass-ppm, dried, oxidized and reduced. The finished catalysts had 4.6 torr water capacities in mass-%, as measured by the previously described McBain water-capacity test, as indicated below: The comparative isomerization performance of the catalysts was evaluated using a pilot plant processing non-equilibrium C8-aromatic feed as described in Example IV. This feed was isomerized at a pressure of a pressure of 1.3 MPa, a mass hourly space velocity of 10 hr"1, a hydrogen/hydrocarbon mole ratio of 4 and a temperature as indicated below. Results of the tests were as follows: Water Ethylbenzene Xylene Catalyst Capacity Temp.. °C Conversion Loss L 3.75 404 61.7% 2.1% M 4.1 415 61.9% 1.15% N 4.2 403 61.1% 1.9% 0 4.2 391 62.6% 1.6% P 4.15 404 65.4% 1.6% Q 4.15 393 67.2% 1.3% Example XI Palladium-containing catalysts of the invention were prepared in the manner described in Example I, except that the steamed spheres were impregnated with tetraamine palladium chloride. The finished catalysts had the following palladium contents in mass-ppm on an elemental basis: Catalyst L 540 Catalyst M 1130 Example XII The isomerization performance of the palladium-containing catalysts of the invention was evaluated using a pilot plant processing non-equilibrium Ca-aromatic feed having the following composition in mol-%: ethylbenzene 7.3% para-xylene 0.1% meta-xylene 71.4% ortho-xylene 21.2% This feed was isomerized at a pressure of 1.3 MPa, a mass hourly space velocity of 10 hr'1, and a hydrogen/hydrocarbon mole ratio of 4. Reactor temperature was adjusted to effect a range of conversion levels, expressed as the disappearance per pass of ethylbenzene. Ethylbenzene, plus the small amount of xylene loss, is converted primarily to benzene and toluene with smaller amounts of light gases. Results of the tests may be summarized as follows at 65% ethylbenzene conversion: Catalyst: L M Temperature, °C 385 382 Product para-xylene/xylenes, % 23.9 23.9 Xylenes loss, % 1.4 1.5 We claim: 1. A process for the isomerization of a non-equilibrium feed mixture of xylenes and ethylbenzene comprising contacting the feed mixture in the presence of hydrogen with a catalyst comprising a zeolitic aluminosilicate comprising a zeolite selected from the group consisting of MFI,MEL,EUO,FER,MFS,MTT,MTW,TON,MOR,FAU and combinations thereof , having a pore diameter of from 5 to 8 Angstroms said finished catalyst having a 4.6 torr water capacity of less than 7 mass-%, a platinum-group metal component and an aluminum phosphate or a silica binder in an isomerization zone at isomeri/ation conditions comprising a temperature of from 300° to 600°C. a pressure of from 100 kPa to 5 MPa, a mass hourly space velocity of from 0.5 to 100 hr"1 to obtain an isomerized product comprising a higher proportion of one xylene isomer selected from the group consisting of para-xylene,meta-xylene, ortho-xylene and combinations thereof than in the feed mixture. 2. The process as claimed in Claim 1 wherein the catalyst contains an amorphous aluminum phosphate binder and is in the form of oil dropped spheres. 3. The process as claimed in Claim 1 wherein the catalyst contains an inert silica binder. 4. The process as claimed in Claim 1 wherein the catalyst comprises oil dropped zeolitic aluminosilicate and an alumina binder. 5. The process as claimed in Claims 1, 2, 3 or 4 wherein the xylene isomer is paraxylene. 6. The process as claimed in Claims 1, 2, 3 or 4 wherein the isomerization conditions comprise a temperature of from 350° to 500°C, a pressure of from 100 kPa to 5 Mpa absolute, and a mass hourly space velocity of from 2 to 50 hr"1. 7. The process as claimed in Claims 1, 2, 3 or 4 wherein the zeolitic aluminosilicate comprise a pentasil zeolite selected from the group consisting of MFI, MEL, MTW and TON. 8. The process as claimed in Claims 1, 2, 3 or 4 wherein the finished catalyst has a 4.6 torr water capacity of 3-5 mass-% or less. 9. The process as claimed in Claim 1 wherein the platinum-group metal component comprises from 200 to 800 mass-ppm platinum on an elemental basis. 10. A process for the isomerization of a non-equilibrium feed mixture of xylenes and ethylbenzene, substantially as hereinbefore described with reference to the foregoing examples and accompanying drawings.

Full Text

This invention relates to a process for the isomerization of a non equiliblem
feed mixtures of xylenes and ethylbenzen

BACKGROUND
The xylenes, para-xylene, meta-xylene and ortho-xylene, are important intermediates which find wide and varied application in chemical syntheses. Para-xylene upon oxidation yields terephthalic acid which is used in the manufacture of synthetic textile fibers and resins. Meta-xylene is used in the manufacture of plasticizers, azo dyes, wood preservers, etc. Ortho-xylene is feedstock for phthalic anhydride production.
Xylene isomers from catalytic reforming or other sources generally do not match demand proportions as chemical intermediates, and further comprise ethylbenzene which is difficult to separate or to convert. Para-xylene in particular is a major chemical intermediate with rapidly growing demand, but amounts to only 20-25% of a typical Cs-aromatics stream. Adjustment of isomer ratio to demand can be effected by combining xylene-isomer recovery, such as adsorption for para-xylene recovery, with isomerization to yield an additional quantity of the desired isomer. Isomerization converts a non-equilibrium mixture of the xylene isomers which is lean in the desired xylene isomer to a mixture which approaches equilibrium concentrations.
Various catalysts and processes have been developed to effect xylene isomerization. In selecting appropriate technology, it is desirable to run the isomerization process as close to equilibrium as practical in order to maximize the para-xylene yield; however, associated with this is a greater cyclic C& loss due to side reactions. The approach to equilibrium that is used is an optimized compromise between high C8 cyclic loss at high conversion (i.e. very close approach to equilibrium) and high utility costs due to the large recycle rate of unconverted Cs aromatics.

Catalysts for isomerization of C8 aromatics ordinarily are classified by the manner of processing ethylbenzene associated with the xylene isomers. Ethylbenzene is not easily isomerized to xylenes, but it normally is converted in the isomerization unit because separation from the xylenes by superfractionation or adsorption is very expensive. One approach is to react the ethylbenzene to form a xylene mixture via conversion to and reconversion from naphthenes in the presence of a solid acid catalyst with a hydrogenation-dehydrogenation function. An alternative widely used approach is to dealkylate ethylbenzene to form principally benzene while isomerizing xylenes to a near-equilibrium mixture. The former approach enhances xylene yield by forming xylenes from ethylbenzene, while the latter approach commonly results in higher ethylbenzene conversion, thus lowering the quantity of recycle to the para-xylene recovery unit and concomitant processing costs.
In the past twenty years or so, crystalline aluminosilicate zeolite-containing catalysts have become prominent for xylene isomerization. US-A-3,856,872,)for example, teaches xylene isomerization and ethylbenzene conversion with a catalyst containing ZSM-5, -12, or -21 zeolite/ US-A-4,626,609 discloses conversion of xylene isomers using a catalyst comprising a composite which has been steamed at 200° to 500°C US-A-4,899,012 teaches the use of a catalyst containing lead, a Group VIII metal, a pentasil zeolite and an inorganic-oxide binder to isomerize xylenes and dealkylate ethylbenzene. Development efforts continue toward realizing economically attractive isomerization catalysts with a superior combination of activity, selectivity and stability.
SUMMARY
A principal object of the present invention is to provide a novel isomerization process for alkylaromatic hydrocarbons. More specifically, this invention is directed to the processing of C8 aromatics to increase the concentration of a desired xylene isomer.
This invention is based on the discovery that improved conversion of Cs aromatics and selectivity for xylene isomerization can be obtained using a zeolitic catalyst component in a finished catalyst composition that has a certain low water

capacity and includes an inert silica or aluminum phosphate binder in the finished composition.
Accordingly, a broad embodiment of the invention is directed toward an alkylaromatics-isomerization process using a catalyst comprising a zeolitic aluminosilicate having a pore diameter of from about 5 to 8Å, a platinum-group metal component and with an inert silica binder or with an aluminum phosphate binder when in the form of an oil dropped spherical catalyst. The process comprises isomerization preferably of a feedstock comprising a non-equilibrium mixture of xylenes and ethylbenzene at isomerization conditions to obtain a product having an increased para-xylene content relative to that of the feedstock. Relevant isomerization conditions comprise a temperature of from about 300° to 600°C, a pressure of from about 100 kPa to 5 MPa, a mass hourly space velocity of from about 0.5 to 100 hr"1. Operation at a temperature of between 350° to 500°C at a mass hourly space velocity of from about 10 to 50 hr"1 is especially favored. MFI-type zeolite is the favored zeolitic aluminosilicate. The catalyst has a low 4.6 torr water capacity of less than about 7 mass-%, and preferably between about 3 and about 5 mass-%. The platinum-group metal preferably comprises platinum in a low concentration of between 100 and 2000 mass-ppm, and optimally between about 200 and 800 mass-ppm, of the catalyst.
These, as well as other objects and embodiments, will become evident from the following detailed description of the invention.
According to the present invention there is provided a process for the isomerization of a non-equilibrium feed mixture of xylenes and ethylbenzene comprising contacting the feed mixture in the presence of hydrogen with a catalyst comprising a zeolitic aluminosilicate comprising a zeolite selected from the group consisting of MFI,MEL,EUO,FER,MFS,MTT,MTW,TON,MOR,FAU and combinations thereof , having a pore diameter of from 5 to 8 Angstroms said finished catalyst having a 4.6 torr water capacity of less than 7 mass-%, a platinum-group metal component and an aluminum phosphate or a silica binder in an isomerization zone at isomerization conditions comprising a temperature of from 300° to 600°C, a pressure of from 100 kPa to 5 MPa, a mass hourly space velocity of from 0.5 to 100 hr" to obtain an isomerized product comprising a higher proportion of one xylene isomer selected from the group consisting of para-xylene,meta-xylene, ortho-xylene and combinations thereof than in the feed mixture.
BRIEF DESCRIPTION OF THE ACCOMPANYING DRAWINGS
Figure 1 shows relative activity and selectivity, in terms of process xylenes losses, of catalysts of the invention and the known art.
Figure 2 shows process xylenes losses as a function of catalyst water capacity.
DETAILED DESCRIPTION OF THE INVENTION
The feedstock to aromatics isomerization comprises isomerizable alkylaromatic hydrocarbons of the general formula C6H(6-n)Rn, where n is an integer from 1 to 5 and R is CH3 C2H5, C3H7, or C4H9, in any combination and including all the isomers thereof to obtain more valuable isomers of the alkylaromatic. Suitable alkylaromatic hydrocarbons include, for example but without so limiting the invention, ortho-xylene, meta-xylene, para-xylene, ethylbenzene, ethyltoluenes, trimethylbenzenes, propylbenzenes, ethyldimethyl-benzenes, diethylbenzenes, methylpropylbenzenes, ethylpropylbenzenes, triethylbenzenes, di-isopropylbenzenes, and mixtures thereof.
Isomerization of a C8-aromatic mixture containing ethylbenzene and xylenes is a particularly preferred application of the invention. Generally such a mixture will have an ethylbenzene content in the approximate range of 5 to 50 mass-%, an ortho-xylene content in the approximate range of 0 to 35 mass-%, a meta-xylene content in the approximate range of 20 to 95 mass-% and a para-xylene content in the approximate range of 0 to 15 mass-%. It is preferred that the feed C8 aromatics comprise a non-equilibrium mixture, i.e., at least one C9-aromatic isomer is present in a concentration that differs substantially from the equilibrium concentration at isomerization conditions. Usually the non-equilibrium mixture is prepared by removal of para- and/or ortho-xylene from a fresh C8-aromatics feed obtained from processes, such as catalytic reforming and/or extraction, for the production and recovery of aromatics from other hydrocarbons.
The alkylaromatic hydrocarbons may be utilized in the present invention as found in appropriate fractions from various refinery petroleum streams, e.g., as individual components or as certain boiling-range fractions obtained by the selective fractionation and distillation of catalytically cracked or reformed hydrocarbons. The isomerizable aromatic hydrocarbons need not be concentrated; the process of this invention allows the isomerization of alkylaromatic-containing streams such as catalytic reformate with or without subsequent aromatics extraction to produce specified xylene isomers and particularly to produce para-xylene. A C8-aromatics feed to the present
process may contain nonaromatic hydrocarbons, i.e., naphthenes and paraffins, in an amount up to 30 mass-%. Preferably the isomerizable hydrocarbons consist essentially of aromatics, however, to ensure pure products from downstream recovery processes.
According to the process of the present invention, an alkylaromatic hydrocarbon feed mixture, preferably in admixture with hydrogen, is contacted with a catalyst of the type hereinafter described in an alkylaromatic hydrocarbon isomerization zone. Contacting may be effected using the catalyst in a fixed-bed system, a moving-bed system, a fluidized-bed system, or in a batch-type operation. In view of the danger of attrition loss of the valuable catalyst and of the simpler operation, it is preferred to use a fixed-bed system. In this system, a hydrogen-rich gas and the feed mixture are preheated by suitable heating means to the desired reaction temperature and then passed into an isomerization zone containing a fixed bed of catalyst. The conversion zone may be one or more separate reactors with suitable means therebetween to ensure that the desired isomerization temperature is maintained at the entrance to each zone. The reactants may be contacted with the catalyst bed in either upward-, downward-, or radial-flow fashion, and the reactants may be in the liquid phase, a mixed liquid-vapor phase, or a vapor phase when contacted with the catalyst.
The alkylaromatic feed mixture, preferably a non-equilibrium mixture of C& aromatics, is contacted with the isomerization catalyst at suitable alkylaromatic-isomerization conditions. Such conditions comprise a temperature ranging from about 100° to 600°C or more, and preferably is in the range of from about 350° to 500°C. The pressure generally is from about 100 kPa to 10 MPa, and more usually no more than about 5 MPa. Sufficient catalyst is contained in the isomerization zone to provide a mass hourly space velocity with respect to the hydrocarbon feed mixture of from about 0.5 to 100 hr"1, and preferably 2 to 50 hr"1; favorable results have been obtained at mass hourly space velocities of at least about 10 hr"1 and higher. The hydrocarbon feed mixture optimally is reacted in admixture with hydrogen at a hydrogen/hydrocarbon mole ratio of about 0.5:1 to about 10:1 or more; other inert diluents such as nitrogen, argon and light hydrocarbons may be present.
The particular scheme employed to recover an isomerized product from the effluent of the reactors of the isomerization zone is not deemed to be critical to the instant invention, and any effective recovery scheme known in the art may be used.
In a separation/isomerization process combination relating to the processing of an ethylbenzene/xylene mixture, a fresh C8-aromatics feed is combined with isomerized product comprising C8 aromatics and naphthenes from the isomerization reaction zone and fed to a para-xylene separation zone from which pure para-xylene is recovered. The para-xylene-depleted stream from the separation zone, comprising a non-equilibrium mixture of C8 aromatics, comprising xylenes and ethylbenzene, is fed to the isomerization reaction zone, where the C8-aromatic isomers are isomerized to near-equilibrium levels to obtain the isomerized product. In this process scheme non-recovered C8-aromatic isomers preferably are recycled to extinction until they are either converted to para-xylene or lost due to side-reactions. Ortho-xylene separation, preferably by fractionation, also may be effected on the fresh C8-aromatic feed or isomerized product, or both in combination, preferably prior to para-xylene separation.
The isomerization catalyst of the present invention comprises a molecular sieve and a refractory inorganic oxide. The preferred molecular sieves are zeolitic alumino-silicates selected from those which have a Si:AI2 ratio greater than about 10, preferably greater than 20, and a pore diameter of about 5 to 8 Angstroms (A). Specific examples of suitable zeolites are the MFI, MEL, EDO, PER, MFS, MTT, MTW, TON, MOR and FAU types of zeolites. Pentasil zeolites MFI, MEL, MTW and TON are preferred, and MFI-type zeolites, often designated ZSM-5, are especially preferred.
The relative proportion of zeolite in the catalyst may range from about 10 to about 99 mass-%, with about 20 to about 90 mass-% being preferred. There is a tradeoff between the zeolite content of the catalyst composite and the pressure, temperature and space velocity of an isomerization operation in maintaining low xylene losses.
A refractory binder or matrix is utilized to facilitate fabrication of the isomerization catalyst. The binder should be uniform in composition and relatively refractory to the conditions used in the process. Suitable binders include inorganic

oxides such as one or more of alumina, magnesia, zirconia, chromia, titania, boria and silica.
A first preferred binder is an amorphous silica. The preferred amorphous silica is a synthetic, white, amorphous silica (silicon dioxide) powder which is classed as wet-process, hydrated silica. This type of silica is produced by a chemical reaction in a water solution, from which it is precipitated as ultra-fine, spherical particles. It is preferred that the BET surface area of the silica is in the range from about 50 to 800 m2/g, especially 120 to 160 m2/g. A low content of sulfate salts is desired, preferably less than 0.3 wt.%. It is especially preferred that the amorphous silica binder be nonacidic, e.g., that the pH of a 5% water suspension be neutral or basic (pH about 7 or above).
A second preferred binder is an amorphous aluminum phosphate. The zeolite and aluminum phosphate binder maybe formed into particles by means well known in the art. A preferred method of preparing the zeolite/aluminum phosphate support involves adding the zeolite either to an alumina sol or a phosphorus compound, forming a mixture of the alumina sol/zeolite/phosphorus compound into particles by employing the oil-drop method described hereinbelow, and calcining the spherical particles.
The preferred oil-drop method-of-preparing the aluminum phosphate bound catalyst is described ia,US-A-4,629,717 Which is incorporated by reference. The technique described in the 717 patent involves the gellation of a hydrosol of alumina which contains a phosphorus compound using the well-known oil-drop method. Generally this technique involves preparing a hydrosol by digesting aluminum in aqueous hydrochloric acid at reflux temperatures of about 80° to 105°C. The ratio of aluminum to chloride in the sol ranges from about 0.7:1 to 1.5:1 mass ratio. A phosphorus compound is now added to the sol. Preferred phosphorus compounds are phosphoric acid, phosphorous acid and ammonium phosphate. The relative amount of phosphorus and aluminum expressed in molar ratios ranges from about 10:1 to 1:100, respectively, on an elemental basis. The zeolite is added to the aluminum phosphate hydrosol and the mixture is gelled. One method of gelling this

mixture involves combining a gelling agent with the mixture and then dispersing the resultant combined mixture into an oil bath or tower which has been heated to elevated temperatures such that gellation occurs with the formation of spheroidal particles. The gelling agents which may be used in this process are hexamethylene tetraamine, urea or mixtures thereof. The gelling agents release ammonia at the elevated temperatures which sets or converts the hydrosol spheres into hydrogel spheres. The spheres are then continuously withdrawn from the oil bath and typically subjected to specific aging and drying treatments in oil and in ammoniacal solution to further improve their physical characteristics. The resulting aged and gelled particles are then washed and dried at a relatively low temperature of about 100° to 150°C and subjected to a calcination procedure at a temperature of about 450° to 700°C for a period of about 1 to 20 hours. The amount of phosphorus-containing alumina component present (as the oxide) in the catalyst can range from about 10 to 70 mass percent and preferably from about 20 to 50 mass percent.
The combined mixture preferably is dispersed into the oil bath in the form of droplets from a nozzle, orifice or rotating disk. Alternatively, the particles may be formed by spray-drying of the mixture at a temperature of from about 425° to 760°C. In any event, conditions and equipment should be selected to obtain small spherical particles; the particles preferably should have an average diameter of less than about 1.0 mm, more preferably from about 0.2 to 0.8 mm, and optimally from about 0.3 to 0.8 mm.
The degree of crystallinity of the aluminum phosphate binder can be controlled by varying the proportion of the phosphorus component. Material that is not in an amorphous phase generally is present as gamma-alumina; as the phosphorus content is decreased, the degree of crystallinity, therefore, is increased. The apparent bulk density of the spheres also varies with the phosphorus content, as a higher proportion of phosphorus decreases the average bulk density. Surface area also is controlled by phosphorus content: gamma-alumina oil-dropped spherical particles typically have surface areas up to about 250 m2/g, while spheroidal particles of aluminum phosphate may have surface areas of up to about 450 m2/g. AI/P atomic

ratios of the binder/matrix generally range from about 1/10 to 100/1, and more typically from about 1/5 to 20/1.
An alternative shape for the catalyst composite is an extrudate. Extrusion is preferred with a silica binder. The well-known extrusion method initially involves mixing of the molecular sieve, either before or after adding metallic components, with the binder and a suitable peptizing agent to form a homogeneous dough or thick paste having the correct moisture content to allow for the formation of extrudates with acceptable integrity to withstand direct calcination. Extrudability is determined from an analysis of the moisture content of the dough, with a moisture content in the range of from 30 to 50 wt. % being preferred. A multitude of different extrudate shapes are possible, including, but not limited to, cylinders, cloverleaf, dumbbell and symmetrical and asymmetrical polylobates.
The catalyst of the present invention may contain a halogen component. The halogen component may be either fluorine, chlorine, bromine or iodine or mixtures thereof, with chlorine being preferred. The halogen component is generally present in a combined state with the inorganic-oxide support. The optional halogen component is preferably well dispersed throughout the catalyst and may comprise from more than 0.2 to about 15 wt.%, calculated on an elemental basis, of the final catalyst. Preferably, however, the catalyst contains no added halogen other than that associated with other catalyst components.
The formed catalyst composite is dried at a temperature of from about 100° to about 320°C for a period of from about 2 to about 24 or more hours and, usually, calcined at a temperature of from 400° to about 650°C in an air atmosphere for a period of from about 0.1 to about 10 hours until the metallic compounds present are converted substantially to the oxide form.
The catalytic composite optimally is subjected to steaming to tailor its acid activity. The steaming may be effected at any stage of the zeolite treatment, but usually is carried out on the composite of zeolite and binder prior to incorporation of the platinum-group metal. Steaming conditions comprise a water concentration of about 5 to 100 volume-%, pressure of from about 100 kPa to 2 MPa, and temperature of from

about 600° to about 1200°C; the steaming temperature preferably is at least about 650°C, more preferably at least about 750°C and optionally may be about 775°C or higher. In some cases, temperatures of about 800° to 850°C or more may be employed. The steaming should be carried out for a period of at least one hour, and periods of 6 to 48 hours are preferred.
Alternatively or in addition to the steaming, the composite may be washed with one or more of a solution of ammonium nitrate, a mineral acid, and/or water. Considering the first alternative, the catalyst may be washed with a solution of about 5 to 30 mass-% ammonium nitrate. When acid washing is employed, a mineral acid such as HCI or HNO3 is preferred; sufficient acid is added to maintain a pH of from more than 1 to about 6, preferably from about 1.5 to 4. The catalyst is maintained in a bed over which the solution and/or water is circulated for a period of from about 0.5 to 48 hours, and preferably from about 1 to 24 hours. The washing may be effected at any stage of the preparation, and two or more stages of washing may be employed.
Prior to addition of the platinum-group metal component, the composite preferably is ion-exchanged with a salt solution containing at least one hydrogen-forming cation such as NH4 or quaternary ammonium. The hydrogen-forming cation replaces principally alkali-metal cations to provide, after calcination, the hydrogen form of the zeolite component.
A platinum-group metal, including one or more of platinum, palladium, rhodium, ruthenium, osmium, and iridium, is an essential component of the present catalyst. The preferred platinum-group metals are platinum and palladium, with platinum being especially preferred. The platinum-group metal component may exist within the final catalyst composite as a compound such as an oxide, sulfide, halide, oxysulfide, etc., or as an elemental metal or in combination with one or more other ingredients of the catalyst composite. It is believed that the best results are obtained when substantially all of the platinum-group metal component exists in a reduced state. The platinum-group metal component generally comprises from about 100 to about 5000 mass-ppm (parts per million) of the final catalyst composite, calculated on an elemental basis, with a level of about 100 to about 2000 mass-ppm being particularly

suitable. When using a platinum component, very low levels of about 200 to 800 mass-ppm of platinum on the catalyst, on an elemental basis, are favored; levels of less than about 600 mass-ppm are especially favored and levels of about 300 to about 500 mass-ppm show excellent results. When using a palladium component, levels of about 400 to 2000 mass-ppm of palladium on the catalyst, on an elemental basis, are favored and levels of from about 500 to about 1200 mass-ppm are especially favored.
The platinum-group metal component may be incorporated into the catalyst composite in any suitable manner. One method of preparing the catalyst involves the utilization of a water-soluble, decomposable compound of a platinum-group metal to impregnate the calcined sieve/binder composite. Alternatively, a platinum-group metal compound may be added at the time of compositing the sieve component and binder. Yet another method of effecting a suitable metal distribution is by compositing the metal component with the binder prior to co-extruding the sieve and binder. Complexes of platinum-group metals which may be employed according to the above or other known methods include chloroplatinic acid, chloropalladic acid, ammonium chloroplatinate, bromoplatinic acid, platinum trichloride, platinum tetrachloride hydrate, platinum dichlorocarbonyl dichloride, tetraamineplatinum chloride, dinitrodiaminoplatinum, sodium tetranitroplatinate (II), palladium chloride, palladium nitrate, palladium sulfate, diaminepalladium (II) hydroxide, tetraaminepalladium (II) chloride, and the like. It is within the scope of the present invention that the catalyst may contain other metal components known to modify the effect of the platinum-group metal component.
After addition of the metal component, the resultant catalytic composite usually is dried at a temperature of about 100° to about 320°C for a period of from about 1 to about 24 or more hours. The dried composite then is calcined at a temperature of from about 400° to about 600°C in an air atmosphere for a period of from about 0.1 to 10 hours to convert the metallic components substantially to the oxide form.
The calcined composite optimally is subjected to a substantially water-free reduction step to insure a uniform and finely divided dispersion of the optional metallic

components. The reduction optionally may be effected on the catalyst as loaded in the isomerization-process reactor of the present invention prior to the startup of the isomerization process. Substantially pure and dry hydrogen (i.e., less than 20 vol. ppm H2O) preferably is used as the reducing agent in this step. The reducing agent contacts the catalyst at conditions, including a temperature of from about 200° to about 650°C and for a period of from about 0.5 to about 10 hours, effective to reduce substantially all of the Group VIII metal component to the metallic state. In some cases the resulting reduced catalyst composite may also be beneficially subjected to presulfiding by a method known in the art to incorporate in the catalyst composite from about 0.01 to about 0.5 mass-% sulfur, on an elemental basis, into the catalyst.
The finished catalyst has a McBain water capacity at 4.6 torr of between about 2 and 7 mass-%, preferably between about 3.0 and about 5.0 mass-%, and with the usual optimum being between about 3.5 and 4.5 mass-%. Water capacity may be measured by the following procedure:
Activation step:
Empty pails readings (W1) are taken, then the catalyst is activated in vacuum for about 16 hours overnight at 375° to 400°C; the vacuum of the system should be less than 1 millitorr. The catalyst is cooled to room temperature and the McBain tubes containing the activated catalyst are closed off; a room-temperature reading (W2) of the activated catalyst then is taken. An ice bath then is assembled around the water reservoir so that the water is maintained at 0°C during the adsorption step
Adsorption step:
The manifold is purged of water vapor by opening the water reservoir; the mercury U-type manometer should read a pressure of 4.6 torr. The tubes are opened and the adsorption starting time recorded. The catalyst is allowed to equilibrate for at least 1.5 hours, the final time is recorded, and the reading (W3) is taken of the catalyst equilibrated with water vapor. The water capacity is calculated as:
Capacity, mass-% = [(W2-W3)/(W1-W2)]*100

The gradual accumulation of coke and other deactivating carbonaceous deposits on the catalyst during the operation of the isomerization process will eventually reduce the activity and selectivity of the process to a level such that regeneration is desirable. When the performance of the catalyst has decayed to the point where it is desired to regenerate the catalyst, the introduction of the hydrocarbon charge stock into the conversion zone containing the catalyst is stopped and the conversion zone purged with a suitable gas stream. Regeneration may be performed to restore catalyst activity and selectivity, either in situ or by unloading and regenerating the catalyst in an off-line facility.
EXAMPLES
Example I
An aluminum-phosphate-bound MFI catalyst was prepared to illustrate the transalkylation process of the invention. A first solution was prepared by adding phosphoric acid to an aqueous solution of hexamethylenetetraamine (HMT) in an amount to yield a phosphorus content of the finished catalyst equal to about 11 mass-%. A second solution was prepared by adding an ammonia-exchanged MFI-type zeolite having an Si/AI2 ratio of about 39 to enough alumina sol, prepared by digesting metallic aluminum in hydrochloric acid, to yield a zeolite content in the finished catalyst equal to about 67 mass-%. These two solutions were commingled to achieve a homogeneous admixture of HMT, phosphorus, alumina sol, and zeolite. This admixture was dispersed as droplets into an oil bath maintained at about 93°C. The droplets remained in the oil bath until they set and formed hydrogel spheres having a diameter of about 1.6 mm. The spheres were removed from the oil bath, water washed, air dried, and calcined at a temperature of about 550°C. The calcined spheres then were subjected to steaming at a temperature of about 660°C in an atmosphere of 40% steam in air for 12 hours.
The steamed spheres then were metal-impregnated using a solution of tetraamine platinum chloride. Upon completion of the impregnation, the catalyst was

dried, oxidized, and reduced to yield a catalyst containing about 460 mass parts per million (ppm) platinum. This isomerization catalyst, utilized to illustrate the process of the invention, was designated as Catalyst A.
Example II
A silica-bound MFI catalyst was prepared to illustrate the transalkylation process of the invention. Ammonia-exchanged MFI-type zeolite having an Si/AI2 ratio of about 38 was blended with Methocel in a muller. Hydrated amorphous silica powder, Ludox AS-40, was added in proportion to effect a final catalyst MFI content of about 67 mass-%. The mixture and sufficient deionized water to effect an extrudable dough having a moisture content of about 40 mass-% was blended thoroughly in the muller. The dough then was extruded through a cylindrical die to form cylindrical extrudates having a diameter of about 1.6 mm. The extrudates then were water washed, air dried, and calcined at a temperature of about 550°C and then subjected to steaming at a temperature of about 660°C in an atmosphere of 40% steam in air for 12 hours.
The steamed extrudates then were column-washed with ammonium nitrate at 88°C for 5 hours, then washed with deionized water and dried at 510°C for about 9 hours. The dried extrudates were metal-impregnated by rolling in a solution of chloroplatinic acid at temperatures of 60-100°C for 6-7 hours. Upon completion of the impregnation, the composite was dried, oxidized, and reduced to yield a catalyst containing about 460 mass parts per million (ppm) platinum. This isomerization catalyst, utilized to illustrate the process of the invention, was designated as Catalyst A'.
Example III
An alumina-bound catalyst was prepared as a control for comparison of isomerization results with Catalyst A. A first solution of aluminum nitrate was prepared to which was added a second solution of NH4OH. The second solution was added slowly maintaining the pH of the first solution at 8 until gellation of the aluminum occurred. The hydrogel of alumina was slurried with water and filtered to obtain a filter

cake having a moisture content of approximately 90 wt.%. A portion of this filter cake was dried at 150°C to a moisture content of about 60 wt. %. This dried material was then ground to produce powdered alumina.
An extrudable dough was prepared by combining and mixing about 67 mass-% MFI zeolite with hydrogel alumina and powdered alumina. The dough then was extruded to form cylindrical extrudates. The extrudates were directly subjected to calcination in flowing air at a temperature of about 600°C.
The calcined extrudates were then subjected to an impregnation procedure using a solution of tetraamine platinum chloride. The catalyst then was dried, oxidized, and reduced to yield a catalyst containing about 400 mass-ppm platinum. This reference catalyst is designated Catalyst X.
Example IV
A second control catalyst was prepared for comparison with the catalyst of the invention. This catalyst consisted essentially of approximately 11 mass-% hydrogen-form ZSM-5 zeolite and 0.29 mass-% platinum, with the remainder being alumina binder. MFI zeolite was added to an alumina sol solution, prepared by digesting metallic aluminum in hydrochloric acid, in an amount sufficient to yield a zeolite content in the finished catalyst of about 11 mass-%. A second solution of hexamethylenetetramine (HMT) was prepared and added to the zeolite/alumina sol mixture to give homogeneous admixture. This admixture was then dispersed as droplets into an oil bath maintained at about 93°C. The droplets remained in the oil bath at 150°C until they set and formed hydrogel spheres. These spheres were removed from the oil bath, water washed with a 0.5% ammonia/water solution, air dried, and calcined at a temperature of about 650°C. These calcined spheres were then coimpregnated with a solution of chloroplatinic acid, lead as Pb(N03)2 and
hydrochloric acid to yield about 0.2 mass-% platinum and 0.8 mass-% lead on the finished catalyst. The impregnated spheres were oxidized, subjected to a reducing environment of H2 at 565°C, and sulfided with H2S. This catalyst of the known art
was designated Catalyst Y.

Example V
The comparative isomerization performance of the catalyst of the invention and the control catalysts were evaluated using a pilot plant processing non-equilibrium Ca-aromatic feed having the following composition in mol-%:
ethylbenzene 7.3-7.4%
para-xylene 0.1%
meta-xylene 70.8-71.3%
ortho-xylene 21.3-21.8%
This feed was isomerized at a pressure of 1.3 MPa, a mass hourly space velocity of 10 hr"1, and a hydrogen/hydrocarbon mole ratio of 4. Reactor temperature was adjusted to effect a range of conversion levels, expressed as the disappearance per pass of ethylbenzene. Ethylbenzene, plus the small amount of xylene loss, is converted primarily to benzene and toluene with smaller amounts of light gases. Results of the tests, comparing the loss of valuable xylenes, may be summarized as follows at 65% ethylbenzene conversion:
Catalyst: A_ A X Y
Temperature, °C 391 364 372 391
Product para-xylene/xylenes, % 23.9 23.7 23.8 24.0
Xylenes loss, % 1.3 2.6 7.4 2.6
Catalyst A of the invention showed substantially lower xylene losses at consistent isomerization conditions than the catalysts of the known art. Catalyst A' of the invention demonstrated exceptional activity as evidenced by the low temperature required to achieve 65% ethylbenzene conversion, along with low xylene losses in comparison to catalysts of the prior art. The relative performance of the catalysts A, X and Y, indicating xylene losses and activity as a function of conversion, is shown in Figure 1.
Example VI
A series of catalysts of the invention were prepared to compare the effect of the concentration of platinum-group metal on performance in an isomerization process.

Calcined spheres having a zeolite content of about 67 mass-% were prepared and steamed according to the procedure described in Example I. The spheres then were impregnated using a solution of tetraamine platinum chloride, dried, oxidized and reduced. The spheres were designated and had platinum contents as follows in mass parts per million:
Catalyst Platinum
A 460 ppm
B 200 ppm
C 390 ppm
D 540 ppm
E 740 ppm
Example VII
The comparative isomerization performance of the catalysts of the invention having varying platinum contents was evaluated using a pilot plant processing non-equilibrium C8-aromatic feed having the following composition in mol-%:
ethylbenzene 7.3%
para-xylene 0.1%
meta-xylene 71.3%
ortho-xylene 21.3%
This feed was isomerized at a pressure of a pressure of 1.3 MPa, a mass hourly space velocity of 10 hr-1, and a hydrogen/hydrocarbon mole ratio of 4. The ratios of para-xylene/xylenes was established at about 23.9%. Reactor temperature was adjusted as shown to effect a range of conversion levels, expressed as the disappearance per pass of ethylbenzene. Results of the tests with respect to loss of valuable xylenes may be summarized as follows at 65% ethylbenzene conversion:
Catalyst: Temperature. °C Xylene Loss
A 392 1.5%
B 408 1.4%
C 382 1.7%
D 392 3.8%
E 388 4.7%
Xylene loss was minimized at catalyst platinum contents of about 400 mass-ppm and less. Catalyst activity was more favorable at catalyst platinum contents of about 400 mass-ppm and above.
Example VIII
The effect of steaming temperature on catalyst properties and performance was studied by preparing and testing a series of catalysts. Calcined spheres having a zeolite content of about 67 mass-% were prepared and steamed according to the procedure described in Example I. Steaming was effected either by ramping to the
temperature indicated ("ramp") or by immediately subjecting the catalyst to the temperature ("flat"). The spheres then were impregnated to effect a platinum content of the catalyst of 350-460 mass-ppm, dried, oxidized and reduced. The finished catalysts had 4.6 torr water capacities in mass-%, as measured by the previously described McBain water-capacity test, as indicated below:
Catalyst Steaming Temp.. °C Water Capacity
A 660 ramp 5.02
F 705 ramp 6.01
G 732 ramp 5.44
H 760 ramp 5.26
J 788 ramp 5.36
K 788 flat 4.29
Example IX
The comparative isomerization performance of the catalysts of Example VII was evaluated using a pilot plant processing non-equilibrium C8-aromatic feed as described in Example IV. This feed was isomerized at a pressure of a pressure of 1.3 MPa, a mass hourly space velocity of 10 hr-1, a hydrogen/hydrocarbon mole ratio of 4 and a temperature as indicated below. Results of the tests may be summarized as follows at 65% ethylbenzene conversion:
Catalyst Temperature. °C Xvlene Loss
A 392 1.5%
F 357 2.7%
G 363 2.5%
H 363 2.0%
J 357 3.3%
K 382 1.4%

Reduced water capacity is a concomitant of catalyst activity, and xylene loss is low when this is achieved with high-temperature steaming without ramping. The results are shown graphically in Figure 2.
Example X
A further series of catalysts was prepared employing high steaming temperatures according to the invention, and performance was studied according to previously described testing procedures. Calcined spheres having a zeolite content of about 67 mass-% were prepared and steamed according to the procedure described in Example I. Steaming was effected in successive zones at temperatures of about 725° and 850°C respectively. Catalysts O and Q were ammonium-exchanged. The spheres then were impregnated to effect a platinum content of the catalyst of 350-460 mass-ppm, dried, oxidized and reduced. The finished catalysts had 4.6 torr water capacities in mass-%, as measured by the previously described McBain water-capacity test, as indicated below: The comparative isomerization performance of the catalysts was evaluated using a pilot plant processing non-equilibrium C8-aromatic feed as described in Example IV. This feed was isomerized at a pressure of a pressure of 1.3 MPa, a mass hourly space velocity of 10 hr"1, a hydrogen/hydrocarbon mole ratio of 4 and a temperature as indicated below. Results of the tests were as follows:
Water Ethylbenzene Xylene
Catalyst Capacity Temp.. °C Conversion Loss
L 3.75 404 61.7% 2.1%
M 4.1 415 61.9% 1.15%
N 4.2 403 61.1% 1.9%
0 4.2 391 62.6% 1.6%
P 4.15 404 65.4% 1.6%
Q 4.15 393 67.2% 1.3%

Example XI
Palladium-containing catalysts of the invention were prepared in the manner described in Example I, except that the steamed spheres were impregnated with tetraamine palladium chloride. The finished catalysts had the following palladium contents in mass-ppm on an elemental basis:
Catalyst L 540
Catalyst M 1130
Example XII
The isomerization performance of the palladium-containing catalysts of the invention was evaluated using a pilot plant processing non-equilibrium Ca-aromatic feed having the following composition in mol-%:
ethylbenzene 7.3%
para-xylene 0.1%
meta-xylene 71.4%
ortho-xylene 21.2%
This feed was isomerized at a pressure of 1.3 MPa, a mass hourly space velocity of 10
hr'1, and a hydrogen/hydrocarbon mole ratio of 4. Reactor temperature was adjusted
to effect a range of conversion levels, expressed as the disappearance per pass of
ethylbenzene. Ethylbenzene, plus the small amount of xylene loss, is converted
primarily to benzene and toluene with smaller amounts of light gases. Results of the
tests may be summarized as follows at 65% ethylbenzene conversion:
Catalyst: L M
Temperature, °C 385 382
Product para-xylene/xylenes, % 23.9 23.9
Xylenes loss, % 1.4 1.5

We claim:
1. A process for the isomerization of a non-equilibrium feed mixture of xylenes and
ethylbenzene comprising contacting the feed mixture in the presence of hydrogen with a
catalyst comprising a zeolitic aluminosilicate comprising a zeolite selected from the
group consisting of MFI,MEL,EUO,FER,MFS,MTT,MTW,TON,MOR,FAU and
combinations thereof , having a pore diameter of from 5 to 8 Angstroms said finished
catalyst having a 4.6 torr water capacity of less than 7 mass-%, a platinum-group metal
component and an aluminum phosphate or a silica binder in an isomerization zone at
isomeri/ation conditions comprising a temperature of from 300° to 600°C. a pressure of
from 100 kPa to 5 MPa, a mass hourly space velocity of from 0.5 to 100 hr"1 to obtain an
isomerized product comprising a higher proportion of one xylene isomer selected from
the group consisting of para-xylene,meta-xylene, ortho-xylene and combinations thereof
than in the feed mixture.
2. The process as claimed in Claim 1 wherein the catalyst contains an amorphous
aluminum phosphate binder and is in the form of oil dropped spheres.
3. The process as claimed in Claim 1 wherein the catalyst contains an inert silica
binder.
4. The process as claimed in Claim 1 wherein the catalyst comprises oil dropped
zeolitic aluminosilicate and an alumina binder.
5. The process as claimed in Claims 1, 2, 3 or 4 wherein the xylene isomer is
paraxylene.
6. The process as claimed in Claims 1, 2, 3 or 4 wherein the isomerization
conditions comprise a temperature of from 350° to 500°C, a pressure of from 100 kPa to 5
Mpa absolute, and a mass hourly space velocity of from 2 to 50 hr"1.

7. The process as claimed in Claims 1, 2, 3 or 4 wherein the zeolitic aluminosilicate
comprise a pentasil zeolite selected from the group consisting of MFI, MEL, MTW and
TON.
8. The process as claimed in Claims 1, 2, 3 or 4 wherein the finished catalyst has a
4.6 torr water capacity of 3-5 mass-% or less.
9. The process as claimed in Claim 1 wherein the platinum-group metal component
comprises from 200 to 800 mass-ppm platinum on an elemental basis.
10. A process for the isomerization of a non-equilibrium feed mixture of xylenes and
ethylbenzene, substantially as hereinbefore described with reference to the foregoing
examples and accompanying drawings.

Documents:

804-del-2000-abstract.pdf

804-del-2000-claims.pdf

804-del-2000-correspondence-others.pdf

804-del-2000-correspondence-po.pdf

804-del-2000-description (complete).pdf

804-del-2000-drawings.pdf

804-del-2000-form-1.pdf

804-del-2000-form-19.pdf

804-del-2000-form-2.pdf

804-del-2000-form-3.pdf

804-del-2000-gpa.pdf

804-del-2000-petition-137.pdf

804-del-2000-petition-138.pdf

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Patent Number

216734

Indian Patent Application Number

804/DEL/2000

PG Journal Number

13/2008

Publication Date

31-Mar-2008

Grant Date

19-Mar-2008

Date of Filing

05-Sep-2000

Name of Patentee

UOP LLC,

Applicant Address

25 EAST ALGONQUIN ROAD, DES PLAINES, ILLINOIS 60017-5017, UNITED STATES OF AMERICA.

Inventors:

#	Inventor's Name	Inventor's Address
1	SANJAY B. SHARMA	25 EAST ALGONQUIN ROAD, DES PLAINES, ILLINOIS 60017-5017, UNITED STATES OF AMERICA, U.S.A.
2	BENJAMIN D. RILEY	25 EAST ALGONQUIN ROAD, DES PLAINES, ILLINOIS 60017-5017, UNITED STATES OF AMERICA
3	SERGEY V. GUREVICH	25 EAST ALGONQUIN ROAD, DES PLAINES, ILLINOIS 60017-5017, UNITED STATES OF AMERICA
4	GREG A. ROSINSKI	25 EAST ALGONQUIN ROAD, DES PLAINES, ILLINOIS 60017-5017, UNITED STATES OF AMERICA

PCT International Classification Number

C07C 15/02

PCT International Application Number

N/A

PCT International Filing date

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1			NA