AU1015100A - Hydrocarbon conversion process using a zeolite bound zeolite catalyst - Google Patents

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Application Number: Lodged: *e 0 *000 *0*e .0.0 Invention Title: HYDROCARBON CONVERSION PROCESS USING A ZEOLITE BOUND ZEOUITE CATALYST 00 000* 0.0.

0 00..

The following statement is a full description of this invention, including the best method of performing it known to us HYDROCARBON CONVERSION PROCESS USING A ZEOLITE BOUND ZEOLITE CATALYST BACKGROUND OF THlE INVENTION This invention relates to zeolite bound zeolites which have enhanced activity, selectivity, and/or activity maintenance when utilized in hydrocarbon conversion processes.

l0 Zeolite materials, both natural and synthetic, have been demonstrated to have catalytic properties for various types of hydrocarbon conversion processes. In addition, zeolite materials have been used as adsorbents, :catalyst carriers for various types of hydrocarbon conversion processes, and other applications. Zeolites are complex crystalline aluininosilicates which form a network of A104 and SiO4 tetrahedra linked by shared oxygen atoms. The negativity of the tetrahedra is balanced by the inclusion of cations such as alkali or alkaline earth metal ions. In the manufacture some zeolites, non-metallic cations, such as tetramethylammonium (TMA) or tetrapropylammonium (TPA), are present in the synthesis. The interstitial spaces or channels formed by the crystalline network enable zeolites to be used as molecular sieves in separation processes and catalysts for chemical reactions and catalysts carriers in a wide variety of hydrocarbon 4 .conversion processes.

Zeolites include materials containing silica and optionally alumina, and materials in which the silica and alumina portions have been replaced in whole or in part with other oxides. For example, germanium oxide, tin oxide, and mixtures thereof can replace the silica portion. Boron oxide, iron oxide, gallium oxide, indium oxide, and mixtures thereof can replace the alumina portion. Unless otherwise specified, the terms "zeolite" and "zeolite material" as used herein, shall mean not only materials containing silicon and, optionally, aluminum atoms in the crystalline lattice structure thereof, but also materials which contain suitable replacement atoms for such silicon and aluminum.

Synthetic zeolites are usually prepared by crystallization from a supersaturated synthesis mixture. The resulting crystalline product is then dried and calcined to produce a zeolite powder. Although the zeolite powder has good adsorptive properties, its practical applications are severely limited because the powder has no significant mechanical strength.

Mechanical strength may be conferred on a zeolite by forming a zeolite aggregate such as a pill, sphere, or extrudate. An extrudate can be 1o formed by extruding the zeolite in the presence of a non-zeolitic binder and drying and calcining the resulting extrudate. Examples of such binders include materials such as alumina, silica, titanium, and various types of days.

a Although such bound zeolite aggregates have much better mechanical strength than the zeolite powder, when the bound zeolite is used in a catalytic conversion process, the activity, selectivity, activity maintenance, or combinations thereof of the catalyst can be reduced because of the binder. For instance, since the binder is typically present in an amount of up to about 60 wt% of zeolite, the binder dilutes the adsorptive properties of the zeolite. In addition, since the bound zeolite is prepared by extruding the zeolite with the binder and subsequently drying and calcining the extrudate, the amorphous binder can penetrate the pores of the zeolite, otherwise block access to the pores of the zeolite, or slow the rate of mass transfer to the pores of the zeolite which can reduce the effectiveness of the zeolite when used in hydrocarbon conversion processes and other applications. Still further, when a bound zeolite is used in catalytic processes, the binder may affect the chemical reactions that are taking place within the zeolite and also may catalyze undesirable reactions which can result in the formation of undesirable products.

Thus, there is a need for a hydrocarbon conversion process which utilizes a zeolite catalyst which overcomes, or at least mitigates the above described problems.

SUMMARY OF THE INVENTION It has been suprisingly discovered that a zeolite catalyst which comprises first zeolite particles and utilizes second zeolite particles as a binder results in a catalyst which provides a means of controlling reactions associated with the binder and has improved mass transfer of reactants to the catalyst, and greater access of the reactants to the pores of the zeolite. The acidity of the second zeolite particles is preferably carefully controlled the acidity of the second zeolite can be the same as the first zeolite particles or the acidity of the second zeolite particles can be higher or lower than the first zeolite particles, so that the performance of the catalyst is further enhanced. The zeolite catalysts of the present invention have enhanced performance when utilized in hydrocarbon conversion processes. The zeolite 15 catalyst of the present invention finds particular application in :..hydrocarbon conversion processes where catalyst acidity in combination with zeolite structure are important for reaction selectivity. Examples of such processes include catalytic cracking, alkylation, dealkylation, dehydrogenation, disproportionation, and transalkylation reactions. The catalyst of the present invention also finds particular application in other hydrocarbon conversion processes in which carbon containing compounds are changed to different carbon containing compounds. Examples of such processes include hydrocracking, isomerization, dewaxing, oligomerization, and 25 reforming processes.

BRIEF DESCRIPTION OF THE DRAWINGS Figures 1-4 are graphs demonstrating the activity, paraxylene selectivity, paraxylene yield and benzene yield respectively for the zeolite bound zeolite catalysts of this invention.

DETAILED DESCRIPTION OF THE INVENTION The present invention is directed to a process for converting organic compounds by contacting the organic compounds under conversion conditions with a zeolite bound zeolite catalyst. The zeolite bound zeolite catalyst comprises first zeolite particles which preferably have an average particle size greater than about 0.1 micron average particle size and a binder comprising second zeolite particles having an average particle size of less than said first particles. Typical zeolite particles used as catalysts in hydrocarbon conversion processes are normally bound with silica or alumina or other commonly used amorphous binders to enhance the mechanical strength of the zeolite. The zeolite bound zeolite catalysts of the present invention preferably do not contain significant amounts of non zeolitic binders. Instead, the first zeolite particles of the present invention are bound by the second zeolite particles. The second zeolite particles have an average particle size that is smaller than the first zeolite particles. Preferably, the second zeolite particles bind the first zeolite particles by adhering to 15 the surface of the first particles thereby forming a matrix or bridge structure which also holds the first crystals particles together. More preferably, the second zeolite particles bind the first zeolite particles by intergrowing so as to form a coating or partial coating on the larger first zeolite crystals.

Although the invention is not intended to be limited to any theory of operation, it is believed that the advantages of the zeolite bound zeolite catalyst are obtained by the second zeolite controlling the accessibility of the acid sites on the external surfaces of the first zeolite to reactants.

Acid sites existing on the external surface of a zeolite catalyst are believed to affect reactants entering the pores of the zeolite and products exiting the pores of the zeolite. In line with this theory, since the acidity of the second zeolite is carefully selected, the second zeolite does not significantly adversely affect the reactants exiting the pores of the first zeolite which can occur with conventionally bound zeolite catalysts and may beneficially affect the reactants exiting the pores of the first zeolite. Still further, since the second zeolite is not amorphous but, instead, is a molecular sieve, hydrocarbons have increased access to the pores of the first zeolite during hydrocarbon conversion processes. Regardless of the theories proposed, the catalyst, when used in catalytic processes, has the improved properties which are disclosed herein.

The term "average particle size" as used herein, means the average diameter of the particles, number average of the major axis and minor axis.

The terms "acidity", "lower acidity" and "higher acidity" as applied to zeolite are known to persons skilled in the art. The acidic properties of lo zeolite are well known. However, with respect to the present invention, a distinction must be made between acid strength and acid site density. Acid sites of a zeolite can be a Bronsted acid or a Lewis acid. The density of the acid sites and the number of acid sites are important in determining the acidity of the zeolite. Factors directly influencing the acid strength are the chemical composition of the zeolite framework, relative concentration and type of tetrahedral atoms, (ii) the concentration of the extra-framework cations and the resulting extra-framework species (iii) the local structure of the zeolite, the pore size and the location, within the crystal or at/near the surface of the zeolite, (iv) the pretreatment conditions and presence of co-adsorbed molecules. The amount of acidity is related to the degree of isomorphous substitution provided, however, such acidity is limited to the loss of acid sites for a pure SiO 2 composition. As used herein, the terms "acidity", "lower acidity" and "higher acidity" refers to the concentration of acid sites irregardless of the strength of such acid sites which can be measured by ammonia adsorption.

Examples of zeolites suitable for use in the present invention include large pore zeolites, medium pore zeolites, and small pore zeolites. A large pore zeolite generally has a pore size of >7 A and includes zeolite L, zeolite Y, zeolite X, MAZ, MEI, FAU, EMT, offretite, omega, Beta, mordenite, ZSM-3, ZSM-4, ZSM-18, and ZSM-20. A medium pore size catalyst generally has a pore size <7A, preferably from about 5A to about 6.8A; and generally the pore apertures consist of about 10 to 12, preferably about 10, membered ring structures and include MFI, MEL, MTW, EUO, MTT, HEU, FER, TON, zeolite beta, ZSM-34, ZSM-38, -3r'EFS501J)OC Page 6 sze zeolite has a pore size from about 3A to about 5.,AK Generally, the por petrsothstructure consist Of from about 8 to 10, preferably about 8. membered ring structurites and smallupoe typles icuch as

HA

ERI, 1(F1 LEV, and, LTA. Examp-Le ofma lezolites includie ans 4, ZK-5, zeolite A, zeolite T1, gmeliflite, dijnoptfoie hb~ n erionite. The zeolites can also comprise gallosi.lcates and titanosilicates.

The silica to al~umina ratio of the first zeolite will generally depend.

upon the particular hydrocarbon, process in which the catalyst is utilized. Generally, however, the :first zeolite will have a silica to alumina ratio of at least 2:1, preferably a silica to alumina ratio in~ the range of from about 10:1 to about 1,000:1, more preferably froma about 20:1 to about 500:1. 'When the catalyst is utilized in the disproportionation of toluene or the cracking of hydiocarbons, the silica to lumnarato i peferably 301 to about 125:1. The average particle size of the first zeoite is preferably from abu .1 toaotb5mcons.

in many applications, the average paicle size is preferably fto bu 2 to about 6 micronS, and more preferably from about 2 to about 4 :20 micronS. In other applications such as the cracking of hydrocarbons, the preferred average Pal-ticle size is from about 0.1 to about microns.

The second zeolite particles are of smaller size than the first zeolite 2S particles. The second zeolite particles generally have an average particle size of less than 1 micron, preferably from about 0.1 to less tha~n 0.5 micron. The silica to alumriina ratio of the second zeolite will generally depend upon the particular hydrocarbon process in which the catalyst is utilized. Generally the silica to aluinfa ratio will be at least 2:1. In applications where low aciditY is desired, the second zeolite preferAlY has a silica to alumina ratio greater than the silica to alumina -ratio of the first zeolite, and more preferably is greater than 200:1, 300:1, 500:1, 1,000:1I, etc. In certain applications, the second zeolite is silicalite, the second zeolite is MIFI substantialy free of Th~e pore size of the second zeolite will preferably be a pore size that does not significantlY restrict access of the hydocarbon feedstreaxli to the pores of the first zeolite. For instance, when the materials of the feedstream which are to be converted have a size from to 6.8A, the second zeolite will preferably be a large pore zeolite or a medium pore zeolite. The second zeolite is preferably present in an amount in the range of from about 10 to about 60 by weight based on the weight of the first zeolite.

The zeolite bound zeolites catalysts of the present invention preferably have an Adsorption Index (AI) greater than 1.00 and more preferably greater than 1.10, and most preferably greater than 1.20 1.25, to 1.30, etc.. The term "Adsorption Index", is defined as the ratio of the weight percent of hydrocarbon (toluene when the first zeolite of the zeolite bound zeolite comprises large pore zeolite or medium pore zeolite and n-hexane when the first zeolite of the zeolite bound zeolite comprises small pore zeolite) adsorbed per amount by weight of zeolite 15 in the zeolite bound zeolite catalyst of the present invention to the weight percent of hydrocarbon (toluene for large pore zeolite and medium pore zeolite and n-hexane for small pore zeolite) adsorbed per amount (by weight) of the first zeolite in the silica bound zeolite catalyst prior to conversion of the silica (after drying and calcination) to the second zeolite of the zeolite bound zeolite catalyst. If the zeolite bound zeolite is not prepared by converting an amorphous silica to a second zeolite, the "Adsorption Index", is defined as the ratio of the weight percent of hydrocarbon (toluene when the first zeolite of the zeolite bound zeolite comprises large pore zeolite or medium pore 25 zeolite and n-hexane when the first zeolite of the zeolite bound zeolite comprises small pore zeolite) adsorbed per amount by weight of zeolite in the zeolite bound zeolite catalyst of the present invention to the weight percent of hydrocarbon (toluene for large pore zeolite and medium pore zeolite and n-hexane for small pore zeolite) adsorped per amount (by weight) of the first zeolite of the zeolite bound zeolite catalyst when the first zeolite is bound by 30% by weight of amorphous silica using the method disclosed in Step B. of Example 1. In the determination of the Adsorption Index, all variables used in the procedure to determine the hydrocarbon adsorption of the catalyst remain constant and only the catalyst differs. The Adsorption Index 8 finds particular application when the second zeolite is a medium pore or large pore zeolite.

Procedures which can be utilized to determine the adsorption of toluene for large pore zeolite and medium pore zeolite and n-hexane for small pore zeolite to measure the Adsorption Index of a zeolite catalyst are known to persons skilled in the art. A preferred procedure, hereinafter referred to as the "ZHA Procedure", involves the use of a thermogravimetric analyzer for measuring the weight of adsorbed hydrocarbon(i.e.,n-hexane or toluene) and comprises first pre-treating a zeolite catalyst, in this example a small pore zeolite, in a 210 mL/min air flow with the following temperature conditions: holding the catalyst at 30 degrees C for one minute, next increasing the temperature at degrees C/min to 150 degrees C; holding the catalyst for 10 minutes at 15 150 degrees C, then increasing the temperature at 20 degrees C/min to 450 degrees C; holding the catalyst at 450 degrees C for 45 minutes, and then cooling the catalyst to 30 degrees C. The weight of the cooled catalyst is then measured and this weight is hereinafter referred to as Next, a gas containing n-hexane (in this example) in nitrogen is 20 introduced into the chamber containing the catalyst at a temperature 30 degrees C (P/Po of 0.26) continuously for 60 minutes. For this procedure, P is the partial pressure of adsorbant hydrocarbon and Po is total pressure. The gas is then switched to nitrogen and the sample is desorbed for 60 minutes at 30 degrees C. The weight of the catalyst is then measured and this weight is hereinafter referred to as The weight percent of hydrocarbon (hexane in this example) adsorbed [(W2-W1) W1] x 100. When toluene is used for catalysts containing a large pore or medium pore zeolite, the process is the same except that the P/Po of the toluene is preferably 0.15. However, other values of P/Po can be used if precautions are taken to prevent condensation in the transfer lines to the sample chamber. The Adsorption Index can be calculated using the following formula: AI W(ZBZ) W(SBZ) 9 wherein W(ZBZ) is weight percent of hydrocarbon (toluene for large and medium pore zeolites or n-hexane for small pore zeolites) adsorbed per amount (by weight) of zeolite bound zeolite (total zeolite weight [excluding any unconverted amorphous silica [excluding any unconverted amorphous silica or other non-zeolite material]); and W(SBZ) is weight percent of hydrocarbon (toluene for large and medium pore zeolites or n-hexane for small pore zeolites) adsorbed per amount (by weight) of zeolite which zeolite is bound with x fraction by weight of amorphous silica. This i weight is calculated by measuring total percent hydrocarbon adsorbed (by zeolite amorphous silica) and dividing that number by W(SBZ) is measured on the same silica bound 15 first zeolite aggregate which is converted to the zeolite bound zeolite which is used to measure W(ZBZ) or, if the zeolite bound zeolite is not prepared by converting an amorphous silica to a second zeolite, is measured on a bound zeolite which zeolite is the same as the first zeolite of the zeolite bound zeolite and is bound with 30% by weight of amorphous silica using the method disclosed in Step B. of Example 1.

The Adsorption Index was calculated for the catalysts set forth below.

With respect to a silica bound ZK5 zeolite containing 70 wt.% ZK5 and 25 a ZK5 bound with ZK5, the procedure to determine the Adsorption Index was carried out under standard conditions of n-hexane uptake (p/po 0.25, T 30*C). The silica bound zeolite had a 6.63 wt.% ofnhexane uptake, while the zeolite bound zeolite (100% zeolite) had a nhexane uptake of 11.10%. These results were converted to the same 3o amount of zeolite. The silica bound ZK5 had a hexane adsorption of 9.45 wt.% (6.63/0.70). The Adsorption Index was determined to be 1.17 (11.10/9.45). A zeolite KL bound zeolite KL and a silica bound zeolite KL containing at least 30% by weight silica were tested using the procedure described above except that toluene was used as the adsorbent. The toluene adsorption was 5.4 wt.% for the silica bound zeolite KL and 10.0 wt.% for the zeolite KL bound zeolite KL. The Adsorption Index was determined to be 1.29.

The catalyst used in the conversion process of the invention can be prepared using various processes but is preferably prepared by a three step procedure. The first step involves the synthesis of a zeolite.

Processes for preparing zeolites are known in the art. For example, with respect to the preparation of a MFI zeolite, a preferred process comprises preparing a solution containing tetrapropyl ammonium to hydroxide or bromide, alkali metal oxide, an oxide of aluminum, an oxide of silicon and water, heating the reaction mixture to a temperature of 80 0 C to 200 0 C for a period of from about four hours to eight days. The resulting gel forms solid crystal particles which are separated from the reaction medium, washed with water and dried.

15 The resulting product may then be optionally calcined in air at temperatures of 400-550 0 C for a period of 10-40 hours to remove tetrapropylammonium (TPA) cations.

o When an MFI is preferred, the MFI can be identified in terms of mole 20 ratios of oxides as follows: 0.9 0.2 M2/nO:Al203:5-500 SiO2:ZH20 wherein M is selected from the group consisting of a mixture of alkali metal cations, preferably sodium, and organic ions such as tetralkylammonium cations, the alkyl groups preferably containing carbon atoms, and z ranges from 0 to 40. In a more preferred form, the MFI zeolite contains a silica to alumina mole ratio of from about 10:1 to about 300:1.

Next, a silica-bound zeolite is prepared preferably by mulling a mixture comprising the zeolite crystals, a silica gel or sol, water and optionally an extrusion aid until a homogeneous composition in the form of an extrudable paste develops. The silica binder used in preparing the silica bound zeolite aggregate is preferably a silica sol and preferably contains only very minor amounts of alumina, less than 2,000 ppm, and more preferably less than 1,000 ppm of alumina.

The amount of silica formulated at this stage is such that the content of the zeolite in the dried extrudate will range from about 30 to 90% by weight, more preferably from about 55 to 85% by weight, with the balance being primarily silica, e.g. about 15 to 45% by weight silica.

The resulting paste is then molded, e.g. extruded, and cut into small strands, 2mm diameter extrudates, which are dried at 100-150 0

C

for a period of 4-12 hours. Preferably the dried extrudates are then lo calcined in air at a temperature of from about 400 0 C to 550 0 C for a period of from about 1 to 10 hours. This calcination step also destroys the extrusion aid if present.

Optionally, the silica-bound aggregate can be made into a very small S. 15 particles which have application in fluid bed processes such as catalytic cracking. This preferably involves mixing the zeolite with a silica containing matrix solution so that an aqueous solution of zeolite and silica binder is formed which can be sprayed dried to result in small fluidizable silica-bound aggregate particles. Procedures for preparing such aggregate particles are known to persons skilled in the art. An example of such a procedure is described by Scherzer (Octaine- Enhancing Zeolitic FCC Catalysts, Julius Scherzer, Marcel Dekker, Inc. New York, 1990). The fluidizable silica-bound aggregate particles, e: like the silica bound extrudates described above, would then undergo the final step described below to convert the silica binder to a second zeolite.

The final step in the three step catalyst preparation process is the conversion of the silica present in the silica-bound catalyst to a second zeolite which serves to bind the residual the zeolite particles together.

The first zeolite crystals are thus held together without the use of a significant amount of non-zeolite binder. The resulting zeolite catalyst preferably contains less than 10% by weight (based on the weight of the first and second zeolite) of non zeolitic binder, more preferably less than 5% by weight, and, most preferably less than 3% by weight of non zeolitic binder.

To prepare the zeolite bound zeolite, the silica-bound aggregate is preferably first aged in an appropriate aqueous solution at elevated temperature. Next, the contents of the solution and the temperature at which the aggregate is aged should be selected to convert the amorphous silica binder into a second zeolite. In certain applications, disproportionation of toluene, it is preferable that the second zeolite be the same as the initially bound zeolite or a crystallographic match for the initially bound zeolite. The newly-formed zeolite is to produced as crystals. The crystals may grow on and/or adhere to the initial zeolite crystals, and may also be produced in the form of new intergrown crystals, which are generally much smaller than the initial crystals, of sub-micron size. These newly formed crystals may grow together and interconnect thereby causing the larger crystals to 15 become bound together.

The nature of the zeolite formed in the secondary synthesis conversion S'of the silica to zeolite may vary as a function of the composition of the secondary synthesis solution and synthesis aging conditions. The 20 secondary synthesis solution is an aqueous ionic solution containing a source of hydroxy ions sufficient to convert the silica to the desired zeolite. For instance, in the manufacture of an MFI-type zeolite, the solution will have an initial molar ratio of OH:ions to SiO2 up to a level of up to about 1.2. An MFI-type zeolite may be formed by aging in a solution containing a source of tetrapropylammonium (TPA) and optionally a source of alumina and optionally a source of Na+; a M1Ltype zeolite may be formed by aging in a solution containing a source of tetrabutyl ammonium and a source of Na+. Suitable aqueous solutions for these and other medium pore zeolites are known to persons skilled in the art. It is important, however, that the aging solution be of a composition which will not cause the silica present in the bound zeolite extrudate to dissolve out of the extrudate. Also, in some instances, it is preferable that the zeolite formed in the secondary synthesis is less acidic than the core zeolite.

In a preferred embodiment of the invention, the aqueous ionic solution in which the bound zeolite is aged contains a source of hydroxy ions (preferably NaOH). When manufacturing an MFI-type zeolite, the initial molar ratio of OH' to SiO2 is preferably at a level of up to about 1.2, more preferably from about 0.05 to 1.2, and most preferably from about 0.07 to 0.15. This treatment causes the silica binder to be converted substantially to a MFI-type zeolite, but of lower acidity as reflected by having a significantly higher silica to alumina ratio. The solution also contains a template source of tetraalkyl ammonium ions for MFI-type zeolite) and may optionally include a source of alumina and a source of Na+ ions. The silica to alumina ratio of the converted binder is thus controlled by controlling the composition of the aqueous solution. If the silica binder material which is converted and the secondary synthesis mixture are substantially free of alumina, 15 the converted material is more appropriately called silicalite.

It important that the aging solution have a pH which is not too alkaline. This may be achieved, when producing a MFI-type bound zeolite, by using a solution having an initial molar ratio of OH':SiO2 of 0.05 to 1.2. Generally ratios of 0.07 to 0.15 are preferred. If the ratio is too high the solution has high alkalinity), the bound crystals will dissolve in the solution. The silica binder, instead of being converted into zeolite crystals on the core zeolite crystals, or forming intergrown crystals, dissolves out of the extrudate and crystallizes 25 outside the zeolite core crystals in the surrounding mother liquor. This weakens or destroys the integrity of the extrudate. The more alkaline the aging solution the more the silica dissolves out of the extrudate. Aging of the zeolite extrudate in the aging solution is preferably conducted at elevated temperatures, generally in the range of from about 95 to 2000C, more preferably in the range of about 130 to 1700C, most preferably in the range of about 145 to 1550C. Aging time may range from about 20 to 140 hours, more preferably from about 60 to 140 hours, most preferably from about 70 to 80 hours.

After aging, the zeolite is separated from solution, washed, dried and calcined.

A preferred process for preparing a binderless MFI-type zeolite comprises mixing a solution containing sodium ions e.g. aqueous sodium hydroxide, with a solution containing TPA ions, a TPA halide solution, such as TPA bromide. The silica-bound extrudate of the second step may then be added and the composition heated to preferably 140 to 160°C, most preferably about 150 0 C. The material is maintained at this temperature for 60 to 140 hours, preferably 70 to hours. The resulting product may then be washed and dried. To 'o remove the TPA+ species, the product is calcined after washing, preferably at a temperature of 450 to 550 0

C.

15 In certain applications, disproportionation of toluene, the most preferred MFI bound catalyst may be described as a two phase catalyst comprising a first phase of particles of MFI-type zeolite having a silica to alumina ratio of from about 10:1 to about 200:1. The second phase is comprised of MFI-type zeolite having a higher silica to alumina ratio 20 in excess of about 200:1. The second phase consists of small intergrown crystals that cover or partially cover the first phase particles and of small crystalline particles that adhere to the surface of the first phase particles. Preferably the first phase particles have a silica to alumina ratio of from about 20:1 to 150:1, more preferably from about 50:1 to 125:1, and the second phase has a silica to alumina ratio greater than about 200:1, more preferably greater than about 300:1. The particle size of the first phase particles may be in the range of conventional MFI-type zeolite particle size, an average particle size of from about 0.1 to 15 microns, more preferably from about microns, and most preferably about 2 to 4 microns. The second phase particles which serve to adhere the first phase particles together are of much smaller size, generally having an average particle size of less than one micron, preferably of from about 0.1 to less than 0.5 micron.

The zeolites of the present invention may be further ion exchanged as is known in the art either to replace at least in part the original alkali metal present in the zeohte with a different cation, e.g. a Group 1B to VIII Periodic Table metal such as nickel, copper, zinc, palladium, platinum, calcium or rare earth metal, or to provide a more acidic form of the zeolite by exchange of alkali metal with intermediate ammonium, followed by calcination of the ammonium form to provide the acidic hydrogen form. The acidic form may be readily prepared by ion exchange using a suitable acidic reagent such as ammonium nitrate. The zeolite may then be calcined at a temperature of 400- 550 0 C for a period of 10-45 hours to remove ammonium cations. Ion lo exchange is preferably' conducted after formation of the two phase zeolite bound zeolite catalyst. Particularly preferred cations are those which render the material catalytically active, especially for certain hydrocarbon conversion reactions. These include hydrogen, rare earth metals, and metals of Groups IA, IIA, IVA, TB, JIB, IIIB, IVB, and VIII of the Periodic Table of the Elements.

The zeolite-bound catalysts as described above have mechanical strength which is at least comparable to and often stronger than that of silica-bound zeolite aggregate. For example typical crush strengths of the silica-bound and zeolite-bound materials compare as follows: CRUSH STRENGTH SiO2 bound extrudate 0.46 kgf/cm 2 IMI-type-bound 1.28 kgf/cm 2 *i The zeolite-bound catalyst also has absorption properties comparable with that of the zeolite powder. 0 The most preferred zeolite-bound MFI catalysts for use in reactions such as toluene disproportionation comprise discrete, rounded core MFI-type crystal particles having crystal size of from about 2-4 microns and a silica/alumina ratio of 60:1 to 100:1 and binder particles of smaller crystal size, generally from about 0.1 to less than 0.5 microns, having a silica/alumina ratio of about 200:1 or greater, from 750:1 to 5,000:1.

06EFS501.DOC Page 16 Processes for preparing the catalysts useful in the present invention are disclosed in the copending U.S. applications 08/335,222, filed November 7, 1994, now U.S. Patent 5,460,769, and 08/344,034, filed November 11, 1994, the disclosures of which are hereby incorporated by reference.

The zeolite bound zeolites of the present invention can be used in processing hydrocarbonaceous feedstocks. Hydrocarbonaceous feedstocks contain carbon compounds and can be from many different to sources, such as virgin petroleum fractions, recycle petroleum fractions, tar sand oil, and, in general, can be any carbon containing fluid susceptible to zeolitic catalytic reactions. Depending on the type of processing the hydrocarbonaceous feed is to undergo, the feed can contain metal or can be free of metals. Also, the feed it can also have 15 high or low nitrogen or sulfur impurities.

The conversion of hydrocarbonaceous feeds can take place in any convenient mode, for example, in fluidized bed, moving bed, or fixed bed reactors depending on the types of process desired.

Since the zeolite bound zeolite catalysts of the present invention have controlled acidity and do not contain a conventional binder which can adversely affect the access and/or contact of reactants to and with the active sites of the catalyst and can also cause undesirable side reactions to occur, the zeolite bound zeolite of the present invention by itself or in combination with one or more catalytically active substances can have high activity, high selectivity, high activity maintenance, or combinations thereof when used as catalysts for a variety of organic, hydrocarbon compound conversion processes.

Examples of such hydrocarbon conversion processes include, as nonlimiting examples, the following: The catalytic cracking of a naphtha feed to produce light olefins. Typical reaction conditions include from about 500°C to about 750°C, pressures of subatmospheric or atmospheric, generally ranging up to about nMENDED SEE L t~ME~DED S~AEE~ 17 atmospheres (gauge) and residence time (volume of the catalyst feed rate from about 10 milliseconds to about seconds.

The catalytic cracking of high molecular weight hydrocarbons to lower weight hydrocarbons. Typical reaction conditions for catalytic cracking include temperatures of from about 400*C to about 700°C, pressures of from about 0.1 atmosphere (bar) to about atmospheres, and weight hourly space velocities of from about 0.1 to about 100.

0*04.0 The transalkylation of aromatic hydrocarbons in the presence of polyalkylaromatic hydrocarbons. Typical 15 reaction conditions include a temperature of from about 200*C to about 500"C, a pressure of from about atmospheric to about 200 atmospheres, a weight hourly space velocity of from about 1 to about 1000 and an aromatic hydrocarbon/polyalkylaromatic hydrocarbon mole ratio of from about 1/1 to about 16/1.

The isomerization of aromatic xylene) feedstock components. Typical reaction conditions for such include a temperature of from about 230°C to about 510*C, a 25 pressure of from about 0.5 atmospheres to about atmospheres, a weight hourly space velocity of from about 0.1 to about 200 and a hydrogen/hydrocarbon mole ratio of from about 0 to about 100.

The dewaxing of hydrocarbons by selectively removing straight chain paraffins. The reaction conditions are dependent in large measure on the feed used and upon the desired pour point. Typical reaction conditions include a temperature between about 200 0 C and 450 0 C, a pressure up to 3,000 psig and a liquid hourly space velocity from 0.1 to 18 The alkylation of aromatic hydrocarbons, benzene and alkylbenzenes, in the presence of an alkylating agent, olefins, formaldehyde, alkyl halides and alcohols having 1 to about 20 carbon atoms. Typical reaction conditions include a temperature of from about 100*C to about 500°C, a pressure of from about atmospheric to about 200 atmospheres, a weight hourly space velocity of from about 1hr 1 to about 2,000hr- I and an aromatic hydrocarbon/alkylating agent mole ratio of from about 1/1 to about 20/1.

The alkylation of aromatic hydrocarbons, benzene, with long chain olefins, C 1 4 olefin. Typical reaction 15 conditions include a temperature of from about 50*C to about 200°C, a pressure of from about atmospheric to about 200 atmospheres, a weight hourly space velocity of from about 2 hr- 1 to about 2000 hr- 1 and an aromatic hydrocarbon/olefin mole ratio of from about 1/1 to about 20 20/1. The resulting product from the reaction are long chain alkyl aromatics which when subsequently sulfonated have particular application as synthetic detergents; The alkylation of aromatic hydrocarbons with light olefins to provide short chain alkyl aromatic compounds, the alkylation of benzene with propylene to provide cumene.

Typical reaction conditions include a temperature of from about 10°C to about 200°C, a pressure of from about 1 to about 30 atmospheres, and an aromatic hydrocarbon weight hourly space velocity (WHSV) of from 1 hr- 1 to about 50 hr- 1 The hydrocracking of heavy petroleum feedstocks, cyclic stocks, and other hydrocrack charge stocks. The zeolite bound zeolite catalyst will contain an effective amount of 19 at least one hydrogenation component of the type employed in hydrocracking catalysts.

The alkylation of a reformate containing substantial quantities of benzene and toluene with fuel gas containing short chain olefins (e.g.,ethylene and propylene) to produce mono- and dialkylates. Typical reaction conditions include temperatures from about 100*C to about 250*C, a pressure of from about 100 to about 800 psig, a WHSV -olefin from about 0.4 hr- 1 to about 0.8 hr- 1 a WHSV -reformate of from about 1 hr- 1 to about 2 hr- 1 and, optionally, a gas recycle from about to 2.5 vol/vol fuel gas feed.

The alkylation of aromatic hydrocarbons, benzene, toluene, xylene, and naphthalene, with long chain olefins,

C

1 4 olefin, to produce alkylated aromatic lube base stocks. Typical reaction conditions include temperatures from about 160*C to about 260*C and pressures from about 350 to 450 psig.

The alkylation of phenols with olefins or equivalent alcohols to provide long chain alkyl phenols. Typical reaction conditions include temperatures from about 25 100"C to about 250*C, pressures from about 1 to 300 psig and total WHSV of from about 2 hr- to about 10 hr- 1 The conversion of light paraffins to olefins and/or aromatics. Typical reaction conditions include temperatures from about 425*C to about 760 C and pressures from about 10 to about 2000 psig.

The conversion of light olefins to gasoline, distillate and lube range hydrocarbons. Typical reaction conditions include temperatures of from about 175C to about 375°C and a pressure of from about 100 to about 2000 psig.

Two-stage hydrocracking for upgrading hydrocarbon streams having initial boiling points above about 200 0 C to premium distillate and gasoline boiling range products or as feed to further fuels or chemicals processing steps in a first stage using in the first stage the zeolite bound zeolite catalyst comprising one or more catalytically active substances, e.g.,a Group VIII metal, and the effluent from the first stage would be reacted in a second stage using a second zeolite, zeolite Beta, comprising one or more catalytically active substances, a Group VIII metal, as the catalyst. Typical reaction conditions include temperatures from about 315°C to about 455*C, a pressure from about 400 to about 2500 psig, hydrogen 15 circulation of from about 1000 to about 10,000 SCF/bbl and a liquid hourly space velocity (LHSV) of from about 0.1 to A combination hydrocracking/dewaxing process in the 20 presence of the zeolite bound zeolite catalyst comprising a hydrogenation component and zeolite Beta. Typical reaction conditions including temperatures from about i' 350*C to about 400 0 C, pressures from about 1400 to about 1500 psig, LHSVs from about 0.4 to about 0.6 and a hydrogen circulation from about 3000 to about 5000 SCF/bbl.

The reaction of alcohols with olefins to provide mixed ethers, the reaction of methanol with isobutene and/or isopentene to provide methyl-t-butyl ether (MTBE) and/or t-amyl methyl ether (TAME). Typical conversion conditions including temperatures from about 20"C to about 200°C, pressures from 2 to about 200 atm, WHSV (gram-olefin per hour gram-zeolite) from about 0.1 hr- 1 to about 200 hr- 1 and an alcohol to olefin molar feed ratio from about 0.1/1 to about 5/1.

96EFS501.DOC Page 21 The disproportionation of toluene to make benzene and paraxylene. Typical reaction conditions including a temperature of from about 200°C to about 760°C, a pressure of from about atmospheric to about atmosphere (bar), and a WHSV of from about 0.1 hr-1 to about 30 hr- 1 The conversion of naphtha C6 C10) and similar mixtures to highly aromatic mixtures. Thus, normal and aslightly branched chained hydrocarbons, preferably having a boiling range above about 40"C, and less than about 2000C, can be converted to products having a substantial higher octane aromatics content by contacting the hydrocarbon feed with the zeolite at a temperature in 15 the range of from about 400*C to 600°C, preferably 480°C S: to 550*C at pressures ranging from atmospheric to 40 bar, and liquid hourly space velocities (LHSV) ranging from 0.1 to The adsorption of alkyl aromatic compounds for the purpose of separating various isomers of the compounds.

The conversion of oxygenates, alcohols, such as methanol, or ethers, such as dimethylether, or mixtures thereof to hydrocarbons including olefins and aromatics ith reaction conditions including a temperature of from about 275°C to about 600°C, a pressure of from about atmosphere to about 50 atmospheres and a liquid'hourly space velocity of from about 0.1 to about 100; The oligomerization of straight and branched chain olefins having from about 2 to about 5 carbon atoms. The oligomers which are the products of the process are medium to heavy olefins which are useful for both fuels, gasoline or a gasoline blending stock, and chemicals.

The oligomerization process is generally carried out by contacting the olefin feedstock in a gaseous state phase with a zeolite bound zeolite at a- temperature in the range of from about 250°C to about 800°C, a LHSV of from about 0.2 to about 50 and a hydrocarbon partial pressure of from about 0.1 to about 50 atmospheres. Temperatures below about 250°C may be used to oligomerize the feedstock when the feedstock is in the liquid phase when contacting the zeolite bound zeolite catalyst. Thus, when the olefin feedstock contacts the catalyst in the liquid phase, temperatures of from about 10°C to about 250°C may be used.

The conversion of C2 unsaturated hydrocarbons (ethylene 15 and/or acetylene) to aliphatic C0612 aldehydes and converting said aldehydes to the corresponding C6-12 alcohols, acids, or esters.

In general, therefore, catalytic conversion conditions over a catalyst 20 comprising the zeolite bound zeolite include a temperature of from about 100*C to about 760°C, a pressure of from about 0.1 atmosphere (bar) to about 200 atmospheres (bar), a weight hourly space velocity of from about 0.08hr 1 to about 2,000hrl.

Although many hydrocarbon conversion processes prefer that the second zeolite crystals have lower acidity to reduce undesirable reactions external to the first zeolite crystals, some processes prefer that the second zeolite crystals have higher acidity, the acidity be tailored so as to catalyze desirable reactions. Such processes are of two types. In the first type, the acidity and the crystallographic type of the second zeolite is tailored to match the acidity and the crystallographic type of the first zeolite. By doing so, the catalytically active material per weight of formed catalyst will be increased thereby resulting in increased apparent catalyst activity. Such a catalyst would also be benefited by the greater adsorption, accessibility and reduced nonselective surface acidity. Toluene disproportionation is an example of a process that would be benefited by this type of catalyst. With toluene disproportionation, a non-selective, equilibrium mixture of xylenes in the product is desired and, therefore, greater formed catalyst apparent activity is more beneficial than improved selectivity.

The second type of process that can be benefited by tailoring the acidity of the second zeolite phase is one where two or more reactions are taking place within the zeolite catalyst. In such a process, the acidity and/or the crystallographic structure of the second phase zeolite may to be tailored so that it is different than that of the first zeolite, but does not have to be essentially void of acidic sites. Such a catalyst would be comprised of two different zeolites that could each be separately tailored to promote or inhibit different reactions. A process using such a catalyst would not only benefit from greater apparent catalyst :i 15 activity, greater zeolite accessibility, and reduced non-selective surface acidity possible with zeolite bound zeolites, it would also benefit from a tailored product.

Combined xylene isomerization/ethylbenzene dealkylation processes 20 would benefit from this type of catalyst. An isomerization/ ethylbenzene dealkylation catalyst could be tailored such that ethylbenzene dealkylation would primarily occur within the first zeolite crystals, and xylenes isomerization would primarily occur within the second zeolite crystals. By tailoring a catalyst in this way, a 25 balance between the two reactions can be achieved that could not otherwise be achieved with a catalyst containing only one zeolite.

The zeolite-bound catalyst of the present invention has particular application in the vapor phase disproportionation of toluene. Such vapor phase disproportionation comprises contacting toluene under disproportionation conditions with the zeolite bound zeolite catalyst to yield a product mixture which comprises a mixture of unreacted (unconverted) toluene, benzene and xylene. In the more preferred embodiment, the catalyst is first selectivated prior to use in the disproportionation process to enhance conversion of toluene to xylene and to maximize the catalyst selectivity towards the production of paraxylene. Processes for selectivating the catalyst are known to persons skilled in the art. For instance, selectivation may be accomplished by exposing the catalyst in a reactor bed to a thermally decomposable organic compound, e.g. toluene, at a temperature in excess of the decomposition temperature of said compound, e.g. from about 480 0 C to about 650 0 C, more preferably 540 0 C to 650 0 C, at a WHSV in the range of from about 0.1 to 20 lbs of feed per pound of catalyst per hour, at a pressure in the range of from about 1 to 100 atmospheres, and in the presence of 0 to about 2 moles of hydrogen, more preferably from about 0.1 to about 2 moles of hydrogen per mole of organic compound, and optionally in the presence of 0-10 moles of nitrogen or another inert gas per mole of organic compound. This process is conducted for a period of time until a sufficient quantity of coke has deposited on the catalyst surface, generally at least about 2% 15 by weight and more preferably from about 8 to about 40% by weight of coke. In a preferred embodiment, such a selectivation process is conducted in the presence of hydrogen in order to prevent rampant formation of coke on the catalyst. The initial mole ratio of hydrogen gas to toluene present in the toluene feed stream can be reduced during S 20 the selectivation process after a significant amount of coke has been deposited on the catalyst surface.

Selectivation of the catalyst can also be accomplished by treating the catalyst with a selectivation agent such as an organosilicon compound.

Organosilicon compounds suitable for use as a selectivation agent are disclosed in United States Patent 5,365,003, which is hereby incorporated by reference.

When used in the vapor phase disproportionation of toluene, the catalyst more preferably comprises a first phase of particles of MFItype zeolite crystallites having a micron average particle size from about 3 to about 4, a silica to alumina mole ratio of from about 70 to about 80:1, having adhered structurally to the surfaces thereof particles of a second MFI or MFI-type binder phase having an average particle size of less than about 0.1 micron and having a alumina to silica ratio in excess of about 300:1 to about 10,000:1 and most preferably greater than 900:1.

Selectivated versions of the zeolite bound zeolite when used in vapor phase disproportionation exhibit a higher selectivity towards the production of paraxylene than conventional selectivated MFI catalysts.

The catalyst of the invention is more resistant to coking than conventional catalysts used in disproportionating. For instance, a selectivation process involving the disproportionation of coke for a conventional catalyst normally requires at least 24 hours until sufficient coke has built up to the point where paraxylene production is maximized. Conventional MFI catalysts are less resistant to coking and can therefore be selectivized in less time. However, because a 15 conventional ZSM-5 catalyst is less resistant to coking, it will be more quickly deactivated during its use in disproportionation, giving rise to shorter run cycles. Thus, one of the major advantages of the use of the zeolite bound- zeolite in vapor phase disproportionation, is longer disproportionation cycle lengths.

Once the catalyst has been selectivated to the desired degree, e.g., greater than 80% paraxylene selectivity at on-oil conditions, reactor selectivation conditions are changed to disproportionation conditions.

These disproportionation conditions include a temperature between about 400 0 C and 550 0 C, more preferably between about 425 0 C and 510 0 C, at a hydrogen to toluene mole ratio of from 0 to about preferably between about 0.1 and 5 and more preferably from about 0.1 to less than 1, at a pressure between about 1 atmosphere and f00 atmospheres and utilizing WHSV of between about 0.5 and 50. One of the particular advantages of the use of the catalyst in disproportionation is that it provides a good paraxylene selectivity at H2/toluene mole ratios of less than 1, e.g. at about The disproportionation process may be conducted as a batch, semicontinuous or continuous operation using a fixed or moving bed catalyst system deposited in a reactor bed. The catalyst may be regenerated after coke deactivation by burning off the coke to a desired extent in an oxygen-containing atmosphere at elevated temperatures as known in the art.

The zeolite bound zeolite of the present invention is also especially useful as a catalyst in a process for isomerizing one or more xylene isomers in a Cs aromatic feed to obtain ortho-, meta-, and para-xylene in a ratio approaching the equilibrium value. In particular, xylene isomerization is used in conjunction with a separation process to to manufacture para-xylene. For example, a portion of the para-xylene in a mixed Cs aromatics stream may be recovered using processes known in the art, crystallization, adsorption, etc. The resulting stream is then reacted under xylene isomerization conditions to restore ortho-, meta-, and paraxylenes to a near equilibrium ratio. At the same time, 15 part of the ethylbenzene in the feed is converted to xylenes or to products which are easily separated by distillation. The isomerate is blended with fresh feed and the combined stream is distilled to remove heavy and light by-products. The resultant Cs aromatics stream is then recycled to repeat the cycle.

It is important that xylene isomerization catalysts produce a near equilibrium mixture of xylenes and it is also sometimes desirable that the catalysts convert ethylbenzene with very little net loss of xylenes. The zeolite bound zeolites find particular application in this regard.

The silica to alumina ratios of the first zeolite and second zeolite can be selected to balance xylene isomerization and ethylbenzene dealkylation while minimining undesirable side reactions. Accordingly, an additional aspect of the present invention is to provide a hydrocarbon conversion process which comprises contacting a Cs aromatic stream containing one or more xylene isomers or ethylbenzene or a mixture thereof, under isomerization conditions with the zeolite bound zeolite.

In the vapor phase, suitable isomerization conditions include a temperature in the range 250 0 C 600 0 C, preferably 300 0 C 550*C, a pressure in the range 0.5 50 atm abs, preferably 10 25 atm abs, and a weight hourly space velocity (WHSV) of 0.1 to 100, preferably 0.5 to Optionally, isomerization in the vapor phase is conducted in the presence of 3.0 to 30.0 moles of hydrogen per mole of alkylbenzene. If hydrogen is used, the catalyst should comprise 0.1 to 2.0 wt% of a hydrogenation/dehydrogenation component selected from Group VIII of the Periodic Table, especially platinum, palladium, or nickel. By Group VIII metal component is meant the metals and their compounds such as oxides and sulfides.

In the liquid phase, suitable isomerization conditions include a o1 temperature in the range 150*C 375 0 C, a pressure in the range 1 200 atm abs, and a WHSV in the range 0.5 50. Optionally, the isomerization feed may contain 10 to 90 wt% of a diluent such as toluene, trimethylbenzenes, naphthenes, or paraffins.

15 The zeolite bound zeolites of the present invention are especially useful as a catalyst in a process for cracking a C4+ naphtha feed, particularly a C4 290*C naphtha feed to produce low molecular weight olefins, e.g., C2 through C 4 olefins, particularly ethylene and propylene. Such a process is preferably carried out by contacting the naphtha feed at temperatures ranging from 500 0 C to about 750 0 C, more preferably 550*C to 675 0 C, at a pressure from subatmospheric up to atmospheres, but preferably from about 1 atmosphere to about 3 atmospheres.

25 The zeolite bound zeolites of the present invention are especially useful as a catalyst in the transalkylation of polyalkylaromatic hydrocarbons.

Examples of suitable polyalkylearomatic hydrocarbons include di-, tri-, and tetra-alkyl aromatic hydrocarbons, such as diethylbenze n e, triethylbenzene, diethylmethylbenzene (diethyltoluene), diisopropylbenzene, triisopropylbenzene, diisopropyltoluene, dibutylbenzene, and the like. Preferred polyalkylaromatic hydrocarbons are the dialkyl benzenes. Particularly preferred polyalkylaromatic hydrocarbons are diisopropylbenzene and diethylbenzene.

The transalkylation process will preferably have a molar ratio of aromatic hydrocarbon to polyalkylaromatic hydrocarbon of preferably from about 0.5:1 to about 50:1, and more preferably from about 2:1 to about 20:1. The reaction temperature will preferably range from about 340 0 C to 500 0 C to maintain at least a partial liquid phase, and the pressure will be preferably in the range of about 50 psig to 1,000 psig, preferably 300 psig to 600 psig. The weight hourly space velocity will range from about 0.1 to The following example illustrates a process for the preparation of a zeolite bound zeolite catalyst useful in the present invention.

29 Example 1 A. PREPARATION OF MFI-TYPE

ZEOLITE:

20.4 kg of a synthesis mixture with a molar composition of: 0.45 Na20/0.9 TPA Br/0.125 A1203/10 SiO 2 /146H20 was aged at 1500C for five days without stirring in a 25 liter stainless steel autoclave. The resulting product was washed with water to pH 10.2 and dried at 120 0 C for about 16 hours. A portion of the product was calcined in air at 4750C for 32 hours.

Characteristics of the calcined product: XRD: Pure NMI.

SEM: -3 micron spherical crystallites.

Elemental: SiO2/A1203 ratio B. PREPARATION SILICA-BOUND

PARTICLES

A portion of the calcined product of above was formed into 2 mm diameter extrudates with silica as follows: COMPONENTS USED FOR

OUANTITY

25 PREPARATION (grams) MFI crystals 200.00 (dried at 2500C for 2 hours) H20 49.75 Si02 gel (AEROSIL 300) 18.82 Silica sol (NALCOAG 1034A) 197.24 Extrusion aid 1.07 (hydroxypropyl methyl cellulose) The above components were mixed in a food processor in the order shown. About 6 minutes after adding the extrusion aid, a thick and smooth paste was obtained. The paste was extruded into 2 mm diameter extrudates. The extrudates were dried overnight at i30C and then calcined. at 510 0 C for 6 hours in air.

Composition of calcined silica-bound extrudates: MFI 69.96 wt% SiO2 binder 30.04 wt% C. CONVERSION TO ZEOLITE BOUND ZEOLITE Preparation synthesis mixture: o COMPONENTS USED FOR QUANTITY PREPARATION (grams) Solution A: NaOH pellets 1.16 H20 24.63 Additional rinse water 10.02 Solution B: Tetrapropylammoniumbromide 8.00 H20 25.47 Additional rinse water 18.89 Solution A was poured together with the additional water into a 300 ml stainless steel autoclave.

Solution B was poured together with the additional water into the contents of the autoclave. The two solutions were mixed.

Finally, 60.04 grams of the silica-bound MFI-type extrudates prepared as above (pre-dried for 2 hours at 150 0 C) were added to the synthesis mixture in the autoclave.

The composition of the mixture in the autoclave was: 0.48 Na20/1.00 TPA Br/10 SiO2/147 (OH':SiO2 ratio -0.1) The amount of IFI crystals in this mixture was 40.5 wt% based on the total weight of the mixture. The autoclave was heated up to 150 0 C and kept at this temperature for 71 hours. After this aging period, the autoclave was opened and the product was io collected.

S-The product was washed in a Beuchner funnel with 4250 ml of water in 11 portions and the pH of the last wash water was 10.2.

The product was dried for three hours at 150 0 C. Weight of product recovered after drying: 62.5 grams. The product was significantly harder than the starting silica-bound extrudates.

The product was calcined in air for 18 hours at 500 0 C to remove the TPA'-speies. Weight loss after calcination was 5.8 wt%.

The product was characterized by x-ray diffraction (XRD), scanning electron microscopy (SEM) and hexane adsorption,.

with the following results: XRD: crystallinity increase vs. starting silica bound 25 extrudates: 32 (height increase of peaks at d values between 3.02 and 2.96 A).

SEM: 10,000 times micrographs showed that the -3 micron MTFI crystallites of preparation were and coated with intergrown, newly formed submicron crystallites. There was no visible trace of the amorphous silica which was plainly visible in the micrographs of the startin g-extru dates.

Silica To Alumina ratio 32 MFI crystallites of preparation A 80:1 Newly formed submicron crystallites 900:1 The following examples illustrate the selectivation and disproportionation processes of the invention.

Example 2 The calcined, zeolite-bound catalyst described in Example 1 was to selectivated by feeding toluene across the catalyst under the following conditions to produce a high selectivity catalyst: Selectivation Conditions Hours 340 Temperature (oF) 1100 Pressure (Psig) 225 WHSV (#Feed/#Cat/hr.) 1 H2:Feed Toluene Ratio (moles) (Ratio Initial 0.5:1 H2:Feed Tol.

decreased during selectivation to Ratio expedite selectivation) Final 0.35:1 H2:Feed Tol. Ratio Hydrocarbon Partial Pressure Initial 60 Psia Final 63 Psia After about 340 hours at selectivation conditions, selectivation was terminated at the point where about 92-94% selectivity to para-xylene would be achieved at normal disproportionation conditions.

Following selectivation, the high selectivity catalyst was used for the selective .disproportionation of toluene (STDP) under the following test conditions: 33 On-Oil Conditions Temperature (oF) Varied within 8050-8600 Pressure (Psig) 300 WHSV 3# feed/lb. cat./hr.

H2:Feed Toluene Ratio (moles) 2:1 Hydrocarbon Partial Pressure 93.4 Psia The on-oil catalyst performance for the high selectivity catalyst is shown in Figs. 1-4.

Upon completion of the test runs described above, the zeolite-bound catalyst used in the tests was once again selectivated under the selectivation conditions described above for an additional 20 hours to 15 produce an ultra-high selective catalyst. Additional STDP tests were then conducted under the STDP conditions described above. These results are also shown in Figures 1-4.

t By selectivating the catalyst further after running at disproportionation conditions, some of the catalyst's activity was lost as demonstrated in Figure 1. The temperature required to achieve a targeted conversion was a few degrees greater than with a conventional ZSM-5 catalyst. However, Figure 2 demonstrates that the para-xylene (PX) selectivity of the zeolite-bound catalyst was 25 increased to 94-95%, an ultra-high selectivity for STDP.

Example 3 A conventional ion exchanged, alumina-bound disproportionation catalyst was selectivated by feeding toluene across the catalyst. The zeolite-bound MFI catalyst of this invention was also selectivated. Selectivation conditions were as follows: CaalstConventional Zeolite-Bound CaalstZSM-5'

-MFI

SELE CTJVATION CONDITIONS Hours 55 163 Temperature( 0 F) 1075 1100 Pressure (Psig) 225 225 WHSV 2 1 H2:Feed Toluene Ratio 0.5:1 0.25:1 Hydrocarbon Partial 60 164.2 Pressure (Psia) Following selectivation, the conventional HZSM-5 catalyst and the zeolite-bound iMII catalyst of this invention were used for the disproportionation of toluene under test conditions shown in Table 1 below. The zeolite bound zeolite catalyst was evaluated under 3 separate test conditions as shown in Table 1. On-oil catalyst performance for each catalyst is also shown in the table.

TABLE 1 On-Oil Conditions Zeolite-bound '.Test Case 1 Test Case 2 Test'Case 3 Temperature(oF) 850 843 827 839 Pressure (Psig) 300 300 300 300 WHSV 3 3 3 4.2 hr.) H2:Feed Toluene 2 2 2 Ratio (moles) Hydrocarbon 93.4 93.4 93.4 196.1 Partial Pressure 5 On-Oil Catalyst Performance Zeolite-boundZSM-5 Toluene Conversion 24.1 28.4 25.0 30.1 Paraxylene Selectivity 82.1 94.0 94.8 93.0 (PX/[PX+MX+OX]X100) Benzene Yield 10.2 13.0 11.1 13.6 Xylene Yield 12.1 13.4 12.4 14.7 Cs-Yield 1.1 0.9 0.6 0.6 Co+Yield 0.5 0.6 0.5 0.8 Selectivation of the conventional catalyst was completed in less than hours. At this point, the conventional catalyst had a coke content of about 34% by weight. By comparison, the zeolite-bound catalysts of this invention typically contained less than 15% by weight coke.

The fact that zeolite-bound MFI catalyst selectivated much slower than conventional MFI catalyst even though more severe selectivation conditions were used is significant. The long time required for the zeolite bound zeolite catalyst selectivation demonstrates that it is very resistant to coking. Since coking is the major cause for catalyst deactivation, the zeolite-bound catalyst deactivates more slowly than conventional ZSM-5 and therefore offers longer cycle lengths. The reason for the zeolite-bound catalyst's resistance to coking is that it has lower MFI nonchannel surface acidity and therefore lower activity for the formation of coke precursors. Lower deactivation rate due to greater resistance to coking is one of the advantages of this invention.

The standard ZSM-5 catalyst was not selectivated as long nor to the degree of the zeolite-bound catalyst because considerable activity loss was apparent during selectivation even though the standard catalyst's selectivation conditions were considerably less severe than those of the zeolite-bound catalyst. The catalyst could have been selectivated to a greater selectivity but at a considerable sacrifice of catalyst activity.

The selectivation was terminated at a point which best balanced catalyst activity and selectivity.

15 The results cearly show that the zeolite-bound catalyst is more active and selective following selectivation. Furthermore, the greater time of selectivation even though greater severity selectivation conditions were used, demonstrates the zeolite-bound catalyst's resistance to coking.

To further demonstrate zeolite-bound catalyst's resistance to coking, the catalyst was subjected to on-oil operations at the severe conditions -of 4 WHSV, 8350 F, 300 psig, and 0.5 H2:oil ratio for a period of 17 days. Initial catalyst lined-out performance at these conditions was: Conversion: 31.0% PX Selectivity: 94.7% BZ Yield: 14.0% PX Yield: 13.9% After 17 days, the catalyst performance was: Conversion: 31.0% PX Selectivity: 95.1% BZ Yield: 14.2% PX Yield: 14.1% 37 This test demonstrates no activity loss (actually a slight gain) during 17 days. Thus, the catalyst is very resistant to coking.

The zeolite-bound MFI catalyst has increased catalyst activity, greater PX selectivity, improved PX yield, and greater resistance to deactivation by coking than does conventional MFI catalyst.

EXAMPLE 4 .0 The zeolite-bound ZSM-5 catalyst of this invention was selectivated and evaluated under the four different test conditions shown in Table 2.

*0 ewe* 00 0 0-004 0 S

S

S

S.

*SSS

TABLE 2 Selectivation Conditions Hours 168 Temperature __1100 Pressure (Psig) _225 WHSV (#feed/#cat./hr.) 1

H

2 :Feed Toluene Ratio (Ratio decreased Initial 0.25:1 during selectivation to expedite selectivation) Final 0.15:1 Hydrocarbon Partial Pressure Initial 64.2 Final 66.0 a.

a..

On-Oil Conditions Ts et et Ts ase C s "Case_ Case-4 Temperature 0 F) 835 I813 835 818 Pressure (Psig) 300 300 300 300 WHSV 4.2 3 3 3 H2:Feed Toluene Ratio 0.5:1 0.5:1 2:1 2:1 Hydrocarbon Partial 196.1 196.1 93.4 93.4 Pressure (Psia) On-Oil Catalyst Test TTest Test Test Performance *Case 1 Case 2 Case 3 Case 4 Feed(100% Toluene) 31.0 30.2 28.2 25.0 Conversion(wt. Paraxylene Selectivity 94.6 94.0 95.6 95.9 (PX/[PX+Mx+OX]X 100) IBenzene Yield 14.0 13.4 12.7 10.9 Xylene Yield 14.7 14.8 12.8 11.9 C.r-Yield 0.9 0.8 1.7 1.3 1 C q+ Yield 0.9 1 0.6 In Example 4, the H 2 :oil ratio was lower during selectivation to reduce selectivation time from the 340 hours shown in Example 2. Cases 1 and 2 demonstrate the very high xylenes production that can b achieved with the zeolite-bound catalyst at very reasonable temperatures and low hydrogen:oil ratios. Case 4 shows how an ultrahigh selectivity of 95.9% can be achieved at a reasonable conversion and temperature.

a Example A zeolite bound zeolite catalyst having substantially the same composition as the catalyst described in Example 1 was evaluated for its ability to crack a light cat naphtha feed.

The test was carried out by first steaming the zeolite bound zeolite catalyst at 704*C for 16 hours for the purpose of aging the catalyst.

Next, the naphtha feed was passed over the zeolite bound zeolite o1 catalyst at 650*C, 1.9 hr-1 WHSV, and at a 0.85 steam to hydrocarbon ratio The tests was repeated except that the catalyst comprised

MFI

bound with 60% by weight of a binder (based on the weight of the catalyst) which comprised silica and alumina.

The results of the tests are shown in Table I below: Table I (raf1vst Conventional MFII Zeolite-Bound MFI Conversion 95.9 Key Product Yields. Wt% Ethvlene 26.9 92.4 31.8

I.

Propylene Butvlenes Aromatics Light Saturates Methane 23.2 7.0 21.1 17.8 6.9 30.3 6.8 12.2 11.4 7.3

I

The results of these tests show that yields of ethylene and propylene were significantly increased and the selectivity to undesirable light saturates and aromatics was significantly reduced using the zeolite bound zeolite as a cracking catalyst.

Claims (5)

1. A process for CO under hg hyrocarbonrin conactin hydrocarbon feedstream udr hdoabn cneso cond-itions with a zeolite bound zeolite catalyst comprising: firSt crystals of a first zeolite; and, a binder Comprising second crystals of a second zeolite having an average particle size less than said first crystals, said second crystals being intergrohrl and form a coating or partial coating On said first crystals.

2. The process recited in Claim 1, wherein said first CrYstalS Of Said' is first zeolite have an average particle size greater than 0.1 micron.

3. The process recited in claims 1 or 2, wherein the hydrocarbon conversion is selected from the group consisting of cracking of hydrocarbonls, isotnerizatiori of ailkyl aromiatics, disproportionation of toluene, transalkylation of aromatics, alkylation of aromatics, reforming of naphtha to aromatics, and conversion of parafflns an3dlor olefins to aromnatics, conversion of oxygenates to hy~drocarbonl products, and cracking of naphtha to light ole~fans.

4. The process of claims 1 to 3, wherein said hydrocarbon conversion is carried out; at Conditions comprising a temfperature of from 100 0 C to about

760-C, a pressure of 0.1 atmosphere to 10aoperSawight hourly space velocity of from about 0.08 hr 1 to about 200 hr-1. The process recited in claims 1. to 4, wherein said second zeolite is selected from the group consisting of a large pore zeolite, a medium pore zeolite, and mixtu~res thereof. 41 6. The process recited in claims 1 to 5, wherein said first zeolite is selected from the group consisting of a large pore zeolite, a medium pore zeolite, and mixtures thereof. 7. The process recited in claims 1 to 6, wherein said second zeolite crystals have an acidity either higher or lower than said first zeolite crystallites. 8. The process recited in claims 1 to 7, wherein said first and second zeolites are selected from the group consisting of L, X, Y, offretite, omega, mordenite, MAZ, MEI, FAO, EMT, ZSM-3, ZSM-4, ZSM-18, ZSM-20, MFI, MEL, MTW, MTT, FER, EUO, HEV, TON, zeolite beta, ZSM-34, ZSM-38, ZSM-48, gallosilicates, and titanosilicates. 9. The process recited in claims 1 to 8, wherein said second zeolite is silicalite. 10. The process recited in claims 1 to 9 wherein said hydrocarbon feed contains aromatics, naphtha, paraffins, olefins, oxygenated, or mixtures thereof. 11. The process recited in claims 1 to 10 wherein said binder contains less than 5% by weight of non-zeolitic binder based on weight of said first zeolite and said second zeolite. 12. The process recited in claims 1 to 11, wherein said second zeolite has a silica to alumina mole ratio of from 300:1 to 5,000:1. 13. A hydrocarbon conversion process as recited in claim 1 comprising transalkylating an aromatic hydrocarbon by contacting under transalkylation conditions an aromatic hydrocarbon with a polyalkylaromatic hydrocarbon in the presence of a zeolite bound zeolite catalyst comprising: first crystals of a first zeolite selected from the group consisting of a large pore zeolite and a medium pore 96EFS50.DOC Page 42 zeolite having an average crystals size greater than about 0.1 micron average particle size; and a binder comprising second crystals of a second zeolite selected from the group consisting of a large pore zeolite and a medium pore zeolite having an average particle size less than said first crystals, said second crystals being intergrown and form a coating or partial coating on said first crystals. 34. The process recited in claim 13, wherein said transalkylation conditions comprise a molar ratio of aromatic hydrocarbon to polyalkylaromatic hydrocarbon of from 0.5:1 to 50:1, a S" temperature from 340*C to 500°C. and a pressure in the range of o 15 from 50 psig to 1,000 psig. 15. The process recited in claims 13 or 14, wherein said polyalkylaromatic hydrocarbon is selected from the group consisting of triethylbenzene, diethylmethylbenzene, diethylbenzene, diisopropylbenzene, triisopropylbenzene, diisopropyltoluene, dibutylbenzene, and mixtures thereof. 16. A hydrocarbon conversion process as recited in claim 1 comprising alkylating an aromatic hydrocarbon by contacting said aromatic hydrocarbon under alkylation conditions with a alkylating agent having 2 to 20 carbon atoms and in the presence of a zeolite bound zeolite catalyst comprising: first crystals of a first zeolite selected from the group consisting of a large pore zeolite and a medium pore zeolite having an average particle size greater than 0.1 micron average particle size: and a binder comprising second crystals of a second zeolite selected from the group consisting of a large pore zeolite and a medium pore zeolite having an average particle size less than said first crystals, said second crystals being 9GEFS501.DOC Page 43 intergrown and form a coating or partial coating on said first crystals. 17. The process recited in claim 16, wherein said aromatic hydrocarbon is benzene or alkylbenzenes. 18. The process recited in claims 16 or 17, wherein said alkylation conditions comprise a mole ratio of aromatic hydrocarbon to alkylation agent of from 1:1 to 20:1 and a reaction temperature from 100"C to 500C. 19. A hydrocarbon conversion process as recited in claim 1 comprising isomerizing a hydrocarbon feed containing an aromatic Ca stream comprising ethylbenzene, xylene isomers, or 15 mixtures thereof by contacting said feed under isomerization conversion conditions with a zeolite bound zeolite catalyst comprising: first crystals of a first zeolite selected from the group 20 consisting of a large pore zeolite and a medium pore zeolite having an average particle size greater than 0.1 micron average particle size; and, a binder comprising second crystals of a second zeolite selected from the group consisting of a large pore zeolite and a medium pore zeolite having an average particle size less than said first crystals, said second crystals being intergrown and form a coating or partial coating on said first crystals. A hydrocarbon conversion process as recited in claim 1 comprising cracking hydrocarbon compounds by contacting a hydrocarbon feed under catalytic cracking conditions with a zeolite bound zeolite catalyst comprising: first crystals of a first medium pore zeolite; and 96ETS501.DOC Page 44 a binder comprising second crystals of a second medium pore zeolite having an average particle size less than said first crystals, said second crystals coating at least a portion of said first crystals. 21. The process of claim 20, wherein said hydrocarbon feed comprises a C 4 naphtha feed. 22. The process of claim 20 or 21, wherein said first crystals have a particle size of from 0.1 to 3 microns. 23. A hydrocarbon conversion process as recited in claim 1 comprising disproportionation of toluene by contacting a hydrocarbon stream under toluene disproportionation conditions 15 with a zeolite bound zeolite catalyst comprising: first crystals of a first medium pore zeolite having an average particle size greater than about 0.1 micron average particle size; and, a binder comprising second crystals of a second medium pore zeolite having an average particle size less than said first crystals and a lower acidity than said first crystals, said second crystals be ig intergrown and form a coating or partial coating on said first crystals. 24. The process recited in claim 23, wherein said catalyst is preselectivated. 3o 25. The process of claim 24. wherein said catalyst is preselectivated by contacting the catalyst with a toluene stream at a temperature in the range of between 480°C and 650 0 C at a pressure within. the range of from 1 to 100 atmospheres and a weight hourly space velocity in the range of 0.1 to 20, and wherein said toluene stream further contains hydrogen at a H-Jcoluene ratio of 0 to about 2. 96EFSGO .DOC Page 26. The process of claim 24 or 25, wherein said toluene disproportionation conditions include contacting said hydrocarbon stream with said catalyst at a temperature in the range of between 400"C to 550 0 C, at a pressure in the range of from 1 to 100 atmospheres and at a weight hourly space velocity in the range of from 0.5 to 50, and wherein said hydrocarbon stream further contains hydrogen at a Hz/toluene mole ratio in the range of 0 to about o1 27. The process of claims 23 to 26, wherein said second zeolite particles are MFI crystals or crystals which are a crystallographic match for MFI having a silica to alumina mole ratio higher than the silica to alumina mole ratio of said first phase MFI crystallites. 28. The process of claims 23 to 27, wherein said second crystals have a silica to alumina mole ratio of from 300:1 to 5,000:1. 29. The process of claims 23 to 28, wherein said catalyst is in the 20 acidic hydrogen form. The process recited in claims 23 to 29, wherein said second zeolite has a silica to alumina mole ratio greater than about 300:1. 31. The process recited in claims 23 to 30, wherein said first zeolite has a silica to alumina mole ratio of from about 2:1 to about 150:1. 32. The process recited in claims 23 to 31. wherein said first zeolite and said second zeolite is a medium pore zeolite. 33. The process recited in claims 23 to 32, wherein said first and second zeolites are selected from the group consisting of L, X, Y, offretite. omega, mordenite, hMAZ, MEI, FAO, EMT. ZSM-3, ZSM-4, ZSM-18, ZSM-20, NMFI, MEL, MTW, MTT, FER, EUO, 4- I S6EFS501.DOC Page 46 HEV, TON, zeolite beta, ZSM-34, ZSM-38, ZSM.48, gallosilicates, and titanosilicates. 34. The process of claims 23 to 33, wherein said first crystals have a particle size of from 2 to 6 microns and said second crystals have a particle size of from 0.1 to less than 0.5 microns. The process recited in claims 23 to 34, wherein said second zeolite is a zeolite of the same type as said first zeolite or is a type which is a crystallographic match for said first zeolite. 36. The process recited in claims 23 to 35, wherein said first crystals have an average particle size of from 3 to 4 microns. 15 37. The process recited in claims 23 to 36, wherein said first zeolite isMFI. *oo* 38. The process recited in claims 23 to 37, wherein said second zeolite is an MFT. 39. The process recited in claims 23 to 38, wherein said second zeolite has a silica to alumina ratio of greater than about 1000:1. 40. The process recited in claims 23 to 39 wherein said zeolite bound zeolite has an Adsorption Index greater than 1.00. 41. The process recited in claims 23 to 40 wherein said second zeolite has a silica to alumina ratio that is greater than the silica to alumina ratio of said first zeolite. 42. The process recited in claims 23 to 41 wherein said zeolite bound zeolite has an Adsorption Index greater than 1. 43. A hydrocarbon conversion process as recited in Claim 1 comprising converting oxygenates to hydrocarbon products containing olefins. aromatics, or mixtures thereof by contacting a hydrocarbon feed containing oxygenates under conditions 96EFS50 1DOC Page 47 sufficient to convert said oxygenates to said hydrocarbon products with a zeolite bound zeolite catalyst comprising: first crystals of a first zeolite; and a binder comprising second crystals of a second zeolite having an average particle size less than said first crystals, said second crystals being intergrown and form a coating or partial coating on said first crystals. 44. The process recited in Claim 43, wherein said first crystals of said first zeolite have an average particle size greater than about 0.1 micron. 15 45. The process recited in Claims 42 to 44, wherein said oxygenate S is an alcohol or ether. 46. The process recited in claims 43 to 45, wherein said first and second zeolites are selected from the group consisting of L, X, Y, offretite, omega, mordenite, MAZ, MEI, FAO, EMT, ZSM-3, ZSM-4, ZSM-18, ZSM-20, MFI, MEL, MTW, MTT, FER, EUO, HEV, TON, zeolite beta, ZSM-34, ZSM-38, ZSM-48, gallosilicates, and titanosilicates. 25 47. The process recited in Claims 43 to 46, wherein said conversion conditions comprise a temperature from about 275 0 C to about 600*C, a pressure from about 0.5 atmosphere to about atmospheres, and a liquid hourly space velocity of from about 0.1 to about 100. 48. The process recited in Claims 43 to 47, wherein said second zeolite has a silica to alumina ratio that is greater than the silica to alumina ratio of said first zeolite. 49. The process of Claims 43 to 48, wherein said second zeolite has a silica to alumina mole ratio greater than 500:1. 48 The process recited in claims 43 to 49, wherein said oxygenate is selected from the group consisting of methanol, dimethylether, and mixtures thereof. 51. The process recited in claims 1 to 50 wherein said zeolite bound zeolite catalyst has an Adsorption Index greater than 1.10. DATED this 5th day of June, 1997. EXXON CHEMICAL PATENTS INC. r r WATERMARK PATENT TRADEMARK ATTORNEYS 290 BURWOOD ROAD HAWTHORN VICTORIA 3122 AUSTRALIA VAX DOC 14 AU4737896.WPC LPS:SE