In order to be used in industrial fixed-bed reactors, zeolitic materials must be contained in catalysts consist- ing of the zeolite itself and an inorganic binder, suitably prepared. Said preparation, in fact, gives to the catalyst new mechanical characteristics, compared to the starting raw materials, which are necessary for avoiding its break- age and consequent production of fine powder during load- ing, running and discharge operations of the industrial re- actor.

The resulting catalysts should also have extra- zeolitic porosity characteristics such as to limit to the minimum the resistance to the mass transfer of reactants

and products from the outside to the inside of the catalyst and vice versa. The extra-zeolitic porosity characteris- tics, and in particular its absolute value and the percent- age distribution of said porosity in relation to the pore dimensions, represent a fundamental aspect for catalyst performances. In addition to the role of these aspects on the catalyst performances, the effect of the catalyst par- ticle size must also be considered: resistance to the dif- fusion of reactants and products inside the porous struc- ture of the catalyst proves to be higher with an increase in the size of the catalyst particles.

With respect to the catalytic performances, it is preferable, in the case, for example, of catalysts in pel- let form, to have a dimension as reduced as possible, which, however, for evident reasons, causes a decrease in the mechanical characteristics of the catalyst, in particu- lar its crushing strength. The mechanical characteristics of the catalyst, moreover, are further reduced with an in- crease in the extra-zeolitic porosity.

It can therefore be asserted that, up until now, the improvement in the diffusion properties of a catalyst was obtained to the detriment of the mechanical characteristics, as the former are positively influenced by an increase in the extra-zeolitic porosity and by a decrease in the diame- ter of the catalyst particle, while the second ones are oth-

erwise negatively influenced by an increase in the extra- zeolitic porosity and by a decrease in the diameter of the catalyst particle.

US 5,118, 896, for example, describes the preparation of a catalyst, starting from a zeolite and an inorganic binder in powder form, characterized by an extra-zeolitic porosity whose fraction with a pore radius having dimensions higher than 450 A is equal to 0.25-0. 50 cc/g and with a diameter of the catalyst particle : 1/32 inch (equal to about 0.8 mm).

U. S. 4,169, 111 describes a process for the production of ethyl benzene characterized in that part of the diethyl benzenes produced in the alkylation section are recycled to the alkylation section itself whereas the remaining part of diethyl benzenes and triethyl benzenes is sent to the tran- salkylation section and wherein, in both the alkylation and transalkylation sections, a catalyst based on zeolite, preferably zeolite Y, and an inorganic binder is used to- gether with an inorganic binder. The catalyst used in both sections is prepared in the form of extrudates in order to provide the necessary mechanical characteristics, so as to have a ratio between the outside surface and the catalyst particle volume preferably within the range of 85-160 inch- 1 and has pores with a radius ranging from 150 to 500 A, the latter however having no role and likewise, no role be- ing attributed to the total pore volume or pore volume

fraction with a radius ranging from 150 to 500 A, which are not even described. With respect to the high ratios between the outside surface and volume of catalysts formed, also obtained be resorting to particular geometries such as di- lobate, tri-lobate cylinders or other curved forms, it is known that they provide better properties in the diffusion of reactants and products inside the mass of the catalytic bed, and not inside the catalyst particle, with a conse- quent modest improvement in the overall performances of the reactors in which said catalysts are used.

U. S. 5,182, 242 describes the preparation of a catalyst consisting of a zeolite and an inorganic binder character- ized by a low acidity. A metal-polymer is used as additive in the preparation, which, as a result of the calcination, is eliminated, leaving as residue the inorganic constituent part in the form of an oxide. All oxides of groups IVA and IVB, as well as mixtures of oxides such as silica/alumina, silica/magnesia, silica/zirconia and silica/titania are suitable as inorganic binder components of the catalyst.

EP 847802 describes the preparation of a catalyst based on beta zeolite and an inorganic binder characterized by a particular extra-zeolitic porosity, i. e. the porosity obtained by summing the mesopore and macropore fraction.

The catalyst described did, in fact, have a fraction equal to at least 25% of said extra-zeolitic porosity consisting

of pores having a radius higher than 100 A and a pore vol- ume, still referring to the extra-zeolitic porosity alone, of not less than 0.8 cc/g. The crushing strength of the catalyst particle indicated in Example 4 of EP 847802 (catalyst Al) proves to be equal to 1.3 kg/mm.

The Applicant has now found a zeolitic catalyst with particular porosity characteristics which are such as to guarantee particularly high catalytic performances in terms of duration and consequently productivity, and at the same time with excellent mechanical characteristics, such as crushing strength and resistance to abrasion.

An object of the present invention therefore relates to a catalytic composition comprising a zeolite having a crystalline structure with openings consisting of 12 tetra- hedrons, i. e. belonging to the group of large-pore zeo- lites, and y-alumina as inorganic binder, said composition being characterized by a pore volume, obtained by adding the mesoporosity and macroporosity fractions present in the catalytic composition itself, greater than or equal to 0.7 cc/g, wherein at least 30% of said volume consists of pores with a diameter greater than 100 nanometers.

The sum of the mesoporosity and macroporosity frac- tions present in the catalytic composition is hereunder in- dicated as extra-zeolitic porosity, whereas the micropo- rosity fraction present in the catalytic composition, which

is due to the contribution of the zeolite alone, is indi- cated as zeolitic porosity.

The terms microporosity, mesoporosity or transitional porosity and macroporosity are used herein in accordance with the Dubinin classification provided in Introduction to Powder Surface Area, Wiley-Interscience publication, authors Lowell and Seymour, chapter 10, page 80 (1979) and correspond to the following porosity ranges: - macroporosity : porosity referring to pores with a ra- dius > 1000 A (diameter 200 nanometers) - mesoporosity : porosity referring to pores with a ra- dius ranging from 1000 A (diameter 200 nanometers) to 15 A (diameter 3 nanometers) - microporosity : porosity referring to pores with a ra- dius < 15 A (diameter 3 nanometers) The zeolite contained in the catalytic composition of the present invention is selected from the group of large-pore zeolites and can, for example, be beta zeo- lite, zeolite Y or zeolite ZSM-12. Beta zeolite is de- scribed in U. S. 3,308, 069, zeolite ZSM-12 is described in U. S. 3,832, 449.

According to a preferred aspect of the present inven- tion, the zeolites contained in the catalytic composition of the present invention are in acidic form, i. e. in the form in which most of the cationic sites are occupied by

hydrogen ions.

The catalytic compositions containing zeolite Y in acidic form represent a preferred aspect of the present in- vention. Zeolite Y is described in US 3,130, 007. The prepa- ration of zeolite Y is described in"Verified Synthesis of Zeolitic Materials"H. Robson Editor, Elsevier, second re- vised edition 2001, whereas the post-synthesis treatments to which zeolite Y can be subjected are described in "Introduction to Zeolite Science and Practice"chapter 5, H. van Bekkum and al. Editors, Studies in Surface Science and Catalysis, Vol. 58, Elsevier.

Zeolites Y having a Si02/Al203 molar ratio ranging from 10 to 20, more preferably ranging from 11 to 17, i. e. zeo- lites Y obtained through de-alumination post-synthesis treatments, are preferably used in the compositions of the present invention. The metal content in the zeolite, ex- pressed as oxides, is lower than or equal to 1000 ppm by weight.

The catalytic compositions of the present invention, and in particular those containing zeolite Y, have a crush- ing strength of the catalyst particle equal to or higher than 1.7 kg/mm (crushing strength/length of the catalyst particle).

The compositions of the present invention, and in par- ticular those containing zeolite Y, have a particularly low

apparent density, not higher than 0.5 g/cc and a catalytic particle diameter in extruded form of not less than 1.8 mm.

Preferably the catalytic particle diameter is higher than or equal to 2.0 mm. The catalyst of the present invention is preferably in the form of regular cylindrical pellets.

The catalysts of the present invention are prepared starting from the zeolite and an inorganic compound precur- sor of y-alumina. Catalytic compositions prepared starting from zeolite Y and an inorganic compound precursor of y- alumina are a preferred aspect of the present invention.

Aluminas in the form of bohemite or pseudo-bohemite, with a metal content, expressed as oxides, lower than or equal to 1000 ppm can be used as precursor.

The relative weight ratio zeolite/binder in the cata- lytic composition is higher than 1: 1 and lower than or equal to 4: 1.

The preparation process of the materials according to the present invention comprises: a) preparing a mixture including a zeolite in acidic form belonging to the class of large-pore zeolites, pref- erably zeolite Y, and a precursor of the binder se- lected from bohemite and pseudo-bohemite, by means of mechanic mixing of the components, using a high speed mixer, at a revolution speed of between 900 and 1100 rpm, for not less than 50 minutes;

b) slowly adding to said mixture, constantly under stir- ring, a solution at a concentration not higher than 0. 5% by weight of an acid and demineralized water, in such a quantity as to have a final ratio between the acid weight and total weight of the mixture prepared in step a) of between 0.25 and 0. 50% ; c) submitting the mixture obtained in the previous step b) to an extrusion forming process; d) submitting the product obtained in step c) to drying in a ventilated oven, at a temperature not higher than 30°C, for not less than 48 hours; e) submitting the product obtained in step d) to an air calcination process starting from room temperature up to temperatures not lower than 550°C and not higher than 600°C for an overall calcination time of not less than 30 hours.

In the mixture prepared in step a), the zeolite, prefera- bly zeolite Y, is mixed with the binder precursor in such a quantity as to obtain, on the basis of the weight loss of the individual components at 550°C previously measured, a relative weight quantity zeolite/binder in the final cata- lyst higher than 1: 1 and lower than or equal to 4: 1.

In step b), the mixing which the mixture undergoes during the addition of the acid, is effected at a much lower rate than that at which step a) is carried out, for

example ranging from 200 to 600 rpm. The acid used in step b) can be selected, for example, from acetic acid, nitric acid and oxalic acid, preferably acetic acid.

At the end of the acid addition, the resulting mixture can be subjected to further mixing, the rate being main- tained constant.

The extrusion in step c) is carried out according to the known techniques. It is possible to use extrusion machines of the gear press extruder type, single screw extruder, double turning screw extruder. A gear press extruder is preferably used.

The specific properties relating to the extra-zeolitic porosity and to the mechanical characteristics of the cata- lytic composition, object of the present invention, are due to the particular preparation procedure of the catalyst.

The catalytic compositions of the present invention can be suitably used in transalkylation processes of aromatic hydrocarbons with polyalkylated aromatic hydrocarbons, par- ticularly of benzene with diethyl benzene and possibly tri- ethyl benzene, to give ethyl benzene. Compositions contain- ing zeolite Y are preferably used.

The transalkylation reaction of polyalkylated aromatic hydrocarbons is of primary industrial interest and, in par- ticular, is currently used for the recovery of polyethyl benzenes in industrial plants for the production of ethyl

benzene. The general design of an industrial plant for the production of ethyl benzene includes a main alkylation re- action section, in which ethylene and benzene are reacted to produce ethyl benzene in the presence of a catalyst of the acidic type, preferably a catalyst containing a zeo- lite. In this reaction, in spite of the high selectivity now reached by the new generation of zeolitic catalysts used for the purpose, significantly high quantities of by- products are formed however, especially polyethyl benzenes, due to the subsequent polyalkylation reactions of benzene with ethylene. In industrial production plants of ethyl benzene based on the use of zeolite-based catalysts, there is consequently, together with the main reaction section, a secondary transalkylation reaction section in which the polyethyl benzenes, mainly diethyl benzenes and triethyl benzenes (recoverable by-products), are recovered by reac- tion with benzene to give ethyl benzene.

In the two alkylation and transalkylation reaction sec- tions, another series of by-products are also formed, in addition to the recoverable by-products, in overall quanti- ties which are lower than that of the recoverable by- products, which form the sum of the unrecoverable impuri- ties and by-products.

The main unrecoverable impurities and by-products formed both in the alkylation and transalkylation reaction mainly

consist of low molecular weight products such as oligomers of ethylene and xylenes (the latter mainly formed in the alkylation section), the group of biphenyl ethanes (1, 1 biphenyl ethane, ethyl-1, 1 biphenyl ethane, diethyl-1, 1 biphenyl ethane, 1,2 biphenyl ethane, ethyl-1,2 biphenyl ethane, diethyl-1,2 biphenyl ethane) and the group of higher polyethyl benzenes (tetraethyl benzenes, pentamethyl benzenes and hexa-ethyl benzenes).

The group of low molecular weight impurities, as already mentioned, cannot be recovered. The impurities belonging to the group of biphenyl ethanes cannot be recovered by means of transalkylation reaction with benzene whereas although the remaining impurities belonging to the group of higher polyethyl benzenes, can in principle be recovered by means of transalkylation reaction with benzene to give ethyl ben- zene, in practice they are unrecoverable, due to the ex- treme difficulty in separating them by distillation from the impurities belonging to the group of biphenyl ethanes.

In an industrial plant for the production of ethyl ben- zene, the sum of all the unrecoverable impurities and by- products therefore represents a direct measurement of the increase in consumption of the benzene and ethylene reac- tants with respect to their stoichiometric quantity neces- sary for the sole production of ethyl benzene.

The sum of all the non-recoverable impurities, with the

exception of the low molecular weight impurities previously specified, is normally indicated with the term Flux oil.

The overall quantity of Flux oil produced in modern produc- tion plants of ethyl benzene based on the use of the new generation of zeolite-based catalysts can vary in relation to the reaction conditions and type of zeolitic catalyst used in the two reaction sections.

It is known however that regardless of the type of zeo- litic catalyst used in the two reaction sections and in spite of the fact that the highest quantity of ethyl ben- zene is produced in the alkylation section and only a mi- nority amount is produced in the transalkylation section, most of the unrecoverable by-products come from the tran- salkylation section (Alkylation of Aromatics with Ethylene and Propylene: Recent Developments in Commercial Processes.

Applied Catalysis A: General 221 (2001) 283-294). The rea- sons for this mainly lie in the different selectivity to unrecoverable impurities and by-products which character- izes the two reaction steps, generally lower in the alkyla- tion step and normally higher in the transalkylation step.

The transalkylation reaction of polyethyl benzenes (di- ethyl benzenes and triethyl benzenes) is, in fact, a less advantageous reaction with respect to the alkylation reac- tion, both with respect to the kinetics and thermodynamics and consequently requires higher operating temperatures

which correspond to lower selectivities. The conversion of polyethyl benzenes per passage in the transalkylation sec- tion is in fact limited by the thermodynamic equilibrium, causing a significant recycling quantity of the latter with a consequent increase in the incidence of secondary reac- tions forming unrecoverable impurities and by-products in this section.

Another aspect which makes the transalkylation step par- ticularly critical with respect to yield and overall pro- ductivity of an industrial plant for the production of ethyl benzene is represented by the deactivation rate of the catalyst which is normally higher for the transalkyla- tion step than for the alkylation step.

This is again due to the higher operating temperature which favours progressive condensation reactions of the aromatic rings responsible for the formation of coke, and also to the higher quantity of heavy compounds already pre- sent in the feeding to the transalkylation step, which also contribute to a more rapid formation of coke precursor im- purities. Some of the problems described above have been solved, for example, as specified in U. S. 5,177, 285, by means of a process for the production of ethyl benzene characterized in that the concentration of water at the in- let of the alkylation section is much higher than the con- centration of water at the inlet of the transalkylation

section and where, in both alkylation and transalkylation sections, a zeolitic catalyst is used, preferably a cata- lyst based on zeolite Y generally bound with alumina. It is known in fact that the catalytic activity of zeolites is generally depressed due to the presence of water, it is therefore convenient to have a less active catalyst in the alkylation section, where the main reaction is kinetically and thermodynamically favoured, in order to reduce the for- mation of by-products and impurities, and a more active catalyst in the transalkylation section, where the main re- action is kinetically and thermodynamically less favoured, in order to have the highest possible conversions of di- ethyl benzenes and triethyl benzenes and consequently re- duce their non-converted quantity to be subjected to recir- culation to the transalkylation reactor itself. The exploi- tation of a catalyst made more active by the use of par- ticular reaction conditions, suitable for increasing its activity, allows the transalkylation reactor to be run at relatively lower temperatures. The reduction in the concen- tration of water is naturally obtained with the disadvan- tage of greater energy costs to reduce the water to concen- trations lower than 100 ppm in the stream at the inlet of the transalkylation section.

A process for the production of ethyl benzene in which the catalyst used in the transalkylation section consists

of a zeolite with larger pore dimensions with respect to the zeolite forming the catalyst used in the alkylation section, is described in U. S. 6,268, 542. The catalyst used in the alkylation section preferably consists of a sili- calite, belonging to the class of small-pore zeolites, in a monoclinic form, whereas the catalyst used in the transal- kylation section consists of zeolite Y.

Also in this case, the specificity of the transalkyla- tion reaction of polyethyl benzenes with respect to the al- kylation reaction of benzene with ethylene, is evident.

The catalytic compositions of the present invention solve the problem of finding a specific catalyst for the transalkylation section, capable of high selectivities and of operating at lower operating temperatures, producing a high yield and overall productivity of transalkylation plants, in particular those for the industrial production of ethyl benzene.

A further object of the present invention therefore re- lates to a process for the transalkylation of aromatic hy- drocarbons with one or more polyalkylated aromatic hydro- carbons catalysed by a catalytic composition comprising a zeolite having a crystalline structure with openings con- sisting of 12 tetrahedra (large-pore zeolites) and y- alumina, as inorganic binder, said composition being char- acterized by a pore volume, obtained by adding the mesopo-

rosity and the macroporosity fractions present in the cata- lytic composition, higher than or equal to 0.7 cc/g, wherein at least 30% of said volume consists of pores hav- ing a diameter greater than 100 nanometers.

Catalytic compositions containing zeolite Y in acidic form are preferably used.

The aromatic hydrocarbon is preferably benzene. The polyalkylated aromatic hydrocarbon is preferably selected from diethyl benzene, and optionally triethyl benzene, and di-isopropyl benzene, and optionally tri-isopropyl benzene.

The transalkylation of benzene with diethyl benzene and op- tionally triethyl benzene, to give ethyl benzene is par- ticularly preferred.

The transalkylation reaction should be carried out under such conditions as to at least partially take place in liq- uid phase and preferably under such conditions as to sub- stantially take place in liquid phase. It is preferably carried out at a temperature ranging from 150 to 300°C, at a pressure ranging from 20 to 50 atms and a space velocity (WHSV) ranging from 0.5 to 10 hours~1. The molar ratio be- tween aromatic hydrocarbon and the sum of the polyalkylated aromatic hydrocarbons in the feeding mixture to the tran- salkylation reaction can vary from 1 to 40, preferably from 3 to 30. The catalytic composition, object of the present invention, is used in all types of reactors in which the

catalyst can be arranged in a fixed bed and is particularly used in chamber reactors having one or more fixed beds of catalyst.

According to a further aspect of the present inven- tion, the transalkylation activity of the catalyst, object of the present invention, can be suitably used for maximiz- ing the production of a mono-alkylated product in the reac- tion of aromatics with light olefins, and in particular benzene with ethylene to give ethyl benzene. According to this particular aspect of the present invention, the prod- uct obtained in the alkylation reaction of aromatics with light olefins is separated into an aromatic hydrocarbon fraction, a mono-alkylated aromatic hydrocarbon fraction, a fraction of polyalkylated aromatic hydrocarbons, preferably prevalently comprising dialkylated aromatics, and a last fraction of heavy aromatic hydrocarbons.

The fraction of polyalkylated aromatic hydrocarbons, preferably prevalently comprising dialkylated aromatic hy- drocarbons, is fed, together with an aromatic hydrocarbon, to a specific reactor, in the presence of the catalyst ob- ject of the present invention.

A further aspect of the present invention therefore relates to a process for preparing mono-alkylated aromatic hydrocarbons, which comprises: a) putting an aromatic hydrocarbon in contact, in the

presence of an acidic catalyst, with a C2-C4 olefin, under alkylation conditions which are such that the reaction takes place at least partially in liquid phase, b) separating the product obtained into a fraction con- taining an aromatic hydrocarbon, a fraction contain- ing a mono-alkylated aromatic hydrocarbon, a fraction containing polyalkylated aromatic hydrocarbons, pref- erably prevalently containing dialkylated aromatic hydrocarbons, and a fraction of heavy aromatic hydro- carbons, c) putting the fraction containing polyalkylated aro- matic hydrocarbons, preferably prevalently containing dialkylated products, in contact with an aromatic hy- drocarbon, in the presence of the catalyst, object of the present invention, under transalkylation condi- tions which are such that the reaction takes place at least partially in liquid phase.

In the alkylation step a), a solid acidic catalyst is preferably used, containing a zeolite of the large-pore class. Zeolites preferably used in the catalytic composi- tion used in the alkylation step are beta zeolite and zeo- lite Y. Beta zeolite is preferably used, as described in EP 432814. Even more preferably, the alkylation step is car- ried out according to EP 687500 or EP 847802 in which a

catalytic composition is used, containing beta zeolite bound with an inorganic binder, characterized by particular porosity and pore volume characteristics.

The olefin which is preferably used in the alkylation step is selected from ethylene and propylene, and is even more preferably ethylene. The aromatic hydrocarbon used in the alkylation step is preferably benzene. A particularly preferred aspect is that benzene and ethylene are put in contact with each other in the alkylation step (a) in the presence of beta zeolite.

When the alkylation product is obtained from the alkyla- tion reaction of benzene with ethylene, in step (b) the first fraction contains benzene, the second contains ethyl benzene, the third preferably prevalently consists of di- ethyl benzene and the last fraction consists of a mixture of heavy hydrocarbons having a boiling point greater than or equal to 260°C.

The third fraction, prevalently consisting of diethyl benzene, is put in contact, in step (c), with benzene, in the presence of the catalyst of the present invention, preferably containing zeolite Y, under transalkylation con- ditions, in at least partially liquid phase.

The fraction of polyalkylated products, in particular diethyl benzenes, fed to step (c) may also contain the un- recoverable by-products, described above, called Flux oil,

preferably in a limited quantity and not higher than 0. 1% by weight with respect to the total weight of the fed mix- ture, consisting of polyalkylated products and the aromatic hydrocarbon. The polyalkylated fraction, in particular di- ethyl benzenes, fed to step (c) may also contain variable quantities of butyl benzenes, up to a maximum of 2% by weight with respect to the total weight of the fed mixture, consisting of polyalkylated products and the aromatic hy- drocarbon.

EXAMPLE 1 260 g of zeolite Y CBV 712 in powder form, produced and supplied by Zeolyst, and 278 g of p-bohemite Versal V- 250 in powder form, produced and supplied by Laroche, are charged into a high-speed mixer (turbo-mixer), equipped with ploughs of the type indicated in figure 1 (of MIX S. r. l.-Modena-Italy).

The powders are dry-mixed for 60 minutes at a rate equal to 1000 rpm. At the end of the dry-mixing of the pow- ders, 310 cc of an aqueous solution at 0. 5% w/w of glacial acetic acid are added through a spray nozzle connected with the mixing chamber. The acetic solution is added at an ap- proximately constant rate in about 36 minutes, during which the rate of the mixer is equal to 400 rpm. At the end of the addition of the acetic solution, a further mixing of the mixture present inside the mixer is effected, maintain-

ing the selected rate of 400 rpm constant, for a further 12 minutes.

The product thus obtained is discharged and submitted to an extrusion process with a gear press extruder, of which a detail is shown in figure 2, taken from Preparation of Solid Catalysts, page 585, edited by G. Ertl, H. Knoz- inger, J. Weitkamp, WILEY-VCH Publishing. At the end of the extrusion, the product thus obtained in the form of regular cylinders is placed in a ventilated oven at 25°C for 48 hours. At the end of the drying, the product obtained is then placed in a muffle to calcinate, in an atmosphere of air, with the following temperature ramp: from room temperature to 120°C in 360 minutes, isotherm at 120°C for 120 minutes, from 120°C to 350°C in 360 minutes, isotherm at 350°C for 240 minutes, from 350°C to 550°C in 240 minutes, isotherm at 550°C for 480 minutes.

The finished catalyst is in the form of regular cylin- ders with a length approximately equal to 7 mm 1 mm and with a diameter equal to 2.1 mm 0.1 mm.

Once the calcination has been completed and the prod- uct has cooled, the extra-zeolitic and mechanical charac- teristics of the catalysts are measured.

Figure 3 indicates the pore size distributions (PSD) obtained by means of mercury porosimetry at the top, nitro- gen porosimetry at the temperature of liquid nitrogen in

the centre and the total extra-zeolitic pore size distribu- tion, obtained by joining the previous two, at the bottom, wherein the porosity of the zeolite itself is not indi- cated. In particular, in abscissa there is the pore diame- ter in nanometers (diameter) and in the ordinate the pore volume in cc/g (Vol. ). The determination of the pore size distributions was effected using a Carlo Erba Porosimeter 2000@ for the mercury porosimetries and an ASAP 2010 Mi- cromeriticsS for the physical adsorption of nitrogen at the temperature of liquid nitrogen.

The total extra-zeolitic porosity proves to be equal to 0.84 cc/g with a fraction of said extra-zeolitic poros- ity having a pore diameter greater than 100 nanometers equal to 34. 5% (0.29 cc/g/0.84 cc/g * 100). The crushing strength measured according to the method ASTM D6175-98 proves to be equal to 2.1 kg/mm. The apparent density is equal to 0.46 g/cc.

The product consists of 49. 99% by weight of y-alumina and 50. 01% by weight of zeolite Y on the basis of the weight loss at 550°C measured on the starting components.

XRD analysis effected on the catalyst confirms the sole presence of the faujasit phases (zeolite Y) and y- alumina.

Figure 4 also shows a series of photographs obtained by means of SEM microscopy and EDS probe for the mapping of

the elements Al and Si, which can be assimilated to the alumina binder and zeolite forming the catalyst, respec- tively. The Si is shown with a dark shade, whereas the Al is indicated with a light shade. Morphological tests were carried out by means of Scanning Electronic Microscopy (SEM), using a Jeol JSM-5400LV scanning electronic micro- scope equipped with a EDAX JSM-5300 microprobe for the EDS (Energy Dispersive Spectroscopy) analysis. The samples were englobed in epoxy resin and subsequently polished until transversal sections of the cylinders were obtained.

Figure 4 shows the distribution of the alumina and zeolite phases in the catalyst prepared according to the present Example 1, at different enlargements. The first up- per photo, obtained at smaller enlargements than the sec- ond, shows an apparently homogeneous phase distribution. In the second photo below, obtained at greater enlargements with respect to the first, a rather heterogeneous phase distribution can be observed, on the contrary, character- ized by alumina and zeolite particles with varying dimen- sions, sometimes differing by at least one order of magni- tude with respect to the average particle sizes.

EXAMPLE 2 A catalytic test is effected in the transalkylation reaction of benzene with polyethyl benzenes. The reactor used for the catalytic test is of the Berty type, consist-

ing of a reaction chamber having a capacity of 250 cc in which there is a 50 cc basket into which the catalyst pre- pared as described in Example 1, is charged. The reactor head is positioned in the upper part of the reaction cham- ber, which supports an impeller which rotates by means of a magnetic joint. The reactor is equipped with a temperature and pressure regulation system.

The feeding mixture, before the reactor inlet, is passed through a column of alumina in order to reduce the quantity of water contained therein to below 50 ppm and is then fed in continuous to the reactor. The test is carried out under the following conditions: reaction temperature equal to 210°C, reaction pressure equal to 50 bar, space velocity expressed as WHSV equal to 4 hours~1, molar ratio [benzene]/ [total polyethyl benzenes] equal to 20. The molar ratio between benzene and total polyethyl benzenes corresponds to the following weight con- centrations with respect to the total weight of the mixture fed: diethyl benzenes equal to 6. 9%, triethyl benzenes equal to 0. 04%, butyl benzenes equal to 1%. The overall concentration of the biphenyl ethanes is lower than 20 ppm by weight.

The effluent from the reactor is collected in a tank and analyzed by means of gaschromatography using an HP 5890 Series 2 instrument equipped with a capillary column with

the stationary phase Carbovax 20M and detector of the flame ionization (FID) type.

After activating the reactor under the above condi- tions, two samplings of the reaction effluent were effected together with the relative Gaschromatographic analyses.

Table 1 indicates the results relating to the two sam- ples.

With a productivity equal to about 24 g of ethyl ben- zene per g of catalyst, the conversion of the polyethyl benzenes and molar yield to ethyl benzene with respect to the polyethyl benzenes converted, were equal to 80. 1% and 71. 4% respectively.

With a productivity equal to 145 g of ethyl benzene per g of catalyst, the conversion of the polyethyl benzenes and molar yield to ethyl benzene with respect to the poly- ethyl benzenes converted were equal to 78. 9% and 69. 1% re- spectively.

The decrease in the yield to ethyl benzene was there- fore equal to 2. 3% as an absolute value and equal to 0. 019% as an absolute value per productivity unit (yield varia- tion/productivity variation).

EXAMPLE 3-COMPARATIVE 260 gr of zeolite Y CBV 712 in powder form, produced and supplied by Zeolyst, and 278 gr of p-bohemite Versal V- 250 in powder form, produced and supplied by Laroche, are

charged into a"Z Blade"-type mixer manufactured by Erweka.

The powders are dry-mixed for 70 minutes at a rate equal to 45 rpm. At the end of the dry-mixing of the pow- ders, 310 cc of an aqueous solution at 0. 3% w/w of glacial acetic acid are added. The acetic solution is added at an approximately constant rate in about 50 minutes, during which the rate of the mixer is equal to 45 rpm. At the end of the addition of the acetic solution, a further mixing of the mixture present inside the mixer is effected, maintain- ing the selected rate of 45 rpm, for a further 30 minutes constant.

The product thus obtained is discharged and submitted to an extrusion process with a gear press extruder, of the type shown in figure 2. At the end of the extrusion, the product thus obtained in the form of regular cylinders is placed in a ventilated oven at 25°C for 24 hours.

At the end of the drying, the product obtained is then placed in a muffle oven to calcinate, in an atmosphere of air, with the following temperature slope: from room temperature to 120°C in 360 minutes, isotherm at 120°C for 120 minutes, from 120°C to 350°C in 360 minutes, isotherm at 350°C for 240 minutes, from 350°C to 550°C in 240 minutes, isotherm at 550°C for 480 minutes.

The catalyst is in the form of regular cylinders with a length approximately equal to 7 mm 1 mm and with a di-

ameter equal to 2.1 mm 0.1 mm.

Once the calcination has been completed and the prod- uct has cooled, the extra-zeolitic and mechanical charac- teristics of the catalysts are measured.

Figure 5 indicates the pore size distributions (PSD) obtained by means of mercury porosimetry at the top, nitro- gen porosimetry at the temperature of liquid nitrogen in the centre and the total extra-zeolitic pore size distribu- tion, obtained by joining the previous two, at the bottom, wherein the porosity of the zeolite itself is not indi- cated. In particular, in abscissa there is the pore diame- ter in nanometers (diameter) and in the ordinate the pore volume in cc/g (Vol. ).

The total extra-zeolitic porosity proves to be equal to 0.44 cc/g with a fraction of said extra-zeolitic poros- ity having a pore diameter greater than 100 nanometers equal to 0. 04% (0.02 cc/g/0.44 cc/g * 100). The crushing strength measured according to the method ASTM D6175-98 proves to be equal to 1.4 kg/mm. The apparent density is equal to 0.74 g/cc.

The product consists of 49. 99% by weight of y-alumina and 50. 01% by weight of zeolite Y on the basis of the weight loss at 550°C measured on the starting components.

XRD analysis effected on the catalyst confirms the sole presence of the zeolite Y and y-alumina phases.

Figure 6 also shows a series of photographs obtained by means of SEM microscopy and EDS probe for the mapping of the elements Al and Si, which can be assimilated to the alumina binder and zeolite forming the catalyst, respec- tively. The Si is shown with a dark shade, whereas the Al is indicated with a light shade. Morphological tests were carried out by means of scanning electronic microscopy (SEM), using a Jeol JSM-5400LV scanning electronic micro- scope equipped with a EDAX JSM-5300 microprobe for the EDS (Energy Dispersive Spectroscopy) analysis. The samples were englobed in epoxy resin and subsequently polished until transversal sections of the cylinders were obtained.

Figure 6 shows the distribution of the alumina and zeolite phases in the catalyst prepared according to the present Example 3, at different enlargements. A homogeneous distribution of the phases can be observed in both photos, with only an occasional presence of particles having higher dimensions. On comparing the two lower photos (at greater enlargements) of figure 6 and figure 4, the latter refer- ring to the catalyst, object of the present invention, the different particle size distribution of the zeolite and alumina particles from both a relative and absolute point of view, is evident.

The particle size in figure 6 is in fact extremely re- duced with respect to the particle size of figure 4 and is

also characterized by a greater homogeneity in the two com- ponents.

EXAMPLE 4-COMPARATIVE A catalytic test is effected in the transalkylation reaction of benzene with polyethyl benzenes. The equipment used and test operating procedures are the same as those of Example 2. The catalyst used is that prepared in Example 3.

Table 1 indicates the results relating to the two samples.

With a productivity equal to about 24 g of ethyl ben- zene per g of catalyst, the conversion of the polyethyl benzenes and molar yield to ethyl benzene with respect to the polyethyl benzenes converted were equal to 78. 3% and 71. 1% respectively.

With a productivity equal to 145 g of ethyl benzene per g of catalyst, the conversion of the polyethyl benzenes and molar yield to ethyl benzene with respect to the poly- ethyl benzenes converted were equal to 73. 9% and 61. 8% re- spectively.

The decrease in the yield to ethyl benzene was there- fore equal to 9. 3% as an absolute value and equal to 0. 077% as an absolute value per productivity unit (yield varia- tion/productivity variation).

The decrease in yield to ethyl benzene was, in this case, higher than the decrease in yield registered in Exam- ple 2 when the catalyst used is a catalyst according to the present invention prepared as described in Example 1.

Table 1 Productivity (g ethyl benzene/g catalyst) 24 145 Example 2 Polyethyl benzenes conversion 80. 1 78. 9 (%) Yield to ethyl benzene 71. 4 69. 1 (molar %) Yield variation/productivity--0. 019 variation [%/ (g/g)] Example 4 Polyethyl benzenes conversion 78. 3 73. 9 (%) Yield to ethyl benzene 71. 1 61. 8 (molar %) Yield variation/productivity--0. 077 variation [%/ (g/g)]