US20020049133A1 - High zeolite content and attrition resistant catalyst, methods for preparing the same and catalyzed processes therewith - Google Patents

High zeolite content and attrition resistant catalyst, methods for preparing the same and catalyzed processes therewith Download PDF

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US20020049133A1
US20020049133A1 US09/260,205 US26020599A US2002049133A1 US 20020049133 A1 US20020049133 A1 US 20020049133A1 US 26020599 A US26020599 A US 26020599A US 2002049133 A1 US2002049133 A1 US 2002049133A1
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catalyst
alumina
weight
zsm
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Michael S. Ziebarth
Terry G. Roberie
Philip S. Deitz
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Priority to US09/260,205 priority Critical patent/US20020049133A1/en
Priority to BRPI0005188-8B1A priority patent/BR0005188B1/pt
Priority to AT00910374T priority patent/ATE275001T1/de
Priority to AU32474/00A priority patent/AU773403B2/en
Priority to PCT/US2000/005065 priority patent/WO2000051731A1/en
Priority to ES00910374T priority patent/ES2226793T3/es
Priority to CA2331123A priority patent/CA2331123C/en
Priority to DE60013376T priority patent/DE60013376T3/de
Priority to KR20007012173A priority patent/KR100694945B1/ko
Priority to CNB008007535A priority patent/CN1134301C/zh
Priority to PT00910374T priority patent/PT1077768E/pt
Priority to MXPA00010489 priority patent/MX226917B/es
Priority to JP2000602390A priority patent/JP4927259B2/ja
Priority to EP00910374A priority patent/EP1077768B2/de
Priority to ZA200005773A priority patent/ZA200005773B/xx
Publication of US20020049133A1 publication Critical patent/US20020049133A1/en
Priority to US10/151,560 priority patent/US6916757B2/en
Abandoned legal-status Critical Current

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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00—Catalysts comprising molecular sieves
    • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/40—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11, as exemplified by patent documents US3702886, GB1334243 and US3709979, respectively
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/14—Phosphorus; Compounds thereof
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00—Catalysts comprising molecular sieves
    • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2229/00—Aspects of molecular sieve catalysts not covered by B01J29/00
    • B01J2229/10—After treatment, characterised by the effect to be obtained
    • B01J2229/26—After treatment, characterised by the effect to be obtained to stabilize the total catalyst structure
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2229/00—Aspects of molecular sieve catalysts not covered by B01J29/00
    • B01J2229/30—After treatment, characterised by the means used
    • B01J2229/42—Addition of matrix or binder particles
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/0009—Use of binding agents; Moulding; Pressing; Powdering; Granulating; Addition of materials ameliorating the mechanical properties of the product catalyst
    • B01J37/0027—Powdering
    • B01J37/0045—Drying a slurry, e.g. spray drying

Definitions

  • the present invention relates to an improved catalyst composition, its manufacture, and a process for reacting hydrocarbon feed over the improved catalyst.
  • Processes such as catalytic cracking operations are commercially employed in the petroleum refining industry to produce gasoline and fuel oils from hydrocarbon-containing feeds. These cracking operations also result in the production of useful lower olefins, e.g., C 3 -C 5 olefins, and it has become increasingly desirable to maximize the yield of such olefins from conversion process operations in general. Endothermic catalytic cracking of hydrocarbons is commonly practiced in fluid catalytic cracking (FCC) processes.
  • FCC fluid catalytic cracking
  • FCC is commercially practiced in a cyclic mode.
  • the hydrocarbon feedstock is contacted with hot, active, solid particulate catalyst without added hydrogen, for example, at pressures of up to about 50 psig and temperatures up to about 650° C.
  • the catalyst is a powder with particle sizes of about 20-200 microns in diameter and with an average size of approximately 60-100 microns.
  • the powder is propelled upwardly through a riser reaction zone, fluidized and thoroughly mixed with the hydrocarbon feed.
  • the hydrocarbon feed is cracked at the aforementioned high temperatures by the catalyst and separated into various hydrocarbon products.
  • Catalysts for FCC are typically large pore aluminosilicate compositions, including faujasite or zeolite Y.
  • the coked catalyst particles are separated from the cracked hydrocarbon products, and after stripping, are transferred into a regenerator where the coke is burned off to regenerate the catalyst.
  • the regenerated catalyst then flows downwardly from the regenerator to the base of the riser.
  • the catalyst particles cannot be too large in diameter, or the particles may not be sufficiently fluidized. Therefore, the catalysts are preferably maintained under 120 to 150 microns in diameter.
  • Particulated catalyst additives are also typically included in the inventory of conventional large pore cracking catalysts for FCC processes and are therefore subject to the same attrition issues. These additives are very useful in enhancing the properties of the resulting gasoline product as well as enhancing octane numbers of the gasoline product. Such additives also are especially suitable for enhancing yields of C 3 -C 5 olefins. Those olefins are useful in making ethers and alkylates which are in high demand as octane enhances for gasoline, as well as useful in making other chemical feedstocks.
  • Particulated catalysts and additives are prepared from a number of compounds in addition to the primary active catalytic species.
  • the catalyst compositions can comprise clay and other inorganic oxides in addition to catalytically active ZSM-5.
  • Alumina is one particular inorganic oxide other than zeolite that can be added.
  • EP 256 875 reports that alumina in conjunction with rare earth compounds improves hydrothermal stability and selectivity of zeolite Y.
  • Phosphorous also is added to “stabilize” ZSM-5 containing catalysts. Additives sold as OlefinsMaxTM by Grace Davison is an example. Stabilization of a catalyst composition means stabilizing the activity of the composition to produce higher yields of light olefins when compared to a composition which has not been stabilized by phosphorus. This comparison is normally made after deactivation with steam.
  • U.S. Pat. No. 5,110,776 teaches a method for preparing FCC catalyst comprising modifying the zeolite, e.g., ZSM-5, with phosphorus.
  • U.S. Pat. No. 5,126,298 teaches manufacture of an FCC catalyst comprising zeolite, e.g., ZSM-5, clay, and phosphorus. See also WO 98/41595 and U.S. Pat. No. 5,366,948.
  • Phosphorus treatment has been used on faujasite-based cracking catalysts for metals passivation (see U.S. Pat. Nos. 4,970,183 and 4,430,199); reducing coke make (see U.S. Pat. Nos.
  • Refiners e.g., FCC refiners, DCC (Deep Catalytic Cracking) refiners, as well as fixed fluidized bed refiners, would also find it advantageous to enhance ethylene yields in order to maximize the yield of valuable products from their refinery operations.
  • Additives or compositions comprising novel catalysts are potential avenues for enhancing ethylene yields. Using those additives or compositions, however, without materially affecting the yield of other olefins can be difficult, especially in light of the other concerns mentioned above with respect to attrition.
  • Attrition resistance and high catalyst content would also benefit processes used to react hydrocarbons other than hydrocarbon cracking processes. Such processes include hydrocarbon isomerization, dimerization and the like.
  • the invention is an attrition resistant zeolite catalyst composition which has high levels of stabilized zeolite (30-85%) thereby effectively increasing the catalytic effect in reactions involving hydrocarbon feedstock. It has been unexpectedly discovered that by limiting the amount of alumina added to the catalyst to 10% or less by weight of the catalyst and further maintaining a phosphorous content between about 6 and 24%, active catalysts containing up to 85% zeolite can be prepared. Acceptable Davison Attrition Indices of 20 or less are achieved by further selecting a phosphorus (as P 2 O 5 ) to total alumina molar ratio sufficient to maintain these attrition indices, while also maintaining acceptable activity, e.g., olefin yields in FCC. Suitable attrition properties are reflected by particles having Davison index attrition numbers of 20 or lower, and preferably less than 10.
  • the catalyst is especially effective for producing light C 3 -C 5 olefins (propylene and butylene) in hydrocarbon cracking processes, such as those in a FCC Unit.
  • the quantity of light olefins produced in a FCC unit is strongly affected by the amount of stabilized zeolite, e.g., ZSM-5 or ZSM-11, in the unit and the unit conversion. Conversion is important since the amount of light olefins produced tends to increase with unit conversion.
  • the advantage of a catalyst which contains a high level of active zeolite is: 1) higher absolute amounts of active zeolite can be put in the unit and/or 2) if the high content catalyst is used as an additive catalyst at constant ZSM-5 or ZSM-11 level, a lower quantity of additive is required and as a result there is less dilution of the standard FCC catalyst, thereby allowing the unit to operate at higher conversion.
  • the invention also provides an improved phosphorus stabilized catalyst composition having a high content of active components, and suitable attrition resistance, which is more selective towards producing ethylene without significantly affecting total olefin yields exhibited by conventional additives in FCC units.
  • FIGS. 1 - 3 illustrates light olefin yields from a FCC process using several embodiments of the inventive catalyst (40% by weight zeolite, 10% or less added alumina).
  • FIG. 4 illustrates the olefin yield of a FCC process using a comparison catalyst comprising more than 10% alumina.
  • FIG. 5 illustrates the effects of added alumina content on attrition resistance and propylene yield in a FCC catalyst.
  • FIG. 6 illustrates the percent change in olefin yield for the invention relative to a conventional phosphorus stabilized ZSM-5 catalyst. These results are taken at 70% conversion of the hydrocarbon.
  • FIG. 7 illustrates total wt. % olefin yield as a function of carbon number as compared against a conventional catalyst. These results are shown for 70% conversion level of the hydrocarbon. This figure as well as FIG. 6 also show the effect the invention has in increasing ethylene yield.
  • FIG. 8 illustrates the invention comprising 80% ZSM-5 and further illustrates how the molar ratio of phosphorous (P 2 O 5 ) and alumina affects propylene yield.
  • FIG. 9 illustrates the propylene yield of an embodiment comprising 80% ZSM-5 compared to a conventional catalyst on a ZSM-5 weight basis and catalyst basis.
  • FIG. 10 illustrates the ethylene yield for an embodiment comprising 80% ZSM-5 compared to a conventional catalyst on both a catalyst and ZSM-5 weight basis.
  • the catalyst composition of this invention can be used, for example, as the primary catalyst for a catalyzed reaction involving hydrocarbon feedstock, as an additive to a fresh catalyst stream, or as an additive to an existing catalyst inventory.
  • the catalyst is prepared from zeolite, alumina, phosphorous and optional additional components.
  • zeolites useful for this purpose are exemplified by intermediate pore (e.g., pore size of from about 4 to about 7 Angstroms) zeolites.
  • ZSM-5 U.S. Pat. No. 3,702,886 and Re. 29,948
  • ZSM-11 U.S. Pat. No. 3,709,979 are preferred. Methods for preparing these synthetic zeolites are well known in the art.
  • the alumina employed to make the invention is referred to herein as “added alumina”.
  • the added alumina component of the catalyst of the present invention therefore is defined herein as alumina separately added to the slurry of starting components and dispersed in the matrix of the catalyst.
  • the alumina primarily serves to act with phosphorous to form binder for the zeolite.
  • Added alumina does not include alumina present in the other components of the additive, e.g., shape selective zeolite or any clay used to prepare the additive.
  • the term “total alumina” as used herein refers to added alumina and alumina present in the other components.
  • Suitable added alumina includes particulate alumina having a total surface area, as measured by the method of Brunauer, Emmett and Teller (BET) greater than 50 square meters per gram (m 2 /g), preferably greater than 140 m 2 /g, for example, from about 145 to 400 m 2 /g.
  • BET Brunauer, Emmett and Teller
  • the pore volume (BET) of the particulate alumina will be greater than 0.35 cc/g.
  • Such alumina may comprise a minor amount of silica or other inorganic oxides such as from about 0.1 to 15 weight percent, preferably from about 0.1 to 6 weight percent silica, based on the weight of the alumina component of the particles.
  • the average particle size of the alumina particles will generally be less than 10 microns, preferably less than 3 microns.
  • the porous alumina will be bulk alumina.
  • the term “bulk” with reference to the alumina is intended herein to designate a material which has been preformed and placed in a physical form such that its surface area and porous structure are stabilized so that when it is added to an inorganic matrix containing residual soluble salts, the salts will not alter the surface and pore characteristics measurably.
  • Suitable particulate aluminas include, but are not limited to, CP3 from Alcoa and Catapal B from Condea Vista.
  • Suitable sources of added alumina include colloidal alumina or alumina sols, reactive alumina, aluminum chlorhydrol and the like.
  • Suitable phosphorus-containing compounds include phosphoric acid (H 3 PO 4 ), phosphorous acid (H 3 PO 3 ), salts of phosphoric acid, salts of phosphorous acid and mixtures thereof.
  • Ammonium salts such as monoammonium phosphate (NH 4 )H 2 PO 4 , diammonium phosphate (NH 4 ) 2 HPO 3 monoammonium phosphite (NH 4 )H 2 PO 3 , diammonium phosphite (NH 4 ) 2 HPO 3 , and mixtures thereof can also be used.
  • Other suitable phosphorous compounds are described in WO 98/41595, the contents of which are incorporated herein by reference. Those compounds include phosphines, phosphonic acid, phosphonates and the like.
  • the catalyst of this invention can include suitable inorganic oxide matrices, such as non-zeolitic inorganic oxides, including silica, silica-alumina, magnesia, boria, titania, zirconia and mixtures thereof.
  • the matrices may include one or more of various known clays, such as montmorillonite, kaolin, halloysite, bentonite, attapulgite, and the like.
  • the inorganic oxide is a clay as described in U.S. Pat. No. 3,867,308; U.S. Pat. No. 3,957,689 and U.S. Pat. No. 4,458,023.
  • the matrix component may be present in the catalyst in amounts ranging from about 0 to about 60 weight percent. In certain embodiments, clay is preferably from about 10 to about 50 wt. % of the total catalyst composition.
  • the catalyst of this invention is manufactured from a slurry of the components mentioned above. Suitable steps comprise:
  • step (b) preparing an aqueous slurry comprising zeolite having a constraint index of 1 to 12, phosphorus-containing compound, alumina and optionally, matrix comprising clay, etc., in amounts which will result in a final dried product of step (b) having from about 30-85% ZSM-5 or ZSM-11, no more than 10% by weight added alumina, about 6-24% by weight phosphorous (as measured P 2 O 5 ) and no more than 30% by weight total alumina;
  • step (b) spray drying the slurry of step (a) at a low pH, such as a pH of less than about 3, preferably less than about 2;
  • the amount of added alumina is 10% or less by weight of the total components making up the particles, with particles comprising 3-8% added alumina being most preferable for FCC processes in terms of the resulting attrition properties and olefin yield.
  • the phosphorus/total alumina ratio wherein the phosphorous is measured as P 2 O 5 , is selected to obtain particles that have an attrition index of about 20 or less.
  • the ratio is also selected to optimize olefin yield. This ratio is calculated using standard techniques and is readily calculated from the amounts of phosphorous added and total alumina present in the additive. The examples below illustrate methods for obtaining the appropriate ratios.
  • total alumina includes added alumina and alumina that may be present in other components, i.e., non-added alumina. Total alumina can be measured by bulk analysis.
  • Ratios for obtaining suitable attrition resistance and preferred activity is dependent upon the content of zeolite. Generally, the higher the zeolite content, the larger the ratio used. Generally suitable ratios, as well as preferred ratios to obtain attrition indices of about 10 or less, are indicated below. All other ranges of ratios within the suitable ranges are also contemplated, e.g., 0.4 to 1.0, 0.25 to 0.7, etc. Zeolite Content Suitable Ratio Preferred Ratio 30-60% zeolite 0.2 to 1.0 0.25 to 0.70 >60-85% zeolite 0.2 to 1.9 0.45 to 1.0
  • the amount of phosphorus is selected to sufficiently harden the particle without causing a loss in activity in terms of olefin yield.
  • the sufficient amount of phosphorus for this purpose is from about 6 to about 24% of the total composition.
  • the amount of phosphorus can also be in all other ranges contained within the range of 6-24%, e.g., 7-23%, 7-15%, etc.
  • alumina affects olefin yield and attrition, and it is shown that 10% or less added alumina provides a balance of those properties. The ratios above are therefore a reflection of the effects alumina and phosphorus have on the resulting particles' properties.
  • the Davison Attrition Index is used to measure attrition of the additive.
  • DI Davison Attrition Index
  • 7.0 cc of sample catalyst is screened to remove particles in the 0 to 20 micron range. Those particles are then contacted in a hardened steel jet cup having a precision bored orifice through which an air jet of humidified (60%) air is passed at 21 liter/minute for 1 hour.
  • Commercially acceptable attrition resistance is indicated by a DI of less than about 20, and preferably less than 10.
  • the invention is suitable for any chemical reaction involving a hydrocarbon feed requiring catalyst to facilitate the reaction.
  • Such reactions include hydrocarbon conversion processes involving molecular weight reduction of a hydrocarbon, e.g., cracking.
  • the invention can also be employed in isomerization, dimerization, polymerization, hydration and aromatization.
  • the conditions of such processes are known in the art. See U.S. Pat. No. 4,418,235 incorporated herein by reference.
  • Other applicable processes include upgradings of reformate, transalkylation of aromatic hydrocarbons, alkylation of aromatics and reduction in the pour point of fuel oils.
  • hydrocarbon feedstock not only includes organic compounds containing carbon and hydrogen atoms, but also includes hydrocarbons comprising oxygen, nitrogen and sulfur heteroatoms.
  • the feedstocks can be those having a wide range of boiling temperatures, e.g., naphtha, distillate, vacuum gas oil and residual oil.
  • Such feedstocks also include those for making heterocyclic compounds such as pyridine.
  • the invention is particularly suitable for fluidized processes, e.g., in which catalyst attrition is a factor.
  • the invention is especially suitable for fluidized catalytic cracking of a hydrocarbon feed to a mixture of products comprising gasoline, alkylate, potential alkylate, and lower olefins, in the presence of conventional cracking catalyst under catalytic cracking conditions.
  • Typical hydrocarbons, i.e., feedstock, to such processes may include in whole or in part, a gas oil (e.g., light, medium, or heavy gas oil) having an initial boiling point above about 204° C., a 50% point of at least about 260° C., and an end point of at least about 315° C.
  • the feedstock may also include deep cut gas oil, vacuum gas oil, thermal oil, residual oil, cycle stock, whole top crude, tar sand oil, shale oil, synthetic fuel, heavy hydrocarbon fractions derived from the destructive hydrogenation of coal, tar, pitches, asphalts, hydrotreated feedstocks derived from any of the foregoing, and the like.
  • distillation of higher boiling petroleum fractions above about 400° C. must be carried out under vacuum in order to avoid thermal cracking.
  • the boiling temperatures utilized herein are expressed in terms of convenience of the boiling point corrected to atmospheric pressure. Resids or deeper cut gas oils having an end point of up to about 700° C., even with high metals contents, can also be cracked using the invention.
  • Catalytic cracking units are generally operated at temperatures from about 400° C. to about 650° C., usually from about 450° C. to about 600° C., and under reduced, atmospheric, or superatmospheric pressure, usually from about atmospheric to about 5 atmospheres.
  • An FCC catalyst (primary or additive) is added to a FCC process as a powder (20-200 microns) and generally is suspended in the feed and propelled upward in a reaction zone.
  • a relatively heavy hydrocarbon feedstock e.g., a gas oil
  • a catalyst is admixed with a catalyst to provide a fluidized suspension and cracked in an elongated reactor, or riser, at elevated temperatures to provide a mixture of lighter hydrocarbon products.
  • the gaseous reaction products and spent catalyst are discharged from the riser into a separator, e.g., a cyclone unit, located within the upper section of an enclosed stripping vessel, or stripper, with the reaction products being conveyed to a product recovery zone and the spent catalyst entering a dense catalyst bed within the lower section of the stripper.
  • a separator e.g., a cyclone unit
  • the catalyst is conveyed to a catalyst regenerator unit.
  • the fluidizable catalyst is continuously circulated between the riser and the regenerator and serves to transfer heat from the latter to the former thereby supplying the thermal needs of the cracking reaction which is endothermic.
  • Gas from the FCC main-column overhead receiver is compressed and directed for further processing and separation to gasoline and light olefins, with C 3 and C 4 product olefins being directed to a petrochemical unit or to an alkylation unit to produce a high octane gasoline by the reaction of an isoparaffin (usually iso-butane) with one or more of the low molecular weight olefins (usually propylene and butylene). Ethylene would be recovered in a similar fashion and processed to additional petrochemical units.
  • isoparaffin usually iso-butane
  • the low molecular weight olefins usually propylene and butylene
  • the FCC conversion conditions include a riser top temperature of from about 500° C. to about 595° C., preferably from about 520° C. to about 565° C., and most preferably from about 530° C. to about 550° C.; catalyst/oil weight ratio of from about 3 to about 12, preferably from about 4 to about 11, and most preferably from about 5 to about 10; and catalyst residence time of from about 0.5 to about 15 seconds, preferably from about 1 to about 10 seconds.
  • the catalyst of this invention is suitable as a catalyst alone, or as an additive to cracking processes which employ conventional large-pore molecular sieve component. The same applies for processes other than cracking processes.
  • Cracking catalysts are large pore materials having pore openings of greater than about 7 Angstroms in effective diameter.
  • Conventional large-pore molecular sieve include zeolite X (U.S. Pat. No. 2,882,442); REX; zeolite Y (U.S. Pat. No. 3,130,007); Ultrastable Y (USY) (U.S. Pat. No. 3,449,070); Rare Earth exchanged Y (REY) (U.S. Pat. No.
  • zeolites such as faujasite, mordenite and the like may also be used (with all patents above in parentheses incorporated herein by reference). These materials may be subjected to conventional treatments, such as impregnation or ion exchange with rare earths to increase stability. In current commercial practice most cracking catalysts contain these large-pore molecular sieves.
  • the preferred molecular sieve of those listed above is a zeolite Y, more preferably an REY, USY or REUSY.
  • SupernovaTM D Catalyst from Grace Davison is a particularly suitable large pore catalyst. Methods for making these zeolites are known in the art.
  • Other large-pore crystalline molecular sieves include pillared silicates and/or clays; aluminophosphates, e.g., ALP04-5, ALPO 4 -8, VPI-5; silicoaluminophosphates, e.g., SAPO-5, SAPO-37, SAPO-40, MCM-9; and other metal aluminophosphates.
  • Mesoporous crystalline material for use as the molecular sieve includes MCM-41.
  • the large-pore molecular sieve catalyst component may also include phosphorus or a phosphorus compound for any of the functions generally attributed thereto, such as, for example, attrition resistance, stability, metals passivation, and coke make reduction.
  • Attrition resistant and active catalyst particles comprising high content, i.e., 30-85%, zeolite.
  • the inventive catalysts are also more selective for ethylene, without substantially reducing the total light olefin, e.g., propylene, yields from catalysts and additives being used commercially, e.g., those containing about 25% ZSM-5.
  • the olefin yield of the invention as measured by propylene yield was equal (on a ZSM-5 basis) to that of conventional phosphorus stabilized ZSM-5 catalysts.
  • the activity of the invention on a ZSM-5 basis in a FCC unit, relative to OlefinsMax additive, is in the range of about 40 to 100% in terms of propylene yields per the MAT test of ASTM 3907. This activity is based on measurements at a constant conversion, e.g., 70%, and as a catalyst additive to Grace's Supernova D faujasite catalyst.
  • Preferred catalysts are at least 50% as active, and more preferably have activity in the range of 70-100% as active as OlefinsMax.
  • the invention can be as active, or two or three times more active than OlefinsMax additive on a particle basis.
  • Attrition resistant and phosphorus stabilized active catalysts having such zeolite e.g., ZSM-5 or ZSM-11, contents greater than 60% zeolite, and particularly up to 85% by weight zeolite, have heretofore not been made. It is believed that limiting the amount of alumina to 10% or less and then optimizing the ratio of phosphorus to total alumina allows one to make such catalysts. In addition to the benefits already noted above, these high content additives allow one to supplement existing catalyst inventories with zeolite catalysts having the desired activity and attrition while at the same time minimizing the amount of non-zeolite material (such as matrix) to the catalyst inventory.
  • non-zeolite material such as matrix
  • Example 1 The calcined catalysts in Example 1 were deactivated by steaming for 4 hours at 1500° F./100% steam in a fluidized bed steamer. The samples were then blended at a 2. 5 % additive level with a steam deactivated Super Nova D (Davison commercial cracking catalyst, 2.5% Re 2 O 3 on catalyst). The admixture was used to crack Feed A (Properties in Table 2) in a Microactivity Test (MAT) as set forth in ASTM 3907. TABLE 2 Feed A Feed B API Gravity @ 60° F. 22.5 23.9 Aniline Point, ° F. 163 198 Sulfur, wt. % 2.59 0.733 Total Nitrogen, wt. % 0.086 0.1 Basic Nitrogen, wt.
  • MAT Microactivity Test
  • the base case catalyst tested with these samples included: 1) steam deactivated Super Nova DTM (SND) 96% steam deactivated SND blended with 4% steam deactivated conventional catalyst additive available as OlefinsMaxTM from Davison which contains 25% of a phosphorus stabilized ZSM-5.
  • SND Super Nova DTM
  • OlefinsMax conventional catalyst additive available as OlefinsMaxTM from Davison which contains 25% of a phosphorus stabilized ZSM-5.
  • the OlefinsMax and SND compositions were steam deactivated separately, each for 4 hours at 1500° F./100% steam in a fluidized bed steamer.
  • the propylene yield (wt. % of feed) as a function of wt. % conversion is shown in FIG. 1.
  • the data shows that on an equal ZSM-5 level (1% ZSM-5), the propylene yield of the catalyst containing Example 1, Sample B, is equal to the sample containing OlefinsMax.
  • Catalysts were prepared in the same manner as Example 1 except with the following compositions:
  • Example 3 The calcined catalysts in Example 3 were deactivated by steaming for 4 hours at 1500° F./100% steam in a fluidized bed steamer. The material was then blended at a 2.5% additive level with a steam deactivated Super Nova® D cracking catalyst, 2.5% Re 2 O 3 on catalyst. The admixture was used to crack Feed A in a Microactivity Test (MAT) as set forth in ASTM 3907.
  • MAT Microactivity Test
  • the base case catalysts tested with these samples included: 1) steam deactivated SND and 2) 96% steam deactivated SND blended with 4% steam deactivated OlefinsMax.
  • the OlefinsMax and SND catalysts were steam deactivated separately, each for 4 hours at 1500° F./100% steam in a fluidized bed steamer.
  • the propylene yield (wt. % of feed) as a function of wt. % conversion is shown in FIG. 2.
  • the data shows that when compared on an equal ZSM-5 basis (1% ZSM-5), the catalysts containing Sample D and Sample E produce 85% of the propylene produced using OlefinsMax additive.
  • Sample F produces 80% of the propylene of OlefinsMax.
  • Example 5 The calcined catalysts in Example 5 were deactivated by steaming for 4 hours at 1500° F./100% steam in a fluidized bed steamer. The material was then blended at a 2.5% additive level with a steam deactivated Super Nova® D cracking catalyst, 2.5% Re 2 O 3 on catalyst. The admixture was used to crack Feed A in a Microactivity Test (MAT) as set forth in ASTM 3907.
  • MAT Microactivity Test
  • the base case catalysts tested with these samples included: 1) steam deactivated SND and 2) 96% steam deactivated SND blended with 4% steam deactivated OlefinsMax additive.
  • the OlefinsMax and SND catalysts were steam deactivated separately, each for 4 hours at 1500° F./100% steam in a fluidized bed steamer.
  • the propylene yield (wt. % of feed) as a function of wt. % conversion is shown in FIG. 3.
  • the data shows that when compared on an equal ZSM-5 basis (1% ZSM-5), the catalysts containing Sample I produces 75% of the propylene of OlefinsMax.
  • Sample G and Sample H produce 70% of the propylene of OlefinsMax.
  • Example 7 The calcined catalysts in Example 7 were deactivated by steaming for 4 hours at 1500° F./100% steam in a fluidized bed steamer. The material was then blended at a 4% additive level with a steam deactivated Super Nova® D cracking catalyst, 2.5% Re 2 O 3 on catalyst. The admixture was used to crack Feed A in a Microactivity Test (MAT) as set forth in ASTM 3907.
  • MAT Microactivity Test
  • the base case catalysts tested with these samples included: 1) steam deactivated SND and 2) 93.6% steam deactivated SND blended with 6.4% steam deactivated OlefinsMax additive.
  • the OlefinsMax and SND catalysts were steam deactivated separately, each for 4 hours at 1500° F./100% steam in a fluidized bed steamer.
  • the data from Examples 1-8 illustrate a correlation between the amount of added Al 2 O 3 in the ZSM-5 (40% by weight) catalyst and the relative propylene yield.
  • the propylene yield is measured as a percent of propylene produced relative to OlefinsMax (equal ZSM-5 level) at 70% conversion.
  • Relative ⁇ ⁇ Propylene ⁇ ⁇ Yield 100 ⁇ % ⁇ [ Propylene ⁇ ⁇ ( Example ) - Propylene ⁇ ⁇ ( SND ⁇ ⁇ Base ⁇ ⁇ Catalyst ) ] [ Propylene ⁇ ⁇ ( OlefinsMax ) - Propylene ⁇ ⁇ ( SND ⁇ ⁇ Base ⁇ ⁇ Catalyst ) ]
  • the propylene yield data for each catalyst used in the correlation was based on the best performance achieved for that catalyst (optimized P 2 O 5 level). The correlation is shown in FIG. 5 which indicates that as the added Al 2 O 3 in the catalyst decreases, the propylene yield increases. At added Al 2 O levels below 10%, the propylene yield increases dramatically. At matrix Al 2 O 3 levels between 3 and 8%, the 40% ZSM-5 catalyst becomes equal in activity to OlefinsMax when compared on an equivalent ZSM-5 basis.
  • FIG. 5 Also shown in FIG. 5 are the DI attrition numbers for the catalyst as a function of added Al 1 2 O 3 .
  • the data shows that the attrition numbers tend to increase as the added Al 2 O 3 content decreases.
  • the amount of alumina added to the slurry of starting components for the catalyst was such that the final catalyst had less than 10% by weight added alumina, acceptable propylene and low attrition numbers were produced.
  • Catalysts having the composition indicated in Table 7 for Samples M-P were prepared in the same manner as in Example 1. As with the other examples, the resulting materials were calcined for two hours at 1000° F. and analyzed for ICP, T-plot surface area, and DI attrition. This data is also reflected in Table 7, below.
  • Example 12 shows that the activity of the catalyst can be optimized with suitable phosphorus to total alumina ratio.
  • TABLE 7 Physical and Chemical Properties of 80% ZSM-5 Catalyst Sample M N 0 P ZSM-5 80 80 80 P 2 O 5 11.6 12.5 12.9 13.2 Aluminum chlorhydrol 8.4 7.5 7.1 6.8 Total 100 100 100 100 Physical Properties 2 hours @ 1000° F. P 2 O 5 /Al 2 O 3 0.67 0.78 0.83 0.88 Dl 21 5 3 3 Total BET Surface Area, m 2 /g 318 316 287 276
  • Example 11 The calcined catalysts in Example 11 were deactivated as with the other examples by steaming for four hours at 1500° F./100% steam in a fluidized bed steamer. The samples were then blended at a 2.5% additive level with a steam deactivated Super Nova® D cracking catalysts, 2.5% Re 2 O 3 on catalysts and used to crack Feed A. The feed was tested as set forth in ASTM 3907. The activity results from these tests on a ZSM-5 basis (1% ZSM-5) are in FIG. 8.
  • the phosphorous to total alumina ratio for the invention can be modified to obtain the desired propylene yields from the very high ZSM-5 content catalyst, i.e., 80% ZSM-5.
  • a catalyst having the composition indicated in Table 8 below was prepared in the manner described in Example 1 and was tested for activity to illustrate the activity on a catalyst particle basis. The previous examples illustrated the activity on a zeolite basis.
  • TABLE 8 Physical and Chemical Properties of 80% ZSM-5 Catalyst Sample Q ZSM-5 79 P 2 O 5 14 Al 2 O 3 2 Clay 0 Aluminum chlorhydrol 5 Total 100 Physical Properties 2 hours @ 1000° F. Dl 9 Al 2 O 3 , wt. % 11.5 P 2 O 5 , wt. % 14.23 SiO 2 , wt. % 76.06 P 2 O 5 /Total Al 2 O 3 0.89 Total BET Surface Area, m 2 /g 263
  • Cat suitable catalysts having a higher activity on a catalyst basis have been difficult to make because of increased attrition occurring in additives containing more than 25% ZSM-5.
  • Table 9 An equilibrium catalyst (ECAT) was also tested as a comparison base catalyst. ECAT is the same equilibrium catalyst referred to earlier in Example 10.
  • FIG. 10 illustrates the specific activity of Catalyst Q for producing ethylene compared to the 25% ZSM-5 additive.
  • Additives were prepared according to the invention using the amounts of components indicated in Tables 10, 11, and 12. The additives were prepared using the preparation methods described in Example 1. As indicated in the tables, the molar ratio of phosphorus (measured as P 2 O 5 ) to total alumina was varied for additives comprising 60, 70 and about 80% ZSM-5.
  • Catalyst R-W comprising the components indicated in Table 10 below comprise 60% by weight ZSM-5 and either 7% added alumina or 9% added alumina.
  • Catalysts X-Z are comparison catalysts which comprise more than 10% added alumina, i.e., 15% by weight added alumina. The propylene yields for each of the above-mentioned catalysts were measured. These results show that even though the comparison catalysts had suitable DI attrition numbers, they did not benefit from the invention's higher activities. These examples illustrate the advantage of catalysts comprising about 10% or less added alumina.
  • Catalysts AA-CC of Table 11 comprise 70% by weight ZSM-5. These examples illustrate modifying the molar ratio of phosphorus to total alumina in order to obtain suitable Dl attrition, as well as maximize activity for the particle.
  • Catalysts DD-GG are additional examples of the invention comprising about 75-80% by weight ZSM-5.
  • TABLE 10 Invention Invention Comparison Formulation R S T U V W X Y Z ZSM-5 60 60 60 60 60 60 60 60 60 P 2 O 5 12 14.5 16 14 16 18 15 18 21 Al 2 O 3 2 2 2 2 2 2 2 2 2 2 Clay 21 18.5 17 17 15 13 10 7 4 Aluminum chlorhydrol 5 5 5 7 7 7 13 13 13 Total 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 Physical Properties 2 hrs @ 100° F.

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US09/260,205 US20020049133A1 (en) 1999-03-02 1999-03-02 High zeolite content and attrition resistant catalyst, methods for preparing the same and catalyzed processes therewith
EP00910374A EP1077768B2 (de) 1999-03-02 2000-02-28 Katalysator mit hohem zeolith-anteil und hohem abreibungswiderstand, herstellungsverfahren und katalytische anwendungen
KR20007012173A KR100694945B1 (ko) 1999-03-02 2000-02-28 제올라이트 함량이 높은 내소모성 촉매, 그의 제조방법 및그를 사용한 촉매화방법
PT00910374T PT1077768E (pt) 1999-03-02 2000-02-28 Catalisador resistente ao atrito, de teor elevado em zeolito, metodos para a suapreparacao e processos por ele catalisados
AU32474/00A AU773403B2 (en) 1999-03-02 2000-02-28 High zeolite content and attrition resistant catalyst, methods for preparing the same and catalyzed processes therewith
PCT/US2000/005065 WO2000051731A1 (en) 1999-03-02 2000-02-28 High zeolite content and attrition resistant catalyst, methods for preparing the same and catalyzed processes therewith
ES00910374T ES2226793T3 (es) 1999-03-02 2000-02-28 Catalizador con alto contenido en zeolita y resistente al rozamiento, procedimiento para prepararlo y procedimiento para procesos catalizados con este.
CA2331123A CA2331123C (en) 1999-03-02 2000-02-28 High zeolite content and attrition resistant catalyst, methods for preparing the same and catalyzed processes therewith
DE60013376T DE60013376T3 (de) 1999-03-02 2000-02-28 Katalysator mit hohem zeolith-anteil und hohem abreibungswiderstand, herstellungsverfahren und katalytische anwendungen
BRPI0005188-8B1A BR0005188B1 (pt) 1999-03-02 2000-02-28 Catalisadores com elevado teor de zeólitos e resistentes ao atrito, métodos para a sua preparação e processos com eles catalisados
CNB008007535A CN1134301C (zh) 1999-03-02 2000-02-28 高沸石含量和耐磨耗催化剂,其制法及用其催化的方法
AT00910374T ATE275001T1 (de) 1999-03-02 2000-02-28 Katalysator mit hohem zeolith-anteil und hohem abreibungswiderstand, herstellungsverfahren und katalytische anwendungen
MXPA00010489 MX226917B (en) 1999-03-02 2000-02-28 High zeolite content and attrition resistant catalyst, methods for preparing the same and catalyzed processes therewith
JP2000602390A JP4927259B2 (ja) 1999-03-02 2000-02-28 高ゼオライト含有量で、かつ耐摩損性の触媒、同触媒の製造方法、および同触媒を用いる接触プロセス
ZA200005773A ZA200005773B (en) 1999-03-02 2000-10-18 High zeolite content and attrition resistant catalyst, methods for preparing the same and catalyzed processes therewith.
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EP1077768B1 (de) 2004-09-01
AU773403B2 (en) 2004-05-27
MXPA00010489A (es) 2001-04-01
JP4927259B2 (ja) 2012-05-09
CN1302228A (zh) 2001-07-04
BR0005188B1 (pt) 2013-11-19
KR20010052293A (ko) 2001-06-25
WO2000051731A1 (en) 2000-09-08
KR100694945B1 (ko) 2007-03-14
US6916757B2 (en) 2005-07-12
AU3247400A (en) 2000-09-21
ZA200005773B (en) 2001-07-11
JP2002537976A (ja) 2002-11-12
CN1134301C (zh) 2004-01-14
CA2331123C (en) 2010-05-04
BR0005188A (pt) 2001-01-09
ATE275001T1 (de) 2004-09-15
DE60013376T3 (de) 2012-12-06
MX226917B (en) 2005-03-23
DE60013376D1 (de) 2004-10-07
CA2331123A1 (en) 2000-09-08
DE60013376T2 (de) 2005-09-08
PT1077768E (pt) 2004-11-30
EP1077768B2 (de) 2012-08-29
ES2226793T3 (es) 2005-04-01

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