Abstract: This invention relates to a new synthetic porous crystalline material, designated MCM-67, a method for its preparation and use thereof in catalytic conversion of organic compounds. MCM-67 appears to be closely related in structure to VPI-8 and SSZ-41 but is synthesized without zinc and in the presence of manganese and/or cobalt ions.

Abstract: A catalytic cracking catalyst, which comprises (1) a zeolite, (2) a silica.cndot.alumina or an alumina and (3) a kaolin, has a pore diameter distribution having a peak at a pore diameter of 450 to 3,000 .ANG., and has 40 to 75% of a pore volume of pores of not less than 200 .ANG. and less than 2,000 .ANG. in pore diameter and 5 to 45% of a pore volume of pores of not less than 2,000 .ANG. and less than 18,000 .ANG. in pore diameter, both based on a pore volume of pores of 40 to 18,000 .ANG. in pore diameter.

Abstract: A process for catalytically cracking a heavy feed in an FCC unit, with large amounts of shape selective cracking additive is disclosed. The catalyst inventory preferably contains at least 10 wt % additive, of 12-40% ZSM-5 on an amorphous support, equivalent to more than 3.0 wt % ZSM-5 crystal circulating with equilibrium catalyst. Large yields of light olefins are produced, without excessive production of aromatics, or loss of gasoline yield. Operating with large amounts of additives allows yields of butadiene and/or methane to be suppressed, and production of a cracked gasoline fraction with an unusually low olefin content, and high ratio of cyclic unsaturates to normal unsaturates.

Abstract: A process for dewaxing middle distillate petroleum products includes the steps of introducing a middle distillate petroleum fraction having a boiling point in the range of from about 160.degree. C. to about 500.degree. C. into a reaction zone and contacting the middle distillate petroleum fraction in the reaction zone at temperatures of from about 500.degree. F. To about 700.degree. F. And pressures of from about 300 psig to about 2000 psig with a nickel-containing silicate catalyst.

Abstract: A process is provided for preparing high quality Group II and Group III lubricating base oils from a sulfur containing feedstock using mild hydrotreating followed by isomerization/dewaxing followed by hydrogenation over a sulfur resistant hydrogenation catalyst.

Abstract: A startup method for a fluidized catalytic cracking (FCC) unit operating with a magnetic catalyst separation means is disclosed. Magnetic strength, or separation severity, is maintained or increased until most of the catalyst has passed through the magnetic separation unit. After this point, magnetic flux and/or centrifugal forces, are decreased for lined-out operation. Preferably a MagnaCat.RTM. catalyst separation unit is used for magnetic fractionation of catalyst.

Abstract: It has been discovered that waxy feeds can be upgraded using a catalyst made by combining powdered dewaxing catalyst with powdered isomerization catalyst said mixture of powdered catalysts being formed into a discrete particle.

Abstract: A porous, crystalline material, designated ERS-10 zeolite, having in its calcined and anhydrous form a molecular composition of oxides corresponding to the formula (I):mM.sub.2/n O.zX.sub.2 O.sub.3.YO.sub.2 (1)wherein m, n, M, z, X and Y are as defined herein, the crystalline material having an X-ray diffraction spectrum shown in Table 1 herein.

Abstract: There is provided a catalyst comprising yttrium containing zeolite Y. The zeolite Y is essentially free of rare earth ions. There is also provided a method for making this catalyst. There is further provided a process for using this catalyst for cracking gas oils. It has been discovered that when yttrium is incorporated into this zeolite Y, and when this catalyst is used to crack gas oils, these results improved gasoline selectivity and reduced dry gas make.

Abstract: A catalytic cracking catalyst and catalytic cracking process for cracking the 650.degree. F.+ portion in a heavy feed to lighter products. The catalytic cracking catalyst contains a Y zeolite in a silica binder that is substantially free of catalytically active alumina. The silica binder contains silica gel as a component.

Abstract: A process for deasphalting a residua feedstock by use of a short vapor contact time thermal process unit comprised of a horizontal moving bed of fluidized hot particles. It is preferred that a mechanical means be used to fluidize a bed of hot particles.

Abstract: The present invention relates to new crystalline zeolite SSZ-41 which comprises oxides of (1) silicon or a mixture of silicon and germanium, and (2) zinc, said zinc being present in an amount from about 2 wt % to about 5 wt % of zinc metal based on the total weight of metals in said zeolite. Zeolite SSZ-41 may also optionally contain oxides of aluminum, iron, gallium or mixtures thereof. Zeolite SSZ-41 has the X-ray diffraction lines of Table I and has an argon adsorption capacity of at least about 0.06 cc/gm at 87.degree. K. Also disclosed are methods of making and using zeolite SSZ-41.

Abstract: A crystalline zeolite high-silica SSZ-37 is prepared using a N,N-dimethyl-4-azoniatricyclo [5.2.2.0.sup.(2,6) ] undec-8-ene cation as a template wherein said zeolite is used in hydrocarbon conversion processes.

Abstract: Methods for preparing phosphorus containing catalysts comprising a large-pore zeolite, e.g., zeolite Beta, zeolite ZSM-12, or zeolite ZSM-20, and a matrix which have improved attrition resistance. The present invention includes the catalyst compositions produced by the above methods. Also included in the present invention are methods for the use of catalysts prepared by the present method in hydrocarbon cracking processes. It is desired to develop cracking catalysts for organic compound conversion that have improved cracking yields and have good attrition resistance. This invention involves the use of large pore siliceous zeolites and a highly siliceous matrix to produce a cracking catalyst with improved cracking yields and good attrition resistance. The invention further involves the use of phosphorus and the use of selected sequences for combining the compounds in the manufacture of the catalyst to enhance the attrition resistance of the catalyst.

Abstract: This invention relates to use of MCM-49 in catalytic cracking. Large amounts of light olefins are produced.

Abstract: Oxides of nitrogen (NO.sub.x) emissions from FCC regenerators in complete CO combustion mode are reduced by degrading regenerator performance to increase the coke on regenerated catalyst. High zeolite content cracking catalyst, regenerated to contain more coke, gives efficient conversion of feed and reduces NO.sub.x emissions from the regenerator. Operating with less catalyst, e.g., 30-60% of the normal amount of catalyst in the bubbling dense bed, can eliminate most NO.sub.x emissions while increasing slightly plant capacity and reducing catalyst deactivation.

Abstract: An FCC process and apparatus for atomizing heavy feed are disclosed. A liquid feed containing stacked asphaltenes is pressurized, and preferably heated, with a gas such as light hydrocarbons. Pressurized gas and liquid discharge at high velocity into an expansion chamber, where shear force and sudden expansion disrupt stacked structures. Preferably, some thermal conversion, visbreaking, occurs in the expansion chamber. The disrupted feed is discharged into an FCC reactor, preferably to the base of a riser reactor, with a lighter feed, such as a gas oil, added higher up in the riser. Improved atomization and vaporization of the heavy feed in the riser increases conversion and reduces coke make.

Abstract: A process for fluidized catalytic cracking of heavy feed to make more catalytically cracked products and less thermally cracked products such as butadiene is disclosed. Operating an upflow riser reactor with a riser top temperature of 1050 to 1150 .degree.F., and a short catalyst residence time, yields large volumes of gasoline and light olefins, but reduced yields of butadiene. Preferably cooled catalyst in large amounts contacts severely preheated feed. FCC catalyst with over 30 wt % Y zeolite is preferred.

Abstract: A process for fluidized catalytic cracking of heavy feed to minimize yields of heavy fuel oil is disclosed. Operating a reactor with a 15:1 to 30:1 cat:oil ratio, at a reactor temperature of 1000.degree. to 1100.degree. F., and 1.5 to 5.0 seconds of catalyst residence time produces large volumes of gasoline and less than 5.0 wt % heavy fuel oil. A catalyst cooler is essential, to provide cool catalyst to the riser while permitting the regenerator to operate at 1200.degree. F. or higher. FCC catalyst with over 25 wt % large pore zeolite is preferred.

Abstract: Catalyst stripping in the fluid catalytic cracking process is improved by cooling the spent catalyst to quench catalytic condensation reactions, then stripping the cooled catalyst in a primary stripper, followed by heating and a stage of hot stripping. Quenched stripping reduces coke make by reducing conversion of light olefins, made during the FCC process, into coke.

Abstract: A fluid catalytic cracking process for producing relatively low emissions fuels. The feedstock is exceptionally low in nitrogen and aromatics and relatively high in hydrogen. The catalyst is an amorphous silica-alumina or a zeolitic material having a relatively small unit cell size. The feedstock can be characterized as having less than about 50 wppm nitrogen; greater than about 13 wt. % hydrogen; less than about 7.5 wt. % 2+ring aromatic cores; and not more than about 15 wt. % aromatic cores overall.

Abstract: Disclosed is a fluid catalytic cracking process for producing low emissions fuels. The feedstock is exceptionally low in nitrogen and aromatics and relatively high in hydrogen. The catalyst is a mixture of zeolite Y and zeolite beta (.beta.). The feedstock can be characterized as having less than about 50 wppm nitrogen; greater than about 13 wt. % hydrogen; less than about 7.5 wt. % 2+ ring aromatic cores; and not more than about 15 wt. % aromatic cores overall.

Abstract: Catalytic cracking catalysts and catalyst additives which contain silica modified bayerite and/or eta alumina.

Abstract: Middle distillates can be produced efficiently in high yields by catalytically cracking petroleum hydrocarbons by contacting the petroleum hydrocarbons at cracking conditions with a catalyst composition comprising a cation-exchanged stevensite.

Abstract: A layered catalyst contains a core of at least one, and preferably three, molecular sieve components within a shell layer of reduced molecular sieve content. A preferred catalyst consists of a core of a large pore molecular sieve, preferably a dealuminized Y-type zeolite, a shape selective paraffin cracking/isomerization component, preferably HZSM-5, and a shape selective aliphatic aromatization component, preferably gallium ZSM-5, within a shell of an alumina-rich, matrix. The shell can capture metals from the feeds being processed, it can act as a metals sink, and can remove metals form the unit by attrition. The catalyst is preferably prepared by forming the core and then coating or encapsulating the core with a shell having a reduced molecular sieve content. The shell may contain a pillared clay or other very large pore cracking component. The shell may be an attritable coating of an amorphous rare earth oxide, aluminum oxide and aluminum phosphate composite, which traps metals.

Abstract: An economic and safe process includes a catalytic cracking of the rubber tires and rubber products in the presence of mica catalyst selected from muscovite, sericite and biotite at a reaction temperature of 230.degree.-400.degree. C. under a pressure of 1-2.5 atmospheres for forming mixed oils, carbon black, gaseous products, and other residual products.

Abstract: A process for thermally and catalytically upgrading a heavy feed in a single riser reactor FCC unit is disclosed. A heavy feed is added to a blast zone in the base of the riser, and sufficient hot regenerated FCC catalyst is added to induce both thermal and catalytic cracking of the heavy feed. A reactive quench material, which cools the material discharged from the blast zone is added to a quench zone downstream of the blast zone, to reduce temperature at least in part by undergoing endothermic reactions in the riser. Quench liquids can be distillable FCC feeds such as gas oil, slack wax, or alcohols or ethers. The quench material is added in an amount equal to 100 to 1000 wt % of the non-distillable material in the heavy feed. A preferred catalyst, with a high zeolite content, is used which retains activity in the quench despite initial contact with the heavy feed, which tends to overwhelm conventional FCC catalysts.

Abstract: A catalytic cracking composition comprising a physical blend of a cracking catalyst component with alcohol treated Sr(OH).sub.2 and alcohol is used to crack hydrocarbon-containing feedstocks that further contain quantities of vanadium.

Abstract: A process and catalyst for catalytic cracking comprising a non-layered, ultra-large pore crystalline material. The crystalline material preferably has a benzene adsorption capacity greater than about 15 grams benzene/100 grams at 50 torr and 25.degree. C. Preferred materials have a hexagonal electron diffraction pattern that can be indexed with a d.sub.100 value greater than about 18 Angstrom Units and a hexagonal arrangement of uniformly sized pores with a maximum perpendicular cross section of at least about 13 Angstrom units. Preferred cracking catalysts comprise ultra-large pore materials having pore openings formed by at least 20 tetrahedrally coordinated members, most preferably with 36 or 42 tetahedrally coordinated members.

Abstract: A process for naphtha cracking employing new synthetic catalyst of ultra-large pore crystalline material. The new crystalline material exhibits unusually large sorption capacity demonstrated by its benzene adsorption capacity of greater than about 15 grams benzene/100 grams at 50 torr and 25.degree. C., a hexagonal electron diffraction pattern that can be indexed with a d.sub.100 value greater than about 18 Angstrom Units and a hexagonal arrangement of uniformly sized pores with a maximum perpendicular cross section of at least about 13 Angstrom units.An improved cracking reaction is provided for catalytic conversion of hydrocarbon feedstock which comprises contacting the feedstock under catalytic conversion conditions with acid metallosilicate solid catalyst having the structure of MCM-41 with hexagonal honeycomb lattice structure consisting essentially of uniform pores in the range of about 20 to 100 Angstroms. The cracking reaction is very selective, especially when conducted at temperature of about 425.

Abstract: A catalytic cracking process for converting a hydrocarbon fraction, preferably boiling in the range of a heavy gas oil, is disclosed in which the cracking catalyst is a large crystal fully crystalline zeolite Beta having a broad range of silica-to-alumina mole ratios, i.e. 20->1000. The zeolite Beta catalyst is synthesized with a nitrogenous organic chelating agent, such as a tertiary alkanolamine, preferably triethanolamine, in the synthesis mixture along with at least one source of organic directing agent such as tetraethylammonium hydroxide, tetraethylammonium bromide and tetraethylammonium fluoride. The zeolite Beta can be used as a stand alone catalyst or an additive catalyst for hydrocarbon cracking reactions along with another molecular seive type catalyst such as a faujasite catalyst or ZSM-5. The large crystal zeolite Beta can also be treated with a source of phosphorus to enhance the properties of the zeolite.

Abstract: A novel shell-coated FCC catalyst is disclosed wherein the shell is a mixture of at least one refractory metal oxide or silicate or precursor thereof (preferably clay) having a particle size of 0.3 to 5 microns and an inorganic refractory binder (preferably silica) having a particle size of less than 0.01 microns and the core is a zeolite-containing microsphere.

Abstract: A process is provided for effecting catalytic conversion of an organic compound-containing feedstock to conversion product which comprises contacting said feedstock under catalytic conversion conditions with a catalyst comprising an active form of a functionalized inorganic, porous, non-layered crystalline phase having uniformly sized pores of at least about 13, e.g., at least about 15, Angstrom Units in diameter.

Abstract: A process is provided for effecting catalytic conversion of an organic compound-containing feedstock to conversion product which comprises contacting said feedstock under catalytic conversion conditions with a catalyst comprising an active form of an inorganic, porous crystalline phase exhibiting, after calcination, a hexagonal arrangement of uniformly-sized pores having diameters of at least about 13, e.g., at least about 15, Angstrom Units and exhibiting a hexagonal electron diffraction pattern that can be indexed with a d.sub.100 value greater than about 18 Angstrom Units.

Abstract: Improved catalytic process for carrying out heavy hydrocarbon conversion in the presence of metal on the catalyst and in the feedstock, by catalytic cracking such heavy carbometallic oils to lighter molecular weight fractions. The discovery of a ferro/superparamagnetic component of older catalyst, which when present, can be employed to achieve enhanced magnetic separation of aged catalyst. This invention utilizes this property to enhance separation of more magnetically active, older, less catalytically active and selective, higher metals-containing catalyst particulates from less magnetically active, lower metal containing particulates. The more catalytically active and selective catalysts fractions, are then recycled back to the process.

Abstract: There is provided a catalyst comprising a layered silicate, such as magadiite, containing interspathic polymeric silica which serves to prop open the layers. The catalyst further comprises rare earth cations which are exchanged with other cations in the silicate. It has been discovered that this rare earth cation exchange imparts enhanced hydrothermal stability to the catalyst. There is also provided a method for making this catalyst and a process for using this catalyst for cracking hydrocarbons. In the cracking process, the catalyst is regenerated.

Abstract: A metals scavenging composition comprising a rare earth component and a layered magnesium silicate, such as sepiolite or attapulgite, is mixed with separate particles of a cracking catalyst and the mixture used to crack hydrocarbon feedstocks containing relatively high concentrations of vanadium and other contaminant metals. The use of the metals scavenger prolongs the life of the catalyst while maintaining (1) relatively high conversions and gasoline yields, and (2) relatively low hydrogen and coke makes.

Abstract: A metals-tolerant FCC catalyst and a process using the catalyst are disclosed. The catalyst matrix comprises bastnaesite and a limited quantity of a large pore boehmite alumina having an average pore diameter greater than 90 Angstroms. The catalyst preferably also contains a molecular sieve component, a siliceous binder and a clay component. The catalyst formulation reduces the harmful effects of accumulated nickel and vanadium on catalyst activity and selectivity. Hydrogen and coke production are reduced.

Abstract: Novel hydrocarbon conversion catalysts and methods for their preparation are disclosed. The catalysts are particularly appropriate for the conversion of hydrocarbon feeds to high octane gasoline, while increasing light cycle oil and decreasing heavy cycle oil yield. The catalyst comprises a zeolite, a cogelled silica-alumina matrix, and clay.

Abstract: One embodiment is an improved process for economically converting carbo-metallic oils by means of catalytic particulates into lighter products, wherein a portion of the particulates is withdrawn and passed through a high strength magnetic field of at least 1 KG and field grandients of at least 10 KG/inch while conveyed on an electrostatic conducting belt to enable separation of the mass of particulates by inertia into at least two fractions; one of which has, in the case of catalyst, higher activity and lower metals content and is recycled back to the unit; a second higher metals, lower activity catalyst which is disposed of or treated for recovery of metals; and optimally, intermediate fraction which can be disposed of, or first treated to remove metals, and then chemically reactivated and returned to the unit.

Abstract: The present invention provides a highly selective catalytic cracking process for the conversion of feedstocks containing a predominant content of C.sub.10 and higher mixed olefins into C.sub.9 and lower olefin products at efficiencies of greater than 20%. said products further characterized in that the content C.sub.6 to C.sub.9 olefins is maximized while the content of C.sub.2 to C.sub.4 olefins is minimized. The process involves contacting an olefin feedstock mixture containing at least about 50 weight %, more preferably at least about 70 weight %, of C.sub.10 and higher olefins under cracking conditions with a catalyst selected from the group consisting of amorphous precipitated silica, selected crystalline silicates and aluminosilicates, namely beta, mordenite and ZSM-5 types, as well as ion exchanged or acid variants thereof. Cracking conditions include a temperature within the range of from about 250.degree. up to about 450.degree. C.

Abstract: A process is provided for catalytic conversion of organic compounds in a conversion zone containing a synthetic, non-composited microporous membrane comprising a continuous array of crystalline molecular sieve material.

Abstract: A composition for use as a road base or levee fill. The composition comprises catalytic cracking catalyst particles in the size range of 1 to 200 microns and a binder the type and amount of which depend on the end use. Hydrated lime is employed as the binder in road base construction while hydrated lime, portland cement, fly ash or mixtures of fly ash and portland cement can be used in levee construction. The spent catalyst particles are present in amounts of 80% to 96% and the binder is present in amounts of 4% to 20%, both percentage ranges being determined according to the dry weight of the composition.

Abstract: There is provided a process for cracking hydrocarbon feedstocks which include large hydrocarbon molecules. Examples of such feedstocks are those which include a large proportion of resids. The catalyst used in this process comprises a layered silicate, such as magadiite, containing interspathic polymeric silica which serves to prop open the layers.

Abstract: A catalytic cracking process is disclosed employing a dual component cracking catalyst system comprising zeolite as a first component and a mixture of a calcium/magnesium-containing material and a magnesium-containing material as a second component. The preferred calcium/magnesium-containing material is dolomite and the preferred magnesium-containing material is sepiolite.

Abstract: Crystalline silica-titania catalyst compositions, optionally containing magnesium, are disclosed; the titanium is introduced through the use of organo-titanate chelates wherein the titanium has a coordination number of at least 5. The compositions are used in acid-catalyzed reactions such as alkylation reactions.

Abstract: A fluid catalytic cracking process wherein a hydrocarbon charge-stock is atomized and injected, in a contactor/reactor, into a vertical curtain of hot regenerated catalyst to vaporize and crack hydrocarbons in the charge-stock, wherein the catalyst preferably contains at least 40% by weight of a zeolitic cracking component and the contact time of the hydrocarbon vapors and the catalyst in the contactor/reactor is ultra-short, preferably not greater than 0.5 second.

Abstract: This invention relates to use of a new improved form of crystalline silicate identified as zeolite ZSM-11 as a catalyst component for organic compound, e.g. hydrocarbon compound, conversion.

Abstract: A process for increasing the volume of feed throughput to the FCC by decreasing coke make under catalytic cracking conditions including a temperature of 950.degree. F. to about 1150.degree. F., a catalyst to feed ratio of 3:1 to 10:1 and a catalyst contact time of from about 1 to about 20 seconds in the presence of catalyst comprising framework silicon enriched ZSM-20.

Abstract: Catalytic cracking catalysts which contain a basic alkaline earth metal component in amounts greater than 5 percent by weight (expressed as the oxides) are used to crack hydrocarbon feedstocks that contain substantial quantities of metals such as vanadium, nickel, copper and iron. In a particularly preferred embodiment natural or synthetic particulate magnesium oxide (MgO) containing composites such as dolomite or a formed particulate coprecipitated magnesia-silica cogel (MgO.SiO.sub.2) having a substantial intra-particle pore volume in pores ranging from about 200-10,000 .ANG. in diameter and an average pore diameter greater than about 400 .ANG. in the 200-10,000 .ANG. diameter range is mixed with a zeolite containing fluid cracking catalyst (FCC) either as an integral component of the catalyst particle or as a separate additive.