Abstract: A new process for the hydrodealkylation of ethylbenzene and the isomerization of xylenes at low pressure and at a low hydrogen to ethylbenzene mole ratio as well as a low hydrogen to hydrocarbon feed mole ratio using a catalyst comprising (a) HZSM-5 having a particle size less than 1.0 microns, (b) a Group VIII metal such as platinum, and (c) an additional element such as magnesium.

Abstract: Disclosed is a method for producing aromatic hydrocarbons, which comprises contacting a light hydrocarbon feedstock comprising olefins and/or paraffins with a zeolite catalyst in a fixed-bed, adiabatic reactor containing a fixed catalyst bed comprised of the zeolite catalyst, to thereby effect a catalytic cyclization reaction of the light hydrocarbon feedstock, wherein the catalytic cyclization reaction is performed under conditions which satisfy the following requirements: (1) the zeolite catalyst has an initial stage-catalytic activity of 0.2 (sec.sup.-1) or more in terms of the initial stage, first-order reaction rate constant of the decomposition of n-hexane catalyzed by the zeolite catalyst; (2) the catalyst bed has a temperature of from 450.degree. C. to 650.degree. C.

Abstract: In the present invention, dimethylbutanes are removed from the raffinate component of the feed to a dehydrocyclization process. Thus, according to a preferred embodiment, a process is provided for producing aromatics by the following steps:(a) contacting fresh paraffins rich feed hydrocarbons, containing 0.1 to 20.0 wt. % dimethylbutanes with a highly selective dehydrocyclization catalyst in a reaction zone, under dehydrocyclization reaction conditions, to convert paraffins to aromatics and obtain an aromatics rich effluent;(b) separating aromatics from the effluent to obtain an aromatics lean raffinate;(c) removing dimethyl butanes from the raffinate to obtain a raffinate of reduced dimethylbutane content; and(d) recycling the raffinate of reduced dimethylbutane content to the reaction zone.Preferably, the dehydrocyclization catalyst used is a nonacidic, monofunctional catalyst. Platinum on L zeolite is a particularly preferred highly selective dehydrocyclization catalyst for use in the process.

Abstract: A process for the hydroisomerization of a predominantly C.sub.8 -C.sub.20 n-paraffinic feed to produce a high purity C.sub.8 -C.sub.20 paraffinic solvent composition having superior low temperature properties, and low viscosities. The feed is contacted, with hydrogen, over a dual functional catalyst to hydroisomerize and convert the feed to a product comprising a mixture of n-paraffins and isoparaffins, the isoparaffins component of which contains greater than 50 percent of mono-methyl species, with the molar ratio of isoparaffins:n-paraffins ranging from about 0.5:1 to 9:1.

Abstract: This is a process for upgrading a petroleum naphtha fraction. The naphtha is subjected to reforming and the reformate is cascaded to a benzene and toluene synthesis zone over a benzene and toluene synthesis catalyst comprising a molecular sieve of low acid activity. The preferred molecular sieve is steamed ZSM-5. The benzene and toluene synthesis zone is operated under conditions compatible with the conditions of the reformer such as pressures of above about 50 psig (446 kPa) and temperatures above about 800.degree. F. (427.degree. C). In one aspect of the invention, the benzene and toluene synthesis catalyst includes a metal hydrogenation component such as cobalt, nickel, platinum or palladium. In one mode of operation, the benzene and toluene synthesis catalyst replaces at least a portion of the catalyst of the reformer. The process produces a product containing an increased proportion of benzene and toluene, and a reduced proportion of C8 aromatics, particularly ethylbenzenes, as compared to the reformate.

Abstract: A catalyst composition and a process for converting a hydrocarbon stream such as, for example, a C.sub.9 + aromatic compound to C.sub.6 to C.sub.8 aromatic hydrocarbons such as xylenes are disclosed. The catalyst composition comprises an aluminosilicate, and a metal wherein the weight ratio of aluminum to silicon is in the range of from about 0.002:1 to about 0.6:1. The process comprises contacting a hydrocarbon stream with the catalyst composition under a condition sufficient to effect the conversion of a hydrocarbon to a C.sub.6 to C.sub.8 aromatic hydrocarbon.

Abstract: A hydrocarbon feedstock is catalytically reformed in a process which comprises at least three catalyst zones. The feedstock contacts a catalyst comprising platinum, a halogen, and a metal promoter on a solid catalyst support in a first catalyst zone. Effluent from the first catalyst zone contacts a catalyst comprising platinum, germanium and halogen on a solid catalyst support in an intermediate catalyst zone to obtain an intermediate effluent, which contacts a catalyst having the essential absence of germanium and comprising platinum, halogen and a metal promoter on a solid catalyst support in a terminal catalyst zone to obtain a reformate.

Abstract: A process for saturating aromatics in a lube range hydrocarbon is disclosed. The process can be used to raise the viscosity index of the lube range products. The process is carried out over a noble metal catalyst under mild process conditions. The catalyst is resistant to sulfur and nitrogen compounds.

Abstract: The present invention provides a catalyst composition, and a hydrocarbon conversion process in which it is used, comprising as first cracking component a zeolite beta having a silica to alumina molar ratio of at least 20 which is in the form of crystals less than 100 nm in size; a second cracking component selected from (i) crystalline molecular sieves having pores with diameters greater than 0.6 nm, (ii) crystalline, mesoporous aluminosilicates having pores with diameters of at least 1.3 nm, and (iii) clays; and at least one hydrogenation component.

Abstract: A catalytic reforming process is disclosed using a catalyst containing a Group VIII metal, low amounts of bismuth, and a zeolite L. The catalyst is a non-acidic, monofunctional reforming catalyst. Preferably, the catalyst contains one or more halogens. Preferably, the feed includes C.sub.8 hydrocarbons. The addition of small amounts of bismuth increase or substantially maintain catalyst stability. Unexpectedly low dealkylation rates are achieved using the catalyst while reforming to produce aromatics, especially to produce xylenes such as paraxylene.

Abstract: A process for reforming a hydrocarbon fraction substantially free of dimethylbutanes. The hydrocarbon is separated into a fraction comprising the C.sub.5 - hydrocarbons and the dimethylbutanes, a light fraction excluding dimethyl butanes, and a heavy fraction. The light fraction is reformed in the presence of a monofunctional catalyst, and the heavy fraction is reformed in the presence of a bifunctional catalyst.

Abstract: Discloses high purity solvent compositions constituted of n-paraffins and isoparaffins, with the isoparaffins containing predominantly methyl branches, and having an isoparaffin:n-paraffin ratio sufficient to provide superior low temperature properties and low viscosities. The solvent compositions are made by a process wherein a waxy, or long chain paraffinic feed, especially a Fischer-Tropsch wax, is reacted over a dual function catalyst to produce hydroisomerization and hydrocracking reactions at 700.degree. F.+ conversion levels ranging from about 20 to 90 wt. % to provide a C.sub.5 -1050.degree. F. crude fraction. The C.sub.5 -1050.degree. F. crude fraction is then topped via atmospheric distillation to produce a low boiling fraction with an upper end point boiling between about 650.degree. F. and 750.degree. F. The low boiling fraction is fractionated and a narrow boiling range solvent obtained therefrom; one which can be further divided into solvent grades of various boiling ranges.

Abstract: A hydrocarbon conversion process wherein austenitic stainless steel portions that are subject to halide stress-corrosion cracking conditions, such as the colder portions of the process equipment including effluent coolers, knockout drums, accumulation drums, and piping low points, are provided with a protective layer having improved halide stress-corrosion cracking resistance. The method comprises applying a metal cladding, plating, paint or other coating to a stressed portion of austenitic stainless steel hydrocarbon conversion process equipment, optionally curing the coated steel to form intermetallic compounds to protect the steel portions; converting hydrocarbons utilizing a halided catalyst or under conditions where a halogen-containing compound is added or evolved or both; and subjecting the protected steel portion to halide stress-corrosion cracking conditions.

Abstract: A catalyst system for treating sulfur and nitrogen contaminated hydrocarbon feedstock includes a matrix, at least one support medium substantially uniformly distributed through said matrix and comprising a silica alumina molecular sieve material having a silica/alumina ratio of at least about 20, a first catalytically active metal phase supported on said support medium, said first catalytically active metal phase comprising a first metal and a second metal each selected from group VIII of the Periodic Table of Elements, said first metal being different from said second metal, a second catalytically active metal phase supported on said matrix, said second catalytically active metal phase comprising a third metal and a fourth metal each selected from group VIII of the Periodic Table of Elements and a fifth metal selected from group VIb of the Periodic Table of Elements, said third metal being different from said fourth metal.

Abstract: A reforming process, selective for the dehydrocyclization of paraffins to aromatics, is effected using a catalyst containing multiple Group VIII (8-10) noble metals having different gradients within the catalyst and a nonacidic large-pore molecular sieve. The use of this bed of catalyst results in greater selectivity of conversion of paraffins to aromatics and improved catalyst stability, particularly in the presence of small amounts of sulfur.

Abstract: A high temperature treatment process is disclosed for increasing conversion and reducing the fouling rate of reforming catalysts. The process comprises reducing the catalyst in a reducing gas atmosphere at a temperature below 1025.degree. F. and then treating the reduced catalyst at a temperature of from 1025.degree. F. to 1275.degree. F. in an inert gas atmosphere.

Abstract: Disclosed is a one-step process intended as an alternative to catalytic reforming which upgrades naphthas by simultaneously saturating aromatics, isomerizing paraffins and selectively cracking heavier hydrocarbons which comprises contacting heavy naphtha feedstock in a reforming zone with a catalyst comprising a solid acid, optionally with a binder of Group III and/or IV of the Periodic Table, having a metal from Group VIII of the Periodic Table deposited thereon, wherein the reaction conditions are much milder than those typically used in catalytic reforming.

Abstract: This invention relates to use of a new and improved form of crystalline material identified as having the structure of SUZ-9 as a sorbent or a catalyst for organic compound, e.g., hydrocarbon compound, conversion.

Abstract: A novel catalyst and the use thereof in a reforming process is disclosed. The catalyst comprises a refractory inorganic oxide, platinum-group metal, Group IVA(IUPAC 14) metal, and europium in a specified ratio. Utilization of this catalyst in the reforming of hydrocarbons, especially in reforming, results in significantly improved selectivity to the desired gasoline or aromatics product.

Abstract: Acidic halides, especially chlorides, are removed from liquid hydrocarbons such as catalytic reformate by contact with solid caustic such as a bed of NaOH pellets covered with a thin film of brine. Hydration of reformate improves removal when large amounts of chlorides are present in reformate. Halides in liquid hydrocarbon are recovered as a brine phase, which can be only slightly alkaline. Hydration of reformate can be controlled based on pH of brine removed from the bed.

Abstract: A difunctional catalyst is disclosed which is constituted by:(a) silica particles partially coated with zirconia, acidified by means of the introduction of sulfate moieties,(b) one or more metal(s) from Group VIIIA.The preparation of said catalyst and its use in wax hydroisomerization are disclosed as well.

Abstract: A reforming process, selective for the dehydrocyclization of paraffins to aromatics, is effected using a catalyst containing multiple Group VIII (8-10) noble metals having different gradients within the catalyst and a nonacidic large-pore molecular sieve. The use of this bed of catalyst results in greater selectivity of conversion of paraffins to aromatics and improved catalyst stability, particularly in the presence of small amounts of sulfur.

Abstract: A catalyst system comprises a physical mixture of a conversion catalyst and a sulfur sorbent to accommodate small quantities of sulfur from a hydrocarbon feedstock. Preferably, the physical mixture comprises a sulfur-sensitive reforming catalyst protected from sulfur deactivation by a manganese-oxide catalyst. The invention shows substantial benefits over prior-art processes in catalyst utilization.

Abstract: Acidic halides, especially chlorides, are removed from dry process vapor and liquid hydrocarbon streams by contact with solid caustic, such as a bed of NaOH. Salt deposits from form on the solid caustic, which are periodically removed by passing a liquid hydrocarbon continuous phase containing a minor amount of dissolved or entrained water over the solid caustic. Salts may be removed from the liquid hydrocarbon by extraction with water, which also saturates the liquid hydrocarbon so that it may be used to remove additional salt deposits.

Abstract: An intermediate pore size molecular sieve supported catalyst includes a platinum group component and a gallium, zinc, indium, iron, tin or boron component. It is used for reforming and aromatization during which it produces a para-xylene enriched product. It comprises an intermediate pore size molecular sieve support, a platinum group component and a component selected from the group consisting of gallium, zinc, indium, iron, tin or boron. One form of the catalyst is first coked and is then contacted with hydrogen. The catalyst is useful in reforming and aromatizing operations.

Abstract: This invention deals with a process for converting aliphatic C.sub.2 -C.sub.6 hydrocarbons into C.sub.6.sup.+ aromatics and C.sub.3.sup.= /C.sub.4.sup.= olefins. The process involves combining dehydrocyclodimerization (DHCD) with dehydrogenation. Thus, the feedstream is first sent to a DHCD zone which produces an effluent stream which contains C.sub.6.sup.+ aromatics along with C.sub.1 -C.sub.5 hydrocarbons. This effluent stream is separated into a stream containing C.sub.1 -C.sub.4 hydrocarbons and one containing C.sub.6.sup.+ aromatics. The C.sub.1 -C.sub.4 containing stream is flowed to a dehydrogenation zone to produce C.sub.3.sup.= /C.sub.4.sup.= olefins.

Abstract: The present invention is directed to an improved isomerization process employing a catalyst wherein the catalyst comprises a pair of catalyst particles of different acidity utilized either as distinct beds of such discrete particles or as a mixture of such discrete particles. The isomerization process utilizing such a catalyst produces a product which exhibits higher VI as compared to products produced using either catalyst component separately or using a single catalyst having the average acidity of the two discrete catalysts.

Abstract: A catalytic reforming process uses a riser reactor with multiple catalyst injection points to obtain high aromatics yields from a naphtha feedstock. Product from the riser reactor typically is discharged into a fluidized-reforming reactor, in which the reforming reaction is completed and catalyst is separated from hydrogen and hydrocarbons. Hydrocarbons from the reactor are separated to recover an aromatized product. Catalyst is regenerated to remove coke and reduced for reuse in the reforming process.

Abstract: Catalytic reforming wherein the lead reactor contains a catalsyt comprised of platinum and a relatively low level of Re on an inorganic oxide support. The tail reactor contains a platinum rhenium catalyst wherein the rhenium content is at higher levels.

Abstract: The invention concerns a process for reducing the benzene content of petrol fractions and isomerizing paraffins in the presence of an isomerization catalyst comprising 4 to 15% of at least one halogen and at least one metal from group VIII deposited on a support composed of a mixture of specific proportions of eta alumina and gamma alumina, in which isomerization is carried out on a mixture of a) a feed with the following composition by weight: 40% to 80% of paraffins, 0.5% to 7% of cyclic hydrocarbons and 6% to 45% of aromatics, and with a maximum distillation temperature of between 70.degree. C. and 90.degree. C., b) a C.sub.5 -C.sub.6 cut which is generally a straight run cut, and c) a chlorine-containing compound providing a concentration of 50-5000 ppm of chlorine in the mixture.

Abstract: A novel zeolite characterized by a large number of secondary pores, a substantially decreased Lattice Constant of below about 24.19 .ANG., and a substantially decreased Acid Site Density is attained by hydrothermal and acid-treating of an ultrastable Y-zeolite.

Abstract: Reforming is effected with a combination of a primary supported noble-metal catalyst and a catalyst containing one or more medium pore non-zeolite molecular sieves (MP-NZMS). The latter reforming and dehydrocyclization comprise a Group VIII metal and at least one bound MP-NZMS characterized in the calcined form by an adsorption of isobutane of at least 2 percent by weight at a partial pressure of 500 torr and a temperature of 20.degree. C. and characterized by an adsorption of triethylamine less than about 5 percent by weight at a partial pressure of 2.6 torr and a temperature of 22.degree. C., The MP-NZMS catalyst binder preferably is alumina and/or silica, and the Group VIII metal preferably is platinum.

Abstract: A process for reducing the amount of down time or yield loss associated with a sulfur upset when using a sulfur-sensitive catalyst. The process comprises applying a metallic coat, cladding, plating or paint to a reactor system which comprises a base metal, so as to form an adherent metallic layer on the base metal and thereby produce a metal-coated reactor system; loading a sulfur-sensitive catalyst into the system; and, after a sulfur upset, using a process comprising sulfur stripping to remove sulfur contaminants from the metal-coated reactor system.

Abstract: An isomerization process is provided which process utilizes a sulfated solid catalyst comprising (1) oxide or hydroxide of Group III or Group IV element, e.g. zirconium, and (2) a first metal comprising a metal or combination of metals selected from the group consisting of platinum, palladium, nickel, platinum and rhenium, and platinum and tin. The sulfated support is calcined prior to incorporation of the first metal and subsequent to said incorporation. The catalyst may further comprise (3) a second metal selected from the group consisting of Group VIII elements, e.g. iron. One embodiment of the invention further comprises (4) a third metal selected from the group consisting of Group V, VI and VII elements, e.g. manganese. Said second and third metals are added prior to the first calcination.

Abstract: A hydrocarbon feedstock is catalytically reformed to effect dehydrocyclization of paraffins in a process combination comprising a first reforming zone, a sulfur-removal zone containing a mixed reforming catalyst and sulfur sorbent comprising a manganese component to preclude sulfur from the feed to a second reforming zone. The process combination shows substantial benefits over prior art processes in achieving reforming-catalyst stability.

Abstract: Catalytic reforming of C.sub.9 + containing naphtha with a high yield of BTX is disclosed. Naphtha is converted under customary reforming conditions on a catalyst which contains at least one platinum group metal at least one metal of the group IV B, and at least one halogen component on an oxidic carrier.

Abstract: A naphtha upgrading process is provided which process utilizes a sulfated solid catalyst comprising (1) oxide or hydroxide of Group III or Group IV element, e.g. zirconium, and (2) a first metal comprising a metal or combination of metals selected from the group consisting of platinum, palladium, nickel, platinum and rhenium, and platinum and tin. The sulfated support is calcined prior to incorporation of the first metal and subsequent to said incorporation. The catalyst may further comprise (3) a second metal selected from the group consisting of Group VIII elements, e.g. iron. One embodiment of the invention further comprises (4) a third metal selected from the group consisting of Group V, VI and VII elements, e.g. manganese. Said second and third metals are added prior to the first calcination.

Abstract: The crystal size and shape of zeolite KL can be improved by forming the zeolite from a synthesis mixture in which the molar ratio of K.sub.2 O/SiO.sub.2 is 0.18 to 0.36, and in which the synthesis mixture comprises iron preferably in an amount such that the molar ratio of Fe.sub.2 O.sub.3 /Al.sub.2 O.sub.3 is 0.015 to 0.3.

Abstract: A hydrocarbon feedstock is catalytically reformed in a sequence comprising a reforming zone containing a catalyst comprising a platinum-group metal and a nonacidic L-zeolite and an aromatics-isomerization zone containing a catalyst comprising a platinum-group metal, a metal attenuator and a refractory inorganic oxide. The process combination features high selectivity in producing a high-purity BTX product from naphtha.

Abstract: A reforming process, selective for the dehydrocyclization of paraffins to aromatics, is effected using a bed of catalyst particles containing multiple Group VIII (8-10) noble metals having different gradients within the catalyst particles and a nonacidic large-pore molecular sieve. The use of this bed of catalyst particles results in greater selectivity of conversion of paraffins to aromatics and improved catalyst stability, particularly in the presence of small amounts of sulfur.

Abstract: Disclosed are reactions for the aromatization of hydrocarbons containing 2 to 9 carbon atoms per molecule, with a composite catalyst containing:an MFI zeolite in hydrogen form, the framework containing at least one of the elements silicon, aluminum and/or gallium; a matrix; gallium; at least one noble metal of the platinum family, at least one additional metal selected from the group made up of tin, germanium, indium, copper, iron, molybdenum, gallium, thallium, gold, silver, ruthenium, chromium, tungsten and lead, and possibly a compound selected from the group made up of alkali and alkaline earth metals.

Abstract: A process and catalyst are provided for dehydrogenating a hydrocarbon feedstock and producing an olefinic product. The process comprises contacting the feedstock at dehydrogenation conditions with a dehydrogenation catalyst comprising from about 0.01 weight percent to about 5.0 weight percent of a platinum group metal, from about 0.02 weight percent to about 10.0 weight percent of zinc, and a support component comprising L zeolite and an alkali metal.

Abstract: Disclosed is a reforming process for the production of gasoline having an increased isoparaffin yield, reduced aromatics content and a constant octane level which comprises passing the gasoline precursor containing greater than 20 vol% aromatics over a reforming catalyst comprising one or more metals from Group VIII and IVA of the Periodic Table on an oxide support, having a total pore volume of about 0.300 to 0.600 cc/g and greater than 85% of the pore volume in pores of diameter less than 100.ANG..

Abstract: A process for reforming a gasoline boiling range naphtha stream using a reforming process unit comprised of two independent process units, each of which are operated in two stages. The first stage is operated in a fixed-bed mode and is comprised of a plurality of serially connected fixed bed reactors, and the second stage is operated in a moving bed continuous catalyst regeneration mode. A hydrogen-rich stream is recycled through both stages for each process unit and the moving-bed reforming zones share a common regeneration zone.

Abstract: A method for producing alkylnaphthalenes in a reformer process unit used to reform a gasoline boiling range hydrocarbonaceous feedstock in the presence of a platinum containing supported catalyst at reforming process conditions, the method comprising spiking said feedstock with up to about 5 vol.% of an additional stream containing a substantial amount of tetralins and decalins, based on the volume of feedstock.

Abstract: Catalytically cracked naphthas containing C.sub.9 + hydrocarbons are hydrocracked over a crystalline zeolite, typically, mildly steamed zeolite beta then subjected to reforming to achieve a gasoline product of reduced end boiling range and higher octane than the feed. A hydrogen stream from the reformer which contains a catalytic promoter, such as chlorine, is separated into a first stream and a second stream. The first stream is treated over a solid sorbent to remove the promoter and recycled promoter to the hydrocracking step while the untreated second hydrogen stream which contains promoter is recycled to the reformer.

Abstract: A method is provided of selecting operating parameters for an aromatization process having at least penultimate and final stages, each containing a respective catalyst, for optimum aromatic barrel per calendar day (AB/CD) production of product having a selected RON and/or over a particular run length. The catalyst lives are determined at constant LHSV for the penultimate and final stage catalysts for a given feed RON to each stage as a function of the change in RON from that of the feed to that of the C.sub.5+ effluent from the respective stage. The penultimate stage C.sub.5+ effluent RON is selected to be such that the lives of the catalysts in each stage are substantially equal. Preferably the yield of C.sub.5+ effluent from each stage and the life of the catalyst used in each stage is determined as a function of the pressure of that stage. The operating pressures of the stages are then selected to be within about 30% of that which gives the highest AB/CD.

Abstract: Provided is a reforming process for producing a high purity benzene product using a non-acidic zeolitic catalyst. The high purity benzene is extracted from a light fraction of reformate that has less than 500 ppm by weight toluene. Generally, a hydrocarbon feed is reformed in a reformer under reforming conditions in the presence of a non-acidic catalyst to produce a reformate. That reformate is separated into a light fraction and a heavy fraction. The extraction unit, preferably an extractive distillation unit, is then used to separate the light fraction into an aromatic extract stream and a nonaromatic raffinate stream.

Abstract: This invention deals with a process for converting aliphatic C.sub.2 -C.sub.6 hydrocarbons into C.sub.6.sup.+ aromatics and C.sub.3.sup.= /C.sub.4.sup.= olefins. The process involves combining dehydrocyclodimerization (DHCD) with dehydrogenation. Thus, the feedstream is first sent to a DHCD zone which produces an effluent stream which contains C.sub.6.sup.+ aromatics along with C.sub.1 -C.sub.5 hydrocarbons. This effluent stream is separated into a stream containing C.sub.1 -C.sub.4 hydrocarbons and one containing C.sub.6.sup.+ aromatics. The C.sub.1 -C.sub.4 containing stream is flowed to a dehydrogenation zone to produce C.sub.3.sup.= /C.sub.4.sup.= olefins.

Abstract: A crystalline low-aluminum boron beta zeolite is prepared using a diquaternary ion as a template.