Abstract: The C.sub.2 -C.sub.4 olefin yield is unexpectedly increased while coke and heavy aromatics production are decreased by the addition of a propane-rich supplemental feedstream in a process for catalytically upgrading C.sub.5 -C.sub.7 paraffinic feedstreams. Further benefits include increased conversion of the C.sub.5 -C.sub.7 paraffinic feedstream, decreased coke production and prolonged catalyst useful life. Udex raffinate is a particularly preferred feedstream.

Abstract: Disclosed is a process for preparing n-hexenes and high octane blending components from a mixture of C.sub.6 olefin isomers. Also disclosed is a process for preparing 1-hexene from a mixture of C.sub.6 olefin isomers which provides high octane blending components as a by-product.

Abstract: Disclosed is a process for preparing C.sub.5 to C.sub.18 straight chain .alpha.-olefins from the corresponding internal olefins. The process comprises reacting a C.sub.5 to C.sub.18 straight chain olefin reactant with an electrophilic compound containing hydrogen followed by selectively cracking the resulting product.

Abstract: Disclosed is a process for preparing 1-hexene from 1-butene. The 1-butene is metathesized to produce 3-hexene which is then subjected to, e.g., an hydration/dehydration procedure to produce a mixture of n-hexenes containing 1-hexene.

Abstract: Processes are disclosed for recovering n-hexenes from a mixture comprising n-hexenes and at least one branched-chain C.sub.6 olefin isomer by oligomerizing the branched-chain C.sub.6 olefin isomers, but not the n-hexenes, and recovering the n-hexenes from the resulting mixture.

Abstract: Disclosed is a process for preparing C.sub.5 to C.sub.18 straight chain .alpha.-olefins from the corresponding internal olefins. The process comprises reacting a C.sub.5 C.sub.18 straight chain olefin reactant with an electrophilic compound containing hydrogen followed by cracking the resulting product.

Abstract: Alcohol feedstock containing water is extracted with olefinic liquid and reacted catalytically to produce tertiary ether. Unreacted alcohol and olefin vapor separated from etherification effluent is converted along with aqueous alcoholic raffinate in a zeolite catalysis step to produce gasoline and paraffinic intermediate. By dehydrogating the C.sub.3 -C.sub.5 paraffins, an olefinic liquid rich in isoalkenes is obtained for recycle to the extractor as solvent for alcohol feedstock.

Abstract: The present invention relates to the conversion of saturated paraffin hydrocarbons having 4 or more carbon atoms to olefins having fewer carbon atoms. In particular, the invention provides for contact of a mixture of 40 to 95 wt % paraffin hydrocarbons having 4 or more carbon atoms and 5 to 60 wt % olefins having 4 or more carbon atoms with solid zeolitic catalyst such as ZSM-5 at conditions effective to form propylene and the separation of light olefins from the reaction mixture.

Abstract: The present invention provides a process for the preparation of propylene from C.sub.4 or higher feed by a combination of cracking and metathesis wherein higher hydrocarbon is cracked to form ethylene and propylene and at least a portion of the ethylene is metathesized to propylene.

Abstract: A method of cracking heavy hydrocarbons into lighter hydrocarbons consisting in providing an advantageously catalytic bed of particles in a reaction chamber, feeding a bed fluidizing gas with a predetermined flow rate to provide a springing fluidized bed and feeding a plasma jet preferably containing argon into the chamber, the jet being directed towards a determined place of the bed so as to provide a reaction space with at least two reaction zones of different temperatures, the zone of higher temperature being the one where the plasma jet is directed; feeding heavy hydrocarbons into the reaction zone of lower temperature and feeding preferably in the zone of higher temperature at least one light alkane for carrying out the cracking of the heavy hydrocarbons within the fluidized bed, the latter effecting a quenching of the reaction medium and catalysing the cracking and consisting in discharging the products obtained downstream of the zone of lower temperature.

Abstract: The present invention provides a process for the preparation of ethylene from C.sub.4 or higher feed by a combination of cracking and metathesis wherein higher hydrocarbon is cracked to form ethylene and propylene and at least a portion of the propylene is metathesized to ethylene.

Abstract: Disclosed is a method for cracking a hydrocarbon material. The method includes introducing a stream including a hydrocarbon fluid into a reaction zone. A microwave discharge plasma is continuously maintained within the reaction zone, and in the presence of the hydrocarbon fluid. Reaction products of the microwave discharge are collected downstream of the reaction zone.

Abstract: A catalyst for promoting the molecular restructuring of the components of hydrocarbons to form desired products. The catalyst comprises copper salts, copper acetate being particularly preferred, in combination with anhydrous aluminum chloride. The catalyst can be used with either gaseous hydrocarbon raw materials such as natural gas, refinery gas, biomass decomposition gases, and similar materials, or with solids, meltable solids, or liquid hydrocarbon-containing raw materials including tar sands, oil shale, waxes, asphaltic compositions and the like. In the case of gaseous raw materials, the gases are preferably brought into contact with the copper salt coated on a catalyst support such as refractory alumina, in the presence of anhydrous aluminum chloride, which can be in vaporous form, in a continuous process.

Abstract: Various fractions of petroleum, including residual oils and crude oils, are catalytically converted to produce gaseous olefins, especially propylene and butylene, in fluidized or moving bed or transfer line reactors with solid, acidic catalysts in the presence of steam at a temperature of 500.degree. to 650.degree. C. and a pressure of 1.5.times.10.sup.5 Pa to 3.times.10.sup.5 Pa, with a weight space velocity of 0.2 to 20 hr.sup.-1 and catalyst-to-oil ratio of 2 to 12. Spent catalyst is continuously removed from the reactor to a regenerator where the coke is burned off and the hot catalyst is returned to the reactor. In a comparison with conventional catalytic cracking and tubular furnance pyrolysis processes, it is found that the process of the present invention produces more propylene and butylene. The total yield of the process of the present invention is about 40 percent by weight of the feedstock.

Abstract: Process and apparatus for upgrading paraffinic naphtha to high octane fuel by contacting a fresh virgin naphtha feedstock stream medium pore acid cracking catalyst under low pressure selective cracking conditions effective to produce at least 10 wt % C4-C5 isoalkene to obtain a light olefinic fraction rich in C4-C5 isoalkene and a C6+ liquid fraction of enhanced octane value. The preferred feedstock is straight run naphtha containing C7+ alkanes, at least 15 wt % C7+ cycloaliphatic hydrocarbons and less than 20% aromatics, which can be converted with a fluidized bed catalyst in a vertical riser reactor during a short contact period.The isoalkene products of cracking are etherified to provide high octane fuel components.

Abstract: C.sub.3 and/or C.sub.4 hydrocarbons (in particular propane and butanes) are converted to less saturated hydrocarbons (in particular ethylene and propylene) in the presence of a catalyst consisting essentially of either (a) zinc oxide and manganese oxide or (b) zinc oxide, manganese oxide and calcium oxide. Compositions of matter (a) and (b), as defined above, are provided in accordance with this invention.

Abstract: A zeolite, its method of preparation and use is disclosed. The zeolite is characterized by a silica to alumina mole ratio greater than 12 and a Constraint Index of 1 to 12. The zeolite undergoes controlled alumina extraction by treatment with, e.g., strong mineral acid or chelating agent. Removal of aluminum increases the acid activity of the zeolite.

Abstract: Crystalline molecular sieves having three-dimensional microporous framework structure of MO.sub.2, AlO.sub.2, and PO.sub.2 tetrahedral oxide units are disclosed. These molecular sieves have an empirical chemical composition on an anhydrous basis are expressed by the formula:mR: (M.sub.x Al.sub.y P.sub.z)O.sub.2wherein "R" represents at least one organic templating agent present in the intracrystalline pore system; "m" represents the molar amount of "R" present per mole of (M.sub.x Al.sub.y P.sub.z)O.sub.2 ; "M" represents at least two elements capable of forming framework tetrahedral oxides and selected from the group consisting of arsenic, beryllium, boron, chromium, gallium, germanium, lithium and vanadium; and "x", "y" and "z" represent the mole fractions of "M", aluminum and phosphorus, respectively, present as tetrahedral oxides. Their use as adsorbents, catalysts, etc. is disclosed. The catalyst is useful in the cracking and hydrocracking of various hydrocarbonaceous feeds.

Abstract: A process for converting heavy hydrocarbons into light hydrocarbons which comprises contacting, in a reaction zone, a heavy hydrocarbon having an API gravity at 25.degree. C. of less than about 20, such as Boscan heavy crude oil or tar sand bitumen, with a liquid comprising water and with an effective amount of selected catalyst materials such as iron (II and/or III) oxides, sulfides or sulfates, in the absence of externally added hydrogen, at a temperature between greater than about 340.degree. and about 480.degree. C. and at a pressure between about 1350 kPa (about 196 psig, about 13.2 atm) and about 15,000 kPa (about 2175 psig, about 148 atm), for a time sufficient to produce a residue and a vapor phase comprising light hydrocarbons, gaseous product and water, withdrawing the residue and said phase from the second zone; and recovering a light hydrocarbon product having an API gravity at 25.degree. C. of greater than about 20 and substantially free of vanadium and nickel values, i.e.

Abstract: The present invention is directed to a method of inhibiting the formation of coke during the elevated temperature cracking of hydrocarbons. The method generally comprises adding to the hydrocarbon an effective amount of an ammonium borate, particularly ammonium biborate and ammonium pentaborate. Preferably, the ammonium borates are in a glycollic solvent or water.

Abstract: Feed hydrocarbons comprising propane and butanes are cracked to selectively maximize the production of ethylene or propylene by contacting the feed hydrocarbons with a cracking catalyst, adapted to convert the feed hydrocarbons to less saturated hydrocarbons, under conditions sufficient to thus crack the feed hydrocarbons, to thereby selectively maximize the production of ethylene, and, at least intervally, hydrogen sulfide or a hydrogen sulfide precursor is added to the feed hydrocarbons to thereby maximize the production of propylene. Preferred catalysts which may be utilized in the process and which are highly selective to the production of ethylene, as opposed to propylene, (in the absence of hydrogen sulfide or hydrogen sulfide precursor) include mixed oxides of manganese and magnesium, mixed oxides of manganese and Lanthanum Series metal and/or niobium, mixed oxides of iron and magnesium and mixed oxides of iron and Lanthanum Series metal and/or niobium.

Abstract: A method for the conversion of C.sub.3 and C.sub.4 hydrocarbons to less saturated hydrocarbons, such as ethylene and propylene and particularly ethylene, includes contacting the feed hydrocarbons with mixed oxides comprising a major proportion of magnesium and a minor proportion of manganese, preferably under conditions which selectively convert the feed hydrocarbons to ethylene and ethane and particularly ethylene, including a temperature between about 625.degree. C. and 850.degree. C. The method is preferably carried out in the presence of steam at a mole ratio of steam/hydrocarbon of less than about 10:1. Selectivity to ethylene and ethane and particularly ethylene is improved and the life of the catalyst, during which the desired selectivity is attained, is extended by adding a promoting amount of at least one oxide of calcium, barium, strontium, tin and antimony. Further improvement can be obtained by limiting the amount of bound or fixed sulfur in the catalyst.

Abstract: Compositions of matter comprise oxides of silicon, aluminum and/or titanium mixed with combinations of manganese oxide and magnesium oxide; iron oxide and magnesium oxide; calcium, strontium, barium, tin and/or antimony oxides, manganese oxide and magnesium oxide; and iron oxide, manganese oxide and magnesium oxide. These compositions are particularly useful as catalysts for selectively converting propane and butanes to ethylene and ethane and particularly to ethylene. A method for converting propane and butanes to less saturated hydrocarbons is also disclosed in which the catalyst life is extended and the selectivity to ethylene and ethane, particularly ethylene, is improved by carrying out the contacting with the catalyst in the presence of steam, when the catalyst contains an oxide of iron and, optionally, when the catalyst does not contain an oxide of iron.

Abstract: Novel compositions of matter include: mixed oxides of (a) at least one oxide of chromium, at least one oxide of manganese and at least one oxide of magnesium, Lanthanum Series metals, preferably lanthanum and cerium, and/or niobium; (b) at least one oxide of chromium, at least one oxide of calcium, strontium, tin and/or antimony, at least one oxide of manganese and at least one oxide of magnesium, Lanthanum Series metals and/or niobium; (c) at least one oxide of chromium, at least one oxide of iron and at least one oxide of magnesium, Lanthanum Series metals and/or niobium; and (d) at least one oxide of chromium, at least one oxide of iron, at least one oxide of manganese and at least one oxide of magnesium, Lanthanum Series metals and/or niobium. These compositions are particularly effective as catalyst compositions for the conversion of C.sub.3 and C.sub.

Abstract: A method of selectively cracking C.sub.3 and C.sub.4 hydrocarbons to C.sub.2 hydrocarbons, particularly ethylene, in which a body of cracking catalyst is established in a reaction zone and the feed hydrocarbons are passed through the body of catalyst while maintaining the conditions sufficient to convert the feed hydrocarbons to product hydrocarbons, including, a temperature in the upstream end of the body of catalyst at least about 100.degree. C. below the temperature in the downstream end of the body of catalyst. The cracking catalyst is preferably selected from the group consisting of: at least one oxide of manganese and at least one oxide of magnesium; at least one oxide of manganese and at least one oxide of at least one metal selected from the group consisting of Lanthanum Series metals, preferably lanthanum or cerium, and niobium; at least one oxide of iron and at least one oxide of magnesium; and at least one oxide of iron and at least one oxide of a Lanthanum Series metals or niobium.

Abstract: The process for the interconversion of "small olefins" selected from the class consisting of ethylene, propylene, butenes and mixtures thereof comprising contacting said small olefin(s) with non-zeolitic molecular sieves.

Abstract: Compositions of matter, including: a composition consisting of iron oxide and magnesium oxide; a composition comprising iron oxide, manganese oxide and magnesium oxide; a composition comprising a small amount of iron oxide and a larger amount of an oxide of a Lanthanum Series metal, particularly lanthanum and cerium; and a composition comprising iron oxide and niobium oxide. The above compositions are particularly useful as catalytic compositions for the conversion of C.sub.3 and C.sub.4 hydrocarbons to less saturated hydrocarbons, particularly ethylene and propylene and preferably ethylene, in the presence of steam. The steam substantially increases the active life of the catalytic composition, before regeneration is necessary, as well as significantly increasing the selectivity to ethylene. Limiting the amount of bound or fixed sulfur in the catalytic compositions also improves the catalysts.

Abstract: C.sub.5.sup.+ hydrocarbons are prepared from C.sub.4.sup.- hydrocarbons by a two-stage process comprising steam reforming followed by Fischer-Tropsch synthesis over a special cobalt-containing catalyst; a gaseous fraction comprising unconverted H.sub.2 and CO as well as C.sub.4.sup.- hydrocarbons and CO.sub.2 formed as by-products is separated from the synthesized product and recycled to the steam reformer.

Abstract: Syngas is subjected to Fischer-Tropsch synthesis over a Co/Zr/SiO.sub.2 catalyst and the C.sub.20.sup.+ fraction of the synthesized product is converted into linear C.sub.10 -C.sub.20 olefins by mild thermal cracking.

Abstract: Compositions of matter, including: A mixture of at least one oxide of manganese and at least one oxide of a Lanthanum Series metal, preferably lanthanum or cerium, or at least one oxide of niobium. The above compositions are particularly useful as catalytic compositions for the conversion of C.sub.3 and C.sub.4 hydrocarbons to less saturated hydrocarbons, particularly ethylene and propylene and preferably ethylene. The life of the catalyst for the selective production of ethylene is extended by carrying out the reaction in the presence of steam. The steam substantially increases the active life of the catalytic composition, before regeneration is necessary, as well as significantly increasing the selectivity to ethylene. Limiting the amount of "bound" or "fixed" sulfur in the catalytic composition also improves the catalyst.

Abstract: Titanium-containing molecular sieves are disclosed having use as molecular sieves and as catalyst compositions in hydrocarbon conversion and other processes. The instant invention employs novel titanium-containing molecular sieves comprising titanium, aluminum, phosphorus and oxygen and are generally employable in hydrocarbon conversion processes, including cracking, hydrocracking and hydrotreating.

Abstract: The process for the interconversion of "small olefins" selected from the class consisting of ethylene, propylene, butenes and mixtures thereof comprising contacting said small olefin(s) with non-zeolitic molecular sieves.

Abstract: Mixed oxides of bismuth with other metals of the perovskite structure and having vacant lattice sites in the same lattice positions occupied by bismuth are disclosed as partial oxidation and ammoxidation catalysts. Such oxides are used as catalysts in the improved method of oxidizing an acyclic hydrocarbon of 1-10 carbons having at most one olefinic unsaturation by reacting the acyclic hydrocarbon in the vapor phase with oxygen in the presence of the solid catalyst to form products having carbon, hydrogen and oxygen.

Abstract: A process for cracking a feed comprising at least one alkane involving contacting said feed with H.sub.2 S and a high surface area contact material under cracking conditions.

Abstract: A process for selectively converting adsorbable hydrocarbon feeds containing straight-chain and slightly branched-chain hydrocarbons to olefins by contacting the feeds with crystalline silicates.

Abstract: A process for treating liquid hydrocarbons to remove toxic, mutagenic and/or carcinogenic aromatic hydrocarbons comprises feeding the hydrocarbons into a reactor where vapors are thermally treated in contact with a catalyst consisting essentially of calcium oxide or a calcium oxide containing mineral. Thermally treating liquid hydrocarbons in contact with calcium oxide preferentially increases the cracking of aromatics thus producing a product having a reduced amount of aromatic compounds.

Abstract: A petroleum distillate feed is upgraded and a substantial C.sub.3 -C.sub.4 olefin product fraction produced by contacting the feed with ZSM-5 type zeolite at (1) a temperature in the 500.degree.-800.degree. F. range, (2) a pressure below about 13 atmospheres gauge, and (3) an LHSV in the 0.1-15 V/V/Hr range, and fractionating the effluent product stream.

Abstract: A petroleum distillate feed is upgraded and a substantial C.sub.3 -C.sub.4 olefin product fraction produced by contacting the feed with ZSM-5 type zeolite at (1) a temperature in the 500.degree.-800.degree. F. range, (2) a pressure below about 13 atmospheres gauge, and (3) an LHSV in the 0.1-15 V/V/Hr range, and fractionating the effluent product stream.

Abstract: A catalytic process for hydrocracking C.sub.5.sup.+ hydrocarbons or mixtures thereof into a C.sub.2 -C.sub.5 mixture paraffin stream in the presence of a palladium/Group IIA, e.g. Be Mg, or IIIB, e.g. Sc, Y, ZSM-20 hydrocracking catalyst, and thermally cracking this mixture to recover ethylene and propylene.

Abstract: A process and catalyst for the catalytic pyrolysis of hydrocarbon to olefins and diolefins at temperatures in the range 600.degree.-750.degree. C. and pressures of 0.1 to 20 atmospheres. The catalyst is a bifunctional synthetic modified mordenite zeolite of the formula (yH.multidot.zM.multidot.uNa) O.multidot.Al.sub.2 O.sub.3 .multidot.SiO.sub.2 wherein M is Cu, Ag or Co/2 and u+y+z approach or equal 2. Good yields of ethylene and propylene are obtained from hydrocarbon feedstocks having boiling points up to 550.degree. C.

Abstract: Olefins are produced by reacting a feedstock containing a hydrocarbon containing 2 or more carbon atoms in the molecule and/or a hydrocarbon derivative containing hydrogen-carbon links over a catalyst comprising "FU-1," which is a zeolite-like silica-containing material characterized inter alia by chemical composition and X-ray diffraction pattern. The feedstock is preferably methanol or dimethyl ether. The predominant olefin product can be controlled according to the reaction conditions used. Conversion to aromatics is very low.

Abstract: A petroleum distillate feed is upgraded and a substantial C.sub.3 -C.sub.4 olefin product fraction produced by contacting the feed with H-ZSM-5 zeolite at (1) a temperature in the 500.degree.-800.degree. F. range, (2) a pressure below about 13 atmospheres gauge, and (3) an LHSV in the 0.1-15 V/V/Hr range, and fractionating the effluent product stream.