Abstract: Apparatuses and processes for converting an oxygenate feedstock, such as methanol and/or dimethyl ether, in a fluidized bed containing a catalyst to hydrocarbons, such as gasoline boiling components, olefins and aromatics are provided herein.

Abstract: Apparatuses and processes for converting an oxygenate feedstock, such as methanol and dimethyl ether, in a fluidized bed containing a catalyst to hydrocarbons, such as gasoline boiling components, olefins and aromatics are provided herein.

Abstract: A Flexicoking™ unit which retains the capability of converting heavy oil feeds to lower boiling liquid hydrocarbon products while making a fuel gas from rejected coke to provide only a minimal coke yield. The heater section of the conventional three section unit (reactor, heater, gasifier) is eliminated and the cold coke from the reactor is passed directly to the gasifier which is modified by the installation of separators to remove coke particles from the product gas which is taken out of the gasifier for ultization. Hot coke from the gasifier is passed directly to the coking zone of the reactor to supply heat to support the endothermic cracking reactions and supply seed nuclei for the formation of coke in the reactor. Coke is withdrawn from the gasifier to remove excess coke and to purge the system of metals and ash.

Abstract: This invention relates to process for producing a reformate or gasoline product. The process involves a rapid cycle of reacting hydrocarbon feedstock to form the product and then regenerating the catalyst used in the reaction. The process can be carried out at relatively high liquid hourly space velocities and preferably at relatively low hydrogen to hydrocarbon ratios to produce a reformed product having relatively high liquid yield and hydrogen content.

Abstract: This invention relates to process for producing a reformate or gasoline product. The process involves a rapid cycle of reacting hydrocarbon feedstock to form the product and then regenerating the catalyst used in the reaction. The process can be carried out at relatively high liquid hourly space velocities and preferably at relatively low hydrogen to hydrocarbon ratios to produce a reformed product having relatively high liquid yield and hydrogen content.

Abstract: The use of rapid cycle pressure swing adsorption having a cycle time of less than 30 s for increasing the hydrogen concentration in hydrogen-containing steams, from a hydrogen source, such as a stream reforming unit.

Abstract: A high solvent power (HSP) crude oil is added to a blend of incompatible oils to proactively address the potential for fouling heat exchange equipment. The HSP component dissolves asphaltene precipitates before coking affects heat exchange surfaces. An HSP oil is also flushed through heat exchange equipment to remove any deposits and/or precipitates on a regular maintenance schedule before coking can affect heat exchange surfaces.

Abstract: HSP crude oil is used as process stream in crude oil storage tanks to address sludge levels both by cleaning sludge accumulations and preventing any significant sludge build up when used on a regular basis. HSP crude oil is also used to optimize cleaning routines. Making HSP oil easily accessible by providing a designated HSP source will make tank maintenance more efficient and allow refineries to use the advantages of the HSP oil to the maximum extent.

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: Oxides of nitrogen (NO.sub.x) emissions from an FCC regenerator are reduced by operating the regenerator in partial CO burn mode to produce flue gas with more CO than O.sub.2 and with NO.sub.x precursors. This flue gas is then enriched with controlled amounts of oxygen and charged over catalyst, preferably Group VIII noble metal on a support, to convert most NO.sub.x precursors to nitrogen. Flue gas may then be charged to a CO boiler. Eliminating more than 90% of NO.sub.x emissions is possible by operating the FCC regenerator in partial CO burn mode, then adding air and catalytically converting NO.sub.x precursors at substoichiometric conditions. Conversion of NO.sub.x, if formed in the regenerator, may be achieved as well.

Abstract: A process is provided for the disproportionation of C.sub.3 -C.sub.5 paraffins. Propane, butanes and/or pentanes are reacted over a zeolite catalyst having a low acid activity in a turbulent fluidized bed reactor regenerator system operating at low to moderate pressures.

Abstract: A condensation reaction process and reactor for converting a plurality of reactants to at least one reaction product having a vapor pressure less than the vapor pressure of the reactants. The process includes heating a liquid phase of the reactants to at least partial vaporization thus forming a vapor phase of the reactants. The vapor phase reactants are passed in a vapor and or condensed state through at least one catalyst bed spaced from the liquid state to form reaction product(s). The reaction product(s) is returned to the liquid phase without additional contact with catalyst.

Abstract: A process is disclosed for alkylating an isoparaffin with an olefin comprising the steps of:(a) reacting an isoparaffin having from 4 to 8 carbon atoms with an olefin having from 2 to 12 carbon atoms in a first alkylation reaction stage at temperature from about -40.degree. C. to about 500.degree. C. and overall isoparaffin:olefin feed weight ratio of from about 1:1 to about 250:1 with a solid alkylation catalyst comprising a synthetic porous crystalline material characterized by an X-ray diffraction pattern including values substantially as set forth in Table I of the specification and having a composition comprising the molar relationshipX.sub.2 O.sub.3 :(n)YO.sub.

Abstract: A low sulfur gasoline of relatively high octane number is produced from a catalytically cracked, sulfur-containing naphtha by hydrodesulfurization followed by octane enhancing treatment in a fluidized bed catalytic process, in the presence of an aromatics-rich feedstream. The process converts the hydrodesulfurized intermediate and the aromatics-rich feedstream to a gasoline boiling range fraction of high octane number. The fluidized bed catalytic process is carried out over zeolite catalyst particles in a turbulent reactor bed at a temperature of about 600.degree. to 800.degree. F. (316.degree. to 427.degree. C.) and pressure of about 100 to 250 psig (790 to 825 kPa. The catalyst has an apparent particle density of about 0.9 to 1.6 g/cm.sup.3 and a size range of about 1 to 150 microns, and average catalyst particle size of about 20 to 100 microns containing about 10 to 25 weight percent of fine particles having a particle size less than 32 microns.

Abstract: A method and operating technique for treating organosulfur compound-containing aliphatic streams by introducing the light hydrocarbon stream at a top portion of a vertical stripping tower having an upper catalytic contact zone containing a bed of solid hydrodesulfurization catalyst particles and a lower contact zone, and introducing a light gas stream containing hydrogen at a lower portion of said stripping tower. Hydrodesulfurization is effected by flowing the light hydrocarbon stream and light gas stream countercurrently in contact with the solid hydrodesulfurization catalyst particles under hydrodesulfurization and stripping conditions, thereby converting the organosulfur compound in the upper contact zone.

Abstract: A system for containing and neutralizing a heavy vapor cloud from a potential source of hazardous vapor, such as HF from an HF alkylation unit, comprising a primary containment enclosure for containing and neutralizing a major portion of the vapor in the event of a leak, and a secondary fence line spaced from the primary enclosure for absorbing the vapor as the cloud passes therethrough.

Abstract: A benzene-rich gasoline stream is alkylated with higher olefins in contact with a fluid bed of shape selective zeolite catalyst to produce a gasoline product stream reduced in benzene content wherein the high octane value alkylaromatics formed by benzene alkylation are of low carbon number, essentially C10-. Concurrently, a portion of olefins in the gasoline stream are converted to gasoline boiling range hydrocarbons and the sulfur content of the gasoline feedstream is lowered. Besides enhancing the octane value of the feedstream, the process results in a lower Reid vapor pressure and lower sulfur content.

Abstract: Aliphatic feeds are converted to olefins and/or aromatics in a multi pressure reactor system. A high pressure first stage reactor generates much or all of the hydrogen needed to reduce catalyst coking in lower pressure downstream reactors. High pressure operation protects catalyst stability in the first reactor, while produced hydrogen helps protect downstream catalyst. Low pressure downstream operation improves yields.

Abstract: A process for desulfurizing a hydrocarbon stream which includes at least 50 ppmw sulfur in the form of organic sulfur compounds, and C.sub.5 + hydrocarbons including benzene. The hydrocarbon stream is contacted in the absence of added hydrogen with a fluidized bed of an acidic catalyst having a structure of ZSM-5, ZSM-11, ZSM-22, ZSM-23, ZSM-35, ZSM-48, MCM-22, MCM-36, MCM-49, zeolite Y, zeolite beta or mixtures thereof to convert the organic sulfur compounds to hydrogen sulfide. The catalyst contacts the hydrocarbon stream at a pressure of from 0.0 psig to about 400 psig, a temperature of from about 400.degree. F. to about 900.degree. F., and a weight hourly space velocity of from about 0.1 hr..sup.-1 to about 10.0 hr..sup.-1. Thereafter, the hydrogen sulfide is removed from the hydrocarbon stream.

Abstract: A method and operating technique for treating diene-containing aliphatic streams by introducing the light hydrocarbon stream at a top portion of a vertical stripping tower having an upper catalytic contact zone containing a bed of solid hydrogenation catalyst particles and a lower contact zone, and introducing a light gas stream containing hydrogen at a lower portion of said stripping tower. Selective hydrogenation is effected by flowing the light hydrocarbon stream and light gas stream countercurrently in contact with the solid hydrogenation catalyst particles under hydrogenation and stripping conditions, thereby converting said diene to mono-alkene in the upper contact zone.