Abstract: A catalyst nominally containing zeolite, preferably HY zeolite and/or ultrastable HY zeolite, clay, alumina and an acidic silica-alumina co-gel matrix. The zeolite is preferably partially exchanged with high La/Ce ratio solution in a wetting step, and rare earths are precipitated onto the matrix. The catalyst has high metals tolerance and is capable of cracking heavy reduced crude oils, producing higher LCO/slurry oil ratio.

Abstract: A fixed-sulfur, solid fuel product is obtained by an improved coking process wherein petroleum fractions are coked in the presence of added alkaline earth metal oxides. The fixed-sulfur, solid fuel product comprises coke and from about 3 to 30 weight percent, preferably from about 5 to 15 weight percent, "ash" (calculated as calcium oxide) derived from the alkaline earth additive. The quantity alkaline earth metal oxide or precursor thereof added to the coking zone is dependent on the sulfur content of the product coke and on the desired ash content of the solid fuel product. The coking zone may comprise delayed, fluid bed, or moving bed cokers.

Abstract: Hydrocarbon feed to a steam cracking furnace is heated to near cracking temperature by indirect heat exchange with steam to permit use of a range of feedstocks.

Abstract: A process for high hydroconversion of heavy hydrocarbon liquid feedstocks such as petroleum residua containing at least about 50 V % material boiling above 975.degree. F. to produce lower boiling hydrocarbon liquid and gas products, wherein heavy RCR materials and metals compounds are removed in-situ from the reactor effluent liquid by solvent vapor extraction using a process-derived solvent vapor at supercritical conditions. In the process, the feedstock is catalytically hydroconverted at 780.degree.-860.degree. F. temperature, and the resulting liquid fraction is contacted with a process-derived solvent vapor fraction having a normal boiling range of 250.degree.-400.degree. F. and heated to supercritical temperature to dissolve and extract substantially all the hydrocarbon liquid fractions, and separate heavy RCR materials and the metals compounds contained therein.

Abstract: The hydrotreatment of hydrocarbons in the liquid phase is effected in a column containing a catalyst bed supported by a grid, wherethrough passes an ascending stream of the charge admixed with hydrogen which expands the catalyst bed, the perforations of the grid being small enough to prevent passage of the catalyst particles but large enough to permit passage of the hydrogen-charge mixture, the reaction effluent being withdrawn from the top of the column.

Abstract: A method for reducing the pour point of a hydrocarbon oil which comprises contacting said oil under dewaxing conditions with a zeolite dewaxing catalyst thereby forming a dewaxed oil that contains olefins, and contacting said dewaxed oil and said contained olefins with a solid acidic catalyst under conditions effective to increase the stability of said oil.

Abstract: A hydrocarbon conversion process is disclosed for the dehydrogenation of alkylaromatic hydrocarbons such as ethylbenzene or ethyltoluene. A subatmospheric pressure is maintained in the reaction zone by the use of two separate compressors. The first compressor pressurizes the vapor phase reactor effluent prior to the final indirect heat exchange step(s) used to partially condense this stream. The second compressor maintains the vapor-liquid separator which receives the partially condensed reactor effluent stream at a subatmospheric pressure. This facilitates operation of the reactor at a subatmospheric pressure.

Abstract: A process for the oligomerization of olefin fractions where boron trifluoride in the gas phase is contacted with such a fraction, in the absence of a catalyst carrier, under such conditions and for such a length of time that the isobutene and/or butadiene present will polymerize; the boron trifluoride and the isobutene and/or butadiene polymers obtained are then conventionally separated from said fraction; and the olefins of the fraction so purified are oligomerized in the presence of a boron trifluoride catalyst comprising a catalyst carrier.

Abstract: Toluene and formaldehyde produce styrene in a gas phase catalytic process using a basic hydroxide of Group I or II, at formaldehyde to toluene mole ratios of from 0.001 to 0.10.

Abstract: The method and means of this invention comprises discharging a suspension of solids (inert or catalytic) in gasiform material (whether hydrocarbon vapors, combustion product flue gases, stripping gases or combinations thereof) from a riser contact zone through a plurality of radiating confined passageway emanating from the upper discharge periphery of the riser each of which is in tangential communication at the outer end of the confined passageway with a cylinder open in the bottom end thereof. The cylinder is closed at the top except for a coaxially aligned conduit of smaller diameter extending downwardly through said cylinder with its bottom open end terminating adjacent a lower portion of the inlet of the confined passageway.

Abstract: A hydrocarbon dewaxing process comprising the steps of:(a) chilling the waxy hydrocarbon feed to be dewaxed in the absence of solvent to crystallize a portion of the hard wax;(b) introducing the hydrocarbon feed to be dewaxed into a centrifuge;(c) centrifuging the solvent free hydrocarbon feed thereby generating two streams, stream (I) comprising a major portion of oil with a minor portion of entrained wax, stream (II) comprising a major portion of wax with a minor portion of entrained oil;(d) adding a dewaxing solvent to stream (II) generating a slurry A;(e) feeding slurry A to a centrifuge thereby separating slurry A into an oil-solvent stream (III) and a wax-solvent stream (IV);(f) passing the oil-solvent stream (III) to a membrane separation unit wherein the stream is separated into a recycle solvent stream and an oil-solvent stream of reduced solvent content (stream V);(g) passing oil-solvent stream (V) to an oil recovery unit wherein the stream is separated into a recycle solvent stream and an oil strea

Abstract: Cracking of hydrocarbons with a mixture of acid dealuminated, rare earth metal exchanged Y-zeolite having a SiO.sub.2 /Al.sub.2 O.sub.3 molar ratio of more than about 6 and not more than about 300, and non-dealuminated rare earth metal exchanged Y-zeolite and a matrix.

Abstract: A method and apparatus is disclosed for retorting particulate solid materials, particularly hydrocarbon-containing materials such as oil shale, oil sands, tar sands, coal shale, coal tailings, and the like, for the recovery of a volatile constituent such as oil or gas. A rotary retorting apparatus is employed which consists of a cylindrical drum, or other similar regularly shaped chamber, with a substantially horizontal axis of rotation and having multiple compartments for retorting and combustion and, optionally, spent solids cooling. The apparatus further includes solids transport chutes for forward and backward circulation of solids, arranged for the intercompartmental transfer of solids with the capability of additions at one or more points in each compartment. Employing the method and apparatus, particulate solids feedstock is heated by recycled spent solids material to remove the volatile constituent of the feedstock in the retort section.

Abstract: Pulverized carbonaceous material such as coal while flowing through a reactor dispersed in a carrier gas substantially transparent to radiant energy and at atmospheric pressure is heated, typically for a few milliseconds to about 1500.degree. K., by thermal radiation while maintained in the cooler carrier gas to selectively heat the pulverized material, while cooling the volatile products as they diffuse into the cooler carrier gas, followed by quenching where necessary. In the case of coal, the principal result of this treatment is a radical increase in the easily soluble fraction of the coal with substantially no net change in the solid ultimate or proximate characteristics and substantially no output gaseous volatile production.

Abstract: A heavy hydrocarbon feed stock is, after being heat-treated in a first cracking zone, introduced into a second thermal cracking zone for obtaining a thermally cracked product and a pitch product. The second cracking zone has a plurality of cracking reactors which are connected in series, through which is successively passed the treated feed stock and to each of which is supplied a gaseous heat transfer medium to maintain the liquid phase therein at a temperature sufficient for effecting the thermal cracking and to strip the resulting distillable, cracked components from the liquid phase. The thermal cracking temperature in one reactor is so controlled as to become higher than that in its adjacent upstream-side reactor. The distillable, cracked components in respective reactors are removed overhead therefrom and separated into a heavy fraction and a light fraction, while the liquid phase in the downstream-end reactor is discharged therefrom for recovery as the pitch product.

Abstract: A method and apparatus for separating regenerated catalyst from gaseous combustion products within a regenerator. The apparatus comprises a downcomer within the regenerator vessel through which the catalyst and gaseous combustion products flow. Means are provided at the lower end of the downcomer for utilizing the momentum of the catalyst particles to separate them from the gaseous combustion products.

Abstract: Petroleum crudes, particularly heavy oil crudes produced by thermal or other enhanced recovery procedures, are treated to break the water-in-oil emulsion and reduce the BS&W content by use of additives, advantageously ammonium bisulfite, which act upon inorganic sulfur contained in the crude.

Abstract: A process for improving the properties of a hydrogen donor coal liquefaction solvent employed in a coal liquefaction process which comprises separating said coal liquefaction solvent into a first fraction boiling in the range from about 350.degree. to about 675.degree. F., and a second fraction boiling in the range from about 675.degree. F. to about 1000.degree. F., hydrogenating said first fraction at a temperature ranging from about 600.degree. to about 800.degree. F., under a pressure of about 500 to 4000 psig, hydrogenating said second fraction at a temperature ranging from about 600.degree. to 700.degree. F. at a pressure from about 500 to 4000 psig and combining said hydrogenated first and second fractions to provide a coal liquefaction solvent having an increased concentration of hydrogen donor components.

Abstract: A process for deashing primary coal liquids with a selective hydrocarbon solvent separation wherein the coal liquids and selective hydrocarbon solvent are contacted initially at a temperature greater than the temperature at which the deashing separation occurs. More particularly, a process for the production of deashed coal liquid which comprises the sequential steps of: (a) admixing a primary coal liquid containing ash and a hydrocarbon deashing solvent having no hydrogen-transferring ability at a selected admixing temperature from about 250.degree. F. to about 575.degree. F.; (b) reducing the temperature of the entire resulting admixture of the primary coal liquid and hydrocarbon deashing solvent to a deashing temperature about 50.degree. F. to about 125.degree. F. less than the admixing temperature of step (a); and deashing the primary coal liquid with the deashing solvent at the deashing temperature of step (b).

Abstract: A process for eliminating and removing impurities including sulfur compounds and microorganisms as well as preventing further microbial contamination is accomplished by treating petroleum products or other hydrocarbon fluids with an aqueous solution of an oxidizing agent such as hydrogen peroxide or ozone together with a metallic ion catalyst, such as a mixture of ferric chloride and cupric chloride, where the metal ion is capable of forming activated oxygen complexes in the presence of such oxidizing agent, or by treatment with an aqueous solution of metallic ion catalyst and activated oxygen complexes formed from permanganate, peroxyborate or chromate ions.