Abstract: A process for preparing a hydrogenated petroleum resin in which a petroleum resin having an aromatic ring is hydrogenated by introducing hydrogen gas and the molten petroleum resin from the upper or lower part of a vertical reactor to parallel-currently pass them through a fixed bed of a supported catalyst containing platinum and/or rhodium which may be used in combination with at most 50% by weight of a metal selected from palladium, ruthenium and rhenium.

Abstract: There is disclosed a system for measuring and controlling the concentration of hydrogen in hydrogen recycle processes used in oil refineries and petrochemical plants. The system is intended to permit reduction in hydrogen use in hydrogen-consuming hydrogen recycle processes. The system is dependent on the recognition that a decrease in cooling medium temperature results in an increase in vent gas flow, which can be decreased to the minimum permissible without endangering catalyst activity and stability and product yield if hydrogen concentration is monitored, and that partial pressure is the key parameter.

Abstract: A process for upgrading carbonaceous materials having low carbon content comprising preheating the carbonaceous material to a temperature above about 200.degree. C. in the absence of a solvent, extracting the heated carbonaceous material under moderate temperature and pressure conditions, and hydrotreating the extract under supercritical solvent conditions.

Abstract: A process for the selective hydrogenation of hydrocarbons having three and more carbon atoms and several double bonds or with triple bonds in monoene-containing hydrocarbon mixtures is described. These compounds are selectively hydrogenated to monoenes in a practically quantitative fashion. Before beginning the hydrogenation, a small amount of carbon monoxide and once to twice the stoichiometric quantity of hydrogen are homogeneously dissolved in the hydrocarbon mixture. The mixture is hydrogenated as a homogeneous liquid phase on a fixed palladium catalyst under a moderately high pressure and at a moderately high temperature. No isomerization can be found in the monoenes and no side reactions or secondary reactions occur.

Abstract: Certain organometallic precursors selectively interact with surface hydroxyl groups on an inorganic oxide support such as silica, alumina or silica-alumina or to provide a uniform distribution of metal complexes on the surfaces of said support. Subsequent reduction of the support results in a high dispersion of uncomplexed metal centers to which other organometallic precursors are subsequently attached. The substantially attached organometallic precursors may be reduced and/or sulfided to yield a highly active hydrogenation catalyst having a plurality of metal species in a highly dispersed distribution.

Abstract: In a process which is catalyzed by a catalyst comprising an active metal on a carrier, said metal being active as a catalyst for the process, an improvement is provided wherein the catalyst is a hydrous, alkali metal or alkaline earth metal titanate, zirconate, niobate or tantalate wherein alkali or alkaline earth metal cations have been exchanged with a catalytically effective amount of cations of said metal.

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 the hydrogenation of aromatic hydrocarbons contained in a hydrocarbonaceous oil feed is provided in which the feed is contacted with hydrogen in a substantially sulfur-free environment in the presence of a catalyst comprising a Group VIII noble metal component, such as palladium, deposited on a steamed support such as steamed tungsten oxide composited with alumina.

Abstract: A selective hydrogenation method for highly saturated hydrocarbons by bringing a mixture of hydrocarbons of low hydrogenation degree having 4 or more carbon atoms containing the highly saturated hydrocarbons in the presence of a catalyst using a fixed bed reaction vessel, which comprises supplying a hydrogen gas in a state of plural splits along the flow direction of the fixed bed reaction vessel is disclosed. In accordance with this mehtod, only the highly unsaturated hydrocarbons are selectively hydrogenated without being accompanied by isomerization of olefins.

Abstract: In the preparation of a heavy oil with a low Ramsbottom Carbon Test (RCT) from a long residue by a two-stage process comprising catalytic hydrotreatment followed by solvent deasphalting and recycle of the asphalt to the first stage the catalytic hydrotreatment for RCT reduction in the first stage is carried out at such a severity that the C.sub.4.sup.- gas production per percent RCT reduction is kept between defined limits.

Abstract: Process for the preparation of a heavy oil with a low Ramsbottom Carbon Test (RCT) from a long residue by (a) catalytic hydrotreatment for RCT reduction at such severity that the C.sub.4.sup.- gas production per percentage RCT reduction is kept between defined limits, followed by (b) solvent deasphalting of the (vacuum or atmospheric) distillation residue of the hydrotreated product.

Abstract: Unreacted hydrogen contained in the gaseous effluent from a high pressure hydrogenation process is reduced in pressure, followed by purification of the hydrogen at the lower pressure, and recompression to a high pressure for use in a hydrogenation process. Liquid effluent is also reduced in pressure, hydrogen stripped therefrom, and combined with the recovered hydrogen gas at the lower pressure for purification.

Abstract: Discloses that in the hydrogenation of liquid, carbonaceous crude material such as bitumen and other heavy oils, a catalyst derived from the addition of Fe.sub.2 (CO).sub.9 is advantageously used to provide a superior yield of distillable oils compared to prior practice.

Abstract: Spent catalysts removed from a catalytic hydrogenation process for hydrocarbon feedstocks, and containing undesired metals contaminants deposits, are regenerated. Following solvent washing to remove process oils, the catalyst is treated either with chemicals which form sulfate or oxysulfate compounds with the metals contaminants, or with acids which remove the metal contaminants, such as 5-50 W % sulfuric acid in aqueous solution and 0-10 W % ammonium ion solutions to substantially remove the metals deposits. The acid treating occurs within the temperature range of 60.degree.-250.degree. F. for 5-120 minutes at substantially atmospheric pressure. Carbon deposits are removed from the treated catalyst by carbon burnoff at 800.degree.-900.degree. F. temperature, using 1-6 V % oxygen in an inert gas mixture, after which the regenerated catalyst can be effectively reused in the catalytic process.

Abstract: A hydrocarbon conversion catalyst is disclosed which comprises a combination of a carrier material, a Group VIB metal component and Group VIII metal component wherein said group VIB metal component and said Group VIII metal component are incorporated in said catalytic composite by means of a non-aqueous organic solution of a Group VIB metal compound and a Group VIII metal compound, wherein said non-aqueous organic solution comprises dimethylformamide, formamide, diethylformamide, ethylformamide, methylformamide, pyridine, aniline or toluene and wherein said catalytic composite is calcined in a non-oxidizing atmosphere. Other embodiments of the present invention describe the use of the catalyst for hydrocarbon conversion and preferred methods of catalyst manufacture.

Abstract: Unsaturated hydrocarbons and mixtures in which the latter are present are treated with anion exchangers prior to hydrogenation and are then hydrogenated catalytically in a known manner. The treatment with anion exchangers is carried out at 0.degree.-120.degree. C. and at a space velocity of 0.1 to 10 l of hydrocarbons to be hydrogenated per l of exchanger, per hour. The process avoids other, energy-intensive pretreatments, for example distillation of the hydrocarbons to be hydrogenated, or washing, and can be carried out in simple equipment. A considerable prolongation of the catalyst operating time is achieved in the subsequent catalytic hydrogenation.

Abstract: Waxy, normal paraffin-type hydrocarbons present in petroleum oil feedstocks are selectively hydrocracked to hydrocarbons boiling below the boiling range of the feedstock by contacting the oil, in the presence of hydrogen, with a catalyst comprising a hydrogen form Zeolite L crystalline alumino-silicate containing at least one catalytic metal component selected from Group VIII and/or Group VI of the Periodic Table. This process is useful for dehazing oils such as white oils, for decreasing the pour point of jet fuels, for dewaxing lube oil feedstocks, including transformer oils and simultaneously reduces the aromatics content of the oil.

Abstract: Process for selectively hydrogenating a diolefin present in a mixture of hydrocarbons having at least 4 carbon atoms per molecule: the hydrocarbon mixture is reacted with hydrogen in contact with a catalyst comprising palladium and silver, the molar ratio of hydrogen to the diolefin being from 1:1 to 5:1.

Abstract: An improved process for hydroconversion of mineral oil is disclosed wherein a spherical hydroconversion catalyst having a diameter greater than 6 mm, a surface area above 200 m.sup.2 /gm, and a crush strength above 70 pounds is used to replace the inert materials which are used to support or retain a fixed bed of suitable hydroconversion catalyst.

Abstract: Hydrogen sulfide is removed from a fluid stream by contacting the fluid stream which contains hydrogen sulfide with an absorbing composition comprising zinc, titanium and at least one promoter selected from the group consisting of vanadium, chromium, manganese, iron, cobalt, nickel, molybdenum, rhenium, and compounds thereof. If organic sulfur compounds are present in the fluid stream, the absorbing composition acts as a hydrodesulfurization catalyst to convert the sulfur in the organic sulfur compounds to hydrogen sulfide which is subsequently removed from the fluid stream by the absorbing composition. If olefin contaminants are present in the fluid stream, the absorbing composition acts as hydrogenation catalyst to hydrogenate the olefin contaminants to paraffins.

Abstract: Fuel oils especially suitable as gas oils for fuelling high speed Diesel engines, are made by hydrogenating a middle oil derived from coal and containing at least 90% of polycyclic hydrocarbons and essentially no paraffinic material, and fractionating the hydrogenated oil to yield the gas oil. The product oil is fully competitive with gas oils from petroleum, and may be blended with petroleum gas oil.

Abstract: Improved method for maximizing jet fuel from shale oil involves hydrotreating the treated oil at a temperature of about 600.degree.-650.degree. F. in the presence of a catalyst having a relatively low metal content and then hydrotreating the oil at a temperature in excess of about 800.degree. F. in the presence of a catalyst having a relatively high metal content. A 480.degree. F. minus boiling point fraction fractionated from the foregoing process can meet JP-4 jet fuel specifications. Hydrocracking the 480.degree. F. plus boiling point fraction results in substantial additional quantities of jet fuel.

Abstract: A process is disclosed for preparation of sulphided fluorine-containing nickel-tungsten catalyst having high activity in hydroconversion processes of hydrocarbons. A process for the conversion of hydrocarbons is also disclosed.

Abstract: The preparation of high quality, e.g., high viscosity index, base lubricating oils and white oils, particularly food grade white mineral oils, of suitable viscosity in high yield from a mineral oil distillate of suitable lubricating oil viscosity comprises contacting the distillate with hydrogen in four catalytic stages. The first reaction stage employs hydrocracking conditions. Subsequent reaction stages employ hydrogenation conditions. The second reaction stage, preferably employs a sulfur-resistant hydrogenation catalyst and produces a product suitable as a high quality lubricating oil base stock. The third reaction stage preferably employs a sulfur-resistant hydrogenation catalyst to obtain further aromatic saturation. The final stage employs a selective hydrogenation catalyst, optionally activated with a halogen, and produces a product suitable as a white oil, preferably a food grade white oil.

Abstract: For thermally cracking heavy liquid hydrocarbons to produce gaseous olefins comprising a catalytic hydrogenating pretreatment, a separation of the hydrogenation product into a lighter fraction and a heavier fraction; passing the heavier fraction at least in part to a thermal cracking step to produce normally gaseous olefins; and withdrawing the lighter fraction, the improvement wherein the hydrogenation is conducted within the shaded area of FIG. 2, whereby said lighter fraction has a higher octane number.

Abstract: The OHP content of an OHP- and THP-containing solvent is enriched by contacting the solvent with hydrogen in the presence of a supported catalyst comprising Group VIB and Group VIII metals under conditions to increase the OHP/THP ratio in the solvent to a level greater than 0.4 and preferably greater than 1. The preferred catalyst contains tungsten where it is desired to provide an OHP/THP ratio greater than 1 in the OHP-enriched solvent, and also contains titanium to improve the hydrogen selectivity of the catalyst so as to enhance the preservation of aromatics in the hydrogenated solvent. The OHP-enriched solvent provides increased solvation of coal and improved yields of liquid fuel product in a coal liquefaction process which utilizes the solvent.

Abstract: A catalytic process for the conversion of hydrocarbons or bituminous shales or carbon monoxide in the liquid phase in contact with hydrogen flowing upwardly through a series of successive stages, each containing a catalyst bed either semi-stationary or dispersed in the charge, the catalyst being maintained at each stage by an upward flow of hydrogen or hydrocarbon supplied below an opening in the partition wall between two successive stages and periodically allowed to pass from one stage to the next through said opening, by discontinuing said upward flow.

Abstract: A method is provided for preparing a synthetic crystalline aluminosilicate zeolite Alpha containing platinum-group metal within the zeolite pores as synthesized, thereby providing shape-selective hydrogenation activity. The method comprises synthesizing the zeolite from a reaction mixture of controlled composition including a source of a cationic platinum-group metal complex. Catalysts made with the zeolite synthesized in accordance hereto are stable, both thermally and in the presence of steam, and exhibit beneficial shape-selectivity in catalysis and absorption.

Abstract: An improvement in the solvent extraction of nonhydrocarbons from a synfuel liquid, e.g., shale oil, involves that the extract from the extractor, rather than being recycled directly back to the extractor, is first hydrotreated. A further improvement involves that a portion of the hydrotreated extract is fractionated and a light fraction is returned to the extractor. Use of the hydrotreated extract as recycle increases the efficiency of the extractor. A still further improvement involves the use as a selective solvent of one of the following: dialkylformamide, aldehydomorpholine, keto-morpholine, morpholine or an aliphatic aromatic ketone. These preferred solvents have the advantage of providing a clear interface between the extract and raffinate in the extractor. Removal of the nonhydrocarbons permits production of more hydrocarbons having enhanced utility as a jet fuel from a synfuel liquid than otherwise would be possible.

Abstract: A mixture of heavy hydrocarbons, hydrogen and fresh catalyst comprising metals from the groups Vb, VIb, VIIb or VIII is passed first in a furnace for a limited heating time and then in a reactor where recycled catalyst is also added; the recycled catalyst is used in the form of a suspension recovered by fractionation of the reaction product.

Abstract: A process for the hydrogenation of unsaturated hydrocarbons comprising contacting said unsaturated hydrocarbons, with hydrogen, at temperatures ranging from about 40.degree. C. to about 160.degree. C., and pressures ranging from about 100 psi to about 3000 psi, with a catalyst comprising an ion exchange resin and an organic linking compound having at least one resin compatible moiety ionically bound to said resin and further having at least one metal complexible moiety selected from the group consisting of trivalent nitrogen, trivalent phosporous, trivalent arsenic, trivalent bismuth and trivalent antimony complexed to a metal selected from the group consisting of ruthenium, rhodium, palladium, osmium, iridium and platinum.

Abstract: A method is described for the preparation of chalcogenides of ruthenium, rhodium, osmium and iridium transition metals of the Periodic Table of the Elements which comprises mixing in the absence of an aqueous solvent a Group VIII transition metal salt with a source of chalcogenide, said chalcogenide being selected from the group consisting of sulfur, selenium, tellurium and mixtures thereof, yielding a precipitate of the formula MX.sub.y wherein M is selected from the group consisting of ruthenium, rhodium, osmium and iridium, X is sulfur, selenium, tellurium and mixtures thereof and y is a number ranging from about 0.1 to about 3, preferably 0.1 to about 2.5. By the practice of the nonaqueous synthesis technique, Group VIII chalcogenides are prepared which are finely divided, have a high surface area, small particle size and small crystallite size which are also free of excess sulfur, water and/or hydrolysis products.

Abstract: Novel, high specific surface area molybdenum oxycarbide catalysts are disclosed. They are prepared by the vapor condensation of molybdenum hexacarbonyl and catalyze the reaction of hydrogen and carbon monoxide to form hydrocarbons. Carburization of the molybdenum oxycarbides increases their activity in the carbon monoxide-hydrogen reaction.

Abstract: In a process for the selective hydrogenation of unsaturated hydrocarbon components of a feedstock, the feedstock is initially passed over a hydrogenation catalyst in the absence of hydrogen to increase hydrogenation selectivity of the catalyst, after which the amount of hydrogen required is then passed over the catalyst along with the feedstock to carry out the desired hydrogenation reaction.

Abstract: A novel catalyst precursor which comprises a Group IV-B transition metal oxide deposited on the surface of an inorganic metal oxide support, preferably alumina; especially where the Group IV-B transition metal oxide is deposited on the support surface as discrete areas separated by areas of support surface which contain little, if any, of said Group IV-B transition metal oxide; and a catalyst composition comprised of a cluster of a Group IV-B transition metal oxide and a Group VIII metal preferably a Group VIII noble metal, deposited on an inorganic metal oxide support, particularly an alumina support, especially where the clusters are deposited on the surface of the support, as discrete clusters separated by areas of support surface which contain little, if any, of said Group VI-B transition metal oxide, or clusters of said Group IV-B and Group VIII metals.

Abstract: A process for the treatment of a hydrocarbon fraction having a boiling point range beginning above 200.degree. C. and obtained in the cracking of hydrocarbons, in which the polymeric component resulting from the cracking pyrolysis is removed and the remaining polymer-free hydrocarbon is subjected to hydrogenation under such reaction conditions that the product is high in monoaromatic components while the polyaromatics are removed therefrom.

Abstract: Olefins and aromatic compounds in mixed hydrocarbon streams boiling above about 200.degree. F. are hydrogenated at a temperature ranging between about 400.degree. F.-720.degree. F. using a zeolite-containing catalyst that has been treated with a hydrocarbon stream relatively high in organic nitrogen compounds to suppress the cracking activity of the catalyst. The catalyst comprises (1) an amorphous base component, (2) a crystalline aluminosilicate component preferably comprising 5-30 wt. % of the total catalyst and having a silica/alumina mole ratio of at least 2.5 and an alkali metal content of less than about 2.0 wt. %, and (3) a transition metal hydrogenation component. The process is particularly useful in the manufacture of jet fuels and technical white oils and white oil bases with a minimum conversion of feed (<20%) to substantially lower boiling products.

Abstract: In a selective hydrogenation process wherein at least two catalyst beds in series are utilized, the temperature of the feed stream to the first catalyst bed and the temperature of the feed stream from the first catalyst bed to the second catalyst bed are manipulated so as to maintain a desired reaction temperature in both catalyst beds. The desired reaction temperature of the first catalyst bed is manipulated so as to insure that a desired percent of a specific feed component is selectively hydrogenated in the first catalyst bed. The reaction temperature of the second catalyst bed is manipulated so as to maintain a desired concentration of the specific feed component in the product stream from the second catalyst bed.

Abstract: Novel catalyst compositions are provided comprising a silica/alumina carrier having a silica content less than about 40% by weight and at least one noble metal component of Group VIII of the Periodic Table and wherein the catalyst contains (1) pores having a diameter of smaller than 600 A occupying at least 90% of the total pore volume and (2) pores having a diameter of 150 to 600 A occupying at least about 40% of the total volume of the pores having a diameter of smaller than 600 A. This catalyst is particularly useful in the production of jet fuels and white oils.

Abstract: A process for hydrotreating a petroleum hydrocarbon feed comprising admixing a quinone compound, or compounds, with said hydrocarbon feed, and contacting said admixture with hydrogen at elevated temperature, suitably at temperatures ranging from about 500.degree. F. to about 1050.degree. F., preferably from about 750.degree. F. to about 900.degree. F. The petroleum hydrocarbon feed is characterized generally as comprised of a full boiling range crude, an atmospheric or vacuum residum, an unconventional whole heavy crude, or fractions boiling within the gasoline and mid-distillate ranges.

Abstract: In a process for the production of olefins in two stages wherein, in the first stage, heavy petroleum fractions are hydrogenated in the presence of hydrogen and a hydrogenation catalyst and, in the second stage, the thus-hydrogenated fractions are subjected to thermal cracking in the presence of steam, the improvement which comprises employing as the hydrogenation catalyst a support-free catalyst consisting essentially of elements from Groups VIb, VIIB, and VIII of the periodic table of the elements in the form of the metals, metal oxides, metal sulfides, or organometal complexes, or mixtures thereof.

Abstract: A process for hydrotreating (hydroprocessing) hydrocarbons and mixtures of hydrocarbons utilizing a catalytic composite comprising an alumina-zeolite support, a rare earth exchange metal component, at least one metal component from Group VIB or Group VIII and from about 0.1 to about 5 weight percent of at least one component from Group IIA based on the weight of the finished catalyst in which process there is effected a chemical consumption of hydrogen. Hydrocarbon hydroprocesses are hydrocracking, the hydrogenation of aromatic nuclei, the ring-opening of cyclic hydrocarbons, desulfurization, denitrification, hydrogenation, etc.

Abstract: A startup method for a moving-bed reactor used in a process for the hydrogenation of olefin-containing hydrocarbons. The reactor is brought on-stream at full capacity while it contains less than a full loading of catalyst, and quantities of catalyst are intermittently added to the reactor while the hydrocarbons are being processed. Catalyst removal is then begun at a rate lower than the rate of catalyst addition and adjusted when the catalyst retention volume of the reactor becomes filled.

Abstract: The invention provides a titania-zirconia or a titania-zirconia-alumina catalyst base containing a system of metals, metal oxides or metal sulfides from Groups VIB, VIIB and VIII of the Periodic Table. Such catalyst are useful in the hydrodesulfurization and denitrogenation of hydrocarbon feed stocks and the saturation of aromatics contained therein.

Abstract: A pyrolysis feedstock, such as a gas oil feed, is hydrotreated in the presence of a bimetallic catalyst which has been promoted by the addition of chlorine and/or fluorine, preferably chlorine, followed by thermal cracking to increase the yields of light olefins and BTX.

Abstract: A process for hydrotreating (hydroprocessing) hydrocarbons and mixtures of hydrocarbons utilizing a catalytic composite comprising a combination of a nickel component, a molybdenum component and a platinum component with a zeolitic carrier material wherein said platinum component is present in an amount sufficient to result in the composite containing, on an elemental basis, about 0.2 to about 0.5 percent by weight platinum, in which process there is effected a chemical consumption of hydrogen. Hydrocarbon hydroprocesses are hydrocracking, the hydrogenation of aromatic nuclei, the ring-opening of cyclic hydrocarbons, desulfurization, denitrification, hydrogenation, etc.

Abstract: UV-unstable hydrocrackate lube oil stock is improved by hydrogenating the stock at a temperature in the 200.degree. to 300.degree. C. range using a hydrogenating component disposed upon an alumina carrier having a substantial pore volume of which a major portion is in pores having diameters in the 80- to 150-Angstrom range.

Abstract: A feedstock comprising olefinic hydrocarbons having more than one double bond per molecule is selectively hydrogenated to produce hydrocarbons having less unsaturation relative to the feedstock by contacting the feedstock in the presence of steam and hydrogen with a catalyst comprising a Group VIII metal or an oxide thereof on a carrier comprising a Group II metal aluminate spinel containing tin or an oxide of tin. The feedstock can be produced by reforming paraffin and cycloparaffin hydrocarbons in the presence of steam with a catalyst comprising a Group VIII metal or an oxide thereof on a carrier comprising a Group II metal aluminate spinel containing tin or an oxide of tin.

Abstract: An unstable heavy hydrocarbon fraction obtained by pyrosis is reacted with hydrogen in contact with three successive catalysts:(a) a group VIII metal catalyst(b) a catalyst comprising nickel and tungsten compounds, and(c) a catalyst comprising alumina, a group VIII noble metal and fluorine or chlorine.

Abstract: This invention relates to a method for making supported nickel catalysts which are characterized as having the nickel in a highly dispersed state, the catalysts and use thereof in hydrogenation, reforming and hydrocarbon synthesis reactions, for example, Fischer-Tropsch reactions. Catalysts prepared by the method of the instant invention, wherein nonaqueous solutions are used in preparing the catalyst, are characterized as having a degree of dispersion of at least 10% greater than similar catalysts prepared by the prior art aqueous impregnation techniques and in some instances show an improved degree of dispersion of more than 50% over the catalysts prepared by the prior art methods.