Abstract: A method for producing a process oil is provided in which an aromatic extract oil is added to a naphthenic rich feed to provide a blended feed. The blended feed is then extracted with an aromatic extract solvent to yield a raffinate which subsequently is hydrotreated to provide a process oil.

Abstract: A hydrotreating apparatus comprising (a') a fixed-bed reactor packed with a hydrotreating catalyst for hydrotreating a heavy oil and (b') a suspended-bed reactor packed with a hydrotreating catalyst for further hydrotreating the heavy oil hydrotreated in the fixed-bed reactor. According to the apparatus of the present invention, (a) feeding of a heavy oil to a fixed-bed reactor is disclosed packed with a hydrotreating catalyst to thereby effect hydrotreating of the heavy oil and (b) feeding of the heavy oil hydrotreated in the fixed-bed reactor to a suspended-bed reactor packed with a hydrotreating catalyst to thereby effect further hydrotreating of the heavy oil can be conducted, and therefore the period of hydrotreating of the heavy oil can be prolonged.

Abstract: In the production of aromatic hydrocarbon from coking crude by-product benzene after a vaporization stage in which the crude benzene is evaporated to leave a residue, the crude benzene is subjected to pressure refining in the presence of hydrogen. The residue is distilled to form high and low boiling fractions and at least the gas pressure and temperature of the distillation stage is controlled so that the sump product apart from styrene is substantially free from aromatic hydrocarbons with less than 9 carbon atoms. The rate of withdrawal of the vaporization residue from the vaporizing column is controlled, depending upon the concentration of polymer formers in the crude benzene to be in the range of 6 to 40% of the rate of feed of the coking by-product benzene to the vaporizing column.

Abstract: A method is provided to remove metals from a residual oil containing an initial amount of a selected metal, the method comprising the steps of:providing a vessel for exposing the residual oil to a DC electric field having a strength of about one kV/inch or greater,passing the residual oils through the vessel whereby at least ten percent by weight of the initial amount of the selected metal is removed by attraction to an electrode; andpassing the residual oil that has been passed through the vessel over a hydrodemetalization catalyst in the presence of hydrogen. Metal containing particles and other toluene insoluble organic and inorganic solids are effectively removed from residual oil streams by treatment with a DC electrical field prior to hydrodemetalization resulting in significant increases in useful lives for downstream hydrodemetalization catalyst.

Abstract: An improved process for producing a low-sulfur fuel oil or gas from used oil and finely divided coal. After mixing, the coal/oil slurry is heated within a pressure vessel to a temperature of approximately 850.degree. F. and the pressure increased to approximately 1500 psi for a time period of more than one hour. A gaseous low-sulfur diesel fuel can be recovered from near the top of the pressure vessel.

Abstract: Nickel-copper catalysts supported on an acidic carrier, preferably containing a binder, are used to hydroisomerize paraffins, particularly Fischer-Tropsch paraffins, boiling at 350.degree. F.+ into lighter, more valuable products.

Abstract: Sulfur species present in cracked naphthas are converted and removed by first passing the naphtha over an acid catalyst to alkylate the thiophenic compounds in the naphtha using the olefins, i.e., monoolefins and diolefins, present in the naphtha as alkylating agent. Alkylated thiophenes are concentrated in the heavy portion of the naphtha by distillation, reducing the amount of naphtha that needs to be hydrodesulfurized. Olefins in cracked naphthas are concentrated in the light portion of the naphtha which is not subsequently hydrotreated. Thus, octane and hydrogen consumption penalties associated with hydrotreating are minimized.

Abstract: A catalytic cracked naphtha is desulfurized with minimum loss of olefins and octane. The naphtha is fed to a first distillation column reactor which acts as a depentanizer or dehexanizer with the lighter material containing most of the olefins and mercaptans being boiled up into a first distillation reaction zone where the mercaptans are reacted with diolefins to form sulfides which are removed in the bottoms along with any higher boiling sulfur compounds. The bottoms are subjected to hydrodesulfurization in a second distillation column reactor where the sulfur compounds are converted to H.sub.2 S and removed. The lighter fraction containing most of the olefins is thus not subjected to the more harsh hydrogenation conditions of the second reactor.

Abstract: Disclosed is a process for hydroconverting a heavy hydrocarbon oil in a reactor under high-temperature and high-pressure conditions,wherein said hydroconversion is carried out through using at least three desulfurization catalysts which each contains as active metals transition metals of Group VI and VIII in the Periodic Table supported on an alumina carrier and which have different SI of 40 or higher, 30 or higher and below 40, and lower than 30, respectively,and wherein said at least three catalysts are packed into the reactor in a descending order of SI from the inlet to the outlet of the reactor, with the proportion of the catalyst having SI of 40 or higher is at least 10% by volume, that of the catalyst having SI of 30 or higher and below 40 is at least 20% by volume, and that of the catalyst having SI of lower than 30 is at least 30% by volume.

Abstract: A process for obtaining a fuel for internal combustion engines from a hydrocarbon charge, comprising a step (a) for distillation (D1) in which a bottom product (Q1) is obtained via a line 3 and in which a top product (T1) is obtained via a line 2, a step (b) of liquid/liquid extraction (LE) using a solvent (S1) to obtain a raffinate to (R1), (line 5) and an extract from which product (Q1) an extract (E1) is obtained (line 6) and a raffinate, a step c) of separating (D2) the raffinate (R1) enabling a product (Q2) to be obtained via line 7, which product has a low solvent (S1) content, and a step (d) of hydrotreatment (HDS) in which the mixture of the products (T1) and (Q2) are subjected to hydrotreatment with a hydrogen partial pressure of less than 10 megapascals, to obtain a product (P) (line 9) which has improved qualities and which contains less than 500 ppm by weight sulphur.

Abstract: Low sulfur gasoline of relatively high octane number is produced from a catalytically cracked, sulfur-containing naphtha by hydrodesulfurization followed by treatment over an acidic catalyst, preferably a catalyst comprising an intermediate pore size zeolite, such as ZSM-5, and a large pore size zeolite, including a metal hydrogenation function, such as a faujasite, preferably USY, which contains nickel and molybdenum. The treatment over the acidic catalyst in the second step restores the octane loss which takes place as a result of the hydrogenative treatment and results in a low sulfur gasoline product with an octane number comparable to that of the feed naphtha. Use of the intermediate pore size zeolite and the large pore size zeolite is expected to provide more boiling point conversion than either zeolite alone under the same conditions.

Abstract: The invention concerns a hydro treatment method in at least two stages, for a heavy hydrocarbon fraction containing asphaltenes, sulphur impurities and metallic impurities, wherein:a) in at least one first stage described as hydrodemetallization, the hydrocarbon charge and hydrogen are passed over a hydrodemetallization catalyst,b) in at least one subsequent stage described as hydrodesulphurization, the product of stage a) and hydrogen are passed over a hydrodesulphurization catalyst.The invention, in which the hydrodemetallization stage comprises one or more zones each containing hydrodemetallization catalyst operating in a fixed bed, is characterised in that this zone or these zones are preceded by two protective zones arranged in parallel, each containing a fixed bed of a hydrodemetallization catalyst, the two protective zones operating alternately.

Abstract: Low sulfur gasoline of relatively high octane number is produced from a catalytically cracked, sulfur-containing naphtha by hydrodesulfurization followed by treatment over an acidic catalyst containing, preferably an intermediate pore size zeolite such as ZSM-5 and a zeolite such as MCM-22. The treatment over the acidic catalyst in the second step restores the octane loss which takes place as a result of the hydrogenative treatment and results in a low sulfur gasoline product with an octane number comparable to that of the feed naphtha. In favorable cases, using feeds of extended end point such as heavy naphthas with 95 percent points above about 380.degree. F. (about 193.degree. C.), improvements in both product octane and yield relative to the feed may be obtained.

Abstract: Low sulfur gasoline of relatively high octane number is produced from a catalytically cracked, sulfur-containing naphtha by hydrodesulfurization followed by treatment in a second step over a a first catalyst zone comprising a large pore size zeolite material and a second catalyst zone comprising an intermediate pore size material. Preferably, the large pore size material is zeolite beta and the intermediate pore size material is ZSM-5. The treatment in the second step restores the octane loss which takes place as a result of the hydrogenative treatment and results in a low sulfur gasoline product with an octane number comparable to that of the feed naphtha. In favorable cases, using feeds of extended end point such as heavy naphthas with 95 percent points above about 380.degree. F. (about 193.degree. C.), improvements in both product octane and yield relative to the feed may be obtained.

Abstract: Low sulfur gasoline of relatively high octane number is produced from a catalytically cracked, sulfur-containing naphtha by hydrodesulfurization followed by treatment over an acidic catalyst, preferably an intermediate pore size zeolite such as ZSM-5. The treatment over the acidic catalyst in the second step restores the octane loss which takes place as a result of the hydrogenative treatment and results in a low sulfur gasoline product with an octane number comparable to that of the feed naphtha. In favorable cases, using feeds of extended end point such as heavy naphthas with 95 percent points above about 380.degree. F. (about 193.degree. C.), improvements in both product octane and yield relative to the feed may be obtained.

Abstract: A process is provided for producing low sulfur gasoline of relatively high octane number from a catalytically cracked, sulfur-containing naphtha by hydrodesulfurization followed by treatment over an acidic catalyst comprising crystals having the structure of ZSM-12. The treatment over the acidic catalyst comprising ZSM-12 in the second step restores the octane loss which takes place as a result of the hydrogenative treatment and results in a low sulfur gasoline product with an octane number comparable to that of the feed naphtha. In favorable cases, using feeds of extended end point such as heavy naphthas with 95 percent points above about 380.degree. F. (about 193.degree. C.), improvements in both product octane and yield relative to the feed may be obtained.

Abstract: Low sulfur gasoline of relatively high octane number is produced from a catalytically cracked, sulfur-containing naphtha by hydrodesulfurization followed by treatment over an acidic catalyst, preferably an intermediate pore size zeolite such as ZSM-5 with controlled diffusion characteristics. The treatment over the acidic catalyst in the second step restores the octane loss which takes place as a result of the hydrogenative treatment and results in a low sulfur gasoline product with an octane number comparable to that of the feed naphtha. In favorable cases, using feeds of extended end point such as heavy naphthas with 95 percent points above about 380.degree. F. (about 193.degree. C.), improvements in both product octane and yield relative to the feed may be obtained.

Abstract: Low sulfur gasoline is produced from a catalytically cracked, sulfur-containing naphtha by fractionating the naphtha feed into a low boiling fraction in which the majority of the sulfur is present in the form of mercaptans and a high-boiling fraction in which the sulfur is predominantly in non-mercaptan form such as thiophenes. The low boiling fraction is desulfurized by a non-hydrogenative mercaptan extraction process which retains the olefins which are present in this fraction. The second fraction is desulfurized by hydrodesulfurization, which results in some saturation of olefins and loss of octane. The octane loss is restored by treatment over an acidic catalyst, preferably an intermediate pore size zeolite such as ZSM-5, to form a low sulfur gasoline product with an octane number comparable to that of the feed naphtha but which contains some recombined sulfur in the form or mercaptans which are removed in the non-hydrogenative mercaptan extraction step.

Abstract: A sulfur-containing catalytically cracked naphtha is upgraded to form a low-sulfur gasoline product by a process which retains the octane contribution from the olefinic front end of the naphtha. Initially, the mercaptan sulfur in the front end of the cracked naphtha is converted to higher boiling disulfides by oxidation. The front end, which is then essentially an olefinic, high octane sulfur-free material, may be blended directly into the gasoline pool. The back end, which now contains the original higher boiling sulfur components such as thiophenes, together with the sulfur transferred from the front end as disulfides, is hydrotreated to produce a desulfurized product. This desulfurized product, which has undergone a loss in octane by saturation of olefins, is then treated in a second stage, by contact with a catalyst of acidic functionality, preferably a zeolite such as ZSM-5, under conditions which produce a product in the gasoline boiling range of higher octane value.

Abstract: Low sulfur gasoline is produced from a catalytically cracked, sulfur-containing naphtha by fractionating the naphtha feed into a low boiling fraction in which the majority of the sulfur is present in the form of mercaptans and a high-boiling fraction in which the sulfur is predominantly in non-mercaptan form such as thiophenes. The low boiling fraction is desulfurized by a non-hydrogenatile mercaptan extraction process which retains the olefins present in this fraction. The second fraction is desulfurized by hydrodesulfurization, which results in some saturation of olefins and loss of octane. The octane loss is restored by treatment over an acidic catalyst, preferably an intermediate pore size zeolite such as ZSM-5, to form a low sulfur gasoline product with an octane number comparable to that of the feed naphtha but which contains some recombined sulfur in the form or mercaptans which are removed in a final hydrotreatment.

Abstract: A resid hydrotreating process hydrotreats a resid bottoms fraction from the reduction of crude oil. The hydrotreated bottoms fraction is then subjected to deep vacuum reduction and in some cases deasphalted by solvent extraction to produce an oil suitable for use as a catalytic cracking feedstock and a resins fraction suitable for solvating resid in a hydrotreating process.

Abstract: A catalyst prepared by the steps which comprise: (a) adding to an asphaltene-containing hydrocarbonaceous oil charge stock a metal compound, a heteropoly acid and water; (b) converting the metal compound and heteropoly acid within the charge stock by heating the oil to a temperature from about 120.degree. F. (43.degree. C.) to about 500.degree. F. (260.degree. C.) to produce at least one organometallic compound within the charge stock; and (c) converting the organometallic compound within the charge stock under hydroconversion conditions to produce the catalyst.

Abstract: Apparatus is provided whereby the heat released from exothermic hydrodemetallization reactions is recovered in order to provide either a lower operating cost of a two-stage hydrotreating process or protection of process equipment against excessive operating temperatures.

Abstract: The hydroprocessing of heavy oils is improved by the use of a high activity slurry catalyst prepared by sulfiding an aqueous Group VIB metal compound with a gas containing hydrogen sulfide to a dosage greater than 8 SCF of hydrogen sulfide per pound of Group VIB metal. After introducing the slurry catalyst into the heavy oil, and subjecting the mixture to elevated temperatures and partial pressures of hydrogen, the mixture is treated in a fixed or ebullated bed of hydrodesulfurization/hydrodemetalation catalyst under hydroprocessing conditions.

Abstract: Method and apparatus are provided whereby the heat released from exothermic hydrodemetallization reactions is recovered in order to provide either a lower operating cost of a two-stage hydrotreating process or protection of process equipment against excessive operating temperatures.

Abstract: A hydrotreating process if provided in which resid and resins are hydrotreated with hydrogen-rich gases in the presence of a hydrotreating catalyst in an ebullated bed reactor.

Abstract: A hydrodesulfurization process for catalytically hydrosulfurizing highly aromatic feeds, especially catalytically cracked feeds such as light cycle oils from catalytic cracking processes and aromatic extracts, employs a hydrodesulfurization catalyst containing zeolite beta. The zeolite beta based catalyst is more effective for effecting desulfurization than comparable amorphous catalysts or catalysts based on other large pore size zeolite and is capable of achieving a high degree of desulfurization at relatively low levels of conversion. The hydrodesulfurization catalyst comprises a transition metal hydrogenation component, preferably Co/Mo, on zeolite beta together with an inert matrix. The zeolite beta based catalyst may be mixed with amorphous catalyst such as Co/Mo/alumina. The low sulfur products are useful as blending components for road diesel fuels and other distillate fuels.

Abstract: A process of concurrently dedusting and upgrading particulate laden raw, whole retort oil is provided which comprises the steps of: retorting solid hydrocarbon-containing material such as oil shale to liberate an effluent stream of dust laden hydrocarbons; injecting the dust-laden retort effluent product stream into a catalytic hydrotreater; agitating the product stream in the hydrotreater to constantly maintain the particulates in suspension within the oil; catalytically hydrotreating the agitated product stream in the presence of a hydroprocessing gas at a pressure of from 500 to 3000 psi, a temperature of from 650.degree. to 850.degree. F. and a space velocity of from 0.1 to 6.0 hr.sup.-1, whereby the suspended particulates are agglomerated to facilitate solid-liquid separation and substantial amounts of sulfur and nitrogen contaminants are simultaneously removed from the resulting ungraded oil; and mechanically separating the agglomerated particulates from the upgraded whole oil.

Abstract: This invention provides a fixed bed of nonuniformly sized grade catalyst particles for hydrocracking or hydrodesulfurization. The graded particles are arranged with the largest particles in either the upstream or the downstream portion of the bed. In either case, when compared with the conventional bed of uniformly sized particles, the graded bed of this invention shows enhanced hydrocarbon conversion activity for heavy oils over a useful range of conversion. Such catalyst bed is particularly useful in moderate hydrocracking operating at less than 1000 psig (7000 kPa) pressure.

Abstract: An enhanced process to reduce the sulfur content in petroleum distillate products through fractionation of a feedstock followed by segregated hydrotreating. Improved performance and more controlled desulfurization is achieved.

Abstract: Desulphurization process for feedstocks in which the sulphur compounds contained therein are first separated into a concentrate stream which is then hydro-desulphurized, and the resulting hydrogen suphide removed using conventional sulphur removal techniques. The initial separation is preferably effected using membrane separation or temperature swing absorption processes.

Abstract: A process for the removal of hydrogenatable hydrocarbonaceous compounds comprising a component selected from the group consisting of halogen, metal, sulfur, oxygen and nitrogen from a hydrocarbonaceous stream which comprises the steps of: (a) contacting the hydrocarbonaceous stream with an adsorbent to remove at least a portion of the hydrogenatable hydrocarbonaceous compounds from the hydrocarbonaceous stream to provide a hydrocarbonaceous stream having a reduced concentration of hydrogenatable hydrocarbonaceous compounds; (b) contacting spent adsorbent with an elution solvent to remove the hydrogenatable hydrocarbonaceous compounds from the spent adsorbent thereby regenerating the adsorbent; (c) contacting the elution solvent in admixture with the hydrogenatable hydrocarbonaceous compounds in the presence of hydrogen with a hydrogenation catalyst; (d) contacting the effluent with an aqueous scrubbing solution; (e) introducing a resulting admixture of the reaction zone effluent and the aqueous scrubbing solu

Abstract: A process is provided in which solvent-extracted oil or other deasphalted oil derived from hydrotreated resid is catalytically cracked to increase the yield of gasoline and other high value products.

Abstract: An improved process for the flexible production of high-quality gas oil from two crude gas oil feedstocks deriving from primary fractionation consisting of subjecting the heavy crude gas oil feedstock to catalytic dewaxing in the presence of hydrogen, adding a lighter crude gas oil feedstock to the actual effluent from the dewaxing stage and subjecting these feedstocks simultaneously to catalytic desulphurization.

Abstract: A heavy crude oil is fractionated into at least three liquid fractions which include a distillate fraction boiling in the 400.degree. F.-650.degree. F. range and a 650.degree. F.+ boiling range residuum. The distillate cut is hydrodesulfurized and the residuum is hydrodemetallized. The cuts thus hydrotreated, and at least a part of the third liquid fraction, are then combined to form an upgraded synthetic crude oil of relatively low sulfur content and relatively low vanadium and nickel content.

Abstract: A process for the production of transportation fuels from heavy hydrocarbonaceous feedstock is provided comprising a two-stage, close-coupled process, wherein the first stage comprises a hydrothermal zone into which is introduced a mixture comprising a feedstock and finely ground hydroprocessing catalyst having coke-suppressing and demetalizing activity, and hydrogen; and the second, close-coupled stage comprises a hydrocatalytic zone into which substantially all the effluent from the first stage is directly passed and processed under hydrocracking conditions. The first-stage ground catalyst may also be spent catalyst from which most metals have been removed.

Abstract: A process for improving the color and oxidation stability of feed characterized as an admixture of liquid hydrocarbon compounds, inclusive of fused multi-ring aromatic and hydroaromatic hydrocarbons. This feed, which boils within a range of from about 224.degree. C. to about 538.degree. C. and contains moderate to high concentrations of organic sulfur and organic nitrogen compounds, is (1) hydrotreated over a hydrotreating catalyst at hydrotreating conditions, or (2) hydrotreated over a hydrotreating catalyst at hydrotreating conditions and the high boiling product therefrom hydrocracked over a hydrocracking catalyst at hydrocracking conditions, to obtain a low sulfur, low nitrogen product which is contacted as a feed in the presence of hydrogen, over a catalyst comprised of elemental iron and one or more alkali or alkaline-earth metals components at hydrogen partial pressure and temperature sufficient to improve product color, or stablize the product against light and oxygen degradation, or both.

Abstract: A process for treating heavy crude oil feedstocks to reduce the asphaltenes, metals and sulfur content thereof while maintaining a high conversion thereof comprising: subjecting the feedstock to an asphaltene separation stage and thereafter subjecting the deasphaltene crude to a first hydrotreatment stage employing a first macroporous catalyst so as to produce an intermediate partially demetallized and desulfurized product and thereafter treating said intermediate product in a second hydrotreatment stage using a microporous catalyst wherein the microporous catalyst exhibits extended life period.

Abstract: A carbonaceous feed, such as a heavy hydrocarbonaceous oil or coal and mixtures thereof, is upgraded by a combination coking and catalytic slurry hydroconversion process which may be integrated with a deasphalting process.

Abstract: In the catalytic processing of hydrocarbons, a hydrocarbon oil is successively contacted with a particulate catalyst in a first reaction zone and contacted at a higher temperature with a second portion of the particulate catalyst in the same reaction zone or in a second reaction zone.

Abstract: The present invention provides for a process for reducing the pour point of a hydrocarbon feedstock containing nitrogen- and sulfur-containing impurities. The hydrocarbon feedstock is contacted with hydrogen and a hydrotreating catalyst under hydrotreating conditions whereby a portion of the nitrogen- and sulfur-containing compounds are converted to hydrogen sulfide and ammonia. A portion of the hydrotreater effluent is then passed to a dewaxing zone and contacted with hydrogen under dewaxing conditions in the presence of a dewaxing catalyst containing a borosilicate molecular sieve on silica-alumina-containing matrix.

Abstract: Disclosed is an improved multi-stage process for the hydroconversion of heavy hydrocarbon feedstocks containing asphaltenes, metals and sulfur compounds. The process is characterized by the use of a relatively inexpensive demetallation catalyst in a first reaction zone comprising a Group VIB and/or a Group VIII metal deposed on a high macropore volume inorganic support followed by the use of a desulfurization catalyst in a second reaction zone comprising a Group VIB and a Group VIII metal on a high macropore volume inorganic oxide support.

Abstract: In a two-stage hydrofining process, hydrogen is utilized as a quench fluid to reduce the temperature of the effluent withdrawn from the hydrodemetallization stage prior to providing such effluent to the hydrodesulfurization stage and the flow of such hydrogen is controlled so as to maintain a desired temperature for the feed to the hydrodesulfurization stage. Also, the flow of fuel to a furnace is controlled so as to maintain a desired temperature for the feed to the hydrodemetallization stage and hydrogen flow rates are manipulated throughout the process so as to maintain desired hydrogen concentrations throughout the hydrofining process.

Abstract: A two-stage process for hydrotreating asphaltenes and metallic contaminants-containing heavy hydrocarbon oils which comprises a demetallization step using a catalyst composition which is smaller in pore size and less in active metal amount than the conventional demetallization catalysts, and a hydrotreating step using a catalyst composition which is larger in pore size and more in active metal amount than the conventional hydrodesulfurization catalysts or hydrocracking catalysts, said hydrotreating step being located downstream of said demetallization step.

Abstract: A process for hydrotreating hydrocarbon feedstocks using shaped catalysts is disclosed. When the catalyst is used for diffusion limited reactions, and particularly when it is used for demetalation, shaped catalysts give longer catalyst lifetimes. Preferred shaped include oval and elliptical shapes, with and without bumps.

Abstract: A process for the removal of trace quantities of hydrocarbonaceous compounds from an aqueous stream which comprises the steps of: (a) contacting a solvent, which in the supercritical state is effective to dissolve the hydrocarbonaceous compounds from the aqueous stream, with the aqueous stream, for a time sufficient at supercritical solvent conditions to dissolve at least a portion of the hydrocarbonaceous compounds and to produce an aqueous stream having a reduced hydrocarbonaceous compound concentration; (b) separating the hydrocarbonaceous compounds from the solvent at subcritical conditions; and (c) recovering the hydrocarbonaceous compounds.

Abstract: An absorbent hydrocarbonaceous oil comprising contaminants, such as sulfur and/or nitrogen, is upgraded by subjecting the contaminated absorbent oil to hydrorefining. The upgraded absorbent may be utilized again as absorbent.

Abstract: A process for the production of transportation fuels from heavy hydrocarbonaceous feedstock is provided comprising a two-stage, close-coupled process, wherein the first stage comprises a hydrothermal zone into which is introduced a mixture comprising the feedstock, dispersed demetalizing contact particles having coke-suppressing activity, and hydrogen; and the second, close-coupled stage comprises a hydrocatalytic zone into which substantially all the effluent from the first stage is directly passed and processed under hydrocatalytic conditions.

Abstract: An improved process for removing metals from heavy oils and other hydrocarbon feed streams is disclosed. The process comprises combining water with the hydrocarbon feed stream at a liquid volume ratio of about 1:50 to about 1:1, and contacting the mixture under suitable demetallizing conditions with hydrogen gas and a catalyst composition comprising (a) AlPO.sub.4 and preferably (b) a Group VIB metal, more preferably molybdenum.

Abstract: A process of recovering the hydrocarbon values from low organic carbon content deposits comprises the hydrotreating of hydrocarbons from those deposits in the presence of supercritical alkane-containing solvent.