Abstract: Process for converting a heavy hydrocarbon feedstock with initial boiling point of at least 300° C. comprising: a) hydroconverting at least part of said feedstock; b) separating the effluent from stage a) to obtain light and heavy liquid fractions; c) at least two stages of deasphalting in series at least part of the heavy liquid fraction originating from stage b), allowing to separate at least one fraction of asphalt, at least one fraction of heavy deasphalted oil (heavy DAO) and at least one fraction of light deasphalted oil (light DAO), at least one deasphalting stage being carried out using a mixture of at least one polar solvent and at least one apolar solvent, said deasphalting stages being under subcritical conditions of the mixture of solvents; d) recycling at least part of said heavy deasphalted oil cut from stage c) upstream of hydroconverting a) and/or of the inlet of separating b).

Abstract: A fuel desulfurization method is provided in the present invention. In the step (a), a fuel is oxidized by adding an ionic liquid, an oxidant, and an acid catalyst. In the step (b), the oxidized fuel is mixed with a desulfurization agent to form a desulfurized fuel. In the step (c), the ionic liquid is recycled. In the recycling step, a first solution is added into the ionic liquid. Then, a second solution is added into the ionic liquid to form a second solution phase and an ionic liquid phase. The second solution phase is separated from the ionic liquid phase. The first solution, the oxidant and the acid catalyst are removed from the remained ionic liquid phase to form a recycled ionic liquid.

Abstract: The present invention relates to a method for treating a feed corresponding to a pyrolysis gasoline, comprising: a) at least one stage of selective hydrogenation of the feed, referred to as HD1, b) fractionating in one or more distillation columns the effluent from stage a) in order to produce at least one light C5 cut, an intermediate C6 or C6-C7 or C6-C8 cut intended for aromatics production, a heavy C7+ or C8+ or C9+ cut intended for gasoline production, c) at least one stage of hydrodesulfurization and deep hydrogenation of the intermediate cut, referred to as HD2, d) at least one stage of alkylation of the heavy C7+, C8+ or C9+ cut consisting of a treatment on an acid catalyst allowing weighting of the sulfur compounds, e) at least one stage of distillation of the effluent from stage d), intended to produce a light fraction that can be directly used as a low-sulfur gasoline base, and a heavy C11+ or C12+ fraction rich in sulfur compounds, used as middle distillate or fuel oil.

Abstract: A method for removing impurities from a feedstock comprising a hydrocarbon oil is provided. The method comprises contacting the feedstock with an oxygen-containing gas under conditions effective to oxidize at least a portion of the impurities, as well as contacting the feedstock with a Lewis acid under conditions effective so that any Lewis base impurity(ies) in the feedstock can react with the Lewis acid. Any impurities so oxidized and/or reacted are then removed.

Abstract: A diesel desulfurization method has various steps including: implementing a modified oxidative desulfurization (UAOD) process. The UAOD has the steps of: mixing diesel fuel with room temperature ionic liquid, oxidant, phase transfer catalyst, and acid catalyst in a tank in a mix; recycling the ionic liquid and recycling the acid catalyst in aqueous phase. A step is to move the sulfur from the diesel fuel in a fluidized bed reactor (FBR) having bed reactor material. The process can be improved with ultrasound during mixing, or a high shear mixer. The bed reactor is preferably acidic alumina for adsorbing oxidized sulfur. The oxidant is preferably hydrogen peroxide (H2O2). The acid catalyst is preferably a mixture of Acetic acid and Tri-fluoro acetic acid.

Abstract: The present invention relates to a process of reducing sulfur- or nitrogen-containing compounds and producing oxygenates, and in particular to a one-pot process of reducing sulfur- or nitrogen-containing compounds and also producing oxygenates in the presence of a homogeneous catalyst such as Mn+/a first solvent or M1n+/a second solvent/M2m+/a third solvent or a mixture thereof, the process herein being useful as an excellent octane booster in the reformulated gasoline and as a cetane booster for the future oxygenated diesel in a one-pot reaction.

Abstract: The instant invention relates to a method for producing low-sulfur, low-nitrogen diesel boiling range products involving contacting a diesel boiling range feedstream with an acidic solution to selectively remove heterocyclic nitrogen-containing compounds before hydrotreating.

Abstract: A sample preparation system provides an automated process that dispenses appropriate amounts of solid material into wells of a microtiter plate for mixing into a suspension. The system utilizes an array of hollow tubes that are lowered into a particle reservoir such that particle material is forced up into the tubes. During loading, solid plungers in the tubes are positioned a known distance from the open end of the tubes. When the particle material is to be dispensed, the plungers are lowered to push the particle material out of the tubes and into receiving wells of the microtiter plate. The plunger stroke and internal diameter of the tubes defines the dispensed volume of particle material.

Abstract: A process for removing sulfur compounds from hydrocarbon streams by contacting the hydrocarbon stream, especially a gasoline stream, with an adsorbent material. The adsorbent material is regenerated with hydrogen or a hydrogen/H2S mixture.

Abstract: Economical processes are disclosed for the production of components for refinery blending of transportation fuels by selective oxidation of feedstocks comprising a mixture of hydrocarbons, sulfur-containing and nitrogen-containing organic compounds. Oxidation feedstock is contacted with a soluble quaternary ammonium salt containing halogen, sulfate, or bisulfate anion, and an immiscible aqueous phase comprising a source of hydrogen peroxide, and at least one member of the group consisting of phosphomolybdic acid and phosphotungstic acid, in a liquid reaction mixture under conditions suitable for reaction of one or more of the sulfur-containing and/or nitrogen-containing organic compounds. Blending components containing less sulfur and/or less nitrogen than the oxidation feedstock are recovered from the reaction mixture. Advantageously, at least a portion of the immiscible acid-containing phase is recycled to the oxidation.

Abstract: Economical processes are disclosed for the production of components for refinery blending of transportation fuels by selective oxidation of feedstocks comprising a mixture of hydrocarbons, sulfur-containing and nitrogen-containing organic compounds. Oxidation feedstock is contacted with an immiscible phase comprising at least one organic peracid or precursors of organic peracid in a liquid phase reaction mixture maintained substantially free of catalytic active metals and/or active metal-containing compounds and under conditions suitable for oxidation of one or more of the sulfur-containing and/or nitrogen-containing organic compounds. Blending components containing less sulfur and/or less nitrogen than the oxidation feedstock are recovered from the reaction mixture. Advantageously, at least a portion of the immiscible acid-containing phase is recycled to the oxidation.

Abstract: A process is disclosed for the production of refinery transportation fuel or components for refinery blending of transportation fuels having a reduced amount of sulfur and/or nitrogen-containing impurities. The process involves contacting a hydrocarbon feedstock containing the above impurities with an immiscible phase containing hydrogen peroxide and acetic acid in an oxidation zone to selectively oxidize the impurities. After a gravity phase separation, the hydrocarbon phase containing any remaining oxidized impurities, is passed to an extraction zone wherein aqueous acetic acid is used to extract a portion of any remaining oxidized impurities. A hydrocarbon stream having reduced impurities can then be recovered. The acetic acid phase effluents from the oxidation and the extraction zones can then be passed to a common separation zone for recovery of the acetic acid and for optional recycle back to the oxidation and extraction zones.

Abstract: A chemical treatment is disclosed for reducing the sulfur content of catalytically processed gasoline and intermediate crude-oil products, by absorbing the sulfur contained in such catalytically processed products on silica gel packed in a filter or assembly of filters, operating at the normal exit pressure from production of catalytically processed gasoline and distillation of intermediate crude-oil products.

Abstract: Economical processes are disclosed for production of components for refinery blending of transportation fuels which are liquid at ambient conditions by selective oxygenation of refinery feedstocks comprising a mixture of organic compounds. The organic compounds are oxygenated in a liquid reaction medium with an oxidizing agent and heterogeneous oxygenation catalyst system which exhibits a capability to enhance the incorporation of oxygen into a mixture of liquid organic compounds to form a mixture comprising hydrocarbons, oxygenated organic compounds, water of reaction, and acidic co-products. The mixture is separated to recover at least a first organic liquid of low density and at least a portions of the catalyst metal, water of reaction and acidic co-products. Advantageously, the organic liquid is washed with an aqueous solution of sodium bicarbonate solution, or other soluble chemical base capable to neutralize and/or remove acidic co-products of oxidation, and recover oxygenated product.

Abstract: A product of reduced sulfur content is produced from an olefin-containing hydrocarbon feedstock which includes sulfur-containing impurities. The feedstock is contacted with an olefin-modification catalyst in a reaction zone under conditions which are effective to produce an intermediate product which has a reduced amount of olefinic unsaturation relative to that of the feedstock as measured by bromine number. The intermediate product is then contacted with a hydrodesulfurization catalyst in the presence of hydrogen under conditions which are effective to convert at least a portion of its sulfur-containing impurities to hydrogen sulfide.

Abstract: A multi-step process for desulfurizing liquid petroleum fuels that also removes nitrogen-containing compounds and aromatics. The process steps are: thiophene extraction; thiophene oxidation; thiophene-oxide and -dioxide extraction; raffinate solvent recovery and polishing; extract solvent recovery; and recycle-solvent purification. The thiophene oxidation is accomplished with hydrogen peroxide and the extraction solvent is acetic acid in combination with secondary solvents. The operating conditions in the process are relatively mild at near ambient pressure and less than 145° C. throughout the process, and the only chemical consumed in the process is hydrogen peroxide. The process design can be modified to accommodate a variety of liquid hydrocarbon feeds.

Abstract: Economical processes are disclosed for production of components for refinery blending of transportation fuels which are liquid at ambient conditions by selective oxygenation of refinery feedstocks comprising a mixture of organic compounds. The organic compounds are oxygenated in a liquid reaction medium with an oxidizing agent and heterogeneous oxygenation catalyst system which exhibits a capability to enhance the incorporation of oxygen into a mixture of liquid organic compounds to form a mixture comprising hydrocarbons, oxygenated organic compounds, water of reaction, and acidic co-products. The mixture is separated to recover at least a first organic liquid of low density and at least a portions of the catalyst metal, water of reaction and acidic co-products. Advantageously, the organic liquid is washed with an aqueous solution of sodium bicarbonate solution, or other soluble chemical base capable to neutralize and/or remove acidic co-products of oxidation, and recover oxygenated product.

Abstract: Economical processes are disclosed for the production of components for refinery blending of transportation fuels by selective oxidation of feedstocks comprising a mixture of hydrocarbons, sulfur-containing and nitrogen-containing organic compounds. Oxidation feedstock is contacted with an immiscible phase comprising at least one organic peracid or precursors of organic peracid in a liquid phase reaction mixture maintained substantially free of catalytic active metals and/or active metal-containing compounds and under conditions suitable for oxidation of one or more of the sulfur-containing and/or nitrogen-containing organic compounds. Blending components containing less sulfur and/or less nitrogen than the oxidation feedstock are recovered from the reaction mixture. Advantageously, at least a portion of the immiscible acid-containing phase is recycled to the oxidation.

Abstract: A product of reduced sulfur content is produced from an olefin-containing hydrocarbon feedstock which includes sulfur-containing impurities. The feedstock is contacted with an olefin-modification catalyst in a reaction zone under conditions which are effective to produce an intermediate product which has a reduced amount of olefinic unsaturation relative to that of the feedstock as measured by bromine number. The intermediate product is then contacted with a hydrodesulfurization catalyst in the presence of hydrogen under conditions which are effective to convert at least a portion of its sulfur-containing impurities to hydrogen sulfide.

Abstract: A multi-step process for desulfurizing liquid petroleum fuels that also removes nitrogen-containing compounds and aromatics. The process steps are: thiophene extraction; thiophene oxidation; thiophene-oxide and -dioxide extraction; raffinate solvent recovery and polishing; extract solvent recovery; and recycle-solvent purification. The thiophene oxidation is accomplished with hydrogen peroxide and the extraction solvent is acetic acid in combination with secondary solvents. The operating conditions in the process are relatively mild at near ambient pressure and less than 145 ° C. throughout the process, and the only chemical consumed in the process is hydrogen peroxide. The process design can be modified to accommodate a variety of liquid hydrocarbon feeds.

Abstract: A process is disclosed for the hydrotreatment of feedstocks for fluidic cat crackers comprising reacting such feedstocks over high-conversion catalyst contain grate nickel-tungsten.

Abstract: A process for improving the performance of heavy oil refining units in a resid hydrotreating unit equipped for resid hydrotreating. The partially refined resid stream issuing from a train of ebullated bed reactor is first separated into high, medium, and low temperature components. The high temperature component is sent through a flash drum and then fractionated by solvent deasphalting in order to provide oil, resin, and asphaltene fractions. Thus, the asphaltene is eliminated before it can foul downstream equipment. This treatment of the heavy oil product has several benefits as compared to treating the vacuum tower bottoms. Among other things, one of these benefits is to debottleneck the resid hydrotreating unit, especially at the atmospheric tower.

Abstract: A refining process uses a two or four stage solvent separator coupled to receive an incoming feedstream of low sulfur resid and a solvent. In the preferred two stage separator, the mixture at the top of the first separator stage is fed to the second stage separator via a heat exchanger. The mixture at the bottom of the first stage separator includes resins and asphaltenes which are fed to a hydrotreater and then, in turn, to a fractionator. The output from the bottom of this fractionator can be fed back to the resid feedstream of the first stage separator for recycled separation. The material at the top of the second stage separator is fed back through the heat exchanger where it helps heat the mixture fed from the top of the first to the second stage separator, this feedback recovers the solvent for reuse in the first stage. The material settling to the bottom of the second stage separator is fed into a catalytic cracker or processed elsewhere.

Abstract: A process for removing S and Fe and to reclaim V, Ni and Co from coal or oil and their derivatives or from minerals. The process is based upon an oxidative extraction performed with hypochlorous acid (HClO) whose oxidizing power is generated and regulated "in situ". The process is particularly applicable to the recovery of V from residual flexi-coke and to the recovery of Ni from coal.

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: Sulfur-bearing liquid hydrocarbon feedstocks such as kerosene undergo desulfurization and deodorization by contacting such feedstocks with sodium hydride at normal atmospheric pressure and at elevated temperatures. The resulting liquid is further contacted with a mineral acid such as sulfuric acid and an alkaline neutralizing agent such as caustic soda. The liquid may also be contacted with an oxidizying agent such as sodium hyprochlorite prior to being contacted with the neutralizing agent and with a dehydrating agent such as soda ash after being contacted with the neutralizing agent.

Abstract: A process for purifying hydrocarbonaceous oils containing heteroatom sulfur and heteroatom nitrogen compound impurities comprising the steps of:(1) reacting said hydrocarbonaceous oil with an oxidizing gas containing at least one nitrogen oxide with more than one oxygen atom for each nitrogen atom while maintaining(a) the molar ratio of the nitrogen oxide to the total of the sulfur heteroatom content and the nitrogen heteroatom content to about 1.5:1 or less,(b) the reaction time to about one hour or less,(c) the temperature to about 100.degree. C.

Abstract: Metals, nitrogen and/or sulfur, particularly vanadium, nickel and nitrogen, are removed from organic compositions, particularly heavy hydrocarbon oils, by contacting the organic composition with a methylating agent, preferably dimethyl sulfate, under conditions sufficient to form a precipitate, including the contaminants, and separating the precipitate from the organic composition as by filtration, decantation, and the like. In another embodiment of the present invention, the treatment with the methylating agent is carried out in conjunction with treatment with an acid gas and water or a solvent, such as a combination of carbon dioxide and water.

Abstract: Metals, nitrogen and/or sulfur, particularly vanadium, nickel and nitrogen, are removed from organic compositions, particularly heavy hydrocarbon oils, by contacting the organic compositions with a halogenating agent, preferably phosphorus oxychloride, under conditions sufficient to form a distinct phase including the contaminants, which is separable from the organic composition and separating the distinct phase from the organic composition as by filtration, decantation, and the like. In another embodiment of the present invention, the treatment with the halogenating agent is carried out in conjunction with treatment with an acid gas and water, as a combination of carbon dioxide and water, or a solvent.