Patent classifications
C10G21/12
Process for oxidative desulfurization and denitrogenation using a fluid catalytic cracking (FCC) unit
A method and apparatus for recovering components from a hydrocarbon feedstock is provided. The method includes the steps of (a) supplying a hydrocarbon feedstock to an oxidation reactor, wherein the hydrocarbon feedstock is oxidized in the presence of a catalyst under conditions sufficient to selectively oxidize sulfur compounds and nitrogen compounds present in the hydrocarbon feedstock; (b) separating the hydrocarbons, the oxidized sulfur compounds, and the oxidized nitrogen compounds by solvent extraction; (c) collecting a residue stream that includes the oxidized sulfur compounds and the oxidized nitrogen compounds; and (d) supplying the residue stream to a fluid catalytic cracking unit.
Process for oxidative desulfurization and denitrogenation using a fluid catalytic cracking (FCC) unit
A method and apparatus for recovering components from a hydrocarbon feedstock is provided. The method includes the steps of (a) supplying a hydrocarbon feedstock to an oxidation reactor, wherein the hydrocarbon feedstock is oxidized in the presence of a catalyst under conditions sufficient to selectively oxidize sulfur compounds and nitrogen compounds present in the hydrocarbon feedstock; (b) separating the hydrocarbons, the oxidized sulfur compounds, and the oxidized nitrogen compounds by solvent extraction; (c) collecting a residue stream that includes the oxidized sulfur compounds and the oxidized nitrogen compounds; and (d) supplying the residue stream to a fluid catalytic cracking unit.
Method for producing non-carcinogenic aromatic process oil
The present invention relates to the chemical or petroleum-processing industry and can be used in the production of petroleum plasticizers for synthetic rubber and tyres. In the method for producing non-carcinogenic aromatic process oil, containing a PCA extract of less than 3.0% according to the IP-346 method, said method comprising purifying the oil fractions of petroleum with selective solvents and separating the extract, additionally processing the extract with a polar solvent and producing a raffinate as the end product, the polar solvent used is a mixture of dimethylsulphoxide and Nmethylpyrrolidone, which is used for preliminary processing of the extract, wherein, after the preliminary processing, the mixture of extract and polar solvent is filtered, divided and the light phase is sent to the additional processing of the extract with the polar solvent, and the heavy phase is sent to a polar solvent regeneration stage. The ratio of dimethylsulphoxide to N-methylpyrrolidone in the mixture is within the range of 1:0.1-0.5. The ratio of polar solvent to extract in the additional processing stage is within the range of 1.5-2.5:1. The ratio of polar solvent to extract in the preliminary processing stage is within the range of 0.1-0.3:1. The technical result consists in increasing the efficiency of the process by preventing the formation of an intermediate layer in the extractor column, by reducing the ratio of solvent:extract, and, as a consequence, by increasing the productivity of the plant, simplifying the process of drying the solvent, and eliminating a paraffin-naphthene solvent, which substantially simplifies the regeneration of extractant from the raffinate solution.
PROCESS FOR SELECTIVE CASCADE DEASPHALTING
The invention describes a process for the deasphalting of a heavy feedstock by liquid/liquid extraction, said process comprising at least two stages of deasphalting in series carried out on the feedstock to be treated making it possible to separate at least one fraction of asphalt, at least one fraction of heavy deasphalted oil, referred to as heavy DAO and at least one fraction of light deasphalted oil, referred to as light DAO, at least one of said stages of deasphalting being carried out by means of a mixture of at least one polar solvent and at least one apolar solvent, said stages of deasphalting being implemented under the subcritical conditions of the mixture of solvents used.
Integrated hydrotreating and isomerization process with aromatic separation
Deep desulfurization of hydrocarbon feeds containing undesired organosulfur compounds to produce a hydrocarbon product having low levels of sulfur, i.e., 15 ppmw or less of sulfur, is achieved by hydrotreating the feed under mild conditions, and separating the hydrotreated effluent into an aromatic-rich fraction which contains a substantial amount of the aromatic refractory and sterically hindered sulfur-containing compounds, and an aromatic-lean fraction. The aromatic-rich fraction is contacted with isomerization catalyst, and the isomerized aromatic-rich fraction is recycled to the mild hydrotreating process.
Integrated hydrotreating and isomerization process with aromatic separation
Deep desulfurization of hydrocarbon feeds containing undesired organosulfur compounds to produce a hydrocarbon product having low levels of sulfur, i.e., 15 ppmw or less of sulfur, is achieved by hydrotreating the feed under mild conditions, and separating the hydrotreated effluent into an aromatic-rich fraction which contains a substantial amount of the aromatic refractory and sterically hindered sulfur-containing compounds, and an aromatic-lean fraction. The aromatic-rich fraction is contacted with isomerization catalyst, and the isomerized aromatic-rich fraction is recycled to the mild hydrotreating process.
Non-aqueous hydrocarbon recovery
The present invention relates to in situ methods of separating, refining and extracting hydrocarbons from an oil formation. In embodiments of the present invention the in situ methods includes: (a) making a perforation in the oil sand formation, (b) disposing a non-polar substance into the perforation without addition of polar fluid, (c) subjecting the non-polar fluid composition disposed in the perforation to ultrasonic vibrations, and (d) extracting the hydrocarbon from the perforation in the oil sand formation. The present invention relates also to methods of separating, refining and extracting hydrocarbons from hydrocarbon matrices such as oil sand or oil shale.
Non-aqueous hydrocarbon recovery
The present invention relates to in situ methods of separating, refining and extracting hydrocarbons from an oil formation. In embodiments of the present invention the in situ methods includes: (a) making a perforation in the oil sand formation, (b) disposing a non-polar substance into the perforation without addition of polar fluid, (c) subjecting the non-polar fluid composition disposed in the perforation to ultrasonic vibrations, and (d) extracting the hydrocarbon from the perforation in the oil sand formation. The present invention relates also to methods of separating, refining and extracting hydrocarbons from hydrocarbon matrices such as oil sand or oil shale.
METHOD AND APPARATUS FOR RECOVERING ABSORBING AGENTS IN ACID GAS TREATMENT
A method and apparatus for continuously treating acid gases including recovering absorbent chemicals by introducing streams leaving a regenerator and/or leaving an absorber into a static mixing zone wherein supplemental washing water is added to recover absorbent chemicals. Improvements to the prior art methods are provided where one or more absorbent chemical recovery units are included to increase the amount of recovered absorbent chemicals exiting the regenerator and/or exiting the absorber are increased and/or maximized. Absorbent chemical recovery units can include mixing units where liquid is added to the stream of sour gas and absorbent chemical to mix with and absorb the absorbent chemical from the stream.
METHOD AND APPARATUS FOR RECOVERING ABSORBING AGENTS IN ACID GAS TREATMENT
A method and apparatus for continuously treating acid gases including recovering absorbent chemicals by introducing streams leaving a regenerator and/or leaving an absorber into a static mixing zone wherein supplemental washing water is added to recover absorbent chemicals. Improvements to the prior art methods are provided where one or more absorbent chemical recovery units are included to increase the amount of recovered absorbent chemicals exiting the regenerator and/or exiting the absorber are increased and/or maximized. Absorbent chemical recovery units can include mixing units where liquid is added to the stream of sour gas and absorbent chemical to mix with and absorb the absorbent chemical from the stream.