Reactive deasphalting process

US11866447B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11866447-B2
Application numberUS-202217591670-A
CountryUS
Kind codeB2
Filing dateFeb 3, 2022
Priority dateFeb 3, 2022
Publication dateJan 9, 2024
Grant dateJan 9, 2024

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A method to convert asphaltenes to partially oxidized asphaltenes comprising the steps of treating the reactor feed in a tubular reactor to produce a reactor effluent, introducing the reactor effluent to a disengagement zone of a vessel reactor, introducing an oxidizing agent stream to the asphaltene collection zone of the vessel reactor, reacting the asphaltenes in the asphaltene-rich fraction with oxygen from the oxidizing agent, withdrawing a bottom reactor effluent from the asphaltene collection zone, reducing a temperature of the bottom reactor effluent to produce a cooled bottom effluent, reducing a pressure of the cooled bottom effluent in a pressure regulator unit to produce a centrifuge feed, separating the centrifuge feed in a centrifuge to produce a centrate, mixing the centrate and the upper upgraded stream in a product mixer to produce a mixed upgraded stream, and separating the mixed upgraded stream in a three-phase separator.

First claim

Opening claim text (preview).

That which is claimed is: 1. A method to convert asphaltenes to partially oxidized asphaltenes, the method comprising the steps of: increasing a pressure of a feedstock in a feedstock pump to produce a pressurized feedstock, wherein the feedstock comprises greater than 0.1 weight percent of carbon 7-asphaltene (C7-asphaltene) content; increasing a temperature of the pressurized feedstock in a feedstock heater to produce a heated feedstock; increasing a pressure of a water stream in a water pump to produce a pressurized water stream; increasing a temperature of the pressurized water stream in a water heater to produce a supercritical water; mixing the heated feedstock and the supercritical water in a feed mixer to produce a mixed feed, wherein a temperature of the mixed feed is between 100° C. and 400° C.; increasing a temperature of the mixed feed in a pre-heater to produce a reactor feed; treating the reactor feed in a tubular reactor to produce a reactor effluent, wherein the tubular reactor comprises one or more pipes in series, wherein the temperature in the tubular reactor is between 374° C. and 500° C., wherein the pressure is between 220 barg and 330 barg, wherein the residence time is between 0.5 minutes and 30 minutes; introducing the reactor effluent to a disengagement zone of a vessel reactor, wherein an asphaltene-rich fraction disengages from a non-asphaltene fraction and flows to an asphaltene collection zone of the vessel reactor, wherein the disengagement zone is positioned at a greater elevation than the asphaltene collection zone, wherein the asphaltene-rich fraction comprises asphaltenes; introducing an oxidizing agent stream to the asphaltene collection zone of the vessel reactor, wherein the oxidizing agent stream comprises an oxidizing agent and water; reacting the asphaltenes in the asphaltene-rich fraction with oxygen from the oxidizing agent to produce partially oxidized asphaltenes, wherein a temperature in the vessel reactor is in the range between 374° C. and 500° C., wherein a pressure in the vessel reactor is between 220 barg and 330 barg; withdrawing an upper reactor effluent from the disengagement zone; withdrawing a bottom reactor effluent from the asphaltene collection zone; reducing a temperature of the upper reactor effluent in an upper cooler to produce a cooled upper effluent, wherein the temperature of the cooled upper effluent is between 50° C. and 150° C.; reducing a pressure of the cooled upper effluent in a pressure control unit to produce an upper upgraded stream, wherein the pressure of the upper upgraded stream is between 1 barg and 5 barg; reducing a temperature of the bottom reactor effluent in a bottom cooler to produce a cooled bottom effluent, wherein the temperature of the cooled bottom effluent is between 70° C. and 150° C.; reducing a pressure of the cooled bottom effluent in a pressure regulator unit to produce a centrifuge feed, wherein the pressure of the centrifuge feed is between 1 barg and 5 barg; separating the centrifuge feed in a centrifuge to produce a centrate and a rejected phase, wherein the temperature in the centrifuge is between 20° C. and 90° C., wherein the rejected phase comprises flocculated asphaltenes, wherein the flocculated asphaltenes comprise partially oxidized asphaltenes; mixing the centrate and the upper upgraded stream in a product mixer to produce a mixed upgraded stream; and separating the mixed upgraded stream in a three-phase separator to a produce gas product, an upgraded oil product, and a water product. 2. The method of claim 1 , wherein a temperature of the heated feedstock is between between 100° C. and 250° C. and a pressure is between 220 barg and 330 barg. 3. The method of claim 1 , wherein a temperature of the supercritical water is between 374° C. and 600° C. and a pressure is between 220 barg and 330 barg. 4. The method of claim 1 , wherein the oxidizing agent is selected from the group consisting of hydrogen peroxide, organic peroxide, oxygen gas, air, or combinations of the same. 5. The method of claim 1 , wherein the tubular reactor comprises 4 pipes in series. 6. The method of claim 1 , wherein a flow rate of oxidizing agent stream is such that an amount oxygen is in the range of 10% to 300% of the mass amount of C7-asphaltene content. 7. The method of claim 1 , wherein the total volume of the vessel reactor is equal to 0.1 to 1 times the volumetric flow rate of the reactor effluent. 8. The method of claim 1 , wherein the ratio of the volume of the disengagement zone to the volume of the asphaltene collection zone is between 1:1 and 10:1. 9. The method of claim 1 , wherein the ratio of the diameter of the disengagement zone to the volume of the asphaltene collection zone is between 2:1 and 5:1. 10. A system to convert asphaltenes to partially oxidized asphaltenes, the system comprising: a feedstock pump configured to increase a pressure of a feedstock to produce a pressurized feedstock, wherein the feedstock comprises greater than 0.1 weight percent of carbon 7-asphaltene (C7-asphaltene) content; a feedstock heater fluidly connected to the feedstock pump, the feedstock heater configured to increase a temperature of the pressurized feedstock to produce a heated feedstock; a water pump configured to increase a pressure of a water stream to produce a pressurized water stream; a water heater fluidly connected to the water pump, the water heater configured to produce a supercritical water; a feed mixer fluidly connected to the feedstock heater and the water heater, the feed mixer configured to mix the heated feedstock and the supercritical water to produce a mixed feed, wherein the feed mixer is selected from the group consisting of an ultrasonic device, agitator-equipped vessel, and a tee fitting; a pre-heater fluidly connected to the feed mixer, the pre-heater configured to produce a reactor feed; a tubular reactor fluidly connected to the pre-heater, the tubular reactor configured to produce a reactor effluent, wherein the tubular reactor comprises one or more pipes in series, wherein the tubular reactor has a residence time between 0.5 minutes and 30 minutes; a vessel reactor fluidly connected to the tubular reactor, the vessel reactor configured to produce an upper reactor effluent and a bottom reactor effluent, wherein the vessel reactor comprises a disengagement zone and an asphaltene collection zone, wherein the disengagement zone is positioned at a greater elevation than the asphaltene collection zone, wherein a distributer in the asphaltene collection zone is configured to distribute oxidizing agent stream into the asphaltene collection zone, wherein the oxidizing agent stream comprises oxidizing agent and water; an upper cooler fluidly connected to the disengagement zone, the upper cooler configured to produce a cooled upper effluent; a pressure control unit fluidly connected to the upper cooler, the pressure control unit configured to produce an upper upgraded stream; a bottom cooler fluidly connected to the asphaltene collection zone, the bottom cooler configured to produce a cooled bottom effluent; a pressure regulator unit fluidly connected to the bottom cooler, the pressure regulator unit configured to produce a centrifuge feed; a centrifuge fluidly connected to the pressure regulator unit, the centrifuge configured to produce a centrate and a rejected phase; a product mixer fluidly connected to the pressure control unit and the centrifuge, the product mixer configured to mix the upper upgraded stream and the centrate to produce a mixed upgraded stream; and a three-phase separator fluidly connected to the product mixer, the three-phase separator configured to produce a ga

Assignees

Inventors

Classifications

  • C07D495/22Primary

    in which the condensed system contains four or more hetero rings · CPC title

  • Separation of non-miscible liquids · CPC title

  • General arrangements, e.g. flowsheets (B01D19/0063 takes precedence) · CPC title

  • Controlling or regulating processes (controlling or regulating in general G05) · CPC title

  • Controlling the temperature of the process · CPC title

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What does patent US11866447B2 cover?
A method to convert asphaltenes to partially oxidized asphaltenes comprising the steps of treating the reactor feed in a tubular reactor to produce a reactor effluent, introducing the reactor effluent to a disengagement zone of a vessel reactor, introducing an oxidizing agent stream to the asphaltene collection zone of the vessel reactor, reacting the asphaltenes in the asphaltene-rich fraction…
Who is the assignee on this patent?
Saudi Arabian Oil Co
What technology area does this patent fall under?
Primary CPC classification C07D495/22. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jan 09 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).