Free fatty acid separation and recovery using resin

US11795403B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11795403-B2
Application numberUS-202217828955-A
CountryUS
Kind codeB2
Filing dateMay 31, 2022
Priority dateMay 28, 2021
Publication dateOct 24, 2023
Grant dateOct 24, 2023

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The disclosure provides various methods for separating and recovering free fatty acids crude oil containing free fatty acids using certain ion-exchange resins to reduce the amount of free fatty acids in the crude oil to 3% or less such that the resultant oil is useable in downstream chemical processes. After separation and removal of the free fatty acids form the crude oil, the ion-exchange resin is reusable in further free fatty acid separation reactions.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for separating free fatty acids (FFA) from crude oil containing FFA comprising: a) contacting an ion-exchange resin with a first alcohol to activate the ion-exchange resin; b) drying the ion-exchange resin to provide an activated ion-exchange resin; c) mixing the activated ion-exchange resin with the crude oil to form a mixture, wherein the mixture comprises the crude oil and the ion-exchange resin, and the ratio of the activated ion-exchange resin and the FFA in the mixture is about 10:1 w/w to about 1.875:1 w/w; d) incubating the mixture to adsorb FFA from the crude oil onto the activated ion-exchange resin; e) filtering the mixture to form a treated oil and a separated ion-exchange resin comprising the adsorbed FAA and residual oil; f) washing the separated ion-exchange resin with a non-polar solvent to partition the residual oil from the separated ion-exchange resin to provide a washed ion-exchange resin and a first FFA fraction, wherein the first FFA fraction comprises the non-polar solvent, the residual oil, and desorbed FFA; g) evaporating the non-polar solvent from the first FFA fraction to provide a second FFA fraction comprising the residual oil and the desorbed FFA; h) combining a second alcohol with the second FFA fraction to separate the desorbed FFA from the residual oil; and i) removing the second alcohol from the residual oil in the second FFA fraction, wherein the second alcohol comprises the desorbed FFA; wherein a FFA content of less than 3% w/w remains in the treated oil. 2. The method of claim 1 further comprising reactivating the washed ion-exchange resin with aqueous sodium hydroxide to reactivate functional groups of the washed ion-exchange resin. 3. The method of claim 1 wherein the ion-exchange resin comprises a styrene-divinylbenzene co-polymer. 4. The method of claim 3 wherein the ion-exchange resin comprises a weakly basic ion-exchange resin comprising secondary or tertiary amine functional groups. 5. The method of claim 1 wherein the first alcohol and the second alcohol are methanol, ethanol, propanol, isopropyl alcohol, butanol, or a combination thereof. 6. The method of claim 1 wherein the treated oil comprises about 1% w/w or less of free fatty acid content. 7. The method of claim 1 wherein the ratio of the activated ion-exchange resin to the FFA in the mixture is about 5:1 w/w to about 1.875:1 w/w. 8. The method of claim 1 wherein the mixture comprises about 0.5% w/w to about 15% w/w of the activated ion-exchange resin. 9. The method of claim 8 wherein the mixture comprises about 2% w/w to about 7.5% w/w of the activated ion-exchange resin. 10. The method of claim 1 wherein the non-polar solvent is pentane, hexane, heptane, benzene, toluene, xylene, chloroform, diethyl ether, ethyl acetate, or pyridine. 11. The method of claim 1 wherein the crude oil is vegetable oil, waste cooking oil, or an oil from vegetative tissue. 12. A method for separating and recovering free fatty acids (FFA) from vegetable oil or waste cooking oil containing FFA comprising: a) activating an ion-exchange resin with a first ethanol for about 1 hour to about 4 hours at about 25° C. to about 35° C. with agitation; b) drying the ion-exchange resin for about 2 hours to about 12 hours at about 45° C. to about 55° C. to provide an activated ion-exchange resin; c) mixing the activated ion-exchange resin with vegetable oil or waste cooking oil to form a mixture, wherein the mixture comprises the vegetable oil or the waste cooking oil and the activated ion-exchange resin, and the ratio of the activated ion-exchange resin and the FFA in the mixture is about 10:1 w/w to about 1.875:1 w/w; d) incubating the mixture for about 4 hours to about 8 hours at about 35° C. to about 45° C. to adsorb FFA from the vegetable oil or the waste cooking oil to the activated ion-exchange resin; e) filtering the mixture to form a treated oil and a separated ion-exchange resin comprising the adsorbed FAA and residual oil; f) washing the separated ion-exchange resin with hexane to partition the residual oil from the separated ion-exchange resin to provide a washed ion-exchange resin and a first FFA fraction, wherein the first FFA fraction comprises the hexane, the residual oil, and desorbed FFA; g) evaporating the hexane from the first FFA fraction to provide a second FFA fraction; h) combining a second ethanol fraction with the second FFA fraction to separate the desorbed FFA from the residual oil remaining in the second FFA fraction; i) removing the second ethanol from the second FFA fraction, wherein the second ethanol comprises the FFA; and j) evaporating the second ethanol fraction to recover the desorbed FFA; wherein a free fatty acid content of less than 3% w/w remains in the treated oil. 13. The method of claim 12 further comprising rinsing the separated ion-exchange resin from step f with an aqueous sodium hydroxide solution for about 20 minutes to about 90 minutes at about 25° C. to about 35° C. with agitation to reactivate functional groups of the separated ion-exchange resin to provide a refreshed ion-exchange resin. 14. The method of claim 13 wherein the refreshed ion-exchange resin is used in a subsequent separation reaction to provide vegetable oil or waste cooking oil with less than 3% FFA, recovered FFA, or both vegetable oil or waste cooking oil with less than 3% FFA and recovered FFA. 15. The method of claim 12 wherein the mixture comprises about 2% w/w to about 7.5% w/w of the activated ion-exchange resin. 16. The method of claim 12 wherein the ion-exchange resin comprises a weakly basic styrene-divinylbenzene co-polymer, and the weakly basic styrene-divinylbenzene co-polymer comprises secondary amine functional groups, tertiary amine functional groups, or both secondary and tertiary amine functional groups. 17. The method of claim 12 wherein the treated oil comprises less than 1% w/w FFA content.

Assignees

Inventors

Classifications

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US11795403B2 cover?
The disclosure provides various methods for separating and recovering free fatty acids crude oil containing free fatty acids using certain ion-exchange resins to reduce the amount of free fatty acids in the crude oil to 3% or less such that the resultant oil is useable in downstream chemical processes. After separation and removal of the free fatty acids form the crude oil, the ion-exchange res…
Who is the assignee on this patent?
Univ Illinois
What technology area does this patent fall under?
Primary CPC classification C10G25/02. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 24 2023 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 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).