Recycling process for the recovery of cotton from polyester-cotton fabrics and/or fibers

US2023416492A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2023416492-A1
Application numberUS-202318244744-A
CountryUS
Kind codeA1
Filing dateSep 11, 2023
Priority dateDec 2, 2020
Publication dateDec 28, 2023
Grant date

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

Polyester-free cotton is obtained from a fabric and/or fibers containing polyester and cotton by reacting the fabric and/or fibers with an amine organocatalyst and/or carboxylic acid salt of same and an alcohol solvent. The reaction, which may be run in batches or as a continuous flow process, recovers (i) polyester-free cotton as a solid inert by-product of the reaction, (ii) the amine organocatalyst and/or carboxylic acid salt of same for reuse, (iii) a polyester monomer product, and (iv) unreacted alcohol. The reaction works on any polyester-cotton fabric and/or fibers, including those that have at least one additional material, such as polyethers polyolefins, polyurethanes, nylon, rayon, acetate, viscose, modal, acrylic, wool, and combinations thereof.

First claim

Opening claim text (preview).

We claim: 1 . A method comprising: placing garneted cotton/polyester fabric in a reaction vessel of a pressure reactor with an amine organocatalyst and/or carboxylic acid salt and an alcohol solvent and heating the reaction vessel to run the reaction; recovering from the reaction vessel (i) polyester-free cotton as a solid inert by-product of the reaction, (ii) the amine organocatalyst and/or carboxylic acid salt of same for reuse, (iii) a polyester monomer product, and (iv) unreacted alcohol solvent; and purifying the recovered polyester-free cotton with a liquid selected from the group consisting of alcohol, acetone, water, and combinations thereof. 2 . The method of claim 1 , wherein the pressure reactor is an autoclave. 3 . The method of claim 1 , wherein the pressure reactor is an extrusion reactor. 4 . The method of claim 1 , wherein the polyester-free cotton is purified with alcohol, wherein the alcohol is the unreacted alcohol solvent recovered from the reaction vessel. 5 . The method of claim 1 , wherein the method is run in batches. 6 . The method of claim 1 , wherein the method is run as a continuous flow process. 7 . The method of claim 1 , wherein the polyester is selected from the group consisting of polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polybutylene terephthalate (PBT), polytrimethylene terephthalate (PTI), polyethylene furanoate (PEF), and combinations thereof. 8 . The method of claim 1 , wherein the amine organocatalyst and/or carboxylic acid salt of same is selected from the group consisting of triethylamine (TEA), tetramethylethylenediamine (TMEDA), pentamethyldiethylenetriamine (PMDETA), trimethyl triaza cyclononane (TACN), 4-(N,N-dimethylamino)pyridine (DMAP), 1,4-diazabicyclo [2.2.2]octane (DABCO), N-methyl imidazole (NMI), and combinations thereof. 9 . The method of claim 1 , wherein the alcohol solvent is a glycol and/or a diol. 10 . The method of claim 1 , wherein the garneted cotton/polyester fabric is a colored fabric and the recovered polyester-free cotton neutral and/or white reusable cotton. 11 . A method comprising: placing a garneted cotton/polyester fabric in a reaction vessel of a non-pressurized chemical reactor with an amine organocatalyst and/or carboxylic acid salt and an alcohol solvent and heating the reaction vessel to run the reaction; recovering from the reaction vessel (i) polyester-free cotton as a solid inert by-product of the reaction, (ii) the amine organocatalyst and/or carboxylic acid salt of same for reuse, (iii) a polyester monomer product, and (iv) unreacted alcohol solvent; and purifying the recovered polyester-free cotton with a liquid selected from the group consisting of alcohol, acetone, water, and combinations thereof. 12 . The method of claim 11 , wherein the non-pressurized reactor is a round-bottom flask. 13 . The method of claim 11 , wherein the polyester-free cotton is purified with alcohol, wherein the alcohol is the unreacted alcohol solvent recovered from the reaction vessel. 14 . The method of claim 11 , wherein the method is run in batches. 15 . The method of claim 11 , wherein the method is run as a continuous flow process. 16 . The method of claim 11 , wherein the polyester is selected from the group consisting of polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polybutylene terephthalate (PBT), polytrimethylene terephthalate (PTI), polyethylene furanoate (PEF), and combinations thereof. 17 . The method of claim 11 , wherein the amine organocatalyst and/or carboxylic acid salt of same is selected from the group consisting of triethylamine (TEA), tetramethylethylenediamine (TMEDA), pentamethyldiethylenetriamine (PMDETA), trimethyl triaza cyclononane (TACN), 4-(N,N-dimethylamino)pyridine (DMAP), 1,4-diazabicyclo [2.2.2]octane (DABCO), N-methyl imidazole (NMI), and combinations thereof. 18 . The method of claim 11 , wherein the alcohol solvent is a glycol and/or a diol. 19 . The method of claim 11 , wherein the garneted cotton/polyester fabric is a colored fabric and the recovered polyester-free cotton neutral and/or white reusable cotton.

Assignees

Inventors

Classifications

  • C08J11/28Primary

    by treatment with organic compounds containing nitrogen, sulfur or phosphorus · CPC title

  • of solvents, plasticisers or unreacted monomers · CPC title

  • Amines · CPC title

  • Amino-carboxylic acids; Betaines; Aminosulfonic acids; Sulfo-betaines · CPC title

  • cellulosic · CPC title

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What does patent US2023416492A1 cover?
Polyester-free cotton is obtained from a fabric and/or fibers containing polyester and cotton by reacting the fabric and/or fibers with an amine organocatalyst and/or carboxylic acid salt of same and an alcohol solvent. The reaction, which may be run in batches or as a continuous flow process, recovers (i) polyester-free cotton as a solid inert by-product of the reaction, (ii) the amine organoc…
Who is the assignee on this patent?
IBM
What technology area does this patent fall under?
Primary CPC classification C08J11/28. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Dec 28 2023 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). 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).