Depolymerization of polyurethanes with organic amine bases

US2025163237A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2025163237-A1
Application numberUS-202318839569-A
CountryUS
Kind codeA1
Filing dateFeb 22, 2023
Priority dateFeb 22, 2022
Publication dateMay 22, 2025
Grant date

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Abstract

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A method for the depolymerization of polyurethanes, produced by reacting an active hydrogen containing polyether and an organic polyisocyanate, hydrolyzes a polyurethane under mild conditions and low salt concentration in the reaction mixture, wherein polyether polyols and polyamines can be recovered in high yields. The recovered active hydrogen containing polyether polyols obtained in the method for the depolymerization of polyurethanes are of excellent quality.

First claim

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1 . A method of hydrolyzing a polyurethane, comprising: contacting said polyurethane with water in the presence of an organic amine base and a phase transfer catalyst to yield an active hydrogen containing polyether, and an organic polyamine, wherein the organic amine base is an aliphatic amine, and a reaction mixture comprising the polyurethane, water and the organic amine base is a stirred homogeneous or heterogeneous mixture, during hydrolysis, and the phase transfer catalyst is selected from the group consisting of quaternary ammonium salts containing an ammonium cation containing 6 to 30 carbon atoms and organic sulfonates containing at least 7 carbon atoms and mixtures thereof. 2 . The method of claim 1 , wherein the organic amine base comprises one or more tertiary nitrogen atom(s) and/or has a boiling point below that of at least one organic polyamine obtained as product of the polyurethane hydrolysis. 3 . The method of claim 1 , wherein the organic amine base is selected from the group consisting of a base according to Formula (1) (((R 3 ) 2 N—R 2 )—(O—R 1 ) x ) y —N(R 4 ) z   (1) wherein the R 1 groups in the molecule may be identical or different, the R 2 groups in the molecule may be identical or different, the R 3 groups in the molecule may be identical or different, and the R 4 groups in the molecule may be identical or different and wherein R 1 are identical or different and are independently from each other selected from the group consisting of linear or branched alkylene radicals with 1 to 10 carbon atoms, R 2 are identical or different and are independently from each other selected from the group consisting of linear or branched alkylene or hydroxy alkylene radicals with 1 to 20 carbon atoms and if R 2 is hydroxy alkylene R 2 comprises 1 to 5 hydroxy group(s), R 3 are identical or different and are independently from each other selected from the group consisting of hydrogen, linear or branched alkyl groups with 1 to 6 carbon atoms, and linear or branched hydroxy alkyl groups with 1 to 6 carbon atoms, R 4 are identical or different and are independently from each other selected from the group consisting of hydrogen, linear or branched, cyclic or alicyclic alkyl groups with 1 to 20 carbon atoms, linear or branched hydroxy alkyl groups with 1 to 6 carbon atoms and cycloalkyl residues having 6 to 18 carbon atoms, and wherein u=1 to 14, v=1 to 14, w=1 to 14, x=0 or 1, y=0 to 3; z=0 to 3, with the proviso that if z=3, at least one R 4 are not hydrogen, y+z=3; a base according to formula (2) (((R 6 ) 2 N—R 5 ) a (H) b N) d —CZ—(N(R 7 ) 2 ) c   (2) wherein the R 5 groups in the molecule may be identical or different, the residues R 6 groups in the molecule may be identical or different and the residues R 7 groups in the molecule may be identical or different and wherein R 5 are identical or different and are independently from each other selected from the group consisting of linear or branched alkylene radicals with 1 to 10 carbon atoms, wherein one or more CH 2 groups may be replaced by O to form ether bonds, R 6 are identical or different and are independently from each other selected from the group consisting of hydrogen, linear or branched alkyl groups with 1 to 6 carbon atoms, linear or branched hydroxy alkyl groups with 1 to 6 carbon atoms, R 7 are identical or different and are independently from each other selected from the group consisting of hydrogen, linear or branched alkyl groups with 1 to 6 carbon atoms, linear or branched hydroxy alkyl groups with 1 to 6 carbon atoms, and wherein Z═O or NH, u=1 to 14, v=1 to 14, w=1 to 14, a=0, 1 or 2, b=0, 1 or 2, a+b=2, c=0, 1 or 2, d=0, 1 or 2, c+d=2, and a cyclic or bicyclic, non-aromatic, nitrogen comprising organic base comprising 4 to 20 carbon atoms, and 1 to 4 nitrogen atoms, optionally the cyclic or bicyclic, non-aromatic, nitrogen comprising organic base comprises one or more O atoms and/or carries one or more substituents, such as linear or branched alkyl or alkenyl groups with 1 to 6, carbon atoms, linear or branched hydroxy alkyl groups with 1 to 6 carbon atoms, or one or more N and or O comprising functional groups and/or two or more cyclic or bicyclic non-aromatic, nitrogen comprising organic rings are bond to each other via alkylene or ether alkylene linkages with 1 to 12 carbon atoms, and mixtures thereof. 4 . The method according to claim 3 , wherein the organic amine base is selected from the group consisting of a trialkylamine according to Formula (3) NR 4 R 4 ′R 4 ″  (3) wherein R 4 , R 4 ′, R 4 ″ are identical or different and are independently selected from the group consisting of hydrogen, linear or branched, cyclic or alicyclic alkyl groups with 1 to 20 carbon atoms, linear or branched hydroxy alkyl groups with 1 to 6 carbon atoms and cycloalkyl residues having 6 to 18 carbon atoms, u=1 to 14, v=1 to 14, w=1 to 14, with the provision at least one, of R 4 , R 4′ and R 4 ″ are not hydrogen; a polyamine according to Formula (4) ((R 3 ) 2 N—R 2 ) 3 N  (4), wherein R 2 are identical or different and are independently from each other selected from the group consisting of linear or branched alkylene or hydroxy alkylene radicals with 1 to 20 carbon atoms and if R 2 is hydroxy alkyl R 2 comprises 1 to 5 hydroxy group(s), R 3 are identical or different and are independently from each other selected from the group consisting of hydrogen, linear or branched alkyl groups with 1 to 6 carbon atoms, linear or branched hydroxy alkyl groups with 1 to 6 carbon atoms, u=1 to 14, v=1 to 14, w=1 to 14, a polyamine according to Formula (5) (((R 3 ) 2 N—R 2 )—(O—R′) x ) y —N(R 4 ) z   (5) wherein x=0 or 1, y=1 or 2, and z=1 or 2, and y+z=3 and wherein R 1 are identical or different and are independently from each other selected from the group consisting of linear or branched alkylene radicals with 1 to 10, carbon atoms, R 2 are identical or different and are independently from each other selected from the group consisting of linear or branched alkylene or hydroxy alkylene radicals with 1 to 20 carbon atoms and if R 2 is hydroxy alkyl R 2 comprises 1 to 5 hydroxy group(s), R 3 are identical or different and are independently from each other selected from the group consisting of hydrogen, linear or branched alkyl groups with 1 to 6 carbon atoms, linear or branched hydroxy alkyl groups with 1 to 6 carbon atoms, R 4 are identical or different and are independently from each other selected from the group consisting of hydrogen, linear or branched, cyclic or alicyclic alkyl groups with 1 to 6 carbon atoms, linear or branched hydroxy alkyl groups with 1 to 6 carbon atoms, u=1 to 14, v=1 to 14, w=1 to 14, a poly aminoalkylurea according to Formula (6) (((R 6 ) 2 N—R 5 ) a (H) b N) d —CO—(N(R 7 ) 2 ) c   (6) wherein R 5 are identical or different and are independently from each other selected from the group consisting of linear or branched alkylene radicals with 1 to 10 carbon atoms, wherein one or more CH 2 groups may be replaced by O to form ether bonds, R 6 are identical or different and are independently from each other selected from the group consisting of hydrogen, linear or branched alkyl groups with 1 to 6 carbon atoms, linear or branched hydroxy alkyl groups with 1 to 6 carbon atoms, R 7 are identical or different and are independently from each other selected from the group consisting of hydrogen, linear or branched alkyl groups with 1 to 6 carbon atoms, linear or branched hydroxy alkyl groups with 1 to 6 carbon atoms, and wherein u=1 to 14, v=1 to 14, w=1 to 14, a=0, 1 or 2, b=0, 1 or 2, a+b=2, c=0, 1 or 2, d=0, 1 or 2, c+d=2, an organic base comprising a guanidino group according to

Assignees

Inventors

Classifications

  • Polyurethanes having carbon-to-carbon unsaturated bonds · CPC title

  • C08J11/14Primary

    by treatment with steam or water · CPC title

  • Polymers modified by chemical after-treatment · CPC title

  • containing oxygen in the form of ether groups · CPC title

  • tin salts of carboxylic acids · CPC title

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What does patent US2025163237A1 cover?
A method for the depolymerization of polyurethanes, produced by reacting an active hydrogen containing polyether and an organic polyisocyanate, hydrolyzes a polyurethane under mild conditions and low salt concentration in the reaction mixture, wherein polyether polyols and polyamines can be recovered in high yields. The recovered active hydrogen containing polyether polyols obtained in the meth…
Who is the assignee on this patent?
Evonik Operations Gmbh
What technology area does this patent fall under?
Primary CPC classification C08J11/14. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu May 22 2025 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).