Waterborne polyurethane dispersion and method for preparing the same

US11981827B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11981827-B2
Application numberUS-201917435593-A
CountryUS
Kind codeB2
Filing dateAug 14, 2019
Priority dateMar 5, 2019
Publication dateMay 14, 2024
Grant dateMay 14, 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 waterborne polyurethane dispersion is provided. The waterborne polyurethane dispersion is prepared by using a tri-functionality polyether polyol as part of the polyols for forming the prepolymer and a hydrophilic amino siloxane co-chain extender, and can exhibit superior performance properties such as enhanced color fastness, improved low temperature stability, good anti-stickiness, bally flex resistance, anti-abrasion and mechanical properties. A laminated synthetic leather article prepared with said waterborne polyurethane dispersion as well the method for preparing the synthetic leather article are also provided.

First claim

Opening claim text (preview).

What is claimed is: 1. A waterborne polyurethane dispersion comprising polyurethane particles dispersed in water, wherein the waterborne polyurethane dispersion is derived from the reaction of: (A) an isocyanate component comprising one or more compounds having at least two isocyanate groups; (B) an isocyanate-reactive component comprising one or more compounds having at least two isocyanate-reactive groups, wherein the isocyanate-reactive component comprises polyether polyols having a hydroxyl functionality of 3.0 and a weight average molecular weight of 1,500 to 12,000 g/mol; (C) a hydrophilic amino siloxane compound represented by Formula I: wherein each R independently represents methyl, ethyl, n-propyl, i-propyl, n-butyl, butyl, sec-butyl, t-butyl, n-pentyl, i-pentyl, tert-pentyl, neo-pentyl, cyclohexyl, phenyl, vinyl, allyl or —(OCH 2 CH 2 ) a —O—CH 2 —CH═CH 2 ; R 1 is —(CH 2 ) m NH 2 or —(CH 2 ) s —NH—(CH 2 ) t NH 2 ; R 2 is —CH 2 CH 2 CH 2 O(CH 2 CH 2 O) n H; and each of R 3 , R 4 , R 5 , R 6 and R 7 is independently selected from the group consisting of methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, t-butyl, n-pentyl, i-pentyl, tert-pentyl, neo-pentyl, cyclohexyl and phenyl; wherein a is an integer of 1 to 10; x is an integer of 20-500; y is an integer of 1-10; z is an integer of 1-10; m is an integer of 1-5; s is an integer of 1, 2, 3, 4 or 5; t is an integer of 1, 2, 3, 4 or 5; and n is an integer of 5-20; and wherein the content of the hydrophilic amino siloxane compound (C) is from 2.0 wt % to 10 wt %, based on the total weight of the isocyanate component (A), the isocyanate-reactive component (B), and the catalyst (D); (D) a catalyst; (E) a surfactant; (F) a chain extender; and (G) water. 2. The waterborne polyurethane dispersion according to claim 1 , wherein there is no cationic or anionic hydrophilic pendant groups covalently attached to the backbone chain of polyurethane in the polyurethane particles or groups which can be converted into the cationic or anionic hydrophilic pendant groups which groups are covalently attached to the backbone chain of polyurethane in the polyurethane particles, and the polyurethane is externally emulsified. 3. The waterborne polyurethane dispersion according to claim 1 , wherein the one or more compounds having at least two isocyanate groups are selected from the group consisting of: a) C4-C12 aliphatic polyisocyanates comprising at least two isocyanate groups, C6-C15 cycloaliphatic or aromatic polyisocyanates comprising at least two isocyanate groups, C7-C15 araliphatic polyisocyanates comprising at least two isocyanate groups, and a combination thereof; and b) an isocyanate prepolymer prepared by reacting one or more polyisocyanates of a) with one or more isocyanate-reactive components selected from the group consisting of C2-C16 aliphatic polyhydric alcohols comprising at least two hydroxy groups, C6-C15 cycloaliphatic or aromatic polyhydric alcohols comprising at least two hydroxy groups, C7-C15 araliphatic polyhydric alcohols comprising at least two hydroxy groups, polyester polyols having a molecular weight from 500 to 5,000, polycarbonate diols having a molecular weight from 200 to 5,000, polyetherdiols having a molecular weight from 200 to 5,000, polyether polyols having a hydroxyl functionality of 3.0 and a weight average molecular weight of 1,500 to 12,000 g/mol, C2 to C10 polyamine comprising at least two amino groups, C2 to C10 polythiol comprising at least two thiol groups, C2-C10 alkanolamine comprising at least one hydroxyl group and at least one amino groups, and a combination thereof, with the proviso that the isocyanate prepolymer comprises at least two free isocyanate terminal groups. 4. The waterborne polyurethane dispersion according to claim 1 , wherein the content of the isocyanate component (A) is from 5 wt % to 50 wt %, based on the total weight of the isocyanate component (A), the isocyanate-reactive component (B) and the catalyst (D). 5. The waterborne polyurethane dispersion according to claim 1 , wherein the one or more compounds having at least two isocyanate-reactive groups are selected from the group consisting of: C2-C16 aliphatic polyhydric alcohols comprising at least two hydroxy groups, C6-C15 cycloaliphatic or aromatic polyhydric alcohols comprising at least two hydroxy groups, C7-C15 araliphatic polyhydric alcohols comprising at least two hydroxy groups, polyester polyols having a molecular weight from 500 to 5,000, polycarbonate diols having a molecular weight from 200 to 5,000, polyetherdiols having a molecular weight from 200 to 5,000, polyether polyols having a hydroxyl functionality of 3.0 and a weight average molecular weight of 1,500 to 12,000 g/mol, C2 to C10 polyamine comprising at least two amino groups, C2 to C10 polythiol comprising at least two thiol groups, C2-C10 alkanolamine comprising at least one hydroxyl group and at least one amino groups, vegetable oil having at least two hydroxyl groups, and a combination thereof. 6. The waterborne polyurethane dispersion according to claim 1 , wherein the content of the isocyanate-reactive component (B) is from 35 wt % to 95 wt %, based on the total weight of the isocyanate component (A), the isocyanate-reactive component (B) and the catalyst (D). 7. The waterborne polyurethane dispersion according to claim 1 , wherein the content of the polyether polyols having a hydroxyl functionality of 3.0 and a weight average molecular weight of 1,500 to 12,000 g/mol is from 10 wt % to 20 wt %, based on the total weight of the isocyanate component (A), the isocyanate-reactive component (B) and the catalyst (D). 8. The waterborne polyurethane dispersion according to claim 1 , wherein the catalyst (D) is selected from the group consisting of: organotin compound, organic bismuth compound, tertiary amine, morpholine derivative, piperazine derivative, and combination thereof; and wherein the content of the catalyst (D) is 1.0 wt % or less, based on the total weight of the isocyanate component (A), the isocyanate-reactive component (B) and the catalyst (D). 9. The waterborne polyurethane dispersion according to claim 1 , wherein the surfactant (E) is selected from the group consisting of: poly(oxy-1,2-ethanediyl) α-sulfo-ω(nonylphenoxy) salt, alkali metal oleates and stearates, alkali metal C 12 -C 16 alkyl sulfates, amine C 12 -C 16 alkyl sulfates, alkali metal C 12 -C 16 alkyl benzene sulfonates, amine C 12 -C 16 alkyl benzene sulfonates, fluorinated C 4 -C 16 alkyl esters, alkali metal C 4 -C 16 perfluoroalkyl sulfonates, and the combination thereof; and wherein the content of the surfactant (E) is 10 wt % or less, based on the total weight of the isocyanate component (A), the isocyanate-reactive component (B) and the catalyst (D). 10. The waterborne polyurethane dispersion according to claim 1 , wherein the chain extender (F) is selected from the group consisting of: C 2 -C 16 aliphatic polyamine comprising at least two amine groups, C 4 -C 15 cycloaliphatic or aromatic polyamine comprising at least two amine groups, C 7 -C 15 araliphatic polyamine comprising at least two amine groups; and wherein the content of the chain extender (F) is from 1.0 wt % to 15 wt %, based on the total weight of the isocyanate component (A), the isocyanate-reactive component (B) and the catalyst (D). 11. A method for preparing the waterborne polyurethane dispersion according to claim 1 , the method comprising (i) reacting the isocyanate component (A) with the isocyanate-reactive

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Classifications

  • Artificial wood or leather grain surface · CPC title

  • C09D175/08Primary

    from polyethers · CPC title

  • characterised by structural features of a {fibrous or filamentary} layer {(layer formed of metallic wires B32B15/02; layer formed of natural mineral fibres B32B19/02; layer formed of wood fibres B32B21/02)} · CPC title

  • Non-woven fabric · CPC title

  • Woven fabric · CPC title

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What does patent US11981827B2 cover?
A waterborne polyurethane dispersion is provided. The waterborne polyurethane dispersion is prepared by using a tri-functionality polyether polyol as part of the polyols for forming the prepolymer and a hydrophilic amino siloxane co-chain extender, and can exhibit superior performance properties such as enhanced color fastness, improved low temperature stability, good anti-stickiness, bally fle…
Who is the assignee on this patent?
Dow Global Technologies Llc
What technology area does this patent fall under?
Primary CPC classification C09D175/08. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 14 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).