Synthetic leather article and method for preparing same

Patent metadata

Field	Value
Publication number	US-12129597-B2
Application number	US-201817285007-A
Country	US
Kind code	B2
Filing date	Nov 15, 2018
Priority date	Nov 15, 2018
Publication date	Oct 29, 2024
Grant date	Oct 29, 2024

Abstract

A synthetic leather article comprising a top coating derived from an internally emulsified PUD, a barrier layer derived from an externally emulsified PUD and a 2K non-solvent PU foam layer is provided. The leather article exhibits high delamination resistance while retaining superior mechanical properties and appearance comparable with those derived from the organic solvent-based PU. A method for preparing the synthetic leather article is also provided.

First claim

What is claimed is:

1. A synthetic leather article, comprising, from top to bottom:
(A) a top coating layer derived from an internally emulsified polyurethane dispersion comprising a first polyurethane derived from (Ai) one or more first isocyanate components comprising at least two isocyanate groups, (Aii) one or more first isocyanate-reactive components comprising at least two isocyanate-reactive groups, and (Aiii) one or more internal emulsifiers, wherein the internal emulsifiers or residual moieties of the internal emulsifiers are covalently attached to a backbone chain of the first polyurethane;
(B) a barrier layer derived from an externally emulsified polyurethane dispersion, wherein the externally emulsified polyurethane dispersion comprising one or more external emulsifiers and a second polyurethane derived from (Bi) one or more second isocyanate components comprising at least two isocyanate groups and (Bii) one or more second isocyanate-reactive components comprising at least two isocyanate-reactive groups, wherein the external emulsifiers or residual moieties of the external emulsifiers are not covalently attached to a backbone chain of the second polyurethane;
(C) a polyurethane foam layer comprising a third foamed polyurethane derived from a solvent-free system comprising (Ci) one or more third isocyanate components comprising at least two isocyanate groups, (Cii) one or more third isocyanate-reactive components comprising at least two isocyanate-reactive groups, and (Ciii) one or more foaming agents; and
(D) a backing substrate.

2. The synthetic leather article according to claim 1 , wherein the second polyurethane does not comprise cationic or anionic hydrophilic pendant group or a group which can be converted into the cationic or anionic hydrophilic pendant group covalently attached to the backbone chain of the second polyurethane.

3. The synthetic leather article according to claim 1 , wherein the first isocyanate components (Ai), the second isocyanate components (Bi) and the third isocyanate components (Ci) are independently select 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 combinations 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, 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 combinations thereof, with the proviso that the isocyanate prepolymer comprise at least two free isocyanate groups; and
the first isocyanate-reactive component (Aii), the second isocyanate-reactive component (Bii) and the third isocyanate-reactive components(Cii) are independently 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, 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 combinations thereof.

4. The synthetic leather article according to claim 1 , wherein the external emulsifier is selected from the group consisting of poly(oxy-1,2-ethanediyl)α-sulfo-ω(nonylphenoxy) salt; alkali metal oleates and stearates; alkali metal C12-C16alkyl sulfates; amine C12-C16alkyl sulfates; alkali metal C12-C16alkylbenzene sulfonates; amine C12-C16alkyl benzene sulfonates; fluorinated C4-C16alkyl esters and alkali metal C4-C16perfluoroalkyl sulfonates; organosilicon emulsifiers; and combinations thereof.

5. The synthetic leather article according to claim 1 , wherein the solvent-free system further comprises a catalyst selected from the group consisting of organotin compounds and strongly basic amines, and the foaming agent (Ciii) is water.

6. A method for producing the synthetic leather article according to claim 1 , comprising:
(1) providing the internally emulsified polyurethane dispersion comprising particles of the first polyurethane and applying the internally emulsified polyurethane dispersion onto a release layer so as to form the top coating layer on the release layer;
(2) providing the externally emulsified polyurethane dispersion comprising particles of the second polyurethane and applying the externally emulsified polyurethane dispersion onto an opposite side of the top coating layer from the release layer so as to form the barrier layer on the top coating layer;
(3) applying the solvent-free system onto an opposite side of the barrier layer from the top coating, curing and foaming the solvent-free system to form the polyurethane foam layer on the barrier layer;
(4) applying the backing substrate onto an opposite side of the polyurethane foam layer from the barrier layer.

7. The method according to claim 6 , wherein in step (3), the solvent-free system is cured by a pre-curing sub-step occurred before step (4) and a post-curing sub-step occurred after step (4),
the pre-curing sub-step comprises heating the solvent-free system at a first temperature to partially cure solvent-free system, and the post-curing sub-step comprises heating the solvent-free system at a second heating temperature higher than the first heating temperature to completely cure solvent-free system.

8. The method according to claim 6 , wherein the externally emulsified polyurethane dispersion is prepared by the steps of:
(i) reacting one or more compounds comprising at least two isocyanate groups or a first prepolymer of the compound with first isocyanate-reactive components comprising at least two hydroxyl groups to produce a second prepolymer comprising two or more free isocyanate groups and having no cationic or anionic hydrophilic pendant group or a group which can be converted into the cationic or anionic hydrophilic pendant group covalently attached to the second prepolymer;
(ii) dispersing the second prepolymer obtained in step (i) in water with the presence of one or more external emulsifiers to form an emulsion; and
optionally (iii) adding one or more isocyanate-reactive components comprising at least two isocyanate-reactive groups into the emulsion obtained in step (ii) and reacting them with the second prepolymer to produce the externally emulsified polyurethane dispersion.

9. The method according to claim 6 , wherein the externally emulsified polyurethane dispersion is prepared by the steps of:
(i) reacting one or more polyisocyanates selected from the group consisting of C4-C12 aliphatic polyisocyanates comprising at least two isocyanate groups, C6-C15 cycloaliphatic or aromatic polyisocyanates comprising at least two isocyanate

Assignees

• Dow Global Technologies Llc

Inventors

• Zhang Chao
• Cai Zetian
• Chen Huan
• Zhang Yi
• Tai Xiangyang
• Qin Shihao

Classifications

• D06N2211/28

  Artificial leather · CPC title

• D06N3/005

  obtained by blowing or swelling agent · CPC title

• D06N3/0002

  characterised by the substrate · CPC title

• C09D175/04

  Polyurethanes · CPC title

• C08G18/80

  Masked polyisocyanates · CPC title