Composite article

Patent metadata

Field	Value
Publication number	US-10830387-B2
Application number	US-201716070087-A
Country	US
Kind code	B2
Filing date	Jan 13, 2017
Priority date	Jan 15, 2016
Publication date	Nov 10, 2020
Grant date	Nov 10, 2020

Abstract

A composite article is formed by disposing a poly(meth)acrylate layer, formed as the reaction product of at least one acrylate that is polymerized in the presence of an organoborane initiator, on and in direct contact with a low surface energy polymer layer, disposing an epoxide layer on and in direct contact with said poly(meth)acrylate layer, and disposing a hydrolytically resistant layer on and in direct contact with said epoxide layer. The hydrolytically resistant layer is a hydrolytically resistant polyurethane elastomer that is the reaction product of an aliphatic isocyanate component and an isocyanate-reactive component that retains at least 90% of its initial tensile strength after submersion in standardized seawater for 24 weeks. The isocyanate-reactive component is a hydroxyl-functional polymer having an average hydroxy functionality ranging from 2 to 3, wherein the hydroxyl-functional polymer is a dimer diol, a trimer triol, or a combination thereof.

First claim

What is claimed is:

1. A composite article comprising:
A. a first layer comprising a low surface energy polymer;
B. a poly(meth)acrylate layer disposed on and in direct contact with said first layer, wherein said poly(meth)acrylate layer comprises a poly(meth)acrylate comprising the reaction product of at least one acrylate polymerized in the presence of an organoborane initiator;
C. an epoxide layer disposed on and in direct contact with said poly(meth)acrylate layer, wherein said epoxide layer comprises an epoxide; and
D. a hydrolytically resistant layer disposed on and in direct contact with said epoxide layer, wherein said hydrolytically resistant layer has an initial tensile strength as measured in accordance with the DIN 53504 S2 standard test method and comprises a hydrolytically resistant polyurethane elastomer comprising the reaction product of:
(1) an aliphatic isocyanate component; and
(2) an isocyanate-reactive component comprising a hydroxyl-functional polymer having an average hydroxy functionality ranging from 2 to 3, said hydroxyl-functional polymer comprising a dimer diol, a trimer triol, or a combination thereof, wherein said hydrolytically resistant layer retains at least 90% of said initial tensile strength as measured in accordance with the DIN 53504 S2 standard test method and after submersion in standardized seawater for 24 weeks in accordance with ASTM D665.

2. The composite article of claim 1 wherein said poly(meth)acrylate is covalently bonded to said low surface energy polymer.

3. The composite article of claim 1 wherein said low surface energy polymer is selected from polypropylene, polyethylene, and combinations thereof.

4. The composite article of claim 1 wherein said poly(meth)acrylate is a self-polymerization product of a C1-C20 alkyl acrylate or methacrylate.

5. The composite article of claim 1 wherein said poly(meth)acrylate is a reaction product of a first C1-C20 alkyl acrylate or methacrylate and a second C1-C20 alkyl acrylate or methacrylate.

6. The composite article of claim 1 wherein said poly(meth)acrylate is a reaction product of a first C1-C20 alkyl acrylate or methacrylate, a second C1-C20 alkyl acrylate or methacrylate, and a third C1-C20 alkyl acrylate or methacrylate.

7. The composite article of claim 1 wherein said epoxide is the reaction product of an epoxy compound and an amine.

8. The composite article claim 1 wherein said organoborane initiator is further defined as an organoborane-organonitrogen complex.

9. The composite article of claim 1 wherein said organoborane initiator is an organoborane-amine complex and said at least one acrylate is polymerized in the presence of said organoborane-amine complex and an amine-reactive compound.

10. The composite article of claim 1 wherein said composite article has a peel strength of at least 50 pli measured between said hydrolytically resistant layer and said epoxide layer using ASTM D6862.

11. The composite article of claim 1 wherein said hydrolytically resistant layer retains at least 99% of said initial tensile strength as measured in accordance with the DIN 53504 S2 standard test method and after submersion in standardized seawater for 24 weeks in accordance with ASTM D665.

12. A subsea structure comprising:
A. a pipe having a length;
B. a first layer disposed on said pipe and comprising a low surface energy polymer;
C. a multilayer coating disposed on and in direct contact with said first layer, wherein said multilayer coating comprises:
(1) a poly(meth)acrylate layer disposed on and in direct contact with said first layer, wherein said poly(meth)acrylate layer comprises a poly(meth)acrylate comprising the reaction product of at least one acrylate polymerized in the presence of an organoborane initiator;
(2) an epoxide layer disposed on and in direct contact with said poly(meth)acrylate layer, wherein said epoxide layer comprises an epoxide; and
(3) a hydrolytically resistant layer disposed on and in direct contact with said epoxide layer, wherein said hydrolytically resistant layer has an initial tensile strength as measured in accordance with the DIN 53504 S2 standard test method and comprises a hydrolytically resistant polyurethane elastomer comprising the reaction product of:
(a) an aliphatic isocyanate component; and
(b) an isocyanate-reactive component comprising a hydroxyl-functional polymer having an average hydroxy functionality ranging from 2 to 3, said hydroxyl-functional polymer comprising a dimer diol, a trimer triol, or a combination thereof;
wherein said hydrolytically resistant layer retains at least 90% of said initial tensile strength as measured in accordance with the DIN 53504 S2 standard test method and after submersion in standardized seawater for 24 weeks in accordance with ASTM D665.

13. The subsea structure of claim 12 wherein the subsea structure has a peel strength of at least 50 pli measured between said hydrolytically resistant layer and said epoxide layer using ASTM D6862.

14. The subsea structure of claim 12 wherein said hydrolytically resistant layer retains at least 99% of said initial tensile strength as measured in accordance with the DIN 53504 S2 standard test method and after submersion in standardized seawater for 24 weeks in accordance with ASTM D665.

15. The subsea structure of claim 12 wherein said first layer comprises a first section and a second section, wherein said first section is spaced apart from said second section along the length of said pipe and said multilayer coating is disposed between said first and second sections.

Assignees

• Basf Se

Inventors

• Dodge Jeffrey A

Classifications

• C08J7/043

  Improving the adhesiveness of the coatings per se, e.g. forming primers (adhesives in the form of films or foils characterised by the primer layers between the polymer carriers and the adhesives C09J7/50) · CPC title

• C08J7/042

  with two or more layers, where at least one layer of a composition contains a polymer binder · CPC title

• C08J2323/06

  Polyethene · CPC title

• C08J2433/10

  Homopolymers or copolymers of methacrylic acid esters · CPC title

• B32B27/40

  comprising polyurethanes · CPC title