Two-component polyurethane adhesive having substantially temperature-independent mechanical properties and high strength

Patent metadata

Field	Value
Publication number	US-11149106-B2
Application number	US-201716321072-A
Country	US
Kind code	B2
Filing date	Jul 28, 2017
Priority date	Aug 3, 2016
Publication date	Oct 19, 2021
Grant date	Oct 19, 2021

Abstract

A two-component polyurethane composition containing at least 55% by weight of polybutadiene polyols based on the total amount of all polyols having an average molecular weight of at least 500 g/mol, and at least one latent hardener, where the ratio of the number of reactive groups in the latent hardener to the number of OH groups present is in the range from 0.02 to 0.4. The composition has a long open time, blister-free curing, a very low glass transition temperature, high elasticity and surprisingly high strength which is very constant over a wide temperature range. Furthermore, it has very good adhesion to metallic and nonmetallic substrates, causing barely any stress cracks on glassy thermoplastics.

First claim

The invention claimed is:

1. A composition consisting of
a first component comprising at least 55% by weight of polybutadiene polyols having an average molecular weight in the range from 2,000 to 10,000 g/mol and an average OH functionality in the range from 2.1 to 4, based on the total amount of all polyols having an average molecular weight of at least 500 g/mol, and
a second component comprising at least one polyisocyanate, where at least one of the two components additionally comprises at least one latent hardener, wherein the ratio of the number of reactive groups in the latent hardener to the number of OH groups present is in the range from 0.02 to 0.4.

2. The composition as claimed in claim 1 , wherein the polyisocyanate comprises diphenylmethane 4,4′- or 2,4′- or 2,2′-diisocyanate or any mixture of these isomers.

3. The composition as claimed in claim 1 , wherein the latent hardener is a blocked amine having a blocked, hydrolytically activatable amino group and at least one further reactive group selected from the group consisting of hydroxyl group, mercapto group, secondary amino group, primary amino group and blocked, hydrolytically activatable amino group.

4. The composition as claimed in claim 1 , wherein the latent hardener is an aldimine of the formula (IV)

where
m is 0 or 1 and n is an integer from 1 to 3, where (m+n) is 2 or 3,
A is an (m+n)-valent hydrocarbyl radical optionally containing ether oxygen and having 2 to 20 carbon atoms, and
Z is an optionally substituted aromatic radical or a radical of the formula

where
R 1 and R 2 are each independently a monovalent hydrocarbyl radical having 1 to 12 carbon atoms, or together are a divalent hydrocarbyl radical having 4 to 12 carbon atoms which is part of an optionally substituted carbocyclic ring having 5 to 8 carbon atoms,
R 3 is a hydrogen atom or an alkyl or arylalkyl or alkoxycarbonyl radical having 1 to 12 carbon atoms, and

Y is where
R 4 is a monovalent hydrocarbyl radical optionally containing ether or aldehyde units and having 6 to 20 carbon atoms, and
R 5 and R 6 are each independently a monovalent aliphatic, cycloaliphatic or arylaliphatic hydrocarbyl radical optionally containing heteroatoms in the form of hydroxyl groups or ether oxygen and having 2 to 20 carbon atoms, or together are a divalent aliphatic radical having 4 to 12 carbon atoms which is part of an optionally substituted heterocyclic ring having 5 to 8 ring atoms and as well as the nitrogen atom optionally contains further heteroatoms in the form of ether oxygen, thioether sulfur or tertiary amine nitrogen.

5. The composition as claimed in claim 4 , wherein Z is a phenyl radical substituted by a branched alkyl group having 10 to 14 carbon atoms.

6. The composition as claimed in claim 4 , wherein Z is a

radical of the formula where R 1 and R 2 are each a methyl radical, R 3 is a hydrogen radical, Y is

and R 4 is a linear alkyl radical having 11 carbon atoms.

7. The composition as claimed in claim 4 , wherein Z is a

radical of the formula where R 1 and R 2 are each a methyl radical, R 3 is a hydrogen radical, Y is

and R 5 and R 6 together are a 3-oxa-1,5-pentylene radical which, together with the nitrogen atom, forms a morpholine ring.

8. The composition as claimed in claim 4 , wherein Z is a

radical of the formula where R 1 and R 2 are each a methyl radical, R 3 is a hydrogen radical, Y is

and R 5 and R 6 are each 2-hydroxyethyl or 2-hydroxypropyl.

9. The composition as claimed in claim 1 , wherein it contains at least one nitrogen-containing compound as catalyst for curing.

10. The composition as claimed in claim 1 , wherein its glass transition temperature is below −45° C.

11. A method comprising applying the composition as claimed in claim 1 as elastic adhesive or sealant.

12. A product from the method as claimed in claim 11 , which is obtained after the curing of the composition.

13. A method of bonding a first substrate to a second substrate, comprising the steps of:
mixing the first and second components of the composition as claimed in claim 1 ,
applying the mixed composition to at least one of the substrate surfaces to be bonded, and
joining the two substrates within the open time of the mixed composition.

14. A method of sealing, comprising the steps of:
mixing the first and second components of the composition as claimed in claim 1 , and
applying the mixed composition to a substrate or between two substrates within the open time of the mixed composition.

15. The method as claimed in claim 13 , wherein at least one of the substrates is a glassy thermoplastic selected from the group consisting of polycarbonate, polymethylmethacrylate and polystyrene.

Assignees

• Sika Tech Ag

Inventors

• Kelch Steffen
• Burckhardt Urs

Classifications

• C08G18/3296

  being in latent form · CPC title

• C08G18/3256

  Reaction products of polyamines with aldehydes or ketones · CPC title

• C08G18/797

  containing carbodiimide and/or uretone-imine groups · CPC title

• C08G18/4238

  derived from dicarboxylic acids and dialcohols · CPC title

• C08G18/222

  metal compounds not provided for in groups C08G18/225 - C08G18/26 · CPC title