Self-wetting adhesive composition

Patent metadata

Field	Value
Publication number	US-9447309-B2
Application number	US-201414896722-A
Country	US
Kind code	B2
Filing date	Jun 16, 2014
Priority date	Jun 24, 2013
Publication date	Sep 20, 2016
Grant date	Sep 20, 2016

Abstract

This disclosure provides novel adhesive compositions comprising a highly crosslinked and plasticized low T g (meth)acrylic copolymer that are self-wetting when applied to a substrate, and peelable therefrom.

First claim

What is claimed is:

1. A syrup polymer composition consisting of:
a) 5 to 40 parts by weight of a solute low T g (meth)acrylate solute (co)polymer component having a T g ≦0° C.;
b) 60 to 95 parts by weight of a low T g solvent monomer component comprising low T g monomers having a T g ≦0° C.;
and a multifunctional acrylate, the sum of a) and b) being 100 parts by weight;

c) 5 to 100 parts of a plasticizer, relative to 100 parts a) and b);
wherein the solute copolymer comprises:
i) 95-100 parts by weight of low T g monomer units;
ii) 0 to 5 parts of acid-functional monomer units;
iii) 0 to 5 parts of a non-acid functional polar monomer;
the sum of i) to iii) being 100 parts by weight

wherein the solvent monomer component comprises:
d) 60 to 90 parts by weight of low T g monomers;
e) 0 to 5 parts of acid functional monomers;
f) 0 to 5 parts of a non-acid functional polar monomer;
g) 10 to 40 parts of a multiacrylate;
the sum of d) to g) being 100 parts by weight.

2. The syrup polymer composition of claim 1 wherein the composition comprises 10 to 40 parts of plasticizer, relative to 100 parts of a) and b).

3. The syrup polymer composition of claim 1 comprising 20 to 50 parts of a plasticizer, relative to 100 parts a) and b).

4. The syrup polymer composition of claim 1 wherein the solute low T g copolymer comprises 1 to 5 parts by weight of acid-functional monomer units and 5 to 95 parts by weight of low T g monomer units.

5. The syrup polymer composition of claim 1 wherein the solute low T g copolymer comprises 1 to 5 parts by weight of non-acid functional polar monomer units.

6. The syrup polymer composition of claim 1 wherein the solvent monomer component comprises 1 to 5 parts by weight of acid-functional monomer units.

7. The syrup polymer composition of claim 1 wherein the solute low T g copolymer comprises 100 parts by weight of low T g monomer units.

8. The syrup polymer composition of claim 1 wherein the solute low T g copolymer has a T g of than −20° C.

9. The syrup polymer composition of claim 1 wherein the plasticizer is selected from monoalkyl esters of aliphatic carboxylic acids, monoalkyl esters of aromatic carboxylic acids, polyalkyl esters of aliphatic carboxylic acids, polyalkyl esters of aromatic carboxylic acids, polyalkyl esters of aliphatic alcohols, polyalkyl esters of phosphonic acids, poly(alkoxylated) esters of aliphatic carboxylic acids, poly(alkoxylated) esters of aromatic carboxylic acids, poly(alkoxylated) ethers of aliphatic alcohols, poly(alkoxylated) ethers of phenols, and mixtures thereof.

10. An adhesive comprising the cured syrup polymer composition of claim 1 .

11. A method of making an adhesive comprising the steps of:
partially polymerizing a low T g monomer and other optional monomers to produce a syrup polymer composition of claim 1 , adding a multifunctional acrylate crosslinker agent, optional additional monomers, and plasticizer, and further photopolymerizing.

12. The method of claim 11 wherein the syrup polymer composition has a viscosity of from 500 to 10,000 cPs at 22° C.

13. The method of claim 11 wherein the syrup copolymer composition comprises up to 30 parts by weight of the solute copolymer in solvent monomers.

14. The method of claim 11 comprising the steps of partially polymerizing a low T g monomer and other optional monomers to produce a syrup polymer composition of claim 1 , adding a multifunctional acrylate crosslinker agent, additional monomers, and plasticizer, and further photopolymerizing.

15. The method of claim 11 where the other optional additional monomers comprise non-acid functional polar monomers.

16. The method of claim 15 wherein up to 20 parts of additional monomers are added relative to 100 parts total monomers.

17. An adhesive article comprising a substrate and a coating of the cured adhesive of claim 1 on a surface thereof.

18. The adhesive article of claim 17 wherein the adhesive has a 180° peel value of ≦5 Newtons/decimeter.

19. The adhesive article of claim 17 wherein the substrate is transparent.

20. The adhesive article of claim 17 wherein the adhesive has a transmissivity of greater than 90% in the visible range.

21. The adhesive article of claim 17 wherein the substrate is a solar control film.

22. The adhesive article of claim 17 having a transmissivity of at least 80% in the visible range.

Assignees

• 3M Innovative Properties Co

Inventors

• Fornof Ann R
• Dizio James P
• Clements George J
• Janoski Jonathan E
• Lewandowski Kevin M
• Runge Michael B
• Seshadri Kannan

Classifications

• C08F220/1808

  C8-(meth)acrylate, e.g. isooctyl (meth)acrylate or 2-ethylhexyl (meth)acrylate · CPC title

• C09J7/385

  Acrylic polymers · CPC title

• C08K5/10

  Esters; Ether-esters · CPC title

• C09J133/08 Primary

  Homopolymers or copolymers of acrylic acid esters · CPC title

• C08F222/102

  of dialcohols, e.g. ethylene glycol di(meth)acrylate or 1,4-butanediol dimethacrylate · CPC title