Multilayer pressure sensitive adhesive assembly

Patent metadata

Field	Value
Publication number	US-9845414-B2
Application number	US-201414889289-A
Country	US
Kind code	B2
Filing date	May 12, 2014
Priority date	May 17, 2013
Publication date	Dec 19, 2017
Grant date	Dec 19, 2017

Abstract

The present disclosure relates to a multilayer pressure sensitive adhesive assembly comprising at least a first pressure sensitive adhesive layer superimposed to a second polymer layer, wherein a curable liquid precursor of the first pressure sensitive adhesive polymer layer comprises a low Tg (meth)acrylate copolymer and a high Tg (meth)acrylate copolymer having a weight average molecular weight (Mw) of above 20,000 Daltons. The present disclosure also relates to a method of manufacturing such a pressure sensitive adhesive assembly and uses thereof.

First claim

What we claim is:

1. A method for manufacturing a multilayer pressure sensitive adhesive assembly comprising at least a first pressure sensitive adhesive polymer layer superimposed to a second polymer layer, the method comprising the steps of:
a) providing a substrate;
b) providing a first curable liquid precursor of the first pressure sensitive adhesive polymer layer and a second curable liquid precursor of the second polymer layer as superimposed layers onto the substrate;
c) optionally, providing one or more solid films and applying these adjacent to and essentially simultaneously with the formation of the superimposed layers; and
d) curing the superimposed layers of the multilayer pressure sensitive adhesive assembly thus obtained;

wherein the first curable liquid precursor of the first pressure sensitive adhesive polymer layer comprises:
a) 60 parts by weight or greater of a low Tg (meth)acrylate copolymer comprising:
i. C 1 -C 32 (meth)acrylic acid ester monomer units;
ii. optionally, acid functional ethylenically unsaturated monomer units;
iii. optionally, non-acid functional, ethylenically unsaturated polar monomer units;
iv. optionally, vinyl monomer units; and
v. optionally, multifunctional (meth)acrylate monomer units, and

b) up to 40 parts by weight of a high Tg (meth)acrylate copolymer having a weight average molecular weight (Mw) of above 20,000 Daltons, and comprising:
i. high Tg (meth)acrylic acid ester monomer units;
ii. optionally, acid functional ethylenically unsaturated monomer units;
iii. optionally, low Tg (meth)acrylic acid ester monomer units;
iv. optionally, non-acid functional, ethylenically unsaturated polar monomer units;
v. optionally, vinyl monomer units; and

c) optionally, up to 20 parts by weight of a hydrogenated hydrocarbon tackifier, based on 100 parts by weight of copolymers a) and b).

2. A method according to claim 1 , wherein the low Tg (meth)acrylate copolymer comprises C 1 -C 24 (meth)acrylic acid ester monomer units.

3. A method according to claim 1 , wherein a layer of the second curable liquid precursor of the second polymer layer is covered by an adjacent layer of the first curable liquid precursor of the first pressure sensitive adhesive polymer layer, respectively, without exposing the layer of a second curable liquid precursor of the second polymer layer.

4. A method according to claim 1 , which further comprises the steps of:
e) providing two or more coating knives which are offset, independently from each other, from the substrate to form two or more gaps normal to a surface of the substrate;
f) moving the substrate relative to the two or more coating knives in a downstream direction;
g) providing the first curable liquid precursor of the first pressure sensitive adhesive polymer layer and the second curable liquid precursor of the second polymer layer to the upstream side of the coating knives thereby coating the first curable liquid precursor through a first gap and the second curable liquid precursor through a second gap as superimposed layers onto the substrate.

5. A method according to claim 1 , wherein the high Tg (meth)acrylate copolymer has a weight average molecular weight (Mw) of above 25,000 Daltons.

6. A method according to claim 1 , wherein the low Tg (meth)acrylate copolymer comprises:
i. 85 to 99.5 parts by weight of an (meth)acrylic acid ester monomer unit of non-tertiary alcohol;
ii. 0.5 to 15 parts by weight of an acid functional ethylenically unsaturated monomer unit;
iii. 0 to 10 parts by weight of a non-acid functional, ethylenically unsaturated polar monomer unit;
iv. 0 to 5 parts vinyl monomer units; and
v. 0 to 5 parts of a multifunctional (meth)acrylate monomer units;
based on 100 parts by weight total monomers of the low Tg (meth)acrylate copolymer.

7. A method according to claim 1 , wherein the high Tg (meth)acrylic acid ester monomer units are selected from the group consisting of t-butyl (meth)acrylate, methyl (meth)acrylate, ethyl (meth)acrylate, isopropyl (meth)acrylate, n-butyl (meth)acrylate, isobutyl (meth)acrylate, s-butyl (meth)acrylate, t-butyl (meth)acrylate, stearyl (meth)acrylate, phenyl (meth)acrylate, cyclohexyl (meth)acrylate, isobornyl (meth)acrylate, isobornyl (meth)acrylate, benzyl (meth)acrylate, 3,3,5 trimethylcyclohexyl (meth)acrylate, cyclohexyl (meth)acrylate, N-octyl acrylamide, propyl (meth)acrylate, and any combinations or mixtures thereof.

8. A method according to claim 1 , wherein the C 1 -C 32 (meth)acrylic acid ester monomer units of the low Tg (meth)acrylate copolymer are selected from the group consisting of (meth)acrylic esters of ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, 1-pentanol, 2-pentanol, 3-pentanol, 2-methyl-1-butanol, 3-methyl-1-butanol, 1-hexanol, 2-hexanol, 2-methyl-1-pentanol, 3-methyl-1-pentanol, 2-ethyl-1-butanol, 3,5,5-trimethyl-1-hexanol, 3-heptanol, 1-octanol, 2-octanol, isooctylalcohol, 2-ethyl-1-hexanol, 1-decanol, 2-propylheptanol, 1-dodecanol, 1-tridecanol, 1-tetradecanol, citronellol, dihydrocitronellol, and any combinations or mixtures thereof.

9. A method according to claim 1 , wherein the C 1 -C 32 (meth)acrylic acid ester monomer units of the low Tg (meth)acrylate copolymer comprise 2-octyl(meth)acrylate.

10. A method according to claim 9 , wherein at least 25 wt % of the chemical structure of the 2-octyl(meth)acrylate is derived from biological material.

11. A method according to claim 1 , wherein the first curable liquid precursor of the first pressure sensitive adhesive polymer layer and/or the second curable liquid precursor of the second polymer layer is derived from biological material.

12. A method according to claim 1 , wherein the first curable liquid precursor of the first pressure sensitive adhesive polymer layer further comprises a chlorinated polyolefinic (co)polymer, which is selected from the group consisting of chlorinated polypropylene, chlorinated polyethylene, chlorinated ethylene/vinyl acetate copolymer, and any combinations, mixtures or copolymers thereof.

13. A multilayer pressure sensitive adhesive assembly obtainable by the method according to claim 1 .

14. A multilayer pressure sensitive adhesive assembly according to claim 13 , exhibiting a decrease in peel strength of less than 40% after heat bond aging on polypropylene, when measured according to the heat bond aging test method described in the experimental section.

Assignees

• 3M Innovative Properties Co

Inventors

• Wieneke Jan U
• Kuester Frank
• Chen Zhong
• Ma Jingjing
• Unverhau Kerstin
• Eckhardt Doreen
• Torre Claudia
• Janoski Jonathan E
• Seth Jayshree
• Weikel Arlin L

Classifications

• B05D7/04

  to surfaces of films or sheets (producing layered products by applying coatings of pasty or pulverulent plastics B29C41/00) · CPC title

• C09J7/385

  Acrylic polymers · CPC title

• B05D7/5423

  the two layers being applied simultaneously · CPC title

• B32B37/26

  with at least one layer which influences the bonding during the lamination process, e.g. release layers or pressure equalising layers · CPC title

• B32B2037/268

  Release layers · CPC title