Curable encapsulants and use thereof

Patent metadata

Field	Value
Publication number	US-10141532-B2
Application number	US-201715590119-A
Country	US
Kind code	B2
Filing date	May 9, 2017
Priority date	May 2, 2012
Publication date	Nov 27, 2018
Grant date	Nov 27, 2018

Abstract

The present invention relates to curable barrier encapsulants or sealants for electronic devices that have pressure sensitive adhesive properties. The encapsulants are especially suitable for organic electronic devices that require lower laminating temperature profiles. The encapsulant protects active organic/polymeric components within an organic electronic device from environmental elements, such as moisture and oxygen.

First claim

We claim:

1. A curable encapsulant comprising:
a) from about 70 to about 90 wt %, based on the total weight of the curable encapsulant, of a polyisobutylene having a Mw of from about 1,000 to about 95,000 Da;
b) from about 10 to about 50 wt %, based on the total weight of the curable encapsulant, of a functionalized polyisobutylene having (i) a Mw of from about 1,000 to about 95,000 Da and (ii) greater than one free-radical reactive functional group per polymer chain, wherein the free-radical reactive functional group is selected from the group consisting of terminal (meth)acrylates and/or, terminal acrylates;
c) a free radical initiator; and
d) a UV absorber;
wherein the curable encapsulant is (i) essentially free of an acrylic monomer with Mw less than about 1,000 Da or volatile organic compound with Mw less than about 1,000 Da, (ii) essentially free of a tackifier, and (iii) a hot melt.

2. The curable encapsulant of claim 1 , wherein the UV absorber is a selected from the group consisting of benzotriazole derivatives, hydroxybenzophenones, hydroxyphenyl triazines, esters of substituted and unsubstituted benzoic acids, hindered amine light stabilizer, and mixtures thereof.

3. The curable encapsulant of claim 2 , wherein the hindered amine light stabilizer is a secondary, tertiary, acetylated, N-hydrocarbyloxy substituted, hydroxyl-substituted N-hydrocarbyloxy substituted, or a substituted cyclic amine characterized by aliphatic substitution on the carbon atoms adjacent to the amine function.

4. The curable encapsulant of claim 1 further comprising a functionalized polyolefin, wherein the functionalized polyolefin has (i) a Mw of from about 1,000 to about 95,000 Da and (ii) greater than 1 free-radical reactive functional group;
wherein the free-radical functional group is selected from the group consisting of terminal (meth)acrylates and/or terminal acrylates.

5. The curable encapsulant of claim 1 further comprising up to 20 wt % of a plurality of desiccant fillers.

6. The curable encapsulant of claim 1 which comprises less than 5,000 ppm of a volatile organic molecule having a Mw less than 1,000 Da.

7. A curable encapsulant comprising:
a) from about 70 to about 90 wt %, based on the total weight of the curable encapsulant, a polyisobutylene having a Mw of from about 1,000 to about 95,000 Da;
b) from about 10 to about 50 wt %, based on the total weight of the curable encapsulant, a functionalized polyolefin having (i) a Mw of from about 1,000 to about 95,000 Da and (ii) greater than one free-radical reactive functional group per polymer chain, wherein the free-radical reactive functional group is selected from the group consisting of terminal (meth)acrylates and/or, terminal acrylates;
c) a free radical initiator; and
d) a UV absorber
wherein the curable encapsulant is (i) essentially free of an acrylic monomer with Mw less than about 1,000 Da or volatile organic compound with Mw less than about 1,000 Da, (ii) essentially free of a tackifier, and (iii) a hot melt.

8. The curable encapsulant of claim 7 , wherein the UV absorber is a selected from the group consisting of benzotriazole derivatives, hydroxybenzophenones, hydroxyphenyl triazines, esters of substituted and unsubstituted benzoic acids, hindered amine light stabilizer, and mixtures thereof.

9. The curable encapsulant of claim 7 , wherein the hindered amine light stabilizer is a secondary, tertiary, acetylated, N-hydrocarbyloxy substituted, hydroxyl-substituted N-hydrocarbyloxy substituted, or a substituted cyclic amine characterized by aliphatic substitution on the carbon atoms adjacent to the amine function.

10. The curable encapsulant of claim 7 wherein the functionalized polyolefin is selected from the group consisting of (meth)acrylate-terminated polybutadiene, hydrogenated (meth)acrylate-terminated polybutadiene, and mixtures thereof.

11. The curable encapsulant of claim 7 further comprising up to 20 wt % of a plurality of desiccant fillers.

12. The curable encapsulant of claim 7 which comprises less than 5,000 ppm of a volatile organic molecule having a Mw less than 1,000 Da.

13. A curable encapsulant comprising:
a) from about 70 to about 90 wt %, based on the total weight of the curable encapsulant, an amorphous polyalphaolefin having a Brookfield viscosity less than 8,000 cps at 190° C.;
b) from about 10 to about 50 wt %, based on the total weight of the curable encapsulant, a functionalized polyisobutylene or functionalized polyolefin having (i) a Mw of from about 1,000 to about 95,000 Da and (ii) greater than one free-radical reactive functional group per polymer chain, wherein the free-radical reactive functional group is selected from the group consisting of terminal (meth)acrylates and/or, terminal acrylates;
c) a free radical initiator;
d) a tackifier; and
e) a UV absorber;
wherein the functionalized polyolefin is selected from the group consisting of (meth)acrylate-terminated polybutadiene, hydrogenated (meth)acrylate-terminated polybutadiene, and mixtures thereof
wherein the curable encapsulant is (i) essentially free of an acrylic monomer with Mw less than about 1,000 Da or volatile organic compound with Mw less than about 1,000 Da and (ii) a hot melt.

14. The curable encapsulant of claim 13 , wherein the UV absorber is a selected from the group consisting of benzotriazole derivatives, hydroxybenzophenones, hydroxyphenyl triazines, esters of substituted and unsubstituted benzoic acids, hindered amine light stabilizer, and mixtures thereof.

15. The curable encapsulant of claim 13 , wherein the hindered amine light stabilizer is a secondary, tertiary, acetylated, N-hydrocarbyloxy substituted, hydroxyl-substituted N-hydrocarbyloxy substituted, or a substituted cyclic amine characterized by aliphatic substitution on the carbon atoms adjacent to the amine function.

16. The curable encapsulant of claim 13 further comprising up to 20 wt % of a plurality of desiccant fillers.

17. An article comprising the curable encapsulant of claim 1 which is an electronic device.

18. An article comprising the curable encapsulant of claim 7 which is an electronic device.

19. An article comprising the curable encapsulant of claim 13 which is an electronic device.

Assignees

• Henkel IP & Holding GmbH
• Henkel Ag & Co Kgaa

Inventors

• Liu Yuxia
• Konarski Mark
• Paul Charles W
• Palasz Peter D

Classifications

• C08L23/22 Primary

  Copolymers of isobutene; Butyl rubber; Homopolymers or copolymers of other iso-olefins · CPC title

• H01L51/56

  Electricity · mapped topic

• H01L51/5259

  Electricity · mapped topic

• C08L2205/03

  containing three or more polymers in a blend · CPC title

• H01B3/441

  from alkenes · CPC title