IP Library Granted Patent US 12,404,355
Granted Patent B2
US 12,404,355 · App. 17/540,824 · Granted Sep 2, 2025

Photopolymerizable composition and cured film and display device using the same

Inventors: Jonghyuk Park (Gyeonggi-do, KR); Hyoc-Min Youn (Gyeonggi-do, KR); Tai Hoon Yeo (Gyeonggi-do, KR); Sang-Hoon Lee (Gyeonggi-do, KR); Wooram Oh (Gyeonggi-do, KR); Jongwook Lee (Gyeonggi-do, KR)
Assignee: DONGJIN SEMICHEM CO., LTD.
C08F20/14C08K3/22C08K2003/2213C08K2003/2241C08K2003/2244C08K2003/2296
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Quick Facts
Patent No.
US 12,404,355
App. No.
17/540,824
Granted
Sep 2, 2025
Kind
B2
Abstract

The present disclosure relates to a photopolymerizable composition capable of improving UV transmittance while maintaining excellent performance such as dielectric constant and sensitivity of a display device, and a cured film and a display device using the same.

Claims (41)

1. A photopolymerizable composition comprising:

one or more olefinic monomers;

metal oxide particles;

a dispersant; and

a photopolymerization initiator,

wherein the olefinic monomer comprises one or more olefinic monomers having an absolute viscosity measured at 25° C. of 1 cP to 30 cP,

wherein the olefinic monomer comprises a mono(meth)acrylate monomer having an absolute viscosity measured at 25° C. of 1 cP or more and 11 cP or less,

wherein the mono(meth)acrylate monomer comprises an aliphatic mono(meth)acrylate having 6 to 20 carbon atoms, and

wherein the aliphatic mono(meth)acrylate comprises at least one selected from the group consisting of isodecyl (meth)acrylate, isobornyl (meth)acrylate, lauryl (meth)acrylate, ethoxy ethyl(meth)acrylate, dicyclopentenyl (meth)acrylate, dicyclopentenyl oxyethyl(meth)acrylate, and dicyclopentanyl(meth)acrylate.

2. The photopolymerizable composition of claim 1 , wherein the olefinic monomer further comprises a glycol di(meth)acrylate monomer having an absolute viscosity measured at 25° C. of 11 cP to 30 cP.

3. The photopolymerizable composition of claim 1 , wherein the mono(meth)acrylate monomer further comprises an aromatic mono(meth)acrylate having 8 to 30 carbon atoms.

4. The photopolymerizable composition of claim 3 , wherein the aromatic mono(meth)acrylate having 8 to 30 carbon atoms comprises at least one selected from the group consisting of benzyl (meth)acrylate, phenoxy ethyl(meth)acrylate, and phenoxy benzyl(meth)acrylate.

5. The photopolymerizable composition of claim 2 , wherein the glycol di(meth)acrylate monomer comprises at least one selected from the group consisting of 1,6-hexanediol di(meth)acrylate, triethylene glycol di(meth)acrylate, tetraethylene glycol di(meth)acrylate, dipropylene glycol di(meth)acrylate, and tripropylene glycol di(meth)acrylate.

6. The photopolymerizable composition of claim 1 , wherein the olefinic monomer further comprises at least one selected from the group consisting of a low-viscosity first olefinic monomer having an absolute viscosity measured at 25° C. of 1 cP to 5 cP, and a high-viscosity second olefinic monomer having an absolute viscosity measured at 25° C. of 8 cP to 30 cP.

7. The photopolymerizable composition of claim 6 , wherein the olefinic monomer comprises the low-viscosity first olefinic monomer and the high-viscosity second olefinic monomer.

8. The photopolymerizable composition of claim 6 ,

wherein content of the low-viscosity first olefinic monomer is 10 parts by weight to 80 parts by weight relative to 100 parts by weight of the high-viscosity second olefinic monomer.

9. The photopolymerizable composition of claim 6 , wherein the second olefinic monomer comprises a high-viscosity olefinic monomer having an absolute viscosity measured at 25° C. of 8 cP to 15 cP.

10. The photopolymerizable composition of claim 6 , wherein the low-viscosity first olefinic monomer comprises at least one selected from the group consisting of benzyl (meth)acrylate, isodecyl (meth)acrylate, lauryl (meth)acrylate, ethoxyethyl (meth)acrylate, dicyclopentenyl (meth)acrylate, and dicyclopentanyl (meth)acrylate.

11. The photopolymerizable composition of claim 6 , wherein the high-viscosity second olefinic monomer comprises at least one selected from the group consisting of dicyclopentenyl oxyethyl (meth)acrylate, phenoxy ethyl(meth)acrylate, phenoxy benzyl(meth)acrylate, isobornyl (meth)acrylate, 1,6-hexanediol di(meth)acrylate, triethylene glycol di(meth)acrylate, tetraethylene glycol di(meth)acrylate, dipropylene glycol di(meth)acrylate, and tripropylene glycol di(meth)acrylate.

12. The photopolymerizable composition of claim 1 , wherein the metal oxide particles comprise a metal element selected from the group consisting of Zn, Zr, Ti, Hf and Ce.

13. The photopolymerizable composition of claim 1 , wherein a D50 particle size of the metal oxide particles is 5 nm to 100 nm.

14. The photopolymerizable composition of claim 1 , which comprises

5% by weight to 85% by weight of the olefinic monomer;

10% by weight to 70% by weight of metal oxide particles;

0.1% by weight to 30% by weight of a dispersant; and

0.1% by weight to 30% by weight of a photopolymerization initiator,

based on 100% by weight of the total content of the photopolymerizable composition.

15. The photopolymerizable composition of claim 1 , wherein the dispersant is at least one selected from the group consisting of acryl-based, epoxy-based and silicone-based compounds.

16. The photopolymerizable composition of claim 1 , wherein the photopolymerization initiator is at least one selected from the group consisting of triazine-based, benzoin-based, benzophenone-based, imidazole-based, xanthone-based, oxime ester-based and acetophenone-based compounds.

17. The photopolymerizable composition of claim 1 , which further comprises any one or more additives selected from the group consisting of 0.1 parts by weight to 30 parts by weight of a melamine crosslinking agent, or 0.1 parts by weight to 30 parts by weight of a silane coupling agent, based on 100 parts by weight of the photopolymerizable composition.

18. A cured film comprising a cured product of the photopolymerizable composition of claim 1 .

19. A photopolymerizable composition comprising:

one or more olefinic monomers;

metal oxide particles;

a dispersant; and

a photopolymerization initiator,

wherein the olefinic monomer comprises one or more olefinic monomers having an absolute viscosity measured at 25° C. of 1 cP to 30 cP,

wherein the olefinic monomer comprises a glycol di(meth)acrylate monomer having an absolute viscosity measured at 25° C. of 11 cP to 30 cP, and

wherein the dispersant is at least one selected from the group consisting of acryl-based, epoxy-based, and silicone-based compounds.

20. A cured film comprising a cured product of the photopolymerizable composition of claim 19 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 2, 2021
From: PARK, JONGHYUK; YOUN, HYOC-MIN; YEO, TAI HOON; LEE, SANG-HOON; OH, WOORAM; LEE, JONGWOOK
To: DONGJIN SEMICHEM CO., LTD.
Reel/Frame 058272/0594 →
Priority Claims (1)
KR 10-2019-0065925 · Jun 4, 2019 · national
Continuity (2)
Continuation PCTKR2020007089 · Jun 1, 2020
Related Publication 20220098334A1 · Mar 31, 2022
References Cited (27)
US 5489621A · Sato · 1996 [cited by examiner]
US 7615581B2 · Choi · 2009 [cited by examiner]
US 7923480B2 · Fujita · 2011 [cited by examiner]
US 7943206B2 · Jones · 2011 [cited by examiner]
US 8007878B2 · Yoneyama · 2011 [cited by examiner]
US 8241755B2 · Jones · 2012 [cited by examiner]
US 8349934B2 · Murofushi · 2013 [cited by examiner]
US 8586154B2 · Hunt · 2013 [cited by examiner]
US 9880322B2 · Hunt · 2018 [cited by examiner]
US 10559777B2 · Galand · 2020 [cited by examiner]
US 20080161444A1 · Hayashi · 2008 [cited by examiner]
US 20100009287A1 · Kodama · 2010 [cited by applicant]
US 20110227008A1 · Jones · 2011 [cited by examiner]
US 20140205771A1 · Huang · 2014 [cited by examiner]
CN 106459316A · 2017 [cited by applicant]
JP 2010189506A · 2010 [cited by applicant]
JP 2013237834A · 2013 [cited by applicant]
JP 2015524494A · 2015 [cited by applicant]
JP 2017082054A · 2017 [cited by applicant]
JP 2017095556A · 2017 [cited by applicant]
JP 2018080322A · 2018 [cited by applicant]
KR 020080005875A · 2008 [cited by applicant]
KR 1020100007737A · 2010 [cited by applicant]
KR 1020100069205A · 2010 [cited by applicant]
KR 1020120040834A · 2012 [cited by applicant]
KR 1020160141022A · 2016 [cited by applicant]
KR 101923209B · 2018 [cited by applicant]