Display device and laminated optical film
US-10126473-B2 · Nov 13, 2018 · US
US10654969B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10654969-B2 |
| Application number | US-201715858424-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 29, 2017 |
| Priority date | Feb 23, 2017 |
| Publication date | May 19, 2020 |
| Grant date | May 19, 2020 |
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A thin film is provided, which includes a polymer formed by reacting (a) p-hydroxybenzoic acid, (b) 6-hydroxy 2-naphthoic acid and (c) branched-monomer. (c) branched-monomer is or a combination thereof, wherein R is aryl group, heteroaryl group, or cycloalkyl group, and each of R 1 is independently —OH, —NH 2 , or —COOH. The molar ratio of (a) p-hydroxybenzoic acid over (b) 6-hydroxy 2-naphthoic acid is between 50:50 and 90:10. The molar ratio of (c) branched-monomer over the sum of (a) p-hydroxybenzoic acid and (b) 6-hydroxy 2-naphthoic acid is between 0.25:100 and 0.5:100. The polymer has an intrinsic viscosity of 4 dL/g to 6 dL/g.
Opening claim text (preview).
What is claimed is: 1. A thin film, comprising: a polymer formed by reacting (a) p-hydroxybenzoic acid, (b) 6-hydroxy 2-naphthoic acid and (c) branched-monomer, wherein (c) branched-monomer is or a combination thereof, wherein R is aryl group, heteroaryl group, or cycloalkyl group, and each of R 1 is independently —OH, —NH 2 , or —COOH; wherein a molar ratio of (a) p-hydroxybenzoic acid over (b) 6-hydroxy 2-naphthoic acid is between 50:50 and 90:10; wherein a molar ratio of (c) branched-monomer over the sum of (a) p-hydroxybenzoic acid and (b) 6-hydroxy 2-naphthoic acid is between 0.25:100 and 0.5:100; and wherein the polymer has an inherent viscosity of 4 dL/g to 6 dL/g. 2. The thin film as claimed in claim 1 , wherein the molar ratio of (a) p-hydroxybenzoic acid over (b) 6-hydroxy 2-naphthoic acid is between 60:40 to 80:20. 3. The thin film as claimed in claim 1 , wherein the molar ratio of (a) p-hydroxybenzoic acid over (b) 6-hydroxy 2-naphthoic acid is between 70:30 to 80:20. 4. The thin film as claimed in claim 1 , wherein (c) branched-monomer is trimesic acid. 5. The thin film as claimed in claim 1 , having a melt strength of 1.4 cN to 1.9 cN. 6. The thin film as claimed in claim 1 , having an elongation ratio of 13% to 25%. 7. The thin film as claimed in claim 1 , having a breaking strength of about 8 kgf/mm 2 to 10 kgf/mm 2 . 8. A method for manufacturing a thin film, comprising: performing a polymerization of (a) p-hydroxybenzoic acid, (b) 6-hydroxy 2-naphthoic acid, and (c) branched-monomer; melting the polymer to form a thin film; and thermally treating the thin film, wherein (c) branched-monomer is or a combination thereof, wherein R is aryl group, heteroaryl group, or cycloalkyl group, and each of R 1 is independently —OH, —NH 2 , or —COOH; wherein a molar ratio of (a) p-hydroxybenzoic acid over (b) 6-hydroxy 2-naphthoic acid is between 50:50 and 90:10; wherein a molar ratio of (c) branched-monomer over the sum of (a) p-hydroxybenzoic acid and (b) 6-hydroxy 2-naphthoic acid is between 0.25:100 and 0.5:100; and wherein the polymer has an inherent viscosity of 4 dL/g to 6 dL/g. 9. The method as claimed in claim 8 , wherein the polymerization further includes anhydride compound, and anhydride groups of the anhydride compound and sum of (a) p-hydroxybenzoic acid and (b) 6-hydroxy 2-naphthoic acid have a molar ratio of 80:100 to 120:100. 10. The method as claimed in claim 8 , wherein the polymerization is performed at a temperature of 280° C. to 330° C. 11. The method as claimed in claim 8 , wherein the step of melting the polymer is performed at a temperature of 100° C. to 160° C. 12. The method as claimed in claim 8 , wherein the step of thermally treating the thin film is performed at a temperature of 250° C. to 300° C. 13. A copper clad laminate, comprising: a thin film; and a copper foil attached to the thin film, wherein the thin film comprises a polymer formed by reacting (a) p-hydroxybenzoic acid, (b) 6-hydroxy 2-naphthoic acid and (c) branched-monomer, wherein (c) branched-monomer is or a combination thereof, wherein R is aryl group, heteroaryl group, or cycloalkyl group, and each of R 1 is independently —OH, —NH 2 , or —COOH; wherein a molar ratio of (a) p-hydroxybenzoic acid over (b) 6-hydroxy 2-naphthoic acid is between 50:50 and 90:10; wherein a molar ratio of (c) branched-monomer over the sum of (a) p-hydroxybenzoic acid and (b) 6-hydroxy 2-naphthoic acid is between 0.25:100 and 0.5:100; and wherein the polymer has an inherent viscosity of 4 dL/g to 6 dL/g. 14. The copper clad laminate as claimed in claim 13 , wherein (c) branched-monomer is trimesic acid.
Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers · CPC title
comprising aluminium or copper {(B32B15/016 and B32B15/017 take precedence)} · CPC title
of synthetic resin · CPC title
Dimensional stability · CPC title
comprising synthetic resins not wholly covered by any one of the sub-groups {B32B27/30 - B32B27/42} · CPC title
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