US2018230271A1PendingUtilityA1
Polyamic acid, polyimide film and fabrication method of the polyimide film
Est. expiryFeb 10, 2037(~10.5 yrs left)· nominal 20-yr term from priority
C08J 5/18C08G 73/1067C08J 2379/08C08L 2201/10C08L 79/08C08G 73/123C08G 73/10C08G 73/1057C08G 73/1042C08G 73/1014C08G 73/1039
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Claims
Abstract
A polyamic acid according to an embodiment is formed by a polymerization reaction of a dianhydride compound, a first diamine compound represented by the following Formula 1, and a second diamine compound, which is different from the first diamine compound. A polyimide film derived from the polyamic acid may exhibit excellent heat resistance and improved optical properties:
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A polyamic acid being a polymerization product of:
a dianhydride compound; a first diamine compound represented by the following Formula 1; and a second diamine compound different from the first diamine compound:
wherein in Formula 1, R 1 and R 2 are each independently selected from a hydrogen atom, a deuterium atom, a halogen atom, and a substituted or unsubstituted alkyl group of 1 to 20 carbon atoms, and
n 1 and n 2 are each independently an integer of 0 to 4.
2 . The polyamic acid of claim 1 , wherein the second diamine compound is represented by the following Formula 2:
wherein in Formula 2, Ar is a substituted or unsubstituted phenyl group, and m is an integer of 1 to 4.
3 . The polyamic acid of claim 1 , wherein the second diamine compound is represented by the following Formula 2-1:
4 . The polyamic acid of claim 1 , wherein in Formula 1,
n 1 and n 2 are each independently an integer of 1 or more, and R 1 and R 2 are each independently an alkyl group of 1 to 20 carbon atoms substituted with at least one fluorine atom.
5 . The polyamic acid of claim 1 , wherein the first diamine compound Formula 1 is represented by the following Formula 1-1:
wherein in Formula 1-1, definitions of R 1 , R 2 , n 1 and n 2 are the same as those in Formula 1.
6 . The polyamic acid of claim 1 , wherein the first diamine compound of Formula 1 is represented by the following Formula 1-2:
7 . The polyamic acid of claim 1 , wherein a molar ratio of a sum of the first diamine compound and the second diamine compound with respect to the dianhydride compound is from 1:0.9 to 1:1.1.
8 . The polyamic acid of claim 7 , wherein a molar ratio of the first diamine compound to the second diamine compound is from 0.01:0.99 to 0.99:0.01.
9 . The polyamic acid of claim 1 , wherein the dianhydride compound comprises at least one selected from 4,4′-(hexafluoroisopropylidene)diphthalic anhydride, 3,3′,4,4′-biphenyltetracarboxylic dianhydride, cyclobutane-1,2,3,4-tetracarboxyl dianhydride and pyromellitic dianhydride.
10 . The polyamic acid of claim 1 , wherein
the dianhydride compound is 3,3′,4,4′-biphenyltetracarboxylic dianhydride, the first diamine compound is 2,2′-bis(trifluoromethyl)benzidine, and the second diamine compound is 3,5-diaminobenzoic acid.
11 . The polyamic acid of claim 1 , wherein the polyamic acid comprises a repeating unit represented by the following Formula 3:
wherein in Formula 3, X and Y are each independently an integer of 1 or more.
12 . A polyimide film comprising a repeating unit derived from the polyamic acid according to claim 1 .
13 . The polyimide film of claim 12 , wherein a thermal expansion coefficient of the polyimide film is from 10 ppm/° C. to 20 ppm/° C.
14 . The polyimide film of claim 12 , wherein a glass transition temperature of the polyimide film is from 300° C. to 420° C.
15 . The polyimide film of claim 12 , wherein a thermal decomposition temperature of the polyimide film is from 400° C. to 500° C.,
wherein the thermal decomposition temperature is a temperature at which a weight reduction ratio of the polyimide film reaches 1%.
16 . The polyimide film of claim 12 , wherein a light transmittance of the polyimide film is 95% or more.
17 . The polyimide film of claim 12 , wherein a yellow index of the polyimide film is from 1 to 10.
18 . The polyimide film of claim 12 , wherein the polyimide film has a light transmittance of 95% or more, a thermal expansion coefficient of 10 ppm/° C. to 20 ppm/° C., and a glass transition temperature of 300° C. to 420° C.
19 . The polyimide film of claim 12 , wherein the polyimide film comprises a repeating unit represented by the following Formula 4:
wherein in Formula 4, A and B are each independently an integer of 1 or more.
20 . A fabrication method of a polyimide film, the method comprising:
preparing a polyamic acid according to claim 1 by a polymerization reaction of a dianhydride compound and at least two kinds of diamine compounds; providing the polyamic acid on a substrate to form a polyamic acid layer; and heat treating the polyamic acid layer.
21 . The fabrication method of a polyimide film of claim 20 , wherein the preparing of the polyamic acid is performed at a temperature range of −10° C. to 80° C.
22 . The fabrication method of a polyimide film of claim 20 , wherein the heat treating of the polyamic acid layer comprises heat treating at a temperature range of 250° C. to 550° C.
23 . The fabrication method of a polyimide film of claim 22 , further comprising cooling after the heat treating of the polyamic acid layer.
24 . The fabrication method of a polyimide film of claim 20 , wherein the heat treating of the polyamic acid layer comprises:
first heat treating at a first temperature; and second heat treating at a second temperature higher than the first temperature.
25 . The fabrication method of a polyimide film of claim 24 , wherein the first temperature is from 250° C. to less than 300° C., and the second temperature is from 300° C. to 550° C.
26 . The fabrication method of a polyimide film of claim 20 , wherein the heat treating of the polyamic acid layer is conducted in a vacuum state.Join the waitlist — get patent alerts
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