US2014363687A1PendingUtilityA1
Aqueous polyimide precursor solution composition and method for producing aqueous polyimide precursor solution
Est. expiryJan 13, 2032(~5.4 yrs left)· nominal 20-yr term from priority
B29K 2079/08B29C 39/38C08J 2379/08C08J 5/18C08G 73/10B29C 39/006C08K 5/3445C08L 79/08Y10T428/31721B29K 2105/0073B29K 2105/0002C08L 2201/08C08L 2201/10B29L 2031/3475C08L 2203/16C08L 2203/20C08G 73/1007C08L 2203/204
50
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
An aqueous polyimide precursor solution composition in which a polyamic acid which is obtained by reacting a tetracarboxylic acid component and a diamine component is dissolved in an aqueous solvent together with an imidazole in an amount of 1.6 moles or more per mole of the tetracarboxylic acid component of the polyamic acid.
Claims
exact text as granted — not AI-modified1 . An aqueous polyimide precursor solution composition, wherein
a polyamic acid, which is formed by the reaction of a tetracarboxylic acid component and a diamine component, and consists of a repeating unit represented by the following formula (1), is dissolved in an aqueous solvent together with an imidazole in an amount of 1.6 mole or more per mole of the tetracarboxylic acid component of the polyamic acid.
wherein
A represents at least one selected from the group consisting of a tetravalent group of an aromatic tetracarboxylic acid containing no fluorine group, from which carboxyl groups have been removed, a tetravalent group of an aliphatic tetracarboxylic acid, from which carboxyl groups have been removed, and a tetravalent group of an aromatic tetracarboxylic acid containing a fluorine group, from which carboxyl groups have been removed, and
B represents at least one selected from the group consisting of a divalent group of an aromatic diamine containing no fluorine group and having a solubility in water at 25° C. of 0.1 g/L or more, from which amino groups have been removed, a divalent group of an aliphatic diamine having a molecular weight of 500 or less, from which amino groups have been removed, and a divalent group of an aromatic diamine containing a fluorine group, from which amino groups have been removed,
with the proviso that
not less than 50 mol % of A is a tetravalent group of an aliphatic tetracarboxylic acid, from which carboxyl groups have been removed, and/or a tetravalent group of an aromatic tetracarboxylic acid containing a fluorine group, from which carboxyl groups have been removed, and not more than 50 mol %, including 0 mol %, of A is a tetravalent group of an aromatic tetracarboxylic acid containing no fluorine group, from which carboxyl groups have been removed, and/or
not less than 50 mol % of B is a divalent group of an aliphatic diamine having a molecular weight of 500 or less, from which amino groups have been removed, and/or a divalent group of an aromatic diamine containing a fluorine group, from which amino groups have been removed, and not more than 50 mol %, including 0 mol %, of B is a divalent group of an aromatic diamine containing no fluorine group and having a solubility in water at 25° C. of 0.1 g/L or more, from which amino groups have been removed.
2 . The aqueous polyimide precursor solution composition of claim 1 , wherein the imidazole is selected from the group consisting of 1,2-dimethylimidazole, 2-ethyl-4-methylimidazole, 4-ethyl-2-methylimidazole, and 1-methyl-4-ethylimidazole.
3 . The aqueous polyimide precursor solution of claim 1 , wherein the aqueous polyimide precursor solution composition has an organic solvent content of less than 5 wt %.
4 . The aqueous polyimide precursor solution composition of claim 3 , wherein the aqueous polyimide precursor solution composition contains substantially no organic solvent.
5 . A polyimide produced by heating the aqueous polyimide precursor solution composition of claim 1 .
6 . The polyimide of claim 5 , wherein the polyimide has a light transmittance at 400 nm of 60% or more when the polyimide is formed into a film having a thickness of 10 μm.
7 . The polyimide of claim 5 , wherein the polyimide has a total light transmittance of 80% or more when the polyimide is formed into a film having a thickness of 10 μm.
8 . A polyimide film obtained from the aqueous polyimide precursor solution composition of claim 1 , wherein the polyimide film has a light transmittance at 400 nm of 60% or more in terms of 10 μm of film thickness.
9 . A polyimide film obtained from the aqueous polyimide precursor solution composition of claim 1 , wherein the polyimide film has a total light transmittance of 80% or more in terms of 10 μm of film thickness.
10 . A method for producing an aqueous polyimide precursor solution composition, comprising
reacting a tetracarboxylic acid component, which comprises an aliphatic tetracarboxylic dianhydride and/or an aromatic tetracarboxylic dianhydride containing a fluorine group in an amount of not less than 50 mol % and comprises an aromatic tetracarboxylic dianhydride containing no fluorine group in an amount of not more than 50 mol %, or alternatively, does not comprise an aromatic tetracarboxylic dianhydride containing no fluorine group, and a diamine component, which comprises an aliphatic diamine having a molecular weight of 500 or less and/or an aromatic diamine containing a fluorine group in an amount of not less than 50 mol % and comprises an aromatic diamine containing no fluorine group and having a solubility in water at 25° C. of 0.1 g/L or more in an amount of not more than 50 mol %, or alternatively, does not comprise an aromatic diamine containing no fluorine group and having a solubility in water at 25° C. of 0.1 g/L or more, in the presence of an imidazole using water as a reaction solvent to provide an aqueous polyimide precursor solution composition.
11 . The method for producing an aqueous polyimide precursor solution composition of claim 10 , wherein the amount of the imidazole used is 1.6 mole or more per mole of the tetracarboxylic dianhydride.
12 . (canceled)
13 . (canceled)
14 . An electrical device, an electronic device, an optical device, a display device, a touch panel, a solar battery, or an LED lighting device comprising the polyimide of claim 5 .
15 . A polyimide precursor resin composition for flexible device substrates, wherein
a polyamic acid, which is formed by the reaction of a tetracarboxylic acid component and a diamine component, and consists of a repeating unit represented by the following formula (1), is dissolved in an aqueous solvent together with an imidazole in an amount of 1.6 mole or more per mole of the tetracarboxylic acid component of the polyamic acid.
wherein
A represents at least one selected from the group consisting of a tetravalent group of an aromatic tetracarboxylic acid containing no fluorine group, from which carboxyl groups have been removed, a tetravalent group of an aliphatic tetracarboxylic acid, from which carboxyl groups have been removed, and a tetravalent group of an aromatic tetracarboxylic acid containing a fluorine group, from which carboxyl groups have been removed, and
B represents at least one selected from the group consisting of a divalent group of an aromatic diamine containing no fluorine group and having a solubility in water at 25° C. of 0.1 g/L or more, from which amino groups have been removed, a divalent group of an aliphatic diamine having a molecular weight of 500 or less, from which amino groups have been removed, and a divalent group of an aromatic diamine containing a fluorine group, from which amino groups have been removed,
with the proviso that
not less than 50 mol % of A is a tetravalent group of an aliphatic tetracarboxylic acid, from which carboxyl groups have been removed, and/or a tetravalent group of an aromatic tetracarboxylic acid containing a fluorine group, from which carboxyl groups have been removed, and not more than 50 mol %, including 0 mol %, of A is a tetravalent group of an aromatic tetracarboxylic acid containing no fluorine group, from which carboxyl groups have been removed, and/or
not less than 50 mol % of B is a divalent group of an aliphatic diamine having a molecular weight of 500 or less, from which amino groups have been removed, and/or a divalent group of an aromatic diamine containing a fluorine group, from which amino groups have been removed, and not more than 50 mol %, including 0 mol %, of B is a divalent group of an aromatic diamine containing no fluorine group and having a solubility in water at 25° C. of 0.1 g/L or more, from which amino groups have been removed.
16 . A method for producing a flexible device which is a display device or a light-receiving device, comprising steps of:
applying the polyimide precursor resin composition for flexible device substrates of claim 15 onto a carrier substrate, and then heating the composition to form a solid polyimide resin film; forming a circuit on the polyimide resin film; and separating the polyimide resin film on which the circuit is formed from the carrier substrate.
17 . A flexible device produced by the method for producing a flexible device of claim 16 , wherein the flexible device is a display device or a light-receiving device.Join the waitlist — get patent alerts
Track US2014363687A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.