POLYIMIDE FILM MANUFACTURING METHOD

Abstract

The present disclosure relates to a method for producing a polyimide film. The method includes: providing a polyamic acid copolymer including at least a semi-aromatic polyamic acid obtained by reacting cyclobutane-1,2,3,4-tetracarboxylic (CBDA) with an aromatic cyclic diamine; and adding dehydrating agent and a pyridine catalyst having an ortho substituent into the polyamic acid copolymer to carry out a chemical imidization reaction of the polyamic acid copolymer to prepare a polyimide film.

Claims

1. A polyimide film manufacturing method comprising following steps: providing a polyamic acid copolymer including at least a semi-aromatic polyamic acid obtained by reacting cyclobutane-1,2,3,4-tetracarboxylic (CBDA) with an aromatic cyclic diamine; and adding a dehydrating agent and a pyridine catalyst having an ortho substituent into the polyamic acid copolymer to carry out a chemical imidization reaction of the polyamic acid copolymer to prepare a polyimide film.

2. The polyimide film manufacturing method according to claim 1, wherein the polyamic acid copolymer further includes an aromatic polyamic acid obtained by reacting an aromatic diamine with an aromatic dianhydride.

3. The polyimide film manufacturing method according to claim 1, wherein the aromatic cyclic diamine is p-phenylenediamine (PDA), 4,4-diaminodiphenyl ether (ODA), 2,2-bis[4-(4-aminophenoxyphenyl)]propane (BAPP), 2,2-bis(trifluoromethyl)benzidine (TFMB), 3,5-diaminobenzoic acid (35DABA), 4,4-diaminobenzanilide (44DABA), 1-(4-aminophenyl)-2,3-dihydro-1,3,3-trimethyl-1H-inden-5-amine (TMDA), bis[4-(4-aminophenoxy)phenyl]sulfone (BAPS), 4,4-bis(4-aminophenoxy)biphenyl (BAPB), 1,4-bis(4-aminophenoxy)benzene (TPEQ), 2,2-bis(trifluoromethyl)-4,4-diaminophenyl ether (6FODA), 2,2-bis[4-(4-aminophenoxy)phenyl]-1,1,1,3,3,3-hexafluoropropane (HFBAPP), 4,4-(9-fluorenylidene)dianiline (BAFL), 2-(4-aminophenyl)-5-aminobenzoxazole (5BPOA), m-phenylenediamine (mPDA), 4,4-diaminodiphenyl sulfone (44DDS), 2,2-bis(4-aminophenyl)hexafluoropropane (Bis-A-AF), 2,2-bis(3-amino-4-hydroxylphenyl) hexafluoropropane (6FAP), or 4,4-[1,4-phenylbis(oxy)]bis[3-(trifluoromethyl)aniline] (FAPB).

4. The polyimide film manufacturing method according to claim 1, wherein the structure of the pyridine catalyst having the ortho substituent is: ##STR00002## wherein, at least one of R1 and R2 is a non-hydrogen substituent.

5. The polyimide film manufacturing method according to claim 1, wherein a number of moles of the pyridine catalyst having the ortho substituent is greater than or equal to a number of moles of the polyamic acid copolymer.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0010] The present disclosure will become more fully understood from the following detailed description and accompanying drawings.

[0011] FIG. 1 is a flow chart of a polyimide film manufacturing method of the present disclosure.

DETAILED DESCRIPTION OF THE EXEMPLARY EMBODIMENTS

[0012] The present disclosure is more particularly described in the following examples that are intended as illustrative only since numerous modifications and variations therein will be apparent to those skilled in the art. Like numbers in the drawings indicate like components throughout the views. As used in the description herein and throughout the claims that follow, unless the context clearly dictates otherwise, the meaning of a, an, and the includes plural reference, and the meaning of in includes in and on. Titles or subtitles can be used herein for the convenience of a reader, which shall have no influence on the scope of the present disclosure.

[0013] The terms used herein generally have their ordinary meanings in the art. In the case of conflict, the present document, including any definitions given herein, will prevail. The same thing can be expressed in more than one way. Alternative language and synonyms can be used for any term(s) discussed herein, and no special significance is to be placed upon whether a term is elaborated or discussed herein. A recital of one or more synonyms does not exclude the use of other synonyms. The use of examples anywhere in this specification including examples of any terms is illustrative only, and in no way limits the scope and meaning of the present disclosure or of any exemplified term. Likewise, the present disclosure is not limited to various embodiments given herein. Numbering terms such as first, second or third can be used to describe various components, signals or the like, which are for distinguishing one component/signal from another one only, and are not intended to, nor should be construed to impose any substantive limitations on the components, signals or the like.

[0014] Referring to FIG. 1, a polyimide film manufacturing method of the present disclosure includes following steps: providing a polyamic acid copolymer (S1) including at least a semi-aromatic polyamic acid obtained by reacting cyclobutane-1,2,3,4-tetracarboxylic (CBDA) with an aromatic cyclic diamine; and adding a dehydrating agent and a pyridine catalyst having an ortho substituent to the polyamic acid copolymer (S2) to carry out an imidization reaction by chemical cyclization (S3) to produce the polyimide film.

[0015] The aromatic cyclic diamine of the semi-aromatic polyamic acid can be p-phenylenediamine (PDA), 4,4-diaminodiphenyl ether (ODA), 2,2-bis[4-(4-aminophenoxyphenyl)]propane (BAPP), 2,2-bis(trifluoromethyl)benzidine (TFMB), 3,5-diaminobenzoic acid (35DABA), 4,4-diaminobenzanilide (44DABA), 1-(4-aminophenyl)-2,3-dihydro-1,3,3-trimethyl-1H-inden-5-amine (TMDA), bis[4-(4-aminophenoxy)phenyl]sulfone (BAPS), 4,4-bis(4-aminophenoxy)biphenyl (BAPB), 1,4-bis(4-aminophenoxy)benzene (TPEQ), 2,2-bis(trifluoromethyl)-4,4-diaminophenyl ether (6FODA), 2,2-bis[4-(4-aminophenoxy)phenyl]-1,1,1,3,3,3-hexafluoropropane (HFBAPP), 4,4-(9-fluorenylidene)dianiline (BAFL), 2-(4-aminophenyl)-5-aminobenzoxazole (5BPOA), m-phenylenediamine (mPDA), 4,4-diaminodiphenyl sulfone (44DDS), 2,2-bis(4-aminophenyl)hexafluoropropane (Bis-A-AF), 2,2-bis(3-amino-4-hydroxylphenyl) hexafluoropropane (6FAP), or 4,4-[1,4-phenylbis (oxy)]bis[3-(trifluoromethyl)aniline] (FAPB).

[0016] The polyamic acid copolymer can include an aromatic polyamic acid obtained by reacting an aromatic diamine with an aromatic dianhydride. The aromatic diamine includes 2,2-bis(trifluoromethyl)benzidine (TFMB), 2,2-bis[4-(4-aminophenoxyphenyl)]propane(BAPP), 2,2-bis[4-(4-aminophenoxy)phenyl]-1,1,1,3,3,3-hexafluoropropane (HFBAPP), 1-(4-aminophenyl)-2,3-dihydro-1,3,3-trimethyl-1H-inden-5-amine (TMDA), p-phenylenediamine (PDA), 4,4-bis(4-aminophenoxy)biphenyl (BAPB), 2,2-bis(trifluoromethyl)-4,4-diaminophenyl ether (6FODA), bis[4-(4-aminophenoxy)phenyl]sulfone (BAPS), 4,4-(9-fluorenylidene)dianiline (BAFL), 4,4-diaminodiphenyl sulfone (44DDS), 4,4-diaminodiphenyl ether (ODA), 4,4-diaminobenzanilide (44DABA), 2,2-bis(4-aminophenyl)hexafluoropropane (Bis-A-AF), m-phenylenediamine (mPDA), 2,2-bis(3-amino-4-hydroxylphenyl) hexafluoropropane (6FAP), 3,5-diaminobenzoic acid (35DABA), 2-(4-aminophenyl)-5-aminobenzoxazole (5BPOA), 1,4-bis(4-aminophenoxy)benzene (TPEQ), and 4,4-[1,4-phenylbis(oxy)]bis[3-(trifluoromethyl)aniline] (FAPB). The aromatic dianhydride includes 1,2,4,5-benzenetetracarboxylic dianhydride (PMDA), 3,3,4,4-biphenyltetracarboxylic dianhydride (BPDA), 4,4-oxydiphthalic anhydride (ODPA), 3,3,4,4-benzophenonetetracarboxylic dianhydride (BTDA), 3,3,4,4-diphenylsulfonetetracarboxylic dianhydride (DSDA), 2,3,3,4-biphenyltetracarboxylic dianhydride (-BPDA), 4,4-hexafluoroisopropyl phthalic anhydride (6FDA) and 4,4-(4,4-isopropyldiphenoxy)diphthalic anhydride (BPADA).

[0017] The polyamic acid copolymer is subjected to chemical cyclization for imidization reaction, the dehydrating agent and the pyridine catalyst having the ortho substituent are added. The pyridine catalyst having the ortho substituent may have the following structure:

##STR00001##

[0018] At least one of R1 and R2 is a non-hydrogen substituent, and a number of moles of the pyridine catalyst having the ortho substituent is greater than or equal to a number of moles of the polyamic acid copolymer.

Testing Method

[0019] Elongation: Measurements are performed using a Hounsfield H10K-S tensile machine in accordance with ASTM D882.

First Embodiment

Manufacture of Polyamic Acid Copolymer

[0020] 42.972 grams of 2,2-bis(trifluoromethyl)benzidine (TFMB, 0.1342 mole, mole fraction 0.625 in diamine solution) is added to 412.5 grams of N,N-dimethylacetamide (DMAc), and after completely dissolving, 21.053 g of cyclobutane-1,2,3,4-tetracarboxylic (CBDA, 0.1074 mole, mole fraction 0.5 in anhydride) is added. The reaction is stirred for six hours and the temperature is maintained at 25 C.

[0021] 25.783 g of TFMB (0.0805 mole) is added to the solution and stirred until being fully dissolved. 47.691 g of 6FDA (0.1074 mole) is added, and the solution is stirred and reacted for a certain period of time, and then stirred for a certain time under a constant temperature of 25 C. to obtain a 25% solid content polyamic acid copolymer solution.

Manufacture of Polyimide Film

[0022] 57 g of the above polyamic acid copolymer solution is taken, and the solid content is diluted to 17.8% using N,N-dimethylacetamide (DMAc). 12.6 ml of acetic anhydride and 19.5 ml of 2-methylpyridine are added respectively, and after uniform stirring, the solution is coated on a glass plate with a scraper having a gap of 900 m. A coated sample is placed in a 50 C. oven for 20 minutes, slowly heated to 170 C. and then heated for 20 minutes. The temperature is raised to 260 C. and then heated for 20 minutes for final treatment to form a polyimide film.

[0023] The polyimide film obtained above has an elongation of 26%.

Second Embodiment

Manufacture of Polyamic Acid Copolymer

[0024] 20.100 grams of 2,2-bis(trifluoromethyl)benzidine (TFMB, 0.0627 mole, mole fraction 0.315 in diamine solution) is added to 412.5 grams of N,N-dimethylacetamide (DMAc), and after completely dissolving, 11.723 g of cyclobutane-1,2,3,4-tetracarboxylic (CBDA, 0.0598 mole, mole fraction 0.3 in anhydride) is added. The solution is stirred for six hours and the temperature is maintained at 25 C.

[0025] 43.711 g of TFMB (0.1365 mole) is added to the solution and stirred until fully dissolved. 61.965 g of 6FDA (0.1395 mole) is added, and the solution is stirred and reacted for a certain period of time, and then stirred for a certain time under a constant temperature of 25 C. to obtain a 25% solid content polyamic acid copolymer solution.

Manufacture of Polyimide Film

[0026] 57 g of the above polyamic acid copolymer solution is taken, and the solid content is diluted to 17.8% using N,N-dimethylacetamide (DMAc). 11.7 ml of acetic anhydride and 4 ml of 2-methylpyridine are added respectively, and after uniform stirring, the solution is coated on a glass plate with a scraper having a gap of 900 m. A coated sample is placed in a 50 C. oven for 20 minutes, slowly heated to 170 C. and then heated for 20 minutes. The temperature is raised to 260 C. and then heated for 20 minutes for final treatment to form a polyimide film.

[0027] The polyimide film obtained above has an elongation of 12%.

COMPARATIVE EXAMPLE 1

Manufacture of Polyamic Acid Copolymer

[0028] 42.972 grams of 2,2-bis(trifluoromethyl)benzidine (TFMB, 0.1342 mole, mole fraction 0.625 in diamine solution) is added to 412.5 grams of N,N-dimethylacetamide (DMAc), and after completely dissolving, 21.053 g of cyclobutane-1,2,3,4-tetracarboxylic (CBDA, 0.1074 mole, mole fraction 0.5 in anhydride) is added. The reaction is stirred for six hours and the temperature is maintained at 25 C.

[0029] 25.783 g of TFMB (0.0805 mole) is added to the solution and stir until fully dissolved. 47.691 g of 6FDA (0.1074 mole) is added, and the solution is stirred and reacted for a certain period of time, and then stirred for a certain time under constant temperature of 25 C. to obtain a 25% solid content polyamic acid copolymer solution.

Manufacture of Polyimide Film

[0030] 57 g of the above polyamic acid copolymer solution is taken, and the solid content is diluted to 17.8% using N,N-dimethylacetamide (DMAc). 12.6 ml of acetic anhydride and 4.3 ml of 3-methylpyridine are added respectively. After stirring, rapid gelation occurs, so that film formation is impossible.

COMPARATIVE EXAMPLE 2

Manufacture of Polyamic Acid Copolymer

[0031] 42.972 grams of 2,2-bis(trifluoromethyl)benzidine (TFMB, 0.1342 mole, mole fraction 0.625 in diamine solution) is added to 412.5 grams of N,N-dimethylacetamide (DMAc), and after completely dissolving, 21.053 g of cyclobutane-1,2,3,4-tetracarboxylic (CBDA, 0.1074 mole, mole fraction 0.5 in anhydride) is added. The reaction is stirred for six hours and the temperature is maintained at 25 C.

[0032] 25.783 g of TFMB (0.0805 mole) is added to the solution and stir until fully dissolved. 47.691 g of 6FDA (0.1074 mole) is added, and the solution is stirred and reacted for a certain period of time, and then stirred for a certain time under constant temperature of 25 C. to obtain a 25% solid content polyamic acid copolymer solution.

Manufacture of Polyimide Film

[0033] 57 g of the above polyamic acid copolymer solution is taken, and the solid content is diluted to 17.8% using N,N-dimethylacetamide (DMAc). The solution is coated on a glass plate with a scraper having a gap of 900 m. A coated sample is placed in a 50 C. oven for 20 minutes, slowly heated to 170 C. and then heated for 20 minutes. The temperature is raised to 260 C. and then heated for 20 minutes for final treatment to form a polyimide film.

[0034] The polyimide film obtained above has a physical property that is fragile, and it is impossible to measure its elongation.

COMPARATIVE EXAMPLE 3

Manufacture of Polyamic Acid Copolymer

[0035] 20.100 grams of 2,2-bis(trifluoromethyl)benzidine (TFMB, 0.0627 mole, mole fraction 0.315 in diamine solution) is added to 412.5 grams of N,N-dimethylacetamide (DMAc), and after completely dissolving, 11.723 g of cyclobutane-1,2,3,4-tetracarboxylic (CBDA, 0.0598 mole, mole fraction 0.3 in anhydride) is added. The reaction is stirred for six hours and the temperature is maintained at 25 C.

[0036] 43.711 g of TFMB (0.1365 mole) is added to the solution and stir until fully dissolved. 61.965 g of 6FDA (0.1395 mole) is added, and the solution is stirred and reacted for a certain period of time, and then stirred for a certain time under constant temperature of 25 C. to obtain a 25% solid content polyamic acid copolymer solution.

Manufacture of Polyimide Film

[0037] 57 g of the above polyamic acid copolymer solution is taken, and the solid content is diluted to 17.8% using N,N-dimethylacetamide (DMAc). The solution is coated on a glass plate with a scraper having a gap of 900 m. A coated sample is placed in a 50 C. oven for 20 minutes, slowly heated to 170 C. and then heated for 20 minutes. The temperature is raised to 260 C. and then heated for 20 minutes for final treatment to form a polyimide film.

[0038] The polyimide film obtained above has an elongation of 2%.

TABLE-US-00001 Experimental comparison table semi-aromatic polyamic acid film- aromatic forming elongation thickness polyamic acid catalyst ability % m Embodiment 1 CBDA TFMB 6FDA 2- 26 50 50 100 50 (mol %)methylpyridine Embodiment 2 CBDA TFMB 6FDA 2- 12 50 30 100 70 (mol %)methylpyridine Comparative CBDA TFMB 6FDA 3- X Example 1 50 100 50 (mol %)methylpyridine Comparative CBDA TFMB 6FDA (mol %) none embrittlement 50 Example 2 50 100 50 Comparative CBDA TFMB 6FDA (mol %) none 2 50 Example 3 30 100 70 X: Unable to form a film; : Able to form a film Pyridine catalyst with ortho substituent: 2-methylpyndme Pyridine catalyst without ortho substituent: 3-methylpyridine

[0039] The foregoing description of the exemplary embodiments of the disclosure has been presented only for the purposes of illustration and description and is not intended to be exhaustive or to limit the disclosure to the precise forms disclosed. Many modifications and variations are possible in light of the above teaching.

[0040] The embodiments were chosen and described in order to explain the principles of the disclosure and their practical application so as to enable others skilled in the art to utilize the disclosure and various embodiments and with various modifications as are suited to the particular use contemplated. Alternative embodiments will become apparent to those skilled in the art to which the present disclosure pertains without departing from its spirit and scope.