Polyimide precursor composition, method for producing polyimide resin, and polyimide resin
A technology of polyimide precursor and polyimide resin, which is applied in the field of polyimide precursor composition, can solve the problems of high skin permeability, high biological toxicity burden, and large environmental burden, and achieve peelability Excellent, excellent coatability and storage stability, excellent solvent resistance and water resistance
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[0206] [Manufacturing method of polyimide precursor composition]
[0207] The preparation method of the polyimide precursor composition of this invention is not specifically limited, For example, it can prepare by implementing the 1st process and 2nd process of the manufacturing method of the polyimide resin of this invention mentioned later.
[0208] [Manufacturing method of polyimide resin]
[0209] The manufacturing method of the polyimide resin of this invention contains the following 1st process, 2nd process, and 3rd process.
[0210] In addition, the manufacturing method of the polyimide resin of this invention also includes using the polyimide precursor composition of this invention instead of the polyimide precursor composition prepared by carrying out a 1st process and a 2nd process. Manufacturing method of polyimide resin.
[0211] 〈The first process〉
[0212] In the first step, a cyclic unsaturated ether compound represented by the following formula (A) (hereinaf...
Embodiment 1
[0329]
[0330] 2,3,3,4-Biphenyltetracarboxylic acid (2.9 g) and water (35.0 g) were added to a detachable flask (100 mL; cylinder type) equipped with a stirrer, stirred and mixed at 25° C. for 10 minutes, and then 2,3-Benzofuran (1.0g) was added, and it stirred and mixed at 25 degreeC for 45 minutes, and obtained the aqueous dispersion liquid of the tetracarboxylic-acid derivative.
[0331] Styrene acrylic polyamine (manufactured by Nippon Shokubai Co., Ltd., Polyment (trademark) NK-200PM; non-volatile content 56% by mass, amine value 2.55mmol / g-solid; m=60) was added to the obtained aqueous dispersion ( 10.0 g), isophthalic acid dihydrazide (0.5 g), and stirred and mixed at 25° C. for 2 hours to obtain a milky white dispersion liquid (polyimide precursor composition) of a polyimide precursor.
Embodiment 2
[0333]
[0334] Water (35.3g) was used instead of water (35.0g), and 2,3-dihydrofuran (0.7g) was used instead of 2,3-benzofuran (1.0g), except that, as in Example 1 Similarly, a milky white dispersion liquid (polyimide precursor composition) of a polyimide precursor was obtained.
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