Thermosetting composition, hardened film, color filter sheet, liquid crystal display device, and touch screen device
A technology of thermosetting and composition, applied in the field of electronic parts, can solve the problems of low dielectric property and loss tangent that have not yet been developed, and achieve display quality and reliability improvement, high practicability, and low dielectric loss Tangent effect
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[0170] Next, the present invention will be specifically described by way of synthesis examples, examples, and comparative examples, but the present invention is not limited by these examples.
[0171] First, the solution of polyesteramic acid (A1) - polyesteramic acid (A4) and polyesteramic acid (A5) containing the reaction product of tetracarboxylic dianhydride, diamine, and polyhydric hydroxyl compound is synthesize|combined as follows.
Synthetic example A-1
[0172] [Synthesis Example A-1] Preparation of a Solution of Polyester Amic Acid (A1)
[0173] In a four-necked flask with a stirrer, dehydrated and purified methyl 3-methoxy propionate (methyl 3-methoxy propionate, hereinafter abbreviated as "MMP"), 3, 3', 3, 3', 4,4'-diphenylether tetracarboxylic dianhydride (3,3',4,4'-diphenylether tetracarboxylic dianhydride, hereinafter abbreviated as "ODPA"), 1,4-butanediol, and benzyl alcohol, Stirring was carried out at 125° C. for 2 hours under a stream of dry nitrogen (first stage of synthesis).
[0174]
[0175] Thereafter, the reaction solution was cooled to 25°C, and 3,3'-diaminodiphenyl sulfone (diaminodiphenyl sulfone, hereinafter abbreviated as "DDS") and MMP were added by the following weight, and the reaction was carried out at 20°C to 30°C. After stirring for 2 hours, stirring was performed at 125° C. for 1 hour (second stage of synthesis).
[0176] DDS 3.26g
[0177] MMP 21.00g
[0178] The solution was cooled to room...
Synthetic example A-2
[0179] [Synthesis Example A-2] Preparation of a Solution of Polyester Amic Acid (A2)
[0180] In a four-necked flask with a stirrer, dehydrated and purified propylene glycol monomethyl ether acetate (propylene glycol monomethyl ether acetate, hereinafter abbreviated as "PGMEA"), 1, 2, 3 , 4-butane tetracarboxylic dianhydride (1,2,3,4-butane tetracarboxylic dianhydride, hereinafter abbreviated as "BT-100"), SMA-1000P (trade name; styrene-maleic anhydride copolymer (Chuanyuan Petrochemical Co., Ltd.), 1,4-butanediol, and benzyl alcohol were stirred for 2 hours at 125° C. under a dry nitrogen stream (the first stage of synthesis).
[0181]
[0182] Thereafter, the reaction solution was cooled to 25° C., DDS and PGMEA were charged in the following weights, and stirred at 20° C. to 30° C. for 2 hours, and then at 125° C. for 1 hour (synthesis second stage).
[0183] DDS 1.20g
[0184] PGMEA 16.51g
[0185] The solution was cooled to room temperature to obtain a 30% by weight ...
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