Thermosetting composition, hard coating film and color filter
A thermosetting and composite technology, applied in the field of electronic parts, can solve the problems of quality degradation and achieve excellent scratch resistance, excellent flatness, and improved display quality
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[0128] Next, the present invention will be specifically described through synthesis examples, examples, and comparative examples, but the present invention is not limited by these examples at all.
[0129] For each component, the compound used in the synthesis example, the example, and the comparative example is described.
[0130] Tetracarboxylic dianhydride:
[0131] 3,3',4,4'-Diphenyl ether tetracarboxylic dianhydride (hereinafter abbreviated as "ODPA")
[0132] 1,2,3,4-Butanetetracarboxylic dianhydride (hereinafter abbreviated as "BT-100")
[0133] Diamine:
[0134] 3,3'-Diaminodiphenylsulfone (hereinafter abbreviated as "DDS")
[0135] Polyhydroxy compound:
[0136] 1,4-butanediol
[0137] Monohydroxy compound:
[0138] Benzyl alcohol
[0139] Styrene-maleic anhydride copolymer:
[0140] Trade name SMA1000P, Sichuan Crude Oil Chemical Co., Ltd., hereinafter abbreviated as "SMA1000P"
[0141] Solvents used in the synthesis reaction of polyester amic acid (A):
[0142] Methyl 3-methoxypropion...
Synthetic example 1
[0168] [Synthesis example 1] Synthesis of polyester amic acid solution (A1)
[0169] In a four-necked flask equipped with a stirrer, the dehydrated purified MMP, ODPA, 1,4-butanediol, and benzyl alcohol were charged with the following weights, and stirred at 130°C for 3 hours under a stream of dry nitrogen.
[0170]
[0171] After that, the reacted solution was cooled to 25°C, 3,3'-diaminodiphenylsulfone (hereinafter abbreviated as "DDS") and MMP were put in the following weight, and stirred at 20°C to 30°C for 2 hours Then, it was stirred at 115°C for 1 hour.
[0172] DDS 29.33g
[0173] MMP 183.04g
[0174] [Z / Y=3.0, (Y+Z) / X=0.8]
[0175] The solution was cooled to room temperature to obtain a 30% by weight solution (A1) of a light yellow transparent polyester amic acid.
[0176] A part of the solution was sampled, and the weight average molecular weight was measured by GPC analysis (polystyrene standard). As a result, the weight average molecular weight of the obtained polyester amic...
Synthetic example 2
[0177] [Synthesis example 2] Synthesis of polyester amic acid solution (A2)
[0178] In a four-necked flask with a stirrer, the dehydrated and purified PGMEA, BT-100, SMA1000P, 1,4-butanediol, and benzyl alcohol were sequentially charged with the following weights, and stirred at 125°C under a stream of dry nitrogen for 3 hour.
[0179]
[0180] After that, the reacted 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 stirred at 125°C for 2 hours.
[0181] DDS 10.50g
[0182] PGMEA 57.69g
[0183] [Z / Y=2.7, (Y+Z) / X=0.9]
[0184] The solution was cooled to room temperature to obtain a 30% by weight solution (A2) of a light yellow transparent polyester amic acid.
[0185] A part of the solution was sampled, and the weight average molecular weight was measured by GPC analysis (polystyrene standard). As a result, the weight average molecular weight of the obtained polyester amic acid (A2) was 10,000.
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