Resin composition and molded article produced from the composition
A resin composition and compound technology, applied in information storage, instruments, optical recording heads, etc., can solve the problems of resin deterioration, difficulty in outdoor use, and decrease in transparency, and achieve deterioration suppression of optical properties, excellent weather resistance, and transparency excellent effect
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[0503] Hereinafter, the present invention will be further specifically described based on examples. First, synthesis examples of hindered amine compounds used in Examples will be described.
[0504] (Hindered Amine Compounds)
Synthetic example 1
[0506] Exemplary compound 1 shown in chemical formula [13] (N, N'-dibutyl-, N"-lauryl-N, N'-bis-(1,2,2,6,6-pentamethyl-4 Synthesis of -piperidin-4-yl)-[1,3,5]-triazine-2,4,6-triamine (LTABM))
[0507] [Chemical 55]
[0508]
[0509] (1) Synthesis of N-butyl-2,2,6,6-tetramethylpiperidin-4-amine (TABA)
[0510] 2,2,6,6-Tetramethyl-4-piperidone (TAA) 108.67g (0.7mol), butylamine 53.76g (0.735g), 2% platinum carbon (50% aqueous product) 2.52g It was poured into 163.0 g of methanol, and the reaction was performed at 50° C. for 2.5 hours at a hydrogen pressure of 0.3 MPa. After filtering the catalyst, solvent removal and distillation were performed to obtain 127.93 g of the title compound as a colorless transparent liquid.
[0511] (2) 2,4-bis(butyl(1,2,2,6,6-pentamethylpiperidin-4-yl)amino)-6-chloro-1,3,5-triazine (CTABM) Synthesis
[0512] TABA127.42g (0.6mol) and 96% sodium hydroxide 27.5g (0.66mol) are dropped in water 175g, after warming up to 60 DEG C, drop the cyanuri...
Synthetic example 2
[0517] Exemplary compound 2 shown in chemical formula [20] (N, N', N"-trilauryl-N, N'-bis-(2,2,6,6-tetramethylpiperidin-4-yl)- Synthesis of [1,3,5]-triazine-2,4,6-triamine (LTADA)
[0518] [Chemical 56]
[0519]
[0520] (1) Synthesis of N-dodecyl-2,2,6,6-tetramethyl-2-piperidin-4-amine (TADA)
[0521] 77.6g (0.5mol) of 2,2,6,6-tetramethyl-4-piperidone (TAA), 97.3g (0.525g) of laurylamine, 1.8g of 2% platinum carbon (50% aqueous product) It was poured into 116.4 g of methanol, and the reaction was performed at 50° C. for 2.5 hours at a hydrogen pressure of 0.3 MPa. After filtering the catalyst, the solvent was removed and distilled to obtain 152.8 g of the title compound as a yellowish liquid.
[0522] (2) 2,4-bis(dodecyl(2,2,6,6-tetramethylpiperidin-4-yl)amino)-6-chloro-1,3,5-triazine (CTADA) Synthesis
[0523] 10.0g (0.339mol) of TADA1 and 14.58g (0.35mol) of 96% sodium hydroxide were dropped into 65g of water, and after the temperature was raised to 60°C, 30.43g (0....
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