Preparation method of supermolecular intercalated structure light-ageing-resistant material
A supramolecular intercalation and anti-photoaging technology, which is applied in the field of preparation of anti-photoaging materials, can solve the problems that the utilization rate of hindered amine light stabilizers does not exceed 40%, it is difficult to control the amount of intercalation, and it is difficult to recycle. The effect of industrial production, mild conditions and less dosage
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Embodiment 1
[0026] Step A: Weigh 1.5g (5.0mmol) Mg(NO 3 ) 2 .6H 2 O and 0.938g (2.5mmol) Al(NO 3 ) 3 .9H 2 O dissolved in 30ml to remove CO 2 salt solution in deionized water. Weigh 0.6g NaOH and 0.825g (5.0mmol) 2-hydroxyl-4-methoxybenzophenone-5-sodium sulfonate and dissolve in 30ml of deionized water in addition to carbon dioxide to form a mixed solution. With stirring, the mixed solution was added to the above-prepared salt solution to mix and react to form a precipitate. The formed precipitate was crystallized at 95°C for 6 hours. After the crystallization was completed, the formed precipitate was centrifuged and washed 3 times, and the wet filter cake was retained.
[0027] Step B: Add 120 ml of deionized water to the wet filter cake retained in step A to prepare a slurry. Weigh 1.18g (2.5mmol) 2-(sodium benzenesulfonate-4-amino)-4-(2,2,6,6-tetramethyl-4-piperidinylamino)-6-ammonia-1,3 , 5-triazine was added to the slurry, and then the precipitate was placed in a water bath ...
Embodiment 2
[0030] Step A: Weigh 2.25g (7.5mmol) Mg(NO 3 ) 2 .6H 2 O and 0.938g (2.5mmol) Al(NO 3 ) 3 .9H 2 O dissolved in 40ml to remove CO 2 salt solution in deionized water. Weigh 0.8g NaOH and 0.8g (5.0mmol) sodium salicylate and dissolve in 30ml deionized water decarbonated to form an alkaline solution. Under nitrogen protection and stirring, the alkali solution was added to the above salt solution to react to form a precipitate, which was crystallized at 80°C for 7 hours. After the crystallization, the formed precipitate was centrifuged and washed 4 times, and the wet filter cake was retained.
[0031] Step B: Add 120 ml of deionized water to the wet filter cake retained in step A to prepare a slurry. Weigh 0.0593g (0.25mmol) sodium 1,2,2,6,6-pentamethylpiperidine-4-oxyacetate and add it to the slurry, then place the precipitate in a water bath at 30°C for 6 hours, after the reaction The reaction product was centrifuged and washed 6 times, and the centrifuged product was dri...
Embodiment 3
[0034] Step A: Weigh 3g (10.0mmol) Mg(NO 3 ) 2 .6H 2 O and 0.938g (2.5mmol) Al(NO 3 ) 3 .9H 2 O dissolved in 45ml to remove CO 2 salt solution in deionized water. Weigh 1g NaOH and 0.3978g (2.5mmol) sodium p-aminobenzoate and dissolve in 45ml of carbon dioxide-deionized deionized water and a mixed solvent of ethylene glycol to form a mixed solution. Under the protection of nitrogen and stirring, the mixed solution was added to the above salt solution and mixed to form a precipitate. The formed precipitate was crystallized at 100°C for 5 hours. After the crystallization, the formed precipitate was centrifuged and washed 6 times, and the wet filter cake was retained. .
[0035] Step B: The wet filter cake retained in Step A was added to 120 ml of deionized water to remove carbon dioxide to prepare a slurry. Weigh 0.0588g (0.25mmol) sodium 2,2,6,6-tetramethylpiperidine-4-aminopropionate and add it to the slurry, then place the precipitate in a water bath at 40°C for 5 hou...
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