Preparation method of imidazole-containing cationic antistatic polyurethane
A technology containing imidazolium cations and ions, which is applied in the field of polymer material preparation and can solve problems such as static electricity accumulation, affecting product quality, and disasters
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[0035] Example 1
[0036] Take 30 g of imidazole (441 mmol) in a flask, dissolve the imidazole with 882 mmol of methanol, add 37.96 g (441 mmol) of methyl acrylate after the imidazole is completely dissolved, stir and react at 0 ℃ for 72 h, and distill off the methanol under reduced pressure Solvent and excess methyl acrylate give imidazole methyl ester derivatives.
[0037] The obtained methylated imidazole and 54.68 g (441 mmol) of 2-bromoethanol were dissolved in 882 mmol of acetone, and reacted at a temperature of 60 ℃ for 1 h. The acetone solvent and excess 2-bromoethanol were removed by distillation under reduced pressure to obtain hydroxyl-terminated methyl Esterified imidazole ionic liquid. Take 11.67 g (50 mmol) hydroxyl-terminated methyl ester imidazole ionic liquid and 50 g (25 mmol) polyethylene glycol with a molecular weight of 1000 to react with stirring at 200 ℃ for 1 h to obtain a dihydroxy-terminated imidazole cationic antistatic polyether Dihydric alcohol.
[003...
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[0039] Example 2
[0040] Take 47 g (691 mmol) of imidazole and place it in the flask. Dissolve the imidazole with 41 mol of methanol. After the imidazole is completely dissolved, add 442 g (3455 mmol) of butyl acrylate. Stir and react at 70 ℃ for 1 h. Distill under reduced pressure to remove the methanol. Solvent and excess butyl acrylate to obtain imidazole butyl esterified derivative.
[0041] The obtained butyl esterified imidazole was dissolved in 41 mol acetone with 428.48 g (3455 mmol) 2-bromoethanol, and reacted at a temperature of 0 ℃ for 72 h. The acetone solvent and excess 2-bromoethanol were removed by distillation under reduced pressure to obtain hydroxy-terminated butyl Esterified imidazole ionic liquid. Take 25 g (90 mmol) of hydroxy-terminated imidazole ionic liquid and 90 g (45 mmol) of hydroxy-terminated polycaprolactone with a molecular weight of 4000, stir and react at a temperature of 80 ℃ for 42 h, to obtain a dihydroxy-terminated imidazole cationic Antistat...
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[0043] Example 3
[0044] Take 20 g of imidazole (294 mmol) in a flask, dissolve the imidazole with 1.2 mol of methanol, add 45.1 g (352 mmol) of butyl acrylate after the imidazole is completely dissolved, stir and react at 45 ℃ for 56 h, and distill under reduced pressure to remove the methanol Solvent and excess butyl acrylate to obtain imidazole butyl esterified derivative.
[0045] The obtained butyl esterified imidazole and 44.7 g (361 mmol) 2-bromoethanol were dissolved in 1.31 mol of acetone, and reacted at a temperature of 30°C for 40 h. The acetone solvent and excess 2-bromoethanol were removed by distillation under reduced pressure to obtain hydroxy-terminated butyl ester. Chemical imidazole ionic liquid. Take 35 g (127 mmol) of hydroxy-terminated imidazole ionic liquid and 63.5 g (63.5 mmol) of double-ended hydroxy-polycaprolactone with a molecular weight of 1000 to react with stirring at a temperature of 160 ℃ for 10 h to obtain a bis-hydroxy-terminated imidazole catio...
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