Modified organosilicon polymer, preparation method and applications thereof
A technology of organosilicon and polymers, applied in the field of modified organosilicon polymers, which can solve the problems of difficult adhesion of marine organisms, limited antifouling effect of antifouling coatings, complex growth mechanism of marine organisms, etc., and achieves low cost and good anti-fouling Stain effect, the effect of convenient synthesis method
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Embodiment 1
[0046] Step 1: In a 500ml round bottom flask, add 44.8g of bis(2-hydroxyethoxy)propyl-terminated polydimethylsiloxane (molecular weight 5300), 2.24g of 4,4'-azobis(4-cyano pentyl valeric acid), 0.96g catalyst 4-dimethylaminopyridine-p-toluenesulfonic acid, 5.00g dehydrating agent N, N'-dicyclohexylcarbodiimide, 150g dichloromethane, 30gDMF, stirring reaction at room temperature for 24h, After the reaction is finished, the precipitate is removed by filtration, and methanol is added to the filtrate to generate a precipitate, and the precipitate is dried at room temperature and under vacuum conditions to obtain the organosilicon macromolecular initiator [ 1 H NMR (CDCl 3 , 400MHz): δ0.1(s, (CH 3 ) 2 Si), 0.6(m, Si-CH 2 ), 1.6-1.7 (s, NC-CH 3 ), 3.5-3.7 (m, -CH 2 -O-CH 2 ), 4.3 (-CH 2 -O-C(=O))];
[0047] Step 2: Add 29.60g of silicone macroinitiator, 31.40g of dimethylaminoethyl methacrylate, 28.8g of 2-carboxyethyl acrylic acid ester, 120g of toluene and 120g of ethanol ...
Embodiment 2
[0050] Step 1: In a 500ml round bottom flask, add 44.8g of bis(2-hydroxyethoxy)propyl-terminated polydimethylsiloxane (molecular weight 10600), 3.36g of 4,4'-azobis(4-cyano pentyl valeric acid), 1.44g catalyst 4-dimethylaminopyridine-p-toluenesulfonic acid, 6.00g dehydrating agent N, N'-dicyclohexylcarbodiimide, 150g dichloromethane, stirred and reacted for 24h at room temperature, and the reaction ended Afterwards, the precipitate is removed by filtration, methanol is added to the filtrate to form a precipitate, and the precipitate is dried at room temperature and under vacuum conditions to obtain an organosilicon macromolecular initiator. [ 1 H NMR (CDCl 3 , 400MHz): δ0.1(s, (CH 3 ) 2 Si), 0.6(m, Si-CH 2 ), 1.6-1.7 (s, NC-CH 3 ), 3.5-3.7 (m, -CH 2 -O-CH 2 ), 4.3 (-CH 2 -O-C(=O))]
[0051] Step 2: Add 29.60g of silicone macroinitiator, 31.40g of dimethylaminoethyl methacrylate, 28.8g of 2-carboxyethyl acrylic acid ester, and 240g of toluene into a 500ml four-neck fla...
Embodiment 3
[0054] Step 1: In a 500ml round bottom flask, add 44.8g of bis(2-hydroxyethoxy)propyl-terminated polydimethylsiloxane (molecular weight 5300), 2.24g of 4,4'-azobis(4-cyano pentyl valeric acid), 0.96g catalyst 4-dimethylaminopyridine-p-toluenesulfonic acid, 5.00g dehydrating agent N, N'-dicyclohexylcarbodiimide, 150g dichloromethane, 30gDMF, stirring reaction at room temperature for 24h, After the reaction is completed, the precipitate is removed by filtration, methanol is added to the filtrate to form a precipitate, and the precipitate is dried at room temperature under vacuum conditions to obtain an organosilicon macromolecular initiator. [ 1 H NMR (CDCl 3 , 400MHz): δ0.1(s, (CH 3 ) 2 Si), 0.6(m, Si-CH 2 ), 1.6-1.7 (s, NC-CH 3 ), 3.5-3.7 (m, -CH 2 -O-CH 2 ), 4.3 (-CH 2 -O-C(=O))].
[0055] Step 2: Add 29.60g of silicone macroinitiator, 47.10g of dimethylaminoethyl methacrylate, 14.40g of 2-carboxyethyl acrylic acid ester, 120g of toluene and 120g of ethanol into a 50...
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