Silanol containing phosphazene compound, flame retardant, epoxy resin composition and composite metallic substrate
A technology of phosphazene compound and epoxy resin, applied in the field of flame retardant substances, can solve the problems of high cost, unfavorable popularization, etc., and achieve the effects of good heat resistance and excellent flame retardancy
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Embodiment 1
[0123]
[0124] Put 1 mol of hexachlorocyclotriphosphazene, 250 ml of acetone, and 3 mol of sodium methoxide into a three-port 2000 ml glass reactor with a stirring device, while stirring, while blowing nitrogen, while raising the temperature to 40 ° C, add 20% sodium hydroxide solution dropwise over 60 minutes 300g, keep the temperature at 45°C, stir and react for 10 hours, then add 3mol of dimethylsilanediol, continue to stir and react for 5 hours. After the reaction, the inorganic components and water in the system were removed by physical methods, and the solvent in the system was distilled off to obtain 1 mol of phosphazene compound with silanol, which was named A.
[0125] The obtained compound A is characterized by proton nuclear magnetic resonance spectrum, and the results are as follows:
[0126] 1 H NMR (CDCl 3 ,500MHz): δ5.0(m,3H,hydrogen on hydroxyl),3.42(s,9H,OC H 3 ),0.2(m,18H,Si-C H 3 ).
[0127] The position of the characteristic peak of the infrared ...
Embodiment 2
[0130]
[0131] Put 1 mol of hexachlorocyclotriphosphazene, 250 ml of acetone, and 1 mol of sodium methoxide into a three-port 2000 ml glass reactor with a stirring device, while stirring, while blowing nitrogen, while raising the temperature to 40 ° C, add 20% sodium hydroxide solution dropwise over 60 minutes 300g, keep the temperature at 45°C, stir and react for 6 hours, then add 5mol of trimethylsilanol, continue to stir and react for 8 hours. After the reaction, the inorganic components and water in the system were removed by physical methods, and the solvent in the system was distilled off to obtain 1 mol of phosphazene compound with silanol, which was named B.
[0132] The obtained compound B is characterized by proton nuclear magnetic resonance spectrum, and the results are as follows:
[0133] 1 H NMR (CDCl 3 ,500MHz):δ3.42(s,3H,OC H 3 ),0.1(m,45H,Si-C H 3 ).
[0134] The position of the characteristic peak of the infrared spectrum: the characteristic absorp...
Embodiment 3
[0137]
[0138] Put 1 mol of hexachlorocyclotriphosphazene, 250 ml of acetone, and 3 mol of sodium methoxide into a three-port 2000 ml glass reactor with a stirring device, while stirring, while blowing nitrogen, while raising the temperature to 40 ° C, add 20% sodium hydroxide solution dropwise over 60 minutes 300g, keep the temperature at 45°C, stir and react for 6 hours, then add 3mol of dimethylphenylsilanol, and continue to stir and react for 8 hours. After the reaction, the inorganic components and water in the system were removed by physical methods, and the solvent in the system was distilled off to obtain 1 mol of phosphazene compound with silanol, which was named C.
[0139] The obtained compound C is characterized by proton nuclear magnetic resonance spectrum, and the results are as follows:
[0140] 1 H NMR (CDCl 3 ,500MHz): δ7.3(m,15H,hydrogen on the benzene ring),3.42(s,9H,OC H 3 ),0.7(m,18H,Si-C H 3 ).
[0141] The position of the characteristic peak o...
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