Polyphosphazene-ether amide material and preparation method thereof
A technology of ether amide and polyphosphazene, which is applied in the field of polyphosphazene-ether amide materials and its preparation, can solve the problems of single material solubility and harsh processing and preparation technology, and achieve good thermal stability, good solubility, good The effect of flame retardancy
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Embodiment 1
[0025] The synthesis of polyphosphazene-ether amide material is realized through the following steps:
[0026] (1) In a 500mL three-neck flask equipped with magnetic rotor stirring, condenser and thermometer, dissolve hexachlorocyclotriphosphazene (17.4g 0.05mol) prepared by multiple sublimation in 50mL tetrahydrofuran (THF) solvent, add dropwise Prepared (2.32g 0.2mol) sodium phenate (under nitrogen protection, (4.6g 0.2mol) sodium metal and (18.822g 0.2mol) phenol reacted in 50mL THF solution at 25°C for 2 hours) THF solution, nitrogen Protected and reacted at 40°C for 12 hours. THF was removed by rotary distillation, washed several times with deionized water, and vacuum-dried at 50°C for 24 hours to obtain a milky white colloid.
[0027] (2) In a 500mL three-neck flask equipped with a magnetic rotor stirring, a condenser, and an HCl absorption device, dissolve the (10.37g 0.018mol) milky white colloid obtained in step (1) in 100mL THF solvent, and add (8g 0.04mol) of 4,4'...
Embodiment 2
[0030] The synthesis of polyphosphazene-ether amide material is realized through the following steps:
[0031] (1) In a 500mL three-neck flask equipped with magnetic rotor stirring, condenser and thermometer, dissolve hexachlorocyclotriphosphazene (13.9g 0.04mol) prepared by multiple sublimation in 50mL tetrahydrofuran (THF) solvent, add dropwise Prepared (1.856g 0.16mol) sodium phenate (under nitrogen protection, (3.68g 0.16mol) metal sodium and (15.06g 0.16mol) phenol reacted in 50mL THF solution at 25°C for 2 hours) THF solution, nitrogen Protected and reacted at 40°C for 12 hours. THF was removed by rotary distillation, washed several times with deionized water, and vacuum-dried at 50°C for 24 hours to obtain a milky white colloid.
[0032] (2) In a 500mL three-neck flask equipped with a magnetic rotor stirring, a condenser, and an HCl absorption device, dissolve the (11.52g 0.02mol) milky white colloid obtained in step (1) in 50mL of THF solvent, and add (8g 0.04mol) of...
Embodiment 3
[0035] The synthesis of polyphosphazene-ether amide material is realized through the following steps:
[0036] (1) In a 500mL three-neck flask equipped with magnetic rotor stirring, condenser and thermometer, hexachlorocyclotriphosphazene prepared by multiple sublimation (34.8g 0.1mol) was dissolved in 100mL tetrahydrofuran (THF) solvent, and added dropwise Prepared (9.28g 0.4mol) sodium phenate (prepared by reacting (9.2g 0.4mol) metal sodium and (37.64g 0.4mol) phenol in 100mL THF solution at 25°C for 2 hours under nitrogen protection) THF solution, nitrogen Protected and reacted at 40°C for 24 hours. THF was removed by rotary distillation, washed several times with deionized water, and vacuum-dried at 50°C for 24 hours to obtain a milky white colloid.
[0037] (2) In the 500mL three-necked flask equipped with magnetic rotor stirring, condenser tube, and HCl absorption device, the (28.81g 0.05mol) milky white colloid obtained in step (1) was dissolved in 100mL THF solvent, an...
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