Polyvinyl alcohol acetal aromatic aldehyde grafting glycidyl azide polymer, preparation method thereof and application thereof
A polyvinyl aromatic acetal and polyvinyl alcohol condensation technology, which is applied in the field of energetic polymers and their preparation, can solve the problems of poor compatibility between TNT and polyurethane, limit the application of molten-cast explosives, reduce the detonation energy of explosives, and the like. Good development potential and market prospects, easy separation and purification, simple and convenient preparation methods
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Embodiment 1
[0023] A 250 mL four-necked flask equipped with a mechanical stirring rod, a reflux condenser and a thermometer was filled with dry argon, and 20 mL of dry DMAc solution, 4.40 g of toluene diisocyanate and 0.30 g of DBTDL were added, the temperature was raised to 60 °C, and the Add the DMAc solution of GAP with an average molecular weight of 700 (10.00 g GAP dissolved in 40 mL dry DMAc) drop by drop under stirring conditions, stir and react at 60°C for 4 hours, and then add polyvinyl acetalization with a degree of acetalization of 60%. DMAc solution of formaldehyde (10.00 g polyvinyl benzal dissolved in 60 mL dry DMAc), continue to stir for 48 hours, after the reaction, pour the reaction solution into 1500 mL distilled water, a large amount of solids precipitated, filtered The obtained solid was washed 3 times with 500 mL of water, and then vacuum-dried at 40 °C to obtain 23.60 g of polyvinyl benzal grafted polyazide glycidyl ether. The infrared spectrum of the product is shown...
Embodiment 2
[0025] A 250 mL four-neck flask equipped with a mechanical stirring rod, a reflux condenser and a thermometer was filled with dry argon, and 20 mL of dry DMAc solution, 0.87 g of toluene diisocyanate and 0.20 g of DBTDL were added, and the temperature was raised to 60 °C, and the Add the DMAc solution of GAP with an average molecular weight of 4000 (10.00 g GAP dissolved in 40 mL dry DMAc) drop by drop under stirring conditions, stir and react at 60°C for 3 hours, and then add polyvinyl alcohol acetalization with a degree of acetalization of 80%. The DMAc solution of nitrobenzaldehyde (10.00 g of polyvinyl m-nitrobenzaldehyde dissolved in 60 mL of dry DMAc), continued stirring for 36 hours, after the reaction was completed, the reaction solution was poured into 1500 mL of distilled water. A large amount of solids precipitated, and after filtering, the obtained solids were washed 3 times with 500 mL of water, and then vacuum-dried at 40 °C to obtain 20.20 g of polyvinyl m-nitrob...
Embodiment 3
[0027] A 250 mL four-necked flask equipped with a mechanical stirring rod, a reflux condenser and a thermometer was filled with dry argon, and 20 mL of dry DMAc solution, 0.35 g of toluene diisocyanate and 0.20 g of DBTDL were added, and the temperature was raised to 70 °C, and the Add the DMAc solution of GAP with an average molecular weight of 10,000 (10.00 g GAP dissolved in 60 mL dry DMAc) drop by drop under stirring conditions, stir and react at 70°C for 2 hours, and then add polyvinyl alcohol acetalization with a degree of acetalization of 80%. DMAc solution of nitrobenzaldehyde (10.00 g of polyvinyl p-nitrobenzaldehyde dissolved in 60 mL of dry DMAc), continued to stir for 24 hours, after the reaction, poured the reaction solution into 1500 mL of distilled water, there was A large amount of solids precipitated, and after filtration, the obtained solids were washed with 500 mL of water for 3 times, and then vacuum-dried at 40 °C to obtain 19.80 g of polyvinyl p-nitrobenza...
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