Remoldable shape memory bismaleimide resin and application thereof
A maleimide resin, bismaleimide technology, applied in the field of thermosetting shape memory polymers and recyclable polymers, can solve the problems of poor heat resistance, poor mechanical properties, and limitations of remodelable thermosetting SMPs , to achieve the effects of outstanding heat resistance, good shape memory performance, and good remodeling performance
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Embodiment 1
[0056] 1) Preparation of 2-allylphenyl glycidyl ether
[0057] On a mass basis, mix 120g of 2-allylphenol, 140g of sodium hydroxide, 10g of tetrabutylammonium bromide and 230g of tetrahydrofuran, and insulate and react at 35°C for 1.5h under stirring conditions to obtain solution A; Slowly add 270 g of epichlorohydrin dropwise, and keep stirring at 35° C. for 6 hours to react; after the reaction, vacuum rotary evaporation removes tetrahydrofuran and epichlorohydrin to obtain a crude product. The crude product was washed successively with saturated ammonium chloride solution (200 mL×2), deionized water (200 mL×2), and finally separated and purified by chromatography to obtain a yellow transparent liquid, namely 2-allylphenyl Glyceryl ether, the yield is about 93%, its reaction formula and 1 H-NMR see attached figure 1 and 2 .
[0058] 2) Preparation of bis(3-(2-allylphenoxy)-2-hydroxypropyl)adipate
[0059] In terms of mass, mix 120g 2-allylphenyl glycidyl ether, 40g adipi...
Embodiment 2
[0098] 1) Preparation of 2-allylphenyl glycidyl ether
[0099] On a mass basis, mix 120g of 2-allylphenol, 100g of sodium hydroxide, 5g of tetramethylammonium bromide and 200g of tetrahydrofuran, and insulate and react for 1 hour at 25°C with stirring to obtain solution A; 250 g of epichlorohydrin was added dropwise, and the mixture was stirred and reacted at 25° C. for 6 hours; after the reaction was completed, tetrahydrofuran and epichlorohydrin were removed by vacuum rotary evaporation to obtain a crude product. The crude product was washed successively with saturated ammonium chloride solution (200 mL×2), deionized water (200 mL×2), and finally separated and purified by chromatography to obtain a yellow transparent liquid, namely 2-allylphenyl Glyceryl ether, the yield is about 90.1%.
[0100] 2) Preparation of bis(3-(2-allylphenoxy)-2-hydroxypropyl)adipate
[0101] By mass, mix 120g of 2-allylphenyl glycidyl ether, 36g of adipic acid, 5g of tetramethylammonium bromide a...
Embodiment 3
[0107] 1) Preparation of 2-allylphenyl glycidyl ether
[0108] On a mass basis, mix 120g of 2-allylphenol, 125g of sodium hydroxide, 7.5g of tetrabutylammonium bromide and 250g of tetrahydrofuran, and insulate and react at 35°C for 1.5h under stirring conditions to obtain solution A; 300g of epichlorohydrin was slowly added dropwise, and the reaction was carried out at 35° C. with stirring for 8 hours; after the reaction was completed, tetrahydrofuran and epichlorohydrin were removed by rotary evaporation under vacuum to obtain a crude product. The crude product was washed successively with saturated ammonium chloride solution (200 mL×2), deionized water (200 mL×2), and finally separated and purified by chromatography to obtain a yellow transparent liquid, namely 2-allylphenyl Glyceryl ether, the yield is about 91.7%.
[0109] 2) Preparation of bis(3-(2-allylphenoxy)-2-hydroxypropyl)adipate
[0110] By mass, 120g of 2-allylphenyl glycidyl ether, 42g of adipic acid, 7.5g of t...
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