Prepolymer for flame-retardant wear-resistant material and application of prepolymer
A technology of wear-resistant materials and prepolymers, applied in the field of thermosetting shape memory polymers and recyclable polymers, can solve the problems of non-wear-resistant materials, waste of resources, environmental pollution, etc., and achieve good shape memory performance and remodeling Performance, simple synthesis process, outstanding effect of heat resistance
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preparation example Construction
[0029] The preparation method of the prepolymer for flame retardant wear-resistant material of the present invention is as follows:
[0030] (1) In the presence of quaternary ammonium salt, react 2-allylphenyl glycidyl ether with adipic acid to prepare bis(3-(2-allylphenoxy)-2-hydroxypropyl)hexyl Diacid ester;
[0031] (2) Stir and mix bis(3-(2-allylphenoxy)-2-hydroxypropyl) adipate, bismaleimide, zinc compound and filler system to obtain flame retardant and wear-resistant Prepolymer for materials; filler system includes epoxy resin, aluminum phosphate and alumina.
Synthetic example
[0033] 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 . In terms of mass, mix 120g 2-allylphenyl glycidyl ether, 40g adipic acid, 10g tetrabutylammonium bromide and 230g acetonitrile, and insulate and react at 70°C for 8h under stirring conditions; after the reac...
Embodiment 1
[0035] Example 1 Preparation of prepolymer for flame-retardant and wear-resistant materials
[0036] 50g N, N'-4,4'-diphenylmethanebismaleimide, 73.41g bis(3-(2-allylphenoxy)-2-hydroxypropyl) adipate and 6.29 g (22.3 mmol) of zinc acetylacetonate hydrate and 6 g of filler system were mixed, stirred and pre-polymerized at 130°C for 90 minutes to obtain a prepolymer for flame-retardant and wear-resistant materials, and samples were taken for DSC testing.
[0037] Cool the above-mentioned prepolymer for flame retardant and wear-resistant materials to room temperature, put it into the preheated mold at 150°C, and perform hot pressing and post-treatment according to the following process: 150°C / 1 h / 1MPa+180°C / 2 h / 3MPa +200 ℃ / 1.5 h / 5MPa+220 ℃ / 1.5 h / 5MPa and 240 ℃ / 2 h; demold after natural cooling to obtain a flame retardant and wear-resistant material. Test TG, DMA, oxygen index and wear resistance.
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