Prepolymer for high performance friction materials and application of prepolymer
A friction material and prepolymer technology, applied in the field of thermosetting shape memory polymers and recyclable polymers, to achieve the effects of good shape memory performance and remodeling performance, low energy consumption, and simple synthesis process
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preparation example Construction
[0027] The preparation method of the high-performance friction material prepolymer of the present invention is as follows:
[0028] (1) In the presence of quaternary ammonium salt, 2-allylphenyl glycidyl ether is reacted with terephthalic acid to prepare bis(3-(2-allylphenoxy)-2-hydroxypropyl) terephthalates;
[0029] (2) Stir and mix bis(3-(2-allylphenoxy)-2-hydroxypropyl) terephthalate, bismaleimide, zinc compound, and filler system to obtain high performance Prepolymers for friction materials; filler systems include epoxy resin, aluminum phosphate and aluminum oxide.
[0030] The high-performance friction material prepolymer is subjected to hot-press curing and post-treatment to obtain a high-performance friction material.
Synthetic example
[0032] By mass, 120g of 2-allylphenol, 140g of sodium hydroxide, 10g of tetrabutylammonium bromide and 230g of tetrahydrofuran were mixed, and the reaction was kept at 35°C and stirred for 1.5h to obtain solution A; Slowly add 270 g of epichlorohydrin dropwise, and keep stirring at 35°C for 6 h; after the reaction, vacuum rotary evaporation to remove 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 a chromatographic column to obtain a yellow transparent liquid, which is 2-allylphenyl acetonitrile Glyceryl ether, the yield is about 93%, and its reaction formula and 1 H-NMR see attached figure 1 and 2 . By mass, 120g of 2-allylphenyl glycidyl ether, 45g of terephthalic acid, 10g of tetrabutylammonium bromide and 230g of acetonitrile were mixed, and the reaction was kept at 70°C under stirring conditions...
Embodiment 1
[0034] Example 1 Preparation of prepolymer for high performance friction material
[0035] 50g N, N'-4,4'-diphenylmethane bismaleimide, 76.17g bis(3-(2-allylphenoxy)-2-hydroxypropyl) terephthalate It was mixed with 6.29g (22.3mmol) of zinc acetylacetonate hydrate and 5.5g of filler system, and prepolymerized under stirring for 90min at 130°C to obtain a prepolymer for high-performance friction materials, which was sampled and tested for DSC.
[0036] The above-mentioned high-performance friction material prepolymer was cooled to room temperature and then added to the mold preheated at 150 °C, and hot pressed and post-treated 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; after natural cooling, demoulding was performed to obtain high-performance friction materials, and TG, DMA, oxygen index and wear resistance were tested.
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