Flame retardant, composite flame retardant and flame retardant polymer material containing the composite flame retardant
A composite flame retardant and flame retardant polymer technology, applied in the field of flame retardant polymer materials, can solve the problems of poor compatibility, easy precipitation of aryl phosphonates, low flame retardant efficiency of flame retardants, etc., and achieve mild conditions , the preparation method is simple, the effect of reducing production cost
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Embodiment 1
[0100] Example 1 Zn(O 3 PH) 0.44 (O 3 PPh) 0.56 preparation of
[0101] Get 31.60 grams (0.20 moles) of phenylphosphonic acid and 16.40 grams (0.20 moles) of phosphorous acid and dissolve in 480 g of water, adjust to pH=11 with 5% sodium hydroxide aqueous solution, obtain mixed acid solution. Another 54.50 g (0.40 mol) of zinc chloride was dissolved in 545 g of water to obtain a zinc chloride solution.
[0102] With stirring at room temperature, the zinc chloride solution was slowly added dropwise to the mixed acid solution to obtain a large amount of white precipitate. The solvent was removed by suction filtration, and the obtained filter cake was washed with ethanol to obtain a white solid.
[0103] The resulting white solid was 31 P NMR test: Part of the white solid is completely dissolved in concentrated hydrochloric acid, and tested according to the aforementioned nuclear magnetic resonance test method, by the obtained 31 P NMR results showed that the ratio of phos...
Embodiment 2
[0113] Example 2 Zn(O 3 PH) 0.57 (O 3 PPh) 0.43 preparation of
[0114] Get 15.80 grams (0.10 moles) of phenylphosphonic acid and 12.30 grams (0.15 moles) of phosphorous acid and dissolve in 281 grams of water, adjust to pH=11 with 5% sodium hydroxide aqueous solution, obtain mixed acid solution. Another 34.08 grams (0.25 moles) of zinc chloride was dissolved in 340 grams of water to obtain a zinc chloride solution.
[0115] With stirring at room temperature, the zinc chloride aqueous solution was slowly added dropwise to the mixed acid solution to obtain a white precipitate. The solvent was removed by suction filtration, and the obtained filter cake was washed with ethanol to obtain a white solid. Then place it in a vacuum oven and dry it under vacuum at 120°C to obtain the product Zn(O 3 PH) 0.57 (O 3 PPh) 0.43 .
[0116] on the sample 31P NMR test: part of the gained white solid is dissolved in concentrated hydrochloric acid, and NMR test is carried out according...
Embodiment 3
[0118] Example 3 Zn(O 3 PH) 0.37 (O 3 PPh) 0.63 preparation of
[0119] Get 23.71 grams (mole) of phenylphosphonic acid and 8.20 grams (0.10 mole) of phosphorous acid and dissolve in 310 grams of water, adjust to pH=11 with 5% sodium hydroxide aqueous solution, obtain mixed acid solution. Another 34.08 grams (0.25 moles) of zinc chloride was dissolved in 340 grams of water to obtain a zinc chloride solution.
[0120] With stirring at room temperature, the zinc chloride aqueous solution was slowly added dropwise to the mixed acid solution to obtain a white precipitate. The solvent was removed by suction filtration, and the obtained filter cake was washed with ethanol to obtain a white solid. Then place it in a vacuum oven and dry it under vacuum at 120°C to obtain the product Zn(O 3 PH) 0.37 (O 3 PPh) 0.63 .
[0121] on the sample 31 P NMR test: the solid sample is dissolved in concentrated hydrochloric acid, and the NMR test is carried out according to the aforement...
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