Removal of environmental pollutant tetrabro-bisphenol A
An environmental pollutant, tetrabromobisphenol technology, applied in the field of environmental restoration, to achieve the effect of easy formation of large-scale production, wide application prospects, and realization of recycling
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Embodiment 1
[0014] Example 1: In a 500 ml three-necked flask, install a thermometer and a stirrer, add tetrabromobisphenol A (1.0 mmol, 624 mg), Ni-Al alloy (10 g), water (100 ml), and then start stirring Heat to 90°C. A 1% aqueous sodium carbonate solution (100 mL) was added dropwise over 1 hour. The reaction temperature is controlled to be 90°C-100°C. After the dropwise addition of the 1% sodium carbonate aqueous solution was completed, the mixture was further stirred at the same temperature for 5 hours. Then, it was cooled to room temperature, filtered, insoluble matter was removed by filtration, the aqueous solution was extracted with ethyl acetate, the organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. Then, the concentrated product was analyzed by high pressure liquid chromatography, and the conversion rate of tetrabromobisphenol A was 100%.
Embodiment 2
[0015] Example 2: In a 500 ml three-necked flask, install a thermometer, a stirrer, tetrabromobisphenol A (1.0 mmol, 624 mg), Ni-Al alloy (8 g), water (100 ml), and then start stirring and heating to 90°C. A 2% aqueous potassium carbonate solution (100 mL) was added dropwise over 2 hours. The reaction temperature is controlled to be 90°C-100°C. After the dropwise addition of the 2% potassium carbonate aqueous solution was completed, the mixture was further stirred at the same temperature for 4 hours. Then, it was cooled to room temperature, filtered, insoluble matter was removed by filtration, the aqueous solution was extracted with ethyl acetate, the organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. Then, the concentrated product was analyzed by high pressure liquid chromatography, and the conversion rate of tetrabromobisphenol A was 100%.
Embodiment 3
[0016] Example 3: In a 500 ml three-necked flask, install a thermometer and a stirrer, add tetrabromobisphenol A (1.0 mmol, 624 mg), Ni-Al alloy (2 g), water (100 ml), and then start stirring Heat to 90°C. Aqueous 0.2% sodium carbonate solution (100 mL) was added dropwise over 1 hour. The reaction temperature is controlled to be 90°C-100°C. After the dropwise addition of the 0.2% sodium carbonate aqueous solution was completed, the mixture was further stirred at the same temperature for 6 hours. Then, it was cooled to room temperature, filtered, insoluble matter was removed by filtration, the aqueous solution was extracted with ethyl acetate, the organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. Then, the concentrated product was analyzed by high pressure liquid chromatography, and the conversion rate of tetrabromobisphenol A was 100%.
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