A method for extracting m-aminobenzenesulfonic acid from dye intermediate waste water
A technology of m-aminobenzenesulfonic acid and dye intermediates, applied in chemical instruments and methods, preparation of organic compounds, organic chemistry and other directions, can solve the problems of increasing waste water treatment costs, waste of resources and the like, and achieves solutions to waste of resources and low cost. , the effect of stable process
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Embodiment a
[0025] S1a, adjust pH
[0026] Under continuous stirring, adding a mass concentration of 30% NaOH aqueous solution to 3487g (3L) m-aminobenzenesulfonic acid wastewater to adjust the wastewater pH to 10;
[0027] S2a, evaporation and concentration
[0028] Evaporate and concentrate the wastewater after pH adjustment of S1a to a solid content of about 40%. At this time, the temperature of the evaporation system is 108°C;
[0029] S3a, cooling and crystallization
[0030] After slowly cooling the evaporation system of S2a to room temperature, solid-liquid separation obtained 546 g of crude salt and 827 g of evaporated mother liquor;
[0031] S4a, frozen crystallization
[0032] The evaporated mother liquor obtained by solid-liquid separation of S3a was frozen at -5°C for 6 hours, and 19 g of frozen salt and 808 g of frozen mother liquor were obtained by solid-liquid separation;
[0033] S5a, acidification precipitation
[0034] Slowly add sulfuric acid aqueous solution with ...
Embodiment b
[0038] S1b, adjust pH
[0039] Under continuous stirring, mix the acidified mother liquor 776g and the refined mother liquor 328g with 3487g (3L) initial m-aminobenzenesulfonic acid wastewater in Example a, and add a NaOH aqueous solution with a mass concentration of 30% therein to adjust the pH of the wastewater to 10;
[0040] S2b, evaporation and concentration
[0041] Evaporate and concentrate the wastewater after adjusting the pH of S1b to a solid content of about 48%. At this time, the temperature of the evaporation system is 108.2°C;
[0042] S3b, cooling and crystallization
[0043] After slowly cooling the S2b evaporation system to room temperature, solid-liquid separation obtained 771 g of crude salt and 824 g of evaporated mother liquor;
[0044] S4b, frozen crystallization
[0045] The evaporated mother liquor obtained by solid-liquid separation of S3b was frozen at -5°C for 6 hours, and 21 g of frozen salt and 803 g of frozen mother liquor were obtained by soli...
Embodiment c
[0051] S1c, adjust pH
[0052] Under continuous stirring, 777g of the acidified mother liquor and 386g of the refined mother liquor in Example b were mixed uniformly with 3487g (3L) of the initial m-aminobenzenesulfonic acid wastewater, and the aqueous solution of NaOH with a mass concentration of 30% was added thereto to adjust the pH of the wastewater to 10;
[0053] S2c, evaporation and concentration
[0054] Evaporate and concentrate the waste water after pH adjustment by S1c to a solid content of about 52%. At this time, the temperature of the evaporation system is 108.5°C;
[0055] S3c, cooling and crystallization
[0056] After slowly cooling the evaporation system of S2c to room temperature, solid-liquid separation obtained 877g of crude salt and 816g of evaporated mother liquor;
[0057] S4c, frozen crystallization
[0058] The evaporated mother liquor obtained by solid-liquid separation of S3c was frozen at -5°C for 6 hours, and 16 g of frozen salt and 800 g of fr...
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