Printing and dyeing wastewater treatment method and preparation method of compound biological flocculant
A biological flocculant and treatment method technology, applied in the field of wastewater treatment, can solve problems such as threats to life and health, secondary pollution of drainage, insufficient stability, etc., and achieve the effects of good removal effect, low production cost, and easy production
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Embodiment 1
[0033] (1) Take 500mL of a certain biochemical printing and dyeing wastewater (COD about 142mg / L, T-P about 0.8mg / L, chroma about 100) in a beaker and place it on a magnetic stirrer;
[0034] (2) Turn on the agitator, add 0.5ml of composite biological flocculant solution, add biological flocculant (concentration 10mg / L) after about 30s, the dosage is 0.1ml, continue to stir for 30s;
[0035] (3) After the coagulation reaction, the beaker was left to stand for about 5 minutes, and the supernatant was taken to measure the COD of 64 mg / L, T-P of 0.25 mg / L, and chromaticity of 40.
Embodiment 2
[0037] (1) Take 500mL of a certain biochemical printing and dyeing wastewater (COD about 142mg / L, T-P about 0.8mg / L, chroma about 100) in a beaker and place it on a magnetic stirrer;
[0038] (2) Turn on the agitator, add 0.625ml of composite biological flocculant solution, add biological flocculant (concentration 10mg / L) after about 30s, the dosage is 0.1ml, continue to stir for 30s;
[0039] (3) After the coagulation reaction, the beaker was left to stand for about 5 minutes, and the supernatant was taken to measure the COD of 54 mg / L, T-P of 0.15 mg / L, and chromaticity of 30.
Embodiment 3
[0041] (1) The rice straw is added into the sodium hydroxide solution with a mass fraction of 1% according to the solid-to-liquid ratio of 1:8, reacted for later use, and the high-efficiency cellulose-degrading bacteria are inserted into the prepared material to complete the saccharification.
[0042] (2) Take 1000ml of straw saccharification solution, K 2 HPO 4 5g, KH 2 PO 4 2g, adjust the pH value to 7.5, and prepare the culture medium;
[0043] (3) Insert the floc-producing flora EM into the culture medium at a ratio of 1:10, put it into a constant temperature water bath shaker, set the temperature at 30°C, and cultivate for 3 days;
[0044] (4) centrifuging the obtained culture solution to separate the bacterial cells and the bacterial liquid. Collect the supernatant, concentrate the supernatant to 1 / 2 of the original volume, add 3 times the volume of 4°C absolute ethanol to the concentrated supernatant, and cool it for 24 hours. Pour off the liquid, retain the precip...
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