A kind of synthetic method of biological preparation for enriching nitrate content in micro-polluted water body
A technology of nitrate content and biological preparations, applied in chemical instruments and methods, biological water/sewage treatment, water/sludge/sewage treatment, etc., can solve the problems of secondary pollution, incomplete removal, difficult operation and management, etc. Achieve the effect of no secondary pollution, low equipment cost and low operating cost
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example 1
[0031] Take 5g of Houttuynia cordata, 10g of sweet potato vine, and 5g of kudzu vine and crush them in a Webster blender, add 10mL of absolute ethanol, pass through the chromatography column, use calcium carbonate particles as the stationary phase, and acetone as the mobile phase to separate and extract chlorophyll a and bacteriochlorophyll mixture; put the above mixture in a 50mL stoppered colorimetric tube, place it in a constant temperature water bath at 60°C for 1.5h, add 1g protein and 0.5g pectin, mix well, transfer to a 100mL volumetric flask, and diethyl ether Constant volume, then sterilize by filtration with 0.05μm filter membrane; dissolve 1.0g sodium dihydrogen phosphate and 0.5g magnesium chloride in 10mL deionized water, stir, and after complete dissolution, sterilize under high temperature and high pressure for 30min, cool at 60°C, and then add filter Into the mixed solution of chlorophyll a and bacteriochlorophyll after membrane sterilization; when the solution ...
example 2
[0035] Take 7g of Houttuynia cordata, 11g of sweet potato vine, and 6.5g of kudzu vine and grind them in a Webster blender, add 12.5mL of absolute ethanol, pass through the chromatography column, use calcium carbonate particles as the stationary phase, and acetone as the mobile phase to separate and extract Produce a mixture of chlorophyll a and bacteriochlorophyll; put the above mixture in a 50mL stoppered colorimetric tube, place it in a constant temperature water bath at 70°C for 1.5h, add 1.5g protein and 0.75g pectin, mix well, and transfer to a 100mL volumetric flask , use diethyl ether to make up the volume, and then use a 0.075μm filter membrane to filter and sterilize; dissolve 1.25g of sodium dihydrogen phosphate and 0.75g of magnesium chloride in 10mL of deionized water, stir, and sterilize under high temperature and high pressure for 30 minutes after completely dissolving, and cool at 70°C. Then add the chlorophyll a and bacteriochlorophyll mixture after filter memb...
example 3
[0039] Take a certain amount of Houttuynia cordata, sweet potato vine, and kudzu vine and crush them in a Webster blender, add absolute ethanol, pass through a chromatographic column, use calcium carbonate particles as the stationary phase, and acetone as the mobile phase to separate and extract chlorophyll a and Bacterial chlorophyll mixture: put the above mixture in a stoppered colorimetric tube, place it in a constant temperature water bath, add protein and pectin, mix well, transfer to a volumetric flask, dilute with ether, and then filter to sterilize; Dissolve sodium dihydrogen phosphate and magnesium chloride in deionized water, stir, sterilize under high temperature and high pressure after being completely dissolved, cool, and then add the mixed solution of chlorophyll a and bacteriochlorophyll after filter membrane sterilization; when the solution is cooled to room temperature, Add 1 succinic acid to adjust pH = 6.0; add methanol and ethyl acetate to the above mixture,...
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