Method of quantitatively detecting contents of endocrine disrupters in water in different occurrence modes
A technology for quantitative detection of endocrine disruptors, applied in the field of environmental analytical chemistry, can solve the problems of unclear distribution mechanism and regulation principle, and achieve good application value
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Embodiment 1
[0019] Example 1: Determination of the content of ethinyl estradiol (EE2) in the granular phase, colloidal phase and true soluble phase of biochemical tail water of a city sewage
[0020] 1) Separation of different forms of EE2: Take 10L of urban sewage biochemical tail water, use 1μm pore size ceramic ultrafiltration membrane, the retentate phase liquid is vacuum freeze-dried and then used as particle phase for further analysis; the filtrate obtained above is further analyzed by TiO2 ceramic nanofiltration membrane (1nm pore size) high-pressure separation, the filtrate is used as the true dissolved phase, and the retentate is saved as the colloidal phase for analysis.
[0021] 2) Extraction of granular phase EE2: Weigh 2 g of the vacuum freeze-dried granular phase sample and place it in a 30 mL round-bottomed test tube, add 100 μL of internal standard (1.0 mg / L), then add 10 mL of methanol and 10 mL of dichloromethane and mix in a vortex Shake on the shaker for 10 minutes. A...
Embodiment 2
[0026] Example 2: Determination of the content of bisphenol A (BPA) in the granular phase, colloidal phase and true soluble phase of a heavily polluted river water body
[0027] 1) Separation of different forms of BPA: Take 10L river water samples, use 1μm pore size ceramic ultrafiltration membrane, and the retentate phase liquid is further analyzed as particle phase after vacuum freeze-drying; pore size) high-pressure separation, the filtrate is used as the true dissolved phase, and the retentate is saved as the colloidal phase for analysis.
[0028] 2) Extraction of granular phase BPA: Weigh 2 grams of vacuum freeze-dried granular phase sample and place it in a 30 mL round bottom test tube, add 100 μL of internal standard (1.0 mg / L), then add 10 mL of methanol and 10 mL of dichloromethane and mix in a vortex Shake on the shaker for 10 minutes. After shaking, ultrasonic for 15min, centrifuged at 3024g for 10min, the separated supernatant was put into a 200mL round-bottomed f...
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