Analysis method for simultaneous determination of 6 kinds of trace phenol environmental endocrine disrupting chemicals in solid environmental sample
A technology for endocrine disruptors and environmental samples, which is applied in the analysis field of simultaneous determination of 6 trace amounts of phenolic environmental endocrine disruptors in solid environmental samples, can solve the problem of not forming phenolic EDCs, etc., and achieves improved chromatographic peak type, precision Good accuracy and good reproducibility
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Embodiment 1
[0066] The collected river silt was dried in a vacuum freeze dryer at -55°C for 4 days, then taken out and returned to normal temperature for use. Weigh 4g of freeze-dried sludge and place it in a 100mL microwave extraction tank, add 10mL of BPA-d 16 After stirring the solution with a glass rod, put it in a cool and dry place and let it stand for 48 hours. Add 25mL of methanol, microwave extraction at 110°C for 20min, then cool to room temperature naturally in a ventilated place, and open the extraction tank. Rinse the extraction tank with methanol 3 times × 5mL / time, and the extract was filtered through absorbent cotton and collected into a 250mL flat-bottomed flask. The extract was concentrated to about 1 mL by a rotary evaporator, gently blown to near dryness with high-purity nitrogen, and then rinsed with 3 mL of cyclohexane / ethyl acetate mixed solvent (1:1, v / v) for three times to rinse the flat-bottomed flask. The solution was transferred to a gel permeation chromatogr...
Embodiment 2
[0068] Weigh the freeze-dried crucian carp sample, peel off the fish muscle, take 4g and put it in a 100mL extraction tank (crush the coarse particles with a mortar), and add 10mL of recovery indicator BPA-d 16 After stirring the solution with a glass rod, put it in a cool and dry place and let it stand for 48 hours. Add 25mL of methanol, microwave extraction at 110°C for 20min, then cool to room temperature naturally in a ventilated place, and open the extraction tank. Rinse the extraction tank with methanol 3 times × 5mL / time, and the extract was filtered through absorbent cotton and collected into a 250mL flat-bottomed flask. The extract was concentrated to about 0.5 mL by a rotary evaporator, blown gently with high-purity nitrogen until nearly dry, and then rinsed the flat-bottomed flask with 3 mL of cyclohexane / ethyl acetate mixed solvent (1:1, v / v) for three times. The washing solution was transferred to a sample tube purified by gel permeation chromatography, and the v...
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