Determination method of amount of phthalic acid esters
A technology for the determination of phthalic acid and its determination method, which is applied in the field of determination of the total amount of phthalates, can solve the problems of complex metabolite components, difficulty in detecting phthalates, etc., and achieve high sensitivity High, stable peak area, good stability
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Embodiment 1
[0038] The determination of the total amount of phthalic acid substances in the oil sample of embodiment 1
[0039] (1) Use phthalic acid standard stock solution to prepare standard solutions with phthalic acid concentrations of 0.05, 0.1, 1, 10, 25, 50, and 100 mg / L. Draw 10 μ L of the standard solution of each concentration and inject it into high-performance liquid chromatography for analysis, and obtain the peak area of the high-performance liquid chromatography obtained from the corresponding concentration, and obtain the standard curve of the peak area-mass concentration of the phthalic acid standard substance and the linear regression equation Y=63331X+ 47465, R 2 =0.9995, and the lowest detection limit was obtained as 0.02mg / L.
[0040] (2) After mixing the sample evenly, weigh 2.0g, put it in a reflux bottle, add 10ml of methanol and mix evenly, then add 10mL of KOH solution with a concentration of 2mol / L, heat it in a water bath at 85°C for 2.5h, and finally remov...
Embodiment 2
[0058] The determination of the total amount of phthalic acid substances in the urine of embodiment 2
[0059] (1) Use phthalic acid standard stock solution to prepare standard solutions with phthalic acid concentrations of 0.05, 0.1, 1, 10, 25, 50, and 100 mg / L. Draw 10 μ L of the standard solution of each concentration and inject it into a high-performance liquid chromatograph for analysis, and obtain the phthalic acid standard substance peak area-mass concentration standard curve and linear regression equation Y=63331X+47465, R 2 =0.9995, and the lowest detection limit was obtained as 0.02mg / L.
[0060] (2) Take the urine sample and centrifuge it at 12000rpm / min for 20min to take the supernatant, take 1ml, add 15μL of β-glucuronide hydrolase, and shake at a constant temperature of 37°C for 12h.
[0061] (3) The enzymolysis solution was inactivated in boiling water at 100°C. After cooling, centrifuge at 12000rpm / min for 20min to take the supernatant, put it in a reflux bott...
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