A kind of detection method of phthalates
A phthalic acid and detection method technology, applied in the detection field, can solve the problems of large amount of organic solvents used, low measurement accuracy, long detection time, etc., and achieve the effect of accurate and reliable results, fast analysis speed and improved detection efficiency
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Embodiment 1
[0029] Example 1: Detection of phthalates by ultra-high performance convergence chromatography-diode array detector method
[0030] First, cut the same plastic sample as the control example into 1mm×1mm fragments, accurately weigh 0.5 g of the sample fragments, place them in a 25 mL stoppered colorimetric tube, add 10 mL of n-hexane accurately, ultrasonically extract for 30 min, and extract the solution through 0.45 After filtration by a μm organic membrane, the sample was injected into ultra-high performance convergence chromatography for analysis. The ultra-high performance convergence chromatography conditions: neutral, C18 SB packing with a particle size of 1.8 μm, the column length is 15 cm; the system back pressure is 12.41 MPa, and the chromatographic conditions are: The column temperature was 65°C, the injection volume was 3 μL, the mobile phase A was supercritical carbon dioxide, the mobile phase B was acetonitrile, and the column flow rate was 1.5 mL / min. Mobile phas...
Embodiment 2
[0032] Example 2: Detection of phthalates by ultra-high performance convergence chromatography-mass spectrometry
[0033] Cut the same plastic sample as the comparative example into fine particles with a single particle ≤ 0.02 g, accurately weigh 0.5 g of the sample particle, put it in a 25 mL stoppered colorimetric tube, add 10 mL of n-hexane accurately, ultrasonically extract for 60 min, and extract The liquid was filtered through a 0.45 μm organic membrane, and then injected into an ultra-high performance convergence chromatography for analysis. The chromatographic conditions: neutral, C18 SB packing with a particle size of 1.8 μm, the column length of the chromatographic column was 15 cm; the system back pressure was 13.10 MPa, and the chromatographic column The temperature was 55°C, the injection volume was 1 μL, the mobile phase A was supercritical carbon dioxide, the mobile phase B was acetonitrile, and the column flow rate was 1.0 mL / min. Mobile phase elution gradient ...
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