Method for detecting 18 kinds of organic chloride pesticide residues in Chinese medicinal material
A technology for pesticide residues and traditional Chinese medicinal materials, applied in the field of pesticide residue detection, can solve the problems of long residue time, complicated purification, different sample matrices, etc., and achieves the effect of quickness, convenience, cost, and simple process.
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example 1
[0012] The following examples help those skilled in the art to better understand the present invention, but do not limit the present invention in any way. Example 1 Multi-residue analysis of 18 organochlorine pesticides in chrysanthemum
[0013] The chrysanthemum samples were dried in the shade, crushed, and passed through a 60-mesh sieve. Accurately weigh 2.0g of the sample, add 2.0g of anhydrous Na 2 SO 4 , fully ground, and transferred to a 100mL Erlenmeyer flask with a stopper. Add acetone:petroleum ether (1:1) 30mL for ultrasonic extraction for 15min, let stand, and filter the supernatant into a 100mL pear-shaped bottle. Then use 20 mL of acetone:petroleum ether (1:1) to repeat the extraction twice, and the operation is the same as above. All the collected filtrates were concentrated in a 40°C water bath to nearly dryness. Quantitatively transfer the concentrated residue to a 10 mL stoppered graduated test tube to 5 mL with petroleum ether, carefully add 1 mL of conc...
example 2
[0015] Example 2 Multi-residue Analysis of 18 Organochlorine Pesticides in Ginkgo Leaf
[0016] Ginkgo biloba samples were dried in the shade, crushed, and sieved. Accurately weigh 2.0g of the sample, add 2.0g of anhydrous Na 2 SO 4 , fully ground, and transferred to a 100mL Erlenmeyer flask with a stopper. Add 30 mL of acetone:petroleum ether (1:1) for ultrasonic extraction for 15 min, let stand, and filter the supernatant into a 100 mL pear-shaped bottle. The extraction was repeated twice with 20 mL of acetone:petroleum ether (1:1), and the operation was the same as above. All the collected filtrates were concentrated in a water bath at 40°C to nearly dryness. Quantitatively transfer the concentrated residue to a 10mL stoppered graduated test tube to 5mL with petroleum ether, carefully add 1mL of concentrated sulfuric acid containing 10% water, shake for 1min, centrifuge at 3000 rpm for 10min, take the supernatant into Gas chromatographic determination.
[0017] Result...
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