A detection kit and method for dicofol
A technology for detecting dicofol and a detection method, which is applied in the field of kits for detecting dicofol, can solve the problems of cumbersome steps, high detection limit of chemical chromogenic method, and high detection cost, so as to simplify the operation process, improve detection efficiency, and save operation steps Effect
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Publication Date
- 2021-02-09
Abstract
Description
technical field
[0001] The invention relates to the field of organic compound detection, in particular to a kit and method for detecting dicofol. Background technique
[0002] Dicofol is a low toxicity and high efficiency organochlorine acaricide, insoluble in water, soluble in various organic solvents, and has low toxicity to humans and animals. This kind of pesticide is a special pesticide for cicada mite pests. It has a good control effect on adults, nymphs and eggs. In addition, its structure is stable, its decomposition is slow, and its residual effect is long. Therefore, it was popularized and applied in my country's tea production in the late last century. . However, the production of most dicofol products uses DDT as the main intermediate, and the residual refining process is not up to standard, resulting in excessive DDT content in a large number of finished products. Therefore, when dicofol is sprayed, a certain amount of DDT is also mixed, so in the tea gardens a...
Examples
Embodiment 1
[0034] 1) Weigh 3g of crushed tea leaves into a centrifuge tube, add 10mL of n-hexane, cover tightly, shake up and down 50 times, and let stand;
[0035] 2) Pour the extract into another centrifuge tube, add 0.5g of silicon-magnesium-type adsorbent, shake it 50 times, and let it stand for stratification;
[0036] 3) Take the supernatant and dry it, add 2mL pH8.0 buffer to redissolve, then add 0.5mL lipase, and pre-react for 5min;
[0037] 4) Add 0.5 mL of 0.15 mg / L p-nitrophenol ester solution, react for 10 min, and detect the absorbance at a wavelength of 405 nm.
Embodiment 2
[0039] 1) Weigh 5g of crushed vegetables into a centrifuge tube, add 8mL of acetone, cover tightly, shake up and down 50 times, and let stand;
[0040] 2) Pour the extract into another centrifuge tube, add 1g of silica gel, shake 50 times, and let stand to separate layers;
[0041] 3) Take the supernatant and dry it, add 1mL pH8.5 buffer to redissolve, then add 0.5mL lipase, and pre-react for 5min;
[0042] 4) Add 1.5 mL of 0.05 mg / L p-nitrophenol ester solution, react for 10 min, and detect the absorbance at a wavelength of 405 nm.
Embodiment 3
[0044] 1) Weigh 10 g of crushed fruit into a centrifuge tube, add 5 mL of ethyl acetate, cover tightly, shake up and down 50 times, and let stand;
[0045] 2) Pour the extract into another centrifuge tube, add 0.2g of neutral alumina, shake 50 times, and let stand to separate layers;
[0046] 3) Take the supernatant and dry it, add 4mL pH7.5 buffer solution to redissolve, then add lipase and nitrophenol ester solution, and detect the absorbance value at a wavelength of 405nm after reaction.
[0047] 1. Detection limit test:
[0048] Get 6 centrifuge tubes, add 5g of pulverized vegetable samples to each, add dicofol pesticide standard substance, the concentration of adding standard is respectively 0, 0.1, 0.2, 0.3, 0.4, 0.5mg / kg, according to the pretreatment method of embodiment 2 of the present invention and Detection method, the reaction solution detects the absorbance value at a wavelength of 405nm, and the following table is obtained:
[0049] Dicofol (mg / kg) 0...