Method for rapidly detecting total amount of paraoxon by ultraviolet spectrophotometry
A technology of spectrophotometry and detection method, which is applied in the field of analytical chemical detection, can solve the problems of difficult specific screening and detection, and achieve the effects of environmental friendliness, convenient use and simple preparation
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Embodiment 1
[0038] Preparation of the rapid hydrolysis reagent: Weigh 40 mg of sodium hydroxide, 5 mg of sodium sulfate, and 7 mg of potassium chloride, dissolve them in ultrapure water, and set the volume to 10 ml to obtain the rapid hydrolysis reagent, mix well and set aside.
Embodiment 2
[0040] The hydrolysis research of methyl paraoxon and ethyl paraoxon was carried out using the rapid hydrolysis reagent prepared in Example 1. Prepare 1000nM methyl paraoxon and 1000nM ethyl paraoxon solutions with rapid hydrolysis reagent, after vortex mixing, take 100 μL at different reaction time points, and carry out UV spectrophotometric detection respectively, the results are shown in Table 1 .
[0041] Changes of paraoxon concentration with time in table 1 hydrolysis system
[0042]
[0043] The results show that the rapid hydrolysis reagent has a strong hydrolysis effect on methyl paraoxon and ethyl paraoxon, and the concentration of paraoxon in the system decreases significantly with the prolongation of the reaction time. After 30 minutes of reaction, 90% of the methyl paraoxon Both phosphorus and ethyl paraoxon were hydrolyzed.
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