Determination method of acraldehyde in electronic cigarette smoke solution
A technology of e-cigarette liquid and measurement method, which is applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve the problems of large differences in additives, complex matrix of e-cigarette liquid, and large difference in matrix, and achieve good solubility , good solubility, anti-polymerization effect
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example 1
[0031] Acrolein-2,4-dinitrophenylhydrazone standard solution was analyzed by LC-MS / MS. Regression analysis was performed on the peak area ratio of the target substance and the internal standard quantitative ion pair and the acrolein concentration to obtain the acrolein standard working curve and regression equation. The limit of detection (LOD) was calculated by 3 times the signal-to-noise ratio (S / N = 3), The specific test results are shown in Table 2:
[0032] Table 2 Test results of acrolein standard working solution
[0033] compound
example 2
[0035] The standard addition recovery experiment was carried out at three concentration levels of low, medium and high. Each standard addition level was repeated 5 times, and the recovery rate and precision of each addition level were calculated according to the measured amount and the standard addition amount. The specific results are shown in the following table:
[0036] Table 3 method recovery and repeatability
[0037]
example 3
[0039] Weigh 0.2 g of an e-cigarette liquid sample, add 0.6-3.0 mL deionized water, 0.4-3.0 mL DNPH derivatization reagent and 50-500 µL HClO 4 Aqueous solution, shake well, place at room temperature for 30-150 min for derivatization reaction, add 50-500 µL pyridine after the reaction, add 100 µL internal standard working solution, and dilute to 10 mL with acetonitrile, shake well, pass through 0.22 µm organic phase filter membrane, into LC-MS / MS analysis.
[0040] Substituting the peak area ratio of the target substance and the internal standard quantitative ion pair into the regression equation, the acrolein content in the sample was calculated to be 0.28 μg / g.
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