Fluorescent detection method of benzo (a) pyrene in edible oil
A technology for fluorescence detection and edible oil, applied in fluorescence/phosphorescence, preparation of test samples, spectrum investigation, etc., can solve the problems of cumbersome processing, lower sensitivity, time-consuming, etc., and achieve short analysis time, good selectivity, and steps simple effect
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Embodiment 1
[0027] Example 1: Sunflower oil: Weigh 0.5g of sunflower oil sample in a 25mL serum bottle, add 4mL of dimethyl sulfoxide, 59kHz, ultrasonic extraction for 6min under the conditions of 250W, take out and let stand for stratification, and separate the upper layer The oil layer was extracted once again under the same conditions, and the dimethyl sulfoxide extract was collected twice as the test solution. Pipette 2mL of the solution to the conventional quartz fluorescence sample cell of the fluorescence photometer, and perform constant energy simultaneous fluorescence spectrum mapping. The instrument parameters are set as follows: constant energy difference In terms of excitation wavelength, the scanning start wavelength is 260nm; the wavelength scanning range is 220nm. like figure 1 The zero-order-constant energy synchronous fluorescence spectrum of figure 1The benzo(a)pyrene spectral peak at 390nm can be used for the identification and rough determination of benzo(a)pyren...
Embodiment 2
[0028] Embodiment 2: Similar to Embodiment 1, the difference is that the second-order derivation function is added to obtain as figure 2 The second derivative-constant energy simultaneous fluorescence spectra are shown. Then add 4 μL of benzo(a)pyrene standard solution with a concentration of 1 mg / L to 2 mL of the sample solution, perform second derivative-constant energy simultaneous fluorescence spectrum mapping, and add the standard 4 times. Use the peak-zero method to read the signal intensity value of the sample at 401nm, and use it as the derivative fluorescence intensity for quantitative calculation. image 3 The standard addition curve, the linear fitting equation of the standard addition curve is Y=405.64+173.03X, the correlation coefficient is 0.9999, and the linearity is good. Thus, the content of benzo(a)pyrene in the sunflower oil sample extract was 2.34 μg / L, and the content of benzo(a)pyrene in sunflower oil was 37.4 μg / kg. Depend on figure 2 It can be seen...
Embodiment 3
[0029] Example 3: Blended oil: Weigh 0.5g blended oil sample into a 25mL serum bottle, add 4mL dimethyl sulfoxide solvent, extract under 59kHz, 250W ultrasonic conditions for 6min, take out and let stand for stratification, and separate the upper layer The oil layer was extracted once again under the same conditions, and the dimethyl sulfoxide extract was collected twice as the test solution. Pipette 2mL of the solution to the conventional quartz fluorescence sample cell of the fluorescence photometer, and perform constant energy simultaneous fluorescence spectrum mapping. The instrument parameters are set as follows: constant energy difference The scanning start excitation wavelength is 260nm; the wavelength scanning range is 220nm. get as Figure 4 The zero-order-constant-energy synchrofluorescence spectrum is shown. Adding the second-order derivation function, we get as Figure 5 The second derivative-constant energy simultaneous fluorescence spectra are shown. The ...
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