Method for fast detection of butylated hydroxyanisole (BHA), 2, 6-ditertbutyl-4 methylphenol (BHT) and tert-butylhydroquinone (TBHQ) of plant oil sample and pre-treatment method
A vegetable oil and sample technology, applied in measuring devices, instruments, scientific instruments, etc., can solve the problems of low recovery rate, cumbersome operation, high labor cost, and achieve the effect of reducing contact time, simple operation steps, and reducing processing cost.
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Embodiment 1
[0059] 0.2g vegetable oil sample, 6g neutral aluminum oxide, 15mL methanol and BHA, BHT, TBHQ standard solution (three concentrations are 100mg / L) 200μL are mixed in a 50mL centrifuge tube to obtain the mixture; Under the condition of a power of 25W, the obtained mixture was vortexed for 1 min to obtain a supernatant; an accurate amount of 7.5 mL of the obtained supernatant was concentrated to 0.2 mL, and then dried by nitrogen blowing, and then Redissolve with 1 mL of methanol solvent to obtain the test solution.
[0060] The obtained liquid to be tested was subjected to chromatographic analysis with an UltiMate3000 liquid chromatograph. According to the peak area of chromatographic analysis, the concentration of BHA, BHT, TBHQ is obtained by linear equation, and then the recovery rate of BHA, BHT, TBHQ is calculated, and the recovery rate is 80%, 77%, 80% respectively.
Embodiment 2
[0062] 0.2g vegetable oil sample, 12g neutral aluminum oxide, 25mL methanol and BHA, BHT, TBHQ standard solution (three concentrations are 100mg / L) 200 μ L are mixed in the centrifuge tube of 50mL, obtain mixture; Under the condition of a power of 30W, the obtained mixture was vortexed for 3 minutes to obtain a supernatant; an accurate amount of 12.5mL of the obtained supernatant was concentrated to 0.2mL, and then dried by nitrogen blowing, and then Redissolve with 1 mL of methanol solvent to obtain the test solution.
[0063] The obtained liquid to be tested was subjected to chromatographic analysis with an UltiMate3000 liquid chromatograph. According to the peak area of chromatographic analysis, the concentration of BHA, BHT, TBHQ is obtained by linear equation, and then the recovery rate of BHA, BHT, TBHQ is calculated, and the recovery rate is 86%, 82%, 87% respectively.
Embodiment 3
[0065] 0.2g vegetable oil sample, 10g neutral aluminum oxide, 20mL methanol and BHA, BHT, TBHQ standard solution (three concentrations are 100mg / L) 200 μ L are mixed in the centrifuge tube of 50mL, obtain mixture; (2) vortex Under the condition that the power of vortex oscillation is 40W, the resulting mixture was vortexed for 2min to obtain a supernatant; accurately measure 10mL of the obtained supernatant, concentrate it to 0.2mL, and then dry it by blowing dry with nitrogen , and then redissolved with 1mL of methanol solvent to obtain the test solution;
[0066] The liquid to be tested obtained in was subjected to chromatographic analysis with an UltiMate3000 liquid chromatograph. According to the peak area of chromatographic analysis, the concentration of BHA, BHT, TBHQ is obtained by linear equation, and then the recovery rate of BHA, BHT, TBHQ is calculated, and the recovery rate is 94%, 90%, 95% respectively.
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