Method for preparing enzyme electrode and rapidly detecting peroxide value of vegetable oil
An enzyme electrode and peroxidation technology, applied in measuring devices, material analysis through electromagnetic means, instruments, etc., can solve the problem of difficulty in adapting to the requirements of accurate, fast, portable, on-site food safety testing, and large fluctuations in measured values , low sensitivity and other issues, to achieve the effect of short response time, improved selectivity and high sensitivity
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Embodiment 1
[0036] Determination of peroxide value of soybean oil
[0037] 1. Preparation method of enzyme electrode
[0038] a. Electrode pretreatment
[0039] Glassy carbon electrode (Glass Carbon Electrode) with Al 2 o 3 The powder is ground and polished, wetted with double distilled water, followed by ultrasonic cleaning, and then washed with double distilled water and acetone to remove the adsorbed substances on the surface to make it a mirror surface; then the glassy carbon electrode is immersed in a concentration of 0.2mol / L In the sulfuric acid solution, use the PAR 270 electrochemical workstation to perform cyclic voltammetry scanning processing, the scanning speed is 50mV / s, the voltage range is -0.5~+1.5V, and the scanning is continued for 10min. After obtaining a stable cyclic voltammogram, take out The glassy carbon electrode was then washed with twice distilled water, dried at room temperature, and used for later use.
[0040] b. Preparation of horseradish peroxidase Naf...
Embodiment 2
[0058] Determination of Peroxide Value of Peanut Oil
[0059] 1. Preparation method of enzyme electrode
[0060] Same as instance 1
[0061] 2. Rapid detection of peroxide value of peanut oil with enzyme electrode
[0062] 1) Standard curve
[0063] Same as instance 1
[0064] 2) Determination
[0065] Get 1.8g peanut oil and place in the electrolytic cell of 25ml, then add the 0.1mol / L ethanol sulfuric acid solution of 0.40ml, the 1.0mol / L ethanol lithium chloride solution of 1.0ml and the 1,2 dichloroethane of 5ml, Then dilute to a final volume of 25ml with acetonitrile, stir and wash with N 2 Purify for 5 minutes, use the PAR 270 electrochemical workstation to measure the cyclic voltammogram of the enzyme electrode, perform three measurements and record the cyclic voltammogram, take the average value of the measured peak current minus the reduction peak current of methylene blue in the blank After that, it is the reduction response current value of the oil sample, and...
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