Method for rapidly identifying camellia oleosa seed oil processing mode based on taste fingerprint spectrum and method for predicting acid value and peroxide value based on taste fingerprint spectrum
A technology of taste fingerprints and camellia oleifera seed oil, which is applied in the direction of testing food, measuring devices, instruments, etc., can solve the problems of few process sources and difficulty in distinguishing adulterated rapeseed oil samples, and achieve the effect of environmental friendliness, simplicity, speed and cost
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Embodiment 1
[0033] In this example, Camellia oleifera seed oil with different processing methods is used as test samples, including 5 parts of commercially available camellia oil, 15 parts of supercritically extracted camellia oil, and 10 parts of solvent-extracted camellia oil, totaling 30 parts. 24 samples were used as testing samples, and the remaining 6 samples were used as verification samples.
[0034] 1) Pretreat 30 camellia seed oils respectively: in a 200mL beaker, mix 12g of oil and 85g of distilled water, keep warm at 60°C, homogenize for 3min, after cooling to room temperature, add 50g of reference solution (KCl and tartaric acid (mass ratio 50:1)), centrifuged at 3000rpm for 10min, removed the supernatant, and refrigerated for later use.
[0035] 2) Electronic tongue detection of Camellia oleifera seed oil samples: At room temperature, the activated taste sensor arrays are respectively contacted with the samples to be tested, and the potential signals between different taste ...
Embodiment 2
[0046] Camellia oil sample pretreatment
[0047] In a 200mL beaker, mix 10g of oil and 100g of distilled water, keep warm at 60°C, and homogenize for 3 minutes. Centrifuge for 10 min, remove the supernatant, and refrigerate for later use.
[0048] Test condition is the same as embodiment 1, and the measurement result obtained is similar to embodiment 1.
Embodiment 3
[0050] Camellia oil sample pretreatment
[0051] In a 200mL beaker, mix 10g of oil and 100g of distilled water, keep warm at 60°C, and homogenize for 3 minutes. Centrifuge for 10 min, remove the supernatant, and refrigerate for later use.
[0052] Test condition is the same as embodiment 1, and the measurement result obtained is similar to embodiment 1.
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