Method for separating plurality of active ingredients from peanut coat
A technology of active ingredients and peanut shells, which is applied in the field of separation of active ingredients of peanut shells, can solve the problems of excessive aflatoxin and other problems, and achieve the effects of low production cost, high yield and strong operability
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Embodiment 1
[0039] (1) Extraction and separation of higher fatty acids: take 1 kg of raw material of peanut shell, crush it to 20 mesh, add organic solvent to heat and reflux to extract twice, the first extraction is to use 10L of petroleum ether and ethyl acetate according to the volume ratio of 4:1 The mixed solvent, the extraction time is 2 hours; the second extraction is to use 7L of 6# solvent oil and 120# solvent oil according to the volume ratio of 1:1 mixed solvent, the extraction time is 1 hour, filter, and combine the two organic solvent extracts , the extraction residue is stand-by; the combined extract is passed through a silica gel chromatography column at a flow rate of 0.5BV / hour (the amount of silica gel used in column chromatography is 0.2L, and the height-to-diameter ratio of the silica gel chromatography column is 5:1), and the silica gel is collected The effluent from the chromatography column was concentrated until there was no solvent to obtain 99.17 g of a light yell...
Embodiment 2
[0046] (1) Extraction and separation of higher fatty acids: take 1 kg of peanut shell raw material, crush it to 20 mesh, add organic solvent to heat and reflux for extraction twice (the first extraction is 9L of petroleum ether and ethyl acetate according to the volume ratio of 6:1) Mixed solvent, the extraction time is 3 hours; the second time 6L of 6# solvent oil and 120# solvent oil are mixed solvents according to the volume ratio of 3:1, the extraction time is 1 hour), filter, and obtain the extraction residue for use. Combine two organic solvent extracts, the extract is passed through a silica gel chromatography column at a flow rate of 0.8BV / hour (the amount of silica gel used in column chromatography is 0.16L, and the height-to-diameter ratio of the silica gel chromatography column is 7:1), and the silica gel is collected. The effluent from the chromatography column was concentrated until there was no solvent to obtain 94.72 g of a light yellow oily substance, which is h...
Embodiment 3
[0053] (1) Extraction and separation of higher fatty acids: Take 1 kg of raw peanut shells, crush them to 20 meshes, add organic solvent to heat and reflux for extraction twice, the first extraction is a mixture of 8L petroleum ether and ethyl acetate at a volume ratio of 5:1 Solvent, the extraction time is 3 hours; the second time 8L of 6# solvent oil and 120# solvent oil are mixed solvents according to the volume ratio of 1:3, the extraction time is 2 hours, filter, and extract the residue for use. Combine two organic solvent extracts, pass the extract through a silica gel chromatography column at a flow rate of 0.6BV / hour (the amount of silica gel used in column chromatography is 0.12L, and the height-to-diameter ratio of the silica gel chromatography column is 8:1), and the silica gel is collected. The effluent from the chromatography column was concentrated until there was no solvent to obtain 95.19 g of a light yellow oily substance, which is higher fatty acid of peanut s...
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