Preparation method of proanthocyanidin
A proanthocyanidin and raw material technology, applied in the field of proanthocyanidin preparation, can solve the problems of inability to carry out large-scale industrial production and immature process, and achieve the effects of easy continuous production operation, short process flow and high separation efficiency
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Embodiment 1
[0038] Add 5 parts by weight of proanthocyanidin raw materials that have been removed, coarsely crushed or cut into sections into a stainless steel reaction tank, add the raw materials and 70% ethanol in a ratio of 1:3 by weight, heat and keep warm for extraction three times, and control the temperature at 50-60°C. The incubation time is 1.2h, and the extracts are combined. Add the extract to a stainless steel reaction kettle, add 2% polyacrylic acid and water or ethanol to the extract, adjust the ethanol content to 30-40% of the solution, stir evenly, let stand for 1.5h to form two phases, and obtain the upper phase extraction liquid, add 4 parts by weight (5:1, v / v) of two-phase extractant ethyl acetate-petroleum ether that is insoluble in water and water-soluble to extract, separate the extract, and distill the filtrate to reclaim the organic solvent, and finally control the temperature to be 60 Below ℃, the vacuum degree is above 0.08Mpa to carry out vacuum drying to obtai...
Embodiment 2
[0041] Add 5 parts by weight of proanthocyanidin raw materials that have been removed, coarsely crushed or cut into sections into a stainless steel reaction tank, add the raw materials and 70% ethanol in a ratio of 1:3 by weight, heat and keep warm for extraction three times, and control the temperature at 50-60°C. The incubation time is 1.2h, and the extracts are combined. Then add the extract of the extract into the enamel reaction kettle, add the extract 3% methyl polypropylene glycol and water or ethanol, adjust the ethanol content to 30-40% ethanol of the solution, stir evenly, and let it stand for 1h to form two phases , to obtain the upper phase extract, add water-insoluble and water-soluble two-phase extractant ethyl acetate-petroleum ether 4 parts by weight (5: 1, v / v) for extraction, separate the extract, distill the filtrate to reclaim the organic solvent, and finally The temperature is controlled below 60°C, and the vacuum degree is above 0.08Mpa for vacuum drying ...
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