Method for extracting chlorogenic acid and hyperoside from lonicera japonica leaves
A technology of honeysuckle leaves and hyperin, which is applied in chemical instruments and methods, separation/purification of carboxylic acid esters, sugar derivatives, etc., can solve the problem that the content of hyperin is not high, only reaches 30%, and the production cost High-level problems, to achieve the effect of abundant reserves, energy saving, and low safety hazards
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Embodiment 1
[0059] Fresh honeysuckle leaves with a moisture content of about 80% are de-enzymed and minced with a tea roller degreening machine (Tea roller degreening machine 6CST-80 produced by Yueyang Agricultural Mechanization Research Institute), and 200kg of fresh honeysuckle leaves with a moisture content of 45% are added to the aqueous solution 1000L, extracted at room temperature for 4 hours, filtered twice with three layers of gauze and once with a ceramic membrane to obtain the filtrate, after solid-liquid separation, add granular activated carbon (provided by Gongyi Hengtai Filter Material Co., Ltd.) for 30 minutes, add 210g of ascorbic acid in Concentrate in vacuum at 50°C to 80L; absorb the concentrated solution on a DM130 macroporous resin column, collect the effluent and washing solution to obtain 240L of solution I; then concentrate the eluate to 20L, and then adjust the pH value with 0.01mol / L hydrochloric acid solution To about 3, add 95% ethanol solution to a final conce...
Embodiment 2
[0061] The fresh honeysuckle leaves with a moisture content of about 75% are de-enzymed and crushed with a tea drum de-greening machine (Tea drum de-greening machine 6CST-80 produced by the Yueyang Agricultural Mechanization Research Institute), and 400kg of fresh honeysuckle leaves with a water content of 48% are weighed and added to the water. 1800L, extract at room temperature for 4 hours, filter twice with three layers of gauze, and filter once with a ceramic membrane to obtain the filtrate. After solid-liquid separation, add granular activated carbon for treatment for 30 minutes, add 400g of ascorbic acid and vacuum concentrate at 50°C to 140L; Adsorb on DM130 macroporous resin column, collect the effluent and washing liquid to obtain 450L of solution I; the eluate is then concentrated to 50L, then 0.01mol / L hydrochloric acid solution is used to adjust the pH value to about 3, and 95% ethanol solution is added to the final The concentration was 50%, crystallized overnight ...
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