A method for extracting and purifying chlorogenic acid from Jerusalem artichoke leaves
A technology of chlorogenic acid and Jerusalem artichoke, which is applied in chemical instruments and methods, preparation of organic compounds, separation/purification of carboxylic acid esters, etc., can solve the problems of unsecured safety, destruction of ecological environment, limited raw materials, etc. Achieve the effect of shortening post-processing time, less control parameters, and fast adsorption rate
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Embodiment 1
[0032] Accurately weigh the above 100g of Jerusalem artichoke leaf coarse powder into the extractor, add 500mL of methanol aqueous solution with a volume fraction of 10%, and heat and reflux at 100°C for extraction twice, each time for 1h. Filter and combine the extracts. The extract is first passed through a hollow fiber ultrafiltration membrane with a molecular weight cut off of 1000 to remove macromolecular impurities, and then the extract is concentrated to 10% of the original volume fraction with a nanofiltration membrane with a molecular weight cut off of 200. The concentrated solution is put on the ADS-7 macroporous resin column at a flow rate of 5BV / h. After the dynamic adsorption is saturated, the macroporous resin column is rinsed with an aqueous hydrochloric acid solution with pH=5-6 at a flow rate of 5BV / h until the effluent is colorless. , and then elute with 40% ethanol at a flow rate of 5BV / h, collect the ethanol eluate, concentrate it under reduced pressure to ...
Embodiment 2
[0034] Accurately weigh 500g of Jerusalem artichoke leaf meal and put it into an extractor, add 3000mL of 30% ethanol aqueous solution, heat and reflux at 80°C to extract twice, each time for 2.5h. Filter and combine the extracts. The extract is first passed through a hollow fiber ultrafiltration membrane with a molecular weight cut off of 1000 to remove macromolecular impurities, and then the extract is concentrated to 10% of the original volume fraction with a nanofiltration membrane with a molecular weight cut off of 200. The concentrated solution is put on the DM130 macroporous resin column at a flow rate of 4BV / h. After the dynamic adsorption is saturated, the macroporous resin column is rinsed with a hydrochloric acid aqueous solution with pH=5-6 at a flow rate of 4BV / h until the effluent is colorless, and then Use ethanol with a volume fraction of 60% to elute at a flow rate of 6BV / h, collect the ethanol eluent, concentrate it under reduced pressure to a paste, and then...
Embodiment 3
[0036] Accurately weigh 1000g of Jerusalem artichoke leaf coarse powder and put it into an extractor, add 8000mL of 60% ethanol aqueous solution, heat and reflux at 50°C to extract twice, each time for 3h. Filter and combine the extracts. The extract is first passed through a hollow fiber ultrafiltration membrane with a molecular weight cut off of 1000 to remove macromolecular impurities, and then the extract is concentrated to 10% of the original volume fraction with a nanofiltration membrane with a molecular weight cut off of 200. The concentrated solution is applied to the HPD-600 macroporous resin column at a flow rate of 3BV / h. After the dynamic adsorption is saturated, the macroporous resin column is rinsed with an aqueous hydrochloric acid solution with pH=5-6 at a flow rate of 3BV / h until the effluent is colorless. , and then eluted with 60% ethanol at a flow rate of 8BV / h, collected the ethanol eluate, concentrated it under reduced pressure to a paste, and then dissol...
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