A method for extracting rubusoside from sweet tea leaves
A technology for sweet tea leaves and sweet tea glycosides, applied in the field of extracting sweet tea glycosides, can solve the problems of low recovery rate, large amount of organic solvent, high equipment and operation requirements
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reference example 1
[0077] The acidic alumina used in the examples of the present invention is activated before use: first activate the acidic alumina at a high temperature of 550°C for 18 hours, and then wash it with an ethanol solution with a volume fraction of 95% until the effluent is colorless Until it is transparent and has no other smell except ethanol, it is finally washed with water until there is no ethanol smell.
Embodiment 1
[0079] (1) Crush and extract: Crush 5t of sweet tea leaves, pass through a 20-mesh sieve, add 50t of water, conduct continuous countercurrent extraction at 85°C for 1 hour, and filter with a 100-mesh filter cloth to obtain 35t of extract;
[0080] (2) Enzymolysis and flocculation: Add 35kg of cellulase preparation and 35kg of protease preparation to the 35t extract obtained in step (1), and carry out enzymolysis for 1 hour at 50°C with a pH value of 5. , under normal pressure, inactivate for 60s, plate cooling to room temperature, and then FeCl 3 Add it to the enzymatic hydrolysis solution for flocculation, stir continuously during the addition until the pH value is 3, then stir for 0.8h, let stand for 1.2h, adjust the pH value to 8 with saturated lime water, stir for 1.2h, let stand for 1h, Use a plate-type filter membrane with a filter membrane pore size of 2.0 μm for plate-and-frame press filtration, then wash the filter residue with 6 t of water until it has no sweet taste...
Embodiment 2
[0088] (1) Crush and extract: Crush 5t of sweet tea leaves, pass through a 30-mesh sieve, add 100t of water, conduct continuous countercurrent extraction at 95°C for 3 hours, and filter with a 300-mesh filter cloth to obtain 95t of extract;
[0089] (2) Enzymolysis and flocculation: Add 47.5kg of hemicellulase preparation and 47.5kg of pectinase preparation to the 95t extract obtained in step (1), carry out enzymolysis at 55°C and pH value of 4 for 2 hours, and enzymatically The solution was inactivated at 100°C under normal pressure for 40 seconds, cooled to room temperature by plate type, and FeSO 4 Add it to the enzymatic hydrolysis solution for flocculation, stir continuously during the addition until the pH value is 5, then stir for 1.2h, let it stand for 0.8h, adjust the pH value to 9 with saturated lime water, stir for another 0.8h, let it stand for 3h, Use a plate filter with a filter membrane pore size of 1.0 μm for plate and frame press filtration, then wash the filt...
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