Method for extracting rubusoside from sweet tea leaves
A technology of sweet tea leaves and rubusoside, which is applied in the field of extracting rubusoside, and can solve the problems of large amount of organic solvent, complicated operation and complex extraction process, etc.
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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, inactivated for 60s, plate cooling to room temperature, then FeCl3 was added to the enzymolysis solution for flocculation, stirring continuously until the pH value was 3, then stirring for 0.8h, standing for 1.2h, using saturated Adjust the pH value to 8 with lime water, then stir for 1.2 hours, let it stand for 1 hour, perform plate and frame pressure filtration with a plate filter membrane with a filter membrane pore size of 2.0 μm, and then wash the filter residue with 6 tons of water until it has no s...
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 hydrolyzate was inactivated at 100°C under normal pressure for 40 seconds, cooled to room temperature by plate cooling, then FeSO4 was added to the enzymatic hydrolyzate for flocculation, stirring continuously until the pH value was 5, then stirred for 1.2 hours, and left to stand 0.8h, use saturated lime water to adjust the pH value to 9, then stir for 0.8h, let it stand for 3h, use a plate filter with a filter membrane pore size of 1.0μm for plate and frame pressure filtration, and then use 8t of wate...
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