Preparation method for dietary fiber based on momordica grosvenori waste
A technology of dietary fiber and Luo Han Guo, which is applied in the direction of food science, can solve the problems that soluble dietary fiber is not separated and collected, the structure of dietary fiber is greatly damaged, and the scope of application is limited, so as to achieve high added value and transformation The effect of high efficiency and elimination of waste of resources
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Embodiment 1
[0048] (1) Beating: Take 183 kg of fresh Luo Han Guo dregs extracted with water as the solvent, and beat to 10 mesh;
[0049] (2) Fermentation: After concentrating the effluent from the upper column to 10 brix, take 2000 kg of the concentrated solution (200 kg converted to solids) and mix with Luo Han pomace, and then add 10 kg of fermentation aids (sucrose: peptone: purine = 3:6: 1) With starter 20kg Trichoderma, ferment for 12h at a temperature of 40℃, and keep stirring during the fermentation.
[0050] (3) Solid-liquid separation: the fermented fermentation broth is subjected to decanter centrifugation and butterfly centrifugation to collect insolubles and solubles respectively.
[0051] (4) Ultrafiltration: Pass the soluble matter through a 400,000 Da ultrafiltration membrane to take the permeate, and then pass the permeate through a 5000 Da nanofiltration membrane to collect the retentate.
[0052] (5) Concentration: The collected retentate is concentrated to 45 brix using a thre...
Embodiment 2
[0058] (1) Beating: Take 183kg of fresh Luo Han Guo dregs extracted with water as solvent, and beat to 60 mesh;
[0059] (2) Fermentation: After concentrating the effluent from the upper column to 8brix, take 5000kg of the concentrated solution (400kg converted to solids) and mix with Luo Han pomace, and then add 15kg of fermentation assistant (sucrose: peptone: purine = 2:4: 2) 15kg of Aspergillus with starter, ferment for 24h at a temperature of 30℃, and keep stirring during the process.
[0060] (3) Solid-liquid separation: Centrifuge the fermented fermentation broth through a three-foot centrifuge to collect insoluble and soluble materials.
[0061] (4) Ultrafiltration: Pass the soluble matter through a 600,000 Da ultrafiltration membrane to take the permeate, and then pass the permeate through a 10,000 Da nanofiltration membrane to collect the retentate.
[0062] (5) Concentration: The collected retentate is concentrated to 40 brix using a scraper evaporative concentrator.
[0063...
Embodiment 3
[0068] (1) Beating: Take 183kg of fresh Luo Han Guo dregs extracted with water as solvent, and beat to 80 mesh;
[0069] (2) Fermentation: After concentrating the effluent from the upper column to 10 brix, take 3500 kg of the concentrated solution (converted to a solid content of 350 kg) and mix it with Luo Han pomace, and then add 13 kg of fermentation aids (sucrose: peptone: purine = 3:5: 1.5) With starter 10kg Trichoderma, 10kg Aspergillus, ferment for 8h at a temperature of 60℃, and keep stirring during the fermentation.
[0070] (3) Solid-liquid separation: the fermented fermentation broth is centrifuged in a decanter to collect insolubles and solubles.
[0071] (4) Ultrafiltration: Pass the soluble matter through a 200,000 Da ultrafiltration membrane to take the permeate, and then pass the permeate through a 3000 Da nanofiltration membrane to collect the retentate.
[0072] (5) Concentration: The collected retentate is concentrated to 50 brix using a five-effect evaporative conc...
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