Method of preparing sugar by utilizing sweet potato residues
A technology of sweet potato residue and sweet potato starch wastewater, applied in the biological field, can solve the problems of incomplete degradation, refractory degradation, low hydrolysis rate, etc., and achieve the effect of improving conversion rate, low cost, and strong specificity
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Embodiment 1
[0034] Sweet potato dregs (moisture content 13.85%, starch content 52.09%) produced by a company in Shanxi, crushed to 60 mesh, weighed 5.0kg, in a 30L enzymolysis tank, added 20kg of sweet potato starch waste water to adjust the slurry (solid-liquid ratio 1:4) , adjust the pH6.5 with 10% NaOH, add high temperature resistant α-amylase (Thermostable α-amylase) by adding 20U of enzyme per gram of feed, the slurry is heated up to 95°C, incubated for 45 minutes, and used I 2 The liquefaction test turns red and the liquefaction is complete. Cool the slurry to 58-60°C, adjust the pH to 4.8 with 10% HCl, add glucoamylase (Glucoamylase) 100U per gram of material, add 100U of cellulase per gram of material and acid protease (Acid) protease) Add enzyme 10U per gram of material, (keep warm for about 40h), stir, the concentration of reducing sugar in the slurry will no longer increase, stop saccharification, extinguish the enzyme at 110°C, cool down to 50°C, and use a centrifuge to separa...
Embodiment 2
[0042] Sweet potato dregs (moisture 13.85%, starch content 52.09%) produced by a company in Shanxi, crushed to 60 mesh, weighed 5.0kg, in a 30L enzymolysis tank, added 22.5kg of sweet potato starch waste water to adjust slurry (solid-liquid ratio 1: 4.5 ), adjust the pH to 5.5 with sodium bicarbonate, add thermostable α-amylase (Thermostable α-amylase) and add 20U of enzyme per gram of feed, the slurry is heated up to 95°C, incubated for 45 minutes, and used I 2 The liquefaction test turns red and the liquefaction is complete. Cool the slurry to 58-60°C, adjust the pH to 3.5 with acetic acid 1, add glucoamylase (Glucoamylase) 250U per gram of material, cellulase (cellulase) 400U per gram of material and acid protease (Acid protease) ) Add 15U of enzyme per gram of material, (keep warm for about 40 hours), stir until the concentration of reducing sugar in the slurry no longer rises, stop saccharification, inactivate the enzyme at 110°C, cool to 65°C, and use a centrifuge for so...
Embodiment 3
[0044] Sweet potato dregs (moisture content 13.85%, starch content 52.09%) produced by a company in Shanxi, crushed to 60 mesh, weighed 5.0kg, in a 30L enzymolysis tank, added 25kg of sweet potato starch waste water to adjust the slurry (solid-liquid ratio 1:5) , adjust the pH to 8.0 with 10% NaOH, add high temperature resistant α-amylase (Thermostable α-amylase) and add 15U of enzyme per gram of feed, the slurry is heated up to 95°C, incubated for 45 minutes, and used I 2 The liquefaction test turns red and the liquefaction is complete. Cool the slurry to 58-60°C, adjust the pH to 5.5 with 10% HCl, add 300U of enzyme per gram of Glucoamylase, 500U of enzyme per gram of cellulase and acid protease at 60°C protease) Add enzyme 12U per gram of material, keep warm for about 40 hours, stir, the concentration of reducing sugar in the slurry will no longer increase, stop saccharification, inactivate the enzyme at 110°C, cool down to 40°C, and use a centrifuge to separate the solid f...
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