Method for producing chitooligo saccharide via acidolysis and enzymolysis by taking shrimp and crab shells as raw material
A technology for shrimp and crab shells and chitosan oligosaccharides, which is applied in the biological field, can solve the problems of high production cost, low degradation efficiency, and inability to degrade chitosan oligosaccharide by chitosan, so as to reduce production costs and solve high-concentration substrates. Effects of Conversion Questions
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Embodiment 1
[0017] Immerse 100g of shrimp and crab shells in water for 1 to 2 days, dry, crush, pass through a 20-mesh sieve, add 1000ml of hydrochloric acid aqueous solution (concentration is 30%), heat up to 75°C, add mixed bacteria (Aspergillus niger: Trichoderma enzyme = 1:0.5) 5g, react for 6 hours; then add potassium hydroxide until the pH value is greater than 8, freeze for 2 hours, melt, add sodium chloride aqueous solution (concentration is 65%), mix, then filter, in a vacuum of - 10mpa, vacuum drying at 60-70°C to obtain.
[0018] The resulting product is tested. The results are as follows: degree of deacetylation: 91%; moisture 6.9%; ash content 0.29%; average molecular weight 1000.
Embodiment 2
[0020] Immerse 100g of shrimp and crab shells in water for 1 to 2 days, dry, crush, pass through a 20-mesh sieve, add 1100ml of hydrochloric acid aqueous solution (concentration is 35%), heat up to 85°C, add mixed bacteria (Aspergillus niger: Trichoderma enzyme = 1:0.7) 20g, react for 7 hours; then add potassium hydroxide until the pH value is greater than 8, freeze for 3 hours, melt, add sodium chloride aqueous solution (concentration is 68%), mix, then filter, in a vacuum of - 10mpa, vacuum drying at 60-70°C to obtain.
[0021] The resulting product is tested. The results are as follows: degree of deacetylation: 88%; moisture 5.9%; ash content 0.25%; average molecular weight 900.
Embodiment 3
[0023] Immerse 100g of shrimp and crab shells in water for 1 to 2 days, dry, crush, pass through a 20-mesh sieve, add 1100ml of hydrochloric acid aqueous solution (concentration is 30%), heat up to 85°C, add mixed bacteria (Aspergillus niger: Trichoderma enzyme = 1:0.7) 20g, react for 6 hours; then add potassium hydroxide until the pH value is greater than 8, freeze for 2 hours, melt, add sodium chloride aqueous solution (concentration is 68%), mix, then filter, in a vacuum of - 10mpa, vacuum drying at 60-70°C to obtain.
[0024] The resulting product is tested. The results are as follows: degree of deacetylation: 89%; moisture 6.1%; ash content 0.28%; average molecular weight 800.
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