Deep-eutectic solvent and microorganism combined degumming method for flax roving
A technology of low eutectic solvent and degumming method, which is applied in bacterial retting, textiles and papermaking, etc., can solve the problems of complicated processing process, long biological degumming time and poor degumming effect.
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Embodiment 1
[0046] S1, deep eutectic solvent pretreatment steps: (1) choline chloride: urea is mixed and heated and melted in a molar ratio of 1:2 to synthesize a deep eutectic solvent; the deep eutectic solvent is mixed with water to obtain a water content of 10% (2) Mix the dried flax roving with the deep eutectic solvent aqueous solution at a mass ratio of 1:60, and treat it in a water bath at a temperature of 90°C for 1 hour. After the treatment, take out the flax roving and wash to remove the flax Aqueous solution of deep eutectic solvent remaining on the surface.
[0047] S2. Seed culture of degummed strains: Inoculate the strains frozen at -80°C into a 500mL Erlenmeyer flask containing 100ml of seed medium at an inoculum size of 2%, and cultivate for 6 hours at a temperature of 37°C and a rotational speed of 150rpm. The formula of the seed medium is peptone 10g / L, yeast powder 5g / L, and NaCl 10g / L.
[0048] S3, scale-up cultivation of degummed bacterial strains: the seed solution ...
Embodiment 2
[0052] S1, deep eutectic solvent pretreatment steps: (1) choline chloride: urea is mixed and heated and melted in a molar ratio of 1:2 to synthesize a deep eutectic solvent; the deep eutectic solvent is mixed with water to obtain a water content of 20% (2) Mix the dried flax roving with the deep eutectic solvent aqueous solution at a mass ratio of 1:60, and treat it in a water bath at 80°C for 1.5 hours. After the treatment, take out the flax roving and rinse to remove Aqueous solutions of deep eutectic solvents remaining on flax surfaces.
[0053] S2. Seed culture of degummed strains: Inoculate the strains frozen at -80°C into a 500mL Erlenmeyer flask containing 200ml of seed medium at an inoculum size of 3%, and cultivate for 8 hours at a temperature of 35°C and a rotation speed of 180rpm. The formula of the seed medium is peptone 10g / L, yeast powder 5g / L, and NaCl 10g / L.
[0054] S3, amplified culture of degummed strains: the seed solution obtained in step S2 is inserted i...
Embodiment 3
[0058] S1, deep eutectic solvent pretreatment steps: (1) choline chloride: urea is mixed and heated and melted in a molar ratio of 1:2 to synthesize a deep eutectic solvent; the deep eutectic solvent is mixed with water to obtain a water content of 30% (2) Mix the dried flax roving with the deep eutectic solvent aqueous solution according to the bath mass ratio of 1:50, and treat it in a water bath at a temperature of 100°C for 1.5h. After the treatment, take out the flax roving and rinse Removal of residual deep eutectic solvent aqueous solution on the surface of flax.
[0059] S2. Seed culture of degummed strains: The strains that will be frozen and stored at -80°C are inoculated into a 500mL triangular flask containing 200ml of seed medium at an inoculum size of 5%, cultivated at a temperature of 36°C and a speed of 170rpm for 6 hours . Wherein the formula of seed medium is peptone 10g / L, yeast powder 5g / L, NaCl 10g / L.
[0060] S3, amplified culture of degummed strains: t...
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