Method for cleaning and separating main components of wood fibers
A main component, wood fiber technology, applied in fiber raw material treatment, textile and papermaking, washing/replacing pulp treatment liquid, etc., can solve the problems of subsequent utilization of unfavorable separation products, large damage of main components, harsh reagent synthesis conditions, etc. problem, achieve the effect of improving component separation efficiency, step-by-step efficient separation, and low price
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Embodiment 1
[0046] Preparation of deep eutectic solvent: weigh choline chloride, imidazole and glycerol in a three-necked flask with a molar ratio of 3:7:2, heat and stir at 60°C to obtain a homogeneous transparent liquid, which is the deep eutectic solvent (DES), cooled to room temperature and stored in a desiccator.
[0047] Weigh 1.00g red poplar wood powder (40-60 mesh) and 20ml deionized water into the autoclave, react at 180°C for 35min, and filter to obtain residue 1 and supernatant 1 after the reaction. The residue is washed and dried for later use. The supernatant was concentrated by vacuum distillation and water was recovered, and one volume of ethyl acetate was added to extract three times. The obtained aqueous phase was separated by a 200 Dalton nanofiltration membrane to separate oligosaccharides, and the filtrate was recovered and the obtained oligosaccharides were dried. Mix the dried residue one with the above-mentioned ternary DES at a mass ratio of 1:20, then raise the ...
Embodiment 2
[0050] Preparation of deep eutectic solvent: Weigh choline chloride, imidazole and 1,4-butanediol in a three-necked flask with a molar ratio of 3:7:1.5, heat and stir at 60°C to obtain a homogeneous transparent liquid. Deep eutectic solvent (DES), cooled to room temperature and stored in a desiccator.
[0051] Weigh 1.00g red poplar wood powder (40-60 mesh) and 30ml deionized water into the autoclave, react at 160°C for 45min, and centrifuge to obtain residue 1 and supernatant 1 after the reaction. The residue is washed and dried for later use. The supernatant was concentrated by vacuum distillation and water was recovered, and one volume of ethyl acetate was added to extract three times. The obtained aqueous phase was separated by a 200 Dalton nanofiltration membrane to separate oligosaccharides, and the filtrate was recovered and the obtained oligosaccharides were dried. Mix the dried residue one with the above ternary DES at a mass ratio of 1:10, then raise the temperature...
Embodiment 3
[0054] Preparation of deep eutectic solvent: Weigh choline chloride, p-hydroxybenzenesulfonic acid and glycerol in a three-necked flask at a molar ratio of 1:0.05:2, heat and stir at 60°C to obtain a homogeneous transparent liquid. Deep eutectic solvent (DES), cooled to room temperature and stored in a desiccator.
[0055] Weigh 1.00g of wheat straw (40-60 mesh) and 25ml of deionized water into the autoclave, react at 170°C for 30min, and filter to obtain residue 1 and supernatant 1 after the reaction. The residue is washed and dried for later use. Concentrate the supernatant by vacuum distillation and recover water, add one volume of ethanol to extract three times, the obtained water phase is separated by 200 Dalton nanofiltration membrane to separate oligosaccharides, the filtrate is recovered and the obtained oligosaccharides are dried. Mix the dried residue one with the above ternary DES at a mass ratio of 1:25, then raise the temperature to 130°C, and react for 3 hours u...
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