Preparation method of hydroxypropyl trimethyl ammonium chloride chitin fiber
A technology of hydroxypropyl trimethyl ammonium chloride and chitosan fiber, which is used in fiber treatment, textiles and papermaking, etc., can solve the problems of weakening the antibacterial property of chitosan fiber, reducing the amino content, and restricting the application, so as to increase the polymer Cationic properties, simple preparation method, and effect of killing bacteria on wound surfaces
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Embodiment 1
[0034] Weigh 5g of chitosan fibers and disperse them in 100mL of methanol, add 0.470g of 2,3-epoxypropyltrimethylammonium chloride, shake and stir at room temperature; then add 10.0g of 20wt% NaOH solution, and After stirring evenly, react in a constant temperature water bath at 50°C for 0.5h, separate the reacted chitosan fibers from the reaction mixture, and disperse the separated chitosan fibers in 80v% methanol aqueous solution, add dropwise 15v% Acetic acid aqueous solution, adjust the pH of the mixture of methanol and acetic acid aqueous solution to 7.1, soak for 30 minutes, then separate the soaked chitosan fibers from the mixed solution, wash twice with 80v% methanol aqueous solution, and dehydrate at 40°C Drying under the hood to obtain hydroxypropyltrimethylammonium chloride chitosan fiber with a substitution degree of 4%.
Embodiment 2
[0036] Weigh 5g of chitosan fiber and disperse it in 100mL of butanol, add 0.470g of 2,3-epoxypropyltrimethylammonium chloride, shake and stir at room temperature; then add 10.0g of NaOH solution with a concentration of 25wt%, and After stirring evenly at high temperature, react in a constant temperature water bath at 50°C for 0.5h, separate the reacted chitosan fibers from the reaction mixture, and disperse the separated chitosan fibers in 80v% acetone aqueous solution, add dropwise 15v % acetic acid aqueous solution, adjust the pH of the mixture of acetone and acetic acid aqueous solution to 6.0, soak for 30 minutes, then separate the soaked chitosan fibers from the mixed solution, wash twice with 80v% acetone aqueous solution, and after dehydration, dry at 40°C drying under the condition to obtain hydroxypropyltrimethylammonium chloride chitosan fiber with a substitution degree of 5%.
Embodiment 3
[0038] Weigh 5g of chitosan fiber and disperse it in 100mL propanol, add 0.470g of 2,3-epoxypropyltrimethylammonium chloride, shake and stir at room temperature; then add 10.0g of 20wt% KOH solution, After stirring evenly at high temperature, react in a constant temperature water bath at 50°C for 0.5h, separate the reacted chitosan fibers from the reaction mixture, and disperse the separated chitosan fibers in 80v% ethanol aqueous solution, and add 15v% acetic acid aqueous solution dropwise , adjust the pH of the mixture of ethanol and acetic acid aqueous solution to 8.0, soak for 30 minutes, then separate the soaked chitosan fibers from the mixed solution, wash twice with 80v% ethanol aqueous solution, dehydrate, and dry at 40°C , to obtain hydroxypropyltrimethylammonium chloride chitosan fibers with a substitution degree of 5%.
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