Preparation method of nitrocellulose diacetate nanofiber membrane capable of adsorbing and desorbing proteins
A technology of cellulose diacetate and nitrodiacetic acid is applied in the field of protein separation and purification, which can solve the problems of complex membrane pore structure, low processing capacity, long operation time, etc., and achieves optimized microstructure, low fiber size, and improved adsorption. Effect
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Embodiment 1
[0037] Weigh 1g of cellulose diacetate, 6mL of acetone and 3mL of DMAc solvent (solvent volume ratio 2:1) into a 20mL Erlenmeyer flask, and stir magnetically at room temperature for 6-8h to form a transparent homogeneous spinning solution; The spinning solution was left to defoam for 4 hours, then poured into a 20mL syringe equipped with a No. At 15-20kV, the needle droplet rapidly formed a Taylor cone, and a cellulose diacetate nanofiber film was formed on the conductive receiving plate covered with aluminum foil. Then, soak the membrane in deionized water for 24 hours to remove residual solvents and impurities, and dry it in an oven at 60° C. to obtain pure cellulose diacetate nanofiber membrane 1 .
[0038] Weigh 0.15g of bovine serum albumin and dissolve it in 0.01M disodium hydrogen phosphate-sodium dihydrogen phosphate buffer solution (pH=7.2), immerse the prepared membrane in the protein solution, shake and adsorb for 4h, centrifuge the solution at 10000 rpm for 5min, a...
Embodiment 2
[0041] Step 1. Dissolve 8g of cellulose diacetate in glacial acetic acid and stir rapidly for 2 hours to fully dissolve and activate it;
[0042] Step 2. After dissolving, add the hydrolyzate (mixed with water / sulfuric acid / glacial acetic acid in a mass ratio of 45 / 30 / 2) in a water bath at 18°C, raise the temperature to 80°C, perform hydrolysis treatment for 3 hours, neutralize and precipitate, wash with water until neutral, Obtain hydrolyzed cellulose diacetate;
[0043] Step 3. Weigh the cellulose diacetate (acetyl substitution degree is 1.8) and nitrating agent (mixing fuming nitric acid and dichloromethane at a mass ratio of 35 / 65) obtained in step 2 and add them into a three-necked flask, and carry out nitration treatment at room temperature for half Hour;
[0044]Step 4, add ethanol after nitration, wash repeatedly to neutrality, obtain nitrocellulose diacetate;
[0045] Step 5, take by weighing 1g of the nitrocellulose diacetate gained in step 4 (the degree of nitro s...
Embodiment 3
[0051] Step 1. Dissolve 8g of cellulose diacetate in glacial acetic acid and stir rapidly for 2 hours to fully dissolve and activate it;
[0052] Step 2. After dissolving, add hydrolyzate (water / sulfuric acid / glacial acetic acid mixed in mass ratio 45 / 30 / 2) in a water bath at 18°C, heat up to 80°C, hydrolyze for 3 hours, neutralize and precipitate, wash with water until neutral, Obtain hydrolyzed cellulose diacetate;
[0053] Step 3: Weigh cellulose diacetate (acetyl substitution degree is 1.8) and nitrating agent (mixing fuming nitric acid and dichloromethane at a mass ratio of 45 / 55) obtained in step 2 into a three-necked flask, and carry out nitration treatment at room temperature for half an hour ;
[0054] Step 4, add ethanol after nitration, wash repeatedly to neutrality, obtain nitrocellulose diacetate;
[0055] Step five, take by weighing 1.198g of the nitrocellulose diacetate gained in step four (the degree of nitro substitution is 0.87) and be dissolved in 6.247gDM...
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