High-strength super-macroporous separating medium for plant polyphenols extraction and preparation method thereof
A separation medium and plant polyphenol technology, applied in chemical instruments and methods, alkali metal oxides/hydroxides, alkali metal compounds, etc., can solve the problems that affect the separation medium reuse, poor mechanical properties, etc., and achieve non-toxic Effects of side effects, fast flow, and simple method
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Embodiment 1
[0019] Dissolve PVA with an average polymer degree of 2000 in hot water, select formaldehyde as a crosslinking agent, use sulfuric acid as a catalyst, use deionized water as a solvent, control the mass fractions of PVA and formaldehyde to 15% and 0.5% respectively, and stir After uniformity, put it in a freezer to cool down to about 0°C, add 0.5ml of sulfuric acid solution with a concentration of 20%, and then pour the mixed solution into a chromatographic column with a diameter of 16mm and a length of 200mm. Lower the temperature from 0°C to -18°C within 1 hour, the system freezes and ice crystals appear, and maintain at -18°C for 12 hours, take out the chromatographic column and thaw it at room temperature, and then wash the bed with 6BV volume of deionized water to remove the non-involved The reacted substances obtain the PVA super-large-pore scaffold.
[0020]Dissolve CTS with a deacetylation degree of 85% in 2% acetic acid solution, select N,N'-methylenebisacrylamide as a...
Embodiment 2
[0024] Dissolve PVA with a polymer degree of 2000 in hot water at 90°C, use glyoxal as a crosslinking agent, use sulfuric acid as a catalyst, and use deionized water as a solvent to control the mass fractions of PVA and glyoxal to 12% respectively and 0.5%, stir evenly and put it in a freezer to cool down to about 0°C, add 0.5ml of sulfuric acid solution with a concentration of 20%, and then pour the mixture into a chromatographic column with a diameter of 16mm and a length of 200mm. Decrease the temperature from 0°C to -20°C within 1h, freeze and crystallize the system, and keep it at -20°C for 15h, then take out the chromatographic column and thaw it at room temperature, then wash the bed layer with 6BV volume of deionized water to remove the non-participating reaction The material obtains the PVA super-large-pore stent.
[0025] Dissolve CTS with a deacetylation degree of 90% in 2% acetic acid solution, select N,N'-methylenebisacrylamide as a crosslinking agent, and use pot...
Embodiment 3
[0029] Dissolve PVA with a polymer degree of 2600 in hot water at 95°C, use glutaraldehyde as a crosslinking agent, use hydrochloric acid as a catalyst, and use deionized water as a solvent to control the mass fractions of PVA and glutaraldehyde to 12% respectively and 1.2%, stir evenly and put it in a freezer to cool down to about 0°C, add 0.5ml of 15% hydrochloric acid solution, and pour the mixture into a chromatographic column with a diameter of 12mm and a length of 200mm. Decrease the temperature from 0°C to -18°C within 1 hour, freeze and crystallize the system, and maintain it at -18°C for 12 hours, then take out the chromatographic column and thaw it at room temperature, then wash the bed with 5BV of deionized water to remove those not involved in the reaction The material obtains the PVA super-large-pore stent.
[0030] Dissolve CTS with a deacetylation degree of 90% in 2% acetic acid solution, select N,N'-methylenebisacrylamide as a crosslinking agent, and use potass...
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