A kind of hydrogel composite material with porous structure and its preparation and application
A composite material and porous structure technology, applied in the direction of luminescent materials, chemical instruments and methods, etc., can solve the problems of rare earth complex hydrogel materials, difficult biodegradation, poor biocompatibility, etc., and achieve good compressive strain Features, easy degradation, and the effect of good mechanical properties
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[0039] The preparation method of the hydrogel composite material of the above-mentioned porous structure comprises the following steps:
[0040] S1. Add CC with a mass percentage concentration of 0.5 to 4% in the CNF sol, and stir at room temperature until fully dissolved;
[0041] S2, adding epichlorohydrin with a volume ratio of 5 to 20% and sodium hydroxide with a molar concentration of 0.4 to 1.5 M into the sol obtained in step S1, and fully stirring it evenly;
[0042] S3. Pour the sol obtained in step S2 into a suitable mold, then put it in a refrigerator, and freeze it at -25°C for 24-72 hours;
[0043] S4, the jelly obtained in step S3 is thawed in water, and washed with a large amount of deionized water to obtain a hydrogel;
[0044] S5, soak the hydrogel obtained in step S4 in a hydrochloric acid solution, and then wash with a large amount of deionized water;
[0045] S6, soak the hydrogel obtained in step S5 in EuCl with a rare earth europium ion molar concentration...
Embodiment 1
[0052] Add 25 mg of CC to 5 mL of CNF sol and stir magnetically at room temperature until the CC is fully dissolved. Subsequently, 0.25 mL of epichlorohydrin was added, and after stirring evenly, 2 mL of 0.4M sodium hydroxide solution was added, and the above sol was stirred evenly and placed in a -25°C refrigerator for 24 hours, and then the obtained jelly was placed in deionized water. Thawed, washed with plenty of deionized water, and soaked the resulting hydrogel material in 20 mL of 0.01 M EuCl 3 In aqueous solution for 12h, then washed the hydrogel with a large amount of deionized water, then soaked the hydrogel material in 20mL of 0.01M 2-thiopheneformyl trifluoroacetone deprotonated sodium salt solution for 12h, and then used a large amount of deionized water. Washed with water to obtain a hydrogel composite.
Embodiment 2
[0054] 30 mg of CC was added to 5 mL of CNF sol, and magnetically stirred at room temperature until the CC was fully dissolved. Subsequently, 0.3 mL of epichlorohydrin was added, and after stirring evenly, 2 mL of 0.5M sodium hydroxide solution was added, and the above sol was stirred evenly and placed in a -25°C refrigerator for 30 hours, and then the obtained jelly was placed in deionized water. Thawed, washed with plenty of deionized water, and soaked the resulting hydrogel material in 20 mL of 0.15 M EuCl 3 In aqueous solution for 12h, the hydrogel was washed with a large amount of deionized water, and then the hydrogel material was soaked in 20mL of 0.1M 2-thiopheneformyl trifluoroacetone deprotonated sodium salt solution for 12h, and then a large amount of deionized water was used. Washed with water to obtain a hydrogel composite.
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