Preparation and regeneration method suitable for large particle diameter activated carbon capable of adsorbing heavy metal ions
A technology for adsorbing heavy metals and activated carbon, which is applied in separation methods, chemical instruments and methods, filter regeneration, etc., and can solve the problems of difficult desorption of microorganisms, long operation cycle of microorganism regeneration methods, and difficult decomposition treatment.
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[0098] The preparation method of the present invention will be further described in detail in conjunction with specific examples below. It should be understood that the following examples are only for illustrating and explaining the present invention, and should not be construed as limiting the protection scope of the present invention. All technologies realized based on the above contents of the present invention are covered within the scope of protection intended by the present invention.
[0099] The experimental methods used in the following examples are conventional methods unless otherwise specified; the reagents and materials used in the following examples can be obtained from commercial sources unless otherwise specified.
Embodiment 1
[0101] 1.1 Preparation of spherical polymer
[0102] Under argon protection, add 0.011mol 2,2 bis(trifluoromethyl)diaminobenzidine to 14.94g polar solvent N,N-dimethylacetamide in a 250mL three-necked flask equipped with mechanical stirring , after stirring to completely dissolve the diamine, add 0.01mol 3,3',4,4'-diphenyl ether tetracarboxylic dianhydride to the reaction system, react for 4 hours, add 0.0005mol norbornene anhydride, and continue the reaction for 24 hours to obtain Polyamic acid soluble.
[0103] The mixture of 2.26g triethylamine and 0.22g pyridine is used as a catalyst, the catalyst is added to the polyamic acid solution, and 9.24g dehydrating agent acetic anhydride is added, and the reaction is continued for 24 hours to obtain a polyimide prepolymer solution, and then the polyimide After diluting the imide prepolymer solution with the polar solvent N-methylpyrrolidone to an equal volume, drop it into methanol to obtain a precipitate, wash and filter the pr...
Embodiment 2
[0120] 2.1 step is the same as 1.1 in embodiment 1
[0121] 2.2 Sulfonation and carbonization
[0122] Carry out sulfonation treatment to the spherical polymer of step 2.1, then mix the spherical polymer after the sulfonation treatment with the mass ratio of 1:3 with concentrated sulfuric acid, then add the mixture into the acid-resistant rotary tube furnace, under nitrogen atmosphere, with 2°C / min heating rate for sulfonation as follows:
[0123] Heat to 60°C and stay for 60 minutes;
[0124] Heat to 110°C and stay for 100 minutes;
[0125] Heat to 150°C and stay for 200 minutes;
[0126] The process can well realize the sulfonation treatment of the spherical polymer after sulfonation treatment;
[0127] Continue to heat up at a heating rate of 3°C / min, and carry out carbonization treatment in a mixed atmosphere with an oxygen volume percentage of 3%:
[0128] Heat to 350°C and stay for 360 minutes;
[0129] Heat to 520°C and hold for 260 minutes. Lower the temperature...
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