Preparation method for cationic-type activated carbon
A cationic activated carbon technology, applied in chemical instruments and methods, other chemical processes, water/sludge/sewage treatment, etc., can solve problems such as cationic activated carbon that has not been found, and achieve good stability
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Embodiment 1
[0027] Embodiment 1, a kind of preparation method of positively charged cationic activated carbon comprises the following steps:
[0028] (1) Activated carbon pretreatment: wash 2g of activated carbon with water, dry at 80°C-100°C, crush to 100-200 mesh, and oxidize the activated carbon with 10mL of 36% hydrochloric acid for 10h to make more hydroxyl groups appear on the surface;
[0029] (2) Put the three-neck flask into the water bath, heat up to 85°C, add the activated carbon pretreated in step (1), then add 5mL epichlorohydrin, 5mL N-N dimethylformamide, and stir for 1h;
[0030] (3) Add 3mL of ethylenediamine, the reaction is violent during this process, so it is advisable to add slowly drop by drop. React for 1 hour; continue to add 5 mL of triethylamine, and react for 30 minutes.
[0031] (4) After the reaction, cool to room temperature, wash, and dry at 70°C to obtain a cationic activated carbon product.
[0032] The scanning electron microscope picture of the cation...
Embodiment 2
[0034] As described in Example 1, the difference is: 40% sulfuric acid was used to oxidize the activated carbon for 10 h during the pretreatment of the activated carbon, so that more hydroxyl groups appeared on the surface.
Embodiment 3
[0035] Embodiment 3, a kind of preparation method of cationic activated carbon comprises the following steps:
[0036] (1) Activated carbon pretreatment
[0037] Wash 6g of activated carbon with water, dry at 80°C-100°C, crush to 100-200 mesh, impregnate with 30mL of 36.5% concentrated hydrochloric acid, and treat for 9h;
[0038] (2) Add the activated carbon pretreated in step (1) into the reaction vessel, raise the temperature to 86°C in a water bath, then add 15mL of epichlorohydrin and 16mL of N-N dimethylformamide, and stir for 1.2h;
[0039] (3) Then add ethylenediamine 10mL dropwise and react for 1.2h; continue to add triethylamine 15mL dropwise and react for 40 minutes.
[0040] (4) After the reaction, cool to room temperature, wash, and dry at 70-75°C to obtain a cationic activated carbon product.
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