Preparation method of super-hydrophobic active carbon
A super-hydrophobic and activated carbon technology, which is applied in chemical instruments and methods, alkali metal oxides/hydroxides, inorganic chemistry, etc., can solve the problems of general effect, limited use, and inability to connect to super-hydrophobic properties, and achieve methyl The effect of large quantity and strong anti-destructive ability
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Embodiment 1
[0018] The invention discloses a preparation method of super-hydrophobic activated carbon. The raw materials used include activated carbon, concentrated nitric acid as an oxidizing agent and trimethylchlorosilane as a modifying agent.
[0019] The preparation method of above-mentioned superhydrophobic gac is:
[0020] (1) Oxidative modification of activated carbon:
[0021] Pretreat the powdery, coal-based activated carbon of Ningxia Coal Group (Shenhua Ningxia Coal Industry Group Co., Ltd.) Dawukou Coal Washing Plant, that is, heat the activated carbon at 120°C for 5 hours; 10g was added to concentrated nitric acid (69% mass fraction) and stirred for 0.5 hours, the temperature was controlled at 25°C, and the stirring rate was 300rpm·min-1, and then the solid was obtained by centrifugation, and the solid was vacuum-dried at 80°C for 6 hours to obtain the oxidative modification. Activated carbon after neutralization.
[0022] (2) Preparation of superhydrophobic activated carb...
Embodiment 2
[0027] Adopt the method for embodiment 1 to obtain superhydrophobic activated carbon.
[0028] According to the amount of 10g / L, superhydrophobic activated carbon was added to water, stirred at 25°C for 1, 2, 3, and 4 hours, respectively, and then filtered to obtain solids, which were vacuum-dried at 88°C for 5 hours, and then measured Solid contact angles are 125°, 119°, 90° and water absorption respectively.
Embodiment 3
[0030] Adopt the method for embodiment 1 to obtain superhydrophobic activated carbon.
[0031] According to the amount of 10g / L, superhydrophobic activated carbon was added to acetic acid, stirred at 25°C for 1, 2, 3, and 4 hours, respectively, and then the solids were obtained by suction filtration, and the solids were vacuum-dried at 100°C for 3 hours, and then The solid contact angles were measured and were 133°, 131°, 130° and 115°, respectively.
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