Uranium adsorbent and preparation method thereof
A technology of adsorbent and adsorption capacity, applied in chemical instruments and methods, other chemical processes, alkali metal oxides/hydroxides, etc., can solve the problems of low selectivity of uranium adsorbent, environmental pollution, small adsorption capacity, etc. , to achieve the effect of fast speed, good environment and large adsorption capacity
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[0036] The preparation method of the above-mentioned uranium adsorbent will be described in detail below.
[0037] The preparation method of uranium adsorbent of the present invention comprises the following steps:
[0038] In step S1, low-temperature plasma is used to treat carbon nanotubes to obtain amidated carbon nanotubes.
[0039] Specifically, the preparation method of amidated carbon nanotubes is as follows: firstly, carbon nanotubes and grafted monomers are mixed, and the resulting mixture is placed in a low-temperature plasma reactor; then, under a protective atmosphere, the aforementioned mixture is placed in a React for at least 30 minutes at a temperature of 200° C. to 400° C. and a discharge power of 10 W to 20 W to obtain amidated carbon nanotubes.
[0040] More specifically, the grafting monomer can be dimethyl diamide or diaminomaleonitrile; when the grafting monomer is dimethyl diamide, then control the ratio of carbon nanotubes and dimethyl diamide to be 1...
Embodiment 1
[0052] First, weigh 4.52g FeCl 3 ·6H 2 O was added to 200mL deionized water to obtain a ferric chloride solution.
[0053] Then, 2 g of unmodified nanotubes were weighed and dispersed in the ferric chloride solution, ultrasonicated for 30 min, and mechanically stirred for 12 h to obtain a stable suspension.
[0054] In the third step, at N 2 Atmosphere, add 1.83g FeCl to the suspension 2 4H 2 O, heat the solution to 70°C, and quickly add 8 mL of ammonia (NH 4 OH, 30%), continued to reflux at 70°C for 1h, cooled to room temperature, washed with deionized water repeatedly until neutral, and then placed in a vacuum drying oven to dry at a constant temperature of 70°C to obtain magnetic carbon nanotubes.
[0055] In the fourth step, magnetic carbon nanotubes are mixed with dimethyl diamide according to the ratio of 0.5g / 200mL, placed in a low-temperature plasma reactor PDC-32G-2, Harrick Plasma), and N 2 , and treated for 30 minutes under the conditions of a temperature of 2...
Embodiment 2
[0060] First, weigh 6.61g FeCl 3 ·6H 2 O was added to 200mL deionized water to obtain a ferric chloride solution.
[0061] Then, 3 g of unmodified nanotubes were weighed and dispersed in the ferric chloride solution, ultrasonicated for 30 min, and mechanically stirred for 12 h to obtain a stable suspension.
[0062] In the third step, at N 2 Atmosphere, add 2.72g FeCl to the suspension 2 4H 2 O, heat the solution to 90°C, quickly add 10mL ammonia water (NH 4 OH, 30%), continued to reflux at 90°C for 1h, cooled to room temperature, washed with deionized water repeatedly until neutral, and then placed in a vacuum drying oven at a constant temperature of 70°C to obtain magnetic carbon nanotubes.
[0063] In the fourth step, magnetic carbon nanotubes are mixed with dimethyl diamide according to the ratio of 0.8g / 300mL, placed in a low-temperature plasma reactor PDC-32G-2, Harrick Plasma), and N 2 , treated for 1 h at a temperature of 320° C. and a discharge power of 15 W to ...
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