A carbon nanotube composite znin 2 s 4 Preparation method of green advanced water treatment agent
A carbon nanotube composite and water treatment agent technology, which is applied in the direction of adsorption water/sewage treatment, light water/sewage treatment, oxidized water/sewage treatment, etc., can solve the problems of unfavorable and sustainable development, and achieve good water treatment effect, The preparation method is simple and the effect of low cost
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Embodiment 1
[0027] (1) Put 10g of carbon nanotubes in 4L of H with a volume ratio of 1:1 2 SO 4 and HNO 4 The mixture was subjected to ultrasonic reaction at room temperature for 30min, washed with water to neutrality, and vacuum-dried at room temperature for 48h to obtain 5g of carboxylated carbon nanotubes; then the above-mentioned 5g of carboxylated carbon nanotubes were dispersed in excess diethylenetriamine, and 100 mg of 2-( 7-Azobenzotriazole)-N,N,N',N'-tetramethylurea hexafluorophosphate, reacted at 40°C for 5h, washed with ethanol, and dried in vacuum at room temperature for 48h to obtain 4g of carbon amide nanoparticles Finally, 4g of aminated carbon nanotubes were ultrasonically dispersed in 1L of a mixture of water and acetone with a volume ratio of 3:1, the pH was adjusted to 5 with sodium carbonate solution, and 4g of 2,4,6- Trifluoro-5-chloropyrimidine was adjusted to pH 6 with sodium carbonate solution, ultrasonically reacted at 20°C for 24h, washed with ethanol, washed ...
Embodiment 2
[0031] (1) Put 10g of carbon nanotubes in 4L of H with a volume ratio of 3:1 2 SO 4 and HNO 4The mixed solution was subjected to ultrasonic reaction at room temperature for 45 min, washed with water until neutral, and vacuum-dried at room temperature for 54 h to obtain 6.5 g of carboxylated carbon nanotubes; then the above 5 g of carboxylated carbon nanotubes were dispersed in excess diethylenetriamine, and 300 mg of 2- (7-Azobenzotriazole)-N,N,N',N'-tetramethylurea hexafluorophosphate, reacted at 45°C for 5h, washed with ethanol, and dried in vacuum at room temperature for 48h to obtain 4.2g of amination Carbon nanotubes; finally, 4.2g of aminated carbon nanotubes were ultrasonically dispersed in 1L of a mixture of water and acetone with a volume ratio of 4:1, the pH was adjusted to 5.5 with sodium carbonate solution, and 5g of 2,4 was added dropwise to an ice-water bath. ,6-trifluoro-5-chloropyrimidine, adjust the pH value with sodium carbonate solution to 6.2, ultrasonica...
Embodiment 3
[0035] (1) Put 10g of carbon nanotubes in 4L of H with a volume ratio of 5:1 2 SO 4 and HNO 4 The mixed solution was subjected to ultrasonic reaction at room temperature for 60min, washed with water to neutrality, and vacuum-dried at room temperature for 60h to obtain 8g of carboxylated carbon nanotubes; then the above-mentioned 8g of carboxylated carbon nanotubes were dispersed in excess diethylenetriamine, and 600mg of 2-( 7-Azobenzotriazole)-N,N,N',N'-tetramethylurea hexafluorophosphate, react at 50°C for 5h, wash with ethanol, and dry in vacuum at room temperature for 48h to obtain 4.5g of carbon amide Nanotubes; finally, 4.5g of carbon nanotubes were ultrasonically dispersed in 1L of a mixture of water and acetone with a volume ratio of 5:1, the pH was adjusted to 6 with sodium carbonate solution, and 6g of 2,4 was added dropwise to an ice-water bath. 6-Trifluoro-5-chloropyrimidine, adjusted to pH 6.5 with sodium carbonate solution, ultrasonically reacted at 30°C for 48...
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