Preparation method for environment-friendly advanced water treatment agent by combining carbon nano tube and ferric vanadate
A technology of carbon nanotube composite and water treatment agent, which is applied in water/sewage treatment, adsorption water/sewage treatment, light water/sewage treatment, etc. It can solve the problems of unfavorable sustainable development and achieve good water treatment effect and low cost. Low cost and low equipment requirements
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Embodiment 1
[0028] (1) 10g of carbon nanotubes in 4L of H with a volume ratio of 1:1 2 SO 4 and HNO 4 The mixture was ultrasonically reacted at room temperature for 30 minutes, washed with water until neutral, and vacuum-dried at room temperature for 48 hours to obtain 5 g of carboxylated carbon nanotubes; then the above 5 g of carboxylated carbon nanotubes were dispersed in excess diethylenetriamine, and 100 mg of 2-( 7-azobenzotriazole)-N,N,N',N'-tetramethyluronium hexafluorophosphate, reacted at 40°C for 5h, washed with ethanol, and dried in vacuum at room temperature for 48h to obtain 4g of aminated carbon nano tube; finally ultrasonically disperse 4g of aminated carbon nanotubes in 1L of a mixture of water and acetone with a volume ratio of 3:1, adjust the pH value to 5 with sodium carbonate solution, add 4g of 2,4,6- Trifluoro-5-chloropyrimidine, adjusted the pH value to 6 with sodium carbonate solution, ultrasonically reacted at 20°C for 24h, washed with ethanol, washed with wate...
Embodiment 2
[0032] (1) 10g of carbon nanotubes in 4L of H with a volume ratio of 3:1 2 SO 4 and HNO 4 Ultrasonic reaction at room temperature in the mixed solution for 45 minutes, washed with water until neutral, and vacuum-dried at room temperature for 54 hours to obtain 6.5 g of carboxylated carbon nanotubes; then disperse the above 5 g of carboxylated carbon nanotubes into excess diethylenetriamine, add 300 mg of 2- (7-Azobenzotriazole)-N,N,N',N'-tetramethyluronium hexafluorophosphate, reacted at 45°C for 5h, washed with ethanol, and dried in vacuum at room temperature for 48h to obtain 4.2g of aminated Carbon nanotubes; finally, ultrasonically disperse 4.2g of aminated carbon nanotubes in 1L of a mixture of water and acetone at a volume ratio of 4:1, adjust the pH value to 5.5 with sodium carbonate solution, and add 5g of 2,4 dropwise in an ice-water bath , 6-trifluoro-5-chloropyrimidine, adjust the pH value to 6.2 with sodium carbonate solution, ultrasonically react at 25°C for 36h...
Embodiment 3
[0036] (1) 10g of carbon nanotubes in 4L of H with a volume ratio of 5:1 2 SO 4 and HNO 4 The mixture was ultrasonically reacted at room temperature for 60 minutes, washed with water to neutrality, and vacuum-dried at room temperature for 60 hours to obtain 8 g of carboxylated carbon nanotubes; then the above 8 g of carboxylated carbon nanotubes were dispersed in excess diethylenetriamine, and 600 mg of 2-( 7-azobenzotriazole)-N,N,N',N'-tetramethyluronium hexafluorophosphate, reacted at 50°C for 5h, washed with ethanol, and dried in vacuum at room temperature for 48h to obtain 4.5g of carbon amides nanotubes; finally ultrasonically disperse 4.5g of aminated carbon nanotubes in 1L of a mixture of water and acetone at a volume ratio of 5:1, adjust the pH value to 6 with sodium carbonate solution, add 6g of 2,4, 6-trifluoro-5-chloropyrimidine, adjust the pH value to 6.5 with sodium carbonate solution, ultrasonically react at 30°C for 48h, wash with ethanol, wash with water, dry...
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