Porous ferric oxide-titanium oxide-activated carbon complex fiber membrane and preparation method
A composite fiber membrane and activated carbon technology, applied in chemical instruments and methods, fiber treatment, special compound water treatment, etc., can solve the problems of unsatisfactory water treatment performance and recyclability, difficulty in uniform control of composite material structure, and particle participation in reactions Probability reduction and other issues, to achieve the effect of simple and controllable equipment, easy large-scale production, and fast processing speed
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Embodiment 1
[0028] (1) Dissolve 4g of polyacrylonitrile PAN and 1g of polyvinyl alcohol PVA in 40g of N,N-dimethylformamide DMF solution, and fully stir to form a transparent sol. At the same time, 0.02 mol of tetrabutyl titanate and 0.02 mol of ferric nitrate were mixed and dissolved in the DMF solution, and fully stirred to form a transparent solution. The two solutions were uniformly mixed and stirred on a magnetic stirrer for 12 hours to obtain a precursor sol with a certain viscosity.
[0029] (2) Inject the precursor sol into the syringe, apply a voltage of 20kV to carry out electrospinning, and collect it by a roller. The distance between the roller and the nozzle is 20cm, and the speed is set at 150r / min. After spinning, the precursor fiber film is obtained. .
[0030] (3) After pretreatment of the precursor fiber membrane in a muffle furnace at 280°C for 4 hours, place it between two graphite plates, put it in a nitrogen atmosphere furnace and bake it at 750°C for 5 hours to obt...
Embodiment 2
[0033](1) Mix and dissolve 4g PAN and 2g PVP in 40g N,N-dimethylformamide DMF solution, stir well to form a transparent sol. At the same time, 0.045 mol of tetrabutyl titanate and 0.01 mol of ferric nitrate were mixed and dissolved in the DMF solution, and fully stirred to form a transparent solution. The two solutions were uniformly mixed and stirred on a magnetic stirrer for 12 hours to obtain a precursor sol with a certain viscosity.
[0034] (2) Inject the precursor sol into the syringe, apply a voltage of 25kV to carry out electrospinning, and collect it by a roller. The distance between the roller and the nozzle is 30cm, and the speed is set at 200r / min. After spinning, the precursor fiber film is obtained. .
[0035] (3) After the precursor fiber membrane was pretreated in a muffle furnace at 280°C for 4 hours, it was placed between two graphite plates and baked in a nitrogen atmosphere furnace at 800°C for 4 hours to obtain nanostructured porous iron oxide -Titanium ...
Embodiment 3
[0038] (1) Dissolve 4g of polyacrylonitrile PAN in 40g of N,N-dimethylformamide DMF solution, stir well to form a transparent sol. At the same time, 0.01 mole of tetrabutyl titanate and 0.06 mole of ferric nitrate were mixed and dissolved in the DMF solution, and fully stirred to form a transparent solution. The two solutions were uniformly mixed and stirred on a magnetic stirrer for 12 hours to obtain a precursor sol with a certain viscosity.
[0039] (2) Inject the precursor sol into the syringe, apply a voltage of 23kV to carry out electrospinning, and collect it by the roller. The distance between the roller and the nozzle is 25cm, and the speed is set at 180r / min. After spinning, the precursor fiber film is obtained. .
[0040] (3) After the precursor fiber membrane was pretreated in a muffle furnace at 280°C for 4 hours, it was placed between two graphite plates and baked in a nitrogen atmosphere furnace at 700°C for 10 hours to obtain nanostructured porous iron oxide ...
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