Method for preparing cyclodextrin/reduced graphene oxide modified ferroferric oxide compound and application
A technology of triiron tetroxide and graphene, which is applied in chemical instruments and methods, special compound water treatment, physical/chemical process catalysts, etc., can solve problems such as the reduction of active sites, achieve a wide pH range, and speed up mass transfer. , the effect of preventing agglomeration
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Embodiment 1
[0021] (1) Disperse 20 mg of graphene oxide in 20 ml of ethylene glycol, sonicate with an ultrasonic cell disruptor for 30 min, and set aside.
[0022] (2) Add 0.4 g FeCl 3 ·6H 2 O, 1.13 g sodium acetate, 0.3 g polyethylene glycol and 20 mg β-CD were added to the dispersion in step (1), and the mixture was magnetically stirred for 30 min, and set aside.
[0023] (3) Transfer the dispersion in step (2) to a 50 mL polytetrafluoroethylene reactor, and react at 200 °C for 8 h.
[0024] (4) Step (3) After the reaction solution was cooled to room temperature, the resulting precipitate was washed with deionized water and ethanol three times repeatedly, and then the sample was vacuum-dried at 50 °C for 12 h.
[0025] (5) The sample obtained in the step (4) of magnetic recovery is ground for later use.
[0026] The prepared β-CD / rGO modified Fe 3 o 4 The complex was placed under a transmission electron microscope (TEM) to observe the morphology of the material, and it was found th...
Embodiment 2
[0028] (1) Disperse 20 mg of graphene oxide in 20 ml of ethylene glycol, sonicate with an ultrasonic cell disruptor for 30 min, and set aside.
[0029] (2) Add 0.4 g FeCl 3 ·6H 2 O, 1.13 g sodium acetate, 0.3 g polyethylene glycol and 20 mg β-CD were added to the dispersion in step (1), and the mixture was magnetically stirred for 30 min, and set aside.
[0030] (3) Transfer the dispersion in step (2) to a 50 mL polytetrafluoroethylene reactor, and react at 200 °C for 8 h.
[0031] (4) Step (3) After the reaction solution was cooled to room temperature, the resulting precipitate was washed with deionized water and ethanol three times repeatedly, and then the sample was vacuum-dried at 50 °C for 12 h.
[0032] (5) The sample obtained in the step (4) of magnetic recovery is ground for later use.
[0033] The prepared catalyst was used to degrade bisphenol A (BPA) to verify its catalytic performance. 20mgL -1 A solution of BPA (20 mL) was placed in a 50 mL Erlenmeyer flask, ...
Embodiment 3
[0035] (1) Disperse 20 mg of graphene oxide in 20 ml of ethylene glycol, sonicate with an ultrasonic cell disruptor for 30 min, and set aside.
[0036] (2) Add 0.4 g FeCl 3 ·6H 2 O, 1.13 g sodium acetate, 0.3 g polyethylene glycol and 20 mg β-CD were added to the dispersion in step (1), and the mixture was magnetically stirred for 30 min, and set aside.
[0037](3) Transfer the dispersion in step (2) to a 50 mL polytetrafluoroethylene reactor, and react at 200 °C for 8 h.
[0038] (4) Step (3) After the reaction solution was cooled to room temperature, the resulting precipitate was washed with deionized water and ethanol three times repeatedly, and then the sample was vacuum-dried at 50 °C for 12 h.
[0039] (5) The sample obtained in the step (4) of magnetic recovery is ground for later use.
[0040] Catalysts were selected Fe 3 o 4 , β-CD / Fe 3 o 4 , rGO and the final composite catalyst, the BPA in Example 2 was catalytically degraded under the same conditions, and it ...
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