Fenton reagent Fe3O4/C as well as preparation method and application thereof
A technology of Fenton's reagent and fe3o4, which is used in catalyst activation/preparation, chemical instruments and methods, water/sludge/sewage treatment, etc., can solve problems such as low efficiency, and achieve simple preparation method, good catalytic performance, and economical recovery. cost effect
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Embodiment 1
[0032] Example 1 Fe 3 o 4 / C nanomaterials
[0033] (1) The preparation method is as follows
[0034] 1. Synthesis of Fe-BTC precursor
[0035] 1.3 g of trimesic acid was dissolved in an aqueous sodium hydroxide solution consisting of 50 g of deionized water and 0.75 g of sodium hydroxide to obtain a colorless solution 1.
[0036] Yellow-orange solution 2 was prepared by dissolving 2.5 g of ferric chloride hexahydrate in 50 g of deionized water.
[0037] Under magnetic stirring, solution 2 was added dropwise into solution 1 to form a brown suspension. The resulting suspension was stirred at room temperature for two hours and the solid product was recovered by centrifugation. The solid product obtained above was washed several times with deionized water and absolute ethanol, and dried at room temperature to obtain an iron-based metal-organic framework Fe-BTC.
[0038] 2. Fe 3 o 4 Synthesis of / C
[0039] The Fe-BTC powder obtained above was evenly spread in a porcelain...
Embodiment 2
[0045] Embodiment 2 Fenton's reagent Fe 3 o 4 Application of / C in Removal of Organic Dyes by Electro-Fenton Process
[0046] (1) MoO 3-x / C / CoO nanocomposites were prepared by the following method
[0047] 1. MoO 3 Synthesis of nanorods
[0048] 4mmol (NH 4 ) 6 Mo 7 o 24 4H 2 O was dissolved in 80ml of deionized water, and magnetically stirred for 30min to obtain a homogeneous solution. Subsequently, 12 ml of nitric acid was added to the above solution, and after stirring for 30 min, the obtained reactant was transferred into an autoclave, and heated in an oven at 180° C. for 24 hours. Take out the autoclave, wait for it to cool to room temperature, and collect the product by centrifugal centrifugation. Then they were washed three times with absolute ethanol and deionized water, and the resultant was dried in an oven at 60°C to obtain MoO 3 Nano stave.
[0049] 2. MoO 3 / Synthesis of ZIF-67 precursor
[0050] 0.6g Co(NO 3 )2·6H 2 O was dispersed in 40 mL of d...
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