Magnetic graphite phase carbon nitride/MIL-125(Ti) composite photocatalyst, and preparation method thereof
A graphitic carbon nitride, composite light technology, applied in the field of photocatalytic materials, can solve the problems of low catalytic activity, limited utilization, lack of visible light response, etc.
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Embodiment 1
[0031] Example 1: Fe 3 o 4 preparation of
[0032] In this embodiment, preferably, 1.08 g of ferric chloride hexahydrate, 0.80 g of polyethylene glycol, and 32 mL of ethylene glycol were mixed with magnetic stirring for 30 minutes, and then 2.88 g of anhydrous sodium acetate was added and magnetically stirred for 30 minutes. This precursor was transferred into a 50mL sealed reaction kettle with polytetrafluoroethylene lining, placed in an electric blast constant temperature drying oven at 200°C for solvothermal reaction for 8 hours, then cooled naturally to room temperature, separated by a magnet, and successively washed with distilled water Wash the product with absolute ethanol 3-5 times, and then place the product at 60°C for 48 hours in vacuum; after grinding, Fe 3 o 4 .
Embodiment 2
[0033] Example 2: Fe 3 o 4 @SiO 2 Preparation of Nanomaterials
[0034] In the present embodiment, preferably, take 100mg of Fe 3 o 4 Place in 80 mL of anhydrous isopropanol, ultrasonically disperse for 15 minutes, then add 7.50 mL of deionized water and 60 μL of tetraethyl silicate, then slowly add 9 mL of concentrated ammonia water to the above solution and ultrasonically for 35 minutes, then separate by magnet And wash the product with distilled water and absolute ethanol for 3-~5 times, and then place the product at 60°C for 48 hours in vacuum; after grinding, Fe 3 o 4 @SiO 2 nanomaterials.
Embodiment 3
[0035] Embodiment 3: the preparation of magnetic graphite phase carbon nitride / MIL-125 (Ti) composite photocatalyst
[0036] In this embodiment, preferably, weigh 0.05g of g-C 3 N 4 Place in 25.53 mL of N,N-dimethylformamide for ultrasonic dispersion, then add 2.84 mL of methanol, 1.76 g of terephthalic acid, and 2.18 mL of n-butyl titanate, mix magnetically for 30 minutes, and then add 50 mg of polyvinylpyrrolidone Continue to stir for 10min, and finally add 50mg of Fe 3 o 4 @SiO 2 The nanomaterials were dispersed in the above solution, and stirred electrically for 10 minutes. Move this precursor into a 50mL sealed reaction kettle with polytetrafluoroethylene lining, place it in an electric blast constant temperature drying oven at 150°C for solvothermal reaction for 16h, then cool it down to room temperature naturally, separate it with a magnet, and use it in sequence Wash the product with distilled water and absolute ethanol for 3-5 times, and then place the product at...
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