Photocatalyst of zinc oxide possessing visible light activity and preparation method
A zinc oxide and catalyst technology, which is applied in the field of zinc oxide photocatalyst and its preparation, can solve the problem of photocatalyst loss of activity, achieve the effects of enriching research and application content, promoting development, and being easy to implement
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Embodiment 1
[0020] In the flask of 500ml, add 1.0g zinc acetate dihydrate, 5g polyvinylpyrrolidone (molecular weight 20,000), be dissolved in ethylene glycol respectively and mix homogeneously, wherein the weight ratio of zinc acetate dihydrate and polyvinylpyrrolidone is 0.2: 1, The weight ratio of ethylene glycol to zinc acetate dihydrate is 300:1; heat up to 140°C under strong stirring, condense and reflux for 5 hours, separate the precipitate by suction filtration while it is hot, wash with absolute ethanol three times, and dry at 120°C 30min, and finally roasted at 300°C to obtain zinc oxide with visible light activity.
Embodiment 2
[0022] Add 1.0g of zinc acetate dihydrate and 2.0g of polyvinylpyrrolidone (molecular weight: 30,000) into a 500ml flask, dissolve them in ethylene glycol and mix well, wherein the weight ratio of zinc acetate dihydrate to polyvinylpyrrolidone is 0.5:1 , the weight ratio of ethylene glycol to zinc acetate dihydrate is 200:1; start to heat up to 195°C under vigorous stirring, condense and reflux for 3 minutes, separate the precipitate by suction filtration while it is hot, wash with absolute ethanol 3 times, and heat up to 120°C Drying for 30 minutes, and finally calcination at 600°C, to obtain zinc oxide with visible light activity.
Embodiment 3
[0024] Add 1.0g of zinc acetate dihydrate and 0.25g of polyvinylpyrrolidone (molecular weight: 60,000) into a 500ml flask, dissolve them in ethylene glycol and mix well, wherein the weight ratio of zinc acetate dihydrate to polyvinylpyrrolidone is 4:1 , the weight ratio of ethylene glycol to zinc acetate dihydrate is 50:1; start to heat up to 200°C under strong stirring, condense and reflux for 1 hour, separate the precipitate by suction filtration while it is hot, wash with absolute ethanol three times, 120°C Dry for 30 minutes, and finally bake at 700°C to obtain zinc oxide with visible light activity.
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