Preparation method for magnetic nanometer microballoon photocatalysis composite materials
A technology of magnetic nano and composite materials, applied in the field of preparation of photocatalytic composite materials, can solve the problems of accelerating the photocorrosion of magnetic materials, reducing the utilization of material light, and poor suspension of catalysts, so as to prevent photocorrosion and photocatalytic performance Good, high magnetic particle content effect
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Embodiment 1
[0037] (1) 24g FeCl 3 ·6H 2 O and 9.82 g FeCl 2 4H 2 O to mix, add 100mL deionized water and stir evenly, after mixing evenly, add 50mL ammonia water, add 3.76g oleic acid after 30 minutes, and continue the reaction for 1.5 hours. The whole process needs to be kept in an oil bath at 80°C. separated, washed three times with ethanol and deionized water, dried, and ground to obtain Fe 3 o 4 particles;
[0038] (2) Take the above Fe 3 o 4 For 0.1 g of particles, measure 3 mL of absolute ethanol (purity: 99.8%) and mix, weigh 0.09 g of TEOS, and add to the solution under ultrasonic treatment. After continuous sonication for 30 min, this solution was transferred to a vapor phase apparatus as the solid phase, and the liquid phase was 5 mL of distilled water and 0.1 mL of anhydrous ethylenediamine. The device was sealed and placed in an oven at 100°C for 12 hours. The solid phase product was washed several times with distilled water and ethanol, magnetically separated, and dr...
Embodiment 2
[0040] (1) 24g FeCl 3 ·6H 2 O and 9.82 g FeCl 2 4H 2 O to mix, add 100mL deionized water and stir evenly, after mixing evenly, add 50mL ammonia water, add 3.76g oleic acid after 30 minutes, and continue the reaction for 1.5 hours. The whole process needs to be kept in an oil bath at 80°C. separated, washed three times with ethanol and deionized water, dried, and ground to obtain Fe 3 o 4 particles;
[0041] (2) Take the above Fe 3 o 4 For 0.1 g of particles, measure 3 mL of absolute ethanol (purity: 99.8%) and mix, weigh 0.09 g of TEOS, and add to the solution under ultrasonic treatment. After continuous sonication for 30 min, this solution was transferred to a vapor phase apparatus as the solid phase, and the liquid phase was 5 mL of distilled water and 0.1 mL of anhydrous ethylenediamine. The device was sealed and placed in an oven at 100°C for 12 hours. The solid phase product was washed several times with distilled water and ethanol, magnetically separated, and dr...
Embodiment 3
[0044] (1) 24g FeCl 3 ·6H 2 O and 9.82 g FeCl 2 4H 2 O to mix, add 100mL deionized water and stir evenly, after mixing evenly, add 50mL ammonia water, add 3.76g oleic acid after 30 minutes, and continue the reaction for 1.5 hours. The whole process needs to be kept in an oil bath at 80°C. separated, washed three times with ethanol and deionized water, dried, and ground to obtain Fe 3 o 4 particles;
[0045] (2) Take the above Fe 3 o 4 For 0.1 g of particles, measure 3 mL of absolute ethanol (purity: 99.8%) and mix, weigh 0.09 g of TEOS, and add to the solution under ultrasonic treatment. After continuous sonication for 30 min, this solution was transferred to a vapor phase apparatus as the solid phase, and the liquid phase was 5 mL of distilled water and 0.1 mL of anhydrous ethylenediamine. The device was sealed and placed in an oven at 100°C for 12 hours. The solid phase product was washed several times with distilled water and ethanol, magnetically separated, and dr...
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