Graphene oxide surface arsenic-antimony double-imprinted polymer capable of being magnetically separated in underground medium and preparation method thereof
A graphene surface and imprinted polymer technology, applied in the direction of alkali metal compounds, chemical instruments and methods, alkali metal oxides/hydroxides, etc., can solve problems such as arsenic and antimony pollution, reduce agglomeration and facilitate elution and recombination, good adsorption effect
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[0040] The preparation method of the arsenic-antimony double imprinted polymer on the surface of graphene oxide that can be magnetically separated in the above-mentioned underground medium comprises the following steps:
[0041] A. Ultrasonic disperse 0.3-0.86g of GO into 0.45L of ultrapure water until GO is evenly dispersed in the ultrapure water to stop, the time is about 1 hour, and then a stable GO suspension is obtained;
[0042] B. Add 2.916g of FeCl 3 and 2.502 g of FeSO 4 ·7H 2 O was dissolved in 50ml of deionized water, and then slowly poured into the suspension of A at room temperature. In order to mix evenly with A, pre-stirring was required for 40 minutes;
[0043] C. Increase the temperature of the solution in step B to 60°C, slowly add ammonia water dropwise to the solution under anaerobic conditions by in-situ precipitation method, so that the pH in the solution is greater than 10, and then continue to increase the temperature to 90°C and continue Stir for 4 ...
Embodiment 1
[0050] A. Ultrasonic disperse 0.3g GO into 450mL of ultrapure water for about 1 hour, and then obtain a stable GO suspension;
[0051] B. Add 2.916g of FeCl 3 and 2.502 g of FeSO 4 ·7H 2 O was dissolved in 50ml of deionized water, then slowly poured into the A suspension at room temperature, and mechanically stirred for 40min;
[0052] C. Increase the temperature of the solution in step B to 60°C, slowly add ammonia water dropwise to the solution under nitrogen protection, so that the pH in the solution is greater than 10, then continue to increase the temperature to 90°C and continue stirring for 4 hours;
[0053] D. Use a magnet to collect the product in the solution of step C, wash it repeatedly with ethanol and ultrapure water for 3 times, and then put the product in a vacuum drying oven at 60°C to dry to obtain Fe 3 o 4 / GO (MGO) material, where GO and Fe 3 o 4 The mass ratio is 0.14:1.
Embodiment 2
[0055] A. Ultrasonic disperse 0.54g GO into 450mL of ultrapure water for about 1 hour, and then obtain a stable GO suspension;
[0056] B. Add 2.916g of FeCl 3 and 2.502 g of FeSO 4 ·7H 2 O was dissolved in 50ml of deionized water, then slowly poured into the A suspension at room temperature, and mechanically stirred for 40min;
[0057] C. Increase the temperature of the solution in step B to 60°C, slowly add ammonia water dropwise to the solution under nitrogen protection, so that the pH in the solution is greater than 10, then continue to increase the temperature to 90°C and continue stirring for 4 hours;
[0058] D. Use a magnet to collect the product in the solution of step C, wash it repeatedly with ethanol and ultrapure water for 3 times, and then put the product in a vacuum drying oven at 60°C to dry to obtain Fe 3 o 4 / GO (MGO) material, where GO and Fe 3 o 4 The mass ratio is 0.25:1.
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