Preparation method of fe3o4/go magnetic composite material
A technology of magnetic composite materials and magnetic microspheres, which can be used in the preparation of microspheres, chemical instruments and methods, microcapsule preparations, etc. Effect
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Embodiment 1
[0044] Preparation of Fe 3 o 4 / GO-A
[0045] 20mgFe 3 o 4 / SiO 2 / SH and 10 mg GO were added to 60 mL of an aqueous solution with a pH of 10.0, ultrasonically dispersed for 5 min, then mechanically stirred at 60 °C for 6 h, then the reaction was stopped and the Fe 3 o 4 / GO was separated from the supernatant, washed 3 times with water and dried in vacuum to obtain a Fe 3 o 4 / GO magnetic composite material Fe 3 o 4 / GO-A.
[0046] Wherein the external magnet is to place a magnet outside the bottom of the beaker; the magnetic microspheres modified by thiol (Fe 3 o 4 / SiO 2 / SH) particle size is about 200nm.
Embodiment 2
[0048] Preparation of Fe 3 o 4 / GO-B
[0049] 20mgFe 3 o 4 / SiO 2 / SH and 10 mg GO were added to 60 mL of an aqueous solution with a pH of 7.0, ultrasonically dispersed for 5 min, then mechanically stirred at 90 °C for 6 h, then the reaction was stopped and the Fe 3 o 4 / GO was separated from the supernatant, washed 3 times with water and dried in vacuum to obtain another Fe 3 o 4 / GO magnetic composite material Fe 3 o 4 / GO-B.
[0050] Wherein the external magnet is to place a magnet outside the bottom of the beaker; the magnetic microspheres modified by thiol (Fe 3 o 4 / SiO 2 / SH) particle size is about 200nm.
[0051] The synthetic reaction schematic diagram of above-mentioned embodiment 1 and embodiment 2 sees figure 1 .
[0052] To the Fe obtained in above-mentioned embodiment 1 and embodiment 2 3 o 4 / GO magnetic composites were analyzed and tested, and their characterizations are as follows.
[0053] SEM analysis
[0054] Fe 3 o 4 / GO-A and Fe 3 o ...
Embodiment 3
[0067] Magnetic solid phase extraction of aromatic amines
[0068] First, weigh 10 mg Fe 3 o 4 / GO was added to a 150mL water sample with a pH of 5.0, and the aromatic amine and Fe 3 o 4 / GO binding and capture to the solid surface. In order to capture the aromatic amine more completely, the mixture was first ultrasonicated for 2 min, and then placed in a water bath at 20°C for 15 min to equilibrate. Then a magnet is added to move the Fe 3 o 4 The / GO-arylamine complex was separated from the water sample, and the aromatic amine was desorbed with 2 mL of acetonitrile (1% NaOH).
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