A kind of preparation method of nanometer rare earth metal oxide/carbon nanotube composite catalyst
A carbon nanotube composite, nano rare earth technology, applied in metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, chemical instruments and methods, etc. Mixed impurities and other problems, to achieve the effect of simple process, easy large-scale production, good crystallinity
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Embodiment 1
[0039] Embodiment 1: Strong acid purifies CNTs
[0040] Add 5 g of pristine CNTs (purchased from Shenzhen Nano Harbor Co., Ltd., with an outer diameter of 40-60 nm, a length of 5-15 μm, and a purity >97%) into 240 ml of concentrated HNO at a volume ratio of 3:1 3 and concentrated H 2 SO 4 In the mixed solution, after ultrasonic dispersion for a certain period of time, reflux at 80°C for 6 hours, dilute, filter with suction, wash and ultrasonically disperse in 200ml HCl (3mol / L) at 65°C for 6 hours, filter with suction and wash with deionized water until pH = 7. Dry at 60°C for 24 hours to obtain purified CNTs. The following examples 2-4 all use the strong acid purified CNTs obtained in this example.
Embodiment 2
[0042] Disperse 0.03g of acid-purified CNTs in 20ml of ethylene glycol (EG) by ultrasonication, and stir for 30min to obtain a homogeneous suspension; at the same time, dissolve 0.25g of yttrium nitrate in another portion of ethylene glycol (20mL) , ultrasonically stirred for 30 minutes to form a uniform solution, mixed with the CNTs ethylene glycol suspension, and stirred at a constant speed for 30 minutes. Then centrifuged, the centrifuged obtained Y 3+ / CNTs were dispersed in 40ml ethylene glycol (EG) solution and ultrasonically dispersed for 1h. Then, 1 g of PEG and 3.6 g of NaAc were dissolved in the above solution, and stirred at a constant speed for 30 min to obtain an in-situ growth reaction precursor. The precursor was put into a three-neck flask with a volume of 100 mL, and reacted in an oil bath at 200° C. for 2.5 h. After the product was cooled to room temperature, the product was repeatedly washed three times with deionized water and absolute ethanol, and suctio...
Embodiment 3
[0044] Disperse 0.03g of acid-purified CNTs in 20ml of ethylene glycol (EG) by ultrasound, and stir for 30min to obtain a homogeneous suspension; at the same time, dissolve 0.2g of neodymium nitrate in another portion of ethylene glycol (20mL), After ultrasonic stirring for 30 minutes to form a uniform solution, mix it with the CNTs ethylene glycol suspension, and stir at a constant speed for 30 minutes. Then centrifuge, the Nd obtained by centrifugation 3+ / CNTs were dispersed in 40ml ethylene glycol (EG) solution and ultrasonically dispersed for 1h. Then, 1 g of PEG and 3.6 g of NaAc were dissolved in the above solution, and stirred at a constant speed for 30 min to obtain an in-situ growth reaction precursor. The precursor was put into a three-neck flask with a volume of 100 mL, and reacted in an oil bath at 200° C. for 2.5 h. After the product was cooled to room temperature, the product was repeatedly washed three times with deionized water and absolute ethanol, and suct...
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