CuO/CeO2 nanorod catalyst and synthesis and application thereof
A nanorod and catalyst technology, applied in CuO/CeO2 nanorod catalyst and its synthesis and application, can solve problems affecting correct cognition
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Embodiment 1
[0042] 1.96 g of cerium nitrate hexahydrate and 16.88 g of sodium hydroxide were dissolved in 40 mL and 30 mL of deionized water, respectively. After the sodium hydroxide solution was cooled to room temperature, it was added dropwise to the cerium nitrate solution, and the solution was uniformly stirred on a magnetic stirrer. After the dropwise addition was completed, the mixed suspension was light purple, and the stirring was continued for 30 minutes. The obtained mixed suspension was transferred to a 100 mL hydrothermal reactor, and heated at 100° C. for 24 hours. After the reaction solution was cooled to room temperature, the obtained precipitate was centrifuged, washed alternately with water and ethanol until the pH was close to 7, and dried at 60°C for 12 hours to obtain CeO 2 Nano stave. Obtained CeO 2 The nanorods were heat-treated at 25 °C, 100 °C, 200 °C, 300 °C, 400 °C, 500 °C, 600 °C for 2 h, and the obtained samples were marked as CeO 2 -T. CeO 2 -25, CeO 2 ...
Embodiment 2
[0044] Get 0.4g CeO gained in Example 1 2 -25 was dispersed in 15mL of deionized water, 5mL of an aqueous solution containing 0.605g of copper nitrate trihydrate was added, stirred for 30 minutes, the resulting mixture was frozen with liquid nitrogen, transferred to a freeze-drying agent for freeze-drying for 24h, and the obtained sample was refrigerated in air for 600 calcined at ℃ for 2h to obtain CuO / CeO 2 -25 catalyst (CuO and CeO 2 mass ratio of 5.0%). CuO / CeO 2 The XRD pattern of -25 is shown in image 3 , see TEM and HRTEM images figure 2 d, It can be seen that the morphology of the cerium oxide support after loading and calcining copper oxide does not change much, but the main exposed crystal planes are changed to {111} planes.
Embodiment 3
[0046] Get 0.4g CeO gained in Example 1 2 -100 was dispersed in 15 mL of deionized water, 5 mL of an aqueous solution containing 0.605 g of copper nitrate trihydrate was added, stirred for 30 minutes, the resulting mixture was frozen with liquid nitrogen, transferred to a freeze-drying agent for freeze-drying for 24 h, and the obtained sample was placed in air for 600 calcined at ℃ for 2h to obtain CuO / CeO 2 -100 catalyst (CuO and CeO 2 mass ratio of 5.0%).
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