Method for preparing nano palladium metal catalyst
A technology of metal catalysts and nano-palladium, applied in metal/metal oxide/metal hydroxide catalysts, chemical instruments and methods, physical/chemical process catalysts, etc., can solve problems such as complex processes and unfavorable large-scale production, and achieve Easy to recover, not easy to deactivate, high activity effect
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Embodiment example 1
[0019]
[0020] Under an argon atmosphere, weigh 0.2g functional additive A1 and dissolve it in 4mL of toluene, stir for 30min, then add 0.8g SiO 2 (Specific surface is 420m 2 / g), stirred at 80°C for 4h, cooled to room temperature, and then added 1mL of Pd(OAc) with a concentration of 0.02g / mL 2 Toluene solution, stirred at 80°C for 6h, filtered, washed the filter cake with toluene, dried the filter cake under vacuum at room temperature, and reduced it under hydrogen atmosphere at 200°C for 3h, added 4mL of toluene to the solid obtained above, and then added 0.1g tetraethyl orthosilicate, Stir at 50°C for another 10h, filter, wash the filter cake with toluene, and vacuum-dry the filter cake at 50°C for 20h to obtain the final catalyst C1.
Embodiment example 2
[0022] Under an argon atmosphere, weigh 0.3g functional additive A1 and dissolve it in 4mL of toluene, stir for 30min, then add 0.7g SiO 2 (Specific surface is 420m 2 / g), stirred at 80°C for 4h, cooled to room temperature, and then added 0.5mL of Pd(OAc) with a concentration of 0.02g / mL 2 Toluene solution, stirred at 50°C for 6h, filtered, washed the filter cake with toluene, dried the filter cake under vacuum at room temperature, and reduced it under hydrogen atmosphere at 200°C for 3h, added 4mL of toluene to the solid obtained above, and then added 0.1g tetraethyl orthosilicate, Stir at 50°C for another 8h, filter, wash the filter cake with toluene, and vacuum-dry the filter cake at 50°C for 20h to obtain the final catalyst C2.
Embodiment example 3
[0024]
[0025] Under an argon atmosphere, weigh 0.1g of functional aid A2 and dissolve it in 4mL of methanol, stir for 30min, then add 0.9g of treated SiO 2 (Specific surface is 420m 2 / g), after stirring at 25°C for 48h, add 0.5mL of Pd(OAc) with a concentration of 0.01g / mL 2 Methanol solution, stirring at 25°C for 8h, filtering, washing the filter cake with methanol, drying the filter cake under vacuum at room temperature, reducing it under hydrogen for 6h at 180°C, adding 4mL of methanol to the reduced catalyst, and then adding 0.1g of orthosilicate Ethyl ester, stirred at 25°C for another 16h, filtered, washed the filter cake with methanol, and vacuum-dried at 50°C for 12h to obtain the final catalyst C3.
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