Reverse water gas shift catalyst, preparation method and application thereof
A reverse water gas and catalyst technology, which is applied in the direction of catalyst activation/preparation, chemical instruments and methods, heterogeneous catalyst chemical elements, etc., can solve the problems of low conversion rate of carbon dioxide and poor thermal stability of catalysts, etc. Poor stability and water resistance, high industrial application value, high activity effect
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Embodiment 1
[0052] 1) make 0.5mol / L solution with zirconium oxynitrate and water, measure 500mL above-mentioned zirconium oxynitrate solution and add in the hydrothermal still of 1L polytetrafluoroethylene lining, add 150g urea to it again, the system is at 120 ℃ Treated under hydrothermal conditions for 48 hours, the obtained solid was washed with water until neutral, and then vacuum-dried at 120 °C to obtain ZrO z (OH) 4-2z (The number of hydroxyl groups on the zirconium hydroxide gel can be adjusted depending on the dry contrast, so the subscript z of the O atom indicates a variable value).
[0053] 2) The obtained zirconium hydroxide precursor ZrO z (OH) 4-2z Disperse in 1000ml of anhydrous toluene solvent, in N 2 Under the protection, 200g of 3-aminopropyltriethoxysilane was heated and stirred under reflux for 8h, filtered and dried under vacuum at 60°C to obtain 90g of solid carrier.
[0054] 3) 60 g of the solid carrier obtained in the above step 2) was placed in N 2 Disperse ...
Embodiment 2
[0056] 1) zirconium oxynitrate and cerium nitrate are made into 0.5mol / L (Zr / Ce mol ratio is 8:2) aqueous solution, measure 500mL of above-mentioned solution and add in the hydrothermal still of 1L polytetrafluoroethylene lining, then to wherein 200g of urea was added, the system was treated under hydrothermal conditions at 120°C for 48 hours, the obtained solid was washed with water until neutral, and then vacuum-dried at 120°C to obtain Zr 0.8 Ce 0.2 O z (OH) 4-2z (According to the degree of drying, the number of hydroxyl groups on the zirconium hydroxide gel can be adjusted, so the subscript z of the O atom represents a variable value).
[0057] 2) Disperse the obtained zirconium hydroxide precursor in 1000 ml of anhydrous toluene solvent, under N 2 Under the protection, 200 g of 3-aminopropyltriethoxysilane was heated and stirred under reflux for 8 h, filtered and dried under vacuum at 60 °C to obtain 90 g of a solid carrier.
[0058] 3) 60 g of the solid carrier obtai...
Embodiment 3
[0060] The preparation process is the same as in Example 2, except that the active metal precursor is selected from bissalicylaldehyde ethylenediamine nickel (II), and the obtained catalyst is 10% Ni / Zr 0.8 Ce 0.2 O z @SiO 2 , the pre-reduction temperature of the catalyst before use was 450 °C.
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