a high performance nh 3 ‑scr catalyst and its preparation method and use
A supported catalyst, tio2-cuo technology, used in chemical instruments and methods, separation methods, dispersed particle separation, etc., can solve problems such as poor low temperature activity and sulfur resistance, limitations, etc. Simple and fast effects
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Embodiment 1
[0021] The preparation of embodiment 1.Ti1 / Ce9 sample
[0022] Accurately measure 0.4437g of n-tetrabutyl titanate and slowly add it dropwise to 22ml of absolute ethanol (containing 2ml of CH 3 COOH, to inhibit the hydrolysis of n-butyl titanate), magnetically stir in an ice-water bath to make it evenly mixed, and then add 2g CeO 2 into the solution and continued to stir for 2h to obtain a suspension. Finally, the suspension was evaporated to dryness in an oil bath to obtain a powdery substance, which was dried in an oven at 110°C for 12 hours, ground evenly, and then calcined at 500°C for 4 hours in an air atmosphere in a muffle furnace to obtain Ti1 / Ce9 supported catalyst. Its XRD, H 2 -TPR and NH 3 -SCR activity results are attached figure 1 -3.
Embodiment 2
[0023] Example 2. Ti1Cu 0.001 / CeO 2 Catalyst preparation
[0024] Accurately measure 0.4437g n-tetrabutyl titanate and 0.116ml 0.1mol / L copper nitrate solution and slowly add it dropwise to 22ml absolute ethanol (containing 2ml CH 3 COOH, to inhibit the hydrolysis of n-butyl titanate), magnetically stir in an ice-water bath to make it evenly mixed, and then add 2g CeO 2into the solution and continued to stir for 2h to obtain a suspension. Finally, the suspension was evaporated to dryness in an oil bath to obtain a powdery substance, which was dried in an oven at 110°C for 12 hours, ground evenly, and then calcined at 500°C for 4 hours in an air atmosphere in a muffle furnace to obtain Ti1Cu 0.001 / CeO 2 supported catalyst. Its XRD, H 2 -TPR and NH 3 -SCR activity results are attached figure 1 -3.
Embodiment 3
[0025] Example 3. Ti1Cu 0.005 / CeO 2 Catalyst preparation
[0026] Accurately measure 0.4437g n-tetrabutyl titanate and 0.581ml 0.1mol / L copper nitrate solution and slowly add it dropwise to 22ml absolute ethanol (containing 2ml CH 3 COOH, to inhibit the hydrolysis of n-butyl titanate), magnetically stir in an ice-water bath to make it evenly mixed, and then add 2g CeO 2 into the solution and continued to stir for 2h to obtain a suspension. Finally, the suspension was evaporated to dryness in an oil bath to obtain a powdery substance, which was dried in an oven at 110°C for 12 hours, ground evenly, and then calcined at 500°C for 4 hours in an air atmosphere in a muffle furnace to obtain Ti1Cu 0.005 / CeO 2 supported catalyst. Its XRD, H 2 -TPR and NH 3 -SCR activity results are attached figure 1 -3.
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