Method for preparing BaFeO3 perovskite catalyst with excellent sulfur resistance for storing nitrogen oxide
A nitrogen oxide and perovskite technology is applied in the field of preparation of nitrogen oxide storage BaFeO3 perovskite catalysts, which can solve the problems of poor sulfur resistance and decreased storage capacity, achieve good sulfur resistance, reduce preparation costs, The effect of storing high amounts of nitrogen oxides
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Embodiment 1
[0010] Prepare Ba(NO 3 ) 2 and Fe(NO 3 ) 3 0.1mol / L solution, according to Ba:Fe molar ratio is that 1:1 ratio gets 100ml and mixes evenly respectively, adds the citric acid solution 40ml of 0.5mol / L dropwise after ultrasonic half an hour (molar ratio is Ba:Fe:CA= 1:1:2), the temperature was maintained at 80°C, and the pH of the solution was controlled to be 9.0 with ammonia solution throughout the process to prevent precipitation in the solution, and the electronic stirrer was used to continuously stir, evaporate, and form a viscous substance; After drying in an oven at 120°C for 13 hours, it was first calcined at 400°C for two hours to completely burn the organic matter, and then calcined in a tube furnace at a heating rate of 4°C / min to 750°C for 6 hours.
[0011] The specific surface area of the prepared sample is 6.5m 2 / g. The NOx storage performance test was carried out on the samples, and the test was carried out in a quartz tubular fixed-bed reactor with an in...
Embodiment 2
[0014] Prepare Ba(NO 3 ) 2 and Fe(NO 3 ) 3 0.1mol / L solution, according to Ba:Fe molar ratio is that 1:1 ratio gets 100ml and mixes evenly respectively, adds the citric acid solution 40ml of 0.5mol / L dropwise after ultrasonic half an hour (molar ratio is Ba:Fe:CA= 1:1:2), the temperature was maintained at 80°C, and the pH of the solution was controlled to be 9.0 with ammonia solution throughout the process to prevent precipitation in the solution, and the electronic stirrer was used to continuously stir, evaporate, and form a viscous substance; After drying in an oven at 120°C for 13 hours, it was first calcined at 400°C for two hours to completely burn the organic matter, and then calcined in a tube furnace at a heating rate of 4°C / min to 850°C for 6 hours.
[0015] The specific surface area of the prepared sample is 5.9m 2 / g. Take 500mg sample at 800ppm NO, 5% O 2 , N 2 For balance gas, the air velocity is 2.52×10 4 h -1 Under the condition of constant temperatu...
Embodiment 3
[0017] Prepare Ba(NO 3 ) 2 and Fe(NO 3 ) 3 0.1mol / L solution, take 100ml each according to the Ba:Fe molar ratio of 1:1 and mix evenly, add 40ml of 0.5mol / L citric acid solution dropwise after ultrasonic half an hour (the molar ratio n / n is Ba:Fe : CA=1: 1: 2), the temperature is maintained at 80°C, the pH of the solution is controlled by ammonia solution to be 9.0 in the whole process to prevent precipitation in the solution, and the electronic stirrer is used to continuously stir, evaporate, and form a viscous substance; After it was dried in an oven at 120°C for 13 hours, it was first calcined at 400°C for two hours to completely burn the organic matter, and then calcined in a tube furnace at a heating rate of 4°C / min to 950°C for 6 hours.
[0018] The specific surface area of the prepared sample is 2.6m 2 / g. Take 500mg sample at 800ppm NO, 5% O 2 , N 2 For balance gas, the air velocity is 2.52×10 4 h -1 Under the condition of constant temperature adsorption of...
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