Catalyst for exhaust gas purification and preparation method thereof
A waste gas purification and catalyst technology, applied in the direction of catalyst activation/preparation, physical/chemical process catalysts, chemical instruments and methods, etc., can solve problems such as high light-off temperature, low catalytic activity of precious metals, and lower light-off temperature, so as to improve Catalytic activity, improved catalytic activity, and easy operation
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Embodiment 1
[0028] A method for preparing a catalyst for exhaust gas purification, the method comprising the following steps:
[0029] (1) by CuFe 1.94 SM 0.03 Er 0.03 o 4 The stoichiometric ratio of 0.5mol copper nitrate, 0.47mol ferric nitrate, 0.015mol samarium nitrate and 0.015mol erbium nitrate were respectively dissolved in 50mL deionized water to form metal nitrate precursor solution A;
[0030] (2) Dissolve 1 mol of citric acid in 50 mL of deionized water to form citric acid precursor solution B;
[0031] (3) Slowly add solution B to solution A, adjust the pH to neutral with ammonia water, and continue to stir at 75°C until the solution is in a sol state; wherein, the stirring speed is 150rpm, and the stirring time is 6h;
[0032] (4) Add cerium oxide to the above sol, and continue to stir for 3 hours; then the sol is aged for 12 hours to form a gel, and then dried at 140°C for 15 hours to form a xerogel; put it in a muffle furnace at 300°C Calcined for 5 h, then calcined at ...
Embodiment 2
[0035] A method for preparing a catalyst for exhaust gas purification, the method comprising the following steps:
[0036] (1) by CuFe 1.94 SM 0.04 Er 0.02 o 4The stoichiometric ratio of 0.5mol copper nitrate, 0.47mol ferric nitrate, 0.02mol samarium nitrate and 0.01mol erbium nitrate were respectively dissolved in 50mL deionized water to form metal nitrate precursor solution A;
[0037] (2) Dissolve 1 mol of citric acid in 50 mL of deionized water to form citric acid precursor solution B;
[0038] (3) Slowly add solution B to solution A, adjust the pH to neutral with sodium hydroxide solution, and continue stirring at 80°C until the solution is in a sol state; the stirring speed is 200rpm, and the stirring time is 3h;
[0039] (4) Add cerium oxide to the above sol, and continue to stir for 4 hours; then the sol is aged for 10 hours to form a gel, and then dried at 160°C for 14 hours to form a xerogel; put it in a muffle furnace at 320°C Calcined for 4 hours, then calcine...
Embodiment 3
[0042] A method for preparing a catalyst for exhaust gas purification, the method comprising the following steps:
[0043] (1) by CuFe 1.94 SM 0.02 Er 0.04 o 4 The stoichiometric ratio of 0.5mol copper nitrate, 0.47mol ferric nitrate, 0.01mol samarium nitrate and 0.02mol erbium nitrate were respectively dissolved in deionized water to form metal nitrate precursor solution A;
[0044] (2) Dissolve 1 mol of citric acid in 50 mL of deionized water to form citric acid precursor solution B;
[0045] (3) Slowly add solution B to solution A, adjust the pH to neutral with sodium carbonate solution, and continue stirring at 70°C until the solution is in a sol state; the stirring speed is 100rpm, and the stirring time is 9h;
[0046] (4) Add cerium oxide to the above sol, and continue to stir for 2 hours; then the sol is aged for 14 hours to form a gel, and then dried at 120°C for 16 hours to form a xerogel; put it in a muffle furnace at 280°C Calcined for 6 hours, then calcined at...
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