High-activity flue gas desulfurization catalyst and preparation method thereof
A desulfurization catalyst and high-activity technology, which is applied in chemical instruments and methods, physical/chemical process catalysts, separation methods, etc., can solve the problems of strong interaction and unfavorable uniform dispersion of active components, so as to improve activity, prolong life, No clogging effect
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Embodiment 1
[0049] (1) Add the carbon black powder to the ethanol solution containing tetraethyl orthosilicate (where the solid-liquid mass ratio is 1:8, and the tetraethyl orthosilicate is SiO 2 The mass ratio of meter to carbon black powder is 2:1), under the condition of ultrasonic dispersion (the energy density of ultrasonic dispersion is 0.6kW / L, the temperature of ultrasonic dispersion is 40°C, and the time of ultrasonic dispersion is 1 hour), mix well, filter, The solid phase was dried at 50° C. for 2 hours, and then dried to obtain silicon source-modified carbon black powder;
[0050] (2) Add 54g of carbon black powder (by weight of carbon black powder) obtained in step (1) and 600g of pseudoboehmite dry rubber powder (65wt% on a dry basis of alumina) to 6g of nitric acid, 3g of citric acid, and 3g of field Cyanine powder and 360g of pure water were kneaded and extruded, then treated in nitrogen at 400°C for 3 hours, and then calcined in air at 500°C for 5 hours to obtain a silico...
Embodiment 2
[0054] (1) Add carbon black powder to ethanol solution containing tetraethyl orthosilicate (wherein the solid-to-liquid mass ratio is 1:15, and tetraethyl orthosilicate is SiO 2 The mass ratio of meter to carbon black powder is 3:1), under the condition of ultrasonic dispersion (the energy density of ultrasonic dispersion is 1kW / L, the temperature of ultrasonic dispersion is 50°C, and the time of ultrasonic dispersion is 0.5 hours), mix evenly, filter, and solidify Drying at 50° C. for 2 hours, followed by drying treatment, to obtain silicon source modified carbon black powder;
[0055] (2) Add 160g of carbon black powder obtained in step (1) (based on the weight of carbon black powder), 1000g of pseudoboehmite dry rubber powder (65wt% alumina dry basis), add 10g of nitric acid, 4g of citric acid, 4g Cylindrical powder and 350g of pure water were kneaded and extruded, then treated in nitrogen at 450°C for 3 hours, and then calcined in air at 500°C for 5 hours to obtain a silic...
Embodiment 3
[0059] (1) Add the carbon black powder to the ethanol solution containing tetraethyl orthosilicate (where the liquid-solid mass ratio is 1:25, and the tetraethyl orthosilicate is SiO 2 The mass ratio of meter to carbon black powder is 4:1), under the condition of ultrasonic dispersion (the energy density of ultrasonic dispersion is 2kW / L, the temperature of ultrasonic dispersion is 30°C, and the time of ultrasonic dispersion is 0.5 hours), mix evenly, filter, and solidify Drying at 50° C. for 2 hours, followed by drying treatment, to obtain silicon source modified carbon black powder;
[0060] (2) Add 160g of carbon black powder obtained in step (1) (based on the weight of carbon black powder), 800g of pseudo-boehmite dry rubber powder (65wt% alumina dry basis), add 7g of nitric acid, 3g of citric acid, 3g Cylindrical powder and 350g of pure water were kneaded and extruded, then treated in nitrogen at 400°C for 3 hours, and then calcined in air at 500°C for 5 hours to obtain a...
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