A kind of cobalt catalyst for synthesizing ammonia and preparation method thereof
A cobalt catalyst, a technology for synthesizing ammonia, applied in catalyst activation/preparation, ammonia preparation/separation, chemical instruments and methods, etc., to achieve the effect of good ammonia synthesis performance and good industrial application prospects
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Embodiment 1
[0021] 1) Dissolve 0.95g of barium nitrate in 20 mL of water to form a barium nitrate aqueous solution; then impregnate the barium nitrate aqueous solution into 5 g of graphitized activated carbon (with a specific surface area of 860 m 2 / g);
[0022] 2) Dissolve 2.47g of cobalt nitrate hexahydrate in 20mL of methanol after drying at 150°C for 24 hours;
[0023] 3) Add the methanol solution of cobalt nitrate obtained in step 2) to the barium-containing activated carbon in step 1), and impregnate at 30 °C for 0.5 hours;
[0024] 4) The obtained solid material was dried under an infrared lamp at 80 °C for 1 hour to remove the methanol solution, and then reduced in pure hydrogen at 450 °C for 6 hours to prepare a cobalt catalyst for ammonia synthesis.
Embodiment 2
[0026] 1) Dissolve 0.95g of barium nitrate and 0.52g of potassium nitrate in 20 mL of water to form a mixed aqueous solution of barium nitrate and potassium nitrate; then impregnate the mixed aqueous solution of barium nitrate and potassium nitrate into 5 g of graphitized activated carbon (specific surface area is 100m 2 / g);
[0027] 2) Dissolve 2.47g of cobalt nitrate hexahydrate in 20mL of ethanol after drying at 150°C for 0.2 hours;
[0028] 3) Add the ethanol solution of cobalt nitrate obtained in step 2) to the barium-containing activated carbon in step 1), and soak at 30 °C for 0.5 hours;
[0029] 4) The obtained solid matter was dried with an infrared lamp at 180 °C for 0.5 hours to remove the ethanol solution, and then placed in 25% H 2 +75%N 2 Reduction treatment at 430 °C for 12 hours in mixed gas to prepare cobalt catalyst for ammonia synthesis.
Embodiment 3
[0031] 1) Dissolve 1.43g of barium nitrate and 1.1g of sodium nitrate in 20 mL of water to form a mixed aqueous solution of barium nitrate and sodium nitrate; then impregnate the mixed aqueous solution of barium nitrate and sodium nitrate into 5 g of graphitized activated carbon (specific surface area is 1020m 2 / g);
[0032] 2) Dissolve 0.69g of cobalt nitrate hexahydrate in 20mL of propanol after drying at 100°C for 40 hours;
[0033] 3) Add the propanol solution of cobalt nitrate obtained in step 2) to the barium-containing activated carbon in step 1), and impregnate at 50 °C for 1.5 hours;
[0034] 4) The obtained solid matter was dried under infrared lamp at 60 °C for 2 hours to remove the propanol solution, and then in 75% H 2 +25%N 2 Reduction treatment at 450 °C for 12 hours in mixed gas to prepare cobalt catalyst for ammonia synthesis.
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