A kind of carbon-supported ruthenium-based ammonia synthesis catalyst and preparation method thereof
A technology of ammonia synthesis and carbon loading, applied in chemical instruments and methods, ammonia preparation/separation, physical/chemical process catalysts, etc., can solve the problem of reducing catalyst stability, affecting the ammonia synthesis performance of ruthenium catalysts, and environmental pollution of waste acid solutions and other problems, to achieve the effect of improving ammonia synthesis activity and heat resistance stability, convenient large-scale application, and good heat resistance stability
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Embodiment 1
[0028] (1) Dissolve 15.2 g of barium nitrate in 180 mL of deionized water as dipping solution A; then weigh 100 g of pretreated coconut shell activated carbon dried to constant weight and add it to dipping solution A. After dipping for 12 h at 25°C , dried to constant weight in a blast drying oven at 120°C;
[0029] (2) placing the dried sample in the step (1) in a tubular furnace, and heating up to 850° C. for 10min under argon atmosphere to obtain barium nitrate modified coconut shell activated carbon;
[0030] (3) get 10g of ruthenium trichloride and dissolve it in 180mL of deionized water as dipping solution B; then add the barium nitrate modified coconut shell activated carbon obtained in step (2) into dipping solution B, dipping under 25 ℃ of conditions After 12 hours, directly add 1000 mL of dilute ammonia solution with a volume concentration of 10% to soak for 12 hours, and finally use deionized water to fully wash until the filtrate is detected with silver nitrate sol...
Embodiment 2
[0032] (1) Dissolve 15.2 g of barium nitrate in 180 mL of deionized water as dipping solution A; then weigh 100 g of pretreated coconut shell activated carbon dried to constant weight and add it to dipping solution A. After dipping for 12 h at 25°C , dried to constant weight in a blast drying oven at 120°C;
[0033] (2) placing the dried sample in the step (1) in a tubular furnace, heating up to 600 DEG C and roasting for 10 min under an argon atmosphere to obtain barium nitrate modified coconut shell activated carbon;
[0034] (3) Dissolve 10 g of ruthenium trichloride in 180 mL of deionized water as dipping solution B; then add the barium nitrate modified coconut shell activated carbon obtained in step (2) into dipping solution B, and dipping at 25°C for 12 h Then, directly add 1000 mL of dilute ammonia solution with a volume concentration of 10% to soak for 12 hours, and finally use deionized water to fully wash until the filtrate is detected with silver nitrate solution wi...
Embodiment 3
[0036] (1) Dissolve 15.2 g of barium nitrate in 180 mL of deionized water as dipping solution A; then weigh 100 g of pretreated coconut shell activated carbon dried to constant weight and add it to dipping solution A. After dipping for 12 h at 25°C , dried to constant weight in a blast drying oven at 120°C;
[0037] (2) placing the dried sample in the step (1) in a tube furnace, heating up to 1000 DEG C and calcining for 10min under an argon atmosphere to obtain barium nitrate modified coconut shell activated carbon;
[0038] (3) Dissolve 10 g of ruthenium trichloride in 180 mL of deionized water as dipping solution B; then add the barium nitrate modified coconut shell activated carbon obtained in step (2) into dipping solution B, and dipping at 25°C for 12 h Then, directly add 1000 mL of dilute ammonia solution with a volume concentration of 10% to soak for 12 hours, and finally use deionized water to fully wash until the filtrate is detected with silver nitrate solution with...
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