Fe/pressed active carbon catalyst and preparation method thereof
A technology for shaping activated carbon and catalysts, applied in physical/chemical process catalysts, chemical instruments and methods, metal/metal oxide/metal hydroxide catalysts, etc., can solve the problem of increasing raw material costs and operating costs, increasing costs and burdens, Catalyst activity and selectivity and other performance degradation problems, to achieve the effect of improving catalytic performance and stability, preventing collapse and expansion, and inexpensive raw materials
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Embodiment 1
[0033] A. According to the mass percentage of elements: Fe=53.8wt%, Mn=38.5wt%, Li=7.7wt%, weigh 10.8214g iron nitrate, 3.4934g manganese nitrate, 2.1161g lithium nitrate, dissolve in 20ml water to make a solution , add a drop of dispersant AEO-3, stir to prepare impregnation solution;
[0034] Divide the impregnating solution into three groups according to the volume ratio of 2:2:1.
[0035] B. Under vacuum conditions, immerse 1.5004g of compressed fruit shell charcoal into the first group of solutions, mix and stir evenly, place in an oven and dry at 50°C for 72 hours, and dry the obtained material in 20ml / min of flowing nitrogen Under protection, calcined at 100°C for 0.5 hours, calcined at 300°C for 3 hours, and passivated for 24 hours.
[0036] C. impregnating the material obtained after step B is dried into the second group of solutions; other steps are the same as step B;
[0037] Then the material obtained by drying is impregnated with the third group of solutions, a...
Embodiment 2
[0040] A. According to the mass percentage of elements: Fe=41.67wt%, Mn=41.67wt%, Mg=8.33wt%, Cu=8.33wt% Weigh 6.241g iron oxalate, 4.8818g manganese nitrate, 3.1985g magnesium nitrate, 1.1291 g copper nitrate, dissolved in 30ml of water and ethanol mixture to make a solution (water:ethanol=2:1), and stirred to make an impregnating solution;
[0041] Divide the impregnating solution into four groups according to the volume ratio of 1:1:1:1.
[0042] B. Under vacuum conditions, immerse 2.4016g of extruded coconut shell charcoal in the first group of solutions, mix and stir evenly, and place in an oven to dry at 90°C for 24 hours. The material obtained after drying was calcined at 400° C. for 2 hours under the protection of flowing helium gas at 20 ml / min, and then passivated for 24 hours.
[0043] C. impregnating the material obtained after step B is dried into the second group of solutions; other steps are the same as step B;
[0044] D. Immerse the material obtained after s...
Embodiment 3
[0048] A. According to element mass percentage content: Fe=71.44wt%, Mn=14.28wt%, Na=7.14wt%, Ca=7.14wt% Weigh 10.8225g ferric nitrate, 0.9758g manganese nitrate, 0.6909g sodium carbonate, 0.8845 g calcium nitrate, dissolved in 20ml water to make a solution, stirred to make an impregnating solution;
[0049] Divide the impregnating solution into three groups according to the volume ratio of 2:2:1.
[0050] B. Under vacuum conditions, immerse 0.6092g of petal shell charcoal into the first group of solutions, mix and stir evenly, and dry naturally at 25-30°C for 150 hours. The material obtained after drying was calcined at 400° C. under the protection of 20 ml / min flowing argon for 1 hour, and then passivated for 24 hours.
[0051] C. impregnating the material obtained after step B is dried into the second group of solutions; other steps are the same as step B;
[0052] Then the material obtained by drying is impregnated with the third group of solutions, after drying, it is c...
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