Cobalt-molybdenum low-temperature sulfur tolerant shift catalyst and preparation method thereof
A sulfur-resistant conversion and catalyst technology, applied in chemical instruments and methods, physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, etc., can solve the problem of poor catalyst structure stability and activity stability, Unavoidable operation of the catalyst, reduction of the specific surface of the catalyst, etc., to achieve good economic benefits, good stability of low-temperature conversion activity, and improvement of activity stability and structural stability
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Embodiment 1
[0043] Dissolve 8.9g of ammonium molybdate in 30.0mL of deionized water to obtain ammonium molybdate solution A; dissolve 11.6g of cobalt nitrate in 30.0mL of deionized water, then add 3.0g of citric acid and 3.0g of oxalic acid to the above cobalt nitrate in sequence solution, stirring and dissolving to obtain solution B containing cobalt. Dissolve 2.7g of lanthanum nitrate in 20mL of deionized water to obtain rare earth additive solution C.
[0044] Weigh 50.0g gibbsite, 8.0g nano zirconia, 30.8g activated carbon, 6g scallop powder and mix evenly, add solution A, knead evenly; then add solution B, knead, shape, dry naturally, and then use high temperature steam Calcined at 380°C for 4h, and then naturally lowered to room temperature to obtain a semi-finished catalyst. The semi-finished catalyst was impregnated with rare earth additive solution C for 3 hours, air-dried, and then fired at 380°C for 4 hours with high-temperature steam to obtain sulfur-tolerant shift catalyst C...
Embodiment 2
[0046] Dissolve 9.2g of ammonium molybdate in 30.0mL of deionized water to obtain ammonium molybdate solution A; dissolve 11.6g of cobalt nitrate in 40.0mL of deionized water, then add 3.0g of citric acid and 3.0g of oxalic acid to the above cobalt nitrate in sequence solution, stirring and dissolving to obtain solution B containing cobalt. Dissolve 2.9g of lanthanum nitrate in 30mL of deionized water to obtain rare earth additive solution C.
[0047] Weigh 51.0g gibbsite, 5.0g nano zirconia, 32.4g activated carbon, 5g scallop powder and mix evenly, add solution A, knead evenly; then add solution B, knead, shape, dry naturally, and then use high temperature steam Calcined at 375°C for 5h, and naturally lowered to room temperature to obtain a semi-finished catalyst. The semi-finished catalyst was impregnated with rare earth additive solution C for 3 hours, dried naturally, and then calcined at 380°C for 4 hours with high-temperature steam to obtain sulfur-tolerant shift cataly...
Embodiment 3
[0049] Dissolve 9.8g of ammonium molybdate in 30.0mL of deionized water to obtain ammonium molybdate solution A; dissolve 11.8g of cobalt nitrate in 30.0mL of deionized water, then add 3.0g of citric acid and 3.0g of carboxymethyl cellulose in sequence into the above-mentioned cobalt nitrate solution, boiled and stirred to dissolve to obtain cobalt-containing solution B. Dissolve 4.0 g of lanthanum nitrate in 35 mL of deionized water to obtain rare earth additive solution C.
[0050] Weigh 52.0g of gibbsite, 7.0g of nano-zirconia, 28.2g of activated carbon, and 8g of scallop powder, mix them evenly, add solution A, and knead evenly; then add solution B, knead, shape, dry naturally, and then use high-temperature steam Calcined at 375°C for 5h, and naturally lowered to room temperature to obtain a semi-finished catalyst. The semi-finished catalyst was impregnated with rare earth additive solution C for 3 hours, dried naturally, and then calcined at 380°C for 4 hours with high-t...
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