CO methanation catalyst and preparation method thereof
A methanation catalyst and catalyst technology, applied in electrical components, battery electrodes, circuits, etc., can solve the problems of reducing hydrogen production efficiency and loss, and achieve the effects of long service life, stable performance, high CO selectivity and conversion rate
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Embodiment 1
[0046] This embodiment provides a method for preparing a CO methanation catalyst, which includes the following steps:
[0047] 1. Take 1000g CeO 2 Carrier, dried at 120°C for 2h, cooled to room temperature for later use, wherein, CeO 2 The particle size of the carrier is 30mm, and the specific surface area is 35m 2 / g;
[0048] 2. Weigh 103.6g nickel chloride hexahydrate, 444.5g nickel nitrate hexahydrate and add water to prepare 1L mixed solution;
[0049] 3. Dry 1000g of CeO 2 The carrier is immersed in the mixed solution, aged for 2 hours, and dried at 120°C for 6 hours;
[0050] 4. The impregnated and dried CeO 2 The carrier was baked in a muffle furnace at 400 °C for 2 h, and then heated in H 2 Reduction at 250°C for 2 hours in the atmosphere, and cooling down to room temperature to obtain CO methanation catalyst A.
[0051] The molar ratio of the main component of CO methanation catalyst A is Ni:Cl obtained by elemental analysis - :CeO 2 = 32.3:12.1:100.0.
Embodiment 2
[0053] This embodiment provides a method for preparing a CO methanation catalyst, which includes the following steps:
[0054] 1. Take 5000g of cerium nitrate, roast it in a muffle furnace at 400°C for 2h, and lower it to room temperature to obtain CeO 2 The carrier is ready for use, and the resulting CeO 2 The particle size of the carrier is 20mm, and the specific surface area is 60m 2 / g;
[0055] 2. Weigh 103.6g nickel chloride hexahydrate, 444.5g nickel nitrate hexahydrate plus ethanol to prepare 1L mixed solution;
[0056] 3. Dry 1000g of CeO 2 The carrier is immersed in the mixed solution, aged for 2 hours, and dried at 150°C for 4 hours;
[0057] 4. The impregnated and dried CeO 2 The carrier was baked in a muffle furnace at 400 °C for 2 h, and then heated in 10 vol% H 2 / 90vol%N 2 Reduction at 250° C. for 2 h in air flow, and cooling down to room temperature to obtain CO methanation catalyst B.
[0058] The molar ratio of the main component of CO methanation ca...
Embodiment 3
[0060] This embodiment provides a method for preparing a CO methanation catalyst, which includes the following steps:
[0061] 1. Take 1000g CeO 2 Carrier, dried at 120°C for 2h, cooled to room temperature for later use, wherein, CeO 2 The particle size of the carrier is 30mm, and the specific surface area is 35m 2 / g;
[0062] 2. Weigh 618.2g nickel nitrate hexahydrate, 46.6g ammonium chloride plus acetone to prepare 1L mixed solution;
[0063] 3. Dry 1000g of CeO 2 The carrier is immersed in the mixed solution, aged for 2 hours, and dried at 100°C for 10 hours;
[0064] 4. The impregnated and dried CeO 2 The carrier was baked in a muffle furnace at 400 °C for 2 h, and then heated in H 2 Reduction at 300°C for 2h in the atmosphere, and cooling down to room temperature to obtain CO methanation catalyst C.
[0065] The molar ratio of the main components contained in the CO methanation catalyst C obtained by elemental analysis is Ni:Cl - :CeO 2 =35.2:12.6:100.0.
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