Preparation method of sulfur-tolerant methanation catalyst
A technology for sulfur-resistant methanation and catalyst, which can be used in catalyst activation/preparation, physical/chemical process catalysts, chemical instruments and methods, etc., and can solve problems such as low conversion rate
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Embodiment 1
[0029] 1.4gH 3 PO 4 Dissolve in 1.0g deionized water, add 2.46g ammonium molybdate and 1.54g nickel nitrate after dissolving, add 1.62g metatungstic acid after dissolving, dissolve with deionized water and an appropriate amount of citric acid, and finally add a certain amount DMSO, then add γ-Al 2 o 3 , impregnated for 24 h, dried at 120°C for 4 h, and calcined at 500°C for 4 h, the components were NiO:2%, MoO 3 :10%, P 2 o 5 :5%, WO 3 : 10% catalyst Cat.1. Take 2g of the catalyst (20~40 mesh) particles and put them into the reactor to carry out the conversion rate of catalyst CO and CH 4 The selectivity evaluation and catalyst activity evaluation experimental results can be seen in Table 1 below.
Embodiment 2
[0031] 0.84gH 3 PO 4 Dissolve in 1.0g deionized water, add 4.92g ammonium molybdate and 2.31g nickel nitrate after dissolving, add 1.62g metatungstic acid after dissolving, dissolve with deionized water and an appropriate amount of citric acid, and finally add a certain amount DMSO, then add γ-Al 2 o 3 , impregnated for 24 h, dried at 120°C for 4 h, and calcined at 500°C for 4 h, the components were NiO:3%, MoO 3 :20%, P 2 o 5 :3%, WO 3 : 10% catalyst Cat.2. Take 2g of the catalyst (20~40 mesh) particles and put them into the reactor to carry out the conversion rate of catalyst CO and CH 4 The selectivity evaluation and catalyst activity evaluation experimental results can be seen in Table 1 below.
Embodiment 3
[0033] 0.56gH 3 PO 4 Dissolve in 1.0g deionized water, add 3.69g ammonium molybdate and 3.08g nickel nitrate after dissolving, add 2.43g metatungstic acid after dissolving, dissolve with deionized water and an appropriate amount of citric acid, and finally add a certain amount DMSO, then add γ-Al 2 o 3 , impregnated for 24 h, dried at 120°C for 4 h, and calcined at 500°C for 4 h, the components were NiO:4%, MoO 3 :15%, P 2 o 5 :2%, WO 3 : 15% catalyst Cat.3. Take 2g of the catalyst (20~40 mesh) particles and put them into the reactor to carry out the conversion rate of catalyst CO and CH 4 The selectivity evaluation and catalyst activity evaluation experimental results can be seen in Table 1 below.
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