Waste hydrotreating catalyst utilization method
A hydrogenation treatment and catalyst technology, applied in the direction of catalysts, physical/chemical process catalysts, carbon compound catalysts, etc., to save costs and improve resource utilization
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Embodiment 1
[0060] (1) Preparation of catalyst precursor A, the steps are as follows:
[0061] Waste Hydrodemetallization MoNi / Al in Fixed Bed Residue Hydrogenation Industrial Plant 2 o 3 Catalyst (with MoO 3 : 9.7 wt%, NiO: 6.2 wt%, V 2 o 3 : 12.1 wt%, Fe 2 o 3 : 0.6 wt%, Al 2 o 3 : 69.9 wt%), the catalyst was ground to 200 mesh, weighed 100 g of powder, added 250 mL of 98 wt% concentrated sulfuric acid, stirred at a constant temperature of 50 °C to dissolve the solid, collected the filtrate by filtration, and added 22.3 g poly Ethylene glycol 200, then add 26.9 mL of tetraethyl orthosilicate, and add ammonia water, control the pH of the system to 8.0, stir at 70°C until a gel is formed, age the gel at room temperature for 8 h, and then cool the gel at 110°C After being dried for 8 h at high temperature, the obtained solid was calcined at 600 °C for 4 h to obtain catalyst precursor A, and the content of silicon oxide in the carrier was 10 wt%.
[0062] (2) Preparation of catalys...
Embodiment 2
[0069] (1) Preparation of catalyst precursor A, the steps are as follows:
[0070] Waste Hydrodemetallization MoNi / Al in Fixed Bed Residue Hydrogenation Industrial Plant 2 o 3 Catalyst (with MoO 3 : 9.7 wt%, NiO: 6.2 wt%, V 2 o3 : 12.1 wt%, Fe 2 o 3 : 0.6 wt%, Al 2 o 3 : 69.9 wt%), the catalyst was ground to 200 mesh, weighed 100 g of powder, added 250 mL of 98 wt% concentrated sulfuric acid, stirred at a constant temperature of 50 °C to dissolve the solid, collected the filtrate by filtration, and added 22.3 g poly Ethylene glycol 200, then add 21.2 mL of tetraethyl orthosilicate, and add ammonia water, control the pH of the system to 8.0, stir at 70°C until a gel is formed, age the gel at room temperature for 8 h, and then cool the gel at 110°C After being dried for 8 h at high temperature, the resulting solid was calcined at 600 °C for 4 h to obtain catalyst precursor A, and the content of silicon oxide in the carrier was 8 wt%.
[0071] (2) Preparation of catalyst:...
Embodiment 3
[0076] (1) Preparation of catalyst precursor A, the steps are as follows:
[0077] Waste Hydrodemetallization MoNi / Al in Fixed Bed Residue Hydrogenation Industrial Plant 2 o 3 Catalyst (with MoO 3 : 9.7 wt%, NiO: 6.2 wt%, V 2 o 3 : 12.1 wt%, Fe 2 o 3 : 0.6 wt%, Al 2 o 3 : 69.9 wt%), the catalyst was ground to 200 mesh, weighed 100 g of powder, added 250 mL of 98 wt% concentrated sulfuric acid, stirred at a constant temperature of 50 °C to dissolve the solid, collected the filtrate by filtration, and added 22.3 g poly Ethylene glycol 200, then add 12.8 mL of tetraethyl orthosilicate, and add ammonia water to control the pH value of the system to 8.0, stir at 70°C until a gel is formed, age the gel at room temperature for 8 h, and then cool the gel at 110°C After being dried for 8 h at high temperature, the obtained solid was calcined at 600 °C for 4 h to obtain the catalyst precursor A, and the content of silicon oxide in the carrier was 5 wt%.
[0078] (2) Preparation...
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