Preparation method of catalyst for partial oxidization of isobutene to prepare methylacrolein
A methacrolein and catalyst technology, which is applied in the preparation of organic compounds, metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, etc., can solve problems such as waste catalyst pollution, and achieve a reasonable process structure. , the method is simple, the effect of low energy consumption
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Embodiment 1
[0034] (1) Preparation of the catalyst, the steps are as follows:
[0035] Selection of waste hydrodesulfurization HDS MoCo / Al in fixed bed residual oil hydrogenation industrial unit 2 o 3 Catalyst, after extracting to remove the oil on the surface of the catalyst, drying and roasting to obtain the treated waste HDS catalyst (containing Mo: 12.7 wt%, Co: 2.2 wt%, V: 2.4 wt%, Ni: 1.7 wt%, Fe : 0.15 wt%, Al 2 o 3 : 71.6 wt%), grind the catalyst to 200 mesh (referring to passing through a 200 mesh sieve), weigh 100 g of powder, add 250 mL of 98 wt% concentrated sulfuric acid, stir at 50 °C until the solid is almost completely dissolved, filter Collect the filtrate, add 10.7 g bismuth nitrate, 19.5 g cobalt nitrate, 1.5 g ammonium metavanadate, 4.1 g nickel nitrate, 4.2 g ferric nitrate to the filtrate, stir and dissolve, add ammonia water to adjust the pH value to 8.0, and stir for 15 min , adding 40 wt% sodium hydroxide solution to adjust the pH value of the solution to 12.0...
Embodiment 2
[0039] Grind the catalyst used in Example 1 to 200 mesh (referring to passing through a 200 mesh sieve), weigh 100 grams of powder, add 300 mL of a mixed solution of 98 wt% concentrated sulfuric acid and 65 wt% nitric acid, and the volume ratio is 2:1 , stirred at a constant temperature at 50°C until the solids were almost completely dissolved, and the filtrate was collected by filtration, 10.7 g of bismuth nitrate, 20.7 g of cobalt nitrate, 1.3 g of ammonium metavanadate, 4.1 g of nickel nitrate, and 4.6 g of iron nitrate were added to the filtrate, and stirred After dissolving, add ammonia water to adjust the pH value to 9.0. After stirring for 15 min, add 40 wt% sodium hydroxide solution to adjust the pH value of the solution to 13.0. After aging for 4 h, filter the precipitate and wash it three times with deionized water. , the filter cake was dried at 110 °C for 8 h, calcined at 600 °C for 4 h, and pressed into pellets to obtain the final catalyst Mo 9 Bi 1.5 co 7.5 V ...
Embodiment 3
[0042] Waste Hydrodesulfurization HDS MoCoNi / Al in Fixed Bed Residue Hydrogenation Industrial Unit 2 o 3 Catalyst (containing Mo: 15.6 wt%, Co: 1.6 wt%, V: 1.7 wt%, Ni: 2.3 wt%, Fe: 0.21 wt%, Al 2 o 3 : 68.5 wt%), the catalyst was ground to 200 mesh (referring to passing through a 200 mesh sieve), weighed 100 grams of powder, added 350 mL of a mixed solution of 98 wt% concentrated sulfuric acid and 65 wt% concentrated nitric acid, and the volume ratio was 1:1 , stirred at a constant temperature at 50°C until the solids were almost completely dissolved, collected the filtrate by filtration, added 8.7 g of bismuth nitrate, 18 g of cobalt nitrate, 0.35 g of ammonium metavanadate, and 2.1 g of ferric nitrate to the filtrate, stirred and dissolved, then added ammonia water Adjust the pH value to 10.0. After stirring for 15 min, add 40 wt% sodium hydroxide solution to adjust the pH value of the solution to 14.0. After aging for 4 h, filter the precipitate and wash it three times w...
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