A kind of catalyst preparation method for oxidative dehydrogenation of propane to produce propylene
A technology for oxidative dehydrogenation and catalysts, applied in the direction of metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, chemical instruments and methods, etc., can solve the problem of low metal utilization in carrier channels and accelerate deep oxidation of products , the contribution of the catalyst is not large, etc., to avoid further oxidation, improve the conversion rate and selectivity of propylene, and improve the effect of utilization
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0035] The spent hydrotreating catalyst (MoCo / Al 2 o 3 ), the oil on the surface of the catalyst was removed by extraction, dried at 110°C for 8 h, and the obtained catalyst was calcined at 450°C for 4 h to obtain the spent catalyst after treatment (containing Mo: 12.8wt%, Co: 2.3 wt%, V: 2.5wt% %, Ni: 1.9 wt%, Al 2 o 3 : 71.2 wt%), grind the catalyst to 200 mesh (referring to passing through a 200 mesh sieve), weigh 100 g of the powder, add 260 mL of 98 wt% concentrated sulfuric acid, stir at 50 °C to dissolve the solid, and collect the filtrate by filtration , add 54.01g of nickel nitrate to the filtrate, stir to dissolve, add 27.31g of citric acid (the molar ratio of citric acid to Mo in the waste agent is 1), add 142.13g of pseudo-boehmite after all dissolved, at 70℃ Stir until the solution is evaporated to dryness, dry the obtained solid at 100°C for 8 h, and calcinate at 600°C for 4 h to obtain catalyst precursor A, wherein Mo accounts for 6 wt% of the weight of catal...
Embodiment 2
[0037] The spent hydrotreating catalyst (MoCo / Al 2 o 3 ), the oil on the surface of the catalyst was removed by extraction, dried at 110°C for 8 h, and the obtained catalyst was calcined at 450°C for 4 h to obtain the spent catalyst after treatment (containing Mo: 12.8wt%, Co: 2.3 wt%, V: 2.5wt% %, Ni: 1.9 wt%, Al 2 o 3 : 71.2 wt%), grind the catalyst 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% concentrated nitric acid, and the volume ratio is 2:1 , stir at a constant temperature at 50°C to dissolve the solid, collect the filtrate by filtration, add 54.01g of nickel nitrate to the filtrate, stir and dissolve, add 40.98g of citric acid (the molar ratio of citric acid to Mo in the waste agent is 1.5), all After dissolving, add 51.65 g of pseudo-boehmite, stir at 70°C until the solution is evaporated to dryness, dry the resulting solid at 100°C for 8 h, an...
Embodiment 3
[0039] The spent hydrotreating catalyst (MoCo / Al 2 o 3 ), the oil on the surface of the catalyst was removed by extraction, dried at 110°C for 8 h, and the obtained catalyst was calcined at 450°C for 4 h to obtain the spent catalyst after treatment (containing Mo: 12.8wt%, Co: 2.3 wt%, V: 2.5wt% %, Ni: 1.9 wt%, Al 2 o 3 : 71.2 wt%), grind the catalyst to 200 mesh (referring to passing through a 200 mesh sieve), weigh 100 grams of powder, add 450 mL of a mixed solution of 35 wt% concentrated hydrochloric acid and 65 wt% concentrated nitric acid, and the volume ratio is 1:1 , stir at a constant temperature at 50°C to dissolve the solid, collect the filtrate by filtration, add 54.01g of nickel nitrate to the filtrate, stir and dissolve, then add 13.66g of citric acid (the molar ratio of citric acid to Mo in the waste agent is 0.5), all After dissolving, add 447g of pseudo-boehmite, stir at 70°C until the solution is evaporated to dryness, dry the obtained solid at 100°C for 8 ...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com