Hydroisomerization catalyst, preparation method and application thereof, and hydroisomerization method for hydrocracked tail oil
A hydroisomerization and catalyst technology, which is applied in the field of hydroisomerization catalysts and its preparation, can solve the problems of reduced processing capacity, reduced device production efficiency, poor utilization of tail oil, etc., and achieves low pour point , high isomerization reaction selectivity, high viscosity index effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0071] (1) Take 70g (on a dry basis, the same below) of ZSM-22 molecular sieve (the ratio of silicon to aluminum is 70), 30g (on a dry basis, the same below) of alumina (provided in the form of pseudo-boehmite, below same), followed by dry mixing and extruding, and the wet strip obtained was dried at 120° C. for 4 hours, and then calcined at 500° C. for 3 hours to obtain a catalyst carrier.
[0072] (2) The 40g catalyst carrier obtained in step (1) was impregnated with a solution containing 60mL of nickel nitrate hexahydrate (5.0% by weight) for 4 hours, and then the impregnated mixture was dried at 120°C for 4 hours to obtain a catalyst carrier loaded with Ni. a. 40 g of the Ni-loaded support was immersed in 60 mL of an aqueous solution containing chloroplatinic acid (concentration: 0.8% by weight) for 4 hours. After filtering the impregnated mixture, the collected solid was dried at 120° C. for 4 hours to obtain a catalyst precursor.
[0073] (3) The catalyst precursor obt...
Embodiment 2
[0075]Adopt the method identical with embodiment 1 to prepare catalyst, difference is, in step (2), the 40g catalyst carrier that step (1) obtains is used 60mL to contain the solution impregnation 4 hours of nickel nitrate hexahydrate (concentration is 5.0% by weight) , and then the impregnated mixture was dried at 120 °C for 4 hours to obtain a Ni-loaded carrier. 40 g of the Ni-loaded support was immersed in 60 mL of an aqueous solution containing chloroplatinic acid (concentration: 0.8% by weight) for 4 hours. The impregnated mixture was placed in an autoclave, and after the autoclave was closed, the temperature in the autoclave was raised to 170° C. and kept at this temperature for 4 hours to perform hydrothermal treatment. After the temperature of the autoclave dropped to room temperature, the autoclave was opened, the hydrothermally treated material was taken out and filtered, and the collected solid was dried at 120° C. for 4 hours to obtain a catalyst precursor. The pr...
Embodiment 3
[0077] Adopt the method identical with embodiment 2 to prepare catalyst, difference is, in step (2), the 40g catalyst carrier that step (1) obtains is used 60mL to contain the solution impregnation 4 hours of nickel nitrate hexahydrate (concentration is 5.0% by weight) , and then the impregnated mixture was dried at 120 °C for 4 hours to obtain a Ni-loaded carrier. 40 g of the Ni-loaded support was immersed in 60 mL of an aqueous solution containing chloroplatinic acid (concentration: 0.8% by weight) for 4 hours. The mixture obtained by impregnation is placed in the autoclave, then ammoniacal liquor is added dropwise in the autoclave, the pH value of the liquid phase in the mixture obtained by the impregnation is adjusted from 6.2 to 9, then the autoclave is closed, and the autoclave is The temperature inside was raised to 170 °C and kept at this temperature for 4 hours for hydrothermal treatment. After the temperature of the autoclave dropped to room temperature, the autocla...
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