A kind of preparation method of hydrocracking catalyst
A hydrocracking and catalyst technology, applied in the field of hydrocracking, can solve problems such as poor product properties, poor catalyst activity, and affecting the operation cycle of hydrocracking units, and achieve high nitrogen resistance and good activity.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0035] The preparation method of the hydrocracking catalyst of the present invention specifically includes the following content:
[0036] (1) Mix the modified Y molecular sieve, amorphous silica-alumina and / or alumina uniformly according to a certain ratio, add dilute nitric acid to form a slurry, extrude into strips, dry and bake to obtain a silica-alumina carrier containing the modified Y molecular sieve; wherein The concentration of the dilute nitric acid is 3wt%~30wt%; the drying conditions are: drying at 80~120 DEG C for 1~5 hours; roasting conditions are: roasting at 400~700 DEG C for 1~5 hours;
[0037] (2) The carrier in step (1) is impregnated with an impregnating liquid containing an active metal, and the impregnated carrier is dried and calcined to obtain a hydrocracking catalyst; wherein the impregnated liquid-solid mass ratio is 1.5:1~3:1 , adopt the saturated impregnation method well known in the art to carry out, the content of VIB group metal compound in the i...
Embodiment 1
[0041] Molecular sieve modification process:
[0042] (1) Take 200g of the original NaY molecular sieve powder prepared in the laboratory, mix it with ammonium nitrate with a concentration of 0.5mol / L according to the liquid-solid ratio of 3:1, exchange it at 60 °C for 2 hours, repeat this process twice, the Y molecular sieve after exchange Na content in Na 2 O counts as 3.5%;
[0043] (2) The molecular sieve obtained in step (1) is mixed with distilled water according to the liquid-solid ratio of 5:1, and then, 180 ml of ammonium fluorosilicate solution with a concentration of 0.8 mol / L is added, and treated at 60 °C for 1.0 hours;
[0044] (3) Hydrothermal treatment of the Y molecular sieve obtained in step (2) at 560°C and 0.2MPa for 2 hours;
[0045] (4) The molecular sieve obtained in step (3) is stirred and mixed with distilled water according to the liquid-solid ratio of 5:1, and then the temperature is raised to 80 ° C, and 400 ml of 0.6 mol / L aluminum sulfate soluti...
Embodiment 2
[0057] Molecular sieve modification process:
[0058] (1) Take 200 g of the original NaY molecular sieve powder prepared in the laboratory, mix it with ammonium nitrate with a concentration of 0.6 mol / L according to the liquid-solid ratio of 3:1, and exchange it at 70 °C for 3 hours. Repeat this process twice. The Na content was 3.0% as Na2O.
[0059] (2) The molecular sieve obtained in step (1) is mixed with distilled water according to the liquid-solid ratio of 6:1, then, 150 ml of ammonium fluorosilicate solution with a concentration of 0.6 mol / L is added, and treated at 70 °C for 1.0 hours;
[0060] (3) Hydrothermal treatment of the Y molecular sieve obtained in step (2) at 540°C and 0.15Mpa for 2 hours;
[0061] (4) The molecular sieve obtained in step (3) is stirred and mixed with distilled water according to the liquid-solid ratio of 6:1, and then the temperature is raised to 80 ° C, and 400 ml of 0.8 mol / L aluminum sulfate solution is added during the stirring process...
PUM
Property | Measurement | Unit |
---|---|---|
specific surface area | aaaaa | aaaaa |
specific surface area | aaaaa | aaaaa |
thickness | aaaaa | aaaaa |
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