A kind of preparation method of mesoporous active material
An active material and mesoporous technology, which is applied in the field of preparation of mesoporous active materials, can solve the problems of uneven distribution of silicon and aluminum, low impurity content, expensive and stable organic silicon, etc., and achieve smooth channels and strong conversion capacity of heavy oil , the effect of small granularity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0022] This example illustrates the preparation method of the mesoporous active material provided by the present invention.
[0023] Take Al 2 (SO 4 ) 3 Solution (concentration 90gAl 2 o 3 / L) and ammonia (mass fraction 25%) are reaction raw materials. Using the method of co-flow gelation, under vigorous stirring, the Al 2 (SO 4 ) 3 Solution and ammoniacal liquor are mixed into gel, 40 DEG C of gel forming temperature, and gel forming pH value is 9.0, simultaneously the water glass solution (concentration 100gSiO 2 / L) mixed with the above-mentioned colloidal slurry in parallel flow to realize the online addition of silicon source. After collecting a certain amount of mixed slurry, raise the temperature to 70°C and age for 2 hours; Base: HCl: H 2 The weight ratio of O=1:0.1:10 was exchanged at 30°C for 0.5 hours, filtered and washed with water to obtain a mesoporous active material, which was designated as SM-1.
Embodiment 2
[0026] This example illustrates the preparation method of the mesoporous active material provided by the present invention.
[0027] Take Al 2 (SO 4 ) 3 The solution and ammonia water are used as the reaction raw materials, and the Al 2 (SO 4 ) 3 The solution and ammonia water are mixed to form a gel, the gelation temperature is 30°C, and the pH value of the gelation is 10.0. At the same time, the metered water glass solution and the above-mentioned gelling slurry are mixed in parallel to realize the online addition of silicon sources. A large amount of mixed slurry was heated to 60°C and aged for 2 hours; after filtration, the obtained solid precipitate was calculated according to the dry basis of the precipitate: HCl: H 2 The weight ratio of O=1:0.08:15 was exchanged at 50°C for 0.3 hours, filtered and washed with water, and the exchange was repeated once. After filtration, the mesoporous active material was obtained, which was designated as SM-2.
[0028] SM-2 has a p...
Embodiment 3
[0030] This example illustrates the preparation method of the mesoporous active material provided by the present invention.
[0031] Take Al 2 (SO 4 ) 3 solution and NaAlO 2 Solution (concentration 190gAl 2 o 3 / L) is the reaction raw material, co-flow gel at room temperature and control the gel pH value to be 10.5, and simultaneously mix the water glass solution and the colloid slurry in proportion to realize the online addition of silicon source, and then the collected The slurry is heated to 60°C and aged for 4 hours; after filtration, the obtained solid precipitate is calculated on a dry basis of the precipitate: H 2 SO 4 :H 2 The weight ratio of O=1:0.12:15 was exchanged at room temperature for 1 hour, filtered and washed with water to obtain a mesoporous active material, which was designated as SM-3.
[0032] SM-3 has a pseudo-boehmite crystal phase structure, and its X-ray diffraction pattern has the characteristics of the attached figure; the chemical compositi...
PUM
Property | Measurement | Unit |
---|---|---|
specific surface area | aaaaa | aaaaa |
pore size | aaaaa | aaaaa |
diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information

- Generate Ideas
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com