Preparation method of core-shell structure nickel base methane dry reforming catalyst
A methane dry reforming and nickel-based methane technology, applied in chemical instruments and methods, inorganic chemistry, non-metallic elements, etc., to achieve the effect of strong resistance to metal agglomeration, improved activity, and easy operation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0021] Weigh 6g of cetyltrimethylammonium bromide, dissolve it in a mixed solution of 80ml of cyclohexane and 15ml of n-butanol, stir, add 4ml of 0.2mol / L nickel nitrate and 0.05mol / L cerium nitrate aqueous solution To the above solution, make it clear, add 0.5ml of hydrazine hydrate and 1.5ml of sodium hydroxide (0.5mol / L) in a water bath at 70°C, and stir for 40 minutes. Then it was lowered to room temperature, and 1ml of ammonia water was added dropwise during vigorous stirring, and then 1ml of tetraethylorthosilicate was slowly added dropwise, stirred for 3 hours, and left to stand for 3 days. Collect by centrifugation, wash with alcohol 5 times to remove excess cetyltrimethylammonium bromide, dry at 120°C, and calcined at 500°C for 2 hours (2°C / min). It is then reduced by using H 2 -TPR, first pass N 2 Pretreated at 300°C for 30 min, cooled to room temperature and treated with H 2 / N 2 Volume ratio 1:9 mixed gas (30mL / min) reduction at 800°C for 1 hour to obtain SiO ...
Embodiment 2
[0024] Weigh 6g of cetyltrimethylammonium bromide, dissolve it in a mixed solution of 80ml of cyclohexane and 15ml of n-butanol, stir, add 4ml of 0.25mol / L nickel nitrate and 0.05mol / L cerium nitrate aqueous solution To the above solution, make it clear, add 0.5ml of hydrazine hydrate and 1.5ml of sodium hydroxide (0.5mol / L) in a water bath at 70°C, and stir for 40 minutes. Then it was lowered to room temperature, and 1 ml of ammonia water was added dropwise during vigorous stirring, and then 1.25 ml of tetraethyl orthosilicate was slowly added dropwise, stirred for 3 hours, and allowed to stand for 3 days. Collect by centrifugation, wash with alcohol 5 times to remove excess cetyltrimethylammonium bromide, dry at 120°C, and calcined at 500°C for 2 hours (2°C / min). It is then reduced by using H 2 -TPR, first pass N 2 Pretreated at 300°C for 30 min, cooled to room temperature and treated with H 2 / N 2 SiO2@NiCe nano-catalysts were obtained by reduction with mixed gas (30mL / ...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More - R&D
- 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

