Method for catalyzing sugar and sugar alcohol hydrocracking reaction through nickel-based catalyst
A catalyst technology for catalyzing sugar and nickel-based catalysts, applied in the direction of heterogeneous catalyst chemical elements, chemical instruments and methods, physical/chemical process catalysts, etc., can solve the problems of high economic cost, non-continuous production, etc., and achieve low environmental pollution , Good product quality, simple operation process
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0026] First, dissolve nickel nitrate in water to make a 3mol / L solution, then react it with ammonia water at a molar ratio of 1:1.5 to form a NiOH precipitate, then filter it, and dry it for later use. Take the dried nickel hydroxide and add γ-Al 2 o 3 Powder, the mass ratio is 1:1, mix the two evenly, add methanol, the mass ratio is 1% of the total mass, stir and knead all the substances, make it evenly mixed and then perform tablet molding. Then carry out high-temperature roasting to decompose NiOH, and the roasting temperature is 650°C. Finally, the calcined catalyst is subjected to hydrogen reduction, the hydrogen pressure is 0.2Mpa, the tail gas flow rate is 10mL / min, the temperature is programmed, the heating rate is 40°C / h, the reduction temperature is 220°C, when the temperature rises to 100°C for 4h, 180°C ℃ for 4 hours, 220 ℃ for 2 hours, the total reduction time is about 15 hours. After the pre-reduction is completed, stop heating, keep the hydrogen pressure of ...
Embodiment 2
[0029] First, nickel nitrate was dissolved in water to prepare a 2mol / L solution, and then reacted with ammonia water at a molar ratio of 1:1 to form a NiOH precipitate, which was then filtered and dried for later use. Take the dried nickel hydroxide and add γ-Al 2 o 3 Powder, the mass ratio is 1:5, mix the two evenly, add deionized water, the mass ratio is 5% of the total mass, stir and knead all the substances, make it evenly mixed and then perform tablet molding. Then carry out high-temperature roasting to decompose NiOH, and the roasting temperature is 450°C. Finally, the calcined catalyst was subjected to hydrogen reduction, the hydrogen pressure was 0.1Mpa, the exhaust gas flow rate was 5mL / min, the temperature was programmed, the heating rate was 20°C / h, and the reduction temperature was 180°C. ℃ for 1h, the total reduction time is about 10h. After the pre-reduction is completed, stop heating, keep the hydrogen pressure of the reaction system above 0.2 MPa, and store...
Embodiment 3
[0032] First, dissolve nickel nitrate in water to make a 1mol / L solution, then react it with ammonia water at a molar ratio of 1:2 to form a NiOH precipitate, then filter it, and dry it for later use. Take the dried nickel hydroxide and add γ-Al 2 o 3Powder, the mass ratio is 1:2.5, mix the two evenly, add talcum powder, the mass ratio is 2.5% of the total mass, stir and knead all the materials, make it evenly mixed and then perform tablet molding. Then carry out high-temperature roasting to decompose NiOH, and the roasting temperature is 500°C. Finally, the calcined catalyst was subjected to hydrogen reduction, the hydrogen pressure was 0.15Mpa, the exhaust gas flow rate was 7mL / min, the temperature was programmed, the heating rate was 30°C / h, and the reduction temperature was 200°C. ℃ for 4 hours, 200 ℃ for 1 hour, the total reduction time is about 20 hours. After the pre-reduction is completed, stop heating, keep the hydrogen pressure of the reaction system above 0.2 MPa...
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