Methanation catalyst for fluidized bed and preparation method of methanation catalyst for fluidized bed
A methanation catalyst, fluidized bed technology, applied in physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, chemical instruments and methods, etc., can solve the problem that the mechanical strength and wear resistance of catalysts need to be improved , the fluidization state is not easy to control, the particle size is not uniform, etc., to achieve the effect of low price, rich porosity, and high catalytic activity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0044] Embodiment 1, preparation and application of fluidized bed methanation catalyst
[0045] (1) will contain 260.5g Al(NO 3 ) 3 9H 2 O, 35.5g Zr(NO 3 ) 4 ·5H 2 O and 15.0g Ni(NO 3 ) 2 ·6H 2 Add 2L of the mixed aqueous solution of O into the constant temperature reaction kettle, stir the reaction at a temperature of 80°C, and add Na with a concentration of 10wt% 2 CO 3 aqueous solution, adjust the pH value to 8.0, and react for 1 hour to obtain a reaction precipitate.
[0046] (2) After the precipitate in step (1) is coarsely filtered and washed with deionized water, the pH value is 7.8, and then the silica-alumina composite sol is added, beaten, sprayed, dried at 80°C for 2 hours, and roasted at 600°C for 5 Hours, the carrier particles with an average particle size of 100 μm were produced.
[0047] (3) Preparation containing 135.0g Ni(NO 3 ) 2 ·6H 2 O and 95.5g Mg(NO 3 ) 2 ·6H 2 O 0.5L mixed aqueous solution, impregnate the carrier particles prepared in st...
Embodiment 2
[0052] Embodiment 2, preparation and application of fluidized bed methanation catalyst
[0053] (1) will contain 290.8g Al(NO 3 ) 3 9H 2 O, 30.5g Zr(NO 3 ) 4 ·5H 2 O and 15.0g Ni(NO 3 ) 2 ·6H 2 Add 2.5L of mixed aqueous solution of O into the constant temperature reaction kettle, stir and react at a temperature of 80°C, and add 10% Na 2 CO 3 aqueous solution, adjust the pH value to 8.0, and react for 1 hour to obtain a reaction precipitate.
[0054] (2) After washing the precipitate in step (1) with deionized water, the pH value is 7.8, then adding silica sol, beating, spray molding, drying at 80°C for 2 hours, and roasting at 600°C for 5 hours to obtain an average The particle size is 200 μm carrier particles.
[0055] (3) Preparation containing 125g Ni(NO 3 ) 2 ·6H 2 O and 55.6g Mn(NO 3 ) 2 4H 2 O 0.5L mixed aqueous solution, impregnate the carrier prepared in step (2), impregnate at 50°C for 6h, then put it in an oven at 80°C for 6h, and bake at 400°C for 6...
Embodiment 3
[0060] Embodiment 3, preparation and application of fluidized bed methanation catalyst
[0061] (1) will contain 260.5g Al(NO 3 ) 3 9H 2 O, 40.6g Zr(NO 3 ) 4 ·5H 2 O and 15.0g Ni(NO 3 ) 2 ·6H 2 Add 2.5L of mixed aqueous solution of O into the constant temperature reaction kettle, stir and react at a temperature of 80°C, and add 10% Na 2 CO 3 aqueous solution, adjust the pH value to 8.0, and react for 1 hour to obtain a reaction precipitate.
[0062] (2) After washing the precipitate in step (1) with deionized water, the pH value is 7.8, then adding silica sol, beating, spray molding, drying at 80°C for 2 hours, and roasting at 600°C for 5 hours to obtain an average The particle size is 250 μm carrier particles.
[0063] (3) Preparation containing 140.7g Ni(NO 3 ) 2 ·6H 2 O and 43.6g Ce(NO 3 ) 3 ·6H 2 O 0.5L mixed aqueous solution, impregnate the carrier prepared in step (2), impregnate at 50°C for 6h, then dry it in an oven at 80°C for 6h, and roast at 400°C f...
PUM
Property | Measurement | Unit |
---|---|---|
particle size | 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