Hexaaluminate, carrier containing hexaaluminate, preparation method of hexaaluminate, and high temperature methanation catalyst
A technology of hexaaluminate and carrier is applied in the field of high temperature methanation catalyst and its preparation, which can solve the problems of low production efficiency, many steps and high discharge, and achieve the effects of high production efficiency, perfect crystal phase and low roasting temperature
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0036]Preparation of barium hexaaluminate: Dissolve 6.57g of barium nitrate in 100ml of distilled water, disperse 20.5g of SB powder in 400ml of water under rapid stirring, raise the temperature of the water bath to 40°C, and add the barium nitrate solution to the SB under continuous stirring. powder suspension, adjust the pH of the mixed solution to 5.0 with 40% nitric acid, and stir for 30 minutes; dissolve 3.0 g of ammonium carbonate in 100 ml of distilled water to prepare an alkali solution, slowly add the alkali solution dropwise to the above mixed solution, and Continue to react for 1 hour, filter, wash with distilled water, dry at 110°C for 5 hours, roast at 1200°C for 3 hours, and grind to obtain 19.5g of barium hexaaluminate.
[0037] The barium hexaaluminate prepared by this method adopts the Japan Rigaku D / max-2200PC X-ray diffractometer to analyze the catalyst phase results as follows figure 2 As shown, with obvious barium hexaaluminate (BaAl 12 o 19 ) crystal s...
Embodiment 2
[0043] Preparation of barium hexaaluminate: Dissolve 6.57g of barium nitrate in 100ml of distilled water, disperse 20.5g of ordinary pseudoboehmite powder in 300ml of water under rapid stirring conditions, raise the temperature of the water bath to 60°C, and dissolve the nitric acid Add the barium solution to the suspension of pseudo-boehmite powder, adjust the pH of the mixture to 1.0 with 40% nitric acid, and stir for 60 minutes; dissolve 3.0 g of ammonium carbonate in 100 ml of distilled water to obtain an alkali solution, and slowly dissolve the alkali solution Add it dropwise into the above mixture, and continue to react for 1 hour, filter, wash with distilled water, dry at 110°C for 5 hours, roast at 1200°C for 3 hours, and grind to obtain 19.5g of barium hexaaluminate.
[0044] The barium hexaaluminate prepared by this method adopts the Japan Rigaku D / max-2200PC X-ray diffractometer to analyze the catalyst phase results as follows image 3 As shown, with obvious barium ...
Embodiment 3
[0050] Preparation of barium hexaaluminate: Dissolve 6.57g of barium nitrate in 100ml of distilled water, disperse 20.5g of SB powder in 400ml of water under rapid stirring, raise the temperature of the water bath to 50°C, and add the barium nitrate solution to the SB under continuous stirring. powder suspension, adjust the pH of the mixed solution to 3.0 with 65% nitric acid, and stir for 30 minutes; dissolve 3.0 g of ammonium carbonate in 100 ml of distilled water to prepare an alkaline solution, slowly drop the alkaline solution into the above mixed solution, and Continue to react for 1 hour, filter, wash with distilled water, dry at 110°C for 5 hours, roast at 1200°C for 3 hours, and grind to obtain 19.5g of barium hexaaluminate.
[0051] The barium hexaaluminate prepared by this method adopts the Japan Rigaku D / max-2200PC X-ray diffractometer to analyze the catalyst phase and finds that the hexaaluminate has obvious barium hexaaluminate (BaAl 12 o 19 ) crystal structure ...
PUM
| Property | Measurement | Unit |
|---|---|---|
| specific surface area | aaaaa | aaaaa |
| specific surface area | aaaaa | aaaaa |
| pore size | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 


