Protective agent for removing carbonyl iron and carbonyl nickel from synthetic gas and preparation method thereof
A technology for forming gas-decarbonylated iron and protective agents, applied in chemical instruments and methods, preparation of hydroxyl compounds, preparation of organic compounds, etc., can solve the problems of complex wet process equipment, difficult handling of absorbents, incomplete adsorption, etc.
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Embodiment 1
[0040]Add potassium bicarbonate solution with a concentration of 0.3mol / L to 0.2mol / L Cu and Zn mixed nitrate aqueous solution to carry out co-precipitation reaction, the co-precipitation temperature is 50°C, the parent precipitate is washed with deionized water, filtered The final pH value of the clear liquid is 7.0, and the parent precipitate slurry is obtained;
[0041] Mix and co-precipitate the soluble salts of metal Zn with aluminum nitrate in a molar ratio of 1:2. According to the different ionization constants of the metal precipitates, adjust the final pH value to 7.2, control the temperature of the mixed solution at 20°C, and then age , washing, and obtaining carrier slurry.
[0042] Then mix and beat the above-mentioned matrix slurry and carrier slurry, let it stand for 30 minutes, filter, dry and granulate to obtain a certain particle size powder, and make decarbonylated iron-nickel protective agent BHJ-101 after molding.
Embodiment 2
[0044] Add the sodium bicarbonate solution with a concentration of 0.5mol / L to the 1mol / L Cu and Zn mixed nitrate aqueous solution to carry out coprecipitation reaction. The coprecipitation temperature is 60°C. The parent precipitate is washed with deionized water and filtered The pH value at the end point of the liquid is 7.1, and the parent precipitate slurry is obtained;
[0045] Mix and co-precipitate the soluble salts of metal Mg with aluminum nitrate in a molar ratio of 1:3. According to the different ionization constants of the metal precipitates, adjust the final pH value to 7.1, control the temperature of the mixed solution at 50°C, and then age , washing, and obtaining carrier slurry.
[0046] Then mix and beat the above-mentioned matrix slurry and carrier slurry, let it stand for 30 minutes, filter, dry and granulate to obtain a certain particle size powder, and make the decarbonylated iron-nickel protective agent BHJ-102 through the molding process.
Embodiment 3
[0048] Add the sodium carbonate solution with a concentration of 0.8mol / L to the 0.2mol / L Cu and Zn mixed nitrate aqueous solution to carry out coprecipitation reaction. The coprecipitation temperature is 50°C. The parent precipitate is washed with deionized water and filtered The pH value at the end point of the liquid is 7.2, and the parent precipitate slurry is obtained;
[0049] Mix and co-precipitate the soluble salts of metal Ca with aluminum nitrate in a molar ratio of 1:4. According to the different ionization constants of the metal precipitates, adjust the final pH value to 7.3, control the temperature of the mixed solution at 30°C, and then age , washing, and obtaining carrier slurry.
[0050] Then mix and beat the above-mentioned matrix slurry and carrier slurry, let it stand for 30 minutes, filter, dry and granulate to obtain a certain particle size powder, and obtain decarbonylated iron-nickel protective agent BHJ-103 after molding.
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