A kind of efficient sulfur dioxide desulfurization agent, preparation method and desulfurization method
A technology of sulfur dioxide and desulfurizer, applied in the field of desulfurization, can solve the problems of adsorption liquid volatilization loss, large by-product output, low adsorption efficiency, etc., and achieve the effect of increasing binding force
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Embodiment 1
[0031] Prepare two 100 mL 1.0mol / L citric acid solutions, dissolve 9.3 g of aniline in one of the citric acid solutions, then add 1 g of common commercial activated carbon to the aniline-citric acid solution, and stir for 30 min in an ice-water bath , put it aside for 1 hour, and set aside; dissolve 22.8 g of ammonium persulfate in another citric acid solution, drop it into the above-mentioned carboaniline-citric acid solution, control the dropping within 1 hour, react in an ice-water bath for 2 hours, and then reduce the pressure Suction filtration, the filter cake was vacuum-dried at 60°C, and finally heated to 350°C in a nitrogen atmosphere at a controlled temperature increase rate of 5°C / min, and kept at this temperature for 2 hours to obtain a carbon material marked C ca-350 .
Embodiment 2
[0033] Prepare two 200 mL 0.75mol / L tartaric acid solutions, dissolve 11.2g of aniline in one of the tartaric acid solutions, then add 1g of common commercial activated carbon into the aniline-tartaric acid solution, stir for 30 min in an ice-water bath, and let stand 0.5h, set aside; dissolve 22.8 g of ammonium persulfate in another part of tartaric acid solution, drop it into the above-mentioned carboaniline-tartaric acid solution, control the dripping within 1 hour, react in an ice-water bath for 1 hour, and then suction filter under reduced pressure. The filter cake was vacuum-dried at 60°C, and finally heated to 350°C in a nitrogen atmosphere at a controlled temperature increase rate of 5°C / min, and kept at this temperature for 1 hour to obtain a carbon material marked C ta-350 .
Embodiment 3
[0035] Prepare two 1000 mL 0.5mol / L sulfuric acid solutions, dissolve 18.6 g of aniline in one of the sulfuric acid solutions, then add 20 g of common commercial activated carbon into the aniline-sulfuric acid solution, and stir for 30 min in an ice-water bath for later use; Dissolve g ammonium persulfate in another part of sulfuric acid solution, drop it into the above-mentioned carboaniline-sulfuric acid solution, control the dripping within 1 hour, react in ice-water bath for 2 hours, then filter under reduced pressure, vacuum the filter cake at 60°C Dry, and finally heat up to 350°C in a nitrogen atmosphere at a controlled temperature increase rate of 5°C / min, and keep the temperature for 0.5h to obtain a carbon material marked C sa-350 .
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