Metal modified La2O2CO3 adsorbent as well as preparation method and application thereof
A metal modification, adsorbent technology, applied in chemical instruments and methods, adsorption water/sewage treatment, water/sludge/sewage treatment, etc., can solve the problem of small number of sites, low phosphorus adsorption capacity, active adsorption sites single order issues
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Embodiment 1
[0015] First, 3.7542g La(NO 3 )·6H 2 O and 0.2524g Ni(NO 3 ) 2 ·6H 2 O dissolved in 20mL deionized water, La(NO 3 )·6H 2 O and Ni(NO 3 ) 2 ·6H 2 The total molar amount of O was fixed at 0.01 mol. In addition, 4.33 g of citric acid monohydrate and 6 g of polyethylene glycol-6000 were dissolved in 20 mL of deionized water as complexing agents for metal ions. After the metal salt is fully dissolved, the metal nitrate mixed solution is added dropwise to the mixed solution of citric acid and polyethylene glycol and fully stirred for 40 minutes. Subsequently, the mixed solution was placed in a magnetically stirred oil bath, the mixed solution was heated from room temperature to 80° C., and the stirring was continued for 6 h. Subsequently, the wet gel was dried in a vacuum oven at 80° C. for 15 hours to form a dry gel. The dry gel was taken out and placed in a muffle furnace, and the temperature was raised to 600 °C at a rate of 5 °C / min and kept for 2.5 h. After cooling ...
Embodiment 2
[0017] First, 3.8864g La(NO 3 )·6H 2 O and 0.3844g Al(NO 3 ) 3 9H 2 O dissolved in 20mL deionized water, La(NO 3 )·6H 2 O and Al(NO 3 ) 3 9H 2 The total molar amount of O was fixed at 0.01 mol. In addition, 4.33 g of citric acid monohydrate and 6 g of polyethylene glycol-6000 were dissolved in 20 mL of deionized water as complexing agents for metal ions. After the metal salt is fully dissolved, the metal nitrate mixed solution is added dropwise to the mixed solution of citric acid and polyethylene glycol and fully stirred for 30 minutes. Subsequently, the mixed solution was placed in a magnetically stirred oil bath, the mixed solution was heated from room temperature to 105° C., and the stirring was continued for 4 h. Subsequently, the wet gel was dried in a vacuum oven at 105°C for 24 hours to form a xerogel. The dry gel was taken out and placed in a muffle furnace, and the temperature was raised to 600 °C at a rate of 5 °C / min and kept for 4 h. After cooling down...
Embodiment 3
[0019] First, 4.2869g La(NO 3 )·6H 2 O and 0.0433g Ce(NO 3 ) 3 ·6H 2 O dissolved in 20mL deionized water, La(NO 3 )·6H 2 O and Ce(NO 3 ) 3 ·6H 2The total molar amount of O was fixed at 0.01 mol. In addition, 4.33 g of citric acid monohydrate and 6 g of polyethylene glycol-6000 were dissolved in 20 mL of deionized water as complexing agents for metal ions. After the metal salt is fully dissolved, the metal nitrate mixed solution is added dropwise to the mixed solution of citric acid and polyethylene glycol and fully stirred for 30 minutes. Subsequently, the mixed solution was placed in a magnetically stirred oil bath, the mixed solution was heated from room temperature to 90° C., and the stirring was continued for 10 h. Subsequently, the wet gel was dried in a vacuum oven at 90°C for 18 hours to form a dry gel. The dry gel was taken out and placed in a muffle furnace, and the temperature was raised to 600 °C at a rate of 5 °C / min and kept for 3 h. After cooling down...
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