Method of using lanthanum ruthenate-bearing perovskite to activate peracetic acid to degrade fluoroquinolone antibiotics
A technology of peracetic acid and fluoroquinolones, which is applied in chemical instruments and methods, chemical/physical processes, catalyst activation/preparation, etc., can solve problems such as secondary pollution and low activation efficiency of peracetic acid, and achieve economic cost reduction, Promote the promotion and application, improve the effect of activation efficiency
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Embodiment 1
[0030] (1) According to the molar ratio La:Ru:CA=1:1:2, weigh La(NO 3 ) 3 ·6H 2 O, RuCl 3 and C 6 h 8 o 7 ·H 2 O After mixing, add water to dissolve it, stir the solution vigorously, while raising the temperature to 65°C, continue to add ethylene glycol and keep it at this temperature until it becomes a viscous gel-like substance due to the slow evaporation of water;
[0031] (2) Transfer the beaker to a heating mantle to provide uniform heating, and the temperature rises to 120° C. for 1 hour, at which time a 3D polymer structure is formed through the reaction of citric acid and ethylene glycol;
[0032] (3) Place the beaker containing the remaining product in an oven (>100°C) to dry thoroughly;
[0033] (4) After drying, the polymer was pulverized and calcined at 800° C. for 8 hours to decompose the polymer and obtain the desired oxide phase.
Embodiment 2
[0035] (1) According to the molar ratio La:Ru:CA=1:5:6, weigh La(NO 3 ) 3 ·6H 2 O, RuCl 3 and C 6 h 8 o 7 ·H 2 O After mixing, add water to dissolve it, stir the solution vigorously, while raising the temperature to 65°C, continue to add ethylene glycol and keep it at this temperature until it becomes a viscous gel-like substance due to the slow evaporation of water;
[0036] (2) Transfer the beaker to a heating mantle to provide uniform heating, and the temperature rises to 120° C. for 1 hour, at which time a 3D polymer structure is formed through the reaction of citric acid and ethylene glycol;
[0037] (3) Place the beaker containing the remaining product in an oven (>100°C) to dry thoroughly;
[0038] (4) After drying, the polymer was pulverized and calcined at 900° C. for 7 hours to decompose the polymer and obtain the desired oxide phase.
Embodiment 3
[0040] (1) According to the molar ratio La:Ru:CA=1:2:3, weigh La(NO 3 ) 3 ·6H 2 O, RuCl 3 and C6 h 8 o 7 ·H 2 O After mixing, add water to dissolve it, stir the solution vigorously, while raising the temperature to 65°C, continue to add ethylene glycol and keep it at this temperature until it becomes a viscous gel-like substance due to the slow evaporation of water;
[0041] (2) Transfer the beaker to a heating mantle to provide uniform heating, and the temperature rises to 120° C. for 4 hours, at which time a 3D polymer structure is formed through the reaction of citric acid and ethylene glycol;
[0042] (3) Place the beaker containing the remaining product in an oven (>100°C) to dry thoroughly;
[0043] (4) After drying, the polymer is pulverized and calcined at 1000° C. for 6 hours to decompose the polymer and obtain the desired oxide phase.
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