A method of catalyzing percarbonate to degrade organic pollutants in wastewater
A technology of organic pollutants and percarbonate, applied in water pollutants, chemical instruments and methods, oxidized water/sewage treatment, etc., can solve the problems of high energy consumption of physical methods, secondary pollution of metal ions, etc., and achieve activation Outstanding effect, uniform dispersion, and large specific surface area
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Embodiment 1
[0035] Raw Materials and Reagents
[0036] Dicyandiamide (C 2 h 4 N 4 ), copper sulfate pentahydrate (CuSO 4 ·5H 2 O), sodium hydroxide (NaOH), and hydrochloric acid (HCl) were of analytical grade (AR), purchased from Sinopharm Chemical Reagent Co., Ltd.; xylitol (C 5 h 12 0 5 ), methyl orange (C 14 h 14 N 3 NaO 3 S) and others were of analytical grade (AR), purchased from Shanghai Aladdin Biochemical Technology Co., Ltd.
[0037] Protonated g-C 3 N 4 Catalyst preparation
[0038] Preparation of g-C by High Temperature Pyrolysis of Dicyandiamide 3 N 4 . Weigh 4g of dicyandiamide and place it in a corundum crucible with a cover, and put the crucible into the muffle furnace, -1 The heating rate was programmed to raise the temperature to 550°C and keep it warm for 4 hours. After the product was naturally cooled, the obtained yellow powder was ground for 30 minutes, and the obtained preliminary product was ground for later use. Mix 10ml of concentrated sulfuric a...
Embodiment 2
[0040] Protonated g-C 3 N 4 Catalyst preparation
[0041] Preparation of g-C by High Temperature Pyrolysis of Dicyandiamide 3 N 4 . Weigh 4g of dicyandiamide and put it in a corundum crucible with a cover, and put the crucible in the muffle furnace, -1 The heating rate was programmed to raise the temperature to 600°C and keep it warm for 3 hours. After the product was naturally cooled, the obtained yellow powder was ground for 30 minutes, and the obtained preliminary product was ground for later use. Mix 10ml of concentrated sulfuric acid and add it into a 50ml flask, stir at room temperature for 8h, and sonicate for 1h. The stirred mixture is slowly poured into 100ml of deionized water while stirring. The obtained milky white suspension was centrifuged at 3000 r for 10 min and washed with deionized water. Dry at 80°C. Weigh the acidified g-C 3 N 4 Pour 0.4g into a 200ml flask, reflux at 75°C for 4h, wash with suction and dry at 80°C to obtain g-C 3 N 4 .
Embodiment 3
[0043] Protonated g-C 3 N 4 Catalyst preparation
[0044] Preparation of g-C by High Temperature Pyrolysis of Dicyandiamide 3 N 4 . Weigh 4g of dicyandiamide and place it in a corundum crucible with a cover, and put the crucible in the muffle furnace, -1 The heating rate was programmed to raise the temperature to 500°C and keep it warm for 5 hours. After the product was cooled naturally, the obtained yellow powder was ground for 30 minutes, and the obtained preliminary product was ground for later use. Mix 10ml of concentrated sulfuric acid and add it into a 50ml flask, stir at room temperature for 8h, and sonicate for 1h. The stirred mixture is slowly poured into 100ml of deionized water while stirring. The obtained milky white suspension was centrifuged at 3000 r for 10 min and washed with deionized water. Dry at 80°C. Weigh the acidified g-C 3 N 4 Pour 0.4g into a 200ml flask, reflux at 50°C for 8h, wash with suction and dry at 80°C to obtain g-C 3 N 4 .
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