Method for degrading rhodamine B and indigo organic pollutant
A technology of organic pollutants and indigo, applied in the field of photocatalytic materials, can solve problems such as application limitations, and achieve the effects of simple synthesis method, good catalytic degradation effect, and low product cost
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[0043] Example 1
[0044] 1.1. Preparation of degradation catalyst
[0045] 0.1mmol CuCl 2 ·2H 2 O, 0.10mmol N , N '-Bis(3-pyridinecarboxyl)-1,2-ethane, 0.10mmolNa 3 [CrMo 6 H 6 O 24 ]·8H 2 O (sodium chromomolybdate octahydrate) and 12.0 mL of deionized water were sequentially added to a 25 mL beaker, and stirred at room temperature for 30 minutes to obtain a suspension mixture. After adjusting the pH of the suspension mixture to 1.8 with 1.0 mol / L HCl solution, transfer to In a 25mL autoclave, heat up to 110°C at a heating rate of 15°C / h, keep the temperature constant for 48 hours under hydrothermal conditions, and then lower to room temperature at a cooling rate of 2.5°C / h to obtain dark green massive crystals. Rinse alternately with water and absolute ethanol twice, and dry naturally at room temperature to obtain the complex H{CuL 1 0.5 [CrMo 6 (OH) 6 O 18 ](H 2 O)}·0.5L 1 , Where L 1 for N , N '-Bis(3-pyridinecarboxyl)-1,2-ethane, the structural formula is: , The yield is 26%,...
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[0049] Example 2
[0050] 1.1. Preparation of degradation catalyst
[0051] Add 0.40mmol CuCl 2 ·2H 2 O, 0.10mmol N , N '-Bis(3-pyridinecarboxyl)-1,2-ethane, 0.30mmol Na 3 [CrMo 6 H 6 O 24 ]·8H 2 O and 7.0 mL of deionized water were added to a 25 mL beaker in turn, stirred at room temperature for 10 min to obtain a suspension mixture. After adjusting the pH of the suspension mixture to 2.5 with 0.5 mol / L HCl solution, it was transferred to a 25 mL autoclave. Heat up to 130°C at a heating rate of 5°C / h, keep for 120h under hydrothermal conditions, and lower to room temperature at a cooling rate of 5°C / h to obtain dark green block crystals, which are washed alternately with deionized water and absolute ethanol 3 Second, let it dry naturally at room temperature to obtain the complex H{CuL 1 0.5 [CrMo 6 (OH) 6 O 18 ](H 2 O)}·0.5L 1 , Where L 1 for N , N '-Bis(3-pyridinecarbonyl)-1,2-ethane, the yield is 28%, and its PXRD diffraction pattern is as figure 1 As shown, the coordination en...
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[0055] Example 3
[0056] 1.1. Preparation of degradation catalyst
[0057] Add 0.5mmol CuCl 2 ·2H 2 O, 0.10mmol N , N '-Bis(3-pyridinecarbonyl)-1,2-ethane, 0.24mmol Na 3 [CrMo 6 H 6 O 24 ]·8H 2 O and 11.0 mL of deionized water were added to a 25 mL beaker in turn, stirred at room temperature for 30 min to obtain a suspension mixture. After adjusting the pH of the suspension mixture to 2.1 with 1.0 mol / L HCl solution, it was transferred to a 25 mL autoclave. Raise the temperature to 120°C at a heating rate of 10°C / h, keep it for 96 hours under hydrothermal conditions, and lower to room temperature at a cooling rate of 10°C / h to obtain dark green block crystals, which are washed alternately with deionized water and absolute ethanol 2 Second, let it dry naturally at room temperature to obtain the complex H{CuL 1 0.5 [CrMo 6 (OH) 6 O 18 ](H 2 O)}·0.5L 1 , L 1 for N , N '-Bis(3-pyridinecarbonyl)-1,2-ethane, the yield is 34%, and its PXRD diffraction pattern is as figure 1 As shown, th...
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