Preparation method and application of super-hydrophobic zeolite imidazole metal-organic framework F-ZIF-90
A metal-organic framework, F-ZIF-90 technology, applied in the field of material chemistry, can solve the problem of poor oil-water separation performance and achieve excellent hydrophobic performance
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Embodiment 1
[0024] Step 1: Organic Ligand Modification
[0025] Dissolve 0.388 g (4 mmol) of imidazole-2-carbaldehyde and 0.732 g (4 mmol) of 2,3,4,5,6-pentafluoroaniline in 20 ml of absolute ethanol, and transfer to a 250 ml single-necked flask after the solution is clarified 0.0088 g (0.0472 mmol) p-toluenesulfonic acid was added, and the reaction was refluxed at 80°C for 12 hours. After the reaction was completed, the solvent was removed by rotary evaporation, and then washed several times with anhydrous methanol to remove the methanol to obtain the organic ligand fluorine-functionalizedimidazole (F-ICA) with a hydrophobic group;
[0026] Step 2: Preparation of superhydrophobic F-ZIF-90
[0027] Dissolve 1.0452 g (4 mmol) of imidazole fluoride and 0.136 g (2 mmol) of sodium formate in 30 mL of anhydrous methanol, and stir the solution magnetically until clear to prepare solution A; 0.136 g (1 mmol) of anhydrous ZnCl 2 Dissolve in 10 mL of anhydrous methanol to prepare solution B; slo...
Embodiment 2
[0030] Step 1: Organic Ligand Modification
[0031] Dissolve 0.388 g (4 mmol) of imidazole-2-carbaldehyde and 0.0.8235 g (4.5 mmol) of 2,3,4,5,6-pentafluoroaniline in 20 ml of absolute ethanol, and transfer to 250 0.0088 g (0.0472 mmol) p-toluenesulfonic acid was added to a single-necked flask, and the reaction was refluxed at 75 °C for 24 hours. After the reaction was completed, the solvent was removed by rotary evaporation, and then washed several times with anhydrous methanol to remove the methanol to obtain the organic ligand fluorine-functionalized imidazole (F-ICA) with a hydrophobic group;
[0032] Step 2: Preparation of superhydrophobic F-ZIF-90
[0033]1.3065 g (5 mmol) of imidazole fluoride and 0.136 g (2 mmol) of sodium formate were dissolved in 30 mL of anhydrous methanol, and the solution was magnetically stirred until clear to prepare solution A; 0.297 g (1 mmol) of Zn(NO 3 ) 2 ·6H 2 O was dissolved in 10 mL of anhydrous methanol to prepare solution B; the cl...
Embodiment 3
[0035] Step 1: Organic Ligand Modification
[0036] Dissolve 0.388 g (4 mmol) of imidazole-2-carbaldehyde and 0.0.8235 g (4.5 mmol) of 2,3,4,5,6-pentafluoroaniline in 20 ml of absolute ethanol, and transfer to 250 0.0088 g (0.0472 mmol) p-toluenesulfonic acid was added to a single-necked flask, and the reaction was refluxed at 60 °C for 30 hours. After the reaction was completed, the solvent was removed by rotary evaporation, and then washed several times with anhydrous methanol to remove the methanol to obtain the organic ligand fluorine-functionalized imidazole (F-ICA) with a hydrophobic group;
[0037] Step 2: Preparation of superhydrophobic F-ZIF-90
[0038] Dissolve 1.0425 g (4 mmol) of imidazole fluoride and 0.219 g (2 mmol) of sodium formate in 30 mL of anhydrous methanol, and stir the solution magnetically until clear to prepare solution A; 0.136 g (1 mmol) of Zn(Ac) 2 2H 2 O was dissolved in 10 mL of anhydrous methanol to prepare solution B; the clear solution A wa...
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