Preparation and application of amino-functionalized MOFs material
A technology of amino functionalization and catalytic reaction, which is applied in the field of metal-organic framework material preparation, can solve the problems of few application reports, and achieve the effect of expanding the application field and making the preparation method simple and feasible.
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Embodiment 1
[0035] 0.370 g organic ligand H 2 ATA and 0.808 g Fe(NO 3 ) 2 9H 2 O was dissolved in 20 mL of DMF solution, ultrasonicated for 20 min at 100 W to disperse and dissolve evenly. The obtained solution was transferred to the lining of a polytetrafluoroethylene autoclave, and the autoclave was sealed and placed in an oven at 140 °C for 6 h. After the reaction dropped to room temperature, the obtained product was washed with methanol, centrifuged several times, dried at 80 °C for 4 h, and then treated under static vacuum at 80 °C for 8 h to finally obtain catalyst A.
Embodiment 2
[0037] 0.370 g organic ligand H 2 ATA and 0.808 g Fe(NO 3 ) 2 9H 2 O was dissolved in 20 mL of DMF solution, ultrasonicated for 20 min at 100 W to disperse and dissolve evenly. The obtained solution was transferred to the lining of a polytetrafluoroethylene autoclave, and the autoclave was sealed and placed in an oven at 150 °C for 6 h. After the reaction was cooled to room temperature, the obtained product was washed with methanol, centrifuged several times, dried at 80 °C for 4 h, and then treated under static vacuum at 80 °C for 8 h to finally obtain catalyst B.
Embodiment 3
[0039] 0.370 g organic ligand H 2 ATA and 0.808 g Fe(NO 3 ) 2 9H 2 O was dissolved in 20 mL of DMF solution, ultrasonicated for 20 min at 100 W to disperse and dissolve evenly. The obtained solution was transferred to the lining of a polytetrafluoroethylene high-pressure reactor, and the reactor was sealed and placed in an oven at 160 °C for 6 h. After the reaction was cooled to room temperature, the obtained product was washed with methanol, centrifuged several times, dried at 80 °C for 4 h, and then treated under static vacuum at 80 °C for 8 h to obtain catalyst C.
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