pH (potential of hydrogen) responsive metal organic framework nanometer crystal, preparation method and application
A metal-organic framework and nanocrystal technology, which is applied in the field of pH-responsive metal-organic framework nanocrystals and its preparation, can solve problems that cannot be transformed into a Pickering emulsion interface catalytic system, and it is difficult to realize in-situ separation, recovery and reuse of catalysts, and separation of surfactants. and purification difficulties, etc., to achieve good chemical reaction performance, easy operation, and mild reaction conditions
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Embodiment 1
[0112] The synthesis of embodiment 1 metal organic framework MOF1
[0113] Dissolve the organic ligand 2-aminoterephthalic acid, zirconium tetrachloride, and acetic acid in N,N-dimethylformamide solvent, keep the temperature at 120°C for 24 hours, and cool down to room temperature to obtain light yellow nano-sized crystals, centrifuge, Drying; the ratio of organic ligand 2-aminoterephthalic acid, zirconium tetrachloride, acetic acid and N,N-dimethylformamide solvent addition is 0.04mmol: 0.04mmol: 2mmol: 1.6mL, the obtained crystal See in description figure 1 .
Embodiment 2
[0114] The synthesis of embodiment 2 metal organic framework MOF2
[0115] Weigh UiO-66-NH-Met crystal (0.6g, 0.002mol), methacrylic anhydride 2.356ml (2.45g, 0.016mol), triethylamine 0.279mL (0.002mol), 50ml of chloroform solution, add Into a 100mL round bottom flask, the chloroform in it was dried, the triethylamine was redistilled, heated to reflux at 55°C for 24h, and a drying device was added to the condenser. After the reaction was completed, it was cooled naturally and then centrifuged, then washed 6 times with fresh chloroform, and dried in vacuum for 5 hours at 100°C. After the treatment, it was taken out for use. figure 2 .
Embodiment 3
[0116] Post-synthesis modification of embodiment 3MOF3 crystal
[0117] Under nitrogen protection, UiO-66-NH-Met crystals (100 mg), diethylaminoethyl methacrylate (0.5 mL, 0.25 mol), potassium persulfate (9 mg, about 1.25 mol%) uniformly dispersed in 20 mL of water , placed in a three-neck flask, heated and stirred at 70°C for 72 hours, centrifuged, washed three times with THF, and dried for use. The obtained crystal morphology is shown in image 3 , after modification, the crystal morphology hardly changed.
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