Two fluorinated metal organic framework materials and preparation and low-carbon hydrocarbon separation application thereof
A technology of copper fluoride and organic ligands, applied in the direction of adsorption purification/separation, organic chemistry, separation methods, etc., can solve the problems of high energy consumption and low selectivity, and achieve reduced energy consumption, low price, and enhanced force Effect
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Embodiment 1
[0028] Example 1: (Cu-FINA-1)
[0029] The first step: Weigh 10 mg of 3-fluoroisonicotinic acid organic ligand and 12 mg of copper nitrate, and dissolve them in 5 mL of N,N-dimethylformamide (DMF). After sonicating and obtaining a homogeneous solution, it was then transferred to a 20 mL glass reaction flask and reacted at 90° C. for 96 hours to obtain the Cu-FINA-1 crystalline sample with a yield of 60% (calculated based on the metal salt).
[0030] The second step: select a single crystal sample with suitable size and good crystallinity, collect the diffraction data with a single crystal diffractometer at 298K, and then refine the crystal structure by using the relevant structure analysis software Olex2. See the attached drawings for the specific structure. The purity of the whole prepared sample was confirmed by X-ray powder diffraction technique.
[0031] Step 3: In order to remove the solvent molecules in the pores of the material, the crystalline sample obtained above was wash...
Embodiment 2
[0038] Example 2: (Cu-FINA-2)
[0039] Step 1: Weigh 10mg 3-fluoroisonicotinic acid organic ligand and 12mg copper nitrate, and dissolve them in a mixed solvent of 2mL N,N-dimethylacetamide (DMA), 2mL acetonitrile, 0.1mL acetic acid and 2mL water . After sonicating and obtaining a homogeneous solution, it was then transferred to a 20 mL glass reaction flask and reacted at 90° C. for 96 hours to obtain the Cu-FINA-2 crystalline sample with a yield of 50% (calculated based on the metal salt).
[0040] The second step: select a single crystal sample with suitable size and good crystallinity, collect the diffraction data with a single crystal diffractometer at 298K, and then refine the crystal structure by using the relevant structure analysis software Olex2. See the attached drawings for the specific structure. The purity of the whole prepared sample was confirmed by X-ray powder diffraction technique.
[0041] The third step: In order to remove the solvent molecules in the pores of ...
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