An iron-based metal-organic framework material with high adsorption selectivity for C6 isomers and its preparation method and application
A technology of isomers and iron-based metals, applied in the field of iron-based metal-organic framework materials and their preparation, can solve the problem of low selectivity of isomers, achieve strong hydrophobicity, good chemical stability, The effect of good adsorption selectivity
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Embodiment 1
[0041] (1) Synthesis of iron clusters: ① 25.4293g of anhydrous sodium acetate and 8.08g of Fe(NO 3 ) 3 9H 2 O was respectively dissolved in 50ml of water; ②The sodium acetate aqueous solution was dropped into the ferric nitrate aqueous solution drop by drop, and stirred for 8 hours to obtain a mixed solution; ③The mixed solution was suction-filtered to obtain a brown solid, and the product was washed with deionized water and ethanol in sequence , the product was dried in a vacuum oven at 70°C for 7 hours at a constant temperature to obtain iron clusters [Fe 3 (CH 3 COO) 6 ].
[0042] (2) Synthesis of Fe-hifpbb: ①Dissolve 450mg ligand 2,2-bis(4-carboxyphenyl)hexafluoropropane and 450mg iron cluster in 30ml (28.44g) N,N-dimethylformamide (DMF); ②Add the DMF solution of 2,2-bis(4-carboxyphenyl)hexafluoropropane dropwise into the DMF solution of iron clusters, then add 5.0ml (5.25g) glacial acetic acid dropwise, and stir 30 min until the mixture is uniform; ③Put the mixture ...
Embodiment 2
[0044] (1) Synthesis of iron clusters: ① 32.32g of anhydrous sodium acetate and 8.08g of Fe(NO 3 ) 3 9H 2 O was respectively dissolved in 50ml of water; ②The sodium acetate aqueous solution was dropped into the ferric nitrate aqueous solution drop by drop, and stirred for 24 hours to obtain a mixed solution; ③The mixed solution was suction-filtered to obtain a brown solid, and the product was washed with deionized water and ethanol in turn , the product was dried in a vacuum oven at 70°C for 7 hours at a constant temperature to obtain iron clusters [Fe 3 (CH 3 COO) 6 ].
[0045] (2) Synthesis of Fe-hifpbb: ①Dissolve 450mg of ligand 2,2-bis(4-carboxyphenyl)hexafluoropropane and 900mg of iron clusters in 35.6ml (33.75g)N,N-dimethylformaldehyde amide (DMF); ②Add the DMF solution of 2,2-bis(4-carboxyphenyl)hexafluoropropane dropwise into the DMF solution of iron clusters, then add 8.57ml (9.0g) glacial acetic acid dropwise, and Stir for 30 minutes until the mixture is unifor...
Embodiment 3
[0047] (1) Synthesis of iron clusters: ① 28.87g of anhydrous sodium acetate and 8.08g of Fe(NO 3 ) 3 9H 2 O was respectively dissolved in 50ml of water; ②The sodium acetate aqueous solution was dropped into the ferric nitrate aqueous solution drop by drop, and stirred for 16 hours to obtain a mixed solution; ③The mixed solution was suction-filtered to obtain a brown solid, and the product was washed with deionized water and ethanol in turn , the product was dried in a vacuum oven at 70°C for 7 hours at a constant temperature to obtain iron clusters [Fe 3 (CH 3 COO) 6 ].
[0048] (2) Synthesis of Fe-hifpbb: ① Dissolve 450mg of the ligand 2,2-bis(4-carboxyphenyl)hexafluoropropane and 675mg of iron clusters in 32.8ml (31.1g) of N,N-dimethylformaldehyde amide (DMF); ②Add the DMF solution of 2,2-bis(4-carboxyphenyl)hexafluoropropane dropwise into the DMF solution of iron clusters, then add 6.785ml (7.125g) of glacial acetic acid dropwise, and Stir for 30 minutes until the mix...
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