A polyacid-based metal-organic framework material that can be used to adsorb antibiotics, its preparation method and use
A metal organic framework and organic framework technology, applied in the field of materials, can solve the problems of poor adsorption performance of antibiotic adsorption materials, and achieve the effects of good antibiotic adsorption performance, easy large-scale production and simple process
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Embodiment 1
[0029] Example 1 Preparation of MIL-101:
[0030] 1.33g (4.90mmol) FeCl 3 ·6H 2 O was dissolved in DMF (50mL), and 0.41g H 2 bdc (2.48 mmol) was added to the brown solution and stirred at room temperature for 10 minutes. The resulting mixture was divided into 10 portions and transferred to a 20 mL autoclave and heated at 383 K for 24 hours. After slow cooling to ambient temperature, the brown powder was centrifuged and washed thoroughly with distilled water and DMF. The product was dried under vacuum at 353K.
Embodiment 2
[0031] Example 2 Preparation of H 3 PMo 12 o 40 @MIL-101(Fe), abbreviated as PM
[0032] (1) 1.33g (4.90mmol) FeCl 3 ·6H 2 O was dissolved in DMF (50mL), and 0.41g H 2 bdc (2.48 mmol) was added to the brown solution and stirred at room temperature for 10 minutes.
[0033] (2) Add 0.2g H 3 PMo 12 o 40 Add in the mixture obtained in step (1) and stir for 0.5 hour;
[0034] (3) The mixture obtained in step (2) was transferred to an autoclave and heated at 383K for 24 hours; after cooling slowly to ambient temperature, the solid powder was separated and washed thoroughly with distilled water and DMF.
[0035] (4) Place the product obtained in step (3) under vacuum and dry at 353K to obtain the target product PM
Embodiment 3
[0036] Example 3 Preparation of PMo 11 VO 40 @MIL-101(Fe), abbreviated as PMV
[0037] (1) 1.33g (4.9mmol) FeCl 3 ·6H 2 O was dissolved in DMF (50mL), and 0.41g H 2 bdc (2.48 mmol) was added to the brown solution and stirred at room temperature for 10 minutes.
[0038] (2) Add 0.2g H 4 PMo 11 VO 40 Add in the mixture obtained in step (1) and stir for 0.5 hour;
[0039] (3) The mixture obtained in step (2) was transferred to an autoclave and heated at 383K for 24 hours; after cooling slowly to ambient temperature, the solid powder was separated and washed thoroughly with distilled water and DMF.
[0040] (4) Place the product obtained in step (3) under vacuum and dry at 353K to obtain the target product PMV
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