Preparation method of aluminum-containing metal organic framework material and material prepared by preparation method
A metal-organic framework and a certain amount of technology are applied in the field of preparation methods and materials, which can solve the problems of inability to observe the reaction intuitively, the long time required for the reaction, and potential safety hazards, and achieve high methane and nitrogen adsorption and separation selectivity. and methane adsorption capacity, high acid resistance, high yield effect
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Embodiment 1
[0036] Aluminum chloride hexahydrate (1.448g, 6mmol), trans-cyclohexane-1,4-dicarboxylic acid (1.002g, 6mmol) and 32ml of N, N dimethylformamide (DMF), 8ml of distilled water were mixed and stirred evenly and placed in 50ml The round-bottomed beaker was continuously stirred at 130 degrees Celsius for 3 minutes to obtain a small amount of precipitate, which was then filtered and washed with N, N dimethylformamide and acetone solvents for two days to remove unreacted organic matter. Ligand, the final product was placed in a vacuum drying oven at 120°C for 12 hours, and the final yield was 90%.
Embodiment 2
[0038] Aluminum chloride hexahydrate (1.448g, 6mmol), trans-cyclohexane-1,4-dicarboxylic acid (1.002g, 6mmol) and 32ml of N, N dimethylformamide (DMF), 8ml of distilled water were mixed and stirred evenly and placed in 50ml The round-bottomed beaker was continuously stirred at 130 degrees Celsius for 5 minutes to obtain a large amount of white precipitate, which was then filtered and washed with N, N dimethylformamide and acetone solvents for two days to remove unreacted Organic ligands, the final product is placed in a vacuum drying oven at 120° C. for 12 hours, and the final yield is 92%-95%.
Embodiment 3
[0040] Aluminum chloride hexahydrate (1.448g, 6mmol), trans-cyclohexane-1,4-dicarboxylic acid (1.002g, 6mmol) and 32ml of N, N dimethylformamide (DMF), 8ml of distilled water were mixed and stirred evenly and placed in 50ml The round-bottomed beaker was continuously stirred at 130 degrees Celsius for 8 minutes to obtain a large amount of white precipitate, which was then filtered and washed with N, N dimethylformamide and acetone solvents for two days to remove unreacted particles. Organic ligands, the final product was placed in a vacuum drying oven at 120°C for 12 hours, and the final yield was 91%.
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