Preparation method for metal organic framework and carbon nitride composite material capable of preferentially adsorbing alkane
A metal-organic framework, preferential adsorption technology, applied in the direction of alkali metal compounds, organic chemistry, adsorption purification/separation, etc., to achieve the effect of good stability
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Embodiment 1
[0034] The ground graphite-like phase g-C 3 N 4 (2.54mg), ZrCl 4 (245mg1.05mmol), biphenyldicarboxylic acid (260mg1.05mmol), glacial acetic acid 2ml, N,N-dimethylformamide (DMF) 40ml, were added to the reaction kettle, stirred and sonicated for 20min. Then the reactor was heated to 100°C for 48h, then cooled to room temperature, and centrifuged. The product obtained by the reaction uses N,N-dimethylformyl
[0035] Rinse the material 3 times with amine; then soak in methanol for 48 hours, replace the methanol every 12 hours, and then keep it at 80°C for 6 hours. Finally, it was activated under vacuum condition at 100° C. for 12 hours to obtain the product, which was labeled as Example 1.
Embodiment 2
[0037] The ground graphite-like phase g-C 3 N 4 (5.08mg), ZrCl 4 (245mg1.05mmol), biphenyldicarboxylic acid (260mg1.05mmol), glacial acetic acid 2ml, N,N-dimethylformamide (DMF) 40ml were added to the reaction kettle, stirred and sonicated for 30min. Afterwards, the reactor was heated to 120° C. for 36 h, then cooled to room temperature, and centrifuged. The product obtained by the reaction was rinsed with N,N-dimethylformamide for 4 times; then soaked in methanol for 48 hours, the methanol was replaced every 12 hours, and then kept at 80°C for 6 hours. Finally, it was activated under vacuum at 120° C. for 8 hours to obtain the product, which was labeled as Example 2.
Embodiment 3
[0039] The ground graphite-like phase g-C 3 N 4 (15.23mg), ZrCl 4 (245mg1.05mmol), biphenyl dicarboxylic acid (260mg1.05mmol), 2ml of glacial acetic acid, 40ml of N,N-dimethylformamide (DMF) were added to the reaction kettle, stirred and ultrasonicated for 60min. Afterwards, the reactor was heated to 150° C. for 24 hours, then cooled to room temperature, and centrifuged. The product obtained by the reaction was rinsed with N,N-dimethylformamide for 5 times; then soaked in methanol for 48 hours, the methanol was replaced every 12 hours, and then kept at 80°C for 6 hours. Finally, the product was activated under vacuum condition at 160° C. for 4 hours to obtain the product, which was labeled as Example 3.
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