A kind of metal organic framework material co-pttic-tpb and its synthesis method and application
A metal-organic framework, co-pttic-tpb technology, applied in the cross field of nanomaterials and coordination chemistry, can solve the problems of large equipment investment and high energy consumption, and achieve stability and gas adsorption capacity, high thermal stability, Good water and alkali resistance
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Embodiment 1
[0029] Example 1: Synthesis of Co-PTTIC of the present invention
[0030] Weigh Co(NO 3 ) 2 ·6H 2 O(18mg), H 6 PTTIC (11mg) is dissolved in a mixed solution of 2mL DMF and 0.5mL deionized water. After the ultrasonic is completely dissolved, add 150μL HBF with a 200μL pipette 4 , Then transfer the mixture to a 25mL stainless steel autoclave, and then react in an oven at 120°C for 3 days (heating time 320min, cooling time 1200min). After cooling to room temperature, red shuttle-like transparent crystals are obtained, filtered and washed with DMF. Obtained pure crystals with a yield of 42%.
Embodiment 2
[0031] Example 2: The present invention adopts precise modification strategy to synthesize Co-PTTIC-TPB
[0032] Weigh Co(NO 3 ) 2 ·6H 2 O(18mg), H 6 PTTIC (11mg), TPB (6mg) are dissolved in a mixed solution of 2mL DMF and 0.5mL deionized water, after the ultrasonic is completely dissolved, add 150μL HBF with a pipette with a volume of 200μL 4 , Then transfer the mixture to a 25mL stainless steel autoclave, and then react in an oven at 120°C for 3 days (heating time 320min, cooling time 1200min). After cooling to room temperature, red square transparent crystals are obtained, filtered and washed with DMF to obtain pure Crystal, the yield is 65%.
[0033] The X-ray powder diffraction (XRD) characterization of the Co-PTTIC and Co-PTTIC-TPB of the present invention: the XRD data obtained by simulating the single crystal structure data of the material and the XRD data measured in the experiment are plotted. {Instrument model: Rigaku D / max-3B diffractometer }.
Embodiment 3
[0034] Example 3: XRD pattern determination of Co-PTTIC of the present invention under different processing conditions
[0035] Take the Co-PTTIC sample of the present invention prepared in Example 1, soak it in fresh methanol for three days, change the methanol twice a day, then dry the sample naturally, then dry the sample in vacuum at 50°C, and measure the XRD patterns respectively . Such as figure 2 , XRD diffraction peaks have gradually shifted, which is a typical feature of the shrinkage of the sample frame structure.
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