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A kind of defective covalent triazine framework material derivative material catalyst and its preparation method and application

A technology of covalent triazine and framework materials, applied in chemical instruments and methods, physical/chemical process catalysts, chemical/physical processes, etc., can solve the problem that the catalytic activity of the catalyst needs to be improved, and achieve good catalytic cycle stability and preparation. Simple method and cheap effect

Active Publication Date: 2022-02-15
ZHEJIANG UNIV OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Moreover, there are few studies on the application of carbon-nitrogen materials based on covalent triazine covalently derived catalysts for electrocatalysis, and the catalytic activity of such catalysts needs to be improved.

Method used

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  • A kind of defective covalent triazine framework material derivative material catalyst and its preparation method and application
  • A kind of defective covalent triazine framework material derivative material catalyst and its preparation method and application
  • A kind of defective covalent triazine framework material derivative material catalyst and its preparation method and application

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] 1) Dissolve 0.64g of terephthalonitrile and 0.64g of 2,6-pyridinedicarbonitrile in 60mL of dichloromethane organic solvent, stir and fully dissolve at room temperature to obtain a dispersion;

[0035] 2) Put the dispersion obtained in step 1) in a round bottom flask, put it in an oil bath, add 10mL of trifluoromethanesulfonic acid, heat to reflux, and stir at 60°C for 40h. After the reaction, put The reaction solution was cooled to room temperature;

[0036]3) Pour the cooled reaction solution in step 2) into a beaker containing 200mL of ultrapure water, and use a pipette to add concentrated ammonia water (the concentration of concentrated ammonia water is 0.5mol / L) drop by drop to adjust the pH value of the solution to 7. Suction filtration is then carried out, and the filter residue is washed with dichloromethane, ultrapure water and ethanol in sequence, and dried in vacuum to finally obtain the defective covalent triazine framework carrier material powder;

[0037] ...

Embodiment 2

[0043] 1) Dissolve 0.64g of terephthalonitrile and 0.64g of 2,6-pyridinedicarbonitrile in 60mL of dichloromethane organic solvent, stir and fully dissolve at room temperature to obtain a dispersion;

[0044] 2) Put the dispersion obtained in step 1) in a round bottom flask, put it in an oil bath, add 10mL of trifluoromethanesulfonic acid, heat to reflux, and stir at 60°C for 40h. After the reaction, put The reaction solution was cooled to room temperature;

[0045] 3) Pour the cooled reaction solution in step 2) into a beaker containing 200mL of ultrapure water, and use a pipette to add concentrated ammonia water (the concentration of concentrated ammonia water is 0.5mol / L) drop by drop to adjust the pH value of the solution to 7. Suction filtration is then carried out, and the filter cake is washed with dichloromethane, ultrapure water and ethanol in sequence, and dried in vacuum to finally obtain the defective covalent triazine framework carrier material powder;

[0046] 4)...

Embodiment 3

[0049] 1) Dissolve 0.64g of terephthalonitrile and 0.64g of 2,6-pyridinedicarbonitrile in 60mL of dichloromethane organic solvent, stir and fully dissolve at room temperature to obtain a dispersion;

[0050] 2) Put the dispersion obtained in step 1) in a round bottom flask, put it in an oil bath, add 10mL of trifluoromethanesulfonic acid, heat to reflux, and stir at 60°C for 40h. After the reaction, put The reaction solution was cooled to room temperature;

[0051] 3) Pour the cooled reaction solution in step 2) into a beaker containing 200mL of ultrapure water, and use a pipette to add concentrated ammonia water (the concentration of concentrated ammonia water is 0.5mol / L) drop by drop to adjust the pH value of the solution to 7. Suction filtration is then carried out, and the filter cake is washed with dichloromethane, ultrapure water and ethanol in sequence, and dried in vacuum to finally obtain the defective covalent triazine framework carrier material powder;

[0052] 4)...

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Abstract

The invention discloses a defect-type covalent triazine framework material derivative material catalyst and its preparation method and application. The preparation process of the catalyst is as follows: a benzonitrile compound and a pyridine derivative are dissolved in a first organic solvent, and a strong acid is added , heated to reflux reaction under oil bath conditions, cooled to room temperature after the reaction, the cooled reaction solution was poured into ultrapure water, added alkali to adjust the pH to neutral, filtered with suction, and the filter residue was washed and dried to obtain defective covalent Triazine framework carrier powder, put the obtained powder, cyano derivatives and ruthenium metal salt into a mortar, add absolute ethanol, grind evenly until the ethanol is completely volatilized, dry, and then perform high-temperature calcination under the protection of inert gas, after calcination The product is washed with ultrapure water and dried to obtain the defect-type covalent triazine framework material-derived material catalyst. The catalyst of the invention has high specific surface area and porous structure, small ruthenium metal particles after loading, high dispersion degree of metal ions, and good effect of catalyzing hydrogen evolution reaction.

Description

technical field [0001] The invention relates to a defect-type covalent triazine frame material derived material catalyst and its preparation method and application. Background technique [0002] At present, with the continuous reduction of fossil fuels and the increasingly serious environmental pollution, human beings must find and develop new renewable energy sources. Hydrogen is clean, sustainable and renewable, making it an ideal alternative. Electrochemical water splitting has the advantages of low cost and high efficiency, and is a promising method for producing high-purity hydrogen. However, the practical application of water splitting for large-scale hydrogen production has been greatly hindered due to the large overpotential required for the two half-reactions (hydrogen evolution reaction and oxygen evolution reaction) in electrochemical water splitting. Among the new energy sources, the fuel cell is also a good new energy source. It is a power generation device th...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J27/24B01J35/10C25B11/091C25B1/04
CPCB01J27/24C25B11/04C25B1/04B01J35/394B01J35/33B01J35/61Y02E60/36
Inventor 庄桂林高旭王建国
Owner ZHEJIANG UNIV OF TECH