WO3/TpPa-1-COF composite material as well as preparation method and application thereof
A tppa-1-cof, composite material technology, applied in organic compound/hydride/coordination complex catalysts, chemical instruments and methods, chemical/physical processes, etc., can solve problems such as limiting solar energy utilization efficiency, and achieve outstanding Catalytic performance, stable catalytic performance, low cost effect
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Embodiment 1
[0056] A kind of WO 3 / TpPa-1-COF composite material, its preparation method comprises the following steps:
[0057] S1. Synthesis of TpPa-1-COF:
[0058] S1.1 First, add 63mg trialdehyde phloroglucinol and 48mg p-phenylenediamine into the Parker heat pipe, and disperse it uniformly by ultrasonic to obtain a mixture;
[0059] S1.2 Add 1.5mL of 1,4-dioxane, 1.5mL of trimesaldehyde and 0.5mL of acetic acid solution (3M) to the mixture obtained in step S1.1, and ultrasonically dissolve it completely to obtain a uniform solution;
[0060] S1.3 The solution obtained in S1.2 was quickly frozen in a liquid nitrogen bath (77K), degassed through three freezing pump thawing cycles, sealed in vacuum, and then heated at 120°C for 3 days, and the precipitate obtained from the reaction was washed with tetrahydrofuran, N, N-dimethylformamide and acetone are filtered to obtain red product;
[0061] S1.4 Activate the red product synthesized in step S1.3 by exchanging the solvent with anhydr...
Embodiment 2
[0078] A kind of WO 3 / TpPa-1-COF composite material, its preparation method comprises the following steps:
[0079] S1. Synthesis of TpPa-1-COF:
[0080] S1.1 First, add 63mg trialdehyde phloroglucinol and 48mg p-phenylenediamine into the Parker heat pipe, and disperse it uniformly by ultrasonic to obtain a mixture;
[0081] S1.2 Add 1.5mL of 1,4-dioxane, 1.5mL of trimesaldehyde and 0.5mL of acetic acid solution (3M) to the mixture obtained in step S1.1, and ultrasonically dissolve it completely to obtain a uniform solution;
[0082] S1.3 The solution obtained in S1.2 was quickly frozen in a liquid nitrogen bath (77K), degassed through three freezing pump thawing cycles, sealed in vacuum, and then heated at 120°C for 3 days, and the precipitate obtained from the reaction was washed with tetrahydrofuran, N, N-dimethylformamide and acetone are filtered to obtain red product;
[0083] S1.4 Activate the red product synthesized in step S1.3 by exchanging the solvent with anhydr...
Embodiment 3
[0096] TpPa-1-COF, WO prepared by comparative examples 1 and 2 3 Materials and WO 3 Differences in photocatalytic performance of / TpPa-1-COF composites:
[0097] Get respectively 10mg powder samples (respectively TpPa-1-COF, WO prepared in embodiment 1 and embodiment 2 3 Materials and WO 3 / TpPa-1-COF composite material) was dispersed in 100mL aqueous solution containing 0.95g ascorbic acid, ultrasonically dispersed for 30min and placed in a photocatalytic reaction vessel for continuous stirring. Vacuum until the reaction system is in an approximate vacuum state (P≤1.0kpa), continue to illuminate with a 300W xenon lamp, and extract the gas in the reaction tank through an autosampler every hour and send it to the gas chromatograph, which is detected online in real time by the gas chromatograph. The peak position and the size of the peak area can be used to judge the reaction product and the amount produced. TpPa-1-COF prepared in embodiment 1, WO 3 Materials and WO 3 / TpP...
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