A kind of nitrogen-doped carbon catalyst and its preparation method and application
A nitrogen-doped carbon and catalyst technology, which is applied in chemical instruments and methods, physical/chemical process catalysts, chemical/physical processes, etc., can solve problems such as homogeneous doping of difficult nitrogen atoms
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[0061] A method for preparing a nitrogen-doped carbon catalyst, the method comprising the steps of:
[0062] 1) The triaryl imidazole benzoxazine monomer (TBZ) is placed in a reactor for thermal polymerization to obtain a triaryl imidazole benzoxazine polymer (TPB).
[0063] 2) The triaryl imidazole benzoxazine polymer (TPB) obtained in step 1) is subjected to a Friedel-Crafts reaction in the presence of a catalyst and a crosslinking agent to synthesize a triaryl imidazole benzoxazine crosslinked polymer (Cross -linked TPB).
[0064] 3) The nitrogen-doped carbon catalyst (NDC) is obtained by heat-treating and acid-treating the triarylimidazole-containing benzoxazine cross-linked polymer (Cross-linked TPB) obtained in step 2).
[0065] Preferably, step 1) specifically includes: putting the triaryl imidazole benzoxazine monomer (TBZ) into a reactor (such as a muffle furnace), and then raising the temperature of the reactor to perform the reaction (the reaction temperature is 15...
Embodiment 1
[0071] 1) Synthesis of triaryl imidazole benzoxazine monomer (TBZ):
[0072] Synthesis of compound A (2-{[4-(4,5-diphenyl-1H-imidazol-2-yl)-phenylimino]-methyl}-phenol): Weigh 10g (32mmol) of 4 -(4,5-Diphenyl-1H-imidazol-2-yl)-aniline and 5.52g (48mmol) of salicylaldehyde were dissolved in 300ml of ethanol, and then heated to 100°C under nitrogen atmosphere for reflux reaction for 24h. After the reaction, the system was poured into 1000ml petroleum ether, suction filtered and washed to obtain bright yellow compound A with a yield of 95%.
[0073] Synthesis of compound B (2-{[4-(4,5-diphenyl-1H-imidazol-2-yl)-phenylamino]-methyl}-phenol): add 1.67 g (43.2mmol) sodium borohydride, 9g (21.6mmol) compound A and 100ml dry tetrahydrofuran were stirred at room temperature for 12h. After the reaction, slowly add 70ml of water, continue to stir for 12h, then pour the system into a large amount of cold water, and filter with suction. The obtained product was first dried under vacuum ...
Embodiment 2
[0082] 1) Synthesis of triaryl imidazole benzoxazine monomer (TBZ):
[0083] Synthesis of compound A (2-{[4-(4,5-diphenyl-1H-imidazol-2-yl)-phenylimino]-methyl}-phenol): Weigh 10g (32mmol) of 4 -(4,5-Diphenyl-1H-imidazol-2-yl)-aniline and 5.52g (48mmol) of salicylaldehyde were dissolved in 300ml of ethanol, and then heated to 100°C under nitrogen atmosphere for reflux reaction for 24h. After the reaction, the system was poured into 1000ml petroleum ether, suction filtered and washed to obtain bright yellow compound A with a yield of 95%.
[0084] Synthesis of compound B (2-{[4-(4,5-diphenyl-1H-imidazol-2-yl)-phenylamino]-methyl}-phenol): add 1.67 g (43.2mmol) sodium borohydride, 9g (21.6mmol) compound A and 100ml dry tetrahydrofuran were stirred at room temperature for 12h. After the reaction, slowly add 70ml of water, continue to stir for 12h, then pour the system into a large amount of cold water, and filter with suction. The obtained product was first dried under vacuum ...
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