Nitrogen-doped attapulgite/carbon/bismuth oxybromide composite nitrogen fixation photocatalyst and preparation method and application thereof
A technology of attapulgite and bismuth oxybromide, which is applied in the direction of metal/metal oxide/metal hydroxide catalyst, physical/chemical process catalyst, preparation/separation of ammonia, etc., which can solve the problem of large energy consumption and achieve cost reduction Low cost, simple process, and the effect of improving charge transfer efficiency
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Embodiment 1
[0027] (1) Take 3g of attapulgite and 1mL of aniline and evenly disperse in 50mL of aqueous solution (solid-to-liquid ratio of attapulgite to aniline (g / mL)=3:1), transfer the system to 0°C and stir for 24h, in-situ polymerization Attapulgite / polyaniline composite material was obtained. Further calcined carbonization (900℃ / 2h, N 2 ), the nitrogen-doped attapulgite / carbon precursor material can be obtained.
[0028] (2) Weigh 91.5 mg of nitrogen-doped attapulgite / carbon prepared in step (1) and 0.119 g of potassium bromide, dissolve in 30 mL of aqueous solution and sonicate for 15 min to obtain a uniform suspension.
[0029] (3) Weigh 0.485 g of bismuth nitrate pentahydrate and disperse it in 20 mL of glycerin with magnetic stirring for 0.5 h to dissolve it to prepare a bismuth nitrate solution.
[0030] (4) The solution prepared in step (2) was slowly added dropwise to step (3) under magnetic stirring conditions, after the dropwise addition was completed and vigorously stirr...
Embodiment 2
[0033] (1) Take 3g of attapulgite and 1mL of aniline and evenly disperse in 50mL of aqueous solution (solid-to-liquid ratio of attapulgite to aniline (g / mL) = 3:1), transfer the system to 0°C and stir for 12h, in situ polymerization Attapulgite / polyaniline composite material was obtained. Further calcined carbonization (900℃ / 2h, N 2 ), the nitrogen-doped attapulgite / carbon precursor material can be obtained.
[0034] (2) Weigh 152.5 mg of nitrogen-doped attapulgite / carbon prepared in step (1) and 0.119 g of potassium bromide, dissolve in 30 mL of aqueous solution and sonicate for 15 min to obtain a uniform suspension.
[0035] (3) Weigh 0.485 g of bismuth nitrate pentahydrate and disperse it in 20 mL of glycerin with magnetic stirring for 0.5 h to dissolve it to prepare a bismuth nitrate solution.
[0036] (4) The solution prepared in step (2) was slowly added dropwise to step (3) under magnetic stirring conditions, after the dropwise addition was completed and vigorously st...
Embodiment 3
[0039] The attapulgite / carbon precursor material was impregnated with bismuth nitrate and potassium bromide respectively to explore the effect of BiOBr crystals on the attapulgite / carbon precursor material in situ growth.
[0040] (1) Take 3g of attapulgite and 1mL of aniline and evenly disperse in 50mL of aqueous solution (solid-to-liquid ratio of attapulgite to aniline (g / mL) = 3:1), transfer the system to 0°C and stir for 12h, in situ polymerization Attapulgite / polyaniline composite material was obtained. Further calcined carbonization (900℃ / 2h, N 2 ), the nitrogen-doped attapulgite / carbon precursor material can be obtained.
[0041] (2) Weigh 427 mg of nitrogen-doped attapulgite / carbon prepared in step (1) and 0.97 g of bismuth nitrate pentahydrate, disperse in 30 mL of glycerin and sonicate for 30 min to obtain a uniform suspension.
[0042] (3) Weigh 0.238 g of potassium bromide in 30 mL of aqueous solution and magnetically stir for 0.5 h to dissolve it to prepare a pota...
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