Graphite-phase-like carbon nitride-(110) crystal face bismuth vanadate Z-type heterojunction photocatalyst and preparation method and application thereof
A technology of graphite phase carbon nitride and photocatalyst, which is applied in the direction of catalyst activation/preparation, physical/chemical process catalyst, chemical instrument and method, etc., which can solve the problem of poor carrier separation efficiency and photogenerated electron-hole pair recombination rate Advanced problems, to achieve the effect of high degradation rate and good application prospects
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[0029] g-C of the present invention 3 N 4 -(110) crystal plane BiVO 4 The preparation method of Z-type heterojunction photocatalyst comprises the following steps:
[0030] Step 1, the Bi(NO 3 ) 3 ·5H 2 O dissolved in HNO 3 solution, after stirring for a certain period of time, NH 4 VO 3 , stirred for 120 minutes to form a precursor solution, and the precursor solution was hydrothermally reacted at 65-75°C for 14-16 hours to prepare BiVO 4 precipitation, the precipitation was washed with water and alcohol and then dried for later use; Bi(NO 3 ) 3 ·5H 2 O. NH 4 VO 3 The mass ratio is 3.54:1;
[0031] Step 2, CO(NH 2 ) 2 Raise the temperature to 540-560°C at a heating rate of 4.5-5.5°C / min, keep the heat for calcination for 2.8-3.2 hours, then lower the temperature to 350°C to obtain pure phase g-C 3 N 4 Powder, the pure phase g-C 3 N 4 Dissolve the powder in deionized water, add 10mL of a certain concentration of H 2 SO 4 The solution was stirred ultrasonica...
Embodiment 1
[0042] Step 1, 6mmol Bi(NO 3 ) 3 ·5H 2 O dissolved in 35 mL of HNO with a concentration of 1 mol / L 3 solution, after stirring for 30min, add 6mmol NH 4 VO 3 , stirred for 120min to form a precursor solution, and the precursor solution was hydrothermally reacted at 65°C for 14h to prepare BiVO 4 Precipitation, washing the precipitate with alcohol and water for later use;
[0043] Step 2, CO(NH 2 ) 2 Raise the temperature to 540°C at a heating rate of 4.5°C / min, and then cool down to 350°C to obtain a pure phase g-C 3 N 4 Powder, the pure phase g-C 3 N 4 Dissolve the powder in deionized water, add 10 mL of H with a concentration of 0.5 mol / L 2 SO 4 The modified g-C was obtained by ultrasonic stirring for 3 h 3 N 4 Powder, washed with alcohol and water for later use;
[0044] Step 3, 0.05g modified g-C 3 N 4 Dissolve in 40mL deionized water, stir, and sonicate for 3.0 h until uniform, to obtain negatively charged g-C 3 N 4 solution and subjected to 25min ultrav...
Embodiment 2
[0048] Step 1, 6mmol Bi(NO 3 ) 3 ·5H 2 O dissolved in 35 mL of HNO with a concentration of 1 mol / L 3 solution, after stirring for 30min, add 6mmol NH 4 VO 3 , stirred for 120min to form a precursor solution, and the precursor solution was hydrothermally reacted at 70°C for 15h to prepare BiVO 4 Precipitation, washing the precipitate with alcohol and water for later use;
[0049] Step 2, CO(NH 2 ) 2 Raise the temperature to 550°C at a rate of 5°C / min, then cool down to 350°C to obtain a pure phase g-C 3 N 4 Powder, the pure phase g-C 3 N 4 Dissolve the powder in deionized water, add 10mL of 1mol / L H 2 SO 4 The modified g-C was obtained by ultrasonic stirring for 3.5h 3 N 4 Powder, washed with alcohol and water for later use;
[0050] Step 3, 0.1g modified g-C 3 N 4 Dissolve in 40mL deionized water, stir, and sonicate for 3.0h until uniform to obtain negatively charged g-C 3 N 4 solution and subjected to 35min ultraviolet light to obtain negatively charged g-C...
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