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A kind of mpg-c3n4 photocatalyst with higher photocatalytic activity and its preparation method and application

A technology of mpg-c3n4 and photocatalytic activity, which is applied in the direction of physical/chemical process catalysts, chemical instruments and methods, chemical/physical processes, etc., to achieve the effects of mild reaction conditions, enhanced photocatalytic activity, and increased specific surface area

Active Publication Date: 2019-01-04
SHAANXI UNIV OF SCI & TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] Currently, mpg-C is prepared by acid / alkali modification + microwave hydrothermal treatment / ultrasonic heat treatment 3 N 4 Photocatalyst work has yet to be reported

Method used

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  • A kind of mpg-c3n4 photocatalyst with higher photocatalytic activity and its preparation method and application
  • A kind of mpg-c3n4 photocatalyst with higher photocatalytic activity and its preparation method and application
  • A kind of mpg-c3n4 photocatalyst with higher photocatalytic activity and its preparation method and application

Examples

Experimental program
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Effect test

Embodiment 1

[0032] Step 1: with 40g melamine and 150mL silica sol (containing the SiO that massfraction is 40%) 2 , the particle size is 12nm) and mix evenly, heat and stir at 90°C until the solvent is evaporated to dryness to obtain a white solid, grind the white solid and put it into a crucible, and heat it up to 2.5°C / min in a muffle furnace. Calcined at 550°C for 4 hours to obtain a yellow powder, and then 4mol / L NH 4 HF 2 The aqueous solution corrodes the yellow powder to remove SiO in the yellow powder 2 , finally washed and dried at 80°C for 10 h to obtain mpg-C 3 N 4 Powder;

[0033] Step 2: Convert 1g mpg-C 3 N 4 Add the powder into 1mol / L, 40mL HCL solution and stir evenly to obtain an acidic modified precursor;

[0034] Step 3: Add the acidic modified precursor liquid into the microwave hydrothermal reactor, place the microwave hydrothermal reactor in the microwave-assisted hydrothermal synthesizer, set the pressure at 1.2MPa, and raise the temperature from room temperat...

Embodiment 2

[0036] Step 1: with 40g melamine and 150mL silica sol (containing the SiO that massfraction is 40%) 2 , the particle size is 12nm) and mix evenly, heat and stir at 90°C until the solvent is evaporated to dryness to obtain a white solid, grind the white solid and put it into a crucible, and heat it up to 2.5°C / min in a muffle furnace. Calcined at 550°C for 4 hours to obtain a yellow powder, and then 4mol / L NH 4 HF 2 The aqueous solution corrodes the yellow powder to remove SiO in the yellow powder 2 , finally washed and dried at 80°C for 10 h to obtain mpg-C 3 N 4 Powder;

[0037] Step 2: Convert 1g mpg-C 3 N 4 Add the powder to 0.5mol / L, 40mL of HNO 3 Stir evenly in the solution to obtain an acidic modified precursor solution;

[0038] Step 3: Add the acidic modified precursor liquid into the microwave hydrothermal reactor, place the microwave hydrothermal reactor in the microwave-assisted hydrothermal synthesizer, set the pressure at 1.2MPa, and raise the temperature ...

Embodiment 3

[0040] Step 1: with 40g melamine and 150mL silica sol (containing the SiO that massfraction is 40%) 2 , the particle size is 12nm) and mix evenly, heat and stir at 90°C until the solvent is evaporated to dryness to obtain a white solid, grind the white solid and put it into a crucible, and heat it up to 2.5°C / min in a muffle furnace. Calcined at 550°C for 4 hours to obtain a yellow powder, and then 4mol / L NH 4 HF 2 The aqueous solution corrodes the yellow powder to remove SiO in the yellow powder 2 , finally washed and dried at 80°C for 10 h to obtain mpg-C 3 N 4 Powder;

[0041] Step 2: Convert 1g mpg-C 3 N 4 Add the powder into a 0.2mol / L, 50mL NaOH solution and stir evenly to obtain an alkaline modified precursor;

[0042] Step 3: Stir the alkaline modified precursor solution for 30 minutes until uniform, then ultrasonically disperse it for 10 minutes, and then heat-preserve it at 100°C for 20 hours. mpg-C 3 N 4 catalyst of light.

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Abstract

The invention discloses a mpg-C3N4 photocatalyst with high photocatalytic activity and its preparation method and application. First, melamine and silica sol are mixed and calcined at high temperature to obtain yellow powder. NH4HF2 aqueous solution is used to remove SiO2 in the yellow powder. The mpg-C3N4 powder is prepared; then the mpg-C3N4 powder is modified using the microwave hydrothermal treatment method in an acid solution or the ultrasonic modification method in an alkali solution to enhance the photocatalytic activity of the mpg-C3N4 powder. The preparation method of the modified mpg-C3N4 photocatalyst with higher photocatalytic activity provided by the invention has a simple process, easy operation, short reaction time, and mild reaction conditions. The synthesized modified mpg-C3N4 photocatalyst With high photocatalytic activity, it is a feasible method to enhance the photocatalytic efficiency of mpg‑C3N4 and has good application prospects.

Description

technical field [0001] The invention belongs to the field of functional materials, in particular to a mpg-C with relatively high photocatalytic activity 3 N 4 Photocatalyst and its preparation method and application. Background technique [0002] With the growth of population and the accelerated pace of industrialization, the problem of pollution has intensified, especially the problem of water pollution, which has gradually threatened the survival of human society. As a sustainable renewable energy source, solar energy is the earliest clean energy source. Photocatalytic technology can not only effectively use sunlight to control environmental pollution, but also convert its energy into other usable energy sources. [0003] mpg-C 3 N 4 (Graphite-like carbon nitride) has a layered structure similar to graphite, and the layers are stacked together through van der Waals interaction. Its structural unit (C 6 N 7 ) are connected to each other to form an infinitely extende...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J27/24C02F1/30
CPCC02F1/30B01J27/24C02F2305/10B01J35/39Y02W10/37
Inventor 谈国强刘婷任慧君折辽娜夏傲
Owner SHAANXI UNIV OF SCI & TECH