Unlock instant, AI-driven research and patent intelligence for your innovation.

Preparation method and application of BN/MoO3 composite photocatalytic material

A technology of composite photocatalysis and preparation steps, which is applied in the field of composite material preparation and photocatalysis technology application, can solve the problems of insufficient quantum efficiency and limited visible light conversion ability, and achieves the improvement of catalytic activity, which is conducive to effective separation and simple method and process. Effect

Inactive Publication Date: 2015-09-23
JIANGSU UNIV
View PDF2 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] With the continuous development of human society, the increasing energy and environmental problems have attracted widespread attention. Semiconductor photocatalysis technology can use the natural light energy available anywhere in the world or artificial indoor lighting to eliminate Environmental pollution, with the advantages of simple reaction conditions, fast reaction speed, low cost and no secondary pollution, has inspired extensive research by scientists; however, this technology has limited visible light conversion capabilities, insufficient quantum efficiency, and insufficient catalysts. It is widely used, so it is of great significance to develop and research efficient visible light catalytic materials

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method and application of BN/MoO3 composite photocatalytic material
  • Preparation method and application of BN/MoO3 composite photocatalytic material
  • Preparation method and application of BN/MoO3 composite photocatalytic material

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0019] Example 1: BN / MoO 3 The preparation and research of its photocatalytic properties include the following steps:

[0020] (1) Dissolve 0.1g of boric acid and 2.4g of urea in 40ml of distilled water and heat to 65°C until the water evaporates completely.

[0021] (2) Dry the mixture under nitrogen (N 2 ) after calcination at medium and high temperature for 5 hours, uniform BN nanosheets were obtained.

[0022] (3) Put 3 g of ammonium molybdate in the ark, put it into the muffle furnace, and under the condition of nitrogen protection, the temperature is controlled at 500 ° C for 2 h to obtain the monomer MoO 3 .

[0023] (4) Weigh 0.015 g BN and 0.485 g MoO respectively 3 Place in 50 mL of absolute ethanol, ultrasonically disperse for 2 h to form a milky white solution, dry at 100 °C for 8 h, take the dried solid powder and grind it in a mortar for 30 min, and then calcinate at 300 °C for 6 h to obtain BN / MoO 3 .

Embodiment 2

[0024] Example 2: BN / MoO 3 The preparation and research of its photocatalytic properties include the following steps:

[0025] (1) Dissolve 0.1g of boric acid and 2.4g of urea in 40ml of distilled water and heat to 65°C until the water evaporates completely.

[0026] (2) Dry the mixture under nitrogen (N 2 ) after calcination at medium and high temperature for 5 hours, uniform BN nanosheets were obtained.

[0027] (3) Put 3g of ammonium molybdate in the ark, put it into the muffle furnace, and under the condition of nitrogen protection, the temperature is controlled at 500°C for 2h to obtain the monomer MoO 3 .

[0028] (4) Weigh 0.005 g BN and 0.495 g MoO respectively 3 Place in 50 mL of absolute ethanol, ultrasonically disperse for 2 h to form a milky white solution, dry at 100 °C for 8 h, take the dried solid powder and grind it in a mortar for 30 min, and then calcinate at 300 °C for 6 h to obtain BN / MoO 3 .

Embodiment 3

[0029] Example 3: BN / MoO 3 The preparation and research of its photocatalytic properties include the following steps:

[0030] (1) Dissolve 0.1g boric acid and 2.4g boric acid in 40ml distilled water, heat to 65℃ and keep constant temperature until the water evaporates completely.

[0031] (2) Dry the mixture under nitrogen (N 2 ) after calcination at medium and high temperature for 5 hours, uniform BN nanosheets were obtained.

[0032] (3) Put 3 g of ammonium molybdate in the ark, put it into a muffle furnace, and calcine at 500 °C for 2 h under nitrogen protection to obtain monomer MoO 3 .

[0033] (4) Weigh 0.025 g BN and 0.475 g MoO respectively 3 Place in 50 mL of absolute ethanol, ultrasonically disperse for 2 h to form a milky white solution, dry at 100 °C for 8 h, take the dried solid powder and grind it in a mortar for 30 min, and then calcinate at 300 °C for 6 h to obtain BN / MoO 3 .

[0034] figure 1 For the prepared BN / MoO of examples 1, 2, and 3 3 Pho...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention relates to a preparation method of a composite photocatalytic material, and particularly relates to a preparation method and an application of a BN / MoO3 composite photocatalytic material. The composite photocatalyst is formed by compositing BN and MoO3 in a mass ratio of 1: 99 to 7: 93. The preparation method comprises the following steps: dissolving boric acid and urea, then heating the boric acid and urea at a constant temperature until water is completely evaporated, calcining an obtained dry mixture in nitrogen (N2) at a high temperature to obtain uniform like-graphene BN, then preparing a monomer MoO3 by a calcining method by adopting ammonium molybdate as a precursor, and mixing and calcining the prepared BN nano-sheets and MoO3, thus obtaining BN / MoO3 composite photocatalysts in different ratios. The BN nano-sheets are used as a supporting material, and the BN / MoO3 composite photocatalyst is synthesized by the calcining method. The preparation method is simple, and pollution to the environment is avoided; moreover, the absorptive spectra range can be enlarged by the composite photocatalyst, the photocatalytic performance can be improved, and the application prospect on the aspect of degrading organic pollutants under visible light is good.

Description

technical field [0001] The present invention relates to the preparation of composite photocatalytic materials, especially a kind of BN / MoO 3 The invention relates to a preparation method and application of a composite photocatalytic material, which belong to the field of composite material preparation and photocatalytic technology application. Background technique [0002] With the continuous development of human society, the increasing energy and environmental problems have attracted widespread attention. Semiconductor photocatalysis technology can use the natural light energy available anywhere in the world or artificial indoor lighting to eliminate Environmental pollution, with the advantages of simple reaction conditions, fast reaction speed, low cost and no secondary pollution, has inspired extensive research by scientists; however, this technology has limited visible light conversion capabilities, insufficient quantum efficiency, and insufficient catalysts. Therefore,...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): B01J27/24B01J35/10B82Y30/00A62D3/17A62D101/28
Inventor 许晖李华明谌佳佳颜佳陈志刚夏杰祥宋艳华
Owner JIANGSU UNIV