Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Method for preparing Bi2S3/BiOCl heterojunction photocatalyst

A photocatalyst and heterojunction technology, applied in physical/chemical process catalysts, chemical instruments and methods, chemical/physical processes, etc., to achieve the effects of easy operation, high purity, and simple operation

Active Publication Date: 2015-04-15
扬州天诗化工科技有限公司
View PDF5 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the synthesis of Bi2S3 / BiOCl heterojunction photocatalysts using triethylenetetramine-type ionic liquids has not been reported in the literature

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
  • Method for preparing Bi2S3/BiOCl heterojunction photocatalyst
  • Method for preparing Bi2S3/BiOCl heterojunction photocatalyst
  • Method for preparing Bi2S3/BiOCl heterojunction photocatalyst

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] (1) Add 50g of triethylenetetramine to 200mL of deionized water and stir to dissolve, weigh diethyl sulfate in a molar ratio of 1:1 and slowly add it dropwise to the aqueous solution of triethylenetetramine, and stir to neutralize it. . An ice bath was set in the reaction process to prevent the solution from volatilizing due to exothermic heat. After stirring for 6 hours, the water in the mixed solution was evaporated using a rotary evaporator to obtain a triethylenetetramine diethyl sulfate ionic liquid.

[0031] (2) Preparation of chlorine-containing imidazole ionic liquid: 40.1799 g of imidazole was weighed into a three-necked flask, and then 48.12 g of hydrochloric acid (37%) was added dropwise to the imidazole solution under stirring, and stirred at 50°C for 3 hours. The imidazolium chloride ionic liquid was isolated by rotary evaporator.

[0032](3) Preparation of BiOCl: 2.4257g of bismuth nitrate was dissolved in 20ml of deionized water, 0.6g of imidazole chlor...

Embodiment 2

[0035] (1) Add 50g of triethylenetetramine to 200mL of deionized water and stir to dissolve, weigh diethyl sulfate in a molar ratio of 1:1 and slowly add it dropwise to the aqueous solution of triethylenetetramine, and stir to neutralize it. . An ice bath was set in the reaction process to prevent the solution from volatilizing due to exothermic heat. After stirring for 6 hours, the water in the mixed solution was evaporated using a rotary evaporator to obtain a triethylenetetramine diethyl sulfate ionic liquid.

[0036] (2) Preparation of chlorine-containing imidazole ionic liquid: weigh 40.1799 g of imidazole in a three-necked flask, add 50 ml of water to dissolve, then take 48.12 g of hydrochloric acid (37%) and add it dropwise to the imidazole solution under stirring, 50 Stir at ℃ for 3h. Impurities such as water were separated by rotary evaporator to obtain imidazolium chloride ionic liquid.

[0037] (3) Preparation of BiOCl: 2.4257g of bismuth nitrate was dissolved in ...

Embodiment 3

[0040] (1) Add 60 g of triethylene tetramine into 200 mL of deionized water and stir to dissolve, weigh diethyl sulfate in a molar ratio of 1:1 and slowly add it dropwise to the aqueous solution of triethylene tetramine, and stir to neutralize it. . An ice bath was set in the reaction process to prevent the solution from volatilizing due to exothermic heat. After stirring for 6 hours, the water in the mixed solution was evaporated using a rotary evaporator to obtain a triethylenetetramine diethyl sulfate ionic liquid.

[0041] (2) Preparation of chlorine-containing imidazole ionic liquid: weigh 40 g of imidazole in a three-necked flask, add 50 ml of water to dissolve, then take 48 g of hydrochloric acid (37%) and add it dropwise to the imidazole solution under stirring, at 50°C Stir for 3h. Impurities such as water were separated by rotary evaporator to obtain imidazolium chloride ionic liquid.

[0042] (3) Preparation of BiOCl: 2.4257g of bismuth nitrate was dissolved in 20...

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 belongs to the preparation field of inorganic material bismuth oxychloride heterojunction photocatalysts and particularly relates to a method for preparing a Bi2S3 / BiOCl heterojunction photocatalyst. The method comprises the following steps of: (1) dropwise adding diethyl sulfate water solution into triethylene tetramine water solution to carry out neutral reaction, stirring, and removing water out of the mixed liquid, so as to prepare triethylene tetramine diethyl sulfate type ionic liquid; (2) dissolving imidazole in water, then dropwise adding hydrochloric acid, and separating out imidazole chloride ion liquid; (3) dissolving bismuth nitrate in deionized water, additionally dissolving imidazole chloride in the deionized water, dropwise adding prepared imidazole chloride water solution into bismuth nitrate water solution, and separating to obtain BiOCl; and (4) preparing triethylene tetramine diethyl sulfate type ionic liquid water solution, and dissolving the BiOCl and thioacetamide into the water solution, so as to prepare Bi2S3 / BiOCl. The photocatalyst disclosed by the invention has good activity, low cost and high purity and can be produced in large scale.

Description

technical field [0001] The invention belongs to the field of preparation of inorganic material bismuth oxychloride (BiOCl) heterojunction photocatalyst, in particular to a kind of combined preparation of Bi by ionic liquid and ultrasonic 2 S 3 / BiOCl heterojunction photocatalyst approach. Background technique [0002] Bismuth oxychloride is a new type of photocatalyst, which has better catalytic activity than commercial P25 under the irradiation of ultraviolet light. However, due to its wide bandgap width (3.5eV), it can only absorb ultraviolet light with a relatively low content in sunlight, which affects its function. [0003] Combining two kinds of semiconductors with matching energy band structures is an effective way to solve the low catalytic activity of single semiconductor catalysts. Its advantages are: (1) It can effectively reduce the recombination of electron-hole pairs; (2) It can increase the operating cycle of carriers; (3) It can increase the amount of sub...

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
Patent Type & Authority Patents(China)
IPC IPC(8): B01J27/10
Inventor 赵荣祥李秀萍
Owner 扬州天诗化工科技有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products