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

Method for photocatalytic degradation of pesticide residues

A technology for degrading pesticides and pesticide residues, applied in the field of degradation and removal of pesticide residues, can solve the problems of difficulty in realization, limited scope of pesticide residues, optical pollution, etc., and achieves the effects of low cost, high absorption strength and simple production process

Active Publication Date: 2015-04-01
CHINA TOBACCO FUJIAN IND
View PDF6 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the above methods are ubiquitous: (1) The synthesized photocatalytic materials have no absorption in the visible light region, and need to be equipped with ultraviolet lamps, resulting in optical pollution; (2) require special equipment, which is difficult to achieve in the production process; (3) can degrade The limited range of pesticide residues and other issues

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 photocatalytic degradation of pesticide residues
  • Method for photocatalytic degradation of pesticide residues
  • Method for photocatalytic degradation of pesticide residues

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] 0.008mol of urea was dissolved in 40ml of absolute ethanol, 0.004mol of butyl titanate and 0.5ml of glacial acetic acid were mixed in a 100ml small beaker, and then the ethanolic solution of urea was added dropwise under the condition of magnetic stirring. Cool and glacial acetic acid in a beaker, after dripping, magnetically stir for 5 minutes, then transfer the transparent mixture to a 50ml PTFE-lined reaction kettle, put it in a thermostat, and keep it at 150°C. After being kept for 18 hours, it was taken out and cooled to room temperature naturally. The white precipitate was washed out by centrifugation with distilled water and absolute ethanol, and dried in a drying box for use.

[0024] Take 1g of synthesized TiO 2 The powder and zinc acetate were added to 120ml of distilled water (the molar ratio of Zn / Ti was 1:1), placed in a sonicator for 20min, and then slowly added 0.35M sodium hydroxide solution under magnetic stirring. After the reaction was completed , a...

Embodiment 2

[0026] 0.016mol of urea was dissolved in 80ml of absolute ethanol, 0.008mol of butyl titanate and 1.0ml of glacial acetic acid were mixed in a 250ml small beaker, and then the ethanolic solution of urea was added dropwise under the condition of magnetic stirring. Cool and glacial acetic acid in a beaker, after dripping, magnetically stir for 10 minutes, then transfer the transparent mixture to a 100ml PTFE-lined reaction kettle, put it in a thermostat, and keep it at 150°C. After being kept for 24 hours, it was taken out and cooled to room temperature naturally. The white precipitate was washed out by centrifugation with distilled water and absolute ethanol, and dried in a drying box for use.

[0027] Take 3g of synthesized TiO 2 The powder and zinc acetate were added to 120ml of distilled water (the molar ratio of Zn / Ti was 1:1), placed in a sonicator for 20min, and then slowly added 0.35M sodium hydroxide solution under magnetic stirring. After the reaction was completed ,...

Embodiment 3

[0029]0.008mol of urea was dissolved in 40ml of absolute ethanol, 0.004mol of butyl titanate and 0.5ml of glacial acetic acid were mixed in a 100ml small beaker, and then the ethanolic solution of urea was added dropwise to the solution containing butyl butyrate under magnetic stirring. Cool and glacial acetic acid in a beaker, after dripping, magnetically stir for 5 minutes, then transfer the transparent mixture to a 50ml PTFE-lined reaction kettle, put it in a thermostat, and keep it at 150°C. After being kept for 18 hours, it was taken out and cooled to room temperature naturally. The white precipitate was washed out by centrifugation with distilled water and absolute ethanol, and dried in a drying box for use.

[0030] Take 8g of synthesized TiO 2 The powder and zinc acetate were added to 120ml of distilled water (the molar ratio of Zn / Ti was 1:1), placed in a sonicator for 30min, and then slowly added 0.35M sodium hydroxide solution under magnetic stirring. After the rea...

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

PropertyMeasurementUnit
particle sizeaaaaaaaaaa
particle sizeaaaaaaaaaa
Login to View More

Abstract

The invention relates to a method for photocatalytic degradation of pesticide residues. The method is characterized by: taking butyl titanate, zinc acetate, urea and the like as raw materials, conducting co-precipitation to synthesize a ZnO / TiO2 composite nano-material with photocatalytic activity, spraying the composite nano-material on plants, and making use of sunlight irradiation to degrade pesticide residues. The material has high absorption strength and strong photocatalytic activity in both ultraviolet and visible ranges, and has the characteristics of obvious degradation effects, simple operation and low cost when used in pesticide residue degradation, thus having wide application and popularization value.

Description

technical field [0001] The invention relates to a method for degradation and removal of pesticide residues, in particular to a method for photocatalytic degradation of pesticide residues. Background technique [0002] Pesticides play an extremely important role in the production and preservation of agriculture and animal husbandry, as well as in the prevention and control of infectious diseases. However, the residual pesticides will also have a negative impact on human health. If the accumulation in the human body reaches a certain dose, it will also cause acute or chronic poisoning in the human body, and even produce highly carcinogenic, teratogenic, and mutagenic effects. At present, some developed countries have formulated regulations on the maximum limit of pesticide residues, which have become an invisible technical barrier. It can be seen that the control and reduction of pesticide residues are necessary both from the point of view of being responsible to consumers an...

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): B01J23/06A62D3/17A62D101/04A62D101/20
Inventor 张建平吴清辉邓其馨黄朝章徐小青叶仲力周培琛许寒春谢卫苏明亮白雪平赵艺强蔡国华赖炜扬
Owner CHINA TOBACCO FUJIAN IND