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

Process for preparing sodium antimony sulfide microwires and array thereof

A technology of antimony sulfide nano and micron wires, which is applied in chemical instruments and methods, inorganic chemistry, antimony compounds, etc., and can solve the problems of inconvenient synthesis

Inactive Publication Date: 2006-12-27
CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI
View PDF0 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, during the hydrothermal preparation of the above-mentioned antimony sulfide one-dimensional materials, a thermal decomposition precursor needs to be synthesized in advance, which brings inconvenience to the synthesis.
In addition, there is no report on the growth of antimony sulfide nano-micron wire arrays on substrates by hydrothermal method.

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
  • Process for preparing sodium antimony sulfide microwires and array thereof
  • Process for preparing sodium antimony sulfide microwires and array thereof
  • Process for preparing sodium antimony sulfide microwires and array thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0014] Weigh 200mg potassium antimony tartrate (0.6mmol), 200mg trisodium citrate dihydrate (0.68mmol), 50mg thiomalic acid (0.33mmol), dissolve them in 50ml secondary water successively under stirring, and put this mixed solution into In the polytetrafluoroethylene lining of a stainless steel autoclave with a capacity of 50ml, the lining containing the solution is sealed in a stainless steel autoclave, and heated at 200° C. for 24 hours to obtain antimony sulfide nano-micron wires.

Embodiment 2

[0016] Weigh 200mg of potassium antimony tartrate (0.6mmol), 200mg of trisodium citrate dihydrate (0.68mmol), and 9mg of thiomalic acid (0.06mmol), dissolve them in 50ml of secondary water successively under stirring, and put this mixed solution into In the polytetrafluoroethylene lining of a stainless steel autoclave with a capacity of 50ml, the lining containing the solution is sealed in a stainless steel autoclave, and heated at 140° C. for 24 hours to obtain antimony sulfide nano-micron wires.

Embodiment 3

[0018] Weigh 200mg of potassium antimony tartrate (0.6mmol), 200mg of trisodium citrate dihydrate (0.68mmol), and 540mg of thiomalic acid (3.6mmol), dissolve them in 50ml of secondary water successively under stirring, and put this mixed solution into In the polytetrafluoroethylene lining of a stainless steel autoclave with a capacity of 50ml, the lining containing the solution is sealed in a stainless steel autoclave, and heated at 240° C. for 3 hours to obtain antimony sulfide nano-micron wires.

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 discloses a preparing method of antimony sulphate nanometer-micrometer line and array, which comprises the following steps: weighing potassium antimony tartrate, dihydrate citric acid trisodium, thiomalic acid at 10:11:1-60 molecular proportion; stirring these raw materials in the secondary distilled water sequently; loading the composition in the polytetrafluoroethylene liner of stainless steel high-pressure autoclave to seal; reacting at 140-240 deg.c for 3-24 h to obtain the product. The beam-shaped antimony sulphate nanometer-micrometer line and array can grow on the surface of substrate with ITO glass, tungsten filament or SiN micrometer fiber in the polytetrafluoroethylene liner simultaneously, which possesses excellent single-crystal structure.

Description

technical field [0001] The invention relates to a preparation method of antimony sulfide nano-micro wire and array thereof. Background technique [0002] One-dimensional nano-micron materials have been extensively studied due to their unique optical, electrical, and thermal properties, and show potential applications in nanodevices. There are many synthetic methods for one-dimensional nano-micron materials, among which hydrothermal method and solvothermal method are very effective synthetic methods. The hydrothermal method and the solvothermal method generally react in an autoclave. The difference between the hydrothermal method and the solvothermal method is only that the former uses water as a solvent, while the latter uses a non-aqueous organic compound as a reaction medium. The reaction solution needs to be contained in the polytetrafluoroethylene lining of the stainless steel autoclave, and then the stainless steel autoclave is sealed and placed in an oven at a tempera...

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 Applications(China)
IPC IPC(8): C01G30/00
Inventor 董绍俊包海峰黄利坚
Owner CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI
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