Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Method for preparing porous spherical stannous oxide nano material

A stannous oxide and nanomaterial technology, applied in the directions of tin oxide and nanotechnology, can solve the problems of increasing the difficulty of stannous oxide nanomaterials, reducing the purity of synthetic products, increasing production costs, etc., and achieving low cost, uniform appearance, The effect of avoiding the formation of impurities

Inactive Publication Date: 2012-09-12
HENAN POLYTECHNIC UNIV
View PDF2 Cites 13 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, since stannous oxide is a metastable compound, it is easily oxidized to other valence tin oxides during the hydrothermal reaction, and divalent tin ions are prone to hydrolysis reactions in aqueous solution, so the oxidation obtained by hydrothermal synthesis Stannous products often contain more impurities, which reduces the purity of the synthetic product
In order to improve the phase purity of stannous oxide nanomaterials, reducing reagents are often added during the synthesis process, which not only increases the production cost, but also complicates the entire synthesis process, increasing the difficulty in the controllable preparation of stannous oxide nanomaterials.

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 porous spherical stannous oxide nano material
  • Method for preparing porous spherical stannous oxide nano material
  • Method for preparing porous spherical stannous oxide nano material

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0022] Accurately weigh 1.128g of stannous oxide dihydrate (SnCl 2 2H 2 O) add in the clean beaker that fills 20mL dehydrated alcohol, be placed on the magnetic stirrer and stir, until the stannous oxide dihydrate crystal dissolves completely. Then accurately weigh 0.6g of sodium hydroxide and add it to a clean beaker filled with 20mL of absolute ethanol, and stir until the sodium hydroxide is completely dissolved. Then, slowly drop the dehydrated ethanol solution dissolved with sodium hydroxide into the dehydrated ethanol solution of stannous oxide, stir while dropping, and continue stirring for 10 min after the dropwise addition to obtain the stannous oxide precursor; The molar concentration of stannous chloride dihydrate in the medium is 0.125mol / L, and the molar ratio of stannous chloride dihydrate to sodium hydroxide is 1:3. The obtained stannous oxide precursor solution was charged into a polytetrafluoroethylene-lined autoclave with a volume of 50 mL. React for 6 hour...

example 2

[0024] Accurately weigh 1.128g of stannous oxide dihydrate and add it to a clean beaker filled with 20mL of absolute ethanol, place it on a magnetic stirrer and stir slowly until the crystals of stannous oxide dihydrate are completely dissolved. Then accurately weigh 0.5 g of solid sodium hydroxide and add it to a clean beaker filled with 20 mL of absolute ethanol, and stir until the sodium hydroxide is completely dissolved. Then, slowly drop the dehydrated ethanol solution that is dissolved with sodium hydroxide into the dehydrated ethanol solution of stannous oxide, stir while dropping, and then stir for 10 min after the dropwise addition to obtain the stannous oxide precursor; The molar concentration of stannous chloride dihydrate in the medium is 0.125mol / L, and the molar ratio of stannous chloride dihydrate to sodium hydroxide is 1:2.5. The configured stannous oxide precursor solution was filled into a polytetrafluoroethylene-lined autoclave with a lining volume of 50 mL....

example 3

[0026] Accurately weigh 1.128g of stannous oxide dihydrate and add it to a clean beaker filled with 20mL of absolute ethanol, place it on a magnetic stirrer and stir slowly until the crystals of stannous oxide dihydrate are completely dissolved. Then accurately weigh 0.7g of sodium hydroxide powder and add it to a clean beaker filled with 20mL of absolute ethanol, and stir until the sodium hydroxide is completely dissolved. Then, slowly drop the dehydrated ethanol solution dissolved with sodium hydroxide into the dehydrated ethanol solution of stannous oxide, stir while dropping, and continue stirring for 10 min after the dropwise addition to obtain the stannous oxide precursor; The molar concentration of stannous chloride dihydrate in the medium is 0.125mol / L, and the molar ratio of stannous chloride dihydrate to sodium hydroxide is 1:3.5. Then the obtained stannous oxide precursor solution was loaded into a polytetrafluoroethylene-lined autoclave with a volume of 50 mL. 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

No PUM Login to View More

Abstract

The invention relates to a method for preparing porous spherical stannous oxide nano material. The method comprises the steps of: slowly dripping a certain amount of prepared sodium hydroxide anhydrous ethanol solution into stannous chloride anhydrous ethanol solution, and stirring while dripping; after dripping, continuously stirring for 10-20min to obtain stannous oxide precursor liquid, wherein in the obtained stannous oxide precursor liquid, the molar concentration of dihydrated stannous chloride is controlled to be 0.125-0.25mol / L and the molar ratio between the dihydrated stannous chloride and sodium hydroxide is controlled to be 1: 2-1: 3.5; putting the prepared stannous oxide precursor liquid into a reaction kettle, wherein the filling degree is 80-90%; sealing the reaction kettle, and carrying out heat preservation on the reaction kettle in an electric constant temperature drying oven for 6-15h at the temperature of 130-170 DEG C; then naturally cooling the reaction kettle to room temperature; and carrying out centrifugation, washing and drying on the product to obtain gray black nano stannous oxide material. The method is simple in operation, mild in condition, easy in control of the condition, low in cost, less in pollution and easy for industrial production; and the prepared porous spherical stannous oxide nano material has the advantages of being even in morphology, high in component purity and the like.

Description

technical field [0001] The invention relates to a method for preparing a nanometer material, in particular to a method for preparing a porous spherical stannous oxide nanometer material. Background technique [0002] After entering the 21st century, energy and environmental issues have become two severe challenges facing mankind. The development and utilization of new clean energy has become an important science and technology related to the sustainable development of human society. As a new type of energy storage battery, lithium-ion battery has been widely used due to its high energy density and environmental friendliness, and it is also considered to be an important energy storage and conversion device in the future. Anode materials are one of the key factors affecting the performance of lithium-ion batteries. At present, commercial lithium-ion batteries are mainly based on carbon anode materials. However, the low theoretical specific capacity of carbon materials (graph...

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): C01G19/02B82Y40/00
Inventor 孙广李彦伟曹建亮王燕付乌有戚凤晓毋乃腾孟哈日巴拉张战营
Owner HENAN POLYTECHNIC UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Eureka Blog
Learn More
PatSnap group products