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Preparation method for tin-based oxide nanorods

A technology of oxides and nanorods, applied in the field of materials, can solve the problems of expensive surfactants, complicated preparation process, uneven mixing, etc., and achieve the effects of reduced preparation cost, low post-treatment temperature and short time

Active Publication Date: 2013-12-04
GANZHOU ZHANHAI IND & TRADING
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Congkang Xu et al. (Large-scale synthesis of rutile SnO 2 nanorods, Solid State Commun. 2003, 125, 301) and Yingkai Liu et al [Improved molten salt synthesis (MSS) for SnO 2 nanorods and nanotwins, Mater. Chem. Physics 2008, 112, 381] The preparation methods related to molten salt all use expensive surfactants without exception, and the preparation process is complicated or there are special requirements for precursors and salts The mixing is uneven, the calcination temperature must be above the melting point of the salt, and the energy consumption is large
At present, there is no simple, fast, low-cost, low-energy method for preparing tin-based nanorods

Method used

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  • Preparation method for tin-based oxide nanorods
  • Preparation method for tin-based oxide nanorods
  • Preparation method for tin-based oxide nanorods

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038] Weigh 0.0929 g of Y 2 o 3 , placed in a beaker with an appropriate amount of 1:1 nitric acid solution, heated to dissolve, and then weighed 2.8042 grams of SnCl 4 ·5H 2 O, 0.211 gram of ethylene glycol, 0.1601 gram of ammonium nitrate and 0.3728 gram of KCl are added therein and heated to dissolve. When the solution is concentrated to a viscous state, it is put into a microwave oven and heated until a self-propagating combustion reaction occurs, and the combustion product is in Incubate at 400°C for 4 hours in the air, wash and dry to obtain Sn0.8 Y 0.2 o 2-δ Nano stave.

Embodiment 2

[0040] Weigh 0.3145 grams of Y (NO 3 ) 3 ·6H 2 O, 3.15477 g SnCl 4 ·5H 2 0, 0.0931 gram of ethylene glycol, 0.1601 gram of ammonium nitrate and 0.3728 gram of KCl are placed in a beaker with an appropriate volume of deionized water, heated while stirring to dissolve the reactant completely, continue heating, and when the solution is concentrated to After it is close to the viscous state, put it into a microwave oven and heat it until the self-propagating combustion reaction occurs. The combustion product is kept at 400°C for 4 hours in the air, washed, and dried to obtain Sn 0.8 Y 0.2 o 2-δ Nano stave.

Embodiment 3

[0042] Weigh 3.5053 grams of SnCl respectively 4 ·5H 2 O, 0.124 gram of ethylene glycol, 0.6404 gram of ammonium nitrate and 0.3728 gram of KCl are placed in a beaker with an appropriate volume of deionized water, heated and stirred to dissolve the reactant completely, continue heating, and when the solution is concentrated to nearly After the viscous state, put it into a microwave oven and heat until the self-propagating combustion reaction occurs. The combustion product is kept at 400°C in the air for 4 hours, washed and dried to obtain tin dioxide nanorods.

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Abstract

A preparation method for tin-based oxide nanorods includes the following steps of weighing one of rare earth nitrate, rare earth oxide, rare earth ocyhydrate or rare earth carbonate according to stoichiometric ratio of metallic elements in Sn1-xREx02-delta, weighing one of rare earth nitrate, rare earth oxide, rare earth ocyhydrate or rare earth carbonate to prepare nitric acid rare earth solution, then weighing SnC14.5H2O to be dissolved to the prepared nitric acid rare earth solution and obtaining mixed solution, then respectively weighing an appropriate amount of organic fuels, a combustion improver of ammonium nitrate and soluble chloride to be dissolved to the mixed solution; after heating the mixed solution to concentrate the solution to a state of being approximately sticky, heating in microwave mode, and initiating self-spreading burning; roasting the self-spreading burning product in the air, after cooling, washing in ultrasonic mode, filtering, removing constitution ions of the chloride, and drying at 80 DEG C. The preparation method shortens technological process, lowers preparation cost, and is simple in synthesis equipment, low in post-treatment temperature and short in time, and easy for achieving industrialized preparation.

Description

technical field [0001] The invention belongs to the technical field of materials and relates to a preparation method of nanometer materials. Background technique [0002] One-dimensional nanomaterials such as nanorods, nanotubes, and nanowires have become a research hotspot and one of the most important research fronts in the fields of physics, chemistry, and materials in recent years. Due to the reduction of material scale and dimension, it presents novel and unique electrical, magnetic, optical, thermal and other physical and chemical properties different from traditional materials, so it has a wide range of applications in optoelectronic materials, sensors, catalysts, composite materials, etc. prospect. Tin dioxide is a typical n-type semiconductor material, its E g =3.6eV (300K), it can be used in the fields of conductive materials, thin film resistors and optoelectronic devices. However, pure SnO 2 It is difficult to meet the requirements of optical, electrical and ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01G19/02B82Y30/00B82Y40/00
Inventor 陈伟凡刘铭李婷林玉翠
Owner GANZHOU ZHANHAI IND & TRADING
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