Preparation method of mesoporous silicon nano particles

A technology of nano-particles and mesoporous silicon, applied in chemical instruments and methods, silicon compounds, inorganic chemistry, etc., can solve the problems of cumbersome preparation process and low yield rate, and achieve the effects of easy promotion, simple operation, and environmentally friendly process

Inactive Publication Date: 2018-04-17
程桂平
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] In the prior art, the preparation method of mesoporous silicon nanoparticles is cumbersome and the yield is low

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Example Embodiment

[0011] Example 1

[0012] A preparation method of mesoporous silicon nanoparticles, the steps are as follows:

[0013] Step 1: add 2g cetyltrimethylammonium bromide in 720mL water, add 7.1mL of 2mol / L sodium hydroxide solution under stirring and heat to 80°C;

[0014] Step 2: Add 15.0 mL of ethyl orthosilicate dropwise, and continue to stir for 2 hours;

[0015] Step 3: Add 5.0 mL of tetrabutyl orthosilicate dropwise, and ultrasonically disperse for 1 hour;

[0016] Step 4: Cool to room temperature, filter the white precipitate, and wash with 2L deionized water for 5 times;

[0017] Step 5: Wash 5 times with 1L, 6mol / L ethanol, and dry at 60°C;

[0018] Step 6: The white powder is calcined at 550°C for 3 hours to remove the surfactant, and the mesoporous silicon nanoparticles can be obtained.

Example Embodiment

[0019] Example 2

[0020] A preparation method of mesoporous silicon nanoparticles, the steps are as follows:

[0021] Step 1: add 2g cetyl trimethyl ammonium bromide in 720mL water, add 7.2mL of 2mol / L sodium hydroxide solution under stirring and heat to 80°C;

[0022] Step 2: Add 15.0 mL of ethyl orthosilicate dropwise, and continue to stir for 2 hours;

[0023] Step 3: Add 5.0 mL of tetrabutyl orthosilicate dropwise, and ultrasonically disperse for 1 hour;

[0024] Step 4: Cool to room temperature, filter the white precipitate, and wash with 2L deionized water for 5 times;

[0025] Step 5: Wash 5 times with 1L, 6mol / L ethanol, and dry at 60°C;

[0026] Step 6: The white powder is calcined at 550°C for 3 hours to remove the surfactant, and the mesoporous silicon nanoparticles can be obtained.

Example Embodiment

[0027] Example 3

[0028] A preparation method of mesoporous silicon nanoparticles, the steps are as follows:

[0029] Step 1: add 2g cetyltrimethylammonium bromide in 720mL water, add 7.3mL of 2mol / L sodium hydroxide solution under stirring and heat to 80°C;

[0030] Step 2: Add 15.0 mL of ethyl orthosilicate dropwise, and continue to stir for 2 hours;

[0031] Step 3: Add 5.0 mL of tetrabutyl orthosilicate dropwise, and ultrasonically disperse for 1 hour;

[0032] Step 4: Cool to room temperature, filter the white precipitate, and wash with 2L deionized water for 5 times;

[0033] Step 5: Wash 5 times with 1L, 6mol / L ethanol, and dry at 60°C;

[0034] Step 6: The white powder is calcined at 550°C for 3 hours to remove the surfactant, and the mesoporous silicon nanoparticles can be obtained.

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Abstract

The invention relates to a preparation method of mesoporous silicon nano particles. The preparation method includes the steps of firstly, adding 2g of cetyl trimethyl ammonium bromide into 720mL of water, adding 7.0mL of 2mol/L sodium hydroxide solution while stirring, and heating to 80 DEG C; secondly, dropwise adding 15.0mL of tetraethyl orthosilicate, and continuing stirring for 2 hours; thirdly, dropwise adding 5.0mL of tetrabutyl orthosilicate, and performing ultrasonic dispersing for an hour; fourthly, cooling to room temperature, filtering white precipitates, and washing with 2L of deionized water five times; fifthly, washing with 1L of 6mol/L ethanol five times, and drying at 60 DEG C; sixthly, calcining white powder under 550 DEG C for 3 hours to remove surfactants to obtain the mesoporous silicon nano particles.

Description

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Claims

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Application Information

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Owner 程桂平
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