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Preparation method of high-temperature-resistant SiOC aerogel

An aerogel and high temperature resistant technology is applied in the field of preparation of high temperature resistant SiOC aerogel materials, which can solve the problems of high cost and complicated preparation, and achieve the effect of simple preparation method and avoiding the disappearance of pore structure.

Inactive Publication Date: 2022-03-18
昆山达富久新材料科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

From the current preparation process of SiOC airgel, it can be seen that the preparation of SiOC airgel precursor requires solvent exchange and supercritical drying process, which is costly and complicated to prepare.

Method used

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  • Preparation method of high-temperature-resistant SiOC aerogel
  • Preparation method of high-temperature-resistant SiOC aerogel
  • Preparation method of high-temperature-resistant SiOC aerogel

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0024] Dissolve dimethyldimethoxysilane, methyltrimethoxysilane and cetyltrimethylammonium bromide in deionized water to obtain a transparent solution, in which methyltrimethoxysilane, dimethyldimethoxy The mol ratio of base silane, cetyltrimethylammonium bromide, and deionized water is 1:1:0.06:40; Add 0.5mol / L ammonia water to adjust the pH value of the solution to form a gel at 7.5 in the above solution, and the The gel was aged at 40°C for 24 hours; the aged gel was soaked in deionized water, soaked for 8 hours each time, and soaked 5 times; the soaked gel was directly put into an oven for normal pressure drying, and the drying temperature was 110°C , The drying time was 48h to obtain polyalkylsiloxane airgel. The polyalkylsiloxane airgel was placed in a tube furnace, and Ar was introduced at a rate of 2 mL / min, then heated to 1200 °C for 4 h at a heating rate of 2 °C / min, and SiOC airgel was obtained after natural cooling.

[0025] The prepared polyalkylsiloxane airgel h...

Embodiment 2

[0028] Dissolve dimethyldimethoxysilane, methyltrimethoxysilane and cetyltrimethylammonium bromide in deionized water to obtain a transparent solution, in which methyltrimethoxysilane, dimethyldimethoxy The molar ratio of base silane, cetyltrimethylammonium bromide, and deionized water is 1:1:0.1:30; 2mol / L ammonia water is added to the above solution to adjust the pH value of the solution to 8.0 to form a gel, and the condensed The gel was aged at 90°C for 12 hours; the aged gel was soaked in deionized water for 12 hours each time and soaked 3 times; the soaked gel was directly put into an oven for normal pressure drying at 200°C. The drying time was 24 hours to obtain polyalkylsiloxane airgel. The polyalkylsiloxane airgel was placed in a tube furnace, passed through Ar at a rate of 5 mL / min, heated to 1200 °C for 4 h at a heating rate of 5 °C / min, and then cooled naturally to obtain SiOC airgel.

[0029]The prepared polyalkylsiloxane airgel has a pore size distribution of 3...

Embodiment 3

[0032] Dissolve dimethyldiethoxysilane, ethyltrimethoxysilane and cetyltrimethylammonium bromide in deionized water to obtain a transparent solution, in which ethyltrimethoxysilane, dimethyldiethoxy The molar ratio of base silane, cetyltrimethylammonium bromide, and deionized water is 1:2:0.1:20; 1mol / L ammonia water is added to the above solution to adjust the pH value of the solution to 8.9 to form a gel, and the condensed The gel was aged at 60°C for 4 hours; the aged gel was soaked in deionized water for 8 hours each time and soaked 5 times; the soaked gel was directly put into an oven for normal pressure drying at 150°C. The drying time was 36 hours to obtain polyalkylsiloxane airgel. The polyalkylsiloxane airgel was placed in a tube furnace, passed through Ar at a rate of 4 mL / min, heated to 1200 °C for 8 h at a heating rate of 4 °C / min, and then cooled naturally to obtain SiOC airgel.

[0033] The pore size distribution of the prepared polyalkylsiloxane airgel is 200-8...

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Abstract

The invention belongs to the technical field of preparation of nano porous materials, and relates to a preparation method of high-temperature-resistant SiOC aerogel. The preparation method comprises the following steps: by taking alkyl trialkoxy silane and dialkyl dialkoxy silane as raw materials, preparing a polyalkyl siloxane aerogel precursor with a macroporous structure by combining a sol-gel method and normal-pressure drying; and then carrying out high-temperature cracking on the polyalkyl siloxane aerogel precursor in an Ar atmosphere to prepare the SiOC aerogel. The preparation method is simple, and the prepared SiOC aerogel is good in block shape, low in density and low in heat conductivity, has a typical mesoporous structure and can be applied to the field of high-temperature heat insulation.

Description

technical field [0001] The invention belongs to the field of porous material preparation, and in particular relates to a preparation method of a high-temperature-resistant SiOC airgel material. Background technique [0002] Airgel is a new material with a three-dimensional nanoporous structure, which has a low density (0.003-0.8g cm -3 ), high porosity (80-99.8%), high specific surface area (200-1000m 2 g -1 ), low thermal conductivity (~0.02W·m -1 K -1 ) and other properties, it has very broad prospects in aerospace, chemical industry, energy-saving buildings, military, communications, electronics, metallurgy and other application fields. However, traditional silica aerogels sinter at high temperatures exceeding 650 °C, resulting in the collapse of the nanopore structure and performance degradation, making it difficult to apply to high-temperature applications. [0003] SiOC ceramic materials have attracted attention because of their ability to withstand high temperatu...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C04B35/571C04B35/622C04B35/624C04B38/00
CPCC04B35/5603C04B35/571C04B35/622C04B35/624C04B38/0045C04B2235/6562C04B2235/6567C04B2235/658C04B2235/77C04B2235/9607C04B38/0067C04B38/0054
Inventor 云山魏鹏
Owner 昆山达富久新材料科技有限公司