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Hybrid aerogels with an ultralight nonparticulate reticulated structure and a method of producing the same

A network structure, aerogel technology, applied in aerogel preparation, chemical instruments and methods, inorganic chemistry, etc., can solve problems such as increasing total thermal conductivity and increasing aerogel density

Inactive Publication Date: 2019-10-18
萨珊雷扎伊 +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although resulting in a significant improvement in the mechanical properties of silica aerogels, this approach increases the density of the aerogels [17,20,23,25,26], thereby increasing their overall thermal conductivity

Method used

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  • Hybrid aerogels with an ultralight nonparticulate reticulated structure and a method of producing the same
  • Hybrid aerogels with an ultralight nonparticulate reticulated structure and a method of producing the same
  • Hybrid aerogels with an ultralight nonparticulate reticulated structure and a method of producing the same

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0091] Example 1: PE-based silica airgel

[0092] This example describes: (i) the synthesis method of a PE-based non-particulate silica airgel precursor with high molecular weight, (ii) the airgel fabrication process, and (iii) the resulting hybrid aircondensation properties of glue. All chemicals were purchased from Sigma-Aldrich.

[0093] An amount of 5.97 g of di-tert-butyl peroxide was added to 60 g of liquid vinyltrimethoxysilane, followed by vigorous stirring at 163° C. for 2 hours under nitrogen. The degree of polymerization under these processing conditions was 130. However, by varying the thermal initiator or processing conditions, different molecular weights can be obtained. for CO 2 To obtain the desired final airgel density after supercritical extraction, a specific amount of polymer precursor and catalyst must be added to a specific amount of solvent (e.g. ethanol). For example, 4 g of the polymer precursor is added to 20 ml of ethanol, and then 5.4 g of ammo...

Embodiment 2

[0094] Example 2: The cost of thermal initiator species using PE-based silica aerogels is significant

[0095] reduce

[0096] This example describes how the synthesis cost of the PE-based silica airgel shown in Example 1 can be significantly reduced by using different thermal initiators with negligible sacrifices for mechanical and thermal properties .

[0097] We added 5.97 g of dicumyl peroxide (instead of di-tert-butyl peroxide) as a thermal initiator to 60 g of vinyltrimethoxysilane, followed by vigorous stirring at 123° C. for 1 hour under nitrogen. The degree of polymerization under this processing condition was 67. for CO 2 To obtain the desired final airgel density after supercritical extraction, a certain amount of polymer precursor and catalyst must be added to a specific solvent such as ethanol. For example, 1.6 g of this polymer precursor was dissolved in 20 ml of ethanol, and then 1.9 g of ammonia were added to the solution at 40°C. After the drying stage, the...

Embodiment 3

[0098] Example 3: Polyether-based silica airgel

[0099] This example describes the synthesis of polyether-based silica airgel precursors and the corresponding hybrid airgel fabrication process.

[0100] To prepare polyether-based silica airgel precursors, (3-glycidyloxypropyl)trimethoxysilane (GPTMS), diethyl etherate boron trifluoride and diethyl ether were used as monomers, respectively, catalysts and solvents. The polymer structure of GPTMS was synthesized by cationic ring-opening polymerization. An amount of 60 g of GPTMS was dissolved in 40 ml of ether and cooled to 0° C. with an ice bath under nitrogen. Then, 0.4 ml of the catalyst was added dropwise to the solution, followed by vigorous stirring for 2 hours. The final mixture was placed under vacuum to remove ether. According to GPC data, the degree of polymerization under this condition was 29. 2 g of the polymer precursor were added to 20 ml of ethanol, then 1.6 g of ammonia were added to the above mixture at 40...

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Abstract

The present invention relates to hybrid aerogels with an ultralight nonparticulate reticulated structure and a method of producing the same. First, the organic and inorganic components of the structure are distributed on a molecular level in such a way that all of the organic components of the precursor are chemically bonded to each other and to the inorganic component. Second, in the new hybrid aerogels, the pores are separated by solid walls like reticulated open-cell foams without the particulate solid parts and also the present invention is a process for preparing a hybrid aerogel withoutaging step having a nonparticulate-reticulated structure comprises of a polymeric precursor that is crosslinked by a linkage without forming particulate structure.

Description

technical field [0001] The present invention relates to hybrid aerogels with a 3-D network structure, and also to a new generation of precursors with polymeric structures. Background technique [0002] Aerogels, such as silica aerogels, are a type of porous material with a 3-D network of aggregated particles. These aerogels are obtained by using, for example, supercritical CO 2 Extractive drying methods such as drying are derived from wet gels with solvents. There are three main classes of aerogels: inorganic, organic, and hybrid. Inorganic aerogels are usually composed of metal oxides such as silica or alumina. Organic aerogels, on the other hand, have a cross-linked polymer framework. Hybrid aerogels include organic and inorganic components. [0003] Silica aerogels are the best known of inorganic aerogels and hybrid aerogels containing inorganic components. This is due to its simple manufacturing process. In 1930, Kistler used sodium silicate [4,5] as a precursor t...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J13/00
CPCB01J13/0091C08J2343/04C01B33/1585C01B33/155C08J9/28C08J2201/05C08J2205/026C08J2300/108C08J2205/05C08F130/08C08J3/075C08L83/10C08G77/20C08K3/22C08J3/24C08K2003/2227C08K2003/2244C08J2383/10C08L2312/08C08L2203/16C08K2003/2241
Inventor 萨珊·雷扎伊舒·B·帕克
Owner 萨珊雷扎伊