Method for preparing bulk-shaped flexible aerogel through normal-pressure drying
A technology of normal pressure drying and shape flexibility, which is applied in the field of airgel materials and atmospheric pressure drying to prepare large flexible airgel. It can solve the problems of pore size and pore structure breakage, and achieve high porosity, excellent support effect, The effect of good compound processability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0029] (1) Evenly mix deionized water and industrial water glass together, stir evenly, add acetic acid solution, adjust the pH value to 5-8, and form a hydrogel after standing for 1 hour;
[0030] (2) Pour the hydrogel obtained in step (1) into a drainable block mold, pass through the ammonia solution containing 25% ammonia continuously for aging, then rinse with water to obtain the aged wet gel, and place it naturally through the drainable Drain the mold naturally;
[0031] (3) The aged wet gel obtained in step (2) is subjected to primary drying at a temperature of 60-80°C, and the drying time is controlled at 35 minutes. The reduction of the volume of the gel is equal to the volume of the liquid evaporation. At this time, the gel network will not collapse and has toughness, and then continuously pass through the calcium chloride solution with a saturated concentration of the fiber crystal nucleus liquid to make the fiber crystal nucleus enter the gel network;
[0032](4) P...
Embodiment 2
[0036] (1) Evenly mix deionized water and industrial water glass together, stir evenly, add sulfuric acid solution, adjust the pH value to 5-8, and form a hydrogel after standing for 1 hour;
[0037] (2) Pour the hydrogel obtained in step (1) into a drainable block mold, aging through ammonia solution continuously, and then rinse with water to obtain an aged wet gel;
[0038] (3) The aged wet gel obtained in step (2) is subjected to primary drying at a temperature of 60-80°C, and the drying time is controlled at 25 minutes. The reduction of the volume of the gel is equal to the volume of the liquid evaporated. At this time, the gel network will not collapse and has toughness, and then continuously pass through the calcium acetate fiber crystal nucleus liquid to make the fiber crystal nucleus enter the gel network;
[0039] (4) Pass the gel obtained in step (3) through sodium silicate aqueous solution and sodium hydroxide aqueous solution continuously, initiated by sodium hydro...
Embodiment 3
[0043] (1) Evenly mix deionized water and industrial water glass together, stir evenly, add citric acid solution, adjust the pH value to 5-8, and form a hydrogel after standing for 1 hour;
[0044] (2) Pour the hydrogel obtained in step (1) into a drainable block mold, aging through ammonia solution continuously, and then rinse with water to obtain an aged wet gel;
[0045] (3) The aged wet gel obtained in step (2) is subjected to primary drying at a temperature of 60-80°C, and the drying time is controlled at 30 minutes. After primary drying, enough liquid phase is filled in the gel pores, and the gel The reduction of the volume of the gel is equal to the volume of the liquid evaporated. At this time, the gel network will not collapse and has toughness, and then continuously pass through the calcium nitrate fiber crystal nucleus liquid to make the fiber crystal nucleus enter the gel network;
[0046] (4) Pass the gel obtained in step (3) through sodium silicate aqueous soluti...
PUM
Property | Measurement | Unit |
---|---|---|
tensile strength | aaaaa | aaaaa |
tensile strength | aaaaa | aaaaa |
tensile strength | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com