Preparation method of magnetic superhydrophobic ethyl cellulose sponge for oil-water separation
A technology of cellulose sponge and ethyl cellulose, applied in water/sewage treatment, chemical instruments and methods, water/sludge/sewage treatment, etc., can solve problems such as secondary pollution, refractory degradation, and environmental pollution, and achieve Effect of high oil-water separation efficiency, high oil-water separation ability, and strong oil-water separation ability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0028] A preparation method for a magnetic superhydrophobic ethyl cellulose sponge for oil-water separation, comprising the following process steps:
[0029] (1) Preparation of silane hydrophobized modified ethyl cellulose:
[0030] Add 1.3 mL of hexadecyltrimethoxysilane (HDTMS) and 4 mL of deionized water to 30 mL of absolute ethanol, stir magnetically for 30 min, then add 1 mL of glacial acetic acid (HAc), and continue stirring for 30 min. Put the reaction device into a 60°C oil bath and connect a spherical condenser, and perform hydrolysis for 60 minutes to obtain HDTMS hydrolyzate. Add 1.2g of ethyl cellulose to the prepared HDTMS hydrolyzate, stir and react at 60°C for 4 hours, take out the flask, wash repeatedly with deionized water to remove solvent and residual glacial acetic acid, and dry to obtain silanized modified Ethyl cellulose.
[0031] (2) Preparation of magnetic Fe3O4 nanoparticles coated with oleic acid:
[0032] Under the protection of high-purity argon,...
Embodiment 2
[0040] A preparation method for a magnetic superhydrophobic ethyl cellulose sponge for oil-water separation, comprising the following process steps:
[0041] (1) Preparation of silane hydrophobized modified ethyl cellulose:
[0042] Add 2.0 mL of hexadecyltrimethoxysilane (HDTMS) and 6 mL of deionized water to 30 mL of absolute ethanol, stir magnetically for 30 min, then add 1 mL of glacial acetic acid (HAc), and continue stirring for 30 min. Put the reaction device into an oil bath at 65°C and connect it with a spherical condenser, and perform a hydrolysis reaction for 60 minutes to obtain HDTMS hydrolyzate. Add 1.8g of ethyl cellulose to the prepared HDTMS hydrolyzate, stir and react at 60°C for 6 hours, take out the flask, wash repeatedly with deionized water to remove solvent and residual glacial acetic acid, and dry to obtain silanized modified Ethyl cellulose.
[0043] (2) Preparation of magnetic Fe3O4 nanoparticles coated with oleic acid:
[0044] Under the protectio...
Embodiment 3
[0052] A preparation method for a magnetic superhydrophobic ethyl cellulose sponge for oil-water separation, comprising the following process steps:
[0053] (1) Preparation of silane hydrophobized modified ethyl cellulose:
[0054] Add 2.2 mL of hexadecyltrimethoxysilane (HDTMS) and 4.5 mL of deionized water to 40 mL of absolute ethanol, stir magnetically for 30 min, then add 2.5 mL of glacial acetic acid (HAc), and continue stirring for 30 min. Put the reaction device into an oil bath at 65°C and connect it with a spherical condenser, and perform a hydrolysis reaction for 60 minutes to obtain HDTMS hydrolyzate. Add 1.2g of ethyl cellulose to the prepared HDTMS hydrolyzate, stir and react at 60°C for 4 hours, take out the flask, wash repeatedly with deionized water to remove solvent and residual glacial acetic acid, and dry to obtain silanized modified Ethyl cellulose.
[0055] (2) Preparation of magnetic Fe3O4 nanoparticles coated with oleic acid:
[0056] Under the prote...
PUM
Property | Measurement | Unit |
---|---|---|
Density | aaaaa | aaaaa |
Separation efficiency | 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