Preparation method of magnetic chitosan and method for adsorbing tannic acid in water
A technology of chitosan and tannic acid, applied in the direction of adsorption water/sewage treatment, chemical instruments and methods, water/sewage treatment, etc., can solve the problem of difficult separation of adsorbent and treated water, and achieve good economic and environmental benefits , good application prospects and low cost
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
preparation example Construction
[0025] The preparation method of magnetic chitosan of the present invention specifically implements according to the following steps:
[0026] Step 1, sodium acetate and FeCl 3 ·6H 2 O dissolved in ethylene glycol (Fe 3+ The molar ratio with sodium acetate is 1:9, Fe 3+ The concentration is 0.1mol / L), magnetically stirred for 30-40min, then transferred to a hydrothermal reaction kettle for 10-15h at 180°C-200°C, cooled to room temperature after the reaction, and deionized water Fe 3 o 4 The nanoparticles are fully washed, then washed three times with absolute ethanol, and vacuum-dried at 45°C to 55°C for 12 hours to obtain magnetic ferric iron tetroxide;
[0027] Step 2, ultrasonically disperse the magnetic iron ferric oxide obtained in step 1, then add it to a mixed solution composed of absolute ethanol and deionized water in a volume ratio of 4:1, then add ammonia water to adjust the pH to 11 2 Under protection, mechanically stir and heat to 50-55°C, then add tetraethy...
Embodiment 1
[0035] Magnetic chitosan (Fe 3 o 4 / SiO 2 / Cs) preparation
[0036] Step 1, weigh 2.7g FeCl respectively 3 ·6H 2 O and 7.2g of sodium acetate were mixed and dissolved in 100ml of ethylene glycol, magnetically stirred for 30min to form a homogeneous yellow solution, then transferred to a hydrothermal reaction kettle, reacted at 190°C for 12h, cooled to room temperature, discarded the supernatant, and removed the bottom black The precipitate was fully rinsed with deionized water, then rinsed three times with absolute ethanol, and dried in a vacuum oven at 50°C for 12 hours to obtain magnetic ferric iron tetroxide;
[0037] Step 2: Add 1.0 g of ultrasonically dispersed magnetic ferric iron tetroxide to a mixed solution composed of 320 mL of absolute ethanol and 80 mL of deionized water, adjust the pH to 11 with ammonia water, and 2 Under protection, mechanically stir and heat to 50°C, add 2 mL of tetraethyl orthosilicate dropwise to the mixed solution, continue to stir for 1...
Embodiment 2
[0040] Magnetic chitosan (Fe 3 o 4 / SiO 2 / Cs) Synthesis of Adsorbent
[0041] Step 1, weigh 2.7g FeCl respectively 3 ·6H 2 O and 7.2g of sodium acetate were mixed and dissolved in 100ml of ethylene glycol, stirred magnetically for 35min to form a uniform yellow solution, then transferred to a hydrothermal reaction kettle, reacted at 180°C for 15h, cooled to room temperature, discarded the supernatant, and removed the black The precipitate was fully rinsed with deionized water, then rinsed three times with absolute ethanol, and dried in a vacuum oven at 45°C for 12 hours to obtain magnetic ferric iron tetroxide;
[0042] Step 2: Add 1.0 g of ultrasonically dispersed magnetic ferric iron tetroxide to a mixed solution composed of 320 mL of absolute ethanol and 80 mL of deionized water, adjust the pH to 11 with ammonia water, and 2 Under protection, mechanically stir and heat to 52°C, add 2mL tetraethyl orthosilicate dropwise to the mixed solution, continue stirring for 11.5...
PUM
Property | Measurement | Unit |
---|---|---|
concentration | aaaaa | aaaaa |
adsorption capacity | aaaaa | aaaaa |
adsorption capacity | 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