Method of preparing bioavailability water-based magnetofluid
A biocompatible, magnetic fluid technology, applied in magnetic liquids, medical preparations with inactive ingredients, inductor/transformer/magnet manufacturing, etc., can solve the problem of poor stability of magnetic liposomes and shell biocompatibility Unsatisfactory, large particle size of magnetic beads, etc., to achieve the effect of easy wide application, good biocompatibility, and small particle size
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0019] Embodiment 1: get the ferric nitrate solution of 10ml 0.12mol / L and the ferrous sulfate solution of 10ml 0.08mol / L, mix and stir evenly, in 40 ℃ constant temperature water bath, add 1.6ml ammoniacal liquor (25%) rapidly, stir 15min , the temperature was raised to 60°C and the reaction was stopped for 5 minutes. Wash the generated black precipitate with distilled water until the upper liquid is neutral, and what is obtained is nano-Fe 3 o 4 . Add 16ml of water to the precipitate, and sonicate for 2 minutes to obtain a uniformly dispersed black solution, which is recorded as solution A; take 4ml of 0.17mol / L sodium gluconate aqueous solution, which is recorded as solution B. Add solution B to solution A, stir at 40°C for 2 hours to fully interact with each other, and sonicate for 2 minutes to finally obtain a stable water-based magnetic fluid. The particle size of the nanocomposite particles prepared by the method is 8.7nm, and the saturation magnetization is 35.3emu / g...
Embodiment 2
[0020] Embodiment 2: get the ferric nitrate solution of 10ml 0.18mol / L and the ferrous sulfate solution of 10ml 0.12mol / L, mix and stir evenly, in 40 ℃ constant temperature water baths, add 2.4ml ammoniacal liquor (25%) rapidly, stir 15min , the temperature was raised to 60°C and the reaction was stopped for 5 minutes. The resulting black precipitate was washed with distilled water until the upper liquid was neutral. Add 24ml of water to the precipitate, and sonicate for 2 minutes to obtain a uniformly dispersed black solution, which is recorded as solution A; take 6ml of 0.17mol / L sodium gluconate aqueous solution, which is recorded as solution B. Add solution B to solution A, stir at 40°C for 2 hours, and sonicate for 2 minutes to finally obtain a stable water-based magnetic fluid. The particle size of the nanocomposite particles prepared by the method is 10nm, and the saturation magnetization is 36.5emu / g.
Embodiment 3
[0021] Embodiment 3: get the ferric nitrate solution of 10ml 0.24mol / L and the ferrous sulfate solution of 10ml 0.16mol / L, mix and stir evenly, in 40 ℃ constant temperature water baths, add 3.2ml ammoniacal liquor (25%) rapidly, stir 15min , the temperature was raised to 60°C and the reaction was stopped for 5 minutes. The resulting black precipitate was washed with distilled water until the upper liquid was neutral. Add 32ml of water to the precipitate, and ultrasonicate for 2 minutes to obtain a uniformly dispersed black solution, which is recorded as solution A; take 8ml of 0.17mol / L sodium gluconate aqueous solution, which is recorded as solution B. Add solution B to solution A, stir at 40°C for 2 hours, and sonicate for 2 minutes to finally obtain a stable water-based magnetic fluid. The particle size of the nanocomposite particles prepared by the method is 12nm, and the saturation magnetization is 38emu / g.
PUM
Property | Measurement | Unit |
---|---|---|
Diameter | aaaaa | aaaaa |
Saturation magnetization | aaaaa | aaaaa |
Particle size | 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