Method for preparing conductive polymer based electromagnetic composite material
An electromagnetic composite material and conductive polymer technology are applied in the field of preparation of conductive polymer-based electromagnetic composite materials, which can solve the problems of limiting the application field of composite materials, poor dispersion of the composite, and many process steps, and achieve a good application prospect. , fast preparation, good reproducibility
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0032] At room temperature, weigh 2.315g Fe 3 o 4 and 2.315g SDS were added to the beaker, then 200ml deionized water was added, and ultrasonically dispersed for 30min to obtain Fe 3 o 4 aqueous suspension. Weigh 0.186g of aniline into a beaker, then add 200ml of deionized water, and ultrasonically disperse for 30min to form a monomer dispersion. Weigh 0.912g of ammonium persulfate into a beaker, then add 200ml of deionized water, and ultrasonically disperse for 30min to form an initiator solution. Will Fe 3 o 4 The aqueous phase suspension, monomer dispersion and initiator solution were added to three syringes, and injected continuously into their respective microtubes at the pushing speed of 50 μl / min, 10 μl / min and 5 μl / min respectively, and the three reaction liquid flows Mix in the reaction tube after passing through the microtube. A polytetrafluoroethylene reaction tube with a diameter of 600 μm was placed in an ultrasonic pool and reacted for 10 min under the con...
Embodiment 2
[0034] At room temperature, weigh 3.315g Fe 3 o 4 and 0.663g SDS were added to the beaker, then 200ml deionized water was added, and ultrasonically dispersed for 60min to obtain Fe 3 o 4 aqueous suspension. Weigh 1.3418g of pyrrole into a beaker, then add 200ml of deionized water, and ultrasonically disperse for 60min to form a monomer dispersion. Weigh 8.109g of ferric chloride into the beaker, then add 200ml of deionized water, and ultrasonically disperse for 60min to form an initiator solution. Will Fe 3 o 4The aqueous phase suspension, monomer dispersion and initiator solution were added to three syringes, and injected continuously into their respective microtubes at the pushing speed of 100 μl / min, 50 μl / min and 20 μl / min respectively, and the three kinds of reaction liquid flow Mix in the reaction tube after passing through the microtube. A polytetrafluoroethylene reaction tube with a diameter of 900 μm was placed in an ultrasonic pool, and reacted for 20 minutes ...
Embodiment 3
[0036] At room temperature, weigh 4.315g Fe 3 o 4 and 1.438g SDS were added to the beaker, then 200ml deionized water was added, and ultrasonically dispersed for 50min to obtain Fe 3 o 4 aqueous suspension. Weigh 1.0814g of o-phenylenediamine into a beaker, then add 200ml of deionized water, and ultrasonically disperse for 50min to form a monomer dispersion. Weigh 6.109g of ferric chloride into the beaker, then add 200ml of deionized water, and ultrasonically disperse for 40min to form an initiator solution. Will Fe 3 o 4 The aqueous phase suspension, monomer dispersion and initiator solution were added to three syringes, and injected continuously into their respective microtubes at the pushing speed of 80 μl / min, 40 μl / min and 15 μl / min respectively, and the three kinds of reaction liquid flow Mix in the reaction tube after passing through the microtube. A polytetrafluoroethylene reaction tube with a diameter of 700 μm was placed in an ultrasonic pool and reacted for 1...
PUM
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