Single-phase multiferroic barium ferrite ceramic material and preparation method thereof
A ceramic material and multiferroic technology, applied in the field of single-phase multiferroic barium ferrite ceramic material and its preparation, can solve the problems of weak ferromagnetism of bismuth ferrite, limited application, difficult ferroelectricity saturation polarization and the like, Achieve the effect of good ferroelectricity and ferromagnetism, low equipment requirements, and uniform particle distribution
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0025] According to the Ba / Fe ratio of 1:10.5, weigh 0.2580g of barium acetate and 3.7082g of iron acetylacetonate and dissolve them in 15ml of deionized water and 200ml of benzene. Reserve in deionized water. The obtained barium precursor solution and iron precursor solution were mixed and stirred for 2 hours, then 100 ml of polyethylene glycol aqueous solution and ammonia water were added and mixed thoroughly at 50° C. for a certain period of time. Centrifuge the obtained suspension solution, place the centrifuged precipitate in a corundum crucible and sinter at 450°C for 1.5h to remove organic matter. Keep warm at 450°C for 1.5h, then cool down to room temperature naturally. Then grind and press the tablet and sinter it into ceramics at 1200°C. The specific steps of sintering are: increase the temperature from room temperature to 1000°C at a rate of 10°C / min, and then increase the temperature from 1000°C at a rate of 5°C / min. to 1200°C, and then kept at this temperature f...
Embodiment 2
[0027] According to the Ba / Fe ratio of 1:9.8, weigh 0.2580g of barium nitrate and 3.4610g of ferric chloride and dissolve them in 15ml of deionized water and 200ml of benzene. Reserve in deionized water. The obtained barium precursor solution and iron precursor solution were mixed and stirred for 2 hours, then 100 ml of polyethylene glycol aqueous solution and ammonia water were added and mixed thoroughly at 50° C. for a certain period of time. Centrifuge the obtained suspension solution, and place the centrifuged precipitate in a corundum crucible to sinter at 350°C for 3 hours to remove organic matter. ℃ for 3 hours, and then cooled down to room temperature naturally. Then grind and press the tablet and sinter it into ceramics at 1100°C. The specific steps of sintering are: from room temperature to 950°C at a heating rate of 10°C / min, and then from 950°C to 950°C at a heating rate of 5°C / min. to 1100°C, and then kept at this temperature for 1h, then dropped from the sinter...
Embodiment 3
[0029]According to the Ba / Fe ratio of 1:10.5, weigh 0.2580g of barium acetate and 3.7082g of iron acetylacetonate and dissolve them in 15ml of deionized water and 200ml of benzene, and weigh 1g of polyethylene glycol (molecular weight: 2000) and dissolve it in 10ml Reserve in deionized water. The obtained barium precursor solution and iron precursor solution were mixed and stirred for 2 hours, then 100 ml of polyethylene glycol aqueous solution and ammonia water were added and mixed thoroughly at 50° C. for a certain period of time. Centrifuge the obtained suspension solution, and place the centrifuged precipitate in a corundum crucible to sinter at 400°C for 2 hours to remove organic matter. ℃ for 2 hours, and then cooled down to room temperature naturally. Then grind and press the tablet and sinter it into ceramics at 1350°C. The specific steps of sintering are: from room temperature to 900°C at a heating rate of 10°C / min, and then from 900°C to 900°C at a heating rate of 5...
PUM
Property | Measurement | Unit |
---|---|---|
Curie point | aaaaa | aaaaa |
particle size | aaaaa | aaaaa |
remanent polarization | 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