• DocumentCode
    823606
  • Title

    Preparation and magnetic properties of barium ferrite fine particles by the coprecipitation salt-catalysis method

  • Author

    Sakai, Hiroshi ; Hanawa, Kenzo ; Aoyagi, Kazumi

  • Author_Institution
    Showa Denko KK, Shiojiri, Nagano, Japan
  • Volume
    28
  • Issue
    6
  • fYear
    1992
  • fDate
    11/1/1992 12:00:00 AM
  • Firstpage
    3355
  • Lastpage
    3362
  • Abstract
    The authors describe catalytic action by NaCl in the reaction between α-Fe2O3 and BaCO3 and the development of a new process for manufacturing barium ferrite fine particles. Pure α-FeOOH and reagent-grade BaCO3 are mixed and heated at temperatures from 300 to 800°C with and without NaCl. The BaCO3 and α-Fe2O3 powders which are formed during heating react and change to barium ferrite at temperatures 100°C lower than NaCl than without it. A hematite defect structure is maintained up to a relatively high temperature due to the presence of the salt, which promotes the formation of barium ferrite. The manufacturing process involves mixing an aqueous solution of metallic chlorides with a mixture of NaOH and Na 2CO3. This alkaline coprecipitate slurry is then neutralized by HCl solution, filtered, and dried. The dried powder, containing salts produced by the reaction, is heated at 840°C. After the salts are dissolved in water, barium ferrite fine particles are obtained
  • Keywords
    barium compounds; ceramics; coercive force; ferrites; magnetic properties of fine particles; magnetisation; powder technology; precipitation (physical chemistry); BaFe12O14; alkaline coprecipitate slurry; catalytic action; coercivity; coprecipitation salt-catalysis method; ferrite fine particles; ferrite preparation; hematite defect structure; magnetic properties; saturation magnetisation; Barium; Ceramics; Ferrites; Heating; Impurities; Magnetic properties; Magnetic recording; Manufacturing processes; Powders; Temperature;
  • fLanguage
    English
  • Journal_Title
    Magnetics, IEEE Transactions on
  • Publisher
    ieee
  • ISSN
    0018-9464
  • Type

    jour

  • DOI
    10.1109/20.179810
  • Filename
    179810