• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    In the process for preparing a magnetically stable, powder comprising the steps of reducing an iron oxide or iron oxide hydrate with a gaseous reduction agent and stabilizing the metallic powder thus produced, the improvement which comprises enhancing its reduction by coating said iron oxide or iron oxide hydrate with an antimony compound at a level of up to about 7 weight percent antimony based on the weight of the iron oxide prior to said reduction.
    公开号:SU1419510A3
    申请号:SU802953002
    申请日:1980-07-29
    公开日:1988-08-23
    发明作者:Джеймс Дизикес Луис；Герман Родриан Ричард
    申请人:Пфайзер Пигментс Инк.(Фирма)；
    IPC主号:
    专利说明:

     cm
    This invention relates to a method for producing magnetically stable iron powder from iron oxide or iron oxide hydrate for magnetic recording with high coercivity to improve workability at wavelength, good orientation and high magnetic moment to achieve high output and good chemical stability for free circulation and long-term storage and can be used in various areas of magnetic multiplication, for example for high-speed reproduction for data storage (in the form of disks if magnetic tapes) and magnetic recording in the form of audio and video tapes.
    The purpose of the invention is to accelerate the recovery process while maintaining high magnetic properties.
    SUMMARY OF THE INVENTION The essence of the invention is to accelerate the rate of recovery by using an antimony compound coating before recovery.
    An increase in the reduction rate can be represented by the term Reduction Factor, which can be defined as the ratio of the reduction of iron oxide or hydrate of iron oxide coated with an antimony compound, by the reduction of iron oxide or hydrate of iron oxide without antimony, both of which are carried out at the same conditions, namely, the weight of the sample, the flow rate of hydrogen, the temperature, and the tod. The reduction time is the amount of time it takes to reduce iron oxide or iron oxide hydrate from magnetite to metal mold.
    Antimony compounds suitable for coatings are antimony oxides, oxychlorides, chlorides, sulphates and antimony hydroxides.
    Small amounts of tin in the coating do not affect the rate of reduction, but they do improve the magnetic properties.
    Preferred iron oxides or iron oxide hydrates, which can be used as starting materials, are powders with needle-like particles. In this group can be included:
    0
    five
    0
    five
    0
    5 0 5
    0
    five
    leza or iron oxide hydrate modified by other metals such as cobalt, chromium and nickel
    As iron oxide or iron oxide hydrate, gamma iron oxide, magnetite, hematite or yellow iron oxide selected from goethite or lepidocrosite are used.
    The method is carried out as follows.
    It is mainly used to precipitate lepidocrosite form of iron oxide hydrate, which is filtered and washed, and then re-suspended in water, the pH of which is set to 1.0 with concentrated hydrochloric acid. An aqueous solution of antimony trichloride containing a sufficient amount of concentrated hydrochloric acid to maintain antimony in solution is added to a suspension of iron oxide hydrate while stirring the mixture, the pH of the mixture is then set to about 1.5 with an aqueous solution of sodium hydroxide to complete the precipitation of the compound antimony on iron oxide hydrate particles An aqueous solution of tin containing stannous chloride and a sufficient amount of concentrated hydrochloric acid to keep the tin in solution Then, it is added to a suspension of iron oxide hydroxide coated with an antimony compound, the pH of the suspension is then set to a value of 2 in order to complete the precipitation of tin hydroxide or tin oxyhydroxide on the coating of the particles.
    The suspension is then filtered, the precipitate is washed and dried. The dried precipitate after filtration is then crushed to the required size. The crushed coated iron oxide hydrate is dehydrated, then reduced to a metal form in a fluidized bed reactor at a temperature of about 350 seconds in a hydrogen atmosphere. After the reduction is complete, the metal particles are stabilized in an air-nitrogen mixture.
    In order to evaluate the properties of the material obtained, magnetic tapes are manufactured using vinyl copolymer of the following composition (all parts of the B composition are indicated in mass percent, using 75% by weight
    the mass of magnetic particles contained in the magnetic material):
     material840
    Ether MeTH. iaCif timlinlope G. schools 60
    Vinyl (1pa resin120
    And the fixer60
    Methylisobutylketok500
    Toluene500
    D and about to with silt with ulgo -
    sodium succinate 33.5
    This mixture is ground in a ball mill for 20 hours. The composition is applied to a polyethylene terephthalate base in the form of a three-inch strip. While the applied coating remains wet, it is passed through a magnetic field to orient the particles, after which the strip is dried and can be calendered, compacted or polished. Finally, it is cut to the required width and then swirled onto rollers or tension drums My Tolii - on the floor of 1 trimer 288-332 micro inches.
    An example, Into a gallon reactor equipped with a stirrer, is placed 60 liters of water. The water is acidified to a pH of 1.5 with concentrated acid; 1 acid.
    During the transfer of the solution, 5.448 kg of sediment is added after
    filtering lepidocrosite containing 1234 g of iron oxide, and then disperse. After 15 minutes, an acidified solution of antimony trichloride containing 6.58 g of antimony is added to the suspension, the pH of the suspension is adjusted to a value of 2.0 with an aqueous solution of 10% sodium hydroxide. Then, an aqueous solution of acidified bivalent tin chloride containing 30% is added. 22 g of tin, the pH of the suspension rises to a value of 3.3 with an aqueous solution of 10% sodium hydroxide. The coated particles are filtered, washed and dried at 82 ° C. The dried coated product is then dehydrated.
    5 about 5
    0
    five
    0 5 0
    It is heated by heating to 408-410 C for about 60 minutes and kept at this temperature for 109 minutes in the presence of air in a rotatable column. Approximately 50 mg of the thus obtained coated dehydrated iron oxide is reduced in hydrogen to a metallic form and passivated. The reduction to metal is carried out within 53 minutes, corresponding to a reduction ratio of 0.58. 600 g of the dehydrated product obtained according to the example is reduced in a fluidized bed column in hydrogen for 51 minutes, then combined with a bonding agent, and a magnetic tape is made from it. The resulting tape has the following magnetic properties: Coercive force, HC, E1176
    Residual Magnetiz, BP, GS2415
    Square, BP / H „0.76
    权利要求:
    Claims (2)
    [1]
    moreover, H is a field strength equal to 3.0 kOe. Invention Formula
    1, A method for producing a magnetic powder for magnetic recording, including the deposition of tin hydroxide or oxyhydroxide on the starting powder of an iron oxide compound selected
    from the group containing iron oxide, iron oxide hydrate, modified iron oxide or modified iron oxide g1-schrat, and subsequent reduction with hydrogen, characterized in that, in order to accelerate the reduction process while maintaining high magnetic properties, before the precipitation of tin hydroxide on the starting compound iron oxides precipitate an antimony compound, with an antimony content of 0.5% and a tin content of 2.4% by weight of iron oxide.
    [2]
    2. Method pop. 1, I differ by the fact that the modified iron oxide hydrate is dehydrated before reduction.
    类似技术:
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    同族专利:
    公开号 | 公开日
    FR2462222A1|1981-02-13|
    SE8004264L|1981-01-31|
    KR830003787A|1983-06-22|
    ES493819A0|1981-08-01|
    PT71622A|1980-08-01|
    JPH0146561B2|1989-10-09|
    FI802370A|1981-01-31|
    BR8004772A|1981-02-10|
    DE3028556C2|1986-04-17|
    FI70339C|1986-09-12|
    CH639014A5|1983-10-31|
    AU522889B2|1982-07-01|
    ES8106267A1|1981-08-01|
    CA1132008A|1982-09-21|
    DE3028556A1|1981-02-12|
    FI70339B|1986-02-28|
    SE454548B|1988-05-09|
    MX152979A|1986-07-11|
    FR2462222B1|1984-01-06|
    JPS5623203A|1981-03-05|
    IN154408B|1984-10-27|
    DD153195A5|1981-12-30|
    NL8004337A|1981-02-03|
    IT1132024B|1986-06-25|
    AU6087080A|1981-06-18|
    US4256484A|1981-03-17|
    IL60693A|1983-02-23|
    PH15943A|1983-04-29|
    IT8023788D0|1980-07-29|
    BE884529A|1981-01-29|
    KR830002684B1|1983-12-07|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    FR1215996A|1957-12-16|1960-04-21|Thomson Houston Comp Francaise|Agglomerated magnetic materials and their manufacture|
    JPS5528129B1|1967-08-10|1980-07-25|
    NL162233C|1968-03-05|1980-04-15|Philips Nv|METHOD FOR PREPARING AN IRON MAGNETIC STABLE POWDER, FOR MAGNETIC REGISTRATION.|
    NL163355C|1969-04-08|1980-08-15|Philips Nv|METHOD FOR PREPARING AN IRON MAGNETIC STABLE METAL POWDER, FOR MAGNETIC REGISTRATION.|
    US3623859A|1970-05-22|1971-11-30|Ampex|Process of making acicular stable magnetic iron particles|
    US3663318A|1970-10-05|1972-05-16|Du Pont|Process for making ferromagnetic metal powders|
    DE2212933A1|1972-03-17|1973-09-20|Philips Nv|Process for the production of a metal powder consisting essentially of iron|
    US4067755A|1974-06-25|1978-01-10|Tdk Electronics Company, Ltd.|Method of making powdered magnetic iron oxide material|
    JPS5133758A|1974-09-17|1976-03-23|Fuji Photo Film Co Ltd|
    JPS5142990A|1974-10-11|1976-04-12|Fuji Photo Film Co Ltd|
    IT1026663B|1974-11-29|1978-10-20|Montedison Spa|PROCEDURE FOR PREPARING IRON-BASED METALLIC POWDERS FOR HAGNETIC REGISTRATION|
    US4020236A|1975-07-22|1977-04-26|Fuji Photo Film Co., Ltd.|Process for producing a magnetic material and magnetic recording medium containing the same|
    DE2909995C2|1978-03-16|1984-06-28|Kanto Denka Kogyo Co., Ltd., Tokyo|Method for producing a magnetic powder|DE2815712A1|1978-04-12|1979-10-25|Bayer Ag|IRON OXIDES FOR MAGNETIC SIGNAL RECORDING AND PROCESS FOR THEIR PRODUCTION|
    JPH0345447B2|1979-11-28|1991-07-11|Tdk Electronics Co Ltd|
    US4826671A|1986-03-14|1989-05-02|Basf Aktiengesellschaft|Preparation of acicular α-Fe2 O3|
    US5219554A|1986-07-03|1993-06-15|Advanced Magnetics, Inc.|Hydrated biodegradable superparamagnetic metal oxides|
    JPS63302420A|1987-01-16|1988-12-09|Nissan Chem Ind Ltd|Production of magnetic iron powder|
    KR100870992B1|2007-04-04|2008-12-01|나노케미칼 주식회사|Zero Valent Fe Powders for Heat Source in Thermal Batteries And Making method of The Same|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    US06/061,797|US4256484A|1979-07-30|1979-07-30|Metallic iron particles for magnetic recording|
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