US3644207A - Lithium-titanium-zinc ferrites - Google Patents

Lithium-titanium-zinc ferrites Download PDF

Info

Publication number
US3644207A
US3644207A US863372A US3644207DA US3644207A US 3644207 A US3644207 A US 3644207A US 863372 A US863372 A US 863372A US 3644207D A US3644207D A US 3644207DA US 3644207 A US3644207 A US 3644207A
Authority
US
United States
Prior art keywords
zinc
ferrites
lithium
titanium
ferrite
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US863372A
Inventor
Paul D Baba
Giltan Michael Argentina
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ampex Corp
Original Assignee
Ampex Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ampex Corp filed Critical Ampex Corp
Application granted granted Critical
Publication of US3644207A publication Critical patent/US3644207A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/26Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on ferrites
    • C04B35/2608Compositions containing one or more ferrites of the group comprising manganese, zinc, nickel, copper or cobalt and one or more ferrites of the group comprising rare earth metals, alkali metals, alkaline earth metals or lead
    • C04B35/2616Compositions containing one or more ferrites of the group comprising manganese, zinc, nickel, copper or cobalt and one or more ferrites of the group comprising rare earth metals, alkali metals, alkaline earth metals or lead containing lithium

Definitions

  • ABSTRACT [52] U.S.Cl ..252/62.59, 252/626, 25266226612, Microwave ferrites with narrow resonance newidths, good Int Cl gg temperature performance, 10w losses, low costs, and rectangula! hysteresis loops are made from a lithiummanium ferrite [58] Fleld of Search ..252/62.59, 62.6, 62.61 62.62 containing a Small amount of zinc. In addition, small amounts [56] References Cited of copper or manganese can be present in the ferrites.
  • garnets are ordinarily employed at microwave frequencies. However, garnets are expensive and have poor temperature performance. Although it has been suggested that ferrites might be used, the losses have been.
  • Oxides of the constituent metal ions are generally employed when possible.
  • the. anhydrous carbonate of the metal ion is used.
  • the raw materials are weighted out in stoichiometric proportions and are wet mixed for 1 hour or more in a ball mill.
  • the resulting slurry is then dried at around -l C. and the dried raw material mixture is then forced through a standard -mesh screen for ease of handling.
  • the screened oxide mixture is then loaded into refractory boats.
  • the boats are placed in a box-type furnace, and heated to a predetermined temperature.
  • the exact temperature can vary from 700 to 900 C.
  • the object of this step is twofold: the primary object is to provide sufficient energy to react the oxide mixture to a 70 percent ferrite 30 percent oxide mixture by a solid state reaction.
  • the secondary objective is the simple thermal'decomposition of any carbonates used.
  • the reacted mixture is generally characterized by a relatively large predominant particle size. Before the mixture can be shaped and sintered into a single phase ferrite body the particle size must be reduced. Ball milling is employed in essentially the same manner as outlined above. The ferrite-oxide slurry is then dried at around 80 C. to a fine powder.
  • a typical binder is polyvinyl alcohol.
  • the addition of the binder can be carried out in the second ball milling step, or in an additional step employing any sort of method facilitating uniform distribution of the substance used as a binder.
  • the binder impregnated powder is then shaped in tool steel dies with enough pressure to facilitate uniform compaction.
  • the pressed shapes are then sintered at temperatures ranging from 950 to l, 1 50 C. in atmospheres of oxygen or air.
  • novel ferrites of the present invention have the following composition.
  • Example I contains zinc while Example 2 does not contain zinc.
  • the material of Example 1 is superior because it exhibits a lower coercive force, a higher remanence, a lower magnetic loss, a narrower resonance linewidth, and a higher density than does 2.
  • Example 3 contains zinc while Example 4 does not contain zinc.
  • the material of Example 1 is superior because it exhibits a lower coercive force, a higher remanence, a lower dielectric loss, a narrower linewidth, and higher density than does 4.
  • a lithium-titanium-zinc ferrite having the formula:

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Magnetic Ceramics (AREA)
  • Soft Magnetic Materials (AREA)

Abstract

Microwave ferrites with narrow resonance linewidths, good temperature performance, low losses, low costs, and rectangular hysteresis loops are made from a lithium-titanium ferrite containing a small amount of zinc. In addition, small amounts of copper or manganese can be present in the ferrites.

Description

O Umted States Patent [151 3,644,207 Baba et a1. Feb. 22, 1972 [54] LlTHIUM-TlTANIUM-ZINC FERRITES 3,177,145 4/1965 Brownlow ..252/62.61 X 72] lnvcmors: Paul D. Balm San Carlos; Gman Michael 3,483,126 12/1969 Sara et a1. ..252/62.6 X
Argentina, Belmont, both of Calif.
- Primary Examiner-Tobias E. Levow od t al f. [73] A'sslgnee Ampex Corporation, Redwo C1 y C Assistant Examiner]. Cooper [22] Filed: Oct. 2, 1969 A"omeiy Rbel-t Clay [21] App1.No.: 863,372
[57] ABSTRACT [52] U.S.Cl ..252/62.59, 252/626, 25266226612, Microwave ferrites with narrow resonance newidths, good Int Cl gg temperature performance, 10w losses, low costs, and rectangula! hysteresis loops are made from a lithiummanium ferrite [58] Fleld of Search ..252/62.59, 62.6, 62.61 62.62 containing a Small amount of zinc. In addition, small amounts [56] References Cited of copper or manganese can be present in the ferrites.
UNITED STATES PATENTS 1 Claims, No Drawings 3,065,182 11/1962 Aghajanian ..252/62.6l X 7 LlTI-IIUM-TITANIUM-ZINC FERRITES The invention described herein was made in the course-of a contract with the United States Department of Air Force.
SUMMARY OF THE INVENTION At the present time, garnets are ordinarily employed at microwave frequencies. However, garnets are expensive and have poor temperature performance. Although it has been suggested that ferrites might be used, the losses have been.
DESCRIPTION OF THE PREFERRED EMBODIMENTS The following preparative procedure is used in compounding ferrite materials in accordance with the present invention:
Oxides of the constituent metal ions are generally employed when possible. In instances where the chemical instability of the oxide of a particular metal ion causes said oxide to be an impure and unreliable compound, the. anhydrous carbonate of the metal ion is used. The raw materials are weighted out in stoichiometric proportions and are wet mixed for 1 hour or more in a ball mill. The resulting slurry is then dried at around -l C. and the dried raw material mixture is then forced through a standard -mesh screen for ease of handling.
The screened oxide mixture is then loaded into refractory boats. The boats are placed in a box-type furnace, and heated to a predetermined temperature. The exact temperature can vary from 700 to 900 C. The object of this step is twofold: the primary object is to provide sufficient energy to react the oxide mixture to a 70 percent ferrite 30 percent oxide mixture by a solid state reaction. The secondary objective is the simple thermal'decomposition of any carbonates used.
The reacted mixture is generally characterized by a relatively large predominant particle size. Before the mixture can be shaped and sintered into a single phase ferrite body the particle size must be reduced. Ball milling is employed in essentially the same manner as outlined above. The ferrite-oxide slurry is then dried at around 80 C. to a fine powder.
The powder is then mixed with a binder as is well known to those skilled in the art. Wide latitude is permissible in the selection of binders. A typical binder is polyvinyl alcohol.
The addition of the binder can be carried out in the second ball milling step, or in an additional step employing any sort of method facilitating uniform distribution of the substance used as a binder. The binder impregnated powder is then shaped in tool steel dies with enough pressure to facilitate uniform compaction.
The pressed shapes are then sintered at temperatures ranging from 950 to l, 1 50 C. in atmospheres of oxygen or air.
The novel ferrites of the present invention have the following composition.
where 0.05 s w s 0.3
and 0.30 s x s 0.95
0 s s 0.2 0 szs0.2
The following nonlimiting examples illustrate various preferred embodiments of the invention. In the examples, Ex
amples l and 3 illustrate com ositiqns which contain zinc whr e Examples 2 and 4 show su stantially the same composition without the addition of zinc, showing the beneficial effect of the zinc addition.
EXAMPLE 1 A ferrite having the composition where x=0.7, y=0, z=0 and w=0.l was prepared by the above procedure. The reaction step was performed at 900 C. The sintering step was performed at 1,100 C. in an oxygen atmosphere. The ferrite had a coercive force of 2.26 oersteds, a remanence of 709 gauss, a saturation magnetization of 825 gauss, a magnetic loss of 0 decibels per inch, a dielectric loss of 0.7 decibels per inch, a resonance linewidth of 360 oersteds, and a density of 3.64 grams per cubic centimeter.
EXAMPLE 2 Example I contains zinc while Example 2 does not contain zinc. The material of Example 1 is superior because it exhibits a lower coercive force, a higher remanence, a lower magnetic loss, a narrower resonance linewidth, and a higher density than does 2. I
EXAMPLE 3 A ferrite was made where x=0.55, y=0. l, z=0.l and w=0. 1. It has a coercive force of 4.02 oersteds, a remanence of 670 gauss, a saturation magnetization of 915 gauss, a dielectric loss of 0.52 decibels per inch, a resonance linewidth of 375 oersteds, and a density of 4.02 grams per cubic centimeter.
EXAMPLE 4 A ferrite was made where x=0.55, y=0.l, z=0.l and w=0. It had a coercive force of 5.15 oersteds, a remanence of 535 gauss, a saturation magnetization of 661 gauss, a dielectric loss of 0.58 decibels per inch, a resonance linewidth of 550 oersteds, and a density of 3.09 grams per cubic centimeter.
Example 3 contains zinc while Example 4 does not contain zinc. The material of Example 1 is superior because it exhibits a lower coercive force, a higher remanence, a lower dielectric loss, a narrower linewidth, and higher density than does 4.
We claim:
1. A lithium-titanium-zinc ferrite having the formula:
US863372A 1969-10-02 1969-10-02 Lithium-titanium-zinc ferrites Expired - Lifetime US3644207A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US86337269A 1969-10-02 1969-10-02

Publications (1)

Publication Number Publication Date
US3644207A true US3644207A (en) 1972-02-22

Family

ID=25340998

Family Applications (1)

Application Number Title Priority Date Filing Date
US863372A Expired - Lifetime US3644207A (en) 1969-10-02 1969-10-02 Lithium-titanium-zinc ferrites

Country Status (1)

Country Link
US (1) US3644207A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5304318A (en) * 1988-02-03 1994-04-19 Tdk Corporation Sintered ferrite materials and chip parts

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3065182A (en) * 1959-11-17 1962-11-20 Ibm Low flux density ferromagnetic material
US3177145A (en) * 1963-02-04 1965-04-06 Ibm Manganese copper ferrite composition containing titanium and germanium and method ofpreparation
US3483126A (en) * 1968-05-15 1969-12-09 Union Carbide Corp Ferrite materials containing titanium or manganese

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3065182A (en) * 1959-11-17 1962-11-20 Ibm Low flux density ferromagnetic material
US3177145A (en) * 1963-02-04 1965-04-06 Ibm Manganese copper ferrite composition containing titanium and germanium and method ofpreparation
US3483126A (en) * 1968-05-15 1969-12-09 Union Carbide Corp Ferrite materials containing titanium or manganese

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5304318A (en) * 1988-02-03 1994-04-19 Tdk Corporation Sintered ferrite materials and chip parts

Similar Documents

Publication Publication Date Title
US3630912A (en) Lithium titanium bismuth ferrites
US3886077A (en) Garnet structure ferrimagnetic material having a saturation magnetisation less than 1000 gauss for microwave applications
US2818387A (en) Square loop ferromagnetic material
US4155863A (en) Soft lithium-titanium-zinc ferrite
US2989473A (en) Ferrite with constricted magnetic hysteresis loop
US2977312A (en) Ferromagnetic material
US3644207A (en) Lithium-titanium-zinc ferrites
US3038860A (en) Lithium nickel ferrites
US3694361A (en) Lithium titanium bismuth cobalt ferrites
US2882235A (en) Method of manufacturing magnetic cores
US3036008A (en) Permanent magnet ferrite
GB839860A (en) Improvements in or relating to ferromagnetic ferrite materials
US3034987A (en) Magnetic cores
US3884823A (en) Ceramic permanent magnet
US3375195A (en) Electromechanical transducer employing piezomagnetic manganese ferrous ferrite
US3380920A (en) Permanent magnet material and process for manufacturing same
US3450635A (en) Nickel ferrites containing cobalt,lead and silicon
US2950251A (en) Magnetic materials having rectangular hysteresis characteristics
US3032503A (en) Composition of magnetic core material and method of producing same
US3030307A (en) Ferrite material containing lithium and aluminum oxides
JPH0761821A (en) Production of garnet-type magnetic material
US3039966A (en) Square loop ferromagnetic material
US2986523A (en) Modified lithium ferrite
Van Uitert Magnesium‐Copper‐Manganese‐Aluminum Ferrites for Microwave Applications
US3072576A (en) Ferrites having rectangular hysteresis loops and method for manufacture of same