US1873155A - Ferromagnetic materials - Google Patents
Ferromagnetic materials Download PDFInfo
- Publication number
- US1873155A US1873155A US446168A US44616830A US1873155A US 1873155 A US1873155 A US 1873155A US 446168 A US446168 A US 446168A US 44616830 A US44616830 A US 44616830A US 1873155 A US1873155 A US 1873155A
- Authority
- US
- United States
- Prior art keywords
- permeability
- nickel
- iron
- alloy
- alloys
- 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
Links
- 239000003302 ferromagnetic material Substances 0.000 title 1
- 230000035699 permeability Effects 0.000 description 32
- 229910045601 alloy Inorganic materials 0.000 description 21
- 239000000956 alloy Substances 0.000 description 21
- UGKDIUIOSMUOAW-UHFFFAOYSA-N iron nickel Chemical class [Fe].[Ni] UGKDIUIOSMUOAW-UHFFFAOYSA-N 0.000 description 16
- 239000006104 solid solution Substances 0.000 description 15
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 12
- 229910052709 silver Inorganic materials 0.000 description 12
- 239000004332 silver Substances 0.000 description 12
- 238000000034 method Methods 0.000 description 11
- 238000010438 heat treatment Methods 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
- 239000013078 crystal Substances 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 229910001004 magnetic alloy Inorganic materials 0.000 description 6
- 238000010791 quenching Methods 0.000 description 6
- 230000000171 quenching effect Effects 0.000 description 6
- 238000002791 soaking Methods 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 229910000640 Fe alloy Inorganic materials 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000000137 annealing Methods 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910001030 Iron–nickel alloy Inorganic materials 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000004698 iron complex Chemical class 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- PSGAAPLEWMOORI-PEINSRQWSA-N medroxyprogesterone acetate Chemical compound C([C@@]12C)CC(=O)C=C1[C@@H](C)C[C@@H]1[C@@H]2CC[C@]2(C)[C@@](OC(C)=O)(C(C)=O)CC[C@H]21 PSGAAPLEWMOORI-PEINSRQWSA-N 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/12—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/78—Combined heat-treatments not provided for above
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/10—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of nickel or cobalt or alloys based thereon
Definitions
- This invention relates to magnetic alloys of the nickel-iron class having a high permeability at low magnetizing forces such as used for loading telephone and tdlegraph 5 conductors or the like in electrical circuits.
- loys of this kind are :((i) high initial per:
- Condition (1)) is fulfilled by an alloy having a comparatively high coercivity, since 'it is well known that the higher the coercivity of alloys of a certain class becomes, the less the dependence of the permeability on the strength of field at small magnetizing forces.
- the present invention provides a generally applicable method of procedure which, in the case of nickel-iron alloys of high initial permeability and small coercivity makes it possible to increase the coercivity and thereby to decrease the change-in-permeability, without unduly-lowering the value of t e initial permeability. It embodies a process in the manufacture or thermal production of alloys with finely distributed heterogeneous iron alloys should be completely in solid solution, and when additional elements have been proposed either to increase the initial permeability or the specific resistance, or else to render mechanical treatment easier, their nature and amount have been selected so as to bring about their complete solid solution. For example, manganese, chromium, cobalt, tungsten, copper, silicon, molybdenum and the like have been added to nickel-iron alloys in such proportions that all formed mixed crystals therewith.
- the separate or heterogeneous particles left in the material (whether they be of micro scopic or sub-microscopicsize) then set up a state of strain therewithin owing to the difference of their thermal coefficients of eXpan-.
- the initial permeability however is affected only within certain limits.
- the value of the initial permeability and of the coercivity may be varied by varying the nature and'quantitv of the added substance as well as by. suitably varying the details of the heat treatment. and within limits any desired combination of both values can be obtained.
- the following table shows the efi'ect of annealinga nickel-iron alloy with an addition of silver, coolingrapidly from 600 C.
- the process of producing magnetic alloys of the nickel-iron class with high initial permeability and with reduced variation of permeability in small magnetic fields characterized by incorporating in the alloy an additional element which does not readily form mixed crystals with the nickel-iron complex, heating the alloy to an annealing temperature, quenching so as to obtain a condition of super-saturation of the element in solid solution, and thereafter soaking the ma terial between about 300 and 500 C. for a substantial period of time in order to precipitate some of the element out of solution in a finely divided state.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Electromagnetism (AREA)
- Manufacturing & Machinery (AREA)
- Soft Magnetic Materials (AREA)
Description
Patented Aug. 23, 1932 amino STATES PATENT OFFICE BEBNHABD SCHARNOW, OF IBERLIN-CEARLOTTENBURG, GERMANY, ASSIGNOB, TO DEUTSOH-ATLANTISCHE TELEGRAPHENGESELLSCEA-FT, OF BERLIN, GERMANY ra'nnomenn'ric surname 30 Drawing. =App1ication filed April 21, 1930, Serial No. 446,168, and in Germany December 10, 1928.
This invention relates to magnetic alloys of the nickel-iron class having a high permeability at low magnetizing forces such as used for loading telephone and tdlegraph 5 conductors or the like in electrical circuits.
It aims to increase the constancy of permeability in low magnetizing fields by increasing the small coercivity of such metals without unduly impairing the general high 19 order of initial permeability, so as to improve their character and applicability to the stated and other uses as will be better understood from the following description.
Chief among the properties required in al-.
loys of this kind are :((i) high initial per:
meability, and (b) a relatively small change I in permeability throughout the largest possible range of small field strengths. Condition (1)) is fulfilled by an alloy having a comparatively high coercivity, since 'it is well known that the higher the coercivity of alloys of a certain class becomes, the less the dependence of the permeability on the strength of field at small magnetizing forces.
In the following description therefore, the
amount of the coercivity will be taken as an inverse measure of the change of the perineability with strength of field.
It is well know that pure nickel-iron al- 0 loys, especially those having approximately 80% nickel content possess an extraordinarily high initial permeability, but these suffer a relatively great change of permeability with changing strength of field. Other alloys, such as those consisting for example of cobalt, iron and nickel, show an extraordi-' narily small increase of permeability with varied strength of field and-accordingly satisfy the above-mentioned condition (6).
However, with these last-mentioned alloys there is alimit to the magnitude of initial permeability, which limit renders the alloy unsuitable for many purposes.
5 The present invention provides a generally applicable method of procedure which, in the case of nickel-iron alloys of high initial permeability and small coercivity makes it possible to increase the coercivity and thereby to decrease the change-in-permeability, without unduly-lowering the value of t e initial permeability. It embodies a process in the manufacture or thermal production of alloys with finely distributed heterogeneous iron alloys should be completely in solid solution, and when additional elements have been proposed either to increase the initial permeability or the specific resistance, or else to render mechanical treatment easier, their nature and amount have been selected so as to bring about their complete solid solution. For example, manganese, chromium, cobalt, tungsten, copper, silicon, molybdenum and the like have been added to nickel-iron alloys in such proportions that all formed mixed crystals therewith.
The behavior of metals is of course known so far as the forming of mixed crystals, or solutions in each other is concerned. For
-. instance, it is known that an alloy of nickel and iron is capable of taking up a considerable percentage of copper in the mixed crys tals of nickel and iron. Only after a certain limit of copper addition is passed are parts of the copper found in the solid body as separate heterogeneous constituents. The conditions under which these constituents are formed have been known for many materials, although tests have not been made for all the different metals and alloys. However,
it was not known that heterogeneous constitu-' tion in nickel-iron alloys of high initial permeability might be used to achieve a special a technical effect and create, so to speak, an r inner tension causing an increase of'the coercivity of the metals.
The discovery of this from prior knowledge and practice, there are produced in the high initial permeability alloys certain materials or elements such as silver out of solid solution and disseminated fact led to this in- 'vention, according to which, as distinguished I in a finely divided state. A particular form I of heat treatment is required to produce the i desired result according .to the invention, which heat treatment comprises heating the alloy, after working it to shape as desired,- to an annealing temperature, e. g. 900. C. or
above, vthen quenching it from that temperature, or from a somewhat lower temperature, e. g. 600 0., in order to obtain a condition of super-saturation of the added element in solid solution, and thereafter soaking the ma-' terial at-a temperature such as 300 to 500 C. for a sufliciently long time.
The separate or heterogeneous particles left in the material (whether they be of micro scopic or sub-microscopicsize) then set up a state of strain therewithin owing to the difference of their thermal coefficients of eXpan-.
sion or to the occurrence of a change of volume, by which state of strain the coerclvity of the material is increased. The initial permeability however is affected only within certain limits. The value of the initial permeability and of the coercivity may be varied by varying the nature and'quantitv of the added substance as well as by. suitably varying the details of the heat treatment. and within limits any desired combination of both values can be obtained. v 4
The coeflicients of solubility of the individ-. ual substances with respect to each other are sufliciently known in science and engineering. Also if several substances are soluble in thereof. arsenic. beryllium. boron. phosphorus, sulphur and zirconium are other possibilities. It is therefore immaterial which of the well known materialsflor elements is added to "the metal or alloy so long as it has or shows, when used in comparatively small amounts, the special behavior of forming heterogeneous constituents which do not pass into or stay in solid solution at room temperature. Elements such as copper, which are comparatively soluble in the nickel-iron solid complex, cannot be usefully employed according to the present invention.
The following table shows the efi'ect of annealinga nickel-iron alloy with an addition of silver, coolingrapidly from 600 C.
I and shows thatthe coercitivity can be increased at will, while retaining a substantially high initial permeability:
Alloy 77.5% m, 20.5% i e/2.5% A
Initial Coerciv- State permeability Rapidly cooled from 600 C 5880 0. Aged (or 1 hour at 350 0..-- 4812 0. Aged for 6 hours at 350 C 4030 0. Aged for 11 hours at 350 C 4100 0. Aged for 16 hours at 350 0..-. 3630 0. Aged for 21 hours at 350 C 3570 0.
Having thus described my invention, what I claim as new and desire to secure by Letters Patent of the United States is 1. The process of producing magnetic alloys of the nickel-iron class with high in1t1al permeability and with reduced variation of permeability in small magnetic fields, char acterized by incorporating'in the alloy an additional element which does not readily form mixed crystals with the nickel-iron complex, heating the alloy and quenching it -from a high temperature so as to obtain a condition of super-saturation of the element in solid solution and thereafter soaking the material at a lower temperature for a substantial period of time, in order to precipitate some of the element out of solution in a finely divided state. 2. The process of producing magnetic alloys of the nickel-iron class with high initial permeability and with reduced variation of permeability in small magnetic fields, characterized by incorporating in the alloy an additional element which does not readily form mixed crystals with the nickel-iron complex, heating the alloy to an annealing temperature, quenching so as to obtain a condition of super-saturation of the element in solid solution, and thereafter soaking the ma terial between about 300 and 500 C. for a substantial period of time in order to precipitate some of the element out of solution in a finely divided state. I
3. The process of producing magnetic alloys of the nickel-iron class with high initial permeability and with reduced variation of permeability in small magnetic fields, characterized by incorporating in the alloy an additional element which does not readily form mixed crystals with the nickel-' iron complex, heating the alloy to an annealing temperature, cooling rather slowly to a lower temperature, such for example as 600 C., quenching so as to obtain a condition of super-saturation of the element in solid solution, and thereafter soaking the material between about 300 and 500 C. for a substantial period of time in order to precipitate some of the element out of solution in a finely divided state.
4. The process of producing magnetic alloys of the nickel-iron class with high initial permeabilityand with reduced variation of permeability in small magnetic fields, characterized by incorporating silver in the' alseminated in a finely divided state "through v 10y, heating the alloy and quenching it from I a high temperature so as to obtain a condition ofsuper-saturation of the silver in-solid solution, and thereafter soaking the'material 6 between about 300 and 500 C. for: a substantial period of time in order to precipitate silver out of solid solution in a finely divided.
- 5. The process l loys ofthe nickel-iron class with high initial permeability and with reduced variation of Permeability n Small magnetic fields, ch ,p Y
V acterized by incorporating silver in the alloy, heating to at least 900? (3., quenching in order 15 to obtain aconditionof super-saturationof Y the silver in solidsolution and thereaflien soaking-the material betweenabout350iand- 400 C. in orderto precipitate silv r'paciot, I solid solution 'in'a finely divided-state." v "6." The process of producing "magnetic a1! loys of the nickel-iron class with highfinitialf' I ample as 600 0., quenehing'irom-thatitem perature in order to obtain acondition of'su-q per-saturation of. the silverin solid solution, 1
8 and thereafter soaking the material between about 350*. and 400 o. in order to-precipitate' 1 a l r out of solid so1utioni afin 1 w state. a
7; Process as claimed in' claim 4; mm 4 the unt of silver incorporated about 0.3% and 5%; a
,8. Process as claimed inthe amount of 2.5%; m 9. Amagnetic havingra high initial permeability and relai-i t y small variation ofpermeflbilityi magnetic field, characterizedby comprising."
an additional element of a kind which does I not readily form, mixed crystals with the k nickel-iron complex, the element being out'of solid solution and disseminated-hm.
finely divided state-throughoutthe'mass at;
'the alloy.
" 10. A magnetic alloy 'ofthe nickel-iron} class having a high initial'permeabilit'y .-and-" j relatively smallvariation of permeability in small magnetic fields,'characteriz'ed by c0'ni'-.
, Prisin 'silver out of solid soluti b h mass of the alloy. 7 A magnetic lloyof;
.7. the ackei ii classhavmg a high initial permeability and relatively small'variationof permeabihty'inj m ll magneticfields, characterized. by v prising between 0.3% and 5% silver outl'of.
solid solution and. ated in. a finely gil'lvided throughout the (if-the I a -12QA magnetic ma the of producing ma gnetic a1- permeability andwith' reduced variationof permeability in small magnetic fields, {char-Iii;
acteri'zed by incorporating'silver inthealloyf' heating-teat .least 900 6;, rather 1 slowly to a lower temperature,,such forfex- 61am 4, n amen; 5 silver incorporated is about:
at of the-nickel iren @1555; F 3
class having'a'highcinitiah rmeability relatively. small'variationo perm bihty in small ma ,etiefields; b com: prising 'a ut2;5%fsilvcrj9utof 01 solui w i a and statethriouglioutthe mas's ofthe a 0y.
and
divided I Intestimon {whe'moflaflixm s1 stud;
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1873155X | 1928-12-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1873155A true US1873155A (en) | 1932-08-23 |
Family
ID=7747009
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US446168A Expired - Lifetime US1873155A (en) | 1928-12-10 | 1930-04-21 | Ferromagnetic materials |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1873155A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3145099A (en) * | 1961-05-22 | 1964-08-18 | Waukesha Foundry Co | Non-galling bearing alloy of silver in nickel base |
| US3350199A (en) * | 1964-10-22 | 1967-10-31 | Bell Telephone Labor Inc | Composition comprising ni-fe-nb with or without silver and magnetic memory element utilizing same |
| US3519498A (en) * | 1966-07-14 | 1970-07-07 | Ibm | Ferromagnetic film |
| US3743550A (en) * | 1970-06-25 | 1973-07-03 | Elect & Magn Alloys Res Inst | Alloys for magnetic recording-reproducing heads |
| US3761904A (en) * | 1970-03-18 | 1973-09-25 | Bell Telephone Labor Inc | Magnetic switching devices comprising ni-mo-fe alloy |
| US3837933A (en) * | 1971-03-13 | 1974-09-24 | Foundation Res Inst Electric A | Heat treated magnetic material |
| US3871927A (en) * | 1971-10-13 | 1975-03-18 | Elect & Magn Alloys Res Inst | Process for producing a high-permeability alloy for magnetic recording-reproducing heads |
-
1930
- 1930-04-21 US US446168A patent/US1873155A/en not_active Expired - Lifetime
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3145099A (en) * | 1961-05-22 | 1964-08-18 | Waukesha Foundry Co | Non-galling bearing alloy of silver in nickel base |
| US3350199A (en) * | 1964-10-22 | 1967-10-31 | Bell Telephone Labor Inc | Composition comprising ni-fe-nb with or without silver and magnetic memory element utilizing same |
| US3519498A (en) * | 1966-07-14 | 1970-07-07 | Ibm | Ferromagnetic film |
| US3761904A (en) * | 1970-03-18 | 1973-09-25 | Bell Telephone Labor Inc | Magnetic switching devices comprising ni-mo-fe alloy |
| US3743550A (en) * | 1970-06-25 | 1973-07-03 | Elect & Magn Alloys Res Inst | Alloys for magnetic recording-reproducing heads |
| US3837933A (en) * | 1971-03-13 | 1974-09-24 | Foundation Res Inst Electric A | Heat treated magnetic material |
| US3871927A (en) * | 1971-10-13 | 1975-03-18 | Elect & Magn Alloys Res Inst | Process for producing a high-permeability alloy for magnetic recording-reproducing heads |
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