US2783170A - Magnetic material and process of making it - Google Patents
Magnetic material and process of making it Download PDFInfo
- Publication number
- US2783170A US2783170A US579324A US57932456A US2783170A US 2783170 A US2783170 A US 2783170A US 579324 A US579324 A US 579324A US 57932456 A US57932456 A US 57932456A US 2783170 A US2783170 A US 2783170A
- Authority
- US
- United States
- Prior art keywords
- mil
- iron
- coercive force
- thickness
- magnetic
- 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
- 238000000034 method Methods 0.000 title claims description 15
- 230000008569 process Effects 0.000 title claims description 14
- 239000000696 magnetic material Substances 0.000 title description 6
- 239000000463 material Substances 0.000 claims description 54
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 17
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 229910052742 iron Inorganic materials 0.000 claims description 8
- 229910052750 molybdenum Inorganic materials 0.000 claims description 8
- 239000011733 molybdenum Substances 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 230000035699 permeability Effects 0.000 claims description 6
- 229910001004 magnetic alloy Inorganic materials 0.000 claims description 4
- 238000000137 annealing Methods 0.000 description 18
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 16
- 229910045601 alloy Inorganic materials 0.000 description 14
- 239000000956 alloy Substances 0.000 description 14
- 239000011162 core material Substances 0.000 description 13
- 229910052759 nickel Inorganic materials 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- 238000005097 cold rolling Methods 0.000 description 8
- 238000005096 rolling process Methods 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 6
- 230000009467 reduction Effects 0.000 description 6
- UGKDIUIOSMUOAW-UHFFFAOYSA-N iron nickel Chemical compound [Fe].[Ni] UGKDIUIOSMUOAW-UHFFFAOYSA-N 0.000 description 5
- 230000005415 magnetization Effects 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 230000006698 induction Effects 0.000 description 4
- XWHPIFXRKKHEKR-UHFFFAOYSA-N iron silicon Chemical compound [Si].[Fe] XWHPIFXRKKHEKR-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000005275 alloying Methods 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910000640 Fe alloy Inorganic materials 0.000 description 2
- 229910000990 Ni alloy Inorganic materials 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000014509 gene expression Effects 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- 238000005121 nitriding Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000287437 Catharus Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000003321 amplification Effects 0.000 description 1
- 230000006399 behavior Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000005255 carburizing Methods 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000003199 nucleic acid amplification method Methods 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- 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
- My invention contemplates and has for its primary object the provision of a magnetic-core material in the form of ultra-thin tape characterized by rectangular hysteresis loops.
- the figure is a typical direct current hysteresis loop of my new material illustrating the degree of rectangularity achieved with magnetic tape of .25 mil thickness.
- Magnetic materials having square hysteresis loops have hitherto been found of value in various fields, such as the field of mechanical rectification of alternating currents and the field of magnetic amplification.
- Hysteresis loop tests using direct current testing equiment are well known.
- a material is said to have a square hysteresis loop if, in such tests, it exhibits a high ratio of residual induction (Br) to maximum induction (Bm).
- the Br/Bm ratio for a given material is not a single value, but varies with the peak magnetizing force and passes through a maximum as saturation is approached.
- a specific object of this invention is the provision of magnetic alloys of high direct current permeability at inductions approaching saturation, characterized by low coercive force, in very thin sections of high resistivity, such that eddy current effects are minimized, and characterized in such thin sections by a high Br/Bm ratio.
- the most important factors involved in the provision of such material appear to be (1) composition, (2) thickness of the ultimate material, (3) the nature of the final heat treatment as respects time, temperature and annealing atmosphere, and (4) processing as respects cold rolling, intermediate anneals and the like.
- the alloy from which my new mate rial is made may contain from to 85% nickel, and from 3 to 6% molybdenum, the balance being primarily iron.
- Manganese can be used for-deoxidation and to improve hot workability and may range from around .3% to 1%, with around .6% being preferred. Silicon may also be used for deoxidation and preferably will not exceed .3% in the metal.
- Sulfur should be as low as possible and preferably less than .005 and lead less than .0O2%.
- Carbon should be low in amount, namely not more than about .l%.
- Aluminum should be as low as possible and preferably below .01%, including all forms present.
- My preferred allow will contain %1-2% nickel, and 4.0% 33% molybdenum.
- Novelty is not claimed in the constitution of the alloy since high permeability alloys within the range stated have hitherto been produced. It has not, however, hitherto been known that such a high Br/Bm ratio could be produced in such materials.
- the alloys can be formed in the electric furnace (using the induction furnace and vacuum melting if desired, although this is not always necessary). Ingots are cast and these are hot rolled to suitable intermediate gauges and prepared for cold rolling. The materials themselves are capable of being cold rolled with very heavy reductions in the absence of intervening annealings; but in the production of very thin materials it is usually easier to,
- stages accomplish the cold rolling reduction in a series of stages. These stages may be widely varied.
- an exemplary routing which can be depended upon to yield my new result, includes the steps of hot rolling the material to a suitable gauge, such as 120 mils; then box annealing it at a temperature of 870 C. in a reducing atmosphere, such as dry hydrogen or dissociated ammonia; cold rolling it to a thickness of 25 mils; open or strand annealing it in a reducing atmosphere at 870 C.; cold rolling it to a thickness Of 1.2 mils; again open annealing it at 870 C. in a reducing atmosphere; and cold rolling it to the final gauge of .25 mil. It is then ready for a final anneal.
- a suitable gauge such as 120 mils
- cold rolling it to a thickness of 25 mils open or strand annealing it in a reducing atmosphere at 870 C.
- An exemplary routing to produce mil material is the same except that the intermediate anneal is practiced at a thickness of .5 mil, after which the strip is rolled directly to .125 mil before final annealing.
- the material treated as described is now in condition to be given its ultimate magnetic characteristics by a final anneal such as that hereinafter described.
- the material is itself very delicate and difficult to handle. may be treated in bulk to give it the ultimate magnetic characteristics, this ordinarily is not desirable because subsequent operations of handling, slitting, winding into cores and the like will very greatly impair these characteristics.
- the formation of complete cores with the materials of this invention normally is practiced prior to the final anneal.
- the fabrication of the material and the cores and the final anneal will most usually be practiced not by the manufacturer and roller of the material itself, but by his vcndee.
- the material, treated as hercinabove described, and coiled or otherwise handled in bulk or in sheets, is a commercial article of manufacture even though its primary utility lies in the fact that when it is given a suitable heat treatment, it will develop or possess the characteristics herein set forth as desirable.
- the cores ordinarily made are quite small, those intended for digital computing machine work being frequently no greater in diameter than about /4 in.
- the alloys are rolled to gauge as single strands in a width of about 2 in. employing work rolls of very small diameter.
- the material, after rolling, is slit into ribbons /8 in. to A in. in width for widening into toroidal cores. Because of the fragile nature of the material itself and of these small cores, which often consist of only a few wraps of the ribbon, it was found advantageous to Wind the cores on tiny ceramic bobbins such as bobbins of steatite.
- These bobbins which have lateral flanges, furnish support for the ribbon during annealing and also provide a frame for the copper windings employed in testing and in many instances in the subsequent use of the cores.
- the convolutions of the metallic ribbon are carefully insulated with a magnesia coating prior to annealing.
- the annealing is conducted in a suitable annealing box in an atmosphere predominantly of hydrogen and substantially free of carburizing, sulfuriziug and nitriding impurities.
- the water vapor should be as low as possible and such that the exit dewpoint will lie below 40 C. and preferably below -50 C.
- the annealing temperature may range from 750 C. to 1050 C., my preference being for temperatures around 850 to 975 C. when the soaking time is two hours.
- my preference is for pure hydrogen, other inert gases may be present in ap preciable quantities.
- I may employ dissociated ammonia. The nitrogen present is dissociated ammonia does no harm; but any substantial quantity of undissociated ammonia should be avoided because of its nitriding effect.
- the preferred annealing temperature represents the optimum balance between maintaining the rectangularity of the hysteresis loop and minimizing the coercive force, in order to obtain the shortest possible switching time with adequate signal-to-noice ratio under pulse excitation. This balance is necessary because while higher temperatures reduce the coercive force they also reduce the rectangularity.
- the material may be furnace cooled, which results in a slow cooling throughout the range substantially to room temperature, or it may be quenched from a temperature not substantially lower than 540 C., provided the cooling is carried out in such a manner as to avoid oxidation harmful to magnetic properties, as for example by maintaining the material in an atmosphere of hydrogen.
- the annealing temperature range, as well as the moisture content of the annealing atmosphere, are critical, and for best results should not be departed from substantially.
- the hysteresis loops can be made quite rectangular at one mil thickness and above, it is not until the thickness is less than one mil that the 4-79 material can be made to exhibit loops of good rectangularity. Hence the high degree of rectangularity of the hysteresis loops which I have obtained in this material at ultra-thin gauges could not have been predicted in advance.
- the coercive force in my preferred materials at .25 mil thickness is about .10 oersted when the tip magnetizing force Hm is .25 oersted.
- the alloy compositions to which my invention is addressed contain the specified percentages of nickel and molybdenum, the balance being substantially all iron, which may contain normal amounts of impurities or minor amounts of other alloying ingredients whether occurring as impurities or added for workability. It has been further pointed out that these minor amounts of other alloying ingredients do not materially or substantially affect the magnetic characteristics of the materials as discussed herein. As a consequence, in the claims which follow, the expression balance substantially all iron has been employed to be inclusive of such minor amounts of these other alloying ingredients as may be present within the scope of my disclosure.
- a process of producing exceedingly thin magnetic alloys having high permeability, low coercive force and rectangular hysteresis loop characteristics which comprises reducing an alloy containing 80:2% nickel and 4.013% molybdenum, balance substantially all iron, to a thickness less than 1 mil and subjecting the reduced material to an anneal in an atmosphere predominantly of hydrogen and having a dew point below 40 C. at a temperature of substantially 750 to 1050 C.
- a process of producing exceedingly thin magnetic alloys having high permeability, low coercive force and rectangular hysteresis loop characteristics which comprises reducing an alloy containing to 85% nickel and 3 to 6% molybdenum, balance substantially all iron, to a thickness less than 1 mil and subjecting the reduced material to an anneal in an atmosphere predominantly of hydrogen and having a dew point below -40 C. at a temperature of substantially 3750" to 1050 C.
- a process of producing a magnetic material of high permeability, low coercive force and of a thickness minimizing eddy current losses at high frequency magnetization which comprises subjecting an alloy consisting of :L-2% nickel, 4.013% molybdenum, balance substantially all iron, to cold rolling from an intermediate gauge to reduce it to a thickness substantially less than 1 mil with intermediate open annealings, and subjecting the material to a final heat treatment in an atmosphere predominantly of hydrogen at about 850 to 975 C. so as to develop a maximum Br/Bm ratio of at least about .90 when tested with direct current at a magnetization parallel to the direction of rolling.
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Soft Magnetic Materials (AREA)
Description
Feb. 26, 1957 M. F. LITTMANN MAGNETIC MATERIAL AND PROCESS OF MAKING IT Filed April 19, 1956 I w R r m W 1 V 3 M I ww I NI WSNRQN v S m m k w -u .w k N W a F N h h .0" k m m .w F 1 n M u I r m w r a w n l b 154: l l I l I l l l l 1 l I I I I lllllllllll p m Nhs R N MAGNETIC MATERIAL AND PROCESS OF MAKING IT Application April 19, 1956, Serial No. 579,324
9 Claims. (Cl. 148-120) This is a continuation-in-part of my copending application, Serial No. 336,734, filed February 13, 1953, and
' entitled Magnetic Material and Process of Making It, to
be abandoned.
My invention contemplates and has for its primary object the provision of a magnetic-core material in the form of ultra-thin tape characterized by rectangular hysteresis loops. This and other objects of the invention which will be apparent to the skilled Worker in the art upon reading these specifications, I accomplish by that procedure and in those alloys of which I shall hereinafter disclose exemplary embodiments.
The figure is a typical direct current hysteresis loop of my new material illustrating the degree of rectangularity achieved with magnetic tape of .25 mil thickness.
Magnetic materials having square hysteresis loops have hitherto been found of value in various fields, such as the field of mechanical rectification of alternating currents and the field of magnetic amplification. Hysteresis loop tests using direct current testing equiment are well known. A material is said to have a square hysteresis loop if, in such tests, it exhibits a high ratio of residual induction (Br) to maximum induction (Bm). The Br/Bm ratio for a given material is not a single value, but varies with the peak magnetizing force and passes through a maximum as saturation is approached. While the terms square or rectangular as applied to hysteresis loops may be susceptible of wide interpretation, the materials to which this invention is addressed have greater utility the higher the maximum Br/Bm ratio becomes; and in general I contemplate materials having Br/Bm ratio greater than .90.
States Patent excessive at the ultra-thin gauges required. Any increase in coercive force is undesirable, since it necessitates an increase in the exciting current, which may exceed that available.
I have made the discovery that an alloy of the 4% Mo79% Ni type, which has a coercive force inherently lower than the other materials useful for this purpose, can be made to have a rectangular hysteresis loop at thicknesses less than one mil by proper processing, which will be described hereinafter. This Was entirely unexpected as, unlike the other materials used, the 4% Mo-'79% Ni alloy does not exhibit a rectangular loop in the heavier gauges. As pointed out hereinafter, some departure from these content values is permissible; but the terms 4% Mo79% Ni or 4-79" are convenient expressions, used herein, for indicating the general type of alloy with which. I am concerned.
This discovery makes it possible to achieve much higher rates of magnetization and shorter switching times Without sacrificing rectangularity of the hysteresis loop or low coercive force. This is achieved not only by reduction in gauge, but also by the higher volume resistivity and other factors not completely understood.
Therefore, a specific object of this invention is the provision of magnetic alloys of high direct current permeability at inductions approaching saturation, characterized by low coercive force, in very thin sections of high resistivity, such that eddy current effects are minimized, and characterized in such thin sections by a high Br/Bm ratio. The most important factors involved in the provision of such material appear to be (1) composition, (2) thickness of the ultimate material, (3) the nature of the final heat treatment as respects time, temperature and annealing atmosphere, and (4) processing as respects cold rolling, intermediate anneals and the like.
, These factors are stated in the order of their apparent High speed digital computing machines have been built I using electronic vacuum tubes. While such machines are capable of solving problems of prodigious length and complexity, a serious disadvantage is to be found in the possibility of unpredictable tube failure, making rechecking impossible even though an error is known. The advent of grain oriented 48% nickel-iron alloys characterized by rectangular hysteresis loops suggested the possibility of using saturable-reactor cores to replace electronic tubes in the memory units of such computers. Successful memory units have been made using the 48% nickel-iron material having rectangular hysteresis loops in thicknesses as low as /2 mil.
Recent developments in digital computers as well as other electronic devices have necessitated higher rates of magnetization or shorter switching times within the cores than were possible with previously available magnetic tapes one mil in thickness. Since increasing the rate of magnetization is dependent upon reducing eddy currents, rolling the magnetic tape to thinner gauges would be indicated. The difiiculty here is that in materials previously known, in which rectangular loops could be produced for this purpose, such as grain oriented 3% silicon-iron and grain oriented 48% nickel-iron, the coercive force increases rapidly with decreasing thickness and becomes importance as respects the securing of rectangular hysteresis loops when the material is reduced to verry small thicknesses.
As to composition, the alloy from which my new mate rial is made may contain from to 85% nickel, and from 3 to 6% molybdenum, the balance being primarily iron. Manganese can be used for-deoxidation and to improve hot workability and may range from around .3% to 1%, with around .6% being preferred. Silicon may also be used for deoxidation and preferably will not exceed .3% in the metal.
Sulfur should be as low as possible and preferably less than .005 and lead less than .0O2%. Carbon should be low in amount, namely not more than about .l%. Aluminum should be as low as possible and preferably below .01%, including all forms present. These and other elements ordinarily present as contaminants of the iron, molybdenum, or nickel, so long as they are low in amount, do not appear to affect to any great extent the characteristics with which this application deals.
My preferred allow will contain %1-2% nickel, and 4.0% 33% molybdenum.
Novelty is not claimed in the constitution of the alloy since high permeability alloys within the range stated have hitherto been produced. It has not, however, hitherto been known that such a high Br/Bm ratio could be produced in such materials.
The alloys can be formed in the electric furnace (using the induction furnace and vacuum melting if desired, although this is not always necessary). Ingots are cast and these are hot rolled to suitable intermediate gauges and prepared for cold rolling. The materials themselves are capable of being cold rolled with very heavy reductions in the absence of intervening annealings; but in the production of very thin materials it is usually easier to,
accomplish the cold rolling reduction in a series of stages. These stages may be widely varied.
Without desiring to limit the invention, an exemplary routing, which can be depended upon to yield my new result, includes the steps of hot rolling the material to a suitable gauge, such as 120 mils; then box annealing it at a temperature of 870 C. in a reducing atmosphere, such as dry hydrogen or dissociated ammonia; cold rolling it to a thickness of 25 mils; open or strand annealing it in a reducing atmosphere at 870 C.; cold rolling it to a thickness Of 1.2 mils; again open annealing it at 870 C. in a reducing atmosphere; and cold rolling it to the final gauge of .25 mil. It is then ready for a final anneal.
An exemplary routing to produce mil material is the same except that the intermediate anneal is practiced at a thickness of .5 mil, after which the strip is rolled directly to .125 mil before final annealing.
These are exemplary routings only, intended for the manufacture of /4 mil and A; mil materials. They can be widely varied even for the production of material of the same final thickness, such as by the omission of the last intermediate anneal. Obviously, it may be varied for the manufacture of stock of other thicknesses, say /2 mil or lighter than /3 mil. The particular sequence of rolling stages and intermediate anneals has been found to be of only secondary importance in producing rectangulari-ty; and this is true also of the number of cold rolling stages by which the material is reduced to final gauge. The reducing annealing atmospheres are to avoid oxidation and pickling.
From the standpoint of securing rectangular hysteresis loops in thin materials of the compositions set forth, there is some advantage in subjecting the material to an intermediate anneal at a gauge which leaves a 70 to 85% reduction still to be accomplished in the final stage of rolling. The use of intermediate anneals also aids materially in softening the material for easier rolling.
The rolling of the materials, at least after they have attained light gauges will, of course, be carried on on suitable precision equipment, which means a rolling mill having very small work rolls and in which deflection of the mill elements transversely of the work piece is minimized. Excellent results can be attained in relatively narrow widths 011 mills of the four-high type where the very small work rolls are backed by backing rolls of large diameter and where means are provided to prevent deflection of the work rolls in the direction of movement of the strip. Where the material is to be handled in wider widths, I prefer to use a mill of the beam backed type such as that shown in Sendzirnir Patent No.
The material treated as described is now in condition to be given its ultimate magnetic characteristics by a final anneal such as that hereinafter described. The material is itself very delicate and difficult to handle. may be treated in bulk to give it the ultimate magnetic characteristics, this ordinarily is not desirable because subsequent operations of handling, slitting, winding into cores and the like will very greatly impair these characteristics. As a consequence, the formation of complete cores with the materials of this invention normally is practiced prior to the final anneal. For this reason and also because the cores themselves are ordinarily quite small and may be made in very large numerical quantities especially for such uses as the memory sections of digital computing machines, the fabrication of the material and the cores and the final anneal will most usually be practiced not by the manufacturer and roller of the material itself, but by his vcndee. Thus the material, treated as hercinabove described, and coiled or otherwise handled in bulk or in sheets, is a commercial article of manufacture even though its primary utility lies in the fact that when it is given a suitable heat treatment, it will develop or possess the characteristics herein set forth as desirable.
While it As indicated, the cores ordinarily made are quite small, those intended for digital computing machine work being frequently no greater in diameter than about /4 in. In my current practice the alloys are rolled to gauge as single strands in a width of about 2 in. employing work rolls of very small diameter. In the formation of the particular exemplary coils, the material, after rolling, is slit into ribbons /8 in. to A in. in width for widening into toroidal cores. Because of the fragile nature of the material itself and of these small cores, which often consist of only a few wraps of the ribbon, it was found advantageous to Wind the cores on tiny ceramic bobbins such as bobbins of steatite. These bobbins, which have lateral flanges, furnish support for the ribbon during annealing and also provide a frame for the copper windings employed in testing and in many instances in the subsequent use of the cores. The convolutions of the metallic ribbon are carefully insulated with a magnesia coating prior to annealing.
The annealing is conducted in a suitable annealing box in an atmosphere predominantly of hydrogen and substantially free of carburizing, sulfuriziug and nitriding impurities. The water vapor should be as low as possible and such that the exit dewpoint will lie below 40 C. and preferably below -50 C. The annealing temperature may range from 750 C. to 1050 C., my preference being for temperatures around 850 to 975 C. when the soaking time is two hours. While my preference is for pure hydrogen, other inert gases may be present in ap preciable quantities. For example, I may employ dissociated ammonia. The nitrogen present is dissociated ammonia does no harm; but any substantial quantity of undissociated ammonia should be avoided because of its nitriding effect.
The preferred annealing temperature represents the optimum balance between maintaining the rectangularity of the hysteresis loop and minimizing the coercive force, in order to obtain the shortest possible switching time with adequate signal-to-noice ratio under pulse excitation. This balance is necessary because while higher temperatures reduce the coercive force they also reduce the rectangularity.
I have found that it is not necessary to hold the material at the annealing temperature except for a sufficient time to insure that all parts of the charge have come to a uniform temperature. Generally one hour is sufiicicnt for the small cores of this material usually being annealed. A relatively brief soak at full temperature may be tolerated, e. g. one to two hours, but a more prolonged soak should be avoided.
The material may be furnace cooled, which results in a slow cooling throughout the range substantially to room temperature, or it may be quenched from a temperature not substantially lower than 540 C., provided the cooling is carried out in such a manner as to avoid oxidation harmful to magnetic properties, as for example by maintaining the material in an atmosphere of hydrogen.
The annealing temperature range, as well as the moisture content of the annealing atmosphere, are critical, and for best results should not be departed from substantially.
It has been found that this treatment results in a material having excellent magnetic characteristics and a very high Br/Bm ratio and low coercive force in spite of the extreme thinness of the material.
This behavior of the particular alloys of the invention is curious and unexpected. in 3% silicon-iron the coercive force increases substantially in proportion to the reduction in thickness. Reducing the thickness of 48% nickel-iron also increases the coercive force but not as rapidly as is the case with silicon-iron. Reducing the thickness of the 4% Mo-79% Ni alloy not only increases the coercive force appreciably less than in these other materials, but this increase is no longer a limiting factor, as the coercive force of this alloy is so much lower at any gauge. Further, while both with the 3% silicon-iron and the 48% nickel-iron alloys the hysteresis loops can be made quite rectangular at one mil thickness and above, it is not until the thickness is less than one mil that the 4-79 material can be made to exhibit loops of good rectangularity. Hence the high degree of rectangularity of the hysteresis loops which I have obtained in this material at ultra-thin gauges could not have been predicted in advance.
The coercive force in my preferred materials at .25 mil thickness is about .10 oersted when the tip magnetizing force Hm is .25 oersted.
Direct current tests performed on an exemplary material of this invention gave values as follows:
Hm Bm Br Br/Bm H c Oersteds Kilogausses Kilogausses Oersted As has been indicated above, the alloy compositions to which my invention is addressed contain the specified percentages of nickel and molybdenum, the balance being substantially all iron, which may contain normal amounts of impurities or minor amounts of other alloying ingredients whether occurring as impurities or added for workability. It has been further pointed out that these minor amounts of other alloying ingredients do not materially or substantially affect the magnetic characteristics of the materials as discussed herein. As a consequence, in the claims which follow, the expression balance substantially all iron has been employed to be inclusive of such minor amounts of these other alloying ingredients as may be present within the scope of my disclosure.
Modifications may be made in my invention without departing from the spirit of it. Having thus described my invention in certain exemplary embodiments, what I claim as new and desire to secure by Letters Patent is:
1. A process of producing exceedingly thin magnetic alloys having high permeability, low coercive force and rectangular hysteresis loop characteristics, which comprises reducing an alloy containing 80:2% nickel and 4.013% molybdenum, balance substantially all iron, to a thickness less than 1 mil and subjecting the reduced material to an anneal in an atmosphere predominantly of hydrogen and having a dew point below 40 C. at a temperature of substantially 750 to 1050 C.
2. A process of producing exceedingly thin magnetic alloys having high permeability, low coercive force and rectangular hysteresis loop characteristics, which comprises reducing an alloy containing to 85% nickel and 3 to 6% molybdenum, balance substantially all iron, to a thickness less than 1 mil and subjecting the reduced material to an anneal in an atmosphere predominantly of hydrogen and having a dew point below -40 C. at a temperature of substantially 3750" to 1050 C.
3. The process claimed in claim 1 wherein the material is reduced to final gauge from an intermediate hot rolled gauge in a series of stages with intermediate annealings, the last of said stages occurring at a gauge requiring about a 70 to 85% reduction to attain final gauge.
4. The process claimed in claim 1 wherein the final gauge of said material is substantially mil.
5. The process claimed in claim 1 wherein the final gauge of said material is substantially A; mil.
6. The process claimed in claim 2 wherein the material is wound into a toroidal coil in the presence of magnesia as an anneal separator and is supported in toroidal form by an internal heat-resistant support prior to the said final heat treatment.
7. A process of producing a magnetic material of high permeability, low coercive force and of a thickness minimizing eddy current losses at high frequency magnetization, which comprises subjecting an alloy consisting of :L-2% nickel, 4.013% molybdenum, balance substantially all iron, to cold rolling from an intermediate gauge to reduce it to a thickness substantially less than 1 mil with intermediate open annealings, and subjecting the material to a final heat treatment in an atmosphere predominantly of hydrogen at about 850 to 975 C. so as to develop a maximum Br/Bm ratio of at least about .90 when tested with direct current at a magnetization parallel to the direction of rolling.
8. The product produced in accordance with the process of claim 1.
9. The product produced in accordance with the process of claim 2.
References Cited in the file of this patent UNITED STATES PATENTS 1,768,443 Elmen June 24, 1930 2,558,104 Schorschu June 26, 1951 2,631,118 Boothby et al. Mar. 10, 1953
Claims (1)
1. A PROCESS OF PRODUCING EXCEEDINGLY THIN MAGNETIC ALLOYS HAVING HIGH PERMEABILITY, LOW COERCIVE FORCE AND RECTANGULAR HYSTERESIS LOOP CHARACTERISTICS, WHICH COMPRISES REDUCING AN ALLOY CONTAINING 80$2% NICKEL AND 4.0$.3% MOLYBDENUM, BALANCE SUBSTANTIALLY ALL IRON, TO A THICKNESS LESS THAN 1 MIL AND SUBJECTING THE REDUCED MATERIAL TO AN ANNEAL IN AN ATMOSPHERE PREDOMINANTLY OF HYDROGEN AND HAVING A DEW POINT BELOW -40*C. AT A TEMPERATURE OF SUBSTANTIALLY 750* TO 1050*C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US579324A US2783170A (en) | 1956-04-19 | 1956-04-19 | Magnetic material and process of making it |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US579324A US2783170A (en) | 1956-04-19 | 1956-04-19 | Magnetic material and process of making it |
Publications (1)
Publication Number | Publication Date |
---|---|
US2783170A true US2783170A (en) | 1957-02-26 |
Family
ID=24316440
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US579324A Expired - Lifetime US2783170A (en) | 1956-04-19 | 1956-04-19 | Magnetic material and process of making it |
Country Status (1)
Country | Link |
---|---|
US (1) | US2783170A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3086280A (en) * | 1959-06-18 | 1963-04-23 | Western Electric Co | Processing of soft magnetic materials |
US3164496A (en) * | 1956-09-20 | 1965-01-05 | Gen Electric | Magnetic material and method of fabrication |
US3225421A (en) * | 1957-01-04 | 1965-12-28 | Lynch Arnold Charles | Method of making a magnetic core for a magnetic switch |
US3247031A (en) * | 1963-10-14 | 1966-04-19 | Armco Steel Corp | Method of hot rolling nickel-iron magnetic sheet stock |
US3368208A (en) * | 1963-01-30 | 1968-02-06 | Siemens Ag | Information carriers for magnetic destination recording in conveying systems |
US3414430A (en) * | 1962-09-18 | 1968-12-03 | Gevaert Photo Prod Nv | Magnetic signal storing elements comprising a vacuum-evaporated magnetizable coatingapplied to a non-magnetic supporting member provided with an elastomeric adhesive layer |
US4854906A (en) * | 1987-12-02 | 1989-08-08 | Zenith Electronics Corporation | Material, and assemblies for tensioned foil shadow masks |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1768443A (en) * | 1930-06-24 | Percent molybdenum | ||
US2558104A (en) * | 1949-02-23 | 1951-06-26 | Allegheny Ludlum Steel | Procedure for making nickel-iron alloys having rectangular hysteresis loops |
US2631118A (en) * | 1949-12-21 | 1953-03-10 | Bell Telephone Labor Inc | Method of producing soft magnetic materials |
-
1956
- 1956-04-19 US US579324A patent/US2783170A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1768443A (en) * | 1930-06-24 | Percent molybdenum | ||
US2558104A (en) * | 1949-02-23 | 1951-06-26 | Allegheny Ludlum Steel | Procedure for making nickel-iron alloys having rectangular hysteresis loops |
US2631118A (en) * | 1949-12-21 | 1953-03-10 | Bell Telephone Labor Inc | Method of producing soft magnetic materials |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3164496A (en) * | 1956-09-20 | 1965-01-05 | Gen Electric | Magnetic material and method of fabrication |
US3225421A (en) * | 1957-01-04 | 1965-12-28 | Lynch Arnold Charles | Method of making a magnetic core for a magnetic switch |
US3086280A (en) * | 1959-06-18 | 1963-04-23 | Western Electric Co | Processing of soft magnetic materials |
US3414430A (en) * | 1962-09-18 | 1968-12-03 | Gevaert Photo Prod Nv | Magnetic signal storing elements comprising a vacuum-evaporated magnetizable coatingapplied to a non-magnetic supporting member provided with an elastomeric adhesive layer |
US3368208A (en) * | 1963-01-30 | 1968-02-06 | Siemens Ag | Information carriers for magnetic destination recording in conveying systems |
US3247031A (en) * | 1963-10-14 | 1966-04-19 | Armco Steel Corp | Method of hot rolling nickel-iron magnetic sheet stock |
US4854906A (en) * | 1987-12-02 | 1989-08-08 | Zenith Electronics Corporation | Material, and assemblies for tensioned foil shadow masks |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP7028290B2 (en) | Manufacturing method of nanocrystal alloy magnetic core | |
US4314594A (en) | Reducing magnetic hysteresis losses in cores of thin tapes of soft magnetic amorphous metal alloys | |
US4150981A (en) | Glassy alloys containing cobalt, nickel and iron having near-zero magnetostriction and high saturation induction | |
US4298409A (en) | Method for making iron-metalloid amorphous alloys for electromagnetic devices | |
JPS6034620B2 (en) | Amorphous alloy with extremely low iron loss and good thermal stability | |
JPS6130404B2 (en) | ||
JPS6056203B2 (en) | Method for manufacturing non-oriented silicon steel sheet with excellent magnetic properties in the rolling direction | |
US5338376A (en) | Iron-nickel based high permeability amorphous alloy | |
US2783170A (en) | Magnetic material and process of making it | |
JPS58139408A (en) | Wound iron core | |
JPS6362579B2 (en) | ||
JP2006045660A (en) | Fe-BASED AMORPHOUS ALLOY THIN STRIP AND MAGNETIC CORE | |
JP3434844B2 (en) | Low iron loss, high magnetic flux density amorphous alloy | |
US5658397A (en) | Iron-based amorphous alloy thin strip and transformers made therefrom | |
US2875114A (en) | Iron-aluminum materials for magnetic applications | |
US4054470A (en) | Boron and copper bearing silicon steel and processing therefore | |
US4082580A (en) | Iron-nickel-molybdenum alloy having improved stability and high initial permeability | |
US1818054A (en) | Magnetic material | |
JPS5833303B2 (en) | iron-nickel alloy | |
JP4207310B2 (en) | Magnetic steel wire with excellent iron loss characteristics and workability | |
US4269634A (en) | Loss reduction in oriented iron-base alloys containing sulfur | |
US2085118A (en) | Magnetic material and manufacture thereof | |
JPH0811818B2 (en) | Heat treatment method for toroidal amorphous magnetic core | |
US1801150A (en) | Magnetic material | |
JPS5942069B2 (en) | Method for manufacturing amorphous alloy with high effective magnetic permeability |