US3868278A - Doubly oriented cobalt iron alloys - Google Patents

Doubly oriented cobalt iron alloys Download PDF

Info

Publication number
US3868278A
US3868278A US401766A US40176673A US3868278A US 3868278 A US3868278 A US 3868278A US 401766 A US401766 A US 401766A US 40176673 A US40176673 A US 40176673A US 3868278 A US3868278 A US 3868278A
Authority
US
United States
Prior art keywords
percent
alloy
cobalt
alloys
iron
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
US401766A
Inventor
Karl Foster
Donald R Thornburg
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.)
CBS Corp
Original Assignee
Westinghouse Electric 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 Westinghouse Electric Corp filed Critical Westinghouse Electric Corp
Priority to US401766A priority Critical patent/US3868278A/en
Priority to US05/532,284 priority patent/US3977919A/en
Application granted granted Critical
Publication of US3868278A publication Critical patent/US3868278A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/12Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/10Ferrous alloys, e.g. steel alloys containing cobalt

Definitions

  • ABSTRACT An alloy and process are described for obtaining improved magnetic characteristics in iron-cobalt alloys.
  • the iron-cobalt alloys described are characterized by a cube-on-face texture, primary recrystallized and normal grain growth microstructure. Processes are described which include both a single stage cold working and a multiple stage cold working in order to obtain the desired texture in the finished alloy.
  • the present invention relates to iron-cobalt alloys especially those iron-cobalt alloys containing between 5 and 35 percent cobalt and which do not undergo an order-disorder transformation phenomenon during heat treatment.
  • the alloy is characterized by a cube-on-face texture which may be described in terms of Miller Indicies as (100) [001] and which also has a primary recrystallized microstructure and normal grain growth.
  • the process for obtaining such cube texture involves either a single or a multiple cold working and the alloys which are produced therefrom find particular use as a magnetic core material for aircraft generators where such rotating machinery is improved by the magnetic laminations having a double orientation of the grain structure.
  • Alloys in the to 30 percent cobalt range which have saturation values similar to the 50 percent cobaltiron, can be much more readily processed.
  • these alloys do not normally possess an oriented structure as commercially produced and consequently, high inductions at low field strengths have not been previously observed in these alloys because of their high positive anisotropy values.
  • the present invention alleviates the shortcomings of the prior art compositions and provides an alloy and a method for manufacturing the same which results in the attainment of a useful degree of cube texture or double orientation in cobalt-iron alloys having between about 5 percent and about 35 percent cobalt which alloys can be most easily cold worked.
  • the present alloy leads to higher operating inductions than can now be obtained in the cube oriented 3% percent silicon-iron alloys or in the non-oriented alloys with similar cobalt contents.
  • the present invention relates to an iron-cobalt alloy which contains between about 5 percent and about 35 percent cobalt, up to 9 percent of at least one of the volume resistivity improving elements and the balance iron with incidental impurities. It is also preferred to maintain the manganese content at less than about 0.3 percent and the carbon content not in excess of 0.03 percent.
  • the alloy when manufactured in accordance with one of the two preferred methods to be set forth hereinafter will exhibit at least 50 percent by volume of the grains having a texture in which the plane is oriented within about 10 of the alloy surface and at least 50 percent of the oriented grains have an [001] direction aligned within 10 of the rolling direction.
  • FIG. 1 is a photo micrograph taken at a magnification of 100X of the surface of an alloy of the present invention illustrating a primary recrystallized microstructure, and;
  • FIG. 2 is a photo micrograph taken at a magnification of 100X of a cross-section of the same alloy further illustrating the microstructure similar to FIG. 1.
  • the alloy of thepresent invention may be essentially described as a binary iron-cobalt alloy in which the cobalt content is maintained with the range between about 5 percent and about 35 percent, the balance being essentially iron with incidental impurities.
  • the alloy preferably contains less than about 0.3 percent manganese, less than about 0.03 percent carbon and less than about 0.01 percent sulphur.
  • at least one other volume resistivity improving element may be added to the essentially binary iron-cobalt composition.
  • this may inelude up to about 1 percent silicon, up to about 1 percent vanadium, up to about 0.5% molybdenum and not over 0.30 percent chromium.
  • the chromium While silicon, vanadium and molybdenum perform the known function of improving the volume resistivity it is highly imperative that the chromium, which also improves volume resistivity, does not exceed 0.3 percent by weight. It hasbeen found that where the chromium content is in excess of about 0.3 percent, while improved volume resistivity is attained, the chromium is highly deleterious to the formation of the doubly oriented, or cube-on-face texture, or a (100) [001] grain orientation.
  • the cobalt content may be as low as 5 percent in order to obtain improved saturation values it is preferred to have a minimum of at least 8 percent and preferably the cobalt should the present within the range between about 18 percent and about 27 percent by weight in order to attain a saturation value which approaches that of the 50 percent cobalt-iron alloy. While amounts of cobalt between about 27 percent and 35 percent will produce a small increase in the saturation value the use of the higher amounts of cobalt is costly, and in the event a combination of other factors are present, this may result in the alloy exhibiting an orderdisorder transformation phenomenon which can prove to be highly deleterious to high degrees of cold work which are imperative for attaining the desired cubic texture in the alloy of the present invention.
  • the alloy of the present invention when manufactured according to one of the processes set forth hereinafter will in its finished form exhibit at least 50 percent of the volume of the'grains having a texture in which the (100) plane is oriented within 10 of the alloy surface and at least 50 percent of the oriented grains having a [001] direction aligned within 10 of the rolling direction. It has been found that as much as 70 and sometimes 80 percent by volume of the microstructure of the alloy will exhibit the (100) plane in the alloy surface aligned within of the [001] direction.
  • the alloy which is manufactured in accordance with the teachings of the present invention is preferably melted employing vacuum technology for attaining the desired degree of purity which is conducive to the formation of the proper texture development.
  • the components may be vacuum induction melted and thereafter cast into ingots which are hot rolled to a convenient intermediate gauge usually between about 0.075 and about 0.200 inch in thickness.
  • the alloy is annealed for a time period of up to about eight hours and preferably for" a time period of about five hours at a temperature within the range between about 850C and the Ac, temperature of the particular alloy which has been melted and hot rolled.
  • a temperature within the range between about 850C and the Ac temperature of the particular alloy which has been melted and hot rolled.
  • the alloy, following hot rolling is anncaled for a time period of about five hours and at a temperature of about 900C.
  • the cold working operation must effect a reduction in the cross sectional area of at least 75 percent from the hot worked gauge to the finished gauge of the material.
  • a suitable schedule within said Process A would include not rolling the ingot to an intermediate gauge of about 0.080 inch which material is thereafter pickled, annealed for five hours at a temperature of 850C in dry hydrogen and then cold rolled to a finished gauge in the range between 0.01 l and 0.012 inch. While it will be appreciated that the final gauge material may be lighter as well as heavier than this thickness, the lighter gauges being down to /sth mil and the heavier gauges may be, for example, about 0.014 inch, the preferred final gauge material will have a thickness within the range between about 0.006 inch and about 0.012 inch, i.e. nominally 6 mil and 12 mil material.
  • the alloys are once again subjected to a final heat treatment at a temperature within the range between about 850C and the Ac, temperature of the alloy for a time period of between about 24 and about 48 hours, the alloy being subjected to a protective atmosphere of dry hydrogen or other suitable protective gas during said final heat treatment.
  • a magnetic field having a strength of between about 5 and about 50 oersted may be employed in order to develop improved magnetic characteristics in the final alloy.
  • the use of a magnetic field does not per se contribute too the cube texture development exhibited by the alloys of the present invention.
  • the hot work material for example having a thickness of about 0.150 inch in thickness is annealed, for example, at 900C for a time period of 5 hours and in an atmosphere of dry hydrogen, that is, hydrogen having a dew point of less than about 40F.
  • the hot worked material which has been annealed is thereafter pickled and subjected to a cold working such initial cold working preferably exceeding a value of about 75 percent reduction in the cross sectional area. This may be done in one or more steps and it is comtemplated that a hot-cold working may be employed especially where higher amounts of cobalt are employed such hot-cold working taking place at a temperature not in excess of about 300C. Hot-cold working,
  • a cold working at temperatures above room temperature and the recrystallization temperature of the alloy typically at temperatures in the range between about 200C and 300C.
  • the cold working which effects preferably at least a 75 percent reduction in the cross sectional area is followed by an annealing heat treatment once again at a temperature within the range between about 850C and the Ac temperature, it having been found that annealing the intermediate gauge material for about 5 hours at 900C has given excellent results.
  • This annealing treatment is also conducted in an atmosphere of dry hydrogen. Thereafter the material may be again cold worked to finish gauge in one or more operations.
  • the material is then subjected to a final heat treatment at a temperature within the range between about 850C and the Ac, temperature for obtaining the desired crystallographic orientation.
  • a final heat treatment at a temperature within the range between about 850C and the Ac, temperature for obtaining the desired crystallographic orientation.
  • the microstructure is characterized by a primary recrystallization which exhibits normal grain growth as will appear more fully hereinafter.
  • Epstein samples and one inch torque discs from the alloys so processed were annealed for 24 to 48 hours at 900 to 950C in dry hydrogen. All samples except alloy M900 were strip annealed at 800C prior to the final anneal. The M900 samples were put into the furnace at temperature.
  • Table II which includes the torque and magnetic test data for the various alloys set forth in Table I and as processed by the different methods as set forth hereinbefore.
  • the silicon iron alloys are normally annealed at 1200C to obtain secondary recrystallization and purification and while all annealing of the cobaltiron alloys is normally done below the A y transformation temperature of about 950C, that is the Ac, temperature, no. secondary recrystallization was observed in any of the cobalt-iron alloys listed in the table.
  • the torque curve data given for the CUBEX material are for the (100) [001] single crystal and the peak torque values are nearly the same for both the (100) [001] and the l [001] textures in silicon iron.
  • the main difference in the torque curve is in the peak ratios.
  • the peak ratio is the absolute value of the small peaks divided by the absolute value of the large peaks. or in the case of the oriented (110) [001] composition the peak ratio for perfect orientation is about 0.34.
  • the (100) [001] torque curve has four equal peaks thereby resulting in a peak ratio of 1.0 for a perfect orientation of the CUBEX'brand material.
  • the commercial HlPERCO 27 brand alloy had no measurable torque peaks and a low B value thereby indicating no appreciable degree of grain orientation or texture exhibited thereby.
  • Alloy M856 which had neither manganese nor chromium additions had no measurable torque peaks for Process 1 and low peaks for Process 2 indicating that without the presence of at least one of these elements good cube texture development is not obtained.
  • the chromium content exceeds about 0.8 percent as will be shown more clearly hereinafter rather than forming good cube texture the alloy has a tendency to be formed with the cube-on-edge orientation.
  • Alloy M859 which had an addition of sulfur demonstrated a high peak torque value and a high peak ratio for Process 1 but a low peak torque value for Process 2 indicating that the double orientation process is not as critical with regard to the sulphur content as is the l 10) [001] texture formation.
  • Alloy M883 is of particular interest because Process 1 and 2 result in very similar peak torque values and almost identical magnetic properties in the rolling direction with quite different torque ratios.
  • Alloy M900 was the only alloy treated by Process 3 which resulted in the same peak ratio as Process 1 together with a higher peaktorque value indicating a high degree of double or cube-on-face orientation. Since the B value for alloy M900 employing Process 3 measured in the rolling direction is higher than tht of commercial cube-on-edge silicon-iron and much higher than the 27 percent cobalt alloy, the degree of final cold reduction appears to .play a major role in determining whether doubly oriented, that is cube-on-face orientation, or the singly oriented cube-on-edge texture is formed. Consequently two or more large cold reductions result in an optimum process for the formation of double orientation in cobalt-iron alloys.
  • Alloy M901 was melted with the same nominal composition namely about 27.4 percent cobalt, about 0.15 percent manganese, about 0.03 percent carbon and the balance iron.
  • This alloy was hot rolled to 0.180 inch in thickness and annealed 5 hours at 900C in dry hydrogen, cold rolled, the first step occurring at a temperature of 300C to 0.080 inches, annealed for a time period of 7 hours at 900C and again cold rolled, the initial step being to a thickness of 0.040 inches and at a temperature of 300C and thereafter at room temperature to a final gauge of 0.012 inches.
  • Torque discs, Epstein samples and punched rings the latter having a threeinch outside diameter by 2% inch inside diameter were annealed for 48 hours at 900C.
  • the material demonstrated a peak torque value of 130,700 ergs/cm and a peak ratio of 0.89 indicating a high degree of doubly oriented or cube-on-face texture.
  • Domain analysis indicated 79 percent by volume of the grains were within 12 of the (100) and 11 percent by volume of the grains were within 12 of the (110); 78 percent of the grains had a [100] direction within of the rolling direction and 88 percent within 15.
  • Table V contains the nominal chemical composition of the alloys so made and tested together with the volume resistivity as exhibited by each of the alloys.
  • the resistivity data set forth in Table V shows a fairly sharp decrease in resistivity with increasing cobalt content in this range for essentially binary alloys.
  • the 0.6 percnet chromium addition increased the resistivity and tended to make it more constant with increasing cobalt content. It is for this reason that chromium is added to commercial l-lIPERCO 27 brand alloy to reduce high frequency losses.
  • the alloys set forth in Table V were hot rolled to 0.180 inch in thickness, annealed 5 hours at 900C in dry hydrogen cold rolled to 0.080 inches in thickness, annealed 5 hours at 900C in dry hydrogen and cold rolled to a finish gauge of 0.012 inches in thickness.
  • Torque and Epstein samples in the rolling direction were strip annealed for about five minutes at 850C and then reannealed for 48- hours at 900C in dry hydrogen.
  • alloy M 904 with a nominal composition of 25.4 percent cobalt, 0.6 percent chromium, 0.15 percent manganese, 0.03 percent carbon and the balance essentially iron was melted and-tested.
  • This alloy was hot rolled to 0.180 inch in thickness, annealed 5 hours at 900C in dry hydrogen, cold rolled with the initial step being at a temperature of 300C to 0.040 inch in thickness, annealed one hour at 900C in dry hydrogen, and cold rolled to 0.004 inch in thickness final gauge.
  • the finished material was annealed for 48 hours at 900C and exhibited a maximum torque value of 128,000 ergs/cm" and a peak ratio of 0.48, indicating a high degree of (1 [001] texture.
  • a tape of this material was strip annealed for about 5 minutes at 815C, coated with alumina, wound into a core and annealed 24 hours at 900C with the following properties. i
  • FIGS. 1 and 2 it is observed that the structure so produced by the process of the present invention exhibits equiaxed grains and of normal grain growth.
  • FIG. 1 closely illustrates a primary recrystallized mocrostructure.
  • Examination of FIG. 2 which is a cross-section of the alloy of FIG. 1, reveals that normal grain growth has occurred. This results from the fact that the grains do not extend completely through the thickness of the alloy as is the observation in secondarily recrystallized microstructures.
  • An alloy member which exhibits improved permeabilities at low field strengths resulting from crystallographic orientation compared to unoriented magnetic material of the same chemical composition consisting essentially of from about 5 percent to about 35 percent cobalt, less than 0.3 percent chromium, up to 0.3 percent manganese, up to 3 percent silicon, less than 0.03 percent carbon and the balance iron with incidental impurities, said alloy having a primary recrystallized microstructure in which a major proportion of the grains exhibit a texture within 10 of the surface of the alloy and in which a major proportion of the oriented grains have cube or edges of their crystal lattices aligned within 10 of the rolling direction.
  • An alloy member which exhibits improved permeabilities at low field strengths resulting from crystallographic orientation compared to unoriented magnetic material of the same chemical composition consisting essentially of from about 5 percent to about 35 percent cobalt, at least one volume resistivity improving element selected from the group of up to 2 percent silicon, up to 1 percent vanadium. up to about 0.5 percent molybdenum, less than 0.3 percent chromium and mixtures thereof, less than 0.03 percent carbon and the balance iron with incidental impurities, the alloy having a primary recrystallized microstructure in which at least 50 percent by volume of the grains exhibit an orientation in which the (100) plane is oriented within 10 of the alloy surface and at least 50 percent of the oriented grains are within 10 of the rolling direction.

Abstract

An alloy and process are described for obtaining improved magnetic characteristics in iron-cobalt alloys. The iron-cobalt alloys described are characterized by a cube-on-face texture, primary recrystallized and normal grain growth microstructure. Processes are described which include both a single stage cold working and a multiple stage cold working in order to obtain the desired texture in the finished alloy.

Description

United States Patent 11 1 Foster et a1.
11] 3,868,278 1 Feb. 25, 1975 1 DOUBLY ORIENTED COBALT IRON ALLOYS [75] Inventors: Karl Foster; Donald R. Thornburg,
both of Pittsburgh, Pa.
[73] Assignee: Westinghouse Electric Corporation,
Pittsburgh, Pa.
22 Filed: Sept. 28, 1973 211 Appl. No.: 401,766
Related U.S. Application Data [63] Continuation of Ser. No. 228,070, Feb. 22, 1972,
abandoned.
[52] U.S. Cl l48/3l.55, 75/123 K, 75/170, 148/120,148/121 [51] Int. Cl C04b 35/00 [58] Field of Search ..148/120,121,110,111, 148/112, 31.55, 3157; 75/123 K, 123 L, 170
[56] References Cited UNITED STATES PATENTS [1917 Becket 75/123 K 5/1933 Smith et a1 148131.57 5/1948 Stanley 75/123 K 11/1962 Wawrousek 148/122 3/1964 Foster 148/31.57
OTHER PUBLICATIONS Bozorth, R.; Ferromagnetism; New York, 1951, pp. 190-200.
Primary ExaminerWa1ter R. Satterfield Attorney, Agent, or Firm-R. T. Randig [57] ABSTRACT An alloy and process are described for obtaining improved magnetic characteristics in iron-cobalt alloys. The iron-cobalt alloys described are characterized by a cube-on-face texture, primary recrystallized and normal grain growth microstructure. Processes are described which include both a single stage cold working and a multiple stage cold working in order to obtain the desired texture in the finished alloy.
4 Claims, 2 Drawing Figures DOUBLY ORIENTED COBALT IRON ALLOYS CROSS-REFERENCE TO RELATED APPLICA- TIONS This is a continuation, of application Ser. No. 228,070 filed Feb. 22, 1972 and now abandoned.
The present application is closely related to application Ser. No. 228,071, filed Feb. 22, 1972, application Ser. No. 480,075 filed June 19, 1974 as a Division of Application Serial No. 228,071, application Ser. No. 228,319, filed Feb. 22, 1972, application Ser. No. 228,320, filed Feb. 22, 1972, now abandoned in favor of Continuation-in-Part Application Ser. No. 430,114 filed Jan. 2, 1974, and Application Ser. No- 228,318 filed Feb. 22, 1972, the latter application being now abandoned in favor of Continuation-in-Par t Application Ser. No. 312,681 filed Dec. 11, 1972.
BACKGROUND OF THE INVENTION 1. Field of the Invention:
The present invention relates to iron-cobalt alloys especially those iron-cobalt alloys containing between 5 and 35 percent cobalt and which do not undergo an order-disorder transformation phenomenon during heat treatment. The alloy is characterized by a cube-on-face texture which may be described in terms of Miller Indicies as (100) [001] and which also has a primary recrystallized microstructure and normal grain growth. The process for obtaining such cube texture involves either a single or a multiple cold working and the alloys which are produced therefrom find particular use as a magnetic core material for aircraft generators where such rotating machinery is improved by the magnetic laminations having a double orientation of the grain structure.
2. Description of the Prior Art:
Great effort has been expended in recent years particularly in the aerospace industry to produce smaller and lighter weight electrical equipment. This has led to increased operating inductions in the magnetic core materials of aircraft electrical generators where, in some designs, cube or doubly oriented silicon steel has replaced nonoriented silicon steel.
Current and future advanced designs are contemplating the use of a 50 percent cobalt-iron alloy which is presently being marketed by the Westinghouse Electric Corporation under-"the trademark HIPERCO 50. This alloy permits higher operating inductions than the 3% percent silicon iron because of its higher saturation value, namely about 24,000 gauss, as well as the low magnetocrystalline anisotropy. However, one of the main deterrents to wider use of the 50 percent cobaltiron alloy is its high cost arising from the 50 percent cobalt content and the difficulty in cold rolling this alloy resulting from the fact that iron-cobalt alloys containing in excess of about 35 percent cobalt undergo, during heat treatment, a transformation phenomenon which is known as an order-disorder phenomenon. This transformation results in the production of an exceedingly brittle material which poses an extreme amount of difficulty in cold working. In order to suppress this transformation phenomenon and its resulting brittleness, elaborate steps must be taken to quench the ironcobalt alloy, containing in excess of 35 percent cobalt, in ice brine before the material has a chance to transform.
Alloys in the to 30 percent cobalt range, which have saturation values similar to the 50 percent cobaltiron, can be much more readily processed. However, these alloys do not normally possess an oriented structure as commercially produced and consequently, high inductions at low field strengths have not been previously observed in these alloys because of their high positive anisotropy values.
The present invention alleviates the shortcomings of the prior art compositions and provides an alloy and a method for manufacturing the same which results in the attainment of a useful degree of cube texture or double orientation in cobalt-iron alloys having between about 5 percent and about 35 percent cobalt which alloys can be most easily cold worked. The present alloy leads to higher operating inductions than can now be obtained in the cube oriented 3% percent silicon-iron alloys or in the non-oriented alloys with similar cobalt contents.
SUMMARY OF THE INVENTION The present invention relates to an iron-cobalt alloy which contains between about 5 percent and about 35 percent cobalt, up to 9 percent of at least one of the volume resistivity improving elements and the balance iron with incidental impurities. It is also preferred to maintain the manganese content at less than about 0.3 percent and the carbon content not in excess of 0.03 percent. The alloy when manufactured in accordance with one of the two preferred methods to be set forth hereinafter will exhibit at least 50 percent by volume of the grains having a texture in which the plane is oriented within about 10 of the alloy surface and at least 50 percent of the oriented grains have an [001] direction aligned within 10 of the rolling direction. This is accomplished by employing either a single stage cold working process with a large cold reduction or a two stage cold reduction process with at least the final step employing a relatively large cold reduction. In addition a cube-on-edge orientation can also be developed by employing the same processes but including from 0.3 percent to about 1.5 percent chromium in the iron-cobalt alloy. The specific processes will be set forth more fully hereinafter.
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a photo micrograph taken at a magnification of 100X of the surface of an alloy of the present invention illustrating a primary recrystallized microstructure, and;
FIG. 2 is a photo micrograph taken at a magnification of 100X of a cross-section of the same alloy further illustrating the microstructure similar to FIG. 1.
DESCRIPTION OF THE PREFERRED EMBODIMENT The alloy of thepresent invention may be essentially described as a binary iron-cobalt alloy in which the cobalt content is maintained with the range between about 5 percent and about 35 percent, the balance being essentially iron with incidental impurities. In this respect it should be noted that the alloy preferably contains less than about 0.3 percent manganese, less than about 0.03 percent carbon and less than about 0.01 percent sulphur. However, where it is desired to improve the volume resistivity of the alloy of the present invention, at least one other volume resistivity improving element may be added to the essentially binary iron-cobalt composition. Advantageously, this may inelude up to about 1 percent silicon, up to about 1 percent vanadium, up to about 0.5% molybdenum and not over 0.30 percent chromium.
While silicon, vanadium and molybdenum perform the known function of improving the volume resistivity it is highly imperative that the chromium, which also improves volume resistivity, does not exceed 0.3 percent by weight. It hasbeen found that where the chromium content is in excess of about 0.3 percent, while improved volume resistivity is attained, the chromium is highly deleterious to the formation of the doubly oriented, or cube-on-face texture, or a (100) [001] grain orientation.
While the cobalt content may be as low as 5 percent in order to obtain improved saturation values it is preferred to have a minimum of at least 8 percent and preferably the cobalt should the present within the range between about 18 percent and about 27 percent by weight in order to attain a saturation value which approaches that of the 50 percent cobalt-iron alloy. While amounts of cobalt between about 27 percent and 35 percent will produce a small increase in the saturation value the use of the higher amounts of cobalt is costly, and in the event a combination of other factors are present, this may result in the alloy exhibiting an orderdisorder transformation phenomenon which can prove to be highly deleterious to high degrees of cold work which are imperative for attaining the desired cubic texture in the alloy of the present invention.
The alloy of the present invention when manufactured according to one of the processes set forth hereinafter will in its finished form exhibit at least 50 percent of the volume of the'grains having a texture in which the (100) plane is oriented within 10 of the alloy surface and at least 50 percent of the oriented grains having a [001] direction aligned within 10 of the rolling direction. It has been found that as much as 70 and sometimes 80 percent by volume of the microstructure of the alloy will exhibit the (100) plane in the alloy surface aligned within of the [001] direction.
The alloy which is manufactured in accordance with the teachings of the present invention is preferably melted employing vacuum technology for attaining the desired degree of purity which is conducive to the formation of the proper texture development. In this respect the components may be vacuum induction melted and thereafter cast into ingots which are hot rolled to a convenient intermediate gauge usually between about 0.075 and about 0.200 inch in thickness.
Following hot rolling, which is done employing conventional equipment and conventional techniques, the alloy is annealed for a time period of up to about eight hours and preferably for" a time period of about five hours at a temperature within the range between about 850C and the Ac, temperature of the particular alloy which has been melted and hot rolled. In no event should such heat treatment take place at a temperature in excess of the Ac, temperature and while lower temperatures can be employed it will become apparent that longer time periods are required for the annealing process. Accordingly, optimum results appear to be obtained where the alloy, following hot rolling, is anncaled for a time period of about five hours and at a temperature of about 900C.
During such annealing heat treatment it is preferred to maintain a protective atmosphere around the alloy and for this reason hydrogen having a dew point of less than about -40C is employed. Thereafter the alloy is cooled to room temperature while maintaining such protective atmosphere and the alloy is then ready for cold working in one of two preferred ways, indicated as Process A and Process B hereinafter.
Process A:
In this method of manufacturing iron-cobalt alloys for producing a cube texture as described herein before, it is preferred to cold work the hot rolled material in one stage or operation without interposing any intermediate heat treatment therebetween. While one operation is desired it will be appreciated that such cold working may involve three or four steps in order to attain the required degree of cold working and such three to four steps are envisaged within the term one cold working operation." Thus, it may be necessary to pass the alloy in a cold rolling mill between the rolls three or four times in order to attain the desired degree of reduction in the cross sectional area but the same is included within the term one cold working operation."
In this Process A, the cold working operation must effect a reduction in the cross sectional area of at least 75 percent from the hot worked gauge to the finished gauge of the material. A suitable schedule within said Process A would include not rolling the ingot to an intermediate gauge of about 0.080 inch which material is thereafter pickled, annealed for five hours at a temperature of 850C in dry hydrogen and then cold rolled to a finished gauge in the range between 0.01 l and 0.012 inch. While it will be appreciated that the final gauge material may be lighter as well as heavier than this thickness, the lighter gauges being down to /sth mil and the heavier gauges may be, for example, about 0.014 inch, the preferred final gauge material will have a thickness within the range between about 0.006 inch and about 0.012 inch, i.e. nominally 6 mil and 12 mil material.
Following cold working to finish gauge the alloys are once again subjected to a final heat treatment at a temperature within the range between about 850C and the Ac, temperature of the alloy for a time period of between about 24 and about 48 hours, the alloy being subjected to a protective atmosphere of dry hydrogen or other suitable protective gas during said final heat treatment. During said final heat treatment it is also comtemplated that a magnetic field having a strength of between about 5 and about 50 oersted may be employed in order to develop improved magnetic characteristics in the final alloy. However, the use of a magnetic field does not per se contribute too the cube texture development exhibited by the alloys of the present invention.
Process B:
In this method of manufacturing the iron-cobalt alloys of the present invention at least two cold working operations are envisaged. Consequently the starting material may be ofa much heavier gauge from that employed in Process A. In this respect while two cold reductions are envisaged each of which effects a substantially large reduction, it is imperative that the second or last of the cold working operations in which the material is cold worked to finish gauge following an annealing after a prior cold working, must effect a reduction in the cross sectional area in excess of about percent from the area of the previous gauge material. Thus for example, if the prior cold working produces a material having a thickness of 0.060 inch which material is thereafter annealed, a suitable final cold reduction would produce a material having a thickness of about 0.012 inch in thickness thus resulting in a final cold reduction of 80 percent of that from the cross-sectional area of the previous gauge material. In Process B the hot work material for example having a thickness of about 0.150 inch in thickness is annealed, for example, at 900C for a time period of 5 hours and in an atmosphere of dry hydrogen, that is, hydrogen having a dew point of less than about 40F. While higher temperatures as well as lower temperatures may be employed for the intermediate annealing once again the limitation is placed that the material does not become heated to a temperature in excess of the AC1 temperature in order to obtain a cube textured material characterized by a primary recrystallized microstructure which exhibits normal grain growth as opposed to some prior art materials.
The hot worked material which has been annealed is thereafter pickled and subjected to a cold working such initial cold working preferably exceeding a value of about 75 percent reduction in the cross sectional area. This may be done in one or more steps and it is comtemplated that a hot-cold working may be employed especially where higher amounts of cobalt are employed such hot-cold working taking place at a temperature not in excess of about 300C. Hot-cold working,
as that term is used herein, contemplates a cold working at temperatures above room temperature and the recrystallization temperature of the alloy, typically at temperatures in the range between about 200C and 300C. The cold working which effects preferably at least a 75 percent reduction in the cross sectional area is followed by an annealing heat treatment once again at a temperature within the range between about 850C and the Ac temperature, it having been found that annealing the intermediate gauge material for about 5 hours at 900C has given excellent results. This annealing treatment is also conducted in an atmosphere of dry hydrogen. Thereafter the material may be again cold worked to finish gauge in one or more operations.
It should be noted however that where more than one operation is performed on the material to reduce the same to finish gauge such operation must be conducted so that the final reduction of the material to finish gauge effects a reduction in the cross sectional area of at least 75 percent. In each of the cold working operations heretofore described in Process B it is envisaged that at the initial step in the cold working operation may take place at an elevated temperature not in excess of about 300C. Thus it has been found that where material which is annealed for five hours at 900C in dry hydrogen and having a hot gauge of 0.060 inch may be cold rolled at a temperature of about 260C to a thickness of about 0.040 inch and thereafter without any intermediate heat treatment the cold working is continued to attain a desired finish gauge of about 0.012 inch in thickness. The material is then subjected to a final heat treatment at a temperature within the range between about 850C and the Ac, temperature for obtaining the desired crystallographic orientation. As thus processed the microstructure is characterized by a primary recrystallization which exhibits normal grain growth as will appear more fully hereinafter.
Both Process A and Process B above-described may be successfully employed in producing a different type of orientation in essentially iron-cobalt alloys, which orientation has useful magnetic characteristics. Essentially, this orientation is described in terms of Miller indices as l 10) [001] on cube-on-edge texture. In order to obtain the 1 10) [001 texture, the chemical composition of the alloy which is subjected to either Process A or Process B must be altered from that of the basic iron-cobalt alloy containing 5 to 35 percent cobalt. In this respect from about 0.3% to about 1.5% chromium must be added to the essentially binary iron-cobalt alloy containing from 5 to 35 percent cobalt. When the alloy is melted to this composition and fabricated employing either Process A or Process B, the texture obtained is that described as [001 1. Ancillary thereto, the addition of 0.3 to 1.5 percent chromium also improves the volume resistivity.
In order to more clearly demonstrate applicants alloy and processes for manufacture, reference may be had to Table I which illustrates the nominal compositions of a series of alloys made and tested employing the teachings of the present invention.
' The alloys having the composition set forth hereinbefore in Table l were processed employing three different processing schedules. Each of the alloys was induction melted in order to obtain a close control over the alloying components as well as purity of the composition. It is noted from Table I that the values set forth therein are nominal compositions and do not reflect the actual chemical composition of the material. The following listed processes were employed in making the alloys set forth in Table 1. Process 1:
Hot roll ingot to 0.080 inch, pickle, anneal 5 hours at 850C in dry hydrogen, cold roll to 0.011 0.012 inch.
Process 2:
Hot roll ingot to 0.080 inch, pickle, anneal five hours at 850C in dry hydrogen, cold roll to 0.025 inch, an-
neal 5 hours at 850C in dry hydrogen, cold roll to 0.011 0.012 inch. Process 3:
Hot roll ingot to 0.150 inch, anneal five hours at 900C in dry hydrogen, pickle, cold roll at 260C to 0.060 inch, anneal 5 hours 900C in dry hydrogen, cold roll (260C to 0.040 inch) to 0.012 inch.
Epstein samples and one inch torque discs from the alloys so processed were annealed for 24 to 48 hours at 900 to 950C in dry hydrogen. All samples except alloy M900 were strip annealed at 800C prior to the final anneal. The M900 samples were put into the furnace at temperature.
Reference may be had to Table II which includes the torque and magnetic test data for the various alloys set forth in Table I and as processed by the different methods as set forth hereinbefore.
TABLE 11 Properties of Oriented Co-Fe Samples Peak Tor ue Peak 11.. B Alloy Process Anneal (ergs/c in" Ratio (e) (0 $8 Cubex 24 hr 1200C 173,00 1.00 0.06 17,300 19,200 HlpCl'Sll 24 hr 1200C 167,000 0.34 0.1 1 18,300 19,800 Hipereu 27 48 hr 900C 1.70 16,100 21,100 M841 l 24 hr 900C 85,600 0.84 0.47 18,500 21,500 M844' 1 24 hr 900C 61,100 0.79 0.54 17,400 20,600 M844' 2 24 hr 900C 83,600 0.42 0.50 18,000 21,100 M85!) 1 24 hr 950C M856 2 24 hr 950'? 33,500 0.42 M85) 1 24 ltr 950C 99,600 0.81 M515! 2 24 hr I00"( 33,000 0.55 M88. 1 40 hr 140"(' 99,300 0.81 0.46 18,300 21,600 M104 2 40 hr 940% 106,800 0.43 0.46 18,500 21,600 M887 1 40 hr 940C 78.400 0.73 0.27 17,100 20,200 M887 2 40 hr 940C 122,300 0.41 0.28 18,000 20,900 M900 1 48 hr 900C 83,100 0.80 l 74 18,400 22,400 M900"-" 2 48 hr 900C 103,200 0.49 M900 3 48 hr 900C 1 18,500 0.80 1.36 19,300 22,900
"No measurable torque peaks. 'Not annealed after hot rolling Annealed at 900C al'tcr hot rolling. rolled at 160C to 0.040 inch "'Hot rolled to 0.100 inch. intermediate anneal 1 hour at 900C. rolled at 260C to 0.040 inch.
Data for the commercial alloys, that is the alloy manufactured and sold under the tradename CUBEX which is 3 percent silicon-iron having a (100) [001] grain texture, an alloy marketed under the name HlPERSlL which is a 3 percent silicon iron composition but having a different texture identified in terms of Miller lndicies as (110) [001] and the composition marketed under the trademark HIPERCO 27 which is an iron-cobalt alloy containing about 27 percent cobalt have been included in the data contained in Table 11 for comparison purposes. Since the silicon iron alloys are normally annealed at 1200C to obtain secondary recrystallization and purification and while all annealing of the cobaltiron alloys is normally done below the A y transformation temperature of about 950C, that is the Ac, temperature, no. secondary recrystallization was observed in any of the cobalt-iron alloys listed in the table.
The torque curve data given for the CUBEX material are for the (100) [001] single crystal and the peak torque values are nearly the same for both the (100) [001] and the l [001] textures in silicon iron. The main difference in the torque curve is in the peak ratios. For the (110) [001] texture there are two large and two small peaks over 180 rotation, thus the peak ratio is the absolute value of the small peaks divided by the absolute value of the large peaks. or in the case of the oriented (110) [001] composition the peak ratio for perfect orientation is about 0.34. On the other hand the (100) [001] torque curve has four equal peaks thereby resulting in a peak ratio of 1.0 for a perfect orientation of the CUBEX'brand material. The commercial HlPERCO 27 brand alloy had no measurable torque peaks and a low B value thereby indicating no appreciable degree of grain orientation or texture exhibited thereby.
An examination of the data contained in Table 11 indicates that the alloys which were made and tested employing Process 1 generally show a relatively high peak ratio of about 0.8 and where high torque values are obtained, indicate a tendency toward (100) [001] texture. Process 2, on the other hand, generally resulted in lower torque ratios of between about 0.4 and 0.5, indicating a high degree of 1 l0) [001] texture for high peak torque values. The tendency toward cube texture formation with a large cold reduction has been further borne out with domain pattern observations in addition to the foregoing magnetic data. Alloy M856 which had neither manganese nor chromium additions had no measurable torque peaks for Process 1 and low peaks for Process 2 indicating that without the presence of at least one of these elements good cube texture development is not obtained. On the other hand where the chromium content exceeds about 0.8 percent as will be shown more clearly hereinafter rather than forming good cube texture the alloy has a tendency to be formed with the cube-on-edge orientation. Alloy M859 which had an addition of sulfur demonstrated a high peak torque value and a high peak ratio for Process 1 but a low peak torque value for Process 2 indicating that the double orientation process is not as critical with regard to the sulphur content as is the l 10) [001] texture formation.
Alloy M883 is of particular interest because Process 1 and 2 result in very similar peak torque values and almost identical magnetic properties in the rolling direction with quite different torque ratios. Alloy M900 was the only alloy treated by Process 3 which resulted in the same peak ratio as Process 1 together with a higher peaktorque value indicating a high degree of double or cube-on-face orientation. Since the B value for alloy M900 employing Process 3 measured in the rolling direction is higher than tht of commercial cube-on-edge silicon-iron and much higher than the 27 percent cobalt alloy, the degree of final cold reduction appears to .play a major role in determining whether doubly oriented, that is cube-on-face orientation, or the singly oriented cube-on-edge texture is formed. Consequently two or more large cold reductions result in an optimum process for the formation of double orientation in cobalt-iron alloys.
Further examination of the test results set forth for the alloys hereinbefore indicate that a fairly high degree of double orientation has been obtained by primary recrystallization and normal grain growth. Since this is obtained in cobalt-iron alloys which can be readily cold' worked, this results in improved induction values over commercially available HIPERCO 27 brand alloys or 3% siliconiron alloysl Moreover, when it is considered that the useful textures have been oburement. The following results were obtained.
TABLE 111 Sample 7((100) 72(110) 71 10-[100] 7r 15-[100] These results are consistent with the torque values.
From the test results set forth in Table 111 it is seen that in excess of 50 percent of the grains by volume had the (100) plane oriented within 10 of the surface of the alloy and 63 percent of the oriented grains were within 10 of the [001] or rolling direction. The actual values for the same characteristics employing Process 3 confirm the operability of Process 3. These results are consistent with the torque values set forth in Table 11 hereinbefore.
Alloy M901 was melted with the same nominal composition namely about 27.4 percent cobalt, about 0.15 percent manganese, about 0.03 percent carbon and the balance iron. This alloy was hot rolled to 0.180 inch in thickness and annealed 5 hours at 900C in dry hydrogen, cold rolled, the first step occurring at a temperature of 300C to 0.080 inches, annealed for a time period of 7 hours at 900C and again cold rolled, the initial step being to a thickness of 0.040 inches and at a temperature of 300C and thereafter at room temperature to a final gauge of 0.012 inches. Torque discs, Epstein samples and punched rings the latter having a threeinch outside diameter by 2% inch inside diameter were annealed for 48 hours at 900C. The material demonstrated a peak torque value of 130,700 ergs/cm and a peak ratio of 0.89 indicating a high degree of doubly oriented or cube-on-face texture. Domain analysis indicated 79 percent by volume of the grains were within 12 of the (100) and 11 percent by volume of the grains were within 12 of the (110); 78 percent of the grains had a [100] direction within of the rolling direction and 88 percent within 15.
Reference is now directed to Table IV and the magnetic properties which were measured on Epstein and ring samples annealed 48 hours at 900C and ring samples which were reannealed for 2 hours at 850C in a 10 oersted. field and thereafter furnace cooled:
From the foregoing test results it is seen that the Epstein sample had very high B value in the rolling direction as expected from the high degree of texture. The as-annealed ring sample had a much lower B value than expected for the cube texture and both had low remanent values. Field annealing the ring sample resulted in a large decrease in the coercive force and an increase in the remanence value while the B value increased to a level consistent with the degree of orientation. These results indicate the large beneficial effect of field annealing cobalt-iron alloys in general and cube textured material in particular.
Another series of alloys were melted to study the effect of the cobalt and chromium contents on the cube texture formation. Table V contains the nominal chemical composition of the alloys so made and tested together with the volume resistivity as exhibited by each of the alloys.
TABLE V p No. 7r Co 7: Cr 7: Mn 7: C (uflcm) M 905 18.0 0.15 0.03 20.0 M 907 19.5 0.15 0.03 19.3 M 909 21.0 0.15 0.03 18.6 M 911 22.5 0.15 0.03 17.6 M 913 24.0 0.15 0.03 16.3 M 915 25.5 0.15 0.03 14.9 M 917 27.0 0.15 0.03 13.8 M 906 18.0 0.6 0.15 0.03 24.6 M 908 19.5 0.6 0.15 0.03 24.4 M 910 21.0 0.6 0.15 0.03 24.1 M 912 22.5 0.6 0.15 0.03 23.6 M 914 24.0 0.6 0.15 0.03 22.9 M 916 25.5 0.6 0.15 0.03 22.6 M 918 27.0 0.6 0.15 0.03 22.2
The resistivity data set forth in Table V shows a fairly sharp decrease in resistivity with increasing cobalt content in this range for essentially binary alloys. The 0.6 percnet chromium addition increased the resistivity and tended to make it more constant with increasing cobalt content. It is for this reason that chromium is added to commercial l-lIPERCO 27 brand alloy to reduce high frequency losses. The alloys set forth in Table V were hot rolled to 0.180 inch in thickness, annealed 5 hours at 900C in dry hydrogen cold rolled to 0.080 inches in thickness, annealed 5 hours at 900C in dry hydrogen and cold rolled to a finish gauge of 0.012 inches in thickness. Torque and Epstein samples in the rolling direction were strip annealed for about five minutes at 850C and then reannealed for 48- hours at 900C in dry hydrogen. Reference is directed to Table VI which sets forth the test results as measured on each of the alloys:
From the test results set forth in Table VI it is seen that the samples with no chromium addition had torque curves indicating a fairly high degree of cube texture as expected. The alloys containing chromium however, had torque curves indicating a high degree of cube-onedge or (1 10) [001] orientation. The B values exhibited by the alloys correlated well with the torque data. These data show unequivocally that the chromium addition tends to promote the (1 10) [001] texture in cobalt-iron alloys and as a result thereof must be limited to a maximum of not in excess of 0.3 percent by weight and preferably less than about 0.15 percent where cube-on-face orientation is desired in the end product. Where, however, cube-on-edge orientation is desired, chromium must be added in the range between 0.3 percent and 1.5 percent by weight.
In order to verify the test results set forth hereinbefore, alloy M 904 with a nominal composition of 25.4 percent cobalt, 0.6 percent chromium, 0.15 percent manganese, 0.03 percent carbon and the balance essentially iron was melted and-tested. This alloy was hot rolled to 0.180 inch in thickness, annealed 5 hours at 900C in dry hydrogen, cold rolled with the initial step being at a temperature of 300C to 0.040 inch in thickness, annealed one hour at 900C in dry hydrogen, and cold rolled to 0.004 inch in thickness final gauge. The finished material was annealed for 48 hours at 900C and exhibited a maximum torque value of 128,000 ergs/cm" and a peak ratio of 0.48, indicating a high degree of (1 [001] texture. A tape of this material was strip annealed for about 5 minutes at 815C, coated with alumina, wound into a core and annealed 24 hours at 900C with the following properties. i
In an attempt to raise the volume resistivity exhibited by the alloy of the present invention the following listed alloys were melted with the additions there indicated and processed in order to attain the desired double orientation or cube texture.
It is noted from the data contained in Table Vlll that all alloys exhibit considerably higher resistivities than the binary 25 percent cobalt-iron alloy. The alloys having the composition set forth in Table V111 were hot rolled to 0.180 inches, annealed 5 hours at 900C, hot cold rolled at 300C to 0.080 inch, annealed 5 hours at 900C and cold rolled at 300C to 0.040 inch and thereafter without any intermediate or additional annealing, cold rolled to both 6 and 12 mils final thicknesses. Torque samples and Epstein samples in the rolling direction were strip annealed for 5 minutes at 850C in dry hydrogen and then annealed 24 hours at 900C in dry hydrogen with the following listed results:
TABLE V11 r r 10 um r r 17/400 20/400 Anneal (08) (G) (B)' l no field 0.83 9,500 19,600 23,500 15.34 20.52 with field 0.36 17,000 19,800 23,500 11.78 17.13
TABLE 1X P,. Thickness Peak Torq ue Torque H,. 13 20/400 Alloy (mils) (ergs/cm') Ratio (0e) (G) (W/lb) M 961 12 112.600 .80 .57 19,500 41.31 M 963 12 120,100 .84 .54 19,400 43.45 M 964 12 115,800 .78 .59 18,800 44.18 M 965 12 1 3,700 .88 .52 19,700 39.89 M 961 6 74,800 .77 .48 18,300 29.17 M 963 6 77,000 .74 .41 19,000 29.13 M 964 6 80,300 .75 .46 19,100 26.21 M 965 6 1 12,300 .84 .43 19,400 28.01
From the data set forth in Table V11 it is seen that the field anneal resulted in a large decrease in the coercive force and an increase in the remanence. In addition, the high frequency watt losses measured at 400 Hz shows a substantial decrease with field annealing while there has been almost no change exhibited in the B or B values.
From the test resulst set forth in Table 1X it is noted that the torque values indicate a high degree of cube texture in all 12 mil samples, and a somewhat lower degree of texture in the thinner samples. X-ray pole figure analyses of the material having a thickness of 12 mils, namely M 961 and M 965 indicated that 65 and 79 percent of the grains were within 15 of respectively. The pole figure also indicated very good directional texture.
Referring now to the photo micrographs of FIGS. 1 and 2, it is observed that the structure so produced by the process of the present invention exhibits equiaxed grains and of normal grain growth. In contrast to seeondarily recrystallized microstructures, in which one or more substantially preferentially oriented grains grow at the expense of the other grains thereby resulting in a duplex grain structure, FIG. 1 closely illustrates a primary recrystallized mocrostructure. Examination of FIG. 2 which is a cross-section of the alloy of FIG. 1, reveals that normal grain growth has occurred. This results from the fact that the grains do not extend completely through the thickness of the alloy as is the observation in secondarily recrystallized microstructures.
The data set forth hereinbefore clearly demonstrates the productionn of an iron cobalt alloy having a high degree of cube-on-face orientation in the microstructure. This orientation is achieved by employing a process of primary recrystallization and normal grain growth. By critically controlling the method of processing the alloys as well as by controlling the chemical composition especially the chromium content. outstanding results are obtained enabling the use of these materials in such applications as aircraft generators where high sat uration values are needed in the alloys forming the magnetic core thereof.
We claim as our invention:
1. An alloy member which exhibits improved permeabilities at low field strengths resulting from crystallographic orientation compared to unoriented magnetic material of the same chemical composition consisting essentially of from about 5 percent to about 35 percent cobalt, less than 0.3 percent chromium, up to 0.3 percent manganese, up to 3 percent silicon, less than 0.03 percent carbon and the balance iron with incidental impurities, said alloy having a primary recrystallized microstructure in which a major proportion of the grains exhibit a texture within 10 of the surface of the alloy and in which a major proportion of the oriented grains have cube or edges of their crystal lattices aligned within 10 of the rolling direction.
2. The alloy of claim 1 in which the cobalt is present within the range between about 18 percent and about 27 percent with not more than 0.25 percent chromium.
3. An alloy member which exhibits improved permeabilities at low field strengths resulting from crystallographic orientation compared to unoriented magnetic material of the same chemical composition consisting essentially of from about 5 percent to about 35 percent cobalt, at least one volume resistivity improving element selected from the group of up to 2 percent silicon, up to 1 percent vanadium. up to about 0.5 percent molybdenum, less than 0.3 percent chromium and mixtures thereof, less than 0.03 percent carbon and the balance iron with incidental impurities, the alloy having a primary recrystallized microstructure in which at least 50 percent by volume of the grains exhibit an orientation in which the (100) plane is oriented within 10 of the alloy surface and at least 50 percent of the oriented grains are within 10 of the rolling direction.
4. The alloy of claim 3 in which the cobalt is present within the range between about 18 percent and about 27 percent.

Claims (4)

1. AN ALLOY MEMBER WHICH EXHIBITS IMPROVED PERMEABILITIES AT LOW FIELD STRENGTHS RESULTING FROM CRYSTALORGAPHIC ORIENTATION COMPARED TO UNORIENTED MAGNETIC MATERIAL OF THE SAME CHEMICAL COMPOSITION CONSISTING ESSENTIALLY OF FROM ABOUT 5 PERCENT TO ABOUT 35 PERCENT COBALT, LESS THAN 0.3 PERCENT CHROMIUM, UP TO 0.3 PERCENT MANGANESE, UP TO 3 PERCENT SILICON, LESS THEN 0.03 PERCENT CARBON AND THE BALANCE IRON WITH INCIDENTAL IMPURITIES, SAID ALLOY HAVING A PRIMARY RECRYSTALLIZED MICROSTRUCTURE IN WHICH A MAJOR PROPORTION OF THE GRAINS EXHIBIT A (100) TEXTURE WITHIN 10* OF THE SURFACE OF THE ALLOY AND IN WHICH A MAJOR PROPORTION OF THE ORIENTED GRAINS HAVE CUBE OR EDGES OF THEIR CRYSTAL LATTICES ALIGNED WITHIN 10* OF THE ROLLING DIRECTION.
2. The alloy of claim 1 in which the cobalt is present within the range between about 18 percent and about 27 percent with not more than 0.25 percent chromium.
3. An alloy member which exhibits improved permeabilities at low field strengths resulting from crystallographic orientation compared to unoriented magnetic material of the same chemical composition consisting essentially of from about 5 percent to about 35 percent cobalt, at least one volume resistivity improving element selected from the group of up to 2 percent silicon, up to 1 percent vanadium, up to about 0.5 percent molybdenum, less than 0.3 percent chromium and mixtures thereof, less than 0.03 percent carbon and the balance iron with incidental impurities, the alloy having a primary recrystallized microstructure in which at least 50 percent by volume of the grains exhibit an orientation in which the (100) plane is oriented within 10* of the alloy surface and at least 50 percent of the oriented grains are within 10* of the rolling direction.
4. The alloy of claim 3 in which the cobalt is present within the range between about 18 percent and about 27 percent.
US401766A 1972-02-22 1973-09-28 Doubly oriented cobalt iron alloys Expired - Lifetime US3868278A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US401766A US3868278A (en) 1972-02-22 1973-09-28 Doubly oriented cobalt iron alloys
US05/532,284 US3977919A (en) 1973-09-28 1974-12-12 Method of producing doubly oriented cobalt iron alloys

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US22807072A 1972-02-22 1972-02-22
US401766A US3868278A (en) 1972-02-22 1973-09-28 Doubly oriented cobalt iron alloys

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US22807072A Continuation 1972-02-22 1972-02-22

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US05/532,284 Division US3977919A (en) 1973-09-28 1974-12-12 Method of producing doubly oriented cobalt iron alloys

Publications (1)

Publication Number Publication Date
US3868278A true US3868278A (en) 1975-02-25

Family

ID=26922023

Family Applications (1)

Application Number Title Priority Date Filing Date
US401766A Expired - Lifetime US3868278A (en) 1972-02-22 1973-09-28 Doubly oriented cobalt iron alloys

Country Status (1)

Country Link
US (1) US3868278A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3977919A (en) * 1973-09-28 1976-08-31 Westinghouse Electric Corporation Method of producing doubly oriented cobalt iron alloys
US4075437A (en) * 1976-07-16 1978-02-21 Bell Telephone Laboratories, Incorporated Composition, processing and devices including magnetic alloy
US4105913A (en) * 1975-08-11 1978-08-08 Sanyo Electric Co., Ltd. Core magnetron and method of manufacturing permanent magnets therefor with low gas emission
US4204887A (en) * 1975-04-04 1980-05-27 The Foundation: The Research Institute Of Electric And Magnetic Alloys High damping capacity alloy
US4208254A (en) * 1976-09-22 1980-06-17 Satoshi Ichioka Method of plating an iron-cobalt alloy on a substrate
US20200325564A1 (en) * 2017-10-27 2020-10-15 Vacuumschmelze Gmbh & Co. Kg High permeability soft magnetic alloy and method for the production of a high permeability soft magnetic alloy
US20210091611A1 (en) * 2019-09-25 2021-03-25 Vacuumschmelze Gmbh & Co. Kg Multi-part stator, electric machine and method for producing a multi-part stator and an electric machine
US11114226B2 (en) 2015-05-04 2021-09-07 Carpenter Technology Corporation Ultra-low cobalt iron-cobalt magnetic alloys
US11827961B2 (en) 2020-12-18 2023-11-28 Vacuumschmelze Gmbh & Co. Kg FeCoV alloy and method for producing a strip from an FeCoV alloy

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1247206A (en) * 1915-04-19 1917-11-20 Electro Metallurg Co Alloy containing iron, cobalt, and silicon.
US1910309A (en) * 1931-07-22 1933-05-23 Telegraph Constr & Main Co Magnetic alloy
US2442219A (en) * 1946-10-30 1948-05-25 Westinghouse Electric Corp Magnetic alloy
US3065118A (en) * 1959-01-16 1962-11-20 Gen Electric Treatment of iron-cobalt alloys
US3124491A (en) * 1960-05-23 1964-03-10 Heavy gauge double oriented magnetic sheet material
US3148092A (en) * 1960-11-17 1964-09-08 Westinghouse Electric Corp Process for producing sheets of magnetic materials
US3164496A (en) * 1956-09-20 1965-01-05 Gen Electric Magnetic material and method of fabrication
US3166408A (en) * 1961-11-16 1965-01-19 Westinghouse Electric Corp Magnetic alloys
US3347718A (en) * 1964-01-20 1967-10-17 Armco Steel Corp Method for improving the magnetic properties of ferrous sheets
US3390443A (en) * 1964-10-20 1968-07-02 Bell Telephone Labor Inc Magnetic material and devices utilizing same
US3418710A (en) * 1963-05-08 1968-12-31 Westinghouse Electric Corp High temperature magnetic cores and process for producing the same

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1247206A (en) * 1915-04-19 1917-11-20 Electro Metallurg Co Alloy containing iron, cobalt, and silicon.
US1910309A (en) * 1931-07-22 1933-05-23 Telegraph Constr & Main Co Magnetic alloy
US2442219A (en) * 1946-10-30 1948-05-25 Westinghouse Electric Corp Magnetic alloy
US3164496A (en) * 1956-09-20 1965-01-05 Gen Electric Magnetic material and method of fabrication
US3065118A (en) * 1959-01-16 1962-11-20 Gen Electric Treatment of iron-cobalt alloys
US3124491A (en) * 1960-05-23 1964-03-10 Heavy gauge double oriented magnetic sheet material
US3148092A (en) * 1960-11-17 1964-09-08 Westinghouse Electric Corp Process for producing sheets of magnetic materials
US3166408A (en) * 1961-11-16 1965-01-19 Westinghouse Electric Corp Magnetic alloys
US3418710A (en) * 1963-05-08 1968-12-31 Westinghouse Electric Corp High temperature magnetic cores and process for producing the same
US3347718A (en) * 1964-01-20 1967-10-17 Armco Steel Corp Method for improving the magnetic properties of ferrous sheets
US3390443A (en) * 1964-10-20 1968-07-02 Bell Telephone Labor Inc Magnetic material and devices utilizing same

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3977919A (en) * 1973-09-28 1976-08-31 Westinghouse Electric Corporation Method of producing doubly oriented cobalt iron alloys
US4204887A (en) * 1975-04-04 1980-05-27 The Foundation: The Research Institute Of Electric And Magnetic Alloys High damping capacity alloy
US4105913A (en) * 1975-08-11 1978-08-08 Sanyo Electric Co., Ltd. Core magnetron and method of manufacturing permanent magnets therefor with low gas emission
US4075437A (en) * 1976-07-16 1978-02-21 Bell Telephone Laboratories, Incorporated Composition, processing and devices including magnetic alloy
US4208254A (en) * 1976-09-22 1980-06-17 Satoshi Ichioka Method of plating an iron-cobalt alloy on a substrate
US11114226B2 (en) 2015-05-04 2021-09-07 Carpenter Technology Corporation Ultra-low cobalt iron-cobalt magnetic alloys
US20200325564A1 (en) * 2017-10-27 2020-10-15 Vacuumschmelze Gmbh & Co. Kg High permeability soft magnetic alloy and method for the production of a high permeability soft magnetic alloy
US20210091611A1 (en) * 2019-09-25 2021-03-25 Vacuumschmelze Gmbh & Co. Kg Multi-part stator, electric machine and method for producing a multi-part stator and an electric machine
US11827961B2 (en) 2020-12-18 2023-11-28 Vacuumschmelze Gmbh & Co. Kg FeCoV alloy and method for producing a strip from an FeCoV alloy

Similar Documents

Publication Publication Date Title
US3977919A (en) Method of producing doubly oriented cobalt iron alloys
US3940299A (en) Method for producing single-oriented electrical steel sheets having a high magnetic induction
US4046602A (en) Process for producing nonoriented silicon sheet steel having excellent magnetic properties in the rolling direction
US5547520A (en) Wear-resistant high permeability magnetic alloy and method of manufacturing the same
US2867559A (en) Method for producing grain oriented silicon steel
CN111566245A (en) Dual-orientation electrical steel sheet and method for manufacturing the same
US3849212A (en) Primary recrystallized textured iron alloy member having an open gamma loop
US3868278A (en) Doubly oriented cobalt iron alloys
US3163564A (en) Method for producing silicon steel strips having cube-on-face orientation
US2801942A (en) Method of rendering an aluminum-iron alloy ductile
US3575739A (en) Secondary recrystallization of silicon iron with nitrogen
US3892604A (en) Method of producing normal grain growth (110) {8 001{9 {0 textured iron-cobalt alloys
US3892605A (en) Method of producing primary recrystallized textured iron alloy member having an open gamma loop
US3351501A (en) Process for producing magnetic sheets with cube-on-face grain texture
US3843424A (en) Normal grain growth(110)(001)textured iron-cobalt alloys
US3597286A (en) Method of treating a high strength high ductility iron-cobalt alloy
US3881967A (en) High saturation cobalt-iron magnetic alloys and method of preparing same
US3214303A (en) Process of retaining a dispersed second phase until after the texture developing anneal
US3148092A (en) Process for producing sheets of magnetic materials
US3096222A (en) Grain oriented sheet metal
US3130092A (en) Process of making cubic texture silicon-iron
US3345219A (en) Method for producing magnetic sheets of silicon-iron alloys
US3105782A (en) Method of producing magnetic material
US3278348A (en) Process for producing doubly oriented cube-on-face magnetic sheet material
US3218202A (en) Method of using a critical cold rolling stage to produce silicon-iron sheets