US2295082A - Permanent magnet and method of making the same - Google Patents
Permanent magnet and method of making the same Download PDFInfo
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- US2295082A US2295082A US281988A US28198839A US2295082A US 2295082 A US2295082 A US 2295082A US 281988 A US281988 A US 281988A US 28198839 A US28198839 A US 28198839A US 2295082 A US2295082 A US 2295082A
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- 238000004519 manufacturing process Methods 0.000 title description 9
- 229910045601 alloy Inorganic materials 0.000 description 72
- 239000000956 alloy Substances 0.000 description 72
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 54
- 230000005291 magnetic effect Effects 0.000 description 49
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 43
- 238000001816 cooling Methods 0.000 description 39
- 229910052759 nickel Inorganic materials 0.000 description 28
- 229910052782 aluminium Inorganic materials 0.000 description 27
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 24
- 239000010941 cobalt Substances 0.000 description 24
- 229910017052 cobalt Inorganic materials 0.000 description 24
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 24
- 229910052742 iron Inorganic materials 0.000 description 22
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 21
- 230000005415 magnetization Effects 0.000 description 15
- 239000010936 titanium Substances 0.000 description 14
- 229910052719 titanium Inorganic materials 0.000 description 13
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 12
- 229910052802 copper Inorganic materials 0.000 description 12
- 239000010949 copper Substances 0.000 description 12
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 11
- 229910000831 Steel Inorganic materials 0.000 description 11
- 230000006872 improvement Effects 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 239000010959 steel Substances 0.000 description 11
- 230000000694 effects Effects 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229910000851 Alloy steel Inorganic materials 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 229910018084 Al-Fe Inorganic materials 0.000 description 2
- 229910018192 Al—Fe Inorganic materials 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 239000004411 aluminium Substances 0.000 description 2
- 229910052787 antimony Inorganic materials 0.000 description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 230000005347 demagnetization Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- 229910017709 Ni Co Inorganic materials 0.000 description 1
- 229910003310 Ni-Al Inorganic materials 0.000 description 1
- 229910003267 Ni-Co Inorganic materials 0.000 description 1
- 229910003262 Ni‐Co Inorganic materials 0.000 description 1
- UQZIWOQVLUASCR-UHFFFAOYSA-N alumane;titanium Chemical compound [AlH3].[Ti] UQZIWOQVLUASCR-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000003302 ferromagnetic material Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/002—Dyes with anthracene nucleus not condensed with any other ring containing onium groups
Definitions
- This invention relates to permanent magnets and to a method of manufacturing them.
- the permanent magnet according to the inventlon exhibits the feature that it consists 01' a Ni-Al-Fe alloy having a cobalt content of 16 to 30%, a nickel content of 12 to 20% and an aluminium content of 6 to 11% and that in one (principal) direction (anisotrope) it has a (BHDm value which is at least 2,000,000, for instance 4,000,000 to 5,000,000, and which is at least 50%, for instance 100 to 200%, higher than that of a permanent magnet which is made from the same alloy, but whose magnetic properties are at least substantially equal in all directions (isotrope). Since, as is well known, the size and weight of magnets are dependent upon the (BH)msx value of the magnet steel used, the advantageous results obtained by the present invention will be readily appreciated.
- the magnets according to the invention preferably have a cobalt content of about 20% to 25%, a nickel content of about 13% to 17% and an aluminum content of about 7% to 10%, and with such compositions it is possible to obtain (BH)nmx values greater than 3,000,000. I have found that such high (BI-I) max values are due to the pronounced arched shape of the demagnetization curves and, as is well known, the fullness factor mma:
- Magnets according to the invention having a (BH)max value of at least 3,000,000 have a fullness factor of at least 0.45, generally 0.50 or more.
- the magnets according to the invention can be made by subjecting the alloys to the action of a magnetic field. during the cooling required for magnetic hardening.
- Figs. 1 and 2 are demagnetization curves of permanent magnets according to the invention.
- This efiect has also been examined with alloys for permanent magnets (see periodical "Nature” dated July 30, 1938, page 209).
- This periodical refers to an iron alloy for permanent magnets of the Ni-Al type which consists of 18% Ni, 10% Al, 12% Co, 6% Cu and 54% Fe and is cooled irom a temperature of 1200 C. in a magnetic field.
- an improvement in the remanence and in the (3mm value is obtained.
- the remanence for instance, was raised from about 7350 to about 7900 Gauss'and the (BH)max from 1,500,000 to 1,800,000. 0
- the material When using a magnetic field during the cooling .operation the material exhibits anisotropy in such manner that, after subsequent magnetisation in a direction corresponding to the direction of the magnetic field during cooling, the magnetic properties in this direction are improved whereas the magnetic properties in other directions are reduced.
- the progress according to the invention is more surprising, because a group of Ni-Al-Fe alloys is used which is very uneconomical and hence unusual in practice viz. alloys having a high cobalt content (more than 16%), while at the same time I obtain permanent magnets aifording maximum economy.
- the permanent magnets according to the invention must be magnetized subsequent to the cooling in the direction oi the lines of magnet force used to magnetize the magnet during the cooling, i. e. the lines of force during the subsequent magnetization should substantially coincide with the magnetic lines of force used during the cooling. If the magnetic lines of force during the subsequent magnetization were perpendicular to the direction of the lines of force used during the cooling, the high (BH)max value of the present invention would not be obtained.
- I refer to the improvement in (BI-I) value of a permanent magnet according to the invention
- I mean the improvement over a permanent magnet of the same composition, but which is subjected to a magnetization only after the heat treatment.
- the magnetic field preferably has an intensity of more than 3,000 Gauss.
- the cooling operation may be effected in a usual manner which is best suited for obtaining favorable magnetic and mechanical properties, and one skilled in the art can select that cooling method which is best suited for use with a certain type of alloy when the cooling is effected without the application of a magnetic field. I employ the same cooling methods when applying the magnetic field during the cooling.
- the action of the magnetic field should take place at least in a temperature-interval which extends from the Curie-temperature to about 150 C. below this temperature and which is a part of the temperature-interval traversed during the cooling of the alloy necessary for hardening.
- a temperature-interval which extends from the Curie-temperature to about 150 C. below this temperature and which is a part of the temperature-interval traversed during the cooling of the alloy necessary for hardening.
- the average cooling speed in the usual cooling operation should be low, i. e. about 10 C. per sec. at the utmost, and preferably about 1 C. to C. per see.
- alloys having a high Curie-point for instance higher than about 780 C.
- the above-described alloys containing more than 16% Co can satisfy this condition.
- the kind of alloy denoted by c which in addition contains copper with respect to the lastmentioned alloy, may also be used for this purpose, and the alloy 41 (without titanium) permits more particularly maximum values and this jointly with remarkable values both for the remanence and for the coercive force.
- Titanium which has also proved to be such a valuable element for various magnetic steel alloys and was present in the best magnetic steels hitherto known, is not an essential element of my alloy, although a total percentage of Al and Ti of less than about 12%, the Al percentage being from 6% to 11%, may be used in my alloy.
- a high titanium content for instance more than about 5%, has proved to be detrimental.
- a magnet of an Al-Fe-Ni-Co alloy when treated in the usual prior art manner has a (BH)max value of 1,500,000 and when treated in the manner of the present invention has a (BH) max value which, due to the anistropy effect, is double, i. e. 3,000,000.
- the (BH)max value will decrease to a value between about 1,000,000 and 1,500,000.
- the anistropy effect is not affected by the addition of these elements and 7 if the alloy is treated in the manner of the present invention, a (1311)., value of about 2,000,000,
- the (BH)max value will be decreased to about 1,000,000 to 1,500,000 but when the alloy is treated by the method of the present invention the (B8)... value will be decreased to about 1,400,000, i. e. to a value less than double the value obtained by the prior art treatment.
- Additions of other elements such as, for instance, calcium and to a lower degree tungsten may give rise to a slight but clearly perceptible increase in a characteristic magnetic value, for instance in remanence, but as a rule they tend to influence the other characteristic magnetic values.
- a permanent magnet consisting of a ferrous alloy containing about 16% to 30% cobalt, about 12% to 20% nickel, about 6% to 11% aluminum and the remainder principally iron, said magnet being magnetically-anisotropic and having a (BH)max value in the principal direction at least about 50% higher than the (31 1):; value of a substantially magnetically-isotropic permanent magnet of the same alloy.
- a permanent magnet consisting of a ferrous alloy containing about 20% to 25% cobalt, about 13% to 17% nickel, about 7% to aluminum and the remainder principally iron, said magnet being magnetically-anisotropic and having 2.
- (BH) max value in the principal direction which is at least 2,500,000 and is at least about 50% higher than the (BIDmax value of a substantially magnetically-isotropic permanent magnet of the same alloy.
- a permanent magnet consisting of a ferrous alloy containing about 20 to cobalt, about 13. to 16.5% nickel, about 7.1% to 8.5% aluminum and the remainder principally iron, said magnet being magnetically-anisotropic and having a (BH)msx value in the principal direction which is equal to at least about 3,000,000 and which is at least 50% greater than that of a substantially magnetically-isotropic permanent magnet of the same composition.
- a permanent magnet consisting of a ferrous alloy containing about 21% to 25% cobalt, about 14% to 20% nickel, about 8% to 10% aluminum and the remainder principally iron, said magnet being magnetically-anisotropic and having a (BI'Dmax value in the principal direction which is at least 2,000,000 and which is at least 50% greater than that of a magnetically-isotropic permanent magnet of the same alloy, and a remanence of at least 8,000 Gausses.
- a permanent magnet consisting of a ferrous alloy containing about 23% to 24% cobalt, about 13.5% to 16% nickel, about 7% to 8.5% aluminum and the remainder substantially iron, said magnet being magnetically-anisotropic and having a (BHMMX value in the principal direction of at least 3,000,000.
- a permanent magnet consisting of a ferrous alloy containing about 16% to cobalt, about 12% to 20% nickel, about 6% to 11% aluminum, the remainder being iron and at least one of the elements titanium in an amount less than about 5% and copper in an amount less than about 7%, said magnet being magnetically anisotropic and having a (BH) max value in the principal direction of at least about 50% higher than the (BH)mx value of a substantially magneticallyisotropic permanent magnet of the same alloy.
- a permanent magnet consisting of a ferrous alloy containing about 20% to 25% cobalt, about 13.5% to 16.5% nickel, about 7.1% to 8.1% aluminum, the optional inclusion of one or both of the elements copper in an amount less than about 6.5% and titanium in an amount less than about 2.8% and the remainder iron, said magnet being magnetically-anisotropic and having a (BH)mu value in the principal direction which is at least 3,000,000 and which is at least 50% greater than that of a magnetically-isotropic permanent magnet of the same alloy, and a remanence of at least 8,000 Gausses.
- BH BH
- a permanent magnet consisting of a ferrous alloy containing about 23% to 24% cobalt, about 13.5% to 16% nickel, about 7% to 8.5% aluminum, the remainder being iron and small quantities of at least one of the elements copper and titanium, said magnet being magneticallyanisotropic and having a (BH)mn value in the principal direction of at least 3,000,000.
- a permanent magnet consisting of a ferrous alloy containing about 16% to 30% cobalt, about 12% to 20% nickel, about 6% to 11% aluminum, not more than 5% titanium and the remainder principally iron, the total aluminum-titanium content being not more than about 12%, said magnet being magnetically-anisotropic and having a (BH)max value in the principal direction at least about 50% higher than the (BHhnu value of a substantially magnetically-isotropic permanent magnet of the same alloy.
- a magnetically-anisotropic permanent magnet consisting of a ferrous alloy containing about 14% to 18% nickel, about 22% to 25% cobalt, about 6% to 8% aluminum, about 0.4% to 4% titanium and the remainder principally iron, said magnet having a coercive force of more than 450 Oersteds and a (BH)max value which is greater than 2,500,000 and which is at least 50% greater than that of a substantially magneticallyisotropic permanent magnet of the same composition.
- a magnetically-anisotropic permanent magnet consisting of a ferrous alloy containing about 14% to 18% nickel, about 22% to 25% cobalt, about 6% to 8% aluminum, about 0.4% to 4% titanium and the remainder principally iron, said magnet having a coercive force of more than 450 Oersteds and a (BH)max value which is greater than 3,000,000 and which is at least 50% greater than that of a substantially magneticallyisotropic permanent magnet of the same composition.
- a permanent magnet consisting of a ferrous alloy containing about 20 to 27.5% cobalt, about 12% to 15% nickel, about 8% to 8.5% aluminum, about 1.5% to 6.5% copper and the remainder principally iron, said magnet being magnetically-anisotropic and having a (BI-Um value in the principal direction which is equal to at least about 3,500,000 and which is atleast 50% greater than that of a substantially magnetically-isotropic permanent magnet of the same composition.
- a magneticallyanisotropic permanent magnet consisting of a ferrous alloy containing about 13% to 16.5% nickel, about 18.5% to 25% cobalt, about 6.5% to 8.5% aluminum, about 1% to 3% titanium, about 1% to 7% copper and the remainder principally iron, said magnet having a (BH)max value which is greater than 3,000,000 and which is at least 50% greater than that of a substantially magnetically-isotropic permanent magnet of the same composition.
- a permanent magnet In the manufacture of a permanent magnet the steps of forming a body of a ferrous alloy containing about 16% to 30% cobalt, about 12% to 20% nickel, about 6% to 11% aluminum and the remainder principally iron, and subjecting the body to a magnetic field during the cooling operation required for magnetic hardening.
- a body of a ferrous alloy containing about 16% to 30% cobalt, about 12% to 20% nickel, about 6% to 11% aluminum, and the remainder principally iron, subjecting the body to a magnetic field during the cooling operation required for magnetic hardening to thereby make the alloy magnetically-anisotropic, and subsequently magnetizing the body in a direction corresponding to the direction of magnetization during cooling to thereby obtain a (BH)max value at least 50% higher than that obtained with the same alloy without magnetization during the cooling.
- a body of a ferrous alloy having a Curie-temperature above about 780 C. and containing about 16% to 30% cobalt, about 12% to 20% nickel, about 6% to 11% aluminum and the remainder principally iron, subjecting the body to a magnetic field during the cooling operation required for magnetic hardening and while the alloy is at a temperature between its Curie-temperature and a temperature lying about 150 below the Curie-temperature to thereby make the alloy magnetically-anisotropic, and subsequently magnetizing the body in a direction corresponding to the direction of magnetization during cooling to thereby obtain a (BB) max value at least 50% higher than that obtained with the same alloy without magnetization during the cooling.
- BB BB max value
- a body of a ferrous alloy containing about 20% to 25% cobalt, about 13% to 17% nickel, about 7% to aluminum and the remainder principally iron subjecting net, the steps of forming a body of a ferrous alloy containing about 20% to 25% cobalt, 13.5% to 16.5% nickel, 7.1% to 8.5% aluminum and the remainder principally iron, subjecting the body to magnetization during the cooling operation required for magnetic hardening, and subsequently magnetizing the body in a direction corresponding to the direction of magnetization during the cooling to thereby obtain a (BH) max value which is greater than 3,000,000 and which is at least 50% greater than that of a substantiallyisotropic permanent magnet of the same composition.
- a body of a ferrous alloy containing about 23% to 24% cobalt, about 13.5% to 16% nickel, about 7% to 8.5% aluminum and the remainder principally iron, subjecting the body to magnetization during the cooling operation required for magnetic hardening and subsequently magnetizing the body in a direction corresponding to the direction of magnetization during the cooling to thereby obtain a (BH) max value greater than 3,000,000.
- a body of a ferrous alloy containing about 20% to 25% cobalt, about 13.5% to 16.5% nickel, about 7.1% to 8.5% aluminum, the optional inclusion of one or both of the elements copper in an amount less than about 6.5% and titanium in an amount less than about 2.8% and the remainder iron, cooling the body in a magnetic field from a temperature of about 1200 C. to a temperature of about 600 C.
- a body of a ferrous alloy containing about 23% to 24% cobalt, about 13.5% to 16% nickel, about 7% to 8.5% aluminum, the remainder being iron and small quantitles of at least one of the elements copper and titanium, subjecting the body to magnetization during the cooling operation required for magnetic hardening and subsequently magnetizing the body in a direction corresponding to the direction of magnetization during the cooling to thereby obtain a (BH)max value greater than 3,000,000.
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Description
G. B. JONAS Sept. 8, 1942.
PERMANENT MAGNET AND METHOD OF MAKlNG THE SAME Filed June 29, 1939 1700 54 70? 63B Jonas firr0 94 y I00 000 900 800 I00 600 500 400 300 200 I00 Patented Sept. 8, 1942 PERMANENT MAGNET AND METHOD OF MAKING THE SAME Elndhoven, Netherlands.
Gottfried Bruno Jonas,
assignments,
assignor, by memo to Hartford National Bank and Trust Company, Hartford,
Conn., as trustee Application June 29, 1939, Serial No. 281,988 In Germany December 6, 1938 21 Claims.
This invention relates to permanent magnets and to a method of manufacturing them.
The permanent magnet according to the inventlon exhibits the feature that it consists 01' a Ni-Al-Fe alloy having a cobalt content of 16 to 30%, a nickel content of 12 to 20% and an aluminium content of 6 to 11% and that in one (principal) direction (anisotrope) it has a (BHDm value which is at least 2,000,000, for instance 4,000,000 to 5,000,000, and which is at least 50%, for instance 100 to 200%, higher than that of a permanent magnet which is made from the same alloy, but whose magnetic properties are at least substantially equal in all directions (isotrope). Since, as is well known, the size and weight of magnets are dependent upon the (BH)msx value of the magnet steel used, the advantageous results obtained by the present invention will be readily appreciated.
The magnets according to the invention preferably have a cobalt content of about 20% to 25%, a nickel content of about 13% to 17% and an aluminum content of about 7% to 10%, and with such compositions it is possible to obtain (BH)nmx values greater than 3,000,000. I have found that such high (BI-I) max values are due to the pronounced arched shape of the demagnetization curves and, as is well known, the fullness factor mma:
B,XHc is decisive for this shape. Magnets according to the invention having a (BH)max value of at least 3,000,000 have a fullness factor of at least 0.45, generally 0.50 or more.
The magnets according to the invention can be made by subjecting the alloys to the action of a magnetic field. during the cooling required for magnetic hardening.
Figs. 1 and 2 are demagnetization curves of permanent magnets according to the invention.
It is already known that the magnetic properties of certain ierro-magnetic materials having a high permeability are greatly influenced when, during the thermal treatment, the cooling from high temperatures is eilected in a magnetic field.
This efiect has also been examined with alloys for permanent magnets (see periodical "Nature" dated July 30, 1938, page 209). This periodical refers to an iron alloy for permanent magnets of the Ni-Al type which consists of 18% Ni, 10% Al, 12% Co, 6% Cu and 54% Fe and is cooled irom a temperature of 1200 C. in a magnetic field. In this case an improvement in the remanence and in the (3mm value is obtained. The remanence, for instance, was raised from about 7350 to about 7900 Gauss'and the (BH)max from 1,500,000 to 1,800,000. 0
As a possible explanation oi-the influence of the magnetic field it is pointedout that when ferro-magnetic materials are not subjected to a magnetic field during the cooling operation, they.
show the same magnetic properties in all directions. When using a magnetic field during the cooling .operation the material exhibits anisotropy in such manner that, after subsequent magnetisation in a direction corresponding to the direction of the magnetic field during cooling, the magnetic properties in this direction are improved whereas the magnetic properties in other directions are reduced.
It appears from the considerations stated in this respect in the above-mentioned periodical that the said process of cooling in a magnetic field yields an improvement of about 7% in remanence and of 20% in (BH)max for magnet steel, but that surprising improvements are not to be expected in this field. This tallies with the prevailing theoretical conceptions and with the fact that most of the alloys used in practice do not show at all or only slightly show this effect.
I have found that treatment in a magnetic field yields quite uneimected results and more particularly permits one to obtain (B3): values up to about 5,000,000, when used for the alloys stated in the preamble. It is remarked in this respect that up until now it has been possible only in special cases to produce a permanent magnet having a (BH)mu value exceeding 2,000,000. None oi the commercial magnets have such values, but have values ranging between about 1.8 10 and 1.9x10'.
The progress according to the invention is more surprising, because a group of Ni-Al-Fe alloys is used which is very uneconomical and hence unusual in practice viz. alloys having a high cobalt content (more than 16%), while at the same time I obtain permanent magnets aifording maximum economy. The permanent magnets according to the invention must be magnetized subsequent to the cooling in the direction oi the lines of magnet force used to magnetize the magnet during the cooling, i. e. the lines of force during the subsequent magnetization should substantially coincide with the magnetic lines of force used during the cooling. If the magnetic lines of force during the subsequent magnetization were perpendicular to the direction of the lines of force used during the cooling, the high (BH)max value of the present invention would not be obtained. when I refer to the improvement in (BI-I) value of a permanent magnet according to the invention, I mean the improvement over a permanent magnet of the same composition, but which is subjected to a magnetization only after the heat treatment. The magnetic field preferably has an intensity of more than 3,000 Gauss.
The cooling operation may be effected in a usual manner which is best suited for obtaining favorable magnetic and mechanical properties, and one skilled in the art can select that cooling method which is best suited for use with a certain type of alloy when the cooling is effected without the application of a magnetic field. I employ the same cooling methods when applying the magnetic field during the cooling.
Furthermore it has been found advisable that the action of the magnetic field should take place at least in a temperature-interval which extends from the Curie-temperature to about 150 C. below this temperature and which is a part of the temperature-interval traversed during the cooling of the alloy necessary for hardening. I have found, that the time during which the temperature of the alloy remains in this interval between the Curie-point and the temperature 150 C. below this point has an influence on the magnitude of the effect. From this it follows that the process is particularly suitable for alloys with which, during the cooling stage of the treatment hitherto used, the time during which the temperature of the alloy remains within this interval has a certain minimum duration, e. g. 30 seconds, for optimum magnetic properties. I have found that in these cases the average cooling speed in the usual cooling operation, say between 1,250 C. and 600 C., should be low, i. e. about 10 C. per sec. at the utmost, and preferably about 1 C. to C. per see. In connection with the internal change of the alloy necessary for the occurrence of the effect, during the action of the magnetic field, it is advantageous to use alloys having a high Curie-point, for instance higher than about 780 C. The above-described alloys containing more than 16% Co can satisfy this condition.
As regards the aluminium content it is to be remarked that this should be adapted by a judicious choice to the contents of the other elements, and primarily to the nickel content.
In order to obtain excellent results as regards the value of (13K):! it is advisable that the nickel content should not exceed 17%.
The use of copper, which is desirable in many modern magnet-steel alloys, is not essential and a high content, 1. e. above 7%, is even inadvisable. However, I have found that in obtaining extremely high (BH) max values it is advisable to admit small quantities of copper, for instance In the following Table I are given several examples from which appears that the whole above-mentioned field of alloys can be split up into sections each of which shows particular magnetic properties.
Table I No. L. Percent negligence 521:; ID-l" ,m-IZ, (I!) 470-765 2. 5-4. 2X10 9, 3(I)-ll, 250 510-71) 3-4Xl0' From this table, which is based on the results obtained from about test-series, it clearly appears that the region of alloys designated by a is preferably to be used when value is attached to extremely high values of the remanence. The kind of alloys designated by b, which contains Ni, Al and Co and in addition Ti should he used if it is attempted to raise the coercive force to the highest possible extent. It is to be remarked that both in the case a and in the case b the (BI-Um obtained with the largest values of the remanence and of the coercive force respectively has at the same time the remarkable value of about 3.5)(10 and 4.2)(10 respectively.
The kind of alloy denoted by c, which in addition contains copper with respect to the lastmentioned alloy, may also be used for this purpose, and the alloy 41 (without titanium) permits more particularly maximum values and this jointly with remarkable values both for the remanence and for the coercive force.
A large number of elements other than those mentioned up till now may be added in considerable quantities as additional alloy constituents such that in each instance the stated improvement of at least 50% in (BH)mnx is obtained. However, a distinction must be made between those metals which do not influence the anistropy effect, but do affect the magnetic properties of the alloys and those other metals 1 to 3%. Generally it is advisable to reduce the nickel content in the case of high copper contents.
Titanium, which has also proved to be such a valuable element for various magnetic steel alloys and was present in the best magnetic steels hitherto known, is not an essential element of my alloy, although a total percentage of Al and Ti of less than about 12%, the Al percentage being from 6% to 11%, may be used in my alloy.
However, a high titanium content, for instance more than about 5%, has proved to be detrimental.
of the periodic system which are usually present in permanent magnets and which affect both the anistropy effect and the magnetic properties of the alloys. As examples of the former metal I might mention, silicon, vanadium, antimony, tin and sulphur, and as examples of the latter metals I may mention chromium and manganese. More particularly, assume that a magnet of an Al-Fe-Ni-Co alloy when treated in the usual prior art manner has a (BH)max value of 1,500,000 and when treated in the manner of the present invention has a (BH) max value which, due to the anistropy effect, is double, i. e. 3,000,000. If an element such as silicon, vanadium, antimony, tin and sulphur is added to this alloy and the alloy is treated in accordance with prior art methods, the (BH)max value will decrease to a value between about 1,000,000 and 1,500,000. However, the anistropy effect is not affected by the addition of these elements and 7 if the alloy is treated in the manner of the present invention, a (1311)., value of about 2,000,000,
a,aas,oss
i. e. approximately double the value obtained when using the prior art treatment, will be obtained.
If. instead of the above mentioned elements, an element such as chromium and manganese. is added to the alloy and the alloy is treated in a prior art manner, the (BH)max value will be decreased to about 1,000,000 to 1,500,000 but when the alloy is treated by the method of the present invention the (B8)... value will be decreased to about 1,400,000, i. e. to a value less than double the value obtained by the prior art treatment. Additions of other elements such as, for instance, calcium and to a lower degree tungsten may give rise to a slight but clearly perceptible increase in a characteristic magnetic value, for instance in remanence, but as a rule they tend to influence the other characteristic magnetic values. It will be understood that neither the anisotropy-eifect nor the magnetic properties are materially influenced by the presence of slight quantitles of other elements, for instance, in the form of impurities (i. e. in quantities of the order of some tenths of a per cent).
When making use of the invention one might expect that the highest attainable (BH)max value would occur with alloys whose (311).; value is about 2,000,000 (which is practically the highest attainable value up till now) without cooling in a magnetic ileld. To my astonishment I have found, however, that with these alloys the anisoa high cobalt-content and which, when heat treated in a manner suitable for obtaining an optimum (BH)max value, have a remanence of more than 10,000 Gauss, the improvement in the (8mm value due to the remarkably strong py-eiiect of the steel is considerable and that in general the remanence has a considerable influence in obtaining high (88)., values. In this manner I have found it possible to obtain the unprecedented (BID-m value of more than 25x10 and even more than x10, while at the same time securing a very high remanence. for instance, more than 12,000 Gauss. Thus, the present invention makes it possible to comply in a practical manner with the frequent desire to have a high (BI-Um together with a high remanence.
In contradistinction to what has been said in the above article in "Nature'. with respect to the change in coercive force I have found that more particularly with alloys according to the invention showing the higher (BIDm values, not only the remanence but also the coercive force, measured in a preferred direction is increased. The enormous. increase in the (3mm value is partly to be ascribed thereto.
In the following Table II are stated, by way of example, various alloys, which have been cooled according to a usual heat treatment (third column) and in a magnetic field (fourth column).
Table II Results obtainedthb o timum (an btained by mak in g mal m g g i Avmgo Fuum Composition in use of a usual therg Improve- No. the p goolnmn, speed factor per cent mal treatment with but in mm the mun ment in out magnetic field, h them 0 In m (13H)... (RH) mean! xmsgneticzl l d s its: between ann g about 1,310 mutant to G10 0 N1 A1 00 Cu Ti (BID-u Ho, Ba (BID-u H 3.-
C.p./sec.
1 10.0 8.5 23 1,211,010 9,050 3,450, 402 12,550 1 183 0.55 2 13.5 8 24 1.5 1,320,000 370 0,450 3,770,)0 505 13,100 2.0 185 0.57 3 13.5 8 84 3 LmiXlO 535 8,300 4,790,000 015 12,700 1.8 185 0.00 4 10 7.8 35 2.8 1,600,000 004 7,000 3,057,000 040 10,000 4 91 0.48 5 14 7.1 24 3 2.4 1,721000 505 7,900 57%,000 050 11, 4 12) 0.52 0 14 7.5 2) 0.5 1.8 1,050,000 020 7,350 3,250,000 570 0,825 4. 97 0.49 7. 15.5 8.1 so 1 1 2.3 1,824,000 640 8,150 3,117,000 585 10,210 4 71 0.45
(BK) max far exceeding the values hitherto attainable by 'means of the best kinds of steel.
Without cooling in a magnetic field higher values 5f (BH)max generally involved hitherto a lower remanence; for instance, (BI-I values of about 2,000,000 could only be attained at comparatively low values of the remanence, for instance not more than 9,000 Gauss. This is due inter alia to the fact that the improvement in (EH) max could only be obtained by raising the coercive force, which increase was obtained to a greater or less extent at the cost of the remanenee.
I have found that with steel alloys which have 7 The average cooling speed stated in the fifth column was used in both of the said cases and is so chosen that in cooling without magnetic field about the highest attainable product of B and H is attained.
Column 6 gives the percentage improvement of the (BH)max value according to column 4 over the (310m value according to column 3. It appears therefrom that, for instance, a composition according to the examples numbered 1 to 3 permits a magnet steel to be obtained which is about three times better than the same steel which has not been cooled in a magnetic field. From the other examples it appears that this composition yields also an improvement of the (BH)max value of at least 50%. From example 2 according to the invention it appears that in contradistinction to the prior art a very high (BH)m-x may quite well be associated with a remanence already high in itself.
The accompanying Figures 1 and 2 show the de-magnetisation curves of the examples numbered 1 and 3 in the table. The curves 1 and 2 correspond to a magnet steel according to the invention, whereas curves 3 and 4 correspond to the same steel treated according to the third column of the table. For comparison both 11gures represent in dotted lines the de-magnetisation curve of a known modern magnet steel having a very high (BI-1m. It appears from the figures that the high (BI'Dmax of the magnets according to the invention primarily results from a highly raised remanence and a more arched shape of the de-magnetisation curve, although the improvement of the coercive force with respect to the same steel cooled without magnetic field (compare curves 1 with 3 and 2 with 4) is also material.
For a proper understanding of the commercial importance of the present invention, it should be noted that the results given in the above tables are not limited to magnets of small dimensions or to testpieces.
I claim:
1. A permanent magnet consisting of a ferrous alloy containing about 16% to 30% cobalt, about 12% to 20% nickel, about 6% to 11% aluminum and the remainder principally iron, said magnet being magnetically-anisotropic and having a (BH)max value in the principal direction at least about 50% higher than the (31 1):; value of a substantially magnetically-isotropic permanent magnet of the same alloy.
2. A permanent magnet consisting of a ferrous alloy containing about 20% to 25% cobalt, about 13% to 17% nickel, about 7% to aluminum and the remainder principally iron, said magnet being magnetically-anisotropic and having 2. (BH) max value in the principal direction which is at least 2,500,000 and is at least about 50% higher than the (BIDmax value of a substantially magnetically-isotropic permanent magnet of the same alloy.
3. A permanent magnet consisting of a ferrous alloy containing about 20 to cobalt, about 13. to 16.5% nickel, about 7.1% to 8.5% aluminum and the remainder principally iron, said magnet being magnetically-anisotropic and having a (BH)msx value in the principal direction which is equal to at least about 3,000,000 and which is at least 50% greater than that of a substantially magnetically-isotropic permanent magnet of the same composition.
4. A permanent magnet consisting of a ferrous alloy containing about 21% to 25% cobalt, about 14% to 20% nickel, about 8% to 10% aluminum and the remainder principally iron, said magnet being magnetically-anisotropic and having a (BI'Dmax value in the principal direction which is at least 2,000,000 and which is at least 50% greater than that of a magnetically-isotropic permanent magnet of the same alloy, and a remanence of at least 8,000 Gausses.
5. A permanent magnet consisting of a ferrous alloy containing about 23% to 24% cobalt, about 13.5% to 16% nickel, about 7% to 8.5% aluminum and the remainder substantially iron, said magnet being magnetically-anisotropic and having a (BHMMX value in the principal direction of at least 3,000,000.
6. A permanent magnet consisting of a ferrous alloy containing about 16% to cobalt, about 12% to 20% nickel, about 6% to 11% aluminum, the remainder being iron and at least one of the elements titanium in an amount less than about 5% and copper in an amount less than about 7%, said magnet being magnetically anisotropic and having a (BH) max value in the principal direction of at least about 50% higher than the (BH)mx value of a substantially magneticallyisotropic permanent magnet of the same alloy.
7. A permanent magnet consisting of a ferrous alloy containing about 20% to 25% cobalt, about 13.5% to 16.5% nickel, about 7.1% to 8.1% aluminum, the optional inclusion of one or both of the elements copper in an amount less than about 6.5% and titanium in an amount less than about 2.8% and the remainder iron, said magnet being magnetically-anisotropic and having a (BH)mu value in the principal direction which is at least 3,000,000 and which is at least 50% greater than that of a magnetically-isotropic permanent magnet of the same alloy, and a remanence of at least 8,000 Gausses.
8. A permanent magnet consisting of a ferrous alloy containing about 23% to 24% cobalt, about 13.5% to 16% nickel, about 7% to 8.5% aluminum, the remainder being iron and small quantities of at least one of the elements copper and titanium, said magnet being magneticallyanisotropic and having a (BH)mn value in the principal direction of at least 3,000,000.
9. A permanent magnet consisting of a ferrous alloy containing about 16% to 30% cobalt, about 12% to 20% nickel, about 6% to 11% aluminum, not more than 5% titanium and the remainder principally iron, the total aluminum-titanium content being not more than about 12%, said magnet being magnetically-anisotropic and having a (BH)max value in the principal direction at least about 50% higher than the (BHhnu value of a substantially magnetically-isotropic permanent magnet of the same alloy.
10. A magnetically-anisotropic permanent magnet consisting of a ferrous alloy containing about 14% to 18% nickel, about 22% to 25% cobalt, about 6% to 8% aluminum, about 0.4% to 4% titanium and the remainder principally iron, said magnet having a coercive force of more than 450 Oersteds and a (BH)max value which is greater than 2,500,000 and which is at least 50% greater than that of a substantially magneticallyisotropic permanent magnet of the same composition.
11. A magnetically-anisotropic permanent magnet consisting of a ferrous alloy containing about 14% to 18% nickel, about 22% to 25% cobalt, about 6% to 8% aluminum, about 0.4% to 4% titanium and the remainder principally iron, said magnet having a coercive force of more than 450 Oersteds and a (BH)max value which is greater than 3,000,000 and which is at least 50% greater than that of a substantially magneticallyisotropic permanent magnet of the same composition.
12. A permanent magnet consisting of a ferrous alloy containing about 20 to 27.5% cobalt, about 12% to 15% nickel, about 8% to 8.5% aluminum, about 1.5% to 6.5% copper and the remainder principally iron, said magnet being magnetically-anisotropic and having a (BI-Um value in the principal direction which is equal to at least about 3,500,000 and which is atleast 50% greater than that of a substantially magnetically-isotropic permanent magnet of the same composition.
13. A magneticallyanisotropic permanent magnet consisting of a ferrous alloy containing about 13% to 16.5% nickel, about 18.5% to 25% cobalt, about 6.5% to 8.5% aluminum, about 1% to 3% titanium, about 1% to 7% copper and the remainder principally iron, said magnet having a (BH)max value which is greater than 3,000,000 and which is at least 50% greater than that of a substantially magnetically-isotropic permanent magnet of the same composition.
14. In the manufacture of a permanent magnet the steps of forming a body of a ferrous alloy containing about 16% to 30% cobalt, about 12% to 20% nickel, about 6% to 11% aluminum and the remainder principally iron, and subjecting the body to a magnetic field during the cooling operation required for magnetic hardening.
15. In the manufacture of a permanent magnet, the steps of forming a body of a ferrous alloy containing about 16% to 30% cobalt, about 12% to 20% nickel, about 6% to 11% aluminum, and the remainder principally iron, subjecting the body to a magnetic field during the cooling operation required for magnetic hardening to thereby make the alloy magnetically-anisotropic, and subsequently magnetizing the body in a direction corresponding to the direction of magnetization during cooling to thereby obtain a (BH)max value at least 50% higher than that obtained with the same alloy without magnetization during the cooling.
16. In the manufacture of a permanent magnet, the steps of forming a body of a ferrous alloy having a Curie-temperature above about 780 C. and containing about 16% to 30% cobalt, about 12% to 20% nickel, about 6% to 11% aluminum and the remainder principally iron, subjecting the body to a magnetic field during the cooling operation required for magnetic hardening and while the alloy is at a temperature between its Curie-temperature and a temperature lying about 150 below the Curie-temperature to thereby make the alloy magnetically-anisotropic, and subsequently magnetizing the body in a direction corresponding to the direction of magnetization during cooling to thereby obtain a (BB) max value at least 50% higher than that obtained with the same alloy without magnetization during the cooling.
17. In the manufacture of a permanent magnet, the steps of forming a body of a ferrous alloy containing about 20% to 25% cobalt, about 13% to 17% nickel, about 7% to aluminum and the remainder principally iron, subjecting net, the steps of forming a body of a ferrous alloy containing about 20% to 25% cobalt, 13.5% to 16.5% nickel, 7.1% to 8.5% aluminum and the remainder principally iron, subjecting the body to magnetization during the cooling operation required for magnetic hardening, and subsequently magnetizing the body in a direction corresponding to the direction of magnetization during the cooling to thereby obtain a (BH) max value which is greater than 3,000,000 and which is at least 50% greater than that of a substantiallyisotropic permanent magnet of the same composition.
19. In the manufacture of a permanent magnet, the steps of forming a body of a ferrous alloy containing about 23% to 24% cobalt, about 13.5% to 16% nickel, about 7% to 8.5% aluminum and the remainder principally iron, subjecting the body to magnetization during the cooling operation required for magnetic hardening and subsequently magnetizing the body in a direction corresponding to the direction of magnetization during the cooling to thereby obtain a (BH) max value greater than 3,000,000.
20. In the manufacture of a permanent magnet, the steps of forming a body of a ferrous alloy containing about 20% to 25% cobalt, about 13.5% to 16.5% nickel, about 7.1% to 8.5% aluminum, the optional inclusion of one or both of the elements copper in an amount less than about 6.5% and titanium in an amount less than about 2.8% and the remainder iron, cooling the body in a magnetic field from a temperature of about 1200 C. to a temperature of about 600 C. at a rate of between about 1 and 4.3 degrees centigrade per second to thereby make the alloy magneticallyanisotropic, and subsequently magnetizing the body in a direction corresponding to the direction of magnetization during cooling to thereby obtain a (BI-Drum: value at least 50% higher than that obtained with the same alloy without magnetization during the cooling.
21. In the manufacture of a permanent magnet, the steps of forming a body of a ferrous alloy containing about 23% to 24% cobalt, about 13.5% to 16% nickel, about 7% to 8.5% aluminum, the remainder being iron and small quantitles of at least one of the elements copper and titanium, subjecting the body to magnetization during the cooling operation required for magnetic hardening and subsequently magnetizing the body in a direction corresponding to the direction of magnetization during the cooling to thereby obtain a (BH)max value greater than 3,000,000.
' GO'I'IFRIED BRUNO JONAS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2295082X | 1938-12-06 |
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| Publication Number | Publication Date |
|---|---|
| US2295082A true US2295082A (en) | 1942-09-08 |
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ID=7993892
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US281988A Expired - Lifetime US2295082A (en) | 1938-12-06 | 1939-06-29 | Permanent magnet and method of making the same |
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Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2427571A (en) * | 1947-09-16 | Magnetic structure for electrical | ||
| US2442762A (en) * | 1943-09-09 | 1948-06-08 | Bell Telephone Labor Inc | Methods of improving the magnetic quality of anisotropic permanent magnets containing iron, nickel, cobalt, and aluminum |
| US2499861A (en) * | 1948-03-16 | 1950-03-07 | Crucible Steel Co America | Permanent magnets and alloys therefor |
| US2499860A (en) * | 1946-10-03 | 1950-03-07 | Crucible Steel Co America | Production of permanent magnets and alloys therefor |
| US2546047A (en) * | 1948-04-13 | 1951-03-20 | Gen Electric | Sintered anisotropic alnico magnet |
| US2683921A (en) * | 1948-03-30 | 1954-07-20 | Gen Electric | Method of making and magetizing encased permanent magnets |
| US2694790A (en) * | 1948-02-17 | 1954-11-16 | Gen Electric | Sintered anisotropic permanent magnet |
| US2695370A (en) * | 1950-07-04 | 1954-11-23 | Hartford Nat Bank & Trust Co | Permanent magnet for dynamoelectric machines |
| US2827437A (en) * | 1951-10-04 | 1958-03-18 | Philips Corp | Method of making a permanent magnet |
| US2961360A (en) * | 1958-12-01 | 1960-11-22 | Gen Electric | Magnets having one easy direction of magnetization |
| US3219496A (en) * | 1962-02-17 | 1965-11-23 | Magnetfabrik Bonn Gewerkschaft | Method of producing columnar crystal texture in sintered permanent magnets |
| US3314828A (en) * | 1964-01-22 | 1967-04-18 | Swift Levick & Sons Ltd | Permanent magnets |
| US3322579A (en) * | 1963-09-18 | 1967-05-30 | Permag Corp | Magnetic hysteresis alloy made by a particular process |
| US3432279A (en) * | 1967-08-30 | 1969-03-11 | Gen Electric | Molded magnetic powdered metal |
| US3471725A (en) * | 1966-03-18 | 1969-10-07 | Squibb & Sons Inc | Oscillating electric motor |
| US3524092A (en) * | 1965-07-23 | 1970-08-11 | Hitachi Ltd | Synchronous motor |
| US3805400A (en) * | 1971-05-05 | 1974-04-23 | Ketcham & Mcdougall | Compass |
| US4273595A (en) * | 1979-03-19 | 1981-06-16 | Inoue-Japax Research Incorporated | Method of preparing thermomagnetically treated magnetically anisotropic objects |
-
1939
- 1939-06-29 US US281988A patent/US2295082A/en not_active Expired - Lifetime
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2427571A (en) * | 1947-09-16 | Magnetic structure for electrical | ||
| US2442762A (en) * | 1943-09-09 | 1948-06-08 | Bell Telephone Labor Inc | Methods of improving the magnetic quality of anisotropic permanent magnets containing iron, nickel, cobalt, and aluminum |
| US2499860A (en) * | 1946-10-03 | 1950-03-07 | Crucible Steel Co America | Production of permanent magnets and alloys therefor |
| US2694790A (en) * | 1948-02-17 | 1954-11-16 | Gen Electric | Sintered anisotropic permanent magnet |
| US2499861A (en) * | 1948-03-16 | 1950-03-07 | Crucible Steel Co America | Permanent magnets and alloys therefor |
| US2683921A (en) * | 1948-03-30 | 1954-07-20 | Gen Electric | Method of making and magetizing encased permanent magnets |
| US2546047A (en) * | 1948-04-13 | 1951-03-20 | Gen Electric | Sintered anisotropic alnico magnet |
| US2695370A (en) * | 1950-07-04 | 1954-11-23 | Hartford Nat Bank & Trust Co | Permanent magnet for dynamoelectric machines |
| US2827437A (en) * | 1951-10-04 | 1958-03-18 | Philips Corp | Method of making a permanent magnet |
| US2961360A (en) * | 1958-12-01 | 1960-11-22 | Gen Electric | Magnets having one easy direction of magnetization |
| US3219496A (en) * | 1962-02-17 | 1965-11-23 | Magnetfabrik Bonn Gewerkschaft | Method of producing columnar crystal texture in sintered permanent magnets |
| US3322579A (en) * | 1963-09-18 | 1967-05-30 | Permag Corp | Magnetic hysteresis alloy made by a particular process |
| US3314828A (en) * | 1964-01-22 | 1967-04-18 | Swift Levick & Sons Ltd | Permanent magnets |
| US3524092A (en) * | 1965-07-23 | 1970-08-11 | Hitachi Ltd | Synchronous motor |
| US3471725A (en) * | 1966-03-18 | 1969-10-07 | Squibb & Sons Inc | Oscillating electric motor |
| US3432279A (en) * | 1967-08-30 | 1969-03-11 | Gen Electric | Molded magnetic powdered metal |
| US3805400A (en) * | 1971-05-05 | 1974-04-23 | Ketcham & Mcdougall | Compass |
| US4273595A (en) * | 1979-03-19 | 1981-06-16 | Inoue-Japax Research Incorporated | Method of preparing thermomagnetically treated magnetically anisotropic objects |
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