US3432369A - Method of making magnetically anisotropic permanent magnets - Google Patents
Method of making magnetically anisotropic permanent magnets Download PDFInfo
- Publication number
- US3432369A US3432369A US549029A US3432369DA US3432369A US 3432369 A US3432369 A US 3432369A US 549029 A US549029 A US 549029A US 3432369D A US3432369D A US 3432369DA US 3432369 A US3432369 A US 3432369A
- Authority
- US
- United States
- Prior art keywords
- melt
- alloy
- seed
- oriented
- axially
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/032—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials
- H01F1/04—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials metals or alloys
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C19/00—Alloys based on nickel or cobalt
- C22C19/07—Alloys based on nickel or cobalt based on cobalt
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/10—Ferrous alloys, e.g. steel alloys containing cobalt
- C22C38/105—Ferrous alloys, e.g. steel alloys containing cobalt containing Co and Ni
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B11/00—Single-crystal growth by normal freezing or freezing under temperature gradient, e.g. Bridgman-Stockbarger method
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B29/00—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
- C30B29/10—Inorganic compounds or compositions
- C30B29/52—Alloys
Definitions
- the invention relates to a method of manufacturing rod-shaped magnetically anisotropic permanent magnet bodies having a cubic crystal structure and a (100) direction of the crystals which is substantially axially oriented from an alloy containing, in addition to, Fe and the normally present impurities, 16-42% of Co, 7-20% of Ni, 6-11% of- Al, 010% of Cu, 110% of Ti, 0-4% of Nb, 08% of Ta, 0l% of Si, 01% of S, a melt of the said alloy being cooled in a temperature gradient.
- Normally-present impurities are to be understood to mean herein those impurities which are already present in the raw materials. In general they total approximately 0.5%.
- alloys in the aforesaid range which contain given quantities of Co and Ti may show very high coercive forces, (up to 2000 oersted)
- Further means are provided to avoid heat flowing away to an undesired extent in a lateral direction, for example, additional heat. It is possible in this manner to obtain a (BH) value of 5.5 10 g.0., which is reproducible in mass production.
- this method consists in that the molten alloy is continuously applied to the top of a vertically arranged pipe, the rod of the molten alloy being continuusly, or discontinuously, drawn out of the pipe on the lower side.
- the desired crystal orientation in axial direction is obtained by withdrawing the heat through the rod itself in one direction-the longitudinal direction of the rodwhich can even be promoted by additionally cooling the part of the rod emerging out of the pipe.
- the pipe be insulated in a transverse direction and/ or heated by additional means so as to check the thermal losses.
- magnets without crystal orientation can be mass produced which show high coercive forces of 1000 0e. and more in a reproducible manner.
- a very good representative of this group is, for example, the alloy consisting of 34% of Co, 14.5% of Ni, 7% of A1, 4.5% of Cu, 5% of Ti, rest Fe and the impurities normally present. With this alloy magnets can be mass-produced without crystal orientation having (BH) values of 4-5 10 go. and coercive forces of 1300-1500 oe.
- Another object of the invention is to provide a method of manufacturing anisotropic permanent magnets consisting of a Co-Ni-Al-Me alloy having a (BH) value of at least 9.0 l g.o.
- the invention is based on the discovery that in order to obtain magnetically anisotropic permanent magnets having a high (BH) value and a high coercive force from the aforesaid group of alloys, the conditions at the solidification front, or points at which solidification of the melt occurs, must be optimum. In addition to the withdrawal of heat in the axial direction, additional measures must be taken to insure formation of the desired crystal orientation, a criterion for which is that the (BH),,,,,,, value must be at least 9X 10 gauss-oersted. Thus, it has been found that the solidification rate R must meet special requirements dependent upon the composition of the alloy and dependent upon quantities determined by the apparatus used.
- the solidification rate R (mm/min.) for a given Ti-content, a given temperature gradient G C/mm.) then is kept below a given maximum value.
- the temperature gradient adjusts in a particular oven, the temperature gradient at the solidification front in the melt-which, ultimately, is decisive of the product to be manufacturedwill differ considerably from the first mentioned gradient. This difference is determined principally by the rate R with which the solidification front moves so that this rate R is the most important variable quantity.
- the solidification of the alloy begin after the melt has been contacted with a seed which has a dendritically formed boundary surface oriented in the direction.
- a seed for example, a cubic monocrystal of an alloy of the composition: 23% of Co, 14% of Ni, 3% of Cu, 8% of Al, and the balance Fe, may be used.
- Such an alloy is also known in the trade at Ticonal G/G.
- the oxide skin which is always present on the surface of such a melt (both of a partially molten seed and on the molten alloy to be contacted therewith) must be removed.
- This oxide skin between the seed and the melt may be removed by means of cryolite (Na AIF which can be provided on the boundary surface of the seed before the melt and the seed are contacted with one another.
- cryolite Na AIF which can be provided on the boundary surface of the seed before the melt and the seed are contacted with one another.
- the oxide skin may also be removed mechanically. This may be done, for example, with a stirring rod.
- the skin can be removed by convection flows in the melt, but convection flows only will be sufiiciently operative when the diameter of the melt is large 10 mm.). The skin may be forced upwards by said flows.
- Example I A rod, 2 cm. long, 20 mm. diameter, of an alloy having the composition:
- a layer of cryolite was provided on the boundary surface between the seed and the rod.
- a ceramic pipe was slid over the rod and the seat, after which the assembly was placed in a vertical oven.
- the rod was melted in an atmosphere of cleaned argon gas.
- the position of the pipe in the oven was chosen to be such that part of the oriented seed also melts.
- the rate R was 0.15 mm./min.
- Example IV A rod, diameter 20 mm., of an alloy having the composition:
- the rate R was 2 mm./ min.
- a method of manufacturing rod-shaped magnetically anisotropic permanent magnet bodies having a cubic crystal structure and a (100) direction of the crystals oriented substantially axially from an alloy consisting of 16-42% of Co, 720% of Ni, 611% of Al, 010% of Cu, 1-10% of Ti, 04% of Nb, 0-8% of Ta, 0l% of Si, 01% of S and the balance principally Fe comprising the steps of forming a melt of the said alloy, contacting the melt with an oxide-free seed having a cubic crystal structure, the (100) direction of which is oriented axially and which is miscible in the liquid phase of the melt, the seed during contact with the melt partially melting and forming a dendritic boundary surface with an axially oriented 100) direction of the crystal, and cooling the melt at a predetermined solidification rate R (mm./min.), which for a given temperature gradient G C./min.) at the solidification front is kept below a predetermined maximum value, which increases as the Ticontent decreases, where
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mechanical Engineering (AREA)
- Power Engineering (AREA)
- Inorganic Chemistry (AREA)
- Hard Magnetic Materials (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
Description
March 11, 1969 P. A. NAASTEPAD 3,432,369
METHOD OF MAKING MAGNETICALLY ANISOTRO PIC PERMANENT MAGNETS Filed May 10, 1966 INVENTOR. P IE TER A. NAASTEPAD AGENT United States Patent 6507303 US. Cl. 148-101 Int. Cl. H01f 1/04 6 Claims The invention relates to a method of manufacturing rod-shaped magnetically anisotropic permanent magnet bodies having a cubic crystal structure and a (100) direction of the crystals which is substantially axially oriented from an alloy containing, in addition to, Fe and the normally present impurities, 16-42% of Co, 7-20% of Ni, 6-11% of- Al, 010% of Cu, 110% of Ti, 0-4% of Nb, 08% of Ta, 0l% of Si, 01% of S, a melt of the said alloy being cooled in a temperature gradient.
Normally-present impurities are to be understood to mean herein those impurities which are already present in the raw materials. In general they total approximately 0.5%.
Known methods of obtaining crystal orientation in magnets of the aforesaid type are all based on the principle that heat is withdrawn from the alloy during soldification only in one direction. From these alloys magnet bodies are formed which in accordance with the method used have a more or less pronounced crystal orientation in that direction. If it is ensured that the preferred direction of magnetization is located in the same direction by subjecting the magnet body to the action of a magnetic field during the thermal treatment, the direction of which field coincides with the (100) direction, it is possible, with the combination of these two factors (crystal-orientation and magnetic field treatment), to obtain magnetic properties in these alloys which far exceed the proper ties which are obtained if only one of these two factors is present. Consequently, in the manufacture of magnets it is sought to obtain optimum results in this manner and in particular by using methods which give reproducible results, and, in addition, are suitable for mass production. The end view in these endeavours is not so much an improvement of the magnetic field treatment, as an improvement of the crystal orientation. Naturally, the choice of the alloy to be used is also decisive for obtaining the desired specific magnetic properties, for example, a high (BH) value combined, or not combined, with a coercive force which is as high as possible- Moreover, the choice of the composition of the alloys determines the properties of the magnet. For example, it is generally known that alloys in the aforesaid range which contain given quantities of Co and Ti, may show very high coercive forces, (up to 2000 oersted) To obtain the desired crystal orientation in alloys which have a titanium content and in which the (100) direction of the crystals is oriented axially, it is conventional to use vertically arranged molds which are provided in the bottom with a so-called chill-plate as a result of which the heat, during solidification of the alloy, is withdrawn substantially in a direction at right angles to said chill-plate. Further means are provided to avoid heat flowing away to an undesired extent in a lateral direction, for example, additional heat. It is possible in this manner to obtain a (BH) value of 5.5 10 g.0., which is reproducible in mass production.
With such alloys (BH) values of 7-9 10 g.o.
can be obtained in'a reproducible manner in mass production if rods of the such alloys are manufactured according to the so-called continuous casting process in which the 100) direction of the crystals is oriented axially. For example, this method consists in that the molten alloy is continuously applied to the top of a vertically arranged pipe, the rod of the molten alloy being continuusly, or discontinuously, drawn out of the pipe on the lower side. The desired crystal orientation in axial direction is obtained by withdrawing the heat through the rod itself in one direction-the longitudinal direction of the rodwhich can even be promoted by additionally cooling the part of the rod emerging out of the pipe. It is also preferable that the pipe be insulated in a transverse direction and/ or heated by additional means so as to check the thermal losses.
In the range of the Ti-containing alloys from the group containing l642% of Co, 720% of Ni, 6-11% of Al, 010% of Cu, 110% of Ti, 0-4% of Nb, 0-8% of Ta, 0-1% of Si, 0-1% of S, rest Fe and the normally present impurities, magnets without crystal orientation can be mass produced which show high coercive forces of 1000 0e. and more in a reproducible manner. A very good representative of this group is, for example, the alloy consisting of 34% of Co, 14.5% of Ni, 7% of A1, 4.5% of Cu, 5% of Ti, rest Fe and the impurities normally present. With this alloy magnets can be mass-produced without crystal orientation having (BH) values of 4-5 10 go. and coercive forces of 1300-1500 oe.
The manufacture of magnets with crystal orientation from an alloy containing little or no Ti presents no difficulties in mass manufacture with reproducible results; this is not the case with magnets containing 1% or more of Ti. With alloys having a maximum Ti content up to 1% it is possible to use the above-described method of molding using a chill-plate. For alloys having higher Ti contents, which are required to obtain the desired very high coercive forces, this method, however, generally cannot be used, since the solidification rates which occur are too large. In addition the simultaneous presence of Ti and Al gives rise to undesired nuclei formation which disturbs the crystal orientation. Nuclei formation can be decreased, however, by adding S or Se to the alloy.
Obtaining crystal orientation in alloys having a high Ti content by means of the above described continuous casting process also presents difficulties. In fact, the high Ti content in the alloy has for its result that the melt more or less sticks to the ceramic material of the wall of the pipe. As a result thereof it is possible only to draw bars of a restricted length, while the very advantage of such a method is that unrestricted lengths can be produced so that continuous manufacture is possible.
Also suitable for mass manufacture is the known and useful but time-consuming and expensive methods of obtaining monocrystals and pseudo-monocrystals by drawing a rod from the Ti-containing melt in an upward direction. However, in this manner only rods a few mms. thick can be obtained and it requires care to be taken that the oxide skin floating on the melt does not disturb the desired crystal orientation. The highly pure atmosphere required for this method, however, requires special measures to be taken which are not very attractive for mass production. It should be noted that it possible in this manner to obtain (BH) values of approximately 1l 10 g.o. combined with coercive forces of 1300-1500 oersted.
An improvement with respect to mass manufacture was obtained using the so-called floating-zone melt method, in which rods of the alloy are moved through a heating zone. Heating is effected by means of a thin high-frequency coil through which the rod extends. In the heating zone the alloy melts after which on cooling in the known manner the desired axial crystal orientation is obtained. This method offers the possibility of using a semior fullyautomatic plant suitable for various alloys.
However, a draw-back of this method, in particular in the method of floating-zone melting without the use of a crucible, is that "during operation the center of the rod does not always coincide with the center of the space enclosed by the high-frequency coil as a result of which an inclined solidification front is obtained which results in that in some parts of the rod not the (100) direction of the crystals, but, for example, the (110) direction Will be oriented axially.
A further drawback is that in spite of the precautions taken, heat will be dissipated in a radial direction which promotes an undesired direction of growth of the crystals, namely from without to within.
A very important drawback of such a magnet is that the molten zone shows convection flows as a result of the presence of the high frequency coil. As a result of this many new crystals are formed with arbitrary orientations, which is very undesirable.
A result of these draw-backs is that the energy product always is smaller than 9x10 go.
It is a principal object of the invention to provide a method of manufacturing a permanent magnet having a high (BH),,,,, value and a high coercive force using an alloy of the aforesaid type.
It is a further object of the invention to provide a method of manufacturing a permanent magnet using alloys of the aforesaid type but having an improved crystal orientation in the (100) direction whereby magnets are obtained which have a higher (BH) value and coercive force than hitherto obtainable.
Another object of the invention is to provide a method of manufacturing anisotropic permanent magnets consisting of a Co-Ni-Al-Me alloy having a (BH) value of at least 9.0 l g.o.
These and further objects of the invention will appear as this specification progresses.
The invention is based on the discovery that in order to obtain magnetically anisotropic permanent magnets having a high (BH) value and a high coercive force from the aforesaid group of alloys, the conditions at the solidification front, or points at which solidification of the melt occurs, must be optimum. In addition to the withdrawal of heat in the axial direction, additional measures must be taken to insure formation of the desired crystal orientation, a criterion for which is that the (BH),,,,,,, value must be at least 9X 10 gauss-oersted. Thus, it has been found that the solidification rate R must meet special requirements dependent upon the composition of the alloy and dependent upon quantities determined by the apparatus used.
Thus, in accordance with the invention the oxide skin which forms between a seed having a cubic crystal structure, the (100) direction of which is oriented axially, and which in the liquid phase is miscible with the melt, and the melt first is removed and then the melt is contacted with the seed during which contact the seed partially melts and forms a dendritic melting face having an axially oriented (100) direction of the crystals. While in contact with the seed, the solidification rate R (mm/min.) for a given Ti-content, a given temperature gradient G C/mm.), and for a given solidification front then is kept below a given maximum value.
According to this method it is possible to mass produce in a fully reproducible manner rods of magnet steel of any desired diameter, the energy product (BH) value of which has values of from 9--12 l0 g.o. These high (BH) values moreover can be obtained with alloys having more than 1% of Ti. The value of the coercive force H may even be 2000 oe. when the composition contains 40% of Co, and 7.5% of Ti.
Although the temperature gradient adjusts in a particular oven, the temperature gradient at the solidification front in the melt-which, ultimately, is decisive of the product to be manufacturedwill differ considerably from the first mentioned gradient. This difference is determined principally by the rate R with which the solidification front moves so that this rate R is the most important variable quantity.
The invention will be described in greater detail with reference to the accompanying drawing, the sole figure of which shows the dependency of the energy product, (BH) value, in relation to the solidification rate, R.
The manner in which maximum admissible solidification rate R for a given temperature gradient G at the solidification front depends upon the percentage of the alloy is shown in the drawing. When combinations of the percentage of Ti and solidification rate R are chosen below the shaded area, a satisfactory crystal orientation is formed in the magnets. Above this area the resulting orientation is bad. With the combination in the shaded transition area, (BH) values of from 49 10 g.o. are obtained.
It is essential in the method according to the invention that the solidification of the alloy begin after the melt has been contacted with a seed which has a dendritically formed boundary surface oriented in the direction. As a seed, for example, a cubic monocrystal of an alloy of the composition: 23% of Co, 14% of Ni, 3% of Cu, 8% of Al, and the balance Fe, may be used. Such an alloy is also known in the trade at Ticonal G/G. Once a part of the melt has solidified, this newly formed magnet steel itself may serve as a seed to obtain the desired crystal orientation in the melt which is still to be solidified.
When the melt has contacted with a seed, first the oxide skin which is always present on the surface of such a melt (both of a partially molten seed and on the molten alloy to be contacted therewith) must be removed. This oxide skin between the seed and the melt may be removed by means of cryolite (Na AIF which can be provided on the boundary surface of the seed before the melt and the seed are contacted with one another. When the oxide skin is contacted with the cryolite, it dissolves therein after which a ready contact is formed between the melt and the seed.
According to a further embodiment of the method of the invention, the oxide skin may also be removed mechanically. This may be done, for example, with a stirring rod. Alternatively, according to another embodiment the skin can be removed by convection flows in the melt, but convection flows only will be sufiiciently operative when the diameter of the melt is large 10 mm.). The skin may be forced upwards by said flows.
Example I A rod, 2 cm. long, 20 mm. diameter, of an alloy having the composition:
35% of Co, 34.5% of Fe, 14.5% of Ni, 7.3% of A1, 4.5% of Cu, 5.2% of Ti,
was placed on a seed consisting of a few crystals oriented with their (100) direction in the direction of the axis of the rod and having the composition:
24% of Co,
14% of Ni,
3% of Cu,
8% of Al,
and the balance Fe.
A layer of cryolite was provided on the boundary surface between the seed and the rod.
A ceramic pipe was slid over the rod and the seat, after which the assembly was placed in a vertical oven. The rod was melted in an atmosphere of cleaned argon gas. The position of the pipe in the oven was chosen to be such that part of the oriented seed also melts.
The ceramic pipe was then lowered on the lower side )max.=X10 go. H 1500 cc.
If the rate R was 2 mm./min., these properties were The rate R was 1.0 mm./min. The resulting magnetic properties were:
If the rate R=3.5 mm./min., these properties were Example III A rod diameter 20 mm., of an alloy of the composition:
40.0% of Co 27.5% of Fe 14.0% of Ni 8.0% of A1 7.5% of Ti 3.0% of Cu was treated in the same manner as described in Example I.
The rate R was 0.15 mm./min.
The resulting magnetic properties were:
( )max.= .g.o. 151 :1980 oe.
If the rate R=1.5 mm./min., the resulting magnetic properties were:
( )max,=7-0X10 g.o.
Example IV A rod, diameter 20 mm., of an alloy having the composition:
29% of Co 14% of Ni 8% of A1 3% of Cu 3% of Ti 2% of Nb and the balance Fe was treated in the same manner as described in Example I.
The rate R was 2 mm./ min.
The resulting magnetic properties were:
( )max.= X10 go. H 1250 0e.
If the rate R was 5 mm./min., the resulting magnetic properties were:
)max.= X10 g.o.
While the invention has been described in connection with specific examples and applications thereof, other modifications will be apparent to those skilled in this art without departing from the spirit and scope of the invention.
What is claimed is:
1. A method of manufacturing rod-shaped magnetically anisotropic permanent magnet bodies having a cubic crystal structure and a (100) direction of the crystals oriented substantially axially from an alloy consisting of 16-42% of Co, 720% of Ni, 611% of Al, 010% of Cu, 1-10% of Ti, 04% of Nb, 0-8% of Ta, 0l% of Si, 01% of S and the balance principally Fe comprising the steps of forming a melt of the said alloy, contacting the melt with an oxide-free seed having a cubic crystal structure, the (100) direction of which is oriented axially and which is miscible in the liquid phase of the melt, the seed during contact with the melt partially melting and forming a dendritic boundary surface with an axially oriented 100) direction of the crystal, and cooling the melt at a predetermined solidification rate R (mm./min.), which for a given temperature gradient G C./min.) at the solidification front is kept below a predetermined maximum value, which increases as the Ticontent decreases, whereby the resulting alloy after thermal treatment in a magnetic field has a (BH) value of at least 9.0)(10 go.
2. A method as claimed in claim 1, in which the oxide skin between the seed and the melt is removed with cryolite, (Na AlF 3. A method as claimed in claim 1, in which the oxide skin between the seed and the melt is removed mechanically.
4. A method as claimed in claim 1, in which the oxide skin between the seed and the melt is removed by convection flows in the melt.
5. A method as claimed in claim 1, in which the seed is an alloy of about 23% of Co, 14% of Ni, 3% of Cu, 8% of Al, and the balance Fe.
6. A method as claimed in claim 2, in which the cryolite is provided on the boundary surface between the seed and the rod.
References Cited UNITED STATES PATENTS 2,673,310 3/1954 Dannijhl 148-3157 XR 2,837,452 6/1958 de Vos et a1. 148-103 2,862,287 12/1958 Koch et a1 148-101 XR 2,933,427 4/ 1960 Marrs et a1. 148-103 3,085,036 4/ 1963 Steinort 148-1.6 XR 3,175,901 3/1965 Jesmont et al -124 3,206,337 9/1965 Walmer 148-3157 3,314,828 4/ 1967 Harrison 148-3157 3,350,240 10/1967 Higuchi et a1. 148-1.6
OTHER REFERENCES Auslegescrift, Germany, 1,160,650, 148-101 Jan. 2, 1964.
Phillips Research Reports, vol. 11, 1956, pp. 489-490.
L. DEWAYNE RUTLEDGE, Primary Examiner. PAUL WEINSTEIN, Assistant Examiner.
U.S. Cl. X.R.
Claims (1)
1. A METHOD OF MANUFACTURING ROD-SHAPED MAGNETICALLY ANISOTROPIC PERMANENT MAGNET BODIES HAVING A CUBIC CRYSTAL STRUCTURE AND A (100) DIRECTION OF THE CRYSTALS ORIENTED SUBSTANTIALLY AXIALLY FROM AN ALLOY CONSISTING OF 16-42% OF CO, 7-20% OF NI, 6-11% OF AL, 0-10% OF CU, 1-10% OF TI, 0-4% OF NB, 0-8% OF TA, 0-1% OF SI, 0-1% OF S AND THE BALANCE PRINCIPALLY FE COMPRISING THE STEPS OF FORMING A MELT OF THE SAID ALLOY, CONTACTING THE MELT WITH AN OXIDE-FREE SEED HAVING A CUBIC CRYSTAL STRUCTURE, THE (100) DIRECTION OF WHICH IS ORIENTED AXIALLY AND WHICH IS MISCIBLE IN THE LIQUID PHASE OF THE MELT, THE SEED DURING CONTACT WITH THE MELT PARTIALLY MELTING AND FORMING A DENDRITIC BOUNDARY SURFACE WITH AN AXIALLY ORIENTED (100) DIRECTION OF THE CRYSTAL, AND COOLING THE MELT AT A PREDETERMINED SOLIDIFICATION RATE R (MM./MIN.), WHICH FOR A GIVEN TEMPERATURE GRADIENT G (*C./MIN.) AT THE SOLIDIFICATION FRONT IS KEPT BELOW A PREDETERMINED MAXIMUM VALUE, WHICH INCREASES AS THE TICONTENT DECREASES, WHEREBY THE RESULTING ALLOY AFTER THERMAL TREATMENT IN A MAGNETIC FIELD HAS A (BH)MAX. VALUE OF AT LEAST 9.0$106 G.0.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL656507303A NL151831B (en) | 1965-06-09 | 1965-06-09 | PROCESS FOR THE MANUFACTURE OF ROD-SHAPED, MAGNETIC ANISOTROPE, PERMANENT MAGNETIC BODIES WITH CUBIC CRYSTAL STRUCTURE AND A MAINLY AXIALLY ORIENTED (100) DIRECTION OF THE CRYSTALS. |
Publications (1)
Publication Number | Publication Date |
---|---|
US3432369A true US3432369A (en) | 1969-03-11 |
Family
ID=19793332
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US549029A Expired - Lifetime US3432369A (en) | 1965-06-09 | 1966-05-10 | Method of making magnetically anisotropic permanent magnets |
Country Status (10)
Country | Link |
---|---|
US (1) | US3432369A (en) |
AT (1) | AT273513B (en) |
BE (1) | BE682208A (en) |
CH (1) | CH488257A (en) |
DE (1) | DE1533335C3 (en) |
DK (1) | DK119470B (en) |
ES (1) | ES327640A1 (en) |
GB (1) | GB1095846A (en) |
NL (1) | NL151831B (en) |
SE (1) | SE331317B (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3908737A (en) * | 1973-07-31 | 1975-09-30 | Nippon Steel Corp | Method for producing grain-oriented electrical steel sheet utilizing a continuous casting process |
US4007065A (en) * | 1975-02-28 | 1977-02-08 | Arnold Engineering Company | Hysteresis alloy |
US4134756A (en) * | 1976-09-07 | 1979-01-16 | Hitachi Metals, Ltd. | Permanent magnet alloys |
US4784703A (en) * | 1983-08-26 | 1988-11-15 | Grumman Aerospace Corporation | Directional solidification and densification of permanent magnets having single domain size MnBi particles |
US10109418B2 (en) | 2013-05-03 | 2018-10-23 | Battelle Memorial Institute | System and process for friction consolidation fabrication of permanent magnets and other extrusion and non-extrusion structures |
US10189063B2 (en) | 2013-03-22 | 2019-01-29 | Battelle Memorial Institute | System and process for formation of extrusion products |
US10695811B2 (en) | 2013-03-22 | 2020-06-30 | Battelle Memorial Institute | Functionally graded coatings and claddings |
US11045851B2 (en) | 2013-03-22 | 2021-06-29 | Battelle Memorial Institute | Method for Forming Hollow Profile Non-Circular Extrusions Using Shear Assisted Processing and Extrusion (ShAPE) |
US11383280B2 (en) | 2013-03-22 | 2022-07-12 | Battelle Memorial Institute | Devices and methods for performing shear-assisted extrusion, extrusion feedstocks, extrusion processes, and methods for preparing metal sheets |
US11549532B1 (en) | 2019-09-06 | 2023-01-10 | Battelle Memorial Institute | Assemblies, riveted assemblies, methods for affixing substrates, and methods for mixing materials to form a metallurgical bond |
US11919061B2 (en) | 2021-09-15 | 2024-03-05 | Battelle Memorial Institute | Shear-assisted extrusion assemblies and methods |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4289570A (en) * | 1978-12-13 | 1981-09-15 | United Technologies Corporation | Seed and method for epitaxial solidification |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2673310A (en) * | 1949-09-07 | 1954-03-23 | Deutsche Edelstahlwerke Ag | Permanent magnet |
US2837452A (en) * | 1955-01-19 | 1958-06-03 | Philips Corp | Method of making anisotropic permanent magnets |
US2862287A (en) * | 1952-12-17 | 1958-12-02 | Philips Corp | Method of making cast alnico magnets |
US2933427A (en) * | 1956-03-28 | 1960-04-19 | Philips Corp | Permanent anisotropic magnet and method of making same |
US3085036A (en) * | 1960-03-11 | 1963-04-09 | Ct Magneti Permanenti | Monocrystalline permanent magnets and method of making them |
US3175901A (en) * | 1962-02-07 | 1965-03-30 | U S Magnet & Alloy Corp | Permanent magnet and alloy therefor |
US3206337A (en) * | 1961-11-08 | 1965-09-14 | Hamilton Watch Co | Cobalt-platinum alloy and magnets made therefrom |
US3314828A (en) * | 1964-01-22 | 1967-04-18 | Swift Levick & Sons Ltd | Permanent magnets |
US3350240A (en) * | 1963-07-05 | 1967-10-31 | Sumitomo Spec Metals | Method of producing magnetically anisotropic single-crystal magnets |
-
1965
- 1965-06-09 NL NL656507303A patent/NL151831B/en unknown
-
1966
- 1966-04-06 SE SE07741/66*A patent/SE331317B/xx unknown
- 1966-05-10 US US549029A patent/US3432369A/en not_active Expired - Lifetime
- 1966-06-04 DE DE1533335A patent/DE1533335C3/en not_active Expired
- 1966-06-06 AT AT534866A patent/AT273513B/en active
- 1966-06-06 DK DK290166AA patent/DK119470B/en unknown
- 1966-06-06 CH CH812866A patent/CH488257A/en not_active IP Right Cessation
- 1966-06-07 BE BE682208D patent/BE682208A/xx unknown
- 1966-06-07 ES ES0327640A patent/ES327640A1/en not_active Expired
- 1966-06-09 GB GB25754/66A patent/GB1095846A/en not_active Expired
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2673310A (en) * | 1949-09-07 | 1954-03-23 | Deutsche Edelstahlwerke Ag | Permanent magnet |
US2862287A (en) * | 1952-12-17 | 1958-12-02 | Philips Corp | Method of making cast alnico magnets |
US2837452A (en) * | 1955-01-19 | 1958-06-03 | Philips Corp | Method of making anisotropic permanent magnets |
US2933427A (en) * | 1956-03-28 | 1960-04-19 | Philips Corp | Permanent anisotropic magnet and method of making same |
US3085036A (en) * | 1960-03-11 | 1963-04-09 | Ct Magneti Permanenti | Monocrystalline permanent magnets and method of making them |
US3206337A (en) * | 1961-11-08 | 1965-09-14 | Hamilton Watch Co | Cobalt-platinum alloy and magnets made therefrom |
US3175901A (en) * | 1962-02-07 | 1965-03-30 | U S Magnet & Alloy Corp | Permanent magnet and alloy therefor |
US3350240A (en) * | 1963-07-05 | 1967-10-31 | Sumitomo Spec Metals | Method of producing magnetically anisotropic single-crystal magnets |
US3314828A (en) * | 1964-01-22 | 1967-04-18 | Swift Levick & Sons Ltd | Permanent magnets |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3908737A (en) * | 1973-07-31 | 1975-09-30 | Nippon Steel Corp | Method for producing grain-oriented electrical steel sheet utilizing a continuous casting process |
US4007065A (en) * | 1975-02-28 | 1977-02-08 | Arnold Engineering Company | Hysteresis alloy |
US4134756A (en) * | 1976-09-07 | 1979-01-16 | Hitachi Metals, Ltd. | Permanent magnet alloys |
US4784703A (en) * | 1983-08-26 | 1988-11-15 | Grumman Aerospace Corporation | Directional solidification and densification of permanent magnets having single domain size MnBi particles |
US10695811B2 (en) | 2013-03-22 | 2020-06-30 | Battelle Memorial Institute | Functionally graded coatings and claddings |
US10189063B2 (en) | 2013-03-22 | 2019-01-29 | Battelle Memorial Institute | System and process for formation of extrusion products |
US11045851B2 (en) | 2013-03-22 | 2021-06-29 | Battelle Memorial Institute | Method for Forming Hollow Profile Non-Circular Extrusions Using Shear Assisted Processing and Extrusion (ShAPE) |
US11383280B2 (en) | 2013-03-22 | 2022-07-12 | Battelle Memorial Institute | Devices and methods for performing shear-assisted extrusion, extrusion feedstocks, extrusion processes, and methods for preparing metal sheets |
US11517952B2 (en) | 2013-03-22 | 2022-12-06 | Battelle Memorial Institute | Shear assisted extrusion process |
US11534811B2 (en) | 2013-03-22 | 2022-12-27 | Battelle Memorial Institute | Method for forming hollow profile non-circular extrusions using shear assisted processing and extrusion (ShAPE) |
US11684959B2 (en) | 2013-03-22 | 2023-06-27 | Battelle Memorial Institute | Extrusion processes for forming extrusions of a desired composition from a feedstock |
US10109418B2 (en) | 2013-05-03 | 2018-10-23 | Battelle Memorial Institute | System and process for friction consolidation fabrication of permanent magnets and other extrusion and non-extrusion structures |
US11549532B1 (en) | 2019-09-06 | 2023-01-10 | Battelle Memorial Institute | Assemblies, riveted assemblies, methods for affixing substrates, and methods for mixing materials to form a metallurgical bond |
US11946504B2 (en) | 2019-09-06 | 2024-04-02 | Battelle Memorial Institute | Assemblies, riveted assemblies, methods for affixing substrates, and methods for mixing materials to form a metallurgical bond |
US11919061B2 (en) | 2021-09-15 | 2024-03-05 | Battelle Memorial Institute | Shear-assisted extrusion assemblies and methods |
Also Published As
Publication number | Publication date |
---|---|
DE1533335B2 (en) | 1974-03-07 |
BE682208A (en) | 1966-12-07 |
ES327640A1 (en) | 1967-07-16 |
GB1095846A (en) | 1967-12-20 |
DE1533335A1 (en) | 1969-12-18 |
SE331317B (en) | 1970-12-21 |
DE1533335C3 (en) | 1974-10-10 |
DK119470B (en) | 1971-01-11 |
NL6507303A (en) | 1966-12-12 |
NL151831B (en) | 1976-12-15 |
CH488257A (en) | 1970-03-31 |
AT273513B (en) | 1969-08-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3432369A (en) | Method of making magnetically anisotropic permanent magnets | |
JP2011080152A (en) | Method of forming molded article of amorphous alloy with high elastic limit | |
GB2112309A (en) | Making a cast single crystal article | |
US4609402A (en) | Method of forming magnetostrictive rods from rare earth-iron alloys | |
US20060086476A1 (en) | Investment casting of bulk-solidifying amorphous alloys | |
US4202400A (en) | Directional solidification furnace | |
US5067551A (en) | Method for manufacturing alloy rod having giant magnetostriction | |
US3529958A (en) | Method for the formation of an alloy composed of metals reactive in their elemental form with a melting container | |
US3189957A (en) | Method of manufacturing permanent magnets by continuous castings | |
US4186046A (en) | Growing doped single crystal ceramic materials | |
US3434892A (en) | Directionally solidified permanent magnet alloys with aligned ferro-magnetic whiskers | |
US4342608A (en) | Mn-Al Permanent magnets and their manufacture | |
JPS627839A (en) | Manufacture of niti alloy | |
US3261722A (en) | Process for preparing semiconductor ingots within a depression | |
US4396441A (en) | Permanent magnet having ultra-high coercive force and large maximum energy product and method of producing the same | |
US2990261A (en) | Processing of boron compact | |
US3234609A (en) | Method of making magnetically anisotropic permanent magnets | |
US3783032A (en) | Method for producing directionally solidified nickel base alloy | |
US4946746A (en) | Novel metal fiber and process for producing the same | |
US5236033A (en) | Method for producing a body from a material susceptible to thermal cracking and casting mold for executing the method | |
JPH049629B2 (en) | ||
US2804415A (en) | Preparation of mnbi bodies | |
US3428498A (en) | Preparation of sintered permanent alnico magnets | |
US3254955A (en) | Method of preparing a tantalum carbide crystal | |
JP3367069B2 (en) | Manufacturing method of giant magnetostrictive alloy rod |