Patent Grant
10562103
The disclosure relates to techniques for forming iron nitride magnetic materials.
Permanent magnets can provide high efficiency and reliability for renewable energy technologies, including electrical vehicles and wind turbines, etc. Because rare earth permanent magnets have supply constraints and high price, a new magnet with more abundant and less strategically important elements is desired to replace rare earth magnets.
Materials including α″-Fe16N2 are promising candidates for rare-earth-free magnets. This disclosure describes techniques that include milling an iron-containing raw material in the presence of a nitrogen source to nitridize the iron-containing raw material and form anisotropically shaped particles including iron nitride. In some examples, the anisotropically shaped particles may include a Fe16N2 phase constitution (e.g., α″-Fe16N2). Anisotropic particles including Fe16N2 may have enhanced magnetic properties, including, for example, at least one of enhanced coercivity, magnetization, magnetic orientation, or energy product, as compared to isotropically shaped particles including Fe16N2.
The disclosure also describes apparatuses configured to mill raw materials and form anisotropic particles. For example, a bar milling apparatus, an electro-discharge assisted milling apparatus, and a magnetic assisted milling apparatus are disclosed. In some examples, such apparatuses may be examples of types of rolling mode milling apparatuses, stirring mode milling apparatuses, or vibration mode milling apparatuses, as described in greater detail below.
In some examples, the disclosure describes a technique that includes milling an iron-containing raw material in the presence of a nitrogen source to generate a powder including a plurality of anisotropic particles, wherein at least some particles of the plurality of anisotropic particles include iron nitride, wherein at least some particles of the plurality of anisotropic particles have an aspect ratio of at least 1.4. Further, an aspect ratio for an anisotropic particle of the plurality of anisotropic particles may include the ratio of the length of a longest dimension to the length of a shortest dimension of the anisotropic particle, where the longest dimension and the shortest dimension are substantially orthogonal. In addition example, the disclosure describes an example bulk permanent magnet formed by any of the techniques described herein.
In another example, the disclosure describes a material that includes an anisotropic particle including at least one iron nitride crystal, where the anisotropic particle has an aspect ratio of at least 1.4. Again, the aspect ratio may include the ratio of the length of a longest dimension of the anisotropic particle to the length of a shortest dimension of the anisotropic particle, where the longest dimension and the shortest dimension are substantially orthogonal.
In another example, the disclosure describes nitridizing an anisotropic particle including iron to form an anisotropic particle including iron nitride, and annealing the anisotropic particle including iron nitride to form at least one α″-Fe16N2 phase domain within the anisotropic particle including iron nitride, where the anisotropic particle including iron nitride has an aspect ratio of at least 1.4, where the aspect ratio for the anisotropic particle including iron nitride comprises the ratio of the length of a longest dimension to the length of a shortest dimension of the anisotropic particle including iron nitride, and where the longest dimension and the shortest dimension are substantially orthogonal.
In another example, the disclosure describes a technique that includes aligning a plurality of anisotropic particles, such that the longest dimensions of respective anisotropic particles of the plurality of anisotropic particles are substantially parallel, where at least some anisotropic particles of the plurality of anisotropic particles comprise iron nitride and have an aspect ratio of at least 1.4. Again, the aspect ratio may include the ratio of the length of the longest dimension of an anisotropic particle to the length of the shortest dimension of the anisotropic particle, where the longest dimension and the shortest dimension are substantially orthogonal. This example technique also may include joining the plurality of anisotropic particles to form a bulk material that includes iron nitride.
This disclosure also describes an example apparatus that includes a plurality of elongated bars, where at least some of elongated bars of the plurality of elongated bars have a width between about 5 millimeters (mm) and about 50 mm, a bin configured to house the plurality of elongated bars, at least one support structure configured to support the bin, and a means for rotating the bin about an axis of the bin.
In addition, the disclosure describes an example apparatus that includes a plurality of milling media, a bin configured to house the plurality of milling media, and a generator that includes at least one of a spark discharge mode or a glow discharge mode, where the generator is configured to generate an electric field within the bin. This example apparatus also may include a first wire including a first end and a second end, wherein the first end of the first wire is affixed to at least one milling medium and the second end of the first wire is electrically coupled to a first terminal of the generator, and a second wire that includes a first end and a second end, wherein the first end of the second wire is electrically coupled to the bin and a ground and the second end of the second wire is electrically coupled to a second terminal of the generator. This example apparatus further may include at least one support structure configured to support the bin, and a means for rotating the bin about an axis of the bin.
Moreover, this disclosure also describes an example apparatus that includes a plurality of milling media, a bin configured to house the plurality of milling media, a means for generating a magnetic field within the bin, at least one support structure configured to support the bin, and a means for rotating the bin about an axis of the bin.
In addition, the disclosure describes workpieces including the anisotropic particles made by any of the techniques described herein. Workpieces may take a number of forms, such as a wire, rod, bar, conduit, hollow conduit, film, sheet, or fiber, each of which may have a wide variety of cross-sectional shapes and sizes, as well as any combinations thereof.
The details of one or more examples are set forth in the accompanying drawings and the description below. Other features, objects, and advantages will be apparent from the description and drawings, and from the claims.
The present disclosure may be understood more readily by reference to the following detailed description taken in connection with the accompanying figures and examples, which form a part of this disclosure. It is to be understood that this disclosure is not limited to the specific devices, methods, applications, conditions or parameters described and/or shown herein, and that the terminology used herein is for the purpose of describing particular examples and is not intended to be limiting of the claims. When a range of values is expressed, another example includes from the one particular value and/or to the other particular value. Similarly, when values are expressed as approximations, by use of the antecedent “about,” it will be understood that the particular value forms another example. All ranges are inclusive and combinable. Further, a reference to values stated in a range includes each and every value within that range.
It is to be appreciated that certain features of the disclosure which are, for clarity, described herein in the context of separate examples, may also be provided in combination in a single example. Conversely, various features of the disclosure that are, for brevity, described in the context of a single example, may also be provided separately or in any subcombination.
The present disclosure describes various milling techniques for forming anisotropically shaped particles that include iron nitride magnetic materials. In some examples, the shape anisotropy of the particles may contribute to increased magnetic anisotropy compared to isotropically shaped particles including the same iron nitride magnetic materials. In some examples, the iron-nitride containing anisotropic particles generated by the various techniques have an aspect ratio of at least 1.4. Anisotropic particles formed by the techniques of this disclosure may be shaped, for example, as needles, flakes, or laminations. The disclosure also describes techniques for joining anisotropically shaped particles to form bulk material, such as a bulk permanent magnet.
In various examples, the disclosure describes techniques for milling iron-containing raw material in the presence of a nitrogen source to generate a powder including anisotropic particles that include iron nitride.
For example, the disclosure describes milling iron-containing raw material in the presence of a nitrogen source for a predetermined period of time, under a predetermined amount of pressure, at a predetermined low temperature, in the presence of a magnetic field, or in the presence of an electric field. In some examples, the milling may be performed, for example, using milling spheres in the bin of a rolling mode, stirring mode, or vibration mode milling apparatus. Iron-containing raw materials also may be milled in the presence of a nitrogen source using elongated bars, alone or in conjunction with other milling media, to form anisotropically shaped particles. For example, iron-containing raw material may be milled in the presence of urea using cylindrical bars housed within a bin of a rolling mode or vibration mode milling apparatus.
In some examples, two or more of the disclosed techniques may be used in combination to form anisotropically shaped particles including iron nitride. For example, and without limitation, an example technique may include milling iron-containing raw material in the presence of a nitrogen source in the presence of an electric field for a predetermined amount of time. As another example, an example technique may include milling iron-containing raw material in the presence of a nitrogen source in the presence of a magnetic field while the contents of a bin of a milling apparatus are under a predetermined amount of pressure. As another example, an example technique may include milling an iron-containing raw material in the presence of a nitrogen source using elongated bars housed in a milling apparatus, while at least the iron-containing raw material is at a predetermined low temperature (e.g., cryo-milling using elongated bars).
Anisotropic particles generated according to techniques of this disclosure may include one or more iron nitride crystals with varying crystal lattice structures or phase domains.
α″-Fe16N2 has high saturation magnetization and magnetic anisotropy constant. The high saturation magnetization and magnetic anisotropy constants result in a magnetic energy product that may be higher than rare earth magnets. For example, experimental evidence gathered from thin film α″-Fe16N2 permanent magnets suggests that bulk Fe16N2 permanent magnets may have desirable magnetic properties, including an energy product of as high as about 134 MegaGauss*Oerstads (MGOe), which is about two times the energy product of NdFeB (which has an energy product of about 60 MGOe). Additionally, iron and nitrogen are abundant elements, and thus are relatively inexpensive and easy to procure.
In some examples, an anisotropically shaped particle generated according to techniques disclosed herein may have at least one Fe16N2 iron nitride crystal. In some examples, such an anisotropic particle may include a plurality of iron nitride crystals, at least some (or all) of which Fe16N2 crystals. As described above, anisotropic particles including Fe16N2 may have enhanced magnetic properties, including, for example, at least one of enhanced coercivity, magnetization, magnetic orientation, or energy product, as compared to isotropically shaped particles including Fe16N2. Thus, for example, materials formed using anisotropic particles including Fe16N2 may be promising candidates for permanent magnet applications.
Although not wishing to be bound by theory, three types of anisotropy may contribute to the magnetic anisotropy energy or magnetic anisotropy field of Fe16N2. These three types of anisotropy include magnetocrystalline anisotropy, shape anisotropy, and strain anisotropy. As described above, magnetocrystalline anisotropy may be related to the distortion of the bcc iron crystalline lattice into the bct iron-nitride crystalline lattice shown in
Strain anisotropy may be related to strain exerted on the α″-Fe16N2 or other iron-based magnetic materials. In some examples, anisotropic particles including at least one Fe16N2 phase domain are disposed or embedded within a matrix that includes grains of iron or other types of iron nitride (e.g., Fe4N). The anisotropic particles including at least one Fe16N2 phase domain may possess a different coefficient of thermal expansion than the grains of iron or other types of iron nitride. This difference can introduce strain into the anisotropic particles including at least one Fe16N2 phase domain due to differential dimensional changes in the particles and the grains of iron or other types of iron nitride during thermal processing. Alternatively or additionally, the material or workpiece may be subjected to mechanical strain or strain due to exposure to an applied magnetic during processing to form anisotropic particles including at least one Fe16N2 phase domain, at least some of which strain may remain in the material or workpiece after processing. Annealing may result in redistribution of the internal stress and local microstructure of the sample in order to reduce the magnetoelastic energy in the stressed state. The magnetic domain structure under strain anisotropy depends on the magnetoelastic energy, magnetostatic energy, and exchange energy.
In connection with various milling techniques described herein, any one or more of a number of forms of iron-containing raw material may be milled in a milling apparatus. Iron-containing raw material may include any material containing iron, including atomic iron, iron oxide, iron chloride, or the like. For example, iron-containing raw material may include iron powder, bulk iron, FeCl3, Fe2O3, or Fe3O4. In some examples, iron-containing raw material may include substantially pure iron (e.g., iron with less than about 10 atomic percent (at. %) dopants or impurities) in bulk or powder form. The dopants or impurities may include, for example, oxygen or iron oxide. Iron-containing raw material may be provided in any suitable form, such as a powder or relatively small particles. In some examples, an average size of particles in iron containing raw material may be between about 50 nanometers (nm) and about 5 micrometers (μm). After milling the iron-containing raw material according to any of the techniques described by this disclosure, a generated powder may include particles that have, on average, dimensions ranging from between about 5 nm and about 50 nm in length.
The described iron-containing raw material may be milled in the presence of one or more sources of nitrogen, in connection with the various milling techniques described in this disclosure. Nitrogen sources may take a number of forms, such as a solid, liquid, or gas source of nitrogen. Moreover, the nitrogen sources described herein may serve as a nitrogen donor for the forming of powders that include particles including iron nitride. For example, iron-containing raw material may be nitridized according to techniques of this disclosure using, as a nitrogen source, ammonia, ammonium nitrate (NH4NO3), an amide-containing material and/or a hydrazine-containing material. Amides include a C—N—H bond, while hydrazine includes an N—N bond. For example, amide-containing materials may include an amide, liquid amide, a solution containing an amide, carbamide ((NH2)2CO, also referred to as urea), methanamide, benzamide, or acetamide, although any amide may be used. Example hydrazine-containing materials may include hydrazine, or a solution containing hydrazine.
In some examples, amides may be derived from carboxylic acids by replacing the hydroxyl group of a carboxylic acid with an amine group. Amides of this type may be referred to as acid amides. An example reaction sequence for forming an acid amide from a carboxylic acid, nitriding iron, and regenerating the acid amide from the hydrocarbon remaining after nitriding the iron is described in International Application No. PCT/US2014/043902, the entire contents of which are incorporated herein by reference.
In addition, in some example techniques of this disclosure, a catalyst may be introduced to the bin of a milling apparatus to assist the formation of anisotropic particles including iron nitride. The catalyst (such as catalyst 22 or 52, shown in
Hence, by mixing sufficient amide and catalyst, iron-containing raw material may be converted to iron nitride containing material according to the techniques described in this disclosure. For example, such a catalyst may be utilized when milling iron-containing raw material in the presence of a nitrogen source at a predetermined low temperature, to assist the formation of anisotropic particles including iron nitride.
In the example illustrated in
In operation, bin 12 of rolling mode milling apparatus 10 may be rotated at a rate sufficient to cause mixing of the components in bin 12 (e.g., milling media 16, iron-containing raw material 18, nitrogen source 20, and, in some examples, catalyst 22) and cause milling media 16 to mill iron-containing raw material 18. In some examples, bin 12 may be rotated at a rotational speed of between about 500 revolutions per minute (rpm) to about 2000 rpm, such as between about 600 rpm and about 650 rpm, about 600 rpm, or about 650 rpm. Further, to facilitate milling of iron-containing raw material 18, in some examples, the mass ratio of the total mass of milling media 16 to the total mass of iron-containing raw material 18 may be between about 1:1 to about 50:1, for example, about 20:1.
In other examples, the milling process may be performed using a different type of milling apparatus.
Stirring mode milling apparatus 30 may be used to mill iron-containing raw material in the presence of a nitrogen source to form a plurality of anisotropic particles in a manner similar to rolling mode milling apparatus 10. For example, shaft 34 may be rotated at a rate between about 500 rpm and about 2,000 rpm, such as between about 600 rpm and about 650 rpm, about 600 rpm, or about 650 rpm. Further, to facilitate milling of the iron-containing raw material, in some examples, the mass ratio of the milling media to the iron-containing raw material may be about 20:1.
Vibration mode milling apparatus 40 may be used to nitridize the iron-containing raw material 48 and form anisotropically shaped particles in a manner similar to milling apparatus 10 illustrated in
A chart 24 of
As used herein, aspect ratio is defined as the ratio of the length of the longest dimension of an anisotropic particle to the length of the shortest dimension of the anisotropic particle, where the longest dimension is substantially orthogonal (e.g., orthogonal or nearly orthogonal) to the shortest dimension. For example, an absolute longest dimension may be measured, and the shortest dimension of the particle in a direction orthogonal to the direction of the absolute longest dimension may be used for the shortest dimension in the determination of the aspect ratio of the particle. Thus, for example, a particle with a length of 14 nanometers (nm) in the z direction, 12 nm in the x direction, and 10 nm in the y direction, has an aspect ratio of 1.4 (14 nm [longest dimension of the particle]:10 nm [shortest dimension of the particle in a direction substantially orthogonal to the longest dimension of the particle]). In general, milling iron-containing raw material in the presence of a nitrogen source according to techniques disclosed herein may generate a powder including a plurality of anisotropic particles that include iron nitride. At least some of the generated anisotropic particles may have an aspect ratio of at least 1.4.
The formation of shape anisotropy in particles including magnetic material, using milling techniques disclosed herein, may enhance magnetic properties and magnetic anisotropy of the particles, e.g., compared to substantially isotropic particles including the same material. For example, anisotropic particles including iron nitride, such as anisotropic particles that have an aspect ratio of at least 1.4, may possess at least one of improved coercivity, magnetization, magnetic orientation, or energy product compared to isotropically shaped particles (e.g., spheres) including the same composition of iron nitride. Some iron nitride phases, such as Fe16N2, have magnetocrystalline anisotropy due to the atomic structure of the iron nitride crystal. Phases such as Fe16N2 have magnetically easy axes, such that magnetization is more energetically favorable or stable along easy axes of the crystal. In some examples, an iron nitride crystal may be oriented within an anisotropic particle such that the easy axis is substantially aligned with the longest dimension of the particle. In some of these examples, an anisotropic particle including a Fe16N2 phase may more readily align its magnetic moment along the longest dimension of the particle, which may substantially align with one or more easy axes of iron nitride crystal(s) in the particle. This may contribute to enhanced magnetic anisotropy and/or magnetic properties compared to isotropically shaped particles including iron nitride.
Further, production of anisotropic particles including iron nitride, according to the techniques of this disclosure, may lead to cost effective mass production of iron nitride-containing material and bulk permanent magnets including iron nitride (e.g., Fe16N2). Moreover, anisotropic particles including iron nitride may, in some examples, be consolidated or joined with other materials (including other magnetic materials) to obtain a higher energy product.
Anisotropically shaped particles including iron nitride may be formed by various milling techniques according to this disclosure. For example, iron-containing raw material may be milled by milling spheres or bars in the presence of a nitrogen source to form anisotropic particles including iron nitride (e.g., Fe16N2). As stated, in some examples, two or more disclosed milling techniques may be combined to form anisotropic particles including iron nitride. In some examples, a technique for forming such anisotropic particles may include milling iron-containing raw material 18 in the presence of nitrogen source 20 for a predetermined period of time. This technique may be implemented using any suitable milling apparatus, such as rolling mode milling apparatus 10, stirring mode milling apparatus 30, or vibration mode milling apparatus 40, described herein with respect to
For instance, iron-containing raw material 18 and nitrogen source 20 (
As another example, a technique of this disclosure may include milling an iron-containing raw material in the presence of a nitrogen source under a predetermined amount of pressure to form anisotropic particles including iron nitride.
Though a high pressure ball milling apparatus 60 is shown in
In some examples, during milling, the pressure within bin 62 of milling apparatus 60 may be increased to between about 0.1 GPa and about 20 GPa to facilitate formation of anisotropically shaped particles that include iron nitride. For example, the pressure within bin 62 may be increased to between about 0.1 GPa and about 1 GPa during milling. In some examples, milling the contents of bin 62 under a predetermined pressure may aid in directing the contents toward an inner surface of bin 62 (e.g., toward liner plates 26 of bin 62) during milling, which may facilitate formation of anisotropically shaped particles. For example, by milling the contents of milling apparatus 60 under a predetermined pressure, a powder including a plurality of anisotropic particles may be formed that include a Fe16N2 phase constitution. In some examples, at least some of the anisotropic particles have an aspect ratio of at least 1.4.
In the example high pressure ball milling apparatus 60, liner plates 67 may be attached to or form an inner surface of bin 62. Liner plates 67 may be composed of, for example, hard metal, such as steel, nickel, chromium, or the like. Further, as shown in
For example, iron-containing powder may be introduced into raw material input 64, and ammonia gas may be input into gas input 66 and bin 62 at a pressure of between about 0.1 GPa and about 20 GPa. The contents of bin 62 may be rotated at a speed of between about 500 rpm and about 2,000 rpm within bin 62 and milled by milling media 63 (e.g., milling spheres), thereby generating a powder including anisotropic particles including iron nitride that exits high pressure ball milling apparatus 60 via powder output 68. In some examples, a temperature within the bin of the milling apparatus used for this technique (such as milling apparatus 60) may be increased, in combination with the introduction of a suitable pressurized gas, to achieve a desired increased pressure between about 0.1 GPa and about 20 GPa within the bin 62.
In some examples, a temperature at which components are milled may be controlled to facilitate formation of anisotropic particles including iron nitride. For example, a technique according to this disclosure may include milling an iron-containing raw material at a predetermined low temperature in the presence of a nitrogen source using milling media. For example, milling the contents of a milling apparatus at a temperature between about 77 Kelvin (K) (about −196.15° C.) and ambient temperature (about 23° C.) may facilitate formation of anisotropically shaped particles that include iron nitride. In some examples, at least the iron-containing raw material, or even all contents of the milling apparatus, may be cooled to a temperature between about −196.15° C. and about ambient temperature by introducing liquid nitrogen to the bin of a milling apparatus, which may cool at least the iron-containing raw material to a temperature of, for example, about −196.15° C. This technique may be implemented using any suitable milling apparatus, such as rolling mode milling apparatus 10, stirring mode milling apparatus 30, or vibration mode milling apparatus 40, described herein with respect to
The rough-milled iron-containing raw material may then be fine milled in a cryo-ball milling apparatus 74. As shown in
Anisotropic particles including iron nitride also may be formed by milling iron-containing raw material in the presence of a nitrogen source and a magnetic field.
In operation, a motor (not shown) that is coupled to bin 88 may cause bin 88 to rotate and/or vibrate to induce milling of the contents of bin 88. Further, one or more sets of bearings (not shown) may be positioned at one or more locations adjacent to bin 88, to facilitate rotation of bin 88 about an axis (e.g., horizontal axis) of bin 88. For example, a set of bearings may be positioned within a support structure of bin 88 and around at least a portion of the circumference of each opposing end of bin 88, such that each bearing may engage at least a portion of an outer circumference of bin 88 on one side, and the support structure and/or a component thereof on an opposing side. In these examples, the set of bearings may rotatably couple bin 88 and a support structure (not shown) for bin 88. An example support structure is described with respect to
When bin 88 rotates in a rolling motion (indicated by arrow 92), magnetic field 87 may substantially maintain (e.g., maintain or nearly maintain) iron-containing raw material 96 in a particular orientation, for at least a portion of the milling time. In such an example, milling media 94 may wear iron-containing raw material 96 in an uneven or anisotropic fashion, such that at least a first surface of iron-containing raw material 96 is worn unevenly in comparison to a second surface (e.g., where the first and second surfaces are substantially orthogonal), instead of being worn in a generally equal or isotropic manner in all dimensions or at all surfaces of iron-containing raw material 96.
For example, iron-containing raw material 96 may align itself such that easy axes of iron crystals within the iron-containing magnetic material (or iron nitride crystals, once the iron-containing raw material is nitridized) are substantially parallel to the direction of the applied magnetic field. In some examples, easy axes of the iron crystals (or iron nitride crystals) are aligned in such a manner at least some (or all) of the time the iron-containing raw material 96 is being milled.
For example, milling media 16 (such as milling spheres) may wear more of a particle of iron-containing raw material 96 from a surface of the particle oriented in an x direction or y direction, and may wear less of a particle of iron-containing raw material 96 in a z direction, such that the length of the particle in the z direction is longer than the length of the particle in an x or y direction. For example, the length of a milled particle in a z direction (which in some examples may be parallel to the <001> crystal axes of iron nitride crystals within the particle) may be about 1.4 times longer than a length of the milled particle in the x or y direction.
This technique may be implemented using any suitable milling apparatus, into or along which a magnetic field is introduced, such as rolling mode milling apparatus 10, stirring mode milling apparatus 30, or vibration mode milling apparatus 40, described herein with respect to
Another example technique for forming anisotropic particles including iron nitride may include utilizing an electric field, alone or in combination with use of a magnetic field or other techniques described herein.
Electro-discharge assisted milling apparatus 100 may include a generator 108 (e.g., a high-voltage generator) that generates an electric field within a bin 106 of electro-discharge assisted milling apparatus 100. For example, generator 108 may apply a voltage within bin 106 along a first wire 109. First wire 109 may include, in some examples, a flexible wire portion 112 connected to first wire 109 via connector 110 that terminates at a milling medium 114 within bin 106. In some examples, first wire 109 may be disposed in an open space within bin 106. In some examples, electro-discharge assisted milling apparatus 100 may include a single milling medium 114 to which first wire 109 is attached via flexible wire portion 112. In other examples, multiple milling media may be attached to wire 109 via multiple respective flexible wire portions 112 that extend from connector 110 to respective milling media. In some examples, first wire 109 may be substantially rigid or have a substantially rigid coating or cladding sufficient to support movement of one or more milling media and respective flexible wire portions as the components move within bin 106 during rotation of bin 106.
In some examples, as shown at
The voltage emanating from generator 108 may be carried by an alternating current, a direct current, or both. For example, generator 108 may generate a direct current voltage between about 10 volts (V) and about 10,000 V. In other examples, an alternating current generator may generate a current with a frequency up to 10 megahertz (MHz), and an output power of between about 0.1 watts (W) and about 100 W.
A high-voltage generator that is electrically coupled (and in some examples, mechanically coupled) to bin 106 of milling apparatus 100 may include a spark discharge mode and/or a glow discharge mode. For example, generator 108 may generate a spark or glow that emanates from milling media 114 via first wire 109 and connector 110. For example, the spark or glow may be conducted from a higher-potential milling media 114 to a lower potential bin 116 coupled to grounded second wire 111. In some examples, the spark or glow may be electrically conducted through iron-containing raw material 116 to bin 106 and/or an electrically conductive component electrically coupled to bin 106, and ultimately to the lower-potential ground 115, as shown in
In some examples, in addition to or as an alternative to using time, temperature, pressure, a magnetic field, or an electric field to facilitate formation of anisotropic particles, a milling technique may utilize elongated milling media to facilitate formation of anisotropic particles.
In some examples, bin 124 of bar milling apparatus 120 may rotate about a horizontal axis (not shown) of bin 124 in a direction 126 (or in the reverse direction), so that elongated bars 122 rotate about their respective horizontal axes and/or the elongated bars 122 roll over one another in bin 124. Before initiating rotation of bin 124, elongated bars 122 may be arranged in any number of suitable manners within bin 124, such as in a triangular arrangement shown in
The elongated shape of elongated bars 122 may cause the iron-containing raw material to wear in an uneven or anisotropic fashion. In some examples, milling iron-containing raw material in the presence of a nitrogen source in bar milling apparatus 120 may form particles in the shape of needles, flakes, or laminations.
In some examples, at least some (or all) of the elongated bars may have a width (e.g., at least one dimension in a plane substantially orthogonal to their horizontal (long) axis) of between about 5 millimeters (mm) and about 50 mm. For example, cylindrically shaped elongated bars 122 may have a circular cross-section with a diameter between about 5 millimeters (mm) and about 50 mm. Elongated bars 122 may have other cross-sectional shapes as well. For example, in a plane substantially orthogonal to a horizontal (long) axis of an elongated bar, the elongated bar may have a square, rectangular, other polygonal, elliptical, or other closed curve shape. Further, in some examples, elongated bars 122 may have lengths along their horizontal (long) axes that are longer than the diameter of bin 124. In some examples, the iron-containing raw material introduced within bin 124 may occupy between about 20% and about 80% of the volume of bin 124 of bar milling apparatus 120.
In addition, in some examples, bin 124 may rotate at a speed of at least 250 rpm. In some of these examples, while bin 124 is rotating at at least this speed, some or all of elongated bars 122 may remain disposed along an inner periphery of bin 124. Further, the iron-containing raw material, nitrogen source, and optional catalyst utilized in this bar milling technique may be the same as or substantially similar to iron-containing raw material 18, nitrogen source 20, and catalyst 22 described with reference to
In some examples, bar milling apparatus 120 may vibrate, for example, in a vertical direction as shown by arrow 127 in
Regardless of the milling technique used to form powder including anisotropic particles that include iron nitride, as described herein, the anisotropic particles may include at least one of FeN, Fe2N (e.g., ξ-Fe2N), Fe3N (e.g., ε-Fe3N), Fe4N (e.g., γ′-Fe4N), Fe2N6, Fe8N, Fe16N2 (e.g., α″-Fe16N2), or FeNx (where x is between about 0.05 and about 0.5). Additionally, in some examples, the iron nitride powder may include other materials, such as pure iron, cobalt, nickel, dopants, or the like. In some examples, the cobalt, nickel, dopants, or the like may be at least partially removed after the milling process using one or more suitable techniques. Dopants within the particles of powder generated from milling may include, for example, at least one of aluminum (Al), manganese (Mn), lanthanum (La), chromium (Cr), cobalt (Co), titanium (Ti), nickel (Ni), zinc (Zn), a rare earth metal, boron (B), carbon (C), phosphorous (P), silicon (Si), or oxygen (O). In some examples, the iron nitride powder may be used in subsequent processes to form a magnetic material, such as a permanent magnet, including an iron nitride phase, such as Fe16N2. Milling an iron-containing raw material in the presence of a nitrogen source, such as ammonium nitrate or an amide- or hydrazine-containing liquid or solution, may be a cost-effective technique for forming an iron-nitride containing material. Further, milling an iron-containing raw material in the presence of a nitrogen source, such as ammonium nitrate or an amide- or hydrazine-containing liquid or solution, may facilitate mass production of iron nitride-containing material, and may reduce iron oxidation.
As described above, any of the milling techniques used to form anisotropic particles including iron nitride may utilize an iron-containing raw material. For any of the milling techniques described, prior to milling the iron-containing raw material in the presence of a nitrogen source, an iron precursor may be converted to the iron-containing raw material using, for example, a rough milling technique or a melting spinning technique. Rough milling an iron precursor material may form, on average, smaller sized particles of iron-containing raw material, for use in further processing, such as any of the fine milling techniques described in this disclosure. In some examples, the iron precursor (e.g., iron precursor 70 shown in
When the iron precursor is rough milled, any of the milling techniques described above may be utilized, for example rolling mode milling, stirring mode milling, vibration mode milling, or variations thereof described herein. In some examples, the iron precursor may be milled in the presence of at least one of calcium (Ca), aluminum (Al), or sodium (Na) under conditions sufficient to cause an oxidation reaction between the at least one of Ca, Al, or Na and any oxygen present in the iron precursor. The at least one of Ca, Al and/or Na may react with, for example, molecular oxygen or oxygen ions present in the iron precursor, if any. The oxidized at least one of Ca, Al, and/or Na then may be removed from the mixture. For example, the oxidized at least one of Ca, Al, and/or Na may be removed using at least one of a deposition technique, an evaporation technique, or an acid cleaning technique.
In some examples, the oxygen reduction process can be carried out by flowing hydrogen gas within the milling apparatus. The hydrogen may react with any oxygen present in the iron-containing raw material, and the oxygen may be removed from the iron-containing raw material. In some examples, this may form substantially pure iron (e.g., iron with less than about 10 at. % dopants). Additionally or alternatively, the iron-containing raw material may be cleaned using an acid cleaning technique. For example, diluted HCl, with a concentration between about 5% and about 50% can be used to wash oxygen from the iron-containing raw material. Milling iron precursors in a mixture with at least one of Ca, Al, and/or Na (or acid cleaning) may reduce iron oxidation and may be effective with many different iron precursors, including, for example, Fe, FeCl3, Fe2O3, or Fe3O4, or combinations thereof. The milling of iron precursors may provide flexibility and cost advantages when preparing iron-containing raw materials for use in forming iron-nitride containing materials.
In other examples, the iron-containing raw material may be formed by melting spinning. In melting spinning, an iron precursor may be melted, e.g., by heating the iron precursor in a furnace to form molten iron precursor. The molten iron precursor then may be flowed over a cold roller surface to quench the molten iron precursor and form a brittle ribbon of material. In some examples, the cold roller surface may be cooled at a temperature below room temperature by a cooling agent, such as water. For example, the cold roller surface may be cooled at a temperature between about 10° C. and about 25° C. The brittle ribbon of material may then undergo a heat treatment step to pre-anneal the brittle iron material. In some examples, the heat treatment may be carried out at a temperature between about 200° C. and about 600° C. at atmospheric pressure for between about 0.1 hour and about 10 hours. In some examples, the heat treatment may be performed in a nitrogen or argon atmosphere. After heat-treating the brittle ribbon of material under an inert gas, the brittle ribbon of material may be shattered to form an iron-containing powder. This powder may be used as iron-containing raw material in the any of the disclosed milling techniques that generate a powder including iron nitride and/or anisotropic particles.
In general, the anisotropic particles including iron nitride generated according to the techniques of this disclosure may include one or more different iron nitride phases (e.g., Fe8N, Fe16N2, Fe2N6, Fe4N, Fe3N, Fe2N, FeN, and FeNx (where x is between about 0.05 and 0.5)). The mixture then may be formed into a bulk material (e.g., a bulk magnetic material) via at least one of a variety of methods.
Prior to being formed into a bulk material, the anisotropically shaped particles including iron nitride generated according to any of the milling techniques of this disclosure may be annealed to enhance the formation of at least one α″-Fe16N2 phase domain within the particles. For example, annealing anisotropic particles including iron nitride may convert at least some Fe8N phase domains in the anisotropic particles including iron nitride to Fe16N2 phase domains.
In some examples, annealing the anisotropic particles including iron nitride may include heating the particles to a temperature between about 100° C. and about 250° C., such as between about 120° C. and about 220° C., for example, between about 180° C. and 220° C. In some examples, annealing the anisotropic particles including iron nitride while straining the particles (e.g., applying a tensile force thereto) may facilitate conversion of at least some of the iron nitride phase domains to α″-Fe16N2 phase domains. The annealing process may continue for a predetermined time that is sufficient to allow diffusion of the nitrogen atoms to the appropriate interstitial spaces in the iron crystal lattice. In some examples, the annealing process continues for between about 20 hours and about 200 hours, such as between about 40 hours and about 60 hours. In some examples, the annealing process may occur under an inert atmosphere, such as Ar, to reduce or substantially prevent oxidation of the iron. Further, in some implementations, while the anisotropic particles including iron nitride are annealed, the temperature is held substantially constant. The annealing (e.g., annealing while straining) of the anisotropic particles including iron nitride may result in an enhanced magnetic material including at least one α″-Fe16N2 phase domain.
In some examples, the anisotropic particles including iron nitride may be exposed to an external magnetic field during the annealing process. Annealing iron nitride materials in the presence of an applied magnetic field may enhance the Fe16N2 phase domain formation in iron nitride materials. Increased volume fractions of α″-Fe16N2 phase domains may improve the magnetic properties of the anisotropic particles including iron nitride. Improved magnetic properties may include, for example, coercivity, magnetization, and magnetic orientation.
In some examples, an applied magnetic field during annealing may be at least 0.2 Tesla (T). The temperature at which the magnetic field annealing is performed may at least partially depend upon further elemental additions to the iron nitride base composition and the approach used to initially synthesize the iron nitride base composition. In some examples, the magnetic field may be at least about 0.2 T, at least about 2 T, at least about 2.5 T, at least about 6 T, at least about 7 T, at least about 8 T, at least about 9 T, at least about 10 T, or higher. In some examples, the magnetic field is between about 5 T and about 10 T. In other examples, the magnetic field is between about 8 T and about 10 T. Further details regarding annealing the materials including iron and nitrogen may be found in U.S. Provisional Application No. 62/019,046, filed Jun. 30, 2014, the entire content of which is incorporated herein by reference.
In some examples, rather than being formed using a milling technique, an anisotropic particle including at least one α″-Fe16N2 phase domain may be formed by nitridizing and annealing anisotropic shaped iron-containing precursors.
The anisotropic particle including iron described in reference to this example technique may include, for instance, the iron-containing raw materials described herein in an anisotropic shape, such as iron powder, bulk iron, FeCl3, Fe2O3, or Fe3O4. In some examples, an anisotropic particle including iron may include substantially pure iron (e.g., iron with less than about 10 atomic percent (at. %) dopants or impurities) in bulk or powder form. The dopants or impurities may include, for example, oxygen or iron oxide. In some examples, the anisotropic particle including iron may have an aspect ratio of at least about 1.4 (e.g., about 1.4), with aspect ratio being defined as described elsewhere in this disclosure. However, other aspect ratios may be suitable.
In some examples, prior to nitridizing an anisotropic particle including iron, the technique of
In some examples, reducing the anisotropic iron precursor may include reducing or removing oxygen content in the anisotropic iron precursor. For example, an oxygen reduction process can be carried out by exposing the anisotropic iron precursor to hydrogen gas. The hydrogen may react with any oxygen present in the anisotropic iron precursor, removing oxygen from the iron-containing raw material. In some examples, such a reduction step may form substantially pure iron within the anisotropic particle including iron (e.g., iron with less than about 10 at. % dopants). Additionally or alternatively, reducing the anisotropic iron precursor may include using an acid cleaning technique. For example, diluted HCl, with a concentration between about 5% and about 50% can be used to wash oxygen from the anisotropic iron precursor to form an anisotropic particle including iron (e.g., substantially pure iron, as described).
Nitridizing of the anisotropic particle including iron to form the anisotropic particle including iron nitride (131) may proceed in a number of manners. In general, nitrogen from a nitrogen source is combined with the anisotropic particle including iron to form an anisotropic particle including iron nitride. Such a nitrogen source may be the same as or similar to nitrogen sources described in elsewhere in this disclosure.
In some examples, nitridizing the anisotropic particle including iron may include heating the anisotropic particle including iron to a temperature for a time sufficient to allow diffusion of nitrogen to a predetermined concentration substantially throughout the volume of the anisotropic particle including iron. In this manner, the heating time and temperature are related, and may also be affected by the composition and/or geometry of the anisotropic particle including iron. For example, iron wire or sheet 28 may be heated to a temperature between about 125° C. and about 600° C. for between about 2 hours and about 9 hours.
In addition to heating the anisotropic particle including iron, nitridizing the anisotropic particle including iron may include exposing the anisotropic particle including iron to an atomic nitrogen substance, which diffuses into the anisotropic particle including iron. In some examples, the atomic nitrogen substance may be supplied as diatomic nitrogen (N2), which is then separated (cracked) into individual nitrogen atoms. In other examples, the atomic nitrogen may be provided from another atomic nitrogen precursor, such as ammonia (NH3). In other examples, the atomic nitrogen may be provided from urea (CO(NH2)2). The nitrogen may be supplied in a gas phase alone (e.g., substantially pure ammonia or diatomic nitrogen gas) or as a mixture with a carrier gas. In some examples, the carrier gas is argon (Ar).
In some examples, nitridizing the anisotropic particle including iron may include a urea diffusion process, in which urea is utilized as a nitrogen source (e.g., rather than diatomic nitrogen or ammonia). Urea (also referred to as carbamide) is an organic compound with the chemical formula CO(NH2)2. To nitridize the anisotropic particle including iron, urea may heated, e.g., within a furnace enclosing the anisotropic particle including iron, to generate decomposed nitrogen atoms which may diffuse into the anisotropic particle including iron. In some examples, the constitution of the resulting nitridized iron material may controlled to some extent by the temperature of the diffusion process as well as the ratio (e.g., the weight ratio) of the iron-containing workpiece to urea used for the process. Further details regarding these nitridizing processes (including urea diffusion) may be found in International Patent Application No. PCT/US12/51382, filed Aug. 17, 2012, the entire content of which is incorporated herein by reference.
The anisotropic particle including iron nitride formed according to the technique of
Upon nitridizing and annealing, the anisotropic particle including iron nitride may have an aspect ratio of at least 1.4, for example, between 1.4 and 2.0. The aspect ratio referenced in this technique is defined in the same way as other examples in this disclosure. Again, the aspect ratio for the anisotropic particle including iron nitride includes the ratio of the length of a longest dimension to the length of a shortest dimension of the anisotropic particle including iron nitride, where the longest dimension and the shortest dimension are substantially orthogonal.
In some examples, the anisotropic particle including iron that is nitridized according to this technique may be a single iron crystal. Hence, once nitridized, in such an example, an anisotropic particle including a single iron nitride crystal is annealed to form a α″-Fe16N2 phase domain within the iron nitride crystal. In some of these examples, the anisotropic particle including the iron nitride crystal may have an aspect ratio of at least 1.4.
In other examples, the anisotropic particle including iron may include a plurality of iron crystals. Hence, once nitridized, the plurality of iron crystals form a plurality of iron nitride crystals within the anisotropic particle. In such an example, annealing the plurality of iron nitride crystals may form at least one α″-Fe16N2 phase domain within some (or all) of the iron nitride crystals of the anisotropic particle. In some of these examples, the anisotropic particle including the iron nitride crystal may have an aspect ratio of at least 1.4.
In some examples, the described technique may be performed starting with a plurality of anisotropic particles including iron. For example, a plurality of anisotropic particles including iron may be nitridized under conditions described herein to form a plurality of anisotropic particles including iron nitride. In such an example, the plurality of anisotropic particles including iron nitride may be annealed under conditions described herein to form at least one α″-Fe16N2 phase domain within at least some (or all) of the anisotropic particles including iron nitride. In some of these examples, at least some (or all) of the plurality of anisotropic particles including iron nitride may have an aspect ratio of at least 1.4.
In some examples, a bulk material, such as a bulk permanent magnet, may be formed by the joining of anisotropic particles including iron nitride.
In some examples, the respective iron-nitride containing particles include at least one iron nitride crystal. In addition, some iron-nitride containing particles may include at least one of Fe8N or Fe16N2 phases. Further, in some examples, the <001> crystal axes of at least some iron nitride crystals of the plurality of iron nitride crystals may be substantially parallel to the respective longest dimensions of the plurality of anisotropic particles. Aligning the <001> crystal axes of the respective anisotropic particles including iron nitride (e.g., a magnetocrystalline easy axis <001> of Fe16N2) may provide uniaxial magnetic anisotropy to a magnetic material formed from the anisotropic particles.
In some examples, aligning the plurality of anisotropic particles may include exposing the anisotropic particles to a magnetic field, such that magnetic material within the anisotropic particles causes the anisotropic particles to align with the magnetic field. In some examples, the applied magnetic field utilized may have a strength between about 0.01 Tesla (T) and about 50 T. In these examples, the applied magnetic field may be, for example, a static magnetic field generated by a direct current (DC) mode electromagnet, a varying magnetic field generated by an alternating current (AC) mode electromagnet, or a pulse field generated by a pulsed magnet. In some examples, the strength of the applied magnetic field may vary along the direction of the magnetic field. For example, a gradient along the direction of the magnetic field may be between about 0.01 T/meter (m) and about 50 T/m.
The example technique of
In some examples, joining a plurality of anisotropic particles including iron nitride, such as a Fe16N2 phase domain, may include alloying the particles using at least one of tin (Sn), Cu, Zn, or Ag to form an iron alloy at the interface of the anisotropic particles. For example, crystallite and/or atomic migration may cause the Sn to agglomerate. The anisotropic particles then may be pressed together and heated to form an iron-tin (Fe—Sn) alloy. The Fe—Sn alloy may be annealed at a temperature between about 150° C. and about 400° C. to join the plurality of anisotropic particles. In some examples, the annealing temperature may be sufficiently low that magnetic properties of the anisotropic particles may be substantially unchanged. In some examples, rather than Sn being used to join the anisotropic particles including iron nitride, copper (Cu), Zinc (Zn), or silver (Ag) may be used.
In some examples, joining the plurality of anisotropic particles to form a bulk material including iron nitride may include disposing the particles within a resin or other adhesive. Examples of resin or other adhesive include natural or synthetic resins, including ion-exchange resins, such as those available under the trade designation Amberlite™, from The Dow Chemical Company, Midland, Mich.; epoxies, such as Bismaleimide-Triazine (BT)-Epoxy; a polyacrylonitrile; a polyester; a silicone; a prepolymer; a polyvinyl buryral; urea-formaldehyde, or the like. Because resin or other adhesives may substantially fully encapsulate the plurality of anisotropic particles including iron nitride, the particles may be disposed substantially throughout the volume of resin or other adhesive. In some examples, the resin or other adhesive may be cured to bond the plurality of anisotropic particles including iron nitride to each other.
In some examples, joining anisotropic particles including iron nitride may include sintering. For example, sintering the anisotropic particles may include at least heating the anisotropic particles at a temperature between ambient temperature (about 23° C.) and about 200° C. In some examples, the sintered bulk material may be aged.
Further, in some examples, joining the plurality of anisotropic particles to form a bulk material may include magnetically coupling a plurality of ferromagnetic particles to iron nitride material, such as Fe16N2 hard magnetic material, within the anisotropic particles via exchange spring coupling. Exchange spring coupling may effectively harden the magnetically soft ferromagnetic particles and provide magnetic properties for the bulk material similar to those of a bulk material consisting essentially of Fe16N2. To achieve exchange spring coupling throughout the volume of the magnetic material, the Fe16N2 domains may be distributed throughout the magnetic structure, e.g., at a nanometer or micrometer scale. The ferromagnetic particles may include, for example, Fe, FeCo, Fe8N, or combinations thereof. In some examples, the bulk material may be annealed at a temperature between about 50° C. and about 200° C. for between about 0.5 hours and about 20 hours to form a solid magnetic bulk material.
In some examples, joining the plurality of anisotropic particles to form a bulk material may include generating a compression shock that joins the anisotropic particles including iron nitride. In some examples, ferromagnetic particles may be disposed about the plurality of anisotropic particles including iron nitride. In other examples, solely a plurality of anisotropic particles including iron nitride may be used. As described above, in some examples, substantially aligning the longest dimensions of anisotropic particles including iron nitride may include substantially aligning the <001> crystal axes of the anisotropic particles, which may provide uniaxial magnetic anisotropy to bulk material or a magnet formed from anisotropic particles. In examples in which ferromagnetic particles are utilized, at least some ferromagnetic particles may be disposed between respective anisotropic particles including iron nitride.
In some examples, shock compression may include placing anisotropic particles including iron nitride (e.g., particles including iron nitride and having an aspect ratio of at least 1.4) between parallel plates. The anisotropic particles may be cooled by flowing liquid nitrogen through a conduit coupled to a back side of one or both of the parallel plates, e.g., to a temperature below 0° C. A gas gun may be used to impact one of the parallel plates with a burst of gas at a high velocity, such as about 850 m/s. In some examples, the gas gun may have a diameter between about 40 mm and about 80 mm.
In some further examples, joining the plurality of anisotropic particles to form a bulk material may include generating an electromagnetic field using a conductive coil through which a current may be applied. The current may be generated in a pulse to generate an electromagnetic force, which may help to consolidate the anisotropic particles including iron nitride, such as Fe16N2 phase domains. In some examples, ferromagnetic particles may be disposed about the anisotropic particles. Further, in some examples, the anisotropic particles including iron nitride may be disposed within an electrically conductive tube or container within the bore of the conductive coil. The conductive coil may be pulsed with a high electrical current to produce a magnetic field in the bore of conductive coil that, in turn, induces electrical currents in the electrically conductive tube or container. The induced currents interact with the magnetic field generated by conductive coil to produce an inwardly acting magnetic force that collapses the electrically conductive tube or container. The collapsing electromagnetic container or tube transmits a force to the anisotropic particles including iron nitride and joins the particles. After the consolidation of the anisotropic particles including iron nitride with the ferromagnetic particles, the ferromagnetic particles may be magnetically coupled to hard magnetic material within the anisotropic particles, such as at least one Fe16N2 phase domain, via exchange spring coupling. In some examples, this technique may be used to produce bulk material that has at least one of cylindrical symmetry, a high aspect-ratio, or a net shape (a shape corresponding to a desired final shape of the workpiece). As stated above, the ferromagnetic particles may include, for example, Fe, FeCo, Fe8N, or combinations thereof.
In any of the above examples, other techniques for assisting consolidation of a plurality of anisotropic particles including iron nitride may be used, such as pressure, electric pulse, spark, applied external magnetic fields, a radio frequency signal, laser heating, infrared heating, for the like. Each of these example techniques for joining a plurality of anisotropic particles including iron nitride may include relatively low temperatures such that the temperatures used may leave any Fe16N2 phase domains substantially unmodified (e.g., such that Fe16N2 phase domains are not converted to other types of iron nitride).
In other examples, a disclosed technique may include joining the plurality of anisotropic particles to form a workpiece. Workpieces may take a number of forms, such as a wire, rod, bar, conduit, hollow conduit, film, sheet, or fiber, each of which may have a wide variety of cross-sectional shapes and sizes, as well as any combinations thereof. One or more of the described joining techniques may be utilized to join anisotropic particles to form the workpiece. In some examples, a workpiece may include a bulk material as described.
The disclosure also describes a material that includes an anisotropic particle including at least one iron nitride crystal. In some examples, the anisotropic particle may have an aspect ratio of at least 1.4, with aspect ratio being defined as described herein. In some examples, the material may include an anisotropic particle having at least one iron nitride crystal, and the anisotropic particle may have an aspect ratio of at least 1.4. Further, in some examples, the at least one iron nitride crystal may include α″-Fe16N2.
Moreover, in some examples of these materials, <001> crystal axes of a plurality of iron nitride crystals may be substantially parallel, and the longest dimension of the anisotropic particle may be substantially parallel to the substantially parallel <001> crystal axes of the iron nitride crystals. Substantially parallel alignment of <001> crystal axes (in some examples, easy axes) of the iron nitride crystals, coupled with substantially parallel alignment of the <001> crystal axes with the longest dimension of an anisotropic particle, may result in enhanced magnetic properties. For example, magnetic anisotropy at the level of crystal units coupled with shape anisotropy of a particle including magnetic material, may result in a particle that exhibits enhanced coercivity, magnetization, magnetic orientation, and/or energy product, as compared to materials having randomly ordered crystals and/or an isotropic shape.
In some example materials according to this disclosure, a length of the anisotropic particle measured in the direction of the substantially parallel <001> crystal axes of the plurality of iron nitride crystals may be at least about 1.4 times the length of the anisotropic particle measured in at least one of the substantially orthogonal direction of the <100> crystal axes of the plurality of iron nitride crystals of the anisotropic particle, or the substantially orthogonal direction of the <010> crystal axes of the plurality of iron nitride crystals of the anisotropic particle, corresponding to an aspect ratio of 1.4. In such an example, the <100> crystal axes of the plurality of iron nitride crystals also may be substantially parallel.
In some examples, a cross-section of the anisotropic particle of the material, taken orthogonal to the substantially parallel <001> crystal axes of the iron nitride crystals, may be substantially circular. For example, the particle may have a needle shape. In other examples, a cross-section of the anisotropic particle taken in a plane orthogonal to the substantially aligned <001> crystal axes of the iron crystals may be substantially rectangular, such that the particle has a flake shape. Other anisotropic particle shapes and cross-sections of those shapes are contemplated by this disclosure as well, as described above.
For example, in some example materials, the length of an anisotropic particle measured in the direction of substantially parallel <001> crystal axes may be about 1 micron (μm), and the length of the anisotropic particle measured in the direction of at least one of the substantially parallel <100> crystal axes or the substantially parallel <010> crystal axes may be between about 200 nm and 500 nm.
In some examples, an example material may include a plurality of anisotropic particles. In some such examples, the longest dimensions of the anisotropic particles may be substantially parallel. For example, the longest dimensions may be aligned by exposure to a magnetic field, such that a magnetic moment along the longest dimension of the anisotropic particles aligns with the applied magnetic field. Further, the plurality of anisotropic particles, including the example when the longest dimensions thereof are aligned, may take the form of a bulk permanent magnet.
The iron nitride materials formed by the techniques described herein may be used as magnetic materials in a variety of applications, including, for example, bulk permanent magnets. Bulk permanent magnets may include a minimum dimension of at least about 0.1 mm. In some examples, the bulk material including iron nitride may be annealed in the presence of an applied magnetic field. In other examples, iron nitride materials annealed in the presence of an applied magnetic field may not be bulk materials (may have a minimum dimension less than about 0.1 mm), and the iron nitride materials may be consolidated with other iron nitride materials to form bulk permanent magnets. Examples of techniques that may be used to consolidate iron nitride magnetic materials are described, for example, in International Patent Application Number PCT/US2012/051382, filed on Aug. 17, 2012, and titled “IRON NITRIDE PERMANENT MAGNET AND TECHNIQUE FOR FORMING IRON NITRIDE PERMANENT MAGNET,” the entire content of which is incorporated herein by reference. Other examples are described in International Patent Application Number PCT/US2014/015104, filed on Feb. 6, 2014, and titled “IRON NITRIDE PERMANENT MAGNET AND TECHNIQUE FOR FORMING IRON NITRIDE PERMANENT MAGNET,” the entire content of which is incorporated herein by reference. Still other examples are described in International Patent Application Number PCT/US2014/043902, filed on Jun. 24, 2014, and titled “IRON NITRIDE MATERIALS AND MAGNETS INCLUDING IRON NITRIDE MATERIALS,” the entire content of which is incorporated herein by reference.
Clause 1: A method comprising: milling an iron-containing raw material in the presence of a nitrogen source to generate a powder including a plurality of anisotropic particles, wherein at least some particles of the plurality of anisotropic particles include iron nitride, wherein at least some particles of the plurality of anisotropic particles have an aspect ratio of at least 1.4, wherein the aspect ratio for an anisotropic particle of the plurality of anisotropic particles comprises the ratio of the length of a longest dimension to the length of a shortest dimension of the anisotropic particle, and wherein the longest dimension and the shortest dimension are substantially orthogonal.
Clause 2: The method of clause 1, wherein milling the iron-containing raw material comprises milling the iron-containing raw material for between about 20 hours and about 65 hours in a bin of a rolling mode milling apparatus, a stirring mode milling apparatus, or a vibration mode milling apparatus.
Clause 3: The method of clause 1, wherein milling the iron-containing raw material comprises milling the iron-containing raw material under a pressure of between about 0.1 gigapascals (GPa) and about 20 GPa in a bin of a rolling mode milling apparatus, a stirring mode milling apparatus, or a vibration mode milling apparatus.
Clause 4: The method of clause 3, wherein a gas flows into the bin to create the pressure, wherein the gas comprises at least one of air, nitrogen, argon, or ammonia.
Clause 5: The method of clause 1, wherein milling the iron-containing raw material comprises milling the iron-containing raw material at a temperature between about −196.15° C. and about 23° C. in a bin of a rolling mode milling apparatus, a stirring mode milling apparatus, or a vibration mode milling apparatus.
Clause 6: The method of clause 5, wherein the iron-containing raw material is cooled by liquid nitrogen to a temperature of about −196.15° C. when milled.
Clause 7: The method of clause 1, wherein milling the iron-containing raw material comprises milling the iron-containing raw material in the presence of a magnetic field in a bin of a rolling mode milling apparatus, a stirring mode milling apparatus, or a vibration mode milling apparatus.
Clause 8: The method of clause 7, wherein the magnetic field has a strength between about 0.1 tesla (T) and about 10 T.
Clause 9: The method of clause 7 or 8, wherein the bin of the rolling mode milling apparatus or the vibration mode milling apparatus rotates at a speed of about 50 revolutions per minute (rpm) to about 500 rpm, or wherein a shaft of the stirring mode milling apparatus rotates at about 50 rpm to about 500 rpm, and wherein at least one paddle extends radially from the shaft.
Clause 10: The method of any one of clauses 7 to 9, wherein the iron-containing raw material comprises an iron-containing powder, and wherein the magnetic field substantially maintains at least one particle of the iron-containing powder in a particular orientation, such that at least a first surface of the at least one particle is worn more than a second surface of the at least one particle.
Clause 11: The method of clause 10, wherein an easy axis of at least one iron nitride crystal of the at least one particle of the iron-containing powder is substantially parallel to a direction of the magnetic field for at least a portion of the time the iron-containing powder is milled.
Clause 12: The method of clause 1, wherein milling the iron-containing raw material comprises milling the iron-containing raw material in the presence of an electric field in a bin of a rolling mode milling apparatus, a stirring mode milling apparatus, or a vibration mode milling apparatus.
Clause 13: The method of clause 12, wherein the electric field comprises an alternating current that has a frequency of up to 10 megahertz (MHz) and a power between about 0.1 watts (W) and 100 W.
Clause 14: The method of clause 12, wherein the electric field comprises a direct current that has a voltage between about 10 volts (V) and about 10,000 V.
Clause 15: The method of clause 1, wherein milling the iron-containing raw material comprises milling the iron-containing raw material with a plurality of elongated bars in a bin of a rolling mode milling apparatus or a vibration mode milling apparatus.
Clause 16: The method of clause 15, wherein at least some particles of the plurality of anisotropic particles have an aspect ratio of at least 5.0.
Clause 17: The method of clause 15 or 16, wherein the plurality of elongated bars comprises a plurality of cylindrical bars, and wherein each cylindrical bar of the plurality of cylindrical bars has a diameter between about 5 millimeters (mm) and about 50 mm.
Clause 18: The method of any one of clauses 15 to 17, wherein the iron-containing raw material occupies between about 20% and about 80% of the volume of the bin of the rolling mode milling apparatus or the vibration mode milling apparatus.
Clause 19: The method of any one of clauses 15 to 18, wherein the bin of the rolling mode milling apparatus or the vibration mode milling apparatus rotates at a speed greater than 250 rpm.
Clause 20: The method of any one of clauses 1 to 19, wherein at least one dimension of at least some particles of the plurality of anisotropic particles is between about 5 nanometers (nm) and about 50 nm in length.
Clause 21: The method of any one of clauses 1 to 20, further comprising, prior to milling the iron-containing raw material in the presence of the nitrogen source, milling an iron precursor to form the iron-containing raw material, wherein the iron precursor comprises at least one of iron (Fe), FeCl3, Fe2O3, or Fe3O4.
Clause 22: The method of clause 21, wherein milling the iron precursor to form the iron-containing raw material comprises milling the iron precursor in the presence of at least one of Ca, Al, or Na under conditions sufficient to cause an oxidation reaction between the at least one of Ca, Al, or Na and oxygen present in the iron precursor.
Clause 23: The method of any one of clauses 1 to 22, wherein the nitrogen source comprises at least one of ammonia, ammonium nitrate, an amide-containing material, or a hydrazine-containing material.
Clause 24: The method of clause 23, wherein the amide-containing material comprises at least one of a liquid amide, a solution containing an amide, carbamide, methanamide, benzamide, or acetamide, and wherein the hydrazine-containing material comprises at least one of a hydrazine or a solution containing the hydrazine.
Clause 25: The method of any one of clauses 1 to 24, further comprising adding a catalyst to the iron-containing raw material.
Clause 26: The method of clause 25, wherein the catalyst comprises at least one of nickel or cobalt.
Clause 27: The method of any one of clauses 1 to 26, wherein the at least some anisotropic particles including iron nitride comprise at least one of FeN, Fe2N, Fe3N, Fe4N, Fe2N6, Fe8N, Fe16N2, or FeNx, wherein x is in the range of from about 0.05 to about 0.5.
Clause 28: The method of clause 27, wherein the iron nitride comprises at least one α″-Fe16N2 phase domain.
Clause 29: The method of any one of clauses 1 to 28, wherein the iron-containing raw material further comprises at least one dopant, wherein at least some of the particles of the plurality of anisotropic particles include the at least one dopant, and wherein the at least one dopant comprises at least one of Al, Mn, La, Cr, Co, Ti, Ni, Zn, a rare earth metal, B, C, P, Si, or O.
Clause 30: An apparatus configured to perform the method of any one of clauses 1 to 29.
Clause 31: A material formed by the method of any one of clauses 1 to 29.
Clause 32: A material comprising: an anisotropic particle comprising at least one iron nitride crystal, wherein the anisotropic particle has an aspect ratio of at least 1.4, wherein the aspect ratio comprises the ratio of the length of a longest dimension of the anisotropic particle to the length of a shortest dimension of the anisotropic particle, and wherein the longest dimension and the shortest dimension are substantially orthogonal.
Clause 33: The material of clause 32, wherein the at least one iron nitride crystal comprises α″-Fe16N2.
Clause 34: The material of clause 32 or 33, wherein the at least one iron nitride crystal comprises a plurality of iron nitride crystals, and wherein the respective <001> crystal axes of the plurality of iron nitride crystals are substantially parallel.
Clause 35: The material of clause 34, wherein the longest dimension of the anisotropic particle is substantially parallel to the substantially parallel respective <001> crystal axes of the plurality of iron nitride crystals.
Clause 36: The material of clause 34 or 35, wherein the length of the anisotropic particle measured in the direction of the substantially parallel <001> crystal axes of the plurality of iron nitride crystals is at least about 1.4 times the length of the anisotropic particle measured in at least one of a substantially orthogonal direction of the <100> crystal axes of the plurality of iron nitride crystals of the anisotropic particle or a substantially orthogonal direction of the <010> crystal axes of the plurality of iron nitride crystals of the anisotropic particle.
Clause 37: The material of clause 36, wherein the length of the anisotropic particle measured in the direction of the substantially parallel <001> crystal axes is about 1 micron (μm) and the length of the anisotropic particle measured in the direction of at least one of the substantially parallel <100> crystal axes or the substantially parallel <010> crystal axes is between about 200 nanometers (nm) and 500 nm.
Clause 38: The material of any one of clauses 34 to 37, wherein at least some iron nitride crystals of the plurality of iron nitride crystals comprise at least one α″-Fe16N2 phase domain.
Clause 39: The material of any one of clauses 32 to 38, wherein the anisotropic particle comprises a plurality of anisotropic particles.
Clause 40: The material of clause 39, wherein the respective longest dimensions of respective particles of the plurality of anisotropic particles are substantially parallel.
Clause 41: A bulk permanent magnet comprising the material of clause 39 or 40.
Clause 42: A method comprising: aligning a plurality of anisotropic particles, such that the longest dimensions of respective anisotropic particles of the plurality of anisotropic particles are substantially parallel, wherein at least some anisotropic particles of the plurality of anisotropic particles comprise iron nitride and have an aspect ratio of at least 1.4, wherein the aspect ratio comprises the ratio of the length of the longest dimension of an anisotropic particle to the length of the shortest dimension of the anisotropic particle, and wherein the longest dimension and the shortest dimension are substantially orthogonal; and joining the plurality of anisotropic particles to form a bulk material comprising iron nitride.
Clause 43: The method of clause 42, wherein each anisotropic particle of the plurality of anisotropic particles includes at least one iron nitride crystal, and wherein the respective <001> crystal axes of at least some of the at least one iron nitride crystals of the plurality of anisotropic particles are substantially parallel to the longest dimensions of the respective anisotropic particles.
Clause 44: The method of clause 42 or 43, wherein aligning the plurality of anisotropic particles comprises exposing the anisotropic particles to a magnetic field.
Clause 45: The method of clause 44, wherein the magnetic field has a strength between about 0.01 Tesla (T) and about 50 T.
Clause 46: The method of any one of clauses 42 to 45, wherein joining the plurality of anisotropic particles comprises at least one of sintering, adhering, alloying, soldering, using a resin or binder on, using shock compression on, or using electrodischarge on the plurality of anisotropic particles.
Clause 47: The method of clause 46, wherein sintering the plurality of anisotropic particles comprises heating the plurality of anisotropic particles at a temperature between about 23° C. and about 200° C.
Clause 48: The method of any one of clauses 42 to 47, wherein the bulk material comprises a bulk permanent magnet.
Clause 49: The method of any one of clauses 42 to 48, wherein the iron nitride comprises at least one α″-Fe16N2 phase domain.
Clause 50: An apparatus comprising: a plurality of elongated bars, wherein at least some of elongated bars of the plurality of elongated bars have a width between about 5 millimeters (mm) and about 50 mm; a bin configured to house the plurality of elongated bars; at least one support structure configured to support the bin; and a means for rotating the bin about an axis of the bin.
Clause 51: The apparatus of clause 50, further comprising a means for vibrating the bin.
Clause 52: The apparatus of clause 50 or 51, further comprising a means for rotatably coupling the support structure and the bin.
Clause 53: The apparatus of any one of clauses 50 to 52, wherein the bin is configured to rotate at a speed greater than 250 revolutions per minute (rpm).
Clause 54: The apparatus of any one of clauses 50 to 53, wherein the means for rotating the bin comprises a motor mechanically coupled to the bin.
Clause 55: The apparatus of any one of clauses 50 to 54, wherein each elongated bar of the plurality of elongated bars has a length along a horizontal axis of the elongated bar that is longer than a diameter of the bin.
Clause 56: An apparatus comprising: a plurality of milling media; a bin configured to house the plurality of milling media; a generator comprising at least one of a spark discharge mode or a glow discharge mode, wherein the generator is configured to generate an electric field within the bin; a first wire comprising a first end and a second end, wherein the first end of the first wire is affixed to at least one milling medium and the second end of the first wire is electrically coupled to a first terminal of the generator; a second wire comprising a first end and a second end, wherein the first end of the second wire is electrically coupled to the bin and a ground and the second end of the second wire is electrically coupled to a second terminal of the generator; at least one support structure configured to support the bin; and a means for rotating the bin about an axis of the bin.
Clause 57: The apparatus of clause 56, further comprising a means for vibrating the bin.
Clause 58: The apparatus of clause 56 or 57, further comprising a means for rotatably coupling the support structure and the bin.
Clause 59: An apparatus comprising: a plurality of milling media; a bin configured to house the plurality of milling media; a means for generating a magnetic field within the bin; at least one support structure configured to support the bin; and a means for rotating the bin about an axis of the bin.
Clause 60: The apparatus of clause 59, further comprising a means for vibrating the bin.
Clause 61: The apparatus of clause 59 or 60, further comprising a means for rotatably coupling the support structure and the bin.
Clause 62: A method comprising: nitridizing an anisotropic particle including iron to form an anisotropic particle including iron nitride; and annealing the anisotropic particle including iron nitride to form at least one α″-Fe16N2 phase domain within the anisotropic particle including iron nitride, wherein the anisotropic particle including iron nitride has an aspect ratio of at least 1.4, wherein the aspect ratio for the anisotropic particle including iron nitride comprises the ratio of the length of a longest dimension to the length of a shortest dimension of the anisotropic particle including iron nitride, and wherein the longest dimension and the shortest dimension are substantially orthogonal.
Clause 63: The method of clause 62, further comprising, prior to nitridizing the anisotropic particle including iron, reducing an anisotropic iron precursor to form the anisotropic particle including iron.
Clause 64: The method of clause 63, wherein the anisotropic iron precursor comprises an anisotropic particle including iron oxide.
Clause 65: The method of clause 63 or 64, wherein reducing the anisotropic iron precursor comprises exposing the iron precursor to hydrogen gas to form the anisotropic particle including iron.
Clause 66: The method of any one of clauses 62 to 65, wherein annealing the anisotropic particle including iron nitride comprises heating the anisotropic particle including iron nitride at a temperature between about 100° C. and about 250° C. for between about 20 hours and about 200 hours.
Clause 67: The method of any one of clauses 62 to 66, wherein the anisotropic particle including iron includes a plurality of anisotropic particles including iron, wherein the plurality of anisotropic particles including iron are nitridized to form a plurality of anisotropic particles including iron nitride, and wherein the plurality of anisotropic particles including iron nitride are annealed to form at least one α″-Fe16N2 phase domain within at least some of the anisotropic particles including iron nitride of the plurality of anisotropic particles including iron nitride.
Clause 68: A workpiece comprising the anisotropic particles made by the method of any one of clauses 1-29, 42-49 or 62-67.
Clause 69: The workpiece of clause 68, wherein the workpiece is a film or wire.
Clause 70: The workpiece of clause 68, wherein the workpiece is a wire, rod, bar, conduit, hollow conduit, film, sheet, or fiber.
Table 1 below presents four samples of powder including anisotropic particles that include iron nitride generated by milling with steel milling spheres in the PM 100 planetary milling apparatus, i.e., FeN 90, FeN 91, FeN 92, and FeN93. For each sample, prior to milling in the PM 100 planetary ball milling apparatus, an iron-containing pieces were pre-annealed in a hydrogen environment at 100° C. for about 2 hours to reduce the carbon content in the iron-containing pieces. The iron-containing pieces were then milled in the PM 100 planetary ball milling apparatus (described above) in the presence of ammonium nitrate (NH4NO3) as a nitrogen source in a 1:1 weight ratio between the iron-containing pieces and the ammonium nitrate. For each sample, 10 steel balls, each having a diameter of about 5 mm, were used. Each time 10 hours of milling was complete, the milling apparatus was stopped for 10 minutes to allow the system to cool. After ball milling, each generated anisotropically shaped iron nitride-containing particles were post-annealed at the temperatures and for the time periods noted in Table 1.
Table 2 below presents the coercivity (Hc) and saturation magnetization (Ms) measured for each of samples FeN 90 through FeN 93, after undergoing carbon reduction and annealing as described above.
Further,
Various examples have been described. These and other examples are within the scope of the following claims.
This application is a National Stage of International Patent Application No. PCT/US2016/014578, filed Jan. 22, 2016, and claims the benefit of U.S. Provisional Patent Application No. 62/107,748, filed Jan. 26, 2015, both applications titled “IRON NITRIDE POWDER WITH ANISOTROPIC SHAPE,” the entire contents of which are incorporated herein by reference for all purposes.
This invention was made with Government support under contract number DE-AR0000199 awarded by DOE, Office of ARPA-E. The government has certain rights in this invention.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2016/014578 | 1/22/2016 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2016/122987 | 8/4/2016 | WO | A |
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| 2013069926 | Apr 2013 | JP |
| 2014210027 | Dec 2014 | WO |
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| Number | Date | Country | |
|---|---|---|---|
| 20180001385 A1 | Jan 2018 | US |
| Number | Date | Country | |
|---|---|---|---|
| 62107748 | Jan 2015 | US |
