• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    PURPOSE: A magnetisable device is provided to be used as a magnetic storage device having improved data storage characteristics. CONSTITUTION: A magnetisable device which comprises a magnetic layer composed of domain-separated, ferromagnetic particles each of which has a largest dimension no greater than 100 nm. And a magnetic recording medium which includes a magnetisable layer thereon, wherein the magnetisable layer comprises a plurality of ferromagnetic particles each having a largest dimension no greater than 100 nm, and each of which particles represents a separate ferromagnetic domain. A magnetic composition comprising a plurality of ferromagnetic particles each of which is fabricated within an organic macromolecule, and each of which ferromagnetic particles has a largest dimension no greater than 100 nm.
    公开号:KR20000053057A
    申请号:KR1019990703966
    申请日:1997-11-17
    公开日:2000-08-25
    发明作者:마에스에릭레이；틸러말빈니콜라스
    申请人:나노마그네틱스 리미티드；
    IPC主号:
    专利说明:

    Magnetization device {MAGNETIZABLE DEVICE}
    Nanoscale particles (1-100 nm) are used between the possible paths for ultra-high density (> = 1 Gbit / in 2 ) magnetic media. Beyond the standard requirements for magnetic media, viable particulate media must not only have particles separated and exchanged, but also have standard horseshoe small in particle size. These requirements are necessary to avoid bad media noise. Typical methods of producing nanoscale particles, such as multiple targets or arc-discharge, which scatter ion beams, do not fully meet these two requirements. In addition, if uniform particles are arranged in the indicated arrays, each particle may be represented by "bit" information at predictable locations that further increase the efficiency of the medium.
    The present invention relates to a magnetization device comprising a magnetic layer made of nanoscale (eg, 1-100 nm) ferromagnetic particles having discrete magnetic domains. The magnetization device of the present invention can be used as a magnetic storage device with improved data storage characteristics. In particular, the present invention relates to a magnetic storage medium comprising uniform nanounits of ferromagnetic particles having discrete single domains that can be arranged in a rated 2-D filled array useful for information storage.
    The present invention describes a method of producing particulate media that meets these requirements for ultra high density recording. The present invention also relates to known systems for producing a variety of magnetic materials, such as media that can be used for other applications.
    In particular, the present invention describes the use of ferritin, an iron storage protein whose inner pores are used to produce nanoparticles. Ferritin is used for iron metabolism of all species and its structure is highly conserved between them. Ferritin consists of 24 subunits arranged to provide a hollow shell approximately 8 nm in diameter. The holes generally store 4500 iron (III) atoms in the form of paramagnetic perihydrate. However, these perhydrates can be eliminated (ferritin without ferrihydrates at all is termed "apoferritin") and other substances can be combined. Examples include ceramics, superparamagnetic magnetite, acetaminophen and sweetener aspartame. In order to match the magnetic medium, the present invention combines ferromagnetically arranged materials.
    According to an example of the present invention, there is provided a magnetization device including a magnetic layer made up of ferromagnetic particles each having a size of up to 100 nm having separate magnetic domains.
    According to a second example of the present invention, there is provided a magnetic recording medium each comprising particles representing ferromagnetic magnetic domains separated from the above magnetic layer each having a size of up to 100 nm. Preferably the magnetic layer is supported on a nonmagnetic adhesive substrate.
    According to a third example of the present invention, there is provided a magnetic construct comprising a plurality of ferromagnetic particles each bonded to an organic molecule and having a size of up to 100 nm or less. In this example of the invention, it is preferred that the organic molecule is a ferritin of ordinary magnetic core perhydrite removed and replaced by ferromagnetic particles.
    As used herein, "ferromagnetic material" includes materials that are one of ferromagnetic and perimagnetic. Such usage is common in the field of electrical engineering.
    Ferromagnetic particles used in the present invention should be a material of a size having ferromagnetic properties at room temperature (for example 15 ℃-30 ℃).
    Preferably the ferromagnetic particles are each of a maximum size not exceeding 50 nm, more preferably 25 nm or less, and most preferably smaller than 15 nm. The maximum size of the ferromagnetic particles should not be so small that the particles lose their ferromagnetic properties and become superparamagnetic at the required operating temperature of the recording medium. In general, operation at room temperature means that magnetic particles normally have their maximum diameter no less than about 3 nm.
    In the magnetization apparatus of one example of the present invention and the magnetic recording medium of the second example of the present invention, the distance between adjacent ferromagnetic magnetic domains is preferably small so as to allow the maximum number of magnetic domains identifiable in a given area and maximum storage in the recording medium Provide the ability. The actual minimum will vary depending on other conditions and other conditions such as the temperature of the recording medium used. The key requirement, however, is that adjacent magnetic domains should not magnetically interfere with each other to the extent that the magnetic arrangement of a magnetic domain can be changed by adjacent magnetic domains. Generally, the minimum for the space of a domain is about 2 nm. The distance between adjacent domains will be determined by the density of the individual domains required. In general, however, the distance between adjacent domains will be less than 10 nm to take advantage of the miniaturization provided by the present invention.
    In general, the particles will be uniform in size, which means that the particles cannot change their maximum diameter by more than about 5%. One of the advantages of using organic molecules in the present invention is that the organic molecules that surround and bind the magnetic particles can be used to select particles of the same size.
    If the particles are ellipsoids, the particle diameter should be smaller than 100 nm.
    In all preferred embodiments of the present invention the respective ferromagnetic particles are enclosed or partially enclosed in organic molecules. A macromolecule is a molecule or group of molecules that has a molecular weight less than 1500kD but is generally less than 500kD. Ferritin has a molecular weight of 400 kD.
    Macromolecules must have the ability to enclose or organize and bind magnetic particles and thus have appropriate cavity to contain them; The hole will generally be completely inside the macromolecule. Optionally, the macromolecule will include a suitable opening that is not fully enclosed but is capable of receiving and supporting magnetic particles; For example, the opening may be defined by a ring in the macromolecule. For example, suitable macromolecules that can be used in the present invention are proteins such as protein apoferritin (empty ferritin), flagella L-P rings, cyclodextrins, cyclic peptides that are self-combining. Alternatively, the magnetic particles may be composed of macromolecules, such as bacterial S-layers, in a manner different from the introduction of magnetic particles into the macromolecules.
    Other materials that can be used in the present invention to construct ferromagnetic particles are inorganic-silica networks such as MCM type materials, dendrimers and colloidal systems.
    Preferred macromolecules for use in the present invention are apoferritin proteins, which usually have pores about 8 nm in diameter. In order to be contained in these proteins, the perimagnetic or ferromagnetic particles must have a diameter of 8 nm or less.
    In this example of the invention the particles which are covered and bound together prevent aggregation and oxidation and also help to have separate domains.
    In the magnetization apparatus of the first example of the present invention and the magnetic recording medium of the second example of the present invention, the particles are preferably arranged in a 2-D designated array that yields an ultrahigh density magnetic medium.
    Ferromagnetic materials include metals such as cobalt, iron or nickel; Metals such as alloys including aluminum, barium, bismuth, cerium, chromium, cobalt, copper iron, manganese, molybdenum, neodymium, nickel, niobium, platinum, praseodymium, samarium, strontium, titanium, vanadium, ytterbium, yttrium or mixtures thereof alloy; Metal ferrites such as ferrite including barium, cobalt or strontium; Or organic ferromagnetic material.
    One important thing when calculating nanoscale particles is that the particles produced should not be superparamagnetic. Superparamagnetic particles have a permanent magnetic dipole moment, but the direction of that moment varies with time with respect to the crystallographic axis. This is not useful for real magnetic storage media. Superparamagnetism depends on volume, temperature and anisotropy of the particles. Taking energy into account, we can obtain equations for these quantities. The volume when the particles become superparamagnetic (V p ) is V p = 25 kT / K where k is the Boltzmann constant, T is the Kelvin temperature of the particle, and K is the anisotropy constant of the material. This equation can be used to determine the temperature (blocking temperature) at which particles become superparamagnetic for a given material at a fixed volume. In a special case of the invention the fixed volume for ferritin is 8 nm. If only cobalt metal particles having crystalline anisotropy are spherical with a diameter of 8 nm, the blocking temperature is 353 o K. It is within the range of temperatures experienced in hard disk drives and it will prove that cobalt particles are useful storage media. Clearly there are other considerations such as coercivity, moment, saturation magnetism and relaxation time of the material. By combining the substances with ferritin they are matched to the conditions.
    Ferritin is used in the iron metabolism of all species and its structure is highly conserved among them. It consists of 24 subunits arranged 432 symmetrically, giving a hollow cell of approximately 8 nm in diameter. In general, the holes store 4500 iron (III) atoms in the form of paramagnetic ferrihydrate. However, these perhydrates can be eliminated (ferritin without ferrihydrates at all is called "apoferritin") and other substances can be combined. The subunits are tightly enclosed in the ferritin but there are channels in the holes in the 3-fold and 4-fold axes. The inner layer of the 3-fold channel is a residue that binds to metals such as cadmium, zinc and calcium. By drawing these divalent ions inwards, they potentially bind with or fertilize the ferritin molecule, or at least stimulate the contiguous arrangement.
    One method of obtaining a 2-D filled array of ferromagnetic particles of uniform size less than 8 nm is to remove the ferrihydrate core from natural ferritin in aqueous solution, and to reduce sodium borohydride of cobalt (II) aqueous solution in the ferritin pore. Binding of ferromagnetically arranged cobalt metal particles, yielding a small distribution through ultracentrifugation, injecting particles into a MES / glucose subphase solution that combines into a 2-D array, and into a carbon-enclosed support layer. Movement of the D array. In this method, the source of ferritin may be produced through vertebrates, invertebrates, plants, fungi, yeast, bacteria or recombinant techniques.
    In the described method the metal alloy core can be produced by sodium borohydride reduction of water soluble metal salts. Other oxidation methods include carbon, carbon monoxide, hydrogen or hydrazine hydroxide solution. Optionally, a suitable solution can be oxidized to obtain a metal ferrite core. Reduction is to obtain metal ferrite chemically or electrochemically.
    Other methods of selecting small distributions in this way may be employed such as short or long column meniscus consumption methods or magnetic field separation.
    In addition, in this method, divalent metal salts containing cadmium, calcium or zinc can be added into the bottom solution to aid in the arrangement of the particles.
    In addition, other methods of arranging the particles in a 2-D array may be employed, such as evaporation of a solution on a solid support layer.
    In addition, the method can cover a 2-D array with a carbon-based film, such as diamond-like carbon treated with hydrogenated or concentrated liquid nitrogen, or a silicon-based film, such as silicon dioxide.
    Ferritin that can be used to enclose the largest ferromagnetic particles in the present invention is limited to an inner diameter of 8 nm. Particles produced by removing the ferrihydrate core yield apoferritin. This is done by dialysis against sodium acetate solution treated with buffer under the influx of nitrogen. Chelation that reduces thioglycolic acid is used to remove the ferrihydrate core. Repeated dialysis against sodium chloride solution completely removes the reduced perhydrate core from the solution. Once apoferritin is produced, permagnetic or ferromagnetic particles are combined in the following methods. First, the metal salt solution in which apoferritin is present is reduced. This is done in an inert atmosphere to protect against oxidation which reduces the magnetism of the metal particles. The compound of metal salt in solution is also reduced to yield an alloy or alloy precursors. Sintering or heat cooling in the magnetic field will be necessary to yield a useful magnetic alloy. Another method is to oxidize the compounds of iron (II) salts and other metal salts. This gives metal ferrite particles which are not affected by reduction from oxidation. Beneficial metal salts include salts of aluminum, barium, bismuth, cerium, chromium, cobalt, copper, iron, manganese, molybdenum, neodymium, nickel, niobium, platinum, praseodymium, samarium, strontium, titanium, vanadium, ytterbium, yttrium .
    Small distribution of particles is necessary to avoid medium noise. Such distribution can be obtained through a variety of methods, including but not limited to density gradient centrifugation or magnetic field separation.
    The production method described uses natural horse spleen ferritin, while the present invention is not limited to its source. Ferritin can be found in vertebrates, invertebrates, plants, fungi, yeast, bacteria or products through recombinant technology. By making apoferritin of a mutant lacking a bivalent binding site, the mutant strains were found to be combined into square aggregates as opposed to dense square hexagons.
    While ferritin is considered an ideal system for producing nanoparticles, it is not a usable system. Flagella L-P rings, for example, are tubular proteins with an internal diameter of 13 nm. By creating a 2-D array of these proteins, a metal film can be placed in the center of the tube to create a magnetic material in the vertical bar. Reduction of the metal in the microemulsion can also be used to make nanoparticles surrounded by a surfactant. The present invention provides another method for producing nanoparticles.
    Finally, an ordered arrangement of the particles is desirable. One way to achieve this is to inject an aqueous solution of the particles into the MES / glucose bottoms solution contained in the Teflon barrel. When the particles are sprayed onto the contact surface of air and the lower part, they are partially modified to form a monolayer film. The 2-D arrangement of the encased particles occurs below this monolayer. After 10 minutes at room temperature the arrangement and monolayer are transferred to the support layer by placing the support layer directly on the monolayer for 5 minutes. After recovering the support layer, it is surrounded by a thin layer of carbon to protect the attached arrangement. It is also possible to obtain a 2-D arrangement by other methods, such as evaporation drying of a solution on a solid support layer, and the present invention is not limited to these arrangement methods.
    (Example 1)
    This example describes a method for obtaining apoferritin from ferritin of a horse's spleen. Thioglye by dialysis (separation of molecular weight 10-14kDaltons) from cadmium free natural horse spleen ferritin (100 mg / ml) under sodium influx buffer (0.2M) at pH 5.5 under nitrogen influx. The perihydrate cores were removed by reduction chelation with cholic acid (0.3M) to yield apoptorit. Dialysis against sodium chloride solution (0.15M) was repeated to completely remove the reduced perhydrate core from the solution.
    (Example 2)
    In this example, a method of obtaining cobalt metal in apoferritin is described. Apoprotein was added to buffered deaired TES / sodium chloride solution (0.1 / 0.4M) at pH7.5 to obtain approximately 1 mg / ml protein working solution. Deaired cobalt (II) [e.g. acetate salt] solution (1 mg / ml) was added incrementally as the total atoms added were approximately 500 atoms / apoprotein molecules. It was stirred in inert atmosphere for one day at room temperature. Cobalt (II) salt was then reduced to cobalt (0) metal using sodium borohydride. The final product yielded a solution of cobalt particles each surrounded by a ferritin shell.
    (Example 3)
    This example describes a method of obtaining a metal alloy, such as yttrium cobalt (YCo 5 ) in apoferritin. The metal alloy is the same as the method of Example 2 but uses yttrium (III) [for example acetate salt] and cobalt (II) [for example acetate salt] in a ratio of 1: 5. The final product yielded a solution of yttrium cobalt particles each surrounded by a ferritin shell.
    (Example 4)
    In this embodiment, a method of obtaining a metal ferrite such as cobalt ferrite (CoO · Fe 2 O 3 ) in apoferritin is described. Apoprotein was added to the pH 6 buffered air MES / sodium chloride solution (0.1 / 0.4M) to obtain a protein processing solution of approximately 1 mg / ml. A solution of cobalt (II) [for example acetate salt] and iron (II) [for example ammonium sulfate salt] depleted in a 1: 2 ratio was added and allowed to oxidize with air. The final product yielded a solution of cobalt ferrite particles each surrounded by a ferritin shell.
    (Example 5)
    This example illustrates the 2-D arrangement of ferritin- wrapped magnetic particles. An aqueous solution of the particles (eg, standardized to a selected size of 2-4) was injected into the MES / glucose bottom solution (0.01 M / 2%) contained in the Teflon barrel. The particles were sprayed onto the contact surface of air and the lower part to denature to form a monolayer film. A 2-D array of encased particles occurs below this monolayer. After 10 minutes at room temperature the arrangement and monolayer were transferred to the support layer by placing the support layer directly on the monolayer for 5 minutes. After the support layer was recovered, it was surrounded by a thin carbon layer to protect the attached arrangement.
    权利要求:
    Claims (10)
    [1" claim-type="Currently amended] The magnetic layer is made up of a plurality of ferromagnetic particles each having a maximum size of 100 nm or less, each of which represents an isolated ferromagnetic domain, and in the process of producing a magnetic recording medium, ferromagnetic particles are put into organic molecules or partially A method for data storage of a magnetic recording medium comprising a magnetic layer characterized in that it is inserted.
    [2" claim-type="Currently amended] The method of claim 1, wherein the distance between adjacent ferromagnetic domains is at least 2 nm.
    [3" claim-type="Currently amended] The method according to claim 1 or 2, wherein the distance between adjacent ferromagnetic domains is 10 nm or less.
    [4" claim-type="Currently amended] The method according to claim 1, wherein the ferromagnetic particles are put into or partially inserted into the pores or openings of the protein macromolecule during the manufacture of the magnetic recording medium.
    [5" claim-type="Currently amended] 5. The method of claim 4 wherein the ferromagnetic particles are incorporated into the apoferritin protein in the manufacture of the magnetic recording medium.
    [6" claim-type="Currently amended] The magnetic layer is made up of a plurality of ferromagnetic particles each having a maximum size of 100 nm or less, each particle represents a separate ferromagnetic domain, and ferromagnetic particles are partially or partially inserted into organic molecules during the manufacture of the magnetic recording medium. And a magnetic recording medium comprising a magnetic layer.
    [7" claim-type="Currently amended] 7. The hard disk drive of claim 6, wherein the distance between adjacent ferromagnetic domains is at least 2 nm.
    [8" claim-type="Currently amended] 8. A hard disk drive according to claim 6 or 7, wherein a distance between adjacent ferromagnetic domains is 10 nm or less.
    [9" claim-type="Currently amended] 9. A hard disk drive according to claim 6, 7, or 8, wherein ferromagnetic particles are inserted or partially inserted into holes or openings of protein macromolecules during the manufacture of the magnetic recording medium.
    [10" claim-type="Currently amended] 10. The hard disk drive of claim 9, wherein ferromagnetic particles are introduced into the apoferritin protein during the manufacture of the magnetic recording medium.
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    同族专利:
    公开号 | 公开日
    GB9623851D0|1997-01-08|
    JP2001504277A|2001-03-27|
    GB2319253A|1998-05-20|
    EP0938728A1|1999-09-01|
    AT270457T|2004-07-15|
    EP0938728B1|2002-08-07|
    DE69714602D1|2002-09-12|
    CN1238059A|1999-12-08|
    DE69714602T2|2003-04-03|
    WO1998022942A1|1998-05-28|
    DE69729761D1|2004-08-05|
    CN1133979C|2004-01-07|
    AT222017T|2002-08-15|
    KR100477428B1|2005-03-23|
    DE69729761T2|2005-07-14|
    BR9713083A|2000-01-18|
    US6896957B1|2005-05-24|
    EP1217616A3|2002-09-11|
    HK1022207A1|2002-10-25|
    EP1217616A2|2002-06-26|
    EP1217616B1|2004-06-30|
    CN1532854A|2004-09-29|
    AU4960097A|1998-06-10|
    CA2271970A1|1998-05-28|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    1996-11-16|Priority to GB9623851A
    1996-11-16|Priority to GB9623851.4
    1997-11-17|Application filed by 나노마그네틱스 리미티드
    2000-08-25|Publication of KR20000053057A
    2005-03-23|Application granted
    2005-03-23|Publication of KR100477428B1
    优先权:
    申请号 | 申请日 | 专利标题
    GB9623851A|GB2319253A|1996-11-16|1996-11-16|Composition, for use in a device, comprising a magnetic layer of domain-separated magnetic particles|
    GB9623851.4|1996-11-16|
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