Synthesis and annealing of manganese bismuth nanoparticles

Abstract

The claimed invention provides a wet chemical method to prepare manganese bismuth nanoparticles having a particle diameter of 5 to 200 nm. When annealed at 550 to 600K in a field of 0 to 3 T the nanoparticles exhibit a coercivity of approximately 1 T and are suitable for utility as a permanent magnet material. A permanent magnet containing the annealed MnBi nanoparticles is also provided.

Claims

1. A MnBi nanoparticle having: a particle size of 5 to 30 nm; a M.sub.r/M.sub.s ratio of from 25% to 45%; and a coercivity of approximately 1 T; wherein the nanoparticle is prepared by a process, comprising: treating Mn powder with a hydride reducing agent in an ether solvent with agitation; adding a solution of a bismuth salt of a long chain carboxylate to the Mn-hydride reducing agent mixture while continuing the agitation; upon completion of the bismuth salt solution addition, adding a an organic amine while continuing the agitation; continuing agitation to form aggregated MnBi nanoparticles; and annealing the MnBi nanoparticles at 550 to 600K in a field of 3 T for from 3 to 40 hours to increase the M.sub.r/M.sub.s ratio from a value less than 9% to a range from 25% to 45%.

2. The MnBi nanoparticle according to claim 1, wherein the annealment is at 600K in a 3 T field for from 3 hours to 11 hours.

3. A hard magnet comprising a plurality of MnBi nanoparticles according to claim 1.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 shows the XRD spectrum of MnBi nanoparticles prepared in Example 1.

(2) FIG. 2a shows the FE-SEM image (10,000) of the MnBi nanoparticles prepared in Example 1.

(3) FIG. 2b shows the FE-SEM image (200,000) of the MnBi nanoparticles prepared in Example 1.

(4) FIG. 3 shows the M(H) curves over the course of annealing the MnBi nanoparticles prepared in Example 1 at 600 K and under a 3 T applied field.

(5) FIG. 4 shows the effect of annealing time and applied field on the H.sub.c value of the MnBi nanoparticles prepared in Example 1.

(6) FIG. 5a shows the MnBi phase diagram.

(7) FIG. 5b shows the M(H) curve of the MnBi nanoparticles of Example 1 heated to form high temperature phase (listed as HTP in phase diagram).

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

(8) In an ongoing study of magnetic materials and particularly nanoparticle magnetic materials, the present inventor has identified manganese bismuth alloy in a nanoparticle form as a material having potential utility as a replacement of neodymium iron borate for manufacture of permanent magnets. MnBi nanoparticles are predicted to express coercivities as high as 4 T. When combined with a soft magnetic nanoparticle matrix, the resulting nanocomposite should yield a rare-earth-element-free alternative to the standard neodymium iron borate permanent magnet.

(9) Conventionally, MnBi nanoparticles have been prepared from a top-down ball milling of MnBi ingots. However, the top-down ball milling of MnBi ingots has shown the limitation of not yielding nanoparticles smaller than 20 nm, just short of the ideal 7 nm nanoparticle diameter. In order to produce nanoparticles having a consistently smaller size than those obtained in a milling process, the inventor has studied nanoparticle wet syntheses, and has discovered the method described in the present invention. Further, the inventor has discovered that annealing treatment of the wet synthesis obtained MnBi nanoparticles results in a material which is equal in performance to neodymium iron borate as a hard magnetic composition. MnBi nanoparticles are predicted to express coercivities as high as 4 T and therefore, when combined with a soft magnetic nanoparticle matrix, the resulting nanocomposite should yield a rare-earth-element-free alternative to the standard neodymium iron borate permanent magnet.

(10) In the first embodiment the present invention provides a method to prepare a manganese-bismuth alloy nanoparticle, comprising: treating Mn powder with a hydride reducing agent in an ether solvent with agitation; adding a solution of a bismuth salt of a long chain carboxylate to the Mn-hydride reducing agent mixture while continuing the agitation; upon completion of the bismuth salt solution addition, adding a an organic amine while continuing the agitation; and continuing agitation to form aggregated MnBi nanoparticles.

(11) The ether solvent for the hydride treatment may be any ether compatible with hydride reaction conditions. Suitable ether solvents include tetrahydrofuran (THF), 2-methyl-tetrahydrofuran, diethyl ether, diisopropyl ether, 1,4-dioxane, dimethoxy ethane, diethylene glycol diethylether, 2-(2-methoxyethoxy)ethanol and methyl tert-butyl ether. THF may be a preferred solvent.

(12) The hydride reducing agent may be any material capable of reacting with the manganese and include NaH, LiH, CaH.sub.2, LiAlH.sub.4 and LiBH.sub.4. LiBH.sub.4 may be a preferred hydride treatment agent.

(13) The hydride treatment comprises at least two stages wherein in an initial stage the mixture is stirred at 20-25 C. for 10 to 48 hours followed by a second stage of treatment at 50 to 70 C. for 10 to 48 hours. Variations of these stages may be optimized to appropriately modify the properties such as size and structure of the nanoparticles obtained as would be understood by one of ordinary skill in the art.

(14) Additionally, the amount of hydride treatment agent may be varied to modify conditions and the properties of the nanoparticles obtained and may vary in an equivalent ratio of hydride to Mn of from 1/1 to 100/1.

(15) The bismuth may be added in any ether soluble salt form and is preferably added as a salt of a long chain carboxylic acid. In a preferred embodiment, the Bi is added as bismuth neodecanoate. The mole ratio of Bi to Mn may vary from 0.8/1 to 1.2/1. Preferably the ratio of Bi/Mn is from 0.9/1 to 1.1/1 and most preferably, the ratio of Bi/Mn is 1/1. The addition time of the bismuth compound may be varied to optimize and modify the properties of the MnBi nanoparticles. Preferably the addition time is less than one hour and in a preferred embodiment the addition time is about 20 minutes.

(16) Upon completion of the addition of the bismuth compound, an organic amine, preferably a primary amine having a carbon chain of from 6 to 12 carbons is added to the alloy reaction mixture to precipitate and aggregate the MnBi nanoparticles. The resulting solids may be removed from the reaction mother liquor and washed free of soluble impurities with water.

(17) XRD analysis (FIG. 1) of the nanoparticles obtained by the wet chemical synthesis according to the present invention indicates the MnBi nanoparticles have a particle diameter of 30 nm or less. This particle size is verified by FE-SEM microscopy (FIGS. 2a and 2b) which also corroborates that the Mn powder is consumed in the synthesis process.

(18) The as-synthesized MnBi nanoparticles have relatively weak magnetic saturation (M.sub.s) and coercivity (H.sub.c). However, the inventor has discovered that annealing the nanoparticles at 600 K, in a 3 T field, produced improvement to both the magnetic saturation (M.sub.s) and coercivity (H.sub.c). M.sub.s is the point where application of an even stronger magnetic field will not make the material being magnetized any more magnetic. Thus, M.sub.s is the maximum point where a material can be magnetized no more. Magnetic remanence (M.sub.r) is the residual magnetization of a material remaining after a secondary/exterior magnetic field is applied and then removed. The smaller the M.sub.r/M.sub.s is for a magnetic material, the greater the oscillation in electric motor performance engineers must struggle with. Ideally in such applications, the M.sub.r/M.sub.s for hard magnetic materials like MnBi would be as large as possible. Thus the inventor has determined that M.sub.r/M.sub.s may be improved with this annealing protocol. H.sub.c values of approximately 1 T were measured, with an M.sub.r/M.sub.s ratio of 45% (FIG. 3).

(19) Thus, in another embodiment, the present invention provides a MnBi nanoparticle having a particle size of 5 to 200 nm and a coercivity of approximately 1 T, wherein the nanoparticle is prepared according to the method described above and further annealed.

(20) The annealing treatment may be conducted at a temperature of from 550 to 600K in a field having a coercivity of from 0 to 5 T. The annealing time will vary depending upon temperature and as indicated in the Examples requires approximately 11 hours at 600K and increases to approximately 40 hours at 550K (FIG. 4). Preferably, the annealing is conducted at 600K in a field of 3 T.

(21) As shown in FIG. 4 annealing at 650K does not increase coercivity or magnetic saturation.

(22) Ferromagnetic MnBi is known to exist in what is referred to as the low temperature phase region of the MnBi phase diagram (FIG. 5a). Above it exists what is referred to as the high temperature phase. The high temperature phase is known to exhibit antiferromagnetic behavior.

(23) The inventor has determined that when the wet synthesis MnBi nanoparticles are heated to temperatures of 800K the change from the ferromagnetic low temperature phase to antiferromagnetic high temperature phase takes place (FIG. 5b).

(24) In an application embodiment, the present invention provides a hard magnet comprising a plurality of MnBi nanoparticles having a particle size of 5 to 200 nm and a coercivity of approximately 1 T. Preferably, the MnBi nanoparticles are obtained by a wet synthesis method according to the invention and the annealed at 600K in a 3 T field for at least 10 hours.

(25) The above description provides a general overview and some preferred embodiments of the present invention. One of ordinary skill in the art will recognize that various permutations and modifications of the present invention are possible and these variations are considered within the scope of the present invention.

(26) Having generally described the invention a further understanding of the invention may be obtained by consideration of the following Examples which are not intended to be limiting unless so specified.

EXAMPLES

Example 1. MnBi Nanoparticle Synthesis

(27) 200 mL of THF, 0.371 g Mn powder and 11.5 mL of 2 M LiBH.sub.4/THF solution are combined. The reaction was first stirred at 23 C. for 24 hrs and then at 60 C. for an additional 24 hrs. To the resulting mixture was added a solution of 4.413 g bismuth neodecanoate dissolved in 200 mL THF. The bismuth neodecanoate solution was added slowly over 20 mins to the stirring Mn/LiBH.sub.4 solution. After the bismuth neodecanoate addition was complete, 0.513 g octylamine were added to the product solution. The nanoparticles aggregated over the following 5 mins and were washed with water to remove reaction side products.

(28) Characterization of the MnBi Nanoparticles

(29) XRD Analysis

(30) The XRD spectrum of the MnBi nanoparticles indicated the presence of three different crystalline materials present in the sample: MnBi alloy, Mn metal, and Bi metal (see FIG. 1). The MnBi nanoparticles were calculated to be approximately 30 nm in diameter based on peak width in this XRD spectrum.

(31) FE-SEM Characterization

(32) High resolution FE-SEM microscopy was conducted on the nanoparticle powder product to further investigate the size of the wet synthesis product (FIGS. 2a and 2b). It was found that the sample was in fact composed of approximately 30 nm diameter features (on average) as indicated by analysis of the XRD spectrum. The FE-SEM data also indicated that large micron-scale pieces of manganese were not present in the sample, also corroborated by the absence for very sharp peaks in the XRD spectrum. If the manganese powder was not being consumed in the synthesis, micron-scale pieces of manganese would be expected to be present in the XRD and FE-SEM data.

Example 2. Annealing Effects on MnBi Nanoparticles

(33) The as-synthesized. MnBi nanoparticles were demonstrated on a very weak coercivity (<100 Oe). Samples of the nanoparticles were annealed in situ with aVSM oven attachment. It was initially found that annealing the nanoparticles at 600 K, in a 3 T field, produced improvement to both the magnetic saturation (M.sub.s) and coercivity (H.sub.c). Additionally, M.sub.r/M.sub.s improved with this annealing protocol. H.sub.c values up to 1 T were measured, with an M.sub.r/M.sub.s ratio of 45% (FIG. 3). M.sub.r/M.sub.s is calculated by the division of M.sub.r by M.sub.s after the empirical measurement of the respective Values from synthesized material (e.g. MnBi). In FIG. 3 M.sub.r is the y-intercept and M.sub.s is the y-value associated with maximum x and y values in the 1.sup.st quadrant of the graph.

(34) Investigation at lower annealing temperature (550 K) showed that a similar 1 T H.sub.c could be reached, but that it required over 40 hrs of annealing, as opposed to 11 hrs at 600 K (FIG. 4). Annealing the same batch of MnBi nanoparticles at 650 K gave very poor results, with a maximum H.sub.c of only approximately 500 Oe.

(35) Ferromagnetic MnBi only exists in what is referred to as the low temperature phase region of the MnBi phase diagram (FIG. 5a). Above it exists what is referred to as the high temperature phase. The high temperature phase is known to exhibit antiferromagnetic behavior. A sample of MnBi nanoparticles was heated to 800 K to induce this change from the ferromagnetic low temperature phase to antiferromagnetic high temperature phase. The M(H) curve (FIG. 5b) is consistent with high temperature phase formation and further supports that alloyed MnBi nanoparticles are being made by the synthesis of Example 1.