Magnetic nanoparticles are known to be very important in a wide variety of applications, such as ultrahigh density magnetic data storage, catalysts, drug delivery, cell separation, diagnostic, hypothermia for cancer treatment, inductive bonding, ferrofluids and magnetic sensors. If such magnetic nanoparticles are to be used with the greatest effectiveness, it is crucial that they be produced with uniform size and shape and in a process that can be easily scaled up for large quantity production.
Existing techniques for the production of magnetic nanoparticles are problematic in that they are very costly, impractical for mass production or involve the use of undesirable toxic materials. For example, monodispersed nanoparticles of transition metals and their alloys may be produced by a polyol process, but it requires the use of expensive noble metals as seeds in order to obtain the desired small size.
Micro-emulsion or reverse micromulsion methods have produced acceptable magnetic nanocrystals but they are unsuitable for large quantity production.
Thermal decomposition methods are also known to produce magnetic nanoparticles but the organic metallic compounds used in this process, such as iron pentacarbonyl [Fe(CO)s], dicobalt octacarbonyl [CO2(C)8], nickel tetracarbonyl [Ni(CO)4], are expensive, unstable and very toxic. Thus, such methods are not conducive for large quantity production.
This invention avoids these problems and produces large quantities of uniformly-sized magnetic nanoparticles by controlling the growth of the emerging nanoparticles as they are formed through the use of an external magnetic field.
In this invention, a novel process is provided for producing nanocrystals of uniform shape and size from magnetic transition metals, salts thereof, alloys of said metals and alloys of said metals with non-magnetic metals.
The process comprises essentially dissolving the selected magnetic transition metal, salt or alloy thereof in a non-aqueous solution and reducing the dissolved transition metal, salt or alloy in the presence of an external magnetic field.
In a preferred embodiment, borohydrides are employed as the reducing agent and the transition metal or alloy is dissolved in ethanol.
By performing the reduction reaction in a non-aqueous medium one is able to avoid the formation of transition metal borides which have much weaker ferromagnetism than pure transition metals and their alloys. By employing an external magnetic field in the reaction solution, one is able to control the nucleation, growth and size of the magnetic nanoparticles so as to achieve very uniform nanoparticles in large quantity. Any non-magnetic particles in the solution will not be attracted by the external magnetic field and may be separated out.
The magnetic nanoparticles produced according to the process of this invention are formed from magnetic transition metals such as iron, cobalt and nickel, salts thereof, their alloys and intermetallic compounds such as Co3Pt, CoPt, CoPt3, Fe3Pt, FePt and FePt3.
It is important to this invention that the metals or their alloys which form the intended magnetic nanoparticles are reduced in a non-aqueous solution, preferably a lower alcohol such as methanol, ethanol, propanol, isopropanol and butanol. Ethanol is especially preferred.
Any of the known reducing agents may be used in the process of this invention, although a strong borohydride such as NaBH4 or KBH4 is preferred.
It is crucial to the formation of magnetic nanoparticles of uniform size and shape that the reaction solution be subjected to an external gradient magnetic field so as to adjust the dwelling time of the newly-formed magnetic nanoparticles in the reaction site, thus controlling their growth.
The materials produced by this invention may be used in exchanged coupled soft and hard magnets, ultrahigh density data storage media, catalysts, biological and medical applications such as cell separation, targeted drug delivery and hyperthermia treatment of tumors and infectious diseases.
CoCl2 and NaBH4 ethanol solutions were first prepared by dissolving appropriate amount of CoCl2 and NaBH4 into ethanol with vigorous stirring. The molar ration of NaBH4 over CoCl2 was purposely made larger than 2 to ensure complete reduction of CoCl2. The CoCl2 ethanol solution was then put on top of a mineral oil layer which has a density larger than the above solution. NaBH4 ethanol solution was added into CoCl2 ethanol solution in a drop-like manner by using a dropping funnel or better using an ultrasonic atomizer that can give rise to small droplets of ˜40 μm. According to Jackelen et al. [A. M. L. Jackelen, M Jungbauer, G. N. Glavee, Langmuir 1999, Vol. 15, PP 2322-2326.], the following chemical reactions take place instantaneously when the NaBH4 ethanol solution is added:
CoCl2+2NaBH4→Co+H2+B2H6+2NaCl
B2H6+6CH3CH2OH→2B(OCH2CH3)3+6H2
The magnetic Co particles were attracted by a permanent magnet placed under the reaction beaker, which create a gradient magnetic field, (see
The resulting nanoparticles are shown in the drawing to have uniform size and shape.
In
M=M1×[coth(μ1H/kBT)−kBT/μ1H]
+M2×[coth(μ2H/kBT)−kBT/μ2H]
where Mi and μi (i=1, 2) are the saturation moment and the effective moments of a unit magnetic cell of each size component, respective and kB is the Boltzmann constant.
The TEMP graph shown in
The zero-field cooled (solid triangles and dotted line) and 5 T-field cooled (solid circles and line) M-H loops (
While there is shown and described certain specific structures embodying the invention, it will be manifest to those skilled in the art that various modifications and rearrangements of the parts may be made without departing from the spirit and scope of the underlying inventive concept and that the same is not limited to the particular forms herein shown and described.
This application claims the benefit of U.S. Provisional Application Ser. No. 60/60,347 filed Sep. 1, 2004, the content of which is incorporated herein by reference in its entirety.
The United States Government has rights in this invention as provided for by U.S. Defense Advanced Program Agency (DARPA) Grant No. F33615-01-2-2166.
Number | Date | Country | |
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60606347 | Sep 2004 | US |