Patent Grant
8697479
1. Field of the Invention
The embodiments described herein are related to inorganic particles such as nanoparticles.
2. Description of the Related Art
Nanoparticles are increasingly finding uses in many applications. Various methods, including thermal plasma synthesis, are available to prepare nanoparticles. One method involves thermal plasma treatment of precursors in a liquid form, such as substantially neat liquids and solutions, introduced into the plasma as droplets. Currently, many believe that when precursor materials are introduced into a plasma as a liquid solution, all materials, both the solutes and liquid components, are completely vaporized in the plasma. After the precursors are vaporized in the plasma, they cool as they begin to pass out of the hotter areas of the plasma. It is believed that when the vapors begin to cool, they become supersaturated and particles start to nucleate, then sometimes agglomerate and/or coagulate. Thus, many currently believe that the size of the particles is a function of the cooling process of the vaporized material, and is not dependent upon any processes that occur before the precursors are vaporized in the plasma. Thus, for example, additives intended to affect the size of droplets introduced into a flame-assisted pyrolysis, such as those described in Purwanto et. al. (J. of Alloys and Compounds 463 (2008) 350-357), would not be expected to affect particle size if used in a plasma process.
Current efforts to control nanoparticle size are directed to quenching processes carried out on the nucleating vapors passing out of the hotter areas of the plasma. According to current models, rapid quenching, on the order of about 50 microseconds, is believed to be required to obtain particles with a diameter of less than 100 nm (see, for example, Leparoux, et. al., Advanced Engineering Materials 2005, 7, No. 5 349-353, esp. FIG. 2). Thus, improved quenching methods are currently being sought to reduce particle size. This application describes a non-quenching based methodology for obtaining nano-sized particles independent of the material system and/or reactor configuration.
Some embodiments provided herein related to a method of preparing a nanoparticle composition comprising: providing an aerosol comprising a plurality of droplets of a precursor solution and a carrier gas; wherein the precursor solution comprises at least one nanoparticle precursor, an expansive component, and a solvent; passing the aerosol through a plasma; and collecting a nanoparticle composition product from the carrier gas which has exited the plasma.
Some embodiments relate to a nanoparticle composition prepared by a method disclosed herein.
Some embodiments relate to a light-emitting device comprising the nanoparticle composition prepared by the method disclosed herein.
These and other embodiments are described in greater detail below.
In the embodiments described herein, a precursor solution comprising at least one nanoparticle precursor, an expansive component, and a solvent is provided. A nanoparticle precursor may include any compound or other chemical species, or combination thereof that may be heated to provide a solid nanoparticle either by itself or in combination with other compounds or chemical species. In some embodiments, the nanoparticle precursor should be soluble in the solvent and stable in the presence of the solvent and any other nanoparticle precursors before the precursor solution is introduced to the plasma.
In some embodiments, a nanoparticle precursor comprises a salt or compound of an element such as, but not limited to: gadolinium, polonium, silver, germanium, aluminum, platinum, arsenic, mercury, rubidium, rhenium, gold, barium, indium, rhodium, beryllium, iridium, potassium, ruthenium, bismuth, antimony, lithium, scandium, selenium, calcium, cadmium, cerium, magnesium, manganese, tin, molybdenum, strontium, cobalt, terbium, chromium, sodium, cesium, niobium, tellurium, copper, neodymium, thorium, titanium, nickel, thallium, vanadium, osmium, tungsten, iron, yttrium, lead, ytterbium, palladium, zinc, gallium, zirconium, lutetium, terbium, lanthanum, praseodymium, holmium, lanthanum, silicon, samarium promethium, dysprosium, etc. For example, salts formed from cations of these elements and anions may be used. Exemplary anions may include, but are not limited to, nitrate, metavanadate, germanate, chromate, manganate, molybdate, sulfate, bisulfate, phosphate, hydrogen phosphate, dihydrogen phosphate, carbonate, bicarbonate, fluoride, chloride, bromide, iodide, manganate, tungstate, an oxy-halide, nitride, an oxynitride, silicate, aluminate, silicide, telluride, borate, gallate, zincate, zirconate, sulfide, phosphide, hydroxide, etc. The conjugate acids of many of these anions, e.g. nitric acid, chromic acid, boric acid, etc., may also be used as nanoparticle precursors. In some embodiments, the cation may be the ammonium ion, while the anion may contain an element which becomes part of the nanoparticle, like chromate, metavanadate, tungstate, titanate, etc. Some precursors comprise soluble organic salts comprising a combination of any element above with one or more anions such as acetates, propionates, acetylacetonates, carbozylates; metallorganic anions which do not decompose in contact with an appropriate solvent; peroxides, such as hydrogen peroxide, methyl ethyl ketone peroxide, benzoyl peroxide, acetone peroxide, tert-butyl hydroperoxide, etc.; peroxy acids such as perbenzoic acid, peracetic acid, performic acid; etc. Appropriate double salts or complex salts of the above elements can also be used as precursors.
In some embodiments, the nanoparticle precursor further comprises an additive, such as a metal nitrate, a non-metal nitrate or an oxidizer. The metal nitrate may include a nitrate of any metallic element listed above. In some embodiments, the metal nitrate may be selected from the group consisting of a nitrate of yttrium, a nitrate of aluminum, and a nitrate of cerium. In some embodiments, non-metal nitrates, such as ammonium nitrate, ammonium salts such as ammonium perchlorate, ammonium chlorate, ammonium peroxide, and peroxides such as hydrogen peroxide and organic peroxides may be additives to the solution. In some embodiments, other oxidizers, such as M-perchlorates, M-chlorate, M-nitrites or M-peroxides where ‘M’ is a desired elemental component of the final nanoparticle may be used.
When the aerosols begin to interact with the plasma, the aerosol droplets may begin to change. The term “droplet relic” as used herein refers to any state of the original droplet from the moment of first interaction with the plasma. The expansive component may include any compound or chemical species that may expand, vaporize, or evolve gas upon heating under conditions in which the droplets of the precursor solution or droplet relics are in a condensed phase. In some embodiments, the expansive component may be non-reactive. For example, the expansive component may be a liquid with a lower boiling point than the solvent or a solid with a lower sublimation temperature than the boiling point of the solvent. Alternatively, the expansive component may be a liquid with a higher boiling point than the solvent or a solid with a higher sublimation temperature than the boiling point of the solvent. In some embodiments, non-reactive solid expansive component may also be used. A non-limiting example of a non-reactive solid expansive component is naphthalene. Additionally or alternatively, the expansive component may vaporize more rapidly than droplets of the precursor solution. In some embodiments, the expansive component may be a dissolved or dispersed gas which expands upon heating under conditions in which the droplets of the precursor solution or droplet relics are in a condensed phase. Non-limiting examples of expansive gases include CO2, Ar, N2, and the like.
In some embodiments, the expansive component may be reactive, such as those that may react by decomposition and/or by reaction with at least one of the nanoparticle precursors or the solvent. For example, some expansive components may include solids or liquids which decompose to produce a gas upon heating, including, but are not limited to, urea, carbohydrazide, glycine, peroxides such as hydrogen peroxide, peroxy acids, thiourea, oxyalyl dihydrazide, tretraformal trisazine, diformyl hydrazine, hydrazine, and the like. In some embodiments, the expansive component comprises at least one of urea, carbohydrazide, and glycine.
In some embodiments, an expansive component may also act as a nanoparticle precursor by reacting with at least one other nanoparticle precursor. The reactivity of an expansive component may depend upon conditions such as the nature of the other nanoparticle precursor, the nature of the solvent, the boiling point of the solvent, the nature of the carrier gas, and various plasma characteristics like degree of ionization within the plasma, plasma power, plasma process gases, reactor pressure, atomization profile, temperature, the rate of temperature change, the maximum temperature, etc. Thus, depending upon the particular conditions, a reactive gas may include, but is not limited to, O2, NH3, air, H2, alkanes (such as methane, ethane, propane isomers, butane isomers, etc.), alkenes (such as ethene, propene isomers, etc.), alkynes (such as acetylene, propyne isomers, etc.), etc. In some embodiments, the expansive component may be a reactive solid.
In some embodiments, the expansive component should expand, vaporize, or evolve a gas under conditions in which the droplets of the precursor solution or droplet relics are in a condensed phase. In some embodiments, the expansive component is a compound or other chemical entity which expands, vaporizes, or evolves a gas when external heat is applied (e.g. the expansive component is in an area which is near to or is a part of the plasma) at a temperature that is at least about 50° C., about 90° C., about 140° C., about 160° C., or 200° C., up to about 240° C., about 260° C., or about 410° C., or about 50° C. to about 410° C., about 90° C. to about 410° C., or about 140° C. to about 240° C.
In some embodiments, the nanoparticle precursors and the expansive component are dissolved in a solvent to provide the precursor solution. The solvent may be any solvent, including, but not limited to water, methanol, ethanol, acetone, isopropanol, dichloromethane, benzene, toluene, ethyl acetate, pentane, hexanes, ethyl ether, dimethylformamide, dimethyl sulfoxide, etc. In some embodiments the solvent is water. In some embodiments, the solvent system may be tuned to adjust the solubility. For example, ethanol or acetone may be added to water to help dissolve a more hydrophobic solute. In some embodiments, one or more components may have more than one function. For example, a solvent may also act as a precursor or an expansive component, or an expansive component may also act as a precursor, etc.
The precursor solution described above may be suspended in a carrier gas to provide an aerosol. The aerosol may include any suspension of a plurality of droplets of the precursor solution in a gas. The size of the individual droplets may vary. In some embodiments, about 95% of the plurality of droplets by number have a diameter in the range of about 20 nm to 200 μm, about 100 nm to about 120 μm, or about 2 μm to about 120 μm. The carrier gas may be any gas suitable for suspending the precursor solution. In some embodiments the carrier gas can be an inert or otherwise non-reactive gas such as helium, neon, argon, krypton, xenon, nitrogen or a combination thereof, wherein the carrier gas is non-reactive with the nanoparticle precursors, solvents, or expansive components. In some embodiments, the carrier gas may comprise a reactive gas such as O2, NH3, air, H2, alkanes, alkenes, alkynes, etc., which may participate in the reaction to form nanoparticles. In some embodiments, the carrier gas can be a mixture comprising at least one reactive gas and at least one inert gas. In some embodiments, the carrier gas is nitrogen, argon, or hydrogen. In some embodiments, the carrier gas comprises argon.
The aerosol may be provided by suspending the precursor solution in the carrier gas by any means known in the art such as using an atomizer or a nebulizer, or via a simple nozzle. Any kind of atomizer or nebulizer can be used for instance, two-fluid, Collison, ultrasonic, eletrospray, spinning disc, filter expansion aerosol generator, etc. In some embodiments, the aerosol may be formed via two-fluid atomization and discharged directly into the plasma. In some embodiments, the aerosol may be formed using a remote nebulizer and then delivered to the plasma.
The aerosol thus provided is passed through a plasma, such as the plasma 25 of
The temperature of the plasma may vary. For example, the temperature in the reaction field may range from at least about 500° C., about 800° C. or about 1000° C., to about 10,000° C. or about 20,000° C. In some embodiments, at least a portion of the reaction field has a temperature of at least about 1000° C.
In some embodiments, as the droplet relics heat up when the aerosol is introduced into the plasma, the expansive component may evolve gas. In some embodiments, the evolved gas may fragment at least a portion of the plurality of droplet relics thereby reducing the size of the droplet relics. In some embodiments, reducing the size of the droplet relics may provide nanoparticles of reduced size via one-droplet-to-one-particle (ODOP) conversion.
Once the aerosol has passed through the plasma (e.g. 25), nanoparticles (e.g. 30) may be collected from the carrier gas which has exited the plasma, as illustrated, for example, in
Once the nanoparticles are collected from the plasma, in some embodiments they may be further subjected to an annealing step. Details of some examples the annealing step can be found in WO2008/112710, WO/2009/105581, and co-pending patent application Ser. Nos. 12/388,936, filed Feb. 19, 2009, and 12/389,177, filed Feb. 19, 2009, all of which are incorporated by reference herein in their entirety. Other methods are also known in the art, and may be used with the methods described herein. In some embodiments, annealing may occur at any temperature of about 500° C. or higher, such as from about 1000° C. to about 1400° C., about 1100° C. to about 1300° C., or from about 1150° C. to about 1250° C. For example, in some embodiments, nanoparticles comprising an undoped or doped (such as cerium doped) mixture of yttrium aluminum garnet (YAG), yittrium aluminium monocyclic (YAM), yttrium aluminium perovskite (YAP) and/or amorphous yttrium aluminum oxide may be heated at a temperature above about 1000° C. but below about 1450° C. to provide a phase pure material.
The annealing may occur in an oxidizing, inert, or reducing atmosphere. In some embodiments, an oxidizing atmosphere may comprise oxidizing gases such as oxygen, chlorine, etc. In some embodiments, an inert atmosphere may be a vacuum or an inert gas such as nitrogen, helium, neon, argon, krypton, xenon, etc., or a mixture thereof In some embodiments, a reducing atmosphere may be an atmosphere that has a greater tendency to reduce a composition as compared to air. Examples of reducing atmospheres may include atmospheres comprising reducing gases such as hydrogen gas, ammonia, hydrazine, carbon monoxide, incomplete carbon combustion products, etc., or mixtures thereof. Any reducing gas may also be diluted in an inert gas. For example a reducing atmosphere may comprise a mixture of nitrogen and hydrogen, or a mixture of argon and hydrogen. In some embodiments, the reducing atmosphere may comprise hydrogen gas (H2) at a concentration of about 1% to about 10%, about 1% to about 5%, about 2% to about 4%, or about 3% by volume in nitrogen or argon. The atmosphere may consist essentially of hydrogen in these concentration ranges diluted in argon or nitrogen. In some embodiments, annealing may occur under a reducing atmosphere comprising about 3% (v/v) H2 and about 97% (v/v) N2 at about 1200° C. for about 2 hrs. In some embodiments, the reducing atmosphere comprises a mixture of at least one inert gas and hydrogen gas.
This method may be used to produce any kind of nanoparticle. Examples may include, but are not limited to, nanoparticles of substantially pure elements, single metal/non-metal or mixed materials, such as single and mixed oxides, nitrides, carbides, sulfides, borides, borates, silicates, tellurides, oxy-nitrides, oxy-carbides, oxy-halides, oxy-sufildes, phosphates, aluminates, borates, cuprates, cobaltates, germanates, vanadates, molybdates, titanates, zirconates, gallates, germanates, chromates, chromites, ferrites, manganates, perovskites, garnets, K2NiF4 like materials and spinels.
In some embodiments, the present method may provide advantages over other methods of producing nanoparticles, such as flame pyrolysis, spray pyrolysis or other flame-based processes. In some embodiments, the present method provides nanoparticles with a lower level of contaminants than would be present if a flame were employed to produce nanoparticles. For example, a nanoparticle composition prepared using a hydrocarbon-oxygen flame may suffer from contamination with residual carbon. In some embodiments, a plasma may provide more enthalpy and higher temperatures (e.g. 10,000° C. for a plasma compared to 2000° C. for a flame) to the reaction zone compared to some flame-based process and may be able to avoid reactive gases such as oxygen if desired. Thus, in some embodiments, the present method provides nanoparticles such as non-oxide nanomaterials like carbides, nitrides or elemental metals, of a composition which may not be prepared using an oxygen-based flame.
Some embodiments provide a nanoparticle composition prepared by a method disclosed herein. In some embodiments, the nanoparticle composition comprises a yttrium aluminum garnet which may be undoped, or doped with a dopant such as cerium. In some embodiments, these nanoparticle compositions may be used in a light-emitting device. For example, some embodiments provide a light emitting device comprising a light-emitting diode, and a phosphor comprising a nanoparticle composition described herein, wherein the phosphor is positioned to receive and convert at least a portion of the light emitted from the light-emitting diode to light of a longer wavelength.
The precursor compositions (Compositions 1, 2, 3 and 4), as well as the control composition (Control) were prepared by dissolving components listed in Table 1 below in water. The total concentration of the metal ions was 2 molal and the urea concentration was 0 molal for the Control, 2 molal for Composition 1, 5 molal for Composition 2, 10 molal for Composition 3, and 15 molal for Composition 4 The amounts of each component of the composition are listed in the Table 1 below.
The precursor compositions were processed in an RF plasma as follows. The precursor was delivered in the form of small droplets (about 2 μm-about 120 μm diameter) using Argon carrier gas (10 slm) through a two-fluid atomizer directly into a radio frequency inductively coupled plasma torch (PL-35 from Tekna Plasma Systems). The precursor flowrate could be varied between about 5 and about 100 ml/min. For all the experiments described here, a flowrate of 10 ml/min was used. After passing through the hot zone of the plasma (operated at 20 kW plate power, Argon central gas of 20 and sheath gas of 60 slm, Hydrogen sheath gas of 3 slm), the resulting Ce-doped Y—Al—O particles were collected from the effluent gas on a porous alumina filter or a glass fiber filter.
It will be appreciated by those skilled in the art that various omissions, additions and modifications may be made to the processes described above without departing from the scope of the invention, and all such modifications and changes are intended to fall within the scope of the invention.
This application is the U.S. National Phase under 35 U.S.C. §371 of International Application No. PCT/US2010/057085, filed Nov. 17, 2010, which claims the benefit of priority to U.S. Application No. 61/262,703, filed Nov. 19, 2009. The contents of these applications are hereby incorporated by reference in their entirety.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US2010/057085 | 11/17/2010 | WO | 00 | 5/17/2012 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2011/063028 | 5/26/2011 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 4575609 | Fassel et al. | Mar 1986 | A |
| 5032568 | Lau et al. | Jul 1991 | A |
| 5077267 | Engler et al. | Dec 1991 | A |
| 5609921 | Gitzhofer et al. | Mar 1997 | A |
| 5989648 | Phillips | Nov 1999 | A |
| 6652967 | Yadav et al. | Nov 2003 | B2 |
| 8137588 | Hafiz et al. | Mar 2012 | B2 |
| 20030094596 | Kijima et al. | May 2003 | A1 |
| 20030116080 | Huang | Jun 2003 | A1 |
| 20050271566 | Yadav | Dec 2005 | A1 |
| 20060051505 | Kortshagen | Mar 2006 | A1 |
| 20060147369 | Bi et al. | Jul 2006 | A1 |
| 20060231795 | Hampden-Smith et al. | Oct 2006 | A1 |
| 20070029291 | Boulos et al. | Feb 2007 | A1 |
| 20070096057 | Hampden-Smith et al. | May 2007 | A1 |
| 20070272664 | Schroder et al. | Nov 2007 | A1 |
| 20090293675 | Mukherjee et al. | Dec 2009 | A1 |
| 20100207065 | Miyagawa et al. | Aug 2010 | A1 |
| 20100207512 | Miyagawa et al. | Aug 2010 | A1 |
| Number | Date | Country |
|---|---|---|
| 1 473 348 | Nov 2004 | EP |
| 2002-523610 | Jul 2002 | JP |
| WO2008112710 | Sep 2008 | WO |
| WO2009105581 | Aug 2009 | WO |
| WO 2011063028 | May 2011 | WO |
| Entry |
|---|
| Fauchais, P, Parameters Controlling Liquid Plasma Spraying: Solutions, Sols, or Suspensions. Journal of Thermal Spray Technology vol. 17(1):31-59, Mar. 2008. |
| Goortani, B, Controlling nanostructure in thermal plasma processing: Moving from highly aggregated porous structure to spherical silica nanoparticles. Science Direct Powder Technology 175:22-32 (2007). |
| International Search Report for PCT/US2010/057085, mailed Feb. 22, 2011. |
| Kagawa, et al., “Preparation of Ultrafine MgO by the Spray-ICP Technique,” Journal of the American Ceramic Society, 64(1): C7-C8 (1981). |
| Kagawa, M. Gas-Phase Synthesis of Ultrafine Particles and Thin Films of Y-AI-O by the Spray-ICP Technique. J. Aerosol Sci., vol. 24, No. 3, pp. 349-355, (1993). |
| Lenggoro, et al,. Preparation of ZnS Nanoparticles by Electrospray Pyrolysis. Journal of Aerosol Science, 31(1): 121-136 (2000). |
| Leparoux M, Induction Plasma Synthesis of Carbide Nanopowders. Advanced Engineering Materials 2005, 7, No. 5:349-353 (2005). |
| McKittrick, J. et al, The influence of processing parameters on luminescent oxides produced by combustion synthesis. Display 19:169-172 (1999). |
| Purwanto, et al, High luminance YAG:Ce nanoparticles fabricated from urea added aqueous precursor by flame process. J Alloys & Compounds, 463:350-357 (2008). |
| Shan Y, et al., Numerical Simulation of Droplet Breakup and Collision in the Solution Precursor Plasma Spraying. Journal of Thermal Spray Technology vol. 16 (5-6):698-704 Dec. 2007. |
| Terashi, Y, et al Role of urea addition in the preparation of tetragonal BaTiO3 nanopartilces using flame-assisted spray pyrolysis. J European Ceramic Soc 28:2573-2580 (2008). |
| Young, R.M, Generation and Behavior of Fine Particles in Thermal Plasmas—A Review. Plasma Chemistry and Plasma Processing, vol. 5, No. 1:1-37 (1985). |
| Zhu H, et al., RF Plasma Synthesis of YBa2Cu3O7-x, Powders. Journal of Superconductivity, vol. 3, No. 2:171-175 (1990). |
| Asakura et al., “Effects of Citric Acid Additive on Photoluminescence Properties of YAG:Ce3+ Nanoparticles Synthesized by Glycothermal Reaction,” Journal of Luminescence, 2007, vol. 127, pp. 416-422. |
| Li et al., “RF Plasma Processing of Er-doped TiO2 Luminescent Nanoparticles,” Thin Solid Films, 2006, vol. 506-507, pp. 292-296. |
| Mangolini et al., “Plasma Synthesis and Liquid-Phase Surface Passivation of Brightly Luminescent Si Nanocrystals,” Journal of Luminescence, 2006, vol. 121, pp. 327-334. |
| Nitto Denko, “Nitto Denko Develops Nano-Scale YAG Phosphor for White LEDs”, Nov. 7, 2005, http://ledsmagazine.com/news/2/11/10. |
| Number | Date | Country | |
|---|---|---|---|
| 20120235203 A1 | Sep 2012 | US |
| Number | Date | Country | |
|---|---|---|---|
| 61262703 | Nov 2009 | US |
