The present invention relates generally to methods for making nanoparticles and, more particularly, to a method for making nanoparticles via reactive precipitation.
Nanoparticles, one of many advanced materials in the field of nanotechnology, have tremendous potential applications in many industries.
In the past decade, significant international research efforts have been directed towards the synthesis of nanoparticles. Many methods for preparing nanoparticles have been developed and reported. The methods can be classified as physical vapor deposition, chemical vapor deposition, sol-gel processing, wet chemical techniques, microemulsion processing, sonochemical processing, supercritical chemical processing, and so forth. However, no current technique can provide a reliable, simple, and low-cost method for production of nanoparticles of a specific size. Some current methods may produce particles of a desirable size, but with high cost. Other techniques suffer from an inability to control the distribution of sizes around a desired nanoparticle size. Still other techniques require specialized equipment, long processing times, or expensive special chemicals.
One potentially attractive wet chemical technique for synthesis of nanoparticles is reactive precipitation. Typical reactive precipitation processes are often carried out by mixing reactants in a stirred tank. A reactive precipitation process consists of three main steps: mixing reactants, chemical reaction, and crystal growth. However, typical reactive precipitation process can only provide macro-scaled mixing, which may limit the size and the homogeneity of the precipitate.
What is needed, therefore, is a simple, and low cost reactive precipitation process for making nanoparticles, which can provide nanoparticles with well-controlled particle-size and particle-size distribution.
In one embodiment thereof, a method for making nanoparticles is provided. Firstly, a reaction chamber and at least two reactants are provided. One of the reactants is a liquid reactant, and at least one high-pressure injector is disposed in the reaction chamber. Secondly, the liquid reactant is atomized by the injector, and simultaneously mixes with the other reactants in the reaction chamber. Thereby, nanoparticles can be precipitated from the mixture of the reactants. Finally, the nanoparticles are isolated from the mixture.
Other advantages and novel features will become more apparent from the following detailed description of preferred embodiments when taken in conjunction with the accompanying drawings.
Many aspects of the method for making nanoparticles can be better understood with reference to the following drawings. The components in the drawings are not necessarily drawn to scale, the emphasis instead being placed upon clearly illustrating the principles of the method for making nanoparticles. Moreover, in the drawings, like reference numerals designate corresponding parts throughout the several views.
Referring to
The first embodiment of the method for making nanoparticles is carried out by spray atomizing two liquid reactants to mix them together. The liquid reactants may be an aqueous sodium carbonate (Na2CO3) solution and an aqueous strontium nitrate (Sr(NO3)2) solution.
Firstly, the sodium carbonate (Na2CO3) solution and the strontium nitrate (Sr(NO3)2) solution are prepared in appropriate molarities and are then each introduced into their respective solution containers 10.
Secondly, the sodium carbonate (Na2CO3) solution and the strontium nitrate (Sr(NO3)2) solution are each atomized by their respective injectors 30, and simultaneously sprayed into the reaction chamber 50 at a rate of 2.0 liters per hour to mix together. The injectors 30 may be high-pressure swirl injectors, and the atomization pressure of the solutions may be in the range of 2˜20 Mpa (megapascals). Therefore, micro-droplets of the sodium carbonate (Na2CO3) solution and the strontium nitrate (Sr(NO3)2) solution are obtained with a diameter in the range of 20˜60 μm (micrometers), which allows the sodium carbonate (Na2CO3) solution and the strontium nitrate (Sr(NO3)2) solution to mix on a molecular scale.
After spray mixing the sodium carbonate (Na2CO3) solution and the strontium nitrate (Sr(NO3)2) solution in the reaction chamber 50, nucleation, which forms nuclei of strontium carbonate (SrCO3) particles, occurs in the chamber 50 according to the following reaction:
Sr(NO3)2(l)+Na2CO3(l)→SrCO3(s)+2NaNO3(l)
Thirdly, the mixture of the sodium carbonate (Na2CO3) solution and the strontium nitrate (Sr(NO3)2) solution is transported into the tank 80 via the pipe 190, and agitated by the stirrer 90. The growth of the nuclei of strontium carbonate (SrCO3) particles may be well controlled with the agitation of the stirrer 90. Thereby a final mixture consisting of sodium nitrate (NaNO3), strontium carbonate (SrCO3) particles, and a small amount of sodium carbonate (Na2CO3) and strontium nitrate (Sr(NO3)2) is obtained. The mixture of the sodium carbonate (Na2CO3) solution and the strontium nitrate (Sr(NO3)2) solution may be returned to the reaction chamber 50 via the valve 60, the pump 70 and the extra injector 40, and be reacted again to precipitate more strontium carbonate (SrCO3).
Finally, the strontium carbonate (SrCO3) particles are separated from the final mixture, and the strontium carbonate (SrCO3) particles are dried to obtain an end-product nano-structured powder.
Referring to
The second embodiment of the method for making nanoparticles is carried out by spray atomizing a liquid reactant and mixing the liquid reactant with a gas reactant. The liquid reactant may be an aqueous sodium aluminate (NaAlO2) solution, and the gas reactant may be carbon dioxide (CO2).
Firstly, the aqueous sodium aluminate (NaAlO2) solution is prepared in an appropriate molarity and introduced into the corresponding solution container 11.
Secondly, the sodium aluminate (NaAlO2) solution is atomized by the injector 12 and sprayed into the reaction chamber 14 at a rate of 2.0 liters per hour. Simultaneously, a carbon dioxide (CO2) gas provided by the gas supply apparatuses 132 is also injected into the reaction chamber 14 via the gas nozzles 13, and meets the atomized sodium aluminate (NaAlO2) solution. The injector 12 may be a high-pressure swirl injector and the atomization pressure of the solution may be in the range of 2˜20 Mpa (megapascals). Therefore, micro-droplets of the sodium aluminate (NaAlO2) solution are obtained with a diameter in the range of 20-60 μm (micrometers), which allows the sodium aluminate (NaAlO2) solution to mix with the carbon dioxide (CO2) on a molecular scale.
After spray mixing the sodium aluminate (NaAlO2) solution and the carbon dioxide (CO2) in the chamber 14, nucleation, which forms nuclei of aluminum hydroxide (Al(OH)3) particles, occurs in the reaction chamber 14 according to the following reaction:
2NaAlO2(l)+3H2O(l)+CO2(g)→Na2CO3(l)+2Al(OH)3(s)
Thirdly, the mixture of the sodium aluminate (NaAlO2) solution and the carbon dioxide (CO2) is transported into the tank 18 via the pipe 19, and agitated by the stirrer 17. The growth of nuclei of the aluminum hydroxide (Al(OH)3) may be well controlled with agitation of the stirrer 17. Thereby a final mixture consisting of sodium carbonate (Na2CO3), aluminum hydroxide (Al(OH)3) particles, and a small amount of aluminate (NaAlO2) that has incompletely reacted with the carbon dioxide (CO2) is obtained. The mixture of the sodium aluminate (NaAlO2) solution and the carbon dioxide (CO2) may be returned into the reaction chamber 14 via the valve 15, the pump 16, the solution container 11 and the injector 12, for reaction with carbon dioxide (CO2) again to precipitate more aluminum hydroxide (Al(OH)3).
Finally, the aluminum hydroxide (Al(OH)3) particles are separated from the final mixture, and the aluminum hydroxide (Al(OH)3) particles are dried to obtain an end-product nano-structured powder.
Referring to
The third embodiment of the method for making nanoparticles is carried out by spray atomizing a liquid reactant and mixing the liquid reactant with a gas reactant and a solid reactant. The liquid reactant, the gas reactant, and the solid reactant may be a distilled water, a carbon dioxide (CO2) gas, and a calcium hydroxide (Ca(OH)2) powder respectively.
Firstly, the distilled water, the carbon dioxide (CO2), and the calcium hydroxide (Ca(OH)2) powder are provided.
Secondly, the water is atomized by the injector 22 and sprayed into the reaction chamber 24 at a rate of 2.0 liters per hour. Simultaneously, the carbon dioxide (CO2) gas and the calcium hydroxide (Ca(OH)2) powder are also injected into the reaction chamber 24 via the gas nozzles 23 and the powder nozzles 30 respectively, and meet the atomized water to mix with each other. The injector 22 may be a high-pressure swirl injector and the atomization pressure of the solution may be in the range of 2˜20 Mpa (megapascals). Therefore, micro-droplets of the water can be obtained with a diameter in the range of 20-60 μm (micrometers), which allows the distilled water to mix with the calcium hydroxide (Ca(OH)2) powder and the carbon dioxide (CO2) on a molecular scale.
After the spray mixing of the distilled water, the calcium hydroxide (Ca(OH)2) powder and the carbon dioxide (CO2) in the reaction chamber 24, nucleation, which forms nuclei of calcium carbonate (CaCO3) particles occurs in the chamber 24 according to the following reaction:
Ca(OH)2(l)+H2O(l)+CO2(g)→CaCO3(s)+2H2O(l)
Thirdly, the mixture of the water, the calcium hydroxide (Ca(OH)2) powder and the carbon dioxide (CO2) is transported into the tank 28 via the pipe 29, and agitated by the stirrer 27. The growth of nuclei of the calcium carbonate (CaCO3) may be well controlled with agitation of the stirrer 17. Thereby a final mixture consisting of water, calcium carbonate (CaCO3) particles, and a small amount of calcium hydroxide (Ca(OH)2) that has incompletely reacted with the carbon dioxide (CO2) is obtained. The mixture of the distilled water, the calcium hydroxide (Ca(OH)2) powder and the carbon dioxide (CO2) may be returned to the reaction chamber 24 via the valve 25, the pump 26, the solution container 21 and the injector 22 in succession, and reacted with carbon dioxide (CO2) again to precipitate more calcium carbonate (CaCO3).
Finally, the calcium carbonate (CaCO3) particles are separated from the final mixture, and the calcium carbonate (CaCO3) particles are dried to obtain an end-product nano-structured powder.
It is to be understood, however, that even though numerous characteristics and advantages of the present embodiments have been set forth in the foregoing description, together with details of the structures and functions of the embodiments, the disclosure is illustrative only, and changes may be made in detail, especially in matters of shape, size, and arrangement of parts within the principles of the invention to the full extent indicated by the broad general meaning of the terms in which the appended claims are expressed.
Number | Date | Country | Kind |
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200510035535.3 | Jun 2005 | CN | national |