Methods and apparatuses for nano-materials powder treatment and preservation

Information

  • Patent Grant
  • 8828328
  • Patent Number
    8,828,328
  • Date Filed
    Wednesday, December 15, 2010
    13 years ago
  • Date Issued
    Tuesday, September 9, 2014
    9 years ago
Abstract
Apparatuses for and methods of nano-material powder preservation and dispersion in liquid, capture, and treatments are disclosed. The applications of the present disclosure ensure powder accountability of the nano-materials preventing the nano material from dispersing into the air. The method of treating a nano-material comprises receiving a nano-material and mixing/dispersing the nano-material with a fluid in a vessel until the nano-material is sealed by the fluid. The apparatus for treating a nano-material comprises a hermetically sealable vessel containing a nano-material and a fluid, wherein the fluid is configured to increase the isolation between particles of the nano-material.
Description
FIELD OF THE INVENTION

The present invention relates to the field of nano-material powder capture and treatment. More specifically, the present invention relates to the apparatus for and method of nano-particle storage, preservation, and treatment.


BACKGROUND OF THE INVENTION

Nano-technologies normally use materials having sizes in the range of nano-meter. In recent years, researchers and industries have demonstrated promising applications of nano-materials to various fields, including bio-medical, fine chemicals, electronics, and catalysts.


The sizes of the nano-materials make them undetectable by human eyes. In addition, the nano-materials often contain active chemicals or bio-reactive substances that are potentially dangerous to the health of human beings and animals and also harmful to the environment. Especially, when the nano-materials are in the powder forms, the likelihood of dispersing the powders into the air is increased. If no apparatus and methods are used to ensure all the nano-materials that are made are properly accounted for, no one can assure that the spaces that are used for handling the nano-materials are free from nano-materials. Accordingly, apparatus and methods to ensure the nano-material powder accountability are needed to ensure the environmental and biological safety of preparing and handling nano-materials.


Nonetheless, current industries and research labs only use regular lab glassware and Schlenk flasks in the traditional wet chemical experiments for nano-materials preparations. Few, if any, apparatuses and methods have been designed for the purposes of nano-materials preservation and accounting for the powders of the nano-materials. Accordingly, apparatuses and methods ensuring nano-materials particles and powders accountability are needed.


SUMMARY OF THE INVENTION

Apparatuses for and methods of nano-material powder preservation, capture, and treatments are disclosed. The applications of the present disclosure ensure powder accountability of the nano-materials by preventing the nano-material from dispersing into the air, thereby preventing the workers and researchers from inhaling the nano-materials and protecting the public from unsafe exposure to the nano-materials.


In one aspect of the present invention, a method of preserving a nano-material is provided. The method comprises receiving a nano-material and mixing the nano-material with a fluid in a vessel until the nano-material is coated/encapsulated by the fluid. In some embodiments, the nano-material is comprised of nano-particles. Alternatively, the nano-material is comprised of nano-tubes, fullerenes, nano-clusters, nanocatalysts, or quantum dots. In some embodiments, the nano-material comprises a biological substance, an enzyme, or a catalyst. In an alternative embodiment, the nano-material comprises titanium carbides. In some embodiments, the method of preserving a nano-material further comprises a step of providing an inert gas. In some embodiments, the vessel is hermetically sealable. In some embodiments, the mixing is performed until the nano-material is substantially evenly distributed in the fluid. In some embodiments, the fluid comprises water and a surfactant. Alternatively, the fluid comprises an organic solvent, an inorganic solvent, or a combination thereof. In some embodiments, the nano-material is substantially evenly distributed in the fluid forming a colloidal fluid. In some embodiments, the step of mixing the nano-material with a fluid comprises a motion of tumbling, shaking, shear mixing, blending, swirling, or sonicating. In some embodiments, the method of preserving a nano-material further comprises a step of sampling using Dynamic Light Scattering (DLS).


In another aspect of the present invention, an apparatus for preserving a nano-material is provided. The apparatus for preserving a nano-material comprises a hermetically sealable vessel; and a nano-material and a fluid contained in the hermetically sealable vessel, wherein the fluid is configured to ensure the nano particles do not agglomerate, coalesce, or adhere to each other in the fluid. In some embodiments, the vessel has a funnel shape bottom. In some embodiments, the nano-material comprises nano-particles, nano-tubes, fullerenes, nano-clusters, nanocatalysts, or quantum dots. Alternatively, the nano-material comprises a biological substance, an enzyme, or a catalyst. In some embodiments, the fluid and the nano-material form a colloidal fluid. In some embodiments, the fluid comprises a surfactant, water, or a combination thereof. Alternatively, the fluid comprises an organic solvent, an inorganic solvent, or a combination thereof. In some embodiments, the hermetically sealable vessel is removably connected with a hermetically sealable receiver. In some embodiments, the hermetically sealable vessel is removably coupled with a fluid source. Alternatively, the hermetically sealable vessel is removably attached to a base. In some embodiments, the hermetically sealable vessel is pivotally rotatable attached to the base, wherein the hermetically sealable vessel is vertically movable from the base. Alternatively, the hermetically sealable vessel is removably coupled with a hermetically sealable mixer, wherein the hermetically sealable mixer is configured to increase the isolation/separation between the particles of the nano-material. In some embodiments, the sealable vessel is removably coupled with a gas inlet, wherein the gas inlet is configured to provide a gas to agitate the fluid, thereby increasing the isolation/separation between particles of the nano-material. Alternatively, the hermetically sealable vessel is removably coupled with a hermetically sealable multi-port switch, thereby forming an integrated sealable apparatus, wherein the hermetically sealable multi-port switch connects any two of the multi-ports. In some embodiments, the hermetically sealable multi-port switch contains three connectable ports, wherein the hermetically sealable multi-port switch connects any two of the three connectable ports, wherein a first connectable port connects to a mixer, wherein a second connectable port connects to a fluid outlet, and wherein a third connectable port connects to a channel configured to re-circulate the fluid in a sealed circle from the hermetically sealable vessel through the mixer and a cooling device back to the hermetically sealable vessel.


In yet another aspect of the present invention, a method of nano-material preservation and dispersion is provided. The method of nano-material preservation and dispersion comprises dispersing powders of a nano-material in a fluid contained in a hermetically sealable vessel until the powder is substantially evenly distributed in the fluid and surrounding the nano material with the fluid, thereby reducing the ability of the nano-material from escaping from the hermetically sealable vessel. In some embodiments, the nano-material comprises a nano-particle. In some embodiments, the fluid comprises water, a surfactant, or a combination thereof.


In another aspect of the present invention, a method of providing particle accountability of a nano-material comprises mixing the powders of the nano-material in a liquid contained in a hermetically sealed vessel until substantially all of the powders become a colloidal suspension in the liquid, and removing the colloid solution from the vessel, thereby making the vessel substantially free from the powders of the nano-material. In some embodiments, the nano-material is received from a hermetically sealable source. In some embodiments, the vessel is removable from the hermetically sealable source, thereby the vessel and hermetically sealable source are able to be concurrently and independently sealed. Alternatively, the vessel is pivotally rotatably secured on a movable base, further wherein the vessel is vertically movable from the base.


In a further aspect, a method of manufacturing nanoparticles comprising dispersing nanoparticles in a solution in an inert gas environment, making the solution into a slurry, and encapsulating the nanoparticles, such that the nanoparticles are prevented from exposing to atmospheric air. In an aspect, a method of nanomaterial treatment comprises producing nanoparticles in a hermetically sealable nanomaterial manufacturing apparatus, transferring the nanoparticles into a hermetically sealable nano-powder collection vessel, hermetically sealing the nanomaterial manufacturing apparatus and the hermetically sealable nano-powder collection vessel, and discoupling the hermetically sealable nano-powder collection vessel with the hermetically sealable nanomaterial manufacturing apparatus, such that the hermeticity of both the hermetically sealable nano-powder collection vessel and hermetically sealable nano-powder collection vessel are able to be maintained. In another aspect, a method of maintaining an inert gas environment for nanomaterial treatment comprises coupling a tubular component between a nanopowder producing device and a nanopowder collector, and purging the tubular component with a gas to eliminate a residual gas in the tubular component. In some embodiments, the gas comprises an inert gas or a reactive gas. In another aspect, a nanomaterial treating vessel comprises a container component, wherein the container component is able to be hermetically sealed and one or more connecting components couple with the container component, such that the vessel is able to receive a nanomaterial from a nanomaterial producing apparatus and is able to process the nanomaterial independently from the nanomaterial producing apparatus.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a flow chart illustrating a method of treating a nano-material in accordance with some embodiments.



FIG. 2 shows a graphic illustration of a nano-materials treatment in accordance with some embodiments.



FIG. 3 illustrates one embodiment of an isometric view of a nano-materials treatment apparatus in accordance with some embodiments.



FIG. 4 is a schematic representation of portions of FIG. 3.



FIGS. 5 and 6 illustrate some of the alternative configurations of the apparatus 300 of FIG. 3.



FIG. 7 illustrates an overall setup of the apparatus for nano-materials treatments in accordance with some embodiments.



FIGS. 8A-D illustrate a method of using the nano-material treatment apparatus in accordance with some embodiments.





DETAILED DESCRIPTION OF THE INVENTION

Embodiments of the present application are directed to devices for and methods of nano-material powder preservation, capture, and treatments. Those of skill in the art will realize that the following detailed description of the devices for and methods of nano-material powder preservation, capture, and treatments are illustrative only and are not intended to be in any way limiting. Other embodiments of the devices, systems, and methods will readily suggest themselves to such skilled persons having the benefit of this disclosure.


Reference will now be made in detail to implementations of the devices for and methods of nano-material powder preservation, capture, and treatments as illustrated in the accompanying drawings. The same reference indicators will be used throughout the drawings and the following detailed description to refer to the same or like parts. In the interest of clarity, not all of the routine features of the implementations described herein are shown and described. It will, of course, be appreciated that in the development of any such actual implementation, numerous implementation-specific decisions must be made in order to achieve the developer's specific goals, such as compliance with application and business related constraints, and that these specific goals will vary from one implementation to another and from one developer to another. Moreover, it will be appreciated that such a development effort might be complex and time-consuming, but would nevertheless be a routine undertaking of engineering for those of skill in the art having the benefit of this disclosure.


Apparatuses for, and methods of, nano-material powder preservation, dispersion, capture, and treatments are disclosed. The applications of the present disclosure ensure powder accountability of the nano-materials preventing the nano-material from dispersing into the air and being lost to collection and treatment. The method of treating a nano-material comprises receiving a nano-material and mixing the nano-material with a fluid in a vessel until the nano-material is sealed by the fluid. The apparatus for treating a nano-material comprises a hermetically sealable vessel containing a nano-material and a fluid, wherein the fluid is configured to increase the isolation between particles of the nano-material.



FIG. 1 is a flow chart illustrating one embodiment of a method 100 of treating a nano-material in accordance with the principles of the present invention.


At step 102, a nano-material is received either in inert gas or in air. The nano-materials include nano-particles, nano-tubes, fullerenes, nano-clusters, nano-catalysts, quantum dots, or any other proper materials in the range of nano-meter-size. Materials that are larger or smaller than the nano-meter-size are also applicable when proper.


At step 104, the received nano-materials are mixed with a liquid in inert gas or in air. The liquid includes water, surfactants, organic solvents, inorganic solvents, solutions that contain biological substance, solutions that contain metals, non-metals, ions, or any combinations thereof. Although the word liquid is used here, present disclosure is also applicable to any substance that has fluid-like movable properties, such as supercritical fluids, gases, aerosol, foam, sol, and gel.


Still referring to step 104, the step of mixing the nano-materials and the liquid can be achieved in many ways. For example, the mixing is able to be achieved by using a mixer to blend, mix, or disturb the liquid that contains the nano-materials until the nano-materials are substantially evenly distributed in the liquid. The mixer can be installed in a main reaction vessel. Alternatively, the mixer can be in a separate unit connected to the main reaction vessel. Further, the mixer can contain various types of mixers including shear mixers, mixers containing blades, vortex mixers, ultrasonic mixer, or any other mixer that can properly mix the liquid and nano-materials to become a homogeneously-like colloid or liquid. In some alternative embodiments, the mixing can be achieved by human labors or mechanical movements, such as manually rotationally tumbling the vessel when mounted in the base 610 (FIG. 6). A person skilled in the art would appreciate that the mixing can be achieved by any motions that can disperse the nano-materials in the liquid. The motions include, but are not limited to, tumbling, shaking, shear mixing, blending, swirling, or sonicating. In some embodiments, further mixing steps are performed to ensure that the nano-materials are thermodynamically and/or homogeneously dispersed in the solution.


At step 105, the mixture is sampled for quality of dispersion. At step 106, the mixing of the nano materials and the liquid are continued until the nano-materials are substantially evenly dispersed in the liquid. The well-dispersed nano-materials in the liquid make the liquid a colloid or colloid-like liquid, emulsion, or solution.


The step(s), in part or as a whole, of method 100 can be operated under inert gas environments, such as nitrogen gas, helium, or argon. Alternatively, the step(s) can be performed under air. The inert gases include argon, nitrogen, helium, or any other non-reactive gas. Alternatively, gases containing chemicals that can form protective layer(s) of the nano-materials can be employed, such as chemicals having single or multi-dentate sites and chemicals having chelating and coordinating abilities. Additional pressure, heating, or cooling can also be applied when required. The nano-materials liquid mixture can be sampled and analyzed. In some embodiments, Dynamic Light Scattering (DLS) is employed to analyze the mixture.



FIG. 2 shows a graphic illustration of one embodiment of nano-materials treatment 200 in accordance with the principles of the present disclosure. At step 202, vessel 208 receives nano-materials 212. At step 204, liquid 218 is added to the nano-material 212. In some embodiments, the liquid 218 includes water 214, surfactants 216, organic solvents, inorganic solvents, any combinations thereof, or any other proper liquids that can make the nano-materials 212 substantially evenly distributed in the liquid 218. At step 206, after the liquid 218 is added, the nano-materials are partially mixed with the liquid 218 forming nano-materials/liquid chunks 226, so the nano-materials are not evenly distributed in the liquid. Some unit of surfactant or solution contains multi-particles of nano-materials 220, some contains one particle of nano-materials 222, and some do not contain any nano-materials 224. The nano-materials can be either enclosed by the liquid or on the surfaces of the liquid. A person skilled in the art will appreciate that surfactants are able to include compounds that are able to lower the surface tension of a liquid, allowing easier spreading, and lowering of the interfacial tension between two liquids, or between a liquid and a solid. Further, surfactants are able to act as detergents, wetting agents, emulsifiers, foaming agents, and dispersants. At step 208, the nano-materials and the solution mixture are further mixed to make the nano-materials more evenly distributed in the liquid. The mixing of step 208 can be achieved by a commercially available mixer, such as the one that has a rotating mixing blade as shown in 208A. Alternatively, the mixing can be achieved by shaking the vessel as shown in 208B. In some embodiments, the shaking of the vessel is performed by human force. In other embodiments, the shaking is performed by any proper mechanical forces. Alternatively, the mixing is achieved by sonication, which is shown in 208D, and such individual mixing methods can be performed either sequentially or simultaneously. The step of mixing the nano-material with a fluid as described above can be any motions that make the nano-material more homogeneously distributed in the liquid. The motion can include, but not limited to, tumbling, shaking, shear mixing, blending, swirling, or sonicating. At step 210, the nano-materials 218 are evenly distributed in the liquid 210 forming a colloid, colloid-like, or emulsion solution 228.



FIG. 3 illustrates one embodiment of an isometric view of a nano-materials treatment apparatus in accordance with the principles of the present disclosure.


An apparatus 300 for treating the nano-materials includes a vessel 302, a receiver 304, and a base 306. The receiver 304 removably attaches to the vessel 302. In some embodiments, the connection between the receiver 304 and the vessel 302 includes valves on both the connector end nearest the receiver 304 and the connector end nearest the vessel 302. When the valves are closed, the vessel 302 and the receiver 304 can be in independent hermetic sealed conditions preventing air from leaking into or the nano-materials getting out of the vessel 302 or receiver 304, which can connect to nano-material preparation chambers. In some embodiments, the receiver 304 is in a funnel-like shape. A narrower end of the receiver 304 is coupled to the vessel 302 to facilitate the transferring of the materials via valves 310, 312, and sliding coupling 308. The wider end of the receiver can attach to other nano-materials reaction chambers or storage places. For example, the receiver can directly attach to a nano-materials preparation chamber 750 (FIG. 7). The valves of the receiver 304 (the valve 312) and the vessel 302 (the valve 310) are closed before the receiver 304 and the vessel 302 attach to each other in order to maintain a hermetically sealed or oxygen free environment. When the receiver 304 is coupled to the vessel 302 via sliding coupling 308, the nano-materials prepared in the chamber 750 (FIG. 7) or other storage places in hermetically sealed or air-free conditions can be transferred into the hermetically sealed or air-free reaction vessel 302 directly without the risks of exposing the nano-materials into the air. This setup provides several advantages that the traditional glassware or traditional Schlenk lines cannot provide. First, the direct connections between the nano-material storage places, handling places, or preparing chambers to the vessel 302 provide a direct transferring channel, which is an isolated transfer channel without the risk of exposing the nano-materials into the environment. After the completion of the transferring, the nano-material residue remaining on the surface of the receiver can be washed down with solution or any other proper solvents or liquid to the vessel 302. As such, no remaining powder is left on the receiver or transferring flask. Accordingly, the methods and apparatus of the present disclosure provide promising powder accountability. Second, the vessel 302 is removably coupled to the receiver 304 via sliding coupling 308. The nano-materials preservation can be performed in the vessel 302 independent from the storage places or preparing chamber 750 (FIG. 7). The feature that the nano-materials treatments can be performed independently from the preparing chamber 750 or storage places prevents the likelihood of contaminating the preparing chamber 750 or storage places with undesired chemicals or solutions. For example, some of the nano-materials treating chemicals contain water, which can be reactive to some of the precursor reactants for preparing the nano-materials. As such, if the nano-materials treating processes are not performed in isolation, the water vapors or molecules used for treating the nano-materials can contaminate the nano-materials preparing chamber 750.


Still referring to FIG. 3, the base 306 is coupled with the vessel 302. In some embodiments, the base 306 includes wheels 305. In some embodiments, the vessel 302 is unmovably attached to the base 306. In some embodiments, the vessel 302 is removably attached to a base 610 (FIG. 6). In FIGS. 5 and 6, one or more bolts 504 secure the position of a mounting arm 570 used to position vessel 502 on the base 610, and the mounting arm 570 is vertically movable on the vessel 502 along a track 506. The bolts 504 are adjustably secured in the track 506. The bolts 504, the tracks 506, and the mounting arm 570 are shown as examples, and various designs to position vessel 502 relative to base 610 can be employed. The tracks, bolts, and mounting arm can be designed to move in any directions and securable in any means as long as the function of positioning and/or securing can be provided. In some embodiments, the vessel 502 includes a pivotal point 503 mounting on the mounting arm 570 (FIG. 5). In some embodiments, the pivotal point 503 comprises a ball bearing allowing a rotational movement of the vessel 502 relative to the base 610. In some embodiments, the pivotal point 503 allows the vessel 502 to rotate in a circular motion, such as rotating 72°, 90°, 180°, 360° or any other angles, such that the content inside the vessel 502 is able to be mixed. For example, a fluid that is inside the vessel 502 is able to be tumbled by a circular movement of the vessel 502. A person skilled in the art would appreciate that the movement is able to be performed in an unidirectional/bidirectional rotation and/or in a constant or irregular speed/motion. In some embodiments, the vessel 502 comprises a handle 512, which is able to be used to transport the vessel 502 by wheels 505. In some embodiments, the vessel 502 comprises a lock 608 (FIG. 6), such as a rotational lock, which is able to be used to secure the vessel 502 from further rotational movements. In some embodiments, the one or more bolts 504 and the track 506 described above are able to provide a function allowing a user to adjust the vessel 502 to a position substantially in the center of gravity to facilitate the circular rotational movements described above.



FIG. 4 is a schematic representation of portions of FIG. 3. FIG. 4 is able to be read together with FIG. 3. The vessels 302 and 402 have conical or funnel shape ends. The funnel shape ends of the vessels 302, 402 can be the bottom of the vessels 302, 402, which facilitate the outputting of the nano-materials from the vessels 302, 402. The contents in the vessel 302, 402 slide down along the angled wall of the funnel shape ends of the vessels. The funnel shape ends connect to outlets 322, 422 for product outputs. The outlets 322, 422 can connect to valves 436 and 336 and/or connect to other containers in a detatchable and sealable manner.


The vessels 302, 402 are able to be connected with various piping ducts or apparatus. As described above, the vessels 302 and 402 can connect to the receivers 304 and 404. Additionally, vessels 302 and 402 can optionally connect to the gas meters 314 and 414, valves 410 and 403, sliding hermetic coupling 308/408, gas inlets 399/499, sealable port 418, and vacuum components 426. In some embodiments, a window 398 is able to be included. In some embodiments, the adaptor to connect the vessel valve 410 with the reactor valve 412 is able to be a sliding coupling 408. The valve 410 is able to be a valve that hermetically isolates the powder collection vessel from atmosphere when the vessel is disconnected and removed from the powder manufacturing tool, such as a nano-material preparation apparatus 750 (FIG. 7). In some embodiments, the valve 412 isolates the manufacturing tool from atmosphere when the vessel is removed. In some embodiments, a valve 497 can be included. The valve 497 can provide inert purge gas to a power collection tube 407 to prevent an oxidation reaction of the air sensitive materials when the valve 410 is opened. The purge flow is able to be measured and regulated by the flow meter 414. The windows 398, 498 allow the status inside the vessel 302 to be observed. A person skilled in the art would appreciate that one or more illuminating devices, such as LED, are able to be equipped on the vessel to facilitate the observation. Any of the above-mentioned components can be included in the channels between the receiver 304, 404 and the vessel 302, 402 or inside the vessel itself. The gas meter 314, 414 and a gas source are able to be coupled with the sliding hermetic coupling 308 via connectors 394 and 396.


In some embodiments, the one or more gas inlets 390/490 provide inert gas, such as argon, nitrogen, and helium to provide an inert gas environment to the vessels 302, 402 and purge the system with the inert gas. Alternatively, the gas inlet 390/490 provides positive pressure protective gases, or reactive gases. In some embodiments, the interstitial space between the o-rings 489 in the sliding hermetic coupling 408 is purged with the gas to eliminate any air ingress in the event of a leak across the o-rings. In some embodiments, the gas meters 314 and 414 regulate the flow required and control the gas release rates. In some embodiments, any residual atmosphere can be purged from powder transfer tube 407 by opening valves 497 and flowing the inert gas through tube 407 and out flow measuring device 414. In some embodiments, the vessels 302 and 402 and other components are made durable to endure a negative pressure (e.g., a vacuum), and a vacuum component 426 is able be included. The vacuum components 426 can further contain pressure gauge 428. Further, the port 418 is able to be a fluid return port and externally coupled to the return lines of one or more stirrers (not shown in the figures). The stirrers are able to be used to mix the nano-materials with the liquids discussed above.



FIG. 5 illustrates a vessel unit 575, which is able to be removably attached to the base 610 (FIG. 6). In some embodiments, the base 610 comprises a pallet lifter, such that the vessel unit 575 is able to be lifted to facilitate the rotational movements described above. (More detail is described in FIG. 8) In some embodiments, the vessel 502 comprise a handle 512, which is able to be used to transport (e.g., pull and/or drag) the vessel 502 by wheels 505.



FIG. 7 illustrates one embodiment of a nano-materials preparation apparatus in accordance with the principles of the present disclosure.


A nano-material treating vessel 702 is similar to vessels 302, 402, 502 in FIGS. 3-6 respectively. The nano-materials can be prepared in the preparation chamber 750. After the nano-materials are made, the powder of the nano-materials can be transferred to the receiver 704. Subsequently, the nano-materials are received by the vessel 702 from the receiver 704. After the vessel 702 receives the nano-materials, the vessel 702 can be sealed at valves 710 and removed from the connection with the receiver 704. In some embodiments, the sliding coupling 708 is used to join the vessel 702 to a manufacturing tool, such as a nano-material preparation apparatus 750, via collection cone 704/404 (FIG. 4) and valve 712/412. The area between the O-rings in the coupling is able to be purged with a flow of inert gas, which is able to be above atmosphere pressure and keeps air from crossing the seal boundary in the event when there is a leak. The supply for the inert gas comes in through 490, 496, and 499 and the flow is able to be regulated by a flow control meter, such as meter 414 (FIG. 4).


Next, the solutions containing surfactants and/or liquids can be introduced from the liquid tank 755 to the vessel 702 to disperse or preserve the nano-materials. After the liquids are introduced from the liquid tank 755, the valves 742A and 742B can be closed and disconnected from one another. The process of mixing, as mentioned above, can be performed. To ensure that the nano-materials are well dispersed in the liquid, the products are optionally transferred to an independent mixer 720. The mixer can further contain a port 738 for sampling. The sample can be analyzed by any particle distribution analytical instruments, such as DSL or any other proper analytical instruments. If the sample passes required quality standard, the products are transferred to a detatchable/removable ship container 726 for further processing or storage. If the sample does not reach required quality standard, the products are transferred back to the vessel 702 for further processing. The mixer 720 can connect to a multi-way adaptor 734. In some embodiments, the adaptor 734 can connect the channels between the mixer 720 and heat exchanger 728 as shown in 734A, mixer 720 and the outlet 724 as shown in 734B, or outlet 724 and heat exchanger 728 as shown in 734C. When the adaptor 734 connects the channel of the mixer 720 and the heat exchanger 728, the solution containing the nano-materials and the liquid in the vessel 702 can be circulated through the mixer 720, heat exchanger 728, and back to vessel 702. By going through the heat exchanger 728, the heat of the solution generated in the mixing can be removed. The heat exchanged in the heat exchanger 728 is subsequently removed in the chiller 732. When the adaptor 734 connects the channel of the mixer 720 and the outlet 724, the products are outputted and sent to be used or stored. When the adaptor 734 connects the channel of the outlet 724 and the heat exchanger 728, the gas from gas supply, such as gas supply inlet 799, can come to push the remaining products out of the outlet 724. In some embodiments, the adaptor 734 comprises a selector valve, which is able to be switched to drain either the collector/mixer or the heat exchanger into a collection vessel via gravity.


Still referring to FIG. 7. In some embodiments, the nano-material treatment apparatus disclosed in the present disclosure is used with a nano-material preparation apparatus 750. In some embodiments, the nano-material preparation apparatus 750 can be the one described in the related U.S. patent application Ser. No. 12/152,097, titled GAS DELIVERY SYSTEM WITH CONSTANT OVERPRESSURE RELATIVE TO AMBIENT TO SYSTEM WITH VARYING VACUUM SUCTION, which is hereby incorporated entirely into present disclosure.



FIGS. 8A-D illustrate a method of using the nano-material treatment apparatus in accordance with some embodiments. The numbers that are used in FIGS. 8A-D for identification are the same numbers that are used in FIGS. 5 and 6. FIG. 8A shows a vessel assembly 575 that is separated/detached from the base 610. The base 610 is able to be a palette lifter. The vessel 575 is able to be rolled to access the base 610 by using the handle 512 and the wheels 505. As shown in FIG. 8B, the pivotal points 503 are able to be placed in the grooves 802, such that the vessel is able to rotate circularly along the pivotal points 503. The rotational lock 508 can be used to secure/lock by using securing means, so that the vessel 575 is prevented from rotating or spinning. In some embodiments, the securing means comprises one or more bolt on the pivotal point 503 capable of protruding into the hole 511 on a metal plate 515, so that the vessel 575 is secured from rotating. In some embodiments, a rotational lock 508 is left unused when the vessel 575 is in an upright position. FIG. 8C shows that the base 610 is in a lifted position and the vessel 575 is in the air having space 521, so that the vessel 575 is able to freely rotate along the pivotal points 503. The rotational lock 508 is able to be in an engaged position, so that the vessel 575 is able to be fixed in a stable position preventing from a rotation. The FIG. 8D shows that the vessel 575 is rotated and flipped in an upside-down position along the pivotal point 503. The vessel is able to be secured in the upside-down position by locking the rotational lock 508.


In the following, some examples in accordance with some embodiments of the present invention are provided. In some embodiments, a system comprised of a hermetically sealed powder manufacturing machine removably coupled to a hermetically sealed powder collection vessel. Once the powder has been collected in the vessel, the vessel can be hermetically disconnected and removed from the manufacturing tool while maintaining the hermeticity (hermetic integrity) of both the manufacturing tool and the vessel.


In some embodiments, other hardware is able to be used to replace the above described vessel onto the powder manufacturing tool. Similar methods are able to be used to maintain an inert gas environment. The hardware is able to comprise a container containing a defined atmosphere (inert or reactive). The interface connection can be purged with inert gas to remove/replace residual atmosphere in the connection of the hardware and proactively/dynamically maintain the inertness of the connection.


In some embodiments, a vessel capable of being moved to a remote processing location is provided. Further processing steps (such as solvating, mixing, dispersing, preserving, coating, quality sampling, cooling, dispensing) can be performed inertly within this vessel or outside the vessel with the aid of external, inert connections to supplemental processing hardware. This vessel is able to be not only an inert powder collection vessel but also able to be an inert processing vessel whereby the powder can be further treated without transfer or risk of disturbing the engineered environment inside the vessel.


The following description is presented to enable one skilled in the art to make and use the invention and is provided in the context of a patent application and its requirements. Various modifications to the described embodiments will be readily apparent to those persons skilled in the art and the generic principles herein may be applied to other embodiments. Thus, the present invention is not intended to be limited to the embodiment shown but is to be accorded the widest scope consistent with the principles and features described herein.


A person skilled in the art would appreciate that the nano-materials contain any material in the size of nano-meter. Although the term “nano-material(s)” is used here, the inventors do not intend to limit the applications of the present disclosure to nano-meter size materials. Any materials that have a size larger or smaller than the nano-materials are applicable with the present disclosure. Further, the term nano-materials used in the present disclosure include both particles and powders. These two terms are used equivalently. The present invention may apply to a wide variety of powders and particles. Powders that fall within the scope of the present invention may include, but are not limited to, any of the following: (a) nano-structured powders (nano-powders), having an average grain size less than 250 nanometers and an aspect ratio between one and one million; (b) submicron powders, having an average grain size less than 1 micron and an aspect ratio between one and one million; (c) ultra-fine powders, having an average grain size less than 100 microns and an aspect ratio between one and one million; and (d) fine powders, having an average grain size less than 500 microns and an aspect ratio between one and one million. Further, the terms of solution(s), liquid(s), solvent(s) disclosed in the present disclosure are all interchangeable.

Claims
  • 1. An apparatus for preparing a nano-material and fluid mixture comprising: a. a hermetically sealable vessel;b. a hermetically sealable receiver coupled to the hermetically sealable vessel and to a nano-material source, wherein the hermetically sealable receiver allows nano-material to transfer from the nano-material source into the hermetically sealable vessel; andc. a fluid source coupled to the hermetically sealable vessel, wherein the hermetically sealable vessel is configured to receive fluid from the fluid source and the fluid increases the isolation between particles of the nano-material transferred into the hermetically sealable vessel.
  • 2. The apparatus of claim 1, wherein the vessel has a funnel shape bottom.
  • 3. The apparatus of claim 1, wherein the nano-material comprises a nano-particle, a nanotube, a fullerene, a nano-cluster, a nanocatalyst, or a quantum dot.
  • 4. The apparatus of claim 1, wherein the nano-material comprises a biological substance, an enzyme, or a catalyst.
  • 5. The apparatus of claim 1, wherein the fluid and the nano-material form a colloidal fluid.
  • 6. The apparatus of claim 1, wherein the fluid comprises a surfactant, water, or a combination thereof.
  • 7. The apparatus of claim 1, wherein the fluid comprises an organic solvent, an inorganic solvent, or a combination thereof.
  • 8. The apparatus of claim 1, wherein the hermetically sealable vessel is removably coupled to the hermetically sealable receiver via a hermetically sealed sliding coupling.
  • 9. The apparatus of claim 1, wherein the hermetically sealable vessel is removably coupled to the fluid source.
  • 10. The apparatus of claim 1, wherein the hermetically sealable vessel is removably attached to a base.
  • 11. The apparatus of claim 10, wherein the hermetically sealable vessel is pivotally rotatable attached to the base, wherein the hermetically sealable vessel is vertically movable from the base.
  • 12. The apparatus of claim 1, wherein the hermetically sealable vessel is removably coupled with a hermetically sealable shear mixer, wherein the hermetically sealable shear mixer is configured to receive the nano-material and fluid mixture from the hermetically sealable vessel and configured to further increase the isolation between the particles of the nano-material.
  • 13. The apparatus of claim 1, wherein the hermetically sealable vessel is removably coupled with a hermetically sealable multi-ports switch comprising a plurality of multi-ports, thereby forming an integrated sealable apparatus, wherein the hermetically sealable multi-ports switch switchably connects any two of the plurality of multi-ports.
  • 14. The apparatus of claim 13, wherein the hermetically sealable multi-ports switch contains three connectable ports, wherein the hermetically sealable multi-ports switch switchably connects any two of the three connectable ports, wherein a first connectable port connects to a mixer, wherein a second connectable port connects to a fluid outlet, and wherein a third connectable port connects to a channel configured to re-circulate the fluid in a sealed loop from the hermetically sealable vessel through the mixer and a cooling device back to the hermetically sealable vessel.
  • 15. The apparatus of claim 1, wherein the nano-material source is a nano-material producing apparatus.
  • 16. The apparatus of claim 15, wherein the nano-material producing apparatus is a plasma production apparatus.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority from U.S. Provisional Patent Application Ser. No. 61/284,329, filed Dec. 15, 2009 and entitled “MATERIALS PROCESSING,” which is hereby incorporated herein by reference in its entirety for all purposes.

US Referenced Citations (458)
Number Name Date Kind
2284554 Beyerstedt May 1942 A
2419042 Todd Apr 1947 A
2519531 Worn Aug 1950 A
2562753 Trost Jul 1951 A
2689780 Rice Sep 1954 A
3001402 Koblin Sep 1961 A
3042511 Reding, Jr. Jul 1962 A
3067025 Chisholm Dec 1962 A
3145287 Siebein et al. Aug 1964 A
3178121 Wallace, Jr. Apr 1965 A
3179782 Matvay Apr 1965 A
3181947 Vordahl May 1965 A
3313908 Unger et al. Apr 1967 A
3401465 Larwill Sep 1968 A
3450926 Kiernan Jun 1969 A
3457788 Miyajima Jul 1969 A
3537513 Austin Nov 1970 A
3552653 Inoue Jan 1971 A
3617358 Dittrich Nov 1971 A
3667111 Chartet Jun 1972 A
3741001 Fletcher et al. Jun 1973 A
3752172 Cohen et al. Aug 1973 A
3761360 Auvil et al. Sep 1973 A
3774442 Gustavsson Nov 1973 A
3804034 Stiglich, Jr. Apr 1974 A
3830756 Sanchez et al. Aug 1974 A
3871448 Vann et al. Mar 1975 A
3892882 Guest et al. Jul 1975 A
3914573 Muehlberger Oct 1975 A
3959094 Steinberg May 1976 A
3959420 Geddes et al. May 1976 A
3969482 Teller Jul 1976 A
4008620 Narato et al. Feb 1977 A
4018388 Andrews Apr 1977 A
4021021 Hall et al. May 1977 A
4127760 Meyer et al. Nov 1978 A
4139497 Castor et al. Feb 1979 A
4157316 Thompson et al. Jun 1979 A
4171288 Keith et al. Oct 1979 A
4174298 Antos Nov 1979 A
4189925 Long Feb 1980 A
4227928 Wang Oct 1980 A
4248387 Andrews Feb 1981 A
4253917 Wang Mar 1981 A
4260649 Dension et al. Apr 1981 A
4284609 deVries Aug 1981 A
4315874 Ushida et al. Feb 1982 A
4344779 Isserlis Aug 1982 A
4369167 Weir Jan 1983 A
4388274 Rourke et al. Jun 1983 A
4419331 Montalvo Dec 1983 A
4431750 McGinnis et al. Feb 1984 A
4436075 Campbell et al. Mar 1984 A
4440733 Lawson et al. Apr 1984 A
4458138 Adrian et al. Jul 1984 A
4459327 Wang Jul 1984 A
4505945 Dubust et al. Mar 1985 A
4513149 Gray et al. Apr 1985 A
4523981 Ang et al. Jun 1985 A
4545872 Sammells et al. Oct 1985 A
RE32244 Andersen Sep 1986 E
4609441 Frese, Jr. et al. Sep 1986 A
4723589 Iyer et al. Feb 1988 A
4731517 Cheney Mar 1988 A
4751021 Mollon et al. Jun 1988 A
4764283 Ashbrook et al. Aug 1988 A
4765805 Wahl et al. Aug 1988 A
4824624 Palicka et al. Apr 1989 A
4836084 Vogelesang et al. Jun 1989 A
4855505 Koll Aug 1989 A
4866240 Webber Sep 1989 A
4885038 Anderson et al. Dec 1989 A
4921586 Molter May 1990 A
4983555 Roy et al. Jan 1991 A
4987033 Abkowitz et al. Jan 1991 A
5006163 Benn et al. Apr 1991 A
5015863 Takeshima et al. May 1991 A
5041713 Weidman Aug 1991 A
5043548 Whitney et al. Aug 1991 A
5070064 Hsu et al. Dec 1991 A
5073193 Chaklader et al. Dec 1991 A
5133190 Abdelmalek Jul 1992 A
5151296 Tokunaga Sep 1992 A
5157007 Domesle et al. Oct 1992 A
5192130 Endo et al. Mar 1993 A
5230844 Macaire et al. Jul 1993 A
5233153 Coats Aug 1993 A
5269848 Nakagawa Dec 1993 A
5330945 Beckmeyer et al. Jul 1994 A
5338716 Triplett et al. Aug 1994 A
5369241 Taylor et al. Nov 1994 A
5371049 Moffett et al. Dec 1994 A
5372629 Anderson et al. Dec 1994 A
5392797 Welch Feb 1995 A
5436080 Inoue et al. Jul 1995 A
5439865 Abe et al. Aug 1995 A
5442153 Marantz et al. Aug 1995 A
5460701 Parker et al. Oct 1995 A
5464458 Yamamoto Nov 1995 A
5485941 Guyomard et al. Jan 1996 A
5534149 Birkenbeil et al. Jul 1996 A
5534270 De Castro Jul 1996 A
5543173 Horn, Jr. et al. Aug 1996 A
5553507 Basch et al. Sep 1996 A
5562966 Clarke et al. Oct 1996 A
5611896 Swanepoel et al. Mar 1997 A
5630322 Heilmann et al. May 1997 A
5652304 Calderon et al. Jul 1997 A
5714644 Irgang et al. Feb 1998 A
5723187 Popoola et al. Mar 1998 A
5726414 Kitahashi et al. Mar 1998 A
5749938 Coombs May 1998 A
5776359 Schultz et al. Jul 1998 A
5788738 Pirzada et al. Aug 1998 A
5804155 Farrauto et al. Sep 1998 A
5811187 Anderson et al. Sep 1998 A
5837959 Muehlberger et al. Nov 1998 A
5851507 Pirzada et al. Dec 1998 A
5853815 Muehlberger Dec 1998 A
5858470 Bernecki et al. Jan 1999 A
5884473 Noda et al. Mar 1999 A
5905000 Yadav et al. May 1999 A
5928806 Olah et al. Jul 1999 A
5935293 Detering et al. Aug 1999 A
5973289 Read et al. Oct 1999 A
5989648 Phillips Nov 1999 A
5993967 Brotzman, Jr. et al. Nov 1999 A
5993988 Ohara et al. Nov 1999 A
6004620 Camm Dec 1999 A
6012647 Ruta et al. Jan 2000 A
6033781 Brotzman, Jr. et al. Mar 2000 A
6045765 Nakatsuji et al. Apr 2000 A
6059853 Coombs May 2000 A
6066587 Kurokawa et al. May 2000 A
6084197 Fusaro, Jr. Jul 2000 A
6093306 Hanrahan et al. Jul 2000 A
6093378 Deeba et al. Jul 2000 A
6102106 Manning et al. Aug 2000 A
6117376 Merkel Sep 2000 A
6168694 Huang et al. Jan 2001 B1
6190627 Hoke et al. Feb 2001 B1
6213049 Yang Apr 2001 B1
6214195 Yadav et al. Apr 2001 B1
6228904 Yadav et al. May 2001 B1
6254940 Pratsinis et al. Jul 2001 B1
6261484 Phillips et al. Jul 2001 B1
6267864 Yadav et al. Jul 2001 B1
6322756 Arno et al. Nov 2001 B1
6342465 Klein et al. Jan 2002 B1
6344271 Yadav et al. Feb 2002 B1
6362449 Hadidi et al. Mar 2002 B1
6379419 Celik et al. Apr 2002 B1
6387560 Yadav et al. May 2002 B1
6395214 Kear et al. May 2002 B1
6398843 Tarrant Jun 2002 B1
6409851 Sethuram et al. Jun 2002 B1
6413781 Geis et al. Jul 2002 B1
6416818 Aikens et al. Jul 2002 B1
RE37853 Detering et al. Sep 2002 E
6444009 Liu et al. Sep 2002 B1
6475951 Domesle et al. Nov 2002 B1
6488904 Cox et al. Dec 2002 B1
6506995 Fusaro, Jr. et al. Jan 2003 B1
6517800 Cheng et al. Feb 2003 B1
6524662 Jang et al. Feb 2003 B2
6531704 Yadav et al. Mar 2003 B2
6548445 Buysch et al. Apr 2003 B1
6554609 Yadav et al. Apr 2003 B2
6562304 Mizrahi May 2003 B1
6562495 Yadav et al. May 2003 B2
6569393 Hoke et al. May 2003 B1
6569397 Yadav et al. May 2003 B1
6569518 Yadav et al. May 2003 B2
6572672 Yadav et al. Jun 2003 B2
6579446 Teran et al. Jun 2003 B1
6596187 Coll et al. Jul 2003 B2
6603038 Hagemeyer et al. Aug 2003 B1
6607821 Yadav et al. Aug 2003 B2
6610355 Yadav et al. Aug 2003 B2
6623559 Huang Sep 2003 B2
6635357 Moxson et al. Oct 2003 B2
6641775 Vigliotti et al. Nov 2003 B2
6652822 Phillips et al. Nov 2003 B2
6652967 Yadav et al. Nov 2003 B2
6669823 Sarkas et al. Dec 2003 B1
6682002 Kyotani Jan 2004 B2
6689192 Phillips et al. Feb 2004 B1
6699398 Kim Mar 2004 B1
6706097 Zornes Mar 2004 B2
6706660 Park Mar 2004 B2
6710207 Bogan, Jr. et al. Mar 2004 B2
6713176 Yadav et al. Mar 2004 B2
6716525 Yadav et al. Apr 2004 B1
6744006 Johnson et al. Jun 2004 B2
6746791 Yadav et al. Jun 2004 B2
6772584 Chun et al. Aug 2004 B2
6786950 Yadav et al. Sep 2004 B2
6813931 Yadav et al. Nov 2004 B2
6817388 Tsangaris et al. Nov 2004 B2
6832735 Yadav et al. Dec 2004 B2
6838072 Kong et al. Jan 2005 B1
6841509 Hwang et al. Jan 2005 B1
6855410 Buckley Feb 2005 B2
6855426 Yadav Feb 2005 B2
6855749 Yadav et al. Feb 2005 B1
6858170 Van Thillo et al. Feb 2005 B2
6886545 Holm May 2005 B1
6896958 Cayton et al. May 2005 B1
6902699 Fritzemeier et al. Jun 2005 B2
6916872 Yadav et al. Jul 2005 B2
6919065 Zhou et al. Jul 2005 B2
6919527 Boulos et al. Jul 2005 B2
6933331 Yadav et al. Aug 2005 B2
6972115 Ballard Dec 2005 B1
6986877 Takikawa et al. Jan 2006 B2
6994837 Boulos et al. Feb 2006 B2
7007872 Yadav et al. Mar 2006 B2
7022305 Drumm et al. Apr 2006 B2
7052777 Brotzman, Jr. et al. May 2006 B2
7073559 O'Larey et al. Jul 2006 B2
7081267 Yadav Jul 2006 B2
7101819 Rosenflanz et al. Sep 2006 B2
7147544 Rosenflanz Dec 2006 B2
7147894 Zhou et al. Dec 2006 B2
7166198 Van Der Walt et al. Jan 2007 B2
7166663 Cayton et al. Jan 2007 B2
7172649 Conrad et al. Feb 2007 B2
7172790 Koulik et al. Feb 2007 B2
7178747 Yadav et al. Feb 2007 B2
7208126 Musick et al. Apr 2007 B2
7211236 Stark et al. May 2007 B2
7217407 Zhang May 2007 B2
7220398 Sutorik et al. May 2007 B2
7255498 Bush et al. Aug 2007 B2
7265076 Taguchi et al. Sep 2007 B2
7282167 Carpenter Oct 2007 B2
7307195 Polverejan et al. Dec 2007 B2
7323655 Kim Jan 2008 B2
7384447 Kodas et al. Jun 2008 B2
7402899 Whiting et al. Jul 2008 B1
7417008 Richards et al. Aug 2008 B2
7494527 Jurewicz et al. Feb 2009 B2
7517826 Fujdala et al. Apr 2009 B2
7534738 Fujdala et al. May 2009 B2
7541012 Yeung et al. Jun 2009 B2
7541310 Espinoza et al. Jun 2009 B2
7557324 Nylen et al. Jul 2009 B2
7572315 Boulos et al. Aug 2009 B2
7576029 Saito et al. Aug 2009 B2
7576031 Beutel et al. Aug 2009 B2
7604843 Robinson et al. Oct 2009 B1
7611686 Alekseeva et al. Nov 2009 B2
7615097 McKechnie et al. Nov 2009 B2
7618919 Shimazu et al. Nov 2009 B2
7622693 Foret Nov 2009 B2
7632775 Zhou et al. Dec 2009 B2
7635218 Lott Dec 2009 B1
7674744 Shiratori et al. Mar 2010 B2
7678419 Kevwitch et al. Mar 2010 B2
7704369 Olah et al. Apr 2010 B2
7709411 Zhou et al. May 2010 B2
7709414 Fujdala et al. May 2010 B2
7745367 Fujdala et al. Jun 2010 B2
7750265 Belashchenko et al. Jul 2010 B2
7803210 Sekine et al. Sep 2010 B2
7851405 Wakamatsu et al. Dec 2010 B2
7874239 Howland Jan 2011 B2
7875573 Beutel et al. Jan 2011 B2
7897127 Layman et al. Mar 2011 B2
7902104 Kalck Mar 2011 B2
7905942 Layman Mar 2011 B1
7935655 Tolmachev May 2011 B2
8051724 Layman et al. Nov 2011 B1
8076258 Biberger Dec 2011 B1
8080494 Yasuda et al. Dec 2011 B2
8089495 Keller Jan 2012 B2
8142619 Layman et al. Mar 2012 B2
8168561 Virkar May 2012 B2
8173572 Feaviour May 2012 B2
8211392 Grubert et al. Jul 2012 B2
8258070 Fujdala et al. Sep 2012 B2
8278240 Tange et al. Oct 2012 B2
8294060 Mohanty et al. Oct 2012 B2
8309489 Cuenya et al. Nov 2012 B2
8349761 Xia et al. Jan 2013 B2
8557727 Yin et al. Oct 2013 B2
20010004009 MacKelvie Jun 2001 A1
20010042802 Youds Nov 2001 A1
20010055554 Hoke et al. Dec 2001 A1
20020018815 Sievers et al. Feb 2002 A1
20020068026 Murrell et al. Jun 2002 A1
20020071800 Hoke et al. Jun 2002 A1
20020079620 DuBuis et al. Jun 2002 A1
20020100751 Carr Aug 2002 A1
20020102674 Anderson Aug 2002 A1
20020131914 Sung Sep 2002 A1
20020143417 Ito et al. Oct 2002 A1
20020182735 Kibby et al. Dec 2002 A1
20020183191 Faber et al. Dec 2002 A1
20020192129 Shamouilian et al. Dec 2002 A1
20030036786 Duren et al. Feb 2003 A1
20030042232 Shimazu Mar 2003 A1
20030047617 Shanmugham et al. Mar 2003 A1
20030066800 Saim et al. Apr 2003 A1
20030108459 Wu et al. Jun 2003 A1
20030110931 Aghajanian et al. Jun 2003 A1
20030129098 Endo et al. Jul 2003 A1
20030139288 Cai et al. Jul 2003 A1
20030143153 Boulos et al. Jul 2003 A1
20030172772 Sethuram et al. Sep 2003 A1
20030223546 McGregor et al. Dec 2003 A1
20040009118 Phillips et al. Jan 2004 A1
20040023302 Archibald et al. Feb 2004 A1
20040023453 Xu et al. Feb 2004 A1
20040077494 LaBarge et al. Apr 2004 A1
20040103751 Joseph et al. Jun 2004 A1
20040109523 Singh et al. Jun 2004 A1
20040119064 Narayan et al. Jun 2004 A1
20040127586 Jin et al. Jul 2004 A1
20040166036 Chen et al. Aug 2004 A1
20040167009 Kuntz et al. Aug 2004 A1
20040176246 Shirk et al. Sep 2004 A1
20040208805 Fincke et al. Oct 2004 A1
20040213998 Hearley et al. Oct 2004 A1
20040238345 Koulik et al. Dec 2004 A1
20040251017 Pillion et al. Dec 2004 A1
20040251241 Blutke et al. Dec 2004 A1
20050000321 O'Larey et al. Jan 2005 A1
20050000950 Schroder et al. Jan 2005 A1
20050066805 Park et al. Mar 2005 A1
20050070431 Alvin et al. Mar 2005 A1
20050077034 King Apr 2005 A1
20050097988 Kodas et al. May 2005 A1
20050106865 Chung et al. May 2005 A1
20050133121 Subramanian et al. Jun 2005 A1
20050163673 Johnson et al. Jul 2005 A1
20050199739 Kuroda et al. Sep 2005 A1
20050220695 Abatzoglou et al. Oct 2005 A1
20050227864 Sutorik et al. Oct 2005 A1
20050233380 Pesiri et al. Oct 2005 A1
20050240069 Polverejan et al. Oct 2005 A1
20050258766 Kim Nov 2005 A1
20050275143 Toth Dec 2005 A1
20060051505 Kortshagen et al. Mar 2006 A1
20060068989 Ninomiya et al. Mar 2006 A1
20060094595 Labarge May 2006 A1
20060096393 Pesiri May 2006 A1
20060105910 Zhou et al. May 2006 A1
20060108332 Belashchenko May 2006 A1
20060153728 Schoenung et al. Jul 2006 A1
20060153765 Pham-Huu et al. Jul 2006 A1
20060159596 De La Veaux et al. Jul 2006 A1
20060166809 Malek et al. Jul 2006 A1
20060211569 Dang et al. Sep 2006 A1
20060213326 Gollob et al. Sep 2006 A1
20060222780 Gurevich et al. Oct 2006 A1
20060231525 Asakawa et al. Oct 2006 A1
20070048206 Hung et al. Mar 2007 A1
20070049484 Kear et al. Mar 2007 A1
20070063364 Hsiao et al. Mar 2007 A1
20070084308 Nakamura et al. Apr 2007 A1
20070084834 Hanus et al. Apr 2007 A1
20070087934 Martens et al. Apr 2007 A1
20070163385 Takahashi et al. Jul 2007 A1
20070173403 Koike et al. Jul 2007 A1
20070178673 Gole et al. Aug 2007 A1
20070221404 Das et al. Sep 2007 A1
20070253874 Foret Nov 2007 A1
20070292321 Plischke et al. Dec 2007 A1
20080006954 Yubuta et al. Jan 2008 A1
20080026041 Tepper et al. Jan 2008 A1
20080031806 Gavenonis et al. Feb 2008 A1
20080038578 Li Feb 2008 A1
20080045405 Beutel et al. Feb 2008 A1
20080047261 Han et al. Feb 2008 A1
20080057212 Dorier et al. Mar 2008 A1
20080064769 Sato et al. Mar 2008 A1
20080104735 Howland May 2008 A1
20080105083 Nakamura et al. May 2008 A1
20080116178 Weidman May 2008 A1
20080125308 Fujdala et al. May 2008 A1
20080125313 Fujdala et al. May 2008 A1
20080138651 Doi et al. Jun 2008 A1
20080175936 Tokita et al. Jul 2008 A1
20080187714 Wakamatsu et al. Aug 2008 A1
20080206562 Stucky et al. Aug 2008 A1
20080207858 Kowaleski et al. Aug 2008 A1
20080248704 Mathis et al. Oct 2008 A1
20080274344 Vieth et al. Nov 2008 A1
20080277092 Layman et al. Nov 2008 A1
20080277264 Sprague Nov 2008 A1
20080277266 Layman et al. Nov 2008 A1
20080277267 Biberger et al. Nov 2008 A1
20080277268 Layman Nov 2008 A1
20080277269 Layman et al. Nov 2008 A1
20080277270 Biberger Nov 2008 A1
20080277271 Layman et al. Nov 2008 A1
20080280049 Kevwitch et al. Nov 2008 A1
20080280751 Harutyunyan et al. Nov 2008 A1
20080280756 Biberger Nov 2008 A1
20080283411 Eastman et al. Nov 2008 A1
20080283498 Yamazaki Nov 2008 A1
20090010801 Murphy et al. Jan 2009 A1
20090054230 Veeraraghavan et al. Feb 2009 A1
20090088585 Schammel et al. Apr 2009 A1
20090092887 McGrath et al. Apr 2009 A1
20090098402 Kang et al. Apr 2009 A1
20090114568 Trevino et al. May 2009 A1
20090162991 Beneyton et al. Jun 2009 A1
20090168506 Han et al. Jul 2009 A1
20090170242 Lin et al. Jul 2009 A1
20090181474 Nagai Jul 2009 A1
20090200180 Capote et al. Aug 2009 A1
20090208367 Calio et al. Aug 2009 A1
20090209408 Kitamura et al. Aug 2009 A1
20090223410 Jun et al. Sep 2009 A1
20090253037 Park et al. Oct 2009 A1
20090274903 Addiego Nov 2009 A1
20090286899 Hofmann et al. Nov 2009 A1
20090324468 Golden et al. Dec 2009 A1
20100089002 Merkel Apr 2010 A1
20100092358 Koegel et al. Apr 2010 A1
20100124514 Chelluri et al. May 2010 A1
20100166629 Deeba Jul 2010 A1
20100180581 Grubert et al. Jul 2010 A1
20100180582 Mueller-Stach et al. Jul 2010 A1
20100186375 Kazi et al. Jul 2010 A1
20100240525 Golden et al. Sep 2010 A1
20100275781 Tsangaris Nov 2010 A1
20110006463 Layman Jan 2011 A1
20110052467 Chase et al. Mar 2011 A1
20110143041 Layman et al. Jun 2011 A1
20110143915 Yin et al. Jun 2011 A1
20110143916 Leamon Jun 2011 A1
20110143926 Yin et al. Jun 2011 A1
20110143930 Yin et al. Jun 2011 A1
20110143933 Yin et al. Jun 2011 A1
20110144382 Yin et al. Jun 2011 A1
20110152550 Grey et al. Jun 2011 A1
20110158871 Arnold et al. Jun 2011 A1
20110174604 Duesel et al. Jul 2011 A1
20110243808 Fossey et al. Oct 2011 A1
20110245073 Oljaca et al. Oct 2011 A1
20110247336 Farsad et al. Oct 2011 A9
20110305612 Müller-Stach et al. Dec 2011 A1
20120023909 Lambert et al. Feb 2012 A1
20120045373 Biberger Feb 2012 A1
20120097033 Arnold et al. Apr 2012 A1
20120122660 Andersen et al. May 2012 A1
20120124974 Li et al. May 2012 A1
20120171098 Hung et al. Jul 2012 A1
20120308467 Carpenter et al. Dec 2012 A1
20130213018 Yin et al. Aug 2013 A1
20130280528 Biberger Oct 2013 A1
20130281288 Biberger et al. Oct 2013 A1
20130316896 Biberger Nov 2013 A1
20130345047 Biberger et al. Dec 2013 A1
20140018230 Yin et al. Jan 2014 A1
Foreign Referenced Citations (47)
Number Date Country
1 134 302 Sep 2001 EP
1 619 168 Jan 2006 EP
1 307 941 Feb 1973 GB
56-146804 Nov 1981 JP
61-086815 May 1986 JP
62-102827 May 1987 JP
63-214342 Sep 1988 JP
1-164795 Jun 1989 JP
05-228361 Sep 1993 JP
05-324094 Dec 1993 JP
6-93309 Apr 1994 JP
6-135797 May 1994 JP
6-272012 Sep 1994 JP
H6-065772 Sep 1994 JP
7031873 Feb 1995 JP
07-256116 Oct 1995 JP
8-158033 Jun 1996 JP
10-130810 May 1998 JP
11-502760 Mar 1999 JP
2000-220978 Aug 2000 JP
2002-88486 Mar 2002 JP
2002-336688 Nov 2002 JP
2003-126694 May 2003 JP
2004-233007 Aug 2004 JP
2004-249206 Sep 2004 JP
2004-290730 Oct 2004 JP
2005-503250 Feb 2005 JP
2005-122621 May 2005 JP
2005-218937 Aug 2005 JP
2005-342615 Dec 2005 JP
2006-001779 Jan 2006 JP
2006-508885 Mar 2006 JP
2006-247446 Sep 2006 JP
2006-260385 Sep 2006 JP
2007-46162 Feb 2007 JP
2007-203129 Aug 2007 JP
493241 Mar 1976 SU
200611449 Apr 2006 TW
201023207 Jun 2010 TW
WO-9628577 Sep 1996 WO
WO 02092503 Nov 2002 WO
WO 2004052778 Jun 2004 WO
WO-2005063390 Jul 2005 WO
WO 2006079213 Aug 2006 WO
WO-2008130451 Oct 2008 WO
WO-2008130451 Oct 2008 WO
WO-2011081833 Jul 2011 WO
Non-Patent Literature Citations (80)
Entry
21 C.F. R. § 113, Thermally Processed Lowacid Foods Packaged in Hermetically Sealed Containers.
Derwent English Abstract for publication No. SU 193241 A, Application No. 1973SU1943286 filed on Jul. 2, 1973, published on Mar. 1, 1976, entitled“Catalyst for Ammonia Synthesis Contains Oxides of Aluminium, Potassium, Calcium, Iron and Nickel Oxide for Increased Activity,” 3 pgs.
A. Gutsch et al., “Gas-Phase Production of Nanoparticles”, Kona No. 20, 2002, pp. 24-37.
Dr. Heike Mühlenweg et al., “Gas-Phase Reactions—Open Up New Roads to Nanoproducts”, Degussa ScienceNewsletter No. 08, 2004, pp. 12-16.
Coating Generation: Vaporization of Particles in Plasma Spraying and Splat Formation, M. Vardelle, A. Vardelle, K-I li, P. Fauchais, Universite de Limoges, 123 Avenue A. Thomas 87000, Limoges, F. , Pure & Chem, vol. 68, No. 5, pp. 1093-1099, 1996.
H. Konrad et al., “Nanostructured Cu—Bi Alloys Prepared by Co-Evaporation in a Continuous Gas Flow,” NanoStructured Materials, vol. 7, No. 6, 1996, pp. 605-610.
Kenvin et al. “Supported Catalysts Prepared from Mononuclear Copper Complexes: Catalytic Properties”, Journal of Catalysis, pp. 81-91,(1992).
J. Heberlein, “New Approaches in Thermal Plasma Technology”, Pure Appl. Chem., vol. 74, No. 3, 2002, pp. 327-335.
M. Vardelle et al., “Experimental Investigation of Powder Vaporization in Thermal Plasma Jets,” Plasma Chemistry and Plasma Processing, vol. 11, No. 2, Jun. 1991, pp. 185-201.
National Aeronautics and Space Administration, “Enthalpy”, http://www.grc.nasa.gov/WWW/K-12/airplane/enthalpy.html, Nov. 23, 2009, 1 page.
P. Fauchais et al., “Plasma Spray: Study of the Coating Generation,” Ceramics International, Elsevier, Amsterdam, NL, vol. 22, No. 4, Jan. 1996, pp. 295-303.
P. Fauchais et al., “Les Dépôts Par Plasma Thermique,” Revue Generale De L'Electricitie, RGE. Paris, FR, No. 2, Jan. 1993, pp. 7-12.
P. Fauchais et al, “La Projection Par Plasma: Une Revue,” Annales De Physique, vol. 14, No. 3, Jun. 1989, pp. 261-310.
T. Yoshida, “The Future of Thermal Plasma Processing for Coating”, Pure & Appl. Chem., vol. 66, No. 6, 1994 pp. 1223-1230.
Hanet al., Deformation Mechanisms and Ductility of Nanostructured Al Alloys, Mat. Res. Soc. Symp. Proc. vol. 821, Jan. 2004, Material Research Society, http://www.mrs.org/s—mrs/bin.asp?CID=2670&DOC=FILE.PDF., 6 pages.
Nagai, Yasutaka, et al., “Sintering Inhibition Mechanism of Platinum Supported on Ceria-based Oxide and Pt-oxide-support Interaction,” Journal of Catalysis 242 (2006), pp. 103-109, Jul. 3, 2006, Elsevier.
Babin, A. et al. (1985). “Solvents Used in the Arts,” Center for Safety in the Arts: 16 pages.
Bateman, J. E. et al. (Dec. 17, 1998). “Alkylation of Porous Silicon by Direct Reaction with Alkenes and Alkynes,” Angew. Chem Int. Ed. 37(19):2683-2685.
Carrot, G. et al. (Sep. 17, 2002). “Surface-Initiated Ring-Opening Polymerization: A Versatile Method for Nanoparticle Ordering,” Macromolecules 35(22):8400-8404.
Chen, H.-S. et al. (Jul. 3, 2001). “On the Photoluminescence of Si Nanoparticles,” Mater. Phys. Mech. 4:62-66.
Chen, W.-J. et al. (Mar. 18, 2008). “Functional Fe3O4/TiO2 Core/Shell Magnetic Nanoparticles as Photokilling Agents for Pathogenic Bacteria,” Small 4(4): 485-491.
Faber, K. T. et al. (Sep. 1988). “Toughening by Stress-Induced Microcracking in Two-Phase Ceramics,” Journal of the American Ceramic Society 71: C-399-C401.
Fojtik, A. et al. (Apr. 29, 1994). “Luminescent Colloidal Silicon Particles,” Chemical Physics Letters 221 :363-367.
Fojtik, A. (Jan. 13, 2006). “Surface Chemistry of Luminescent Colloidal Silicon Nanoparticles,” J. Phys. Chem. B. 110(5):1994-1998.
Gangeri, M. et al. (2009). “Fe and Pt Carbon Nanotubes for the Electrocatalytic Conversion of Carbon Dioxide to Oxygenates,” Catalysis Today 143: 57-63.
Hua, F. et al. (Mar. 2006). “Organically Capped Silicon Nanoparticles With Blue Photoluminescence Prepared by Hydrosilylation Followed by Oxidation,” Langmuir 22(9):4363-4370.
Ji, Y. et al. (Nov. 2002) “Processing and Mechanical Properties of Al2O3—5 vol.% Cr Nanocomposites,” Journal of the European Ceramic Society 22(12):1927-1936.
Jouet, R. J. et al. (Jan. 25, 2005). “Surface Passivation of Bare Aluminum Nanoparticles Using Perfluoroalkyl Carboxylic Acids,” Chem. Mater.17(11):2987-2996.
Kim, N. Y. et al. (Mar. 5, 1997). “Thermal Derivatization of Porous Silicon with Alcohols,” J. Am. Chem. Soc. 119(9):2297-2298.
Kwon, Y.-S. et al. (Apr. 30, 2003). “Passivation Process for Superfine Aluminum Powders Obtained by Electrical Explosion of Wires,” Applied Surface Science 211:57-67.
Langner, A. et al. (Aug. 25, 2005). “Controlled Silicon Surface Functionalization by Alkene Hydrosilylation,” J. Am. Chem. Soc. 127(37):12798-12799.
Li, D. et al. (Apr. 9, 2005). “Environmentally Responsive “Hairy” Nanoparticles: Mixed Homopolymer Brushes on Silica Nanoparticles Synthesized by Living Radical Polymerization Techniques,” J. Am. Chem. Soc. 127(7):6248-6256.
Li, X. et al. (May 25, 2004). “Surface Functionalization of Silicon Nanoparticles Produced by Laser-Driven Pyrolysis of Silane Followed by HF—HNO3 Etching,” Langmuir 20(11):4720-4727.
Liao, Y.-C. et al. (Jun. 27, 2006). “Self-Assembly of Organic Monolayers on Aerosolized Silicon Nanoparticles,” J.Am. Chem. Soc. 128(28):9061-9065.
Liu, S.-M. et al. (Jan. 13, 2006). “Enhanced Photoluminescence from Si Nano-Organosols by Functionalization With Alkenes and Their Size Evolution,” Chem. Mater. 18(3):637-642.
Luo, J. et al. (2008). “Core/Shell Nanoparticles as Electrocatalysts for Fuel Cell Reactions,” Advanced Materials 20: 4342-4347.
Mignard, D. et al. (2003). “Methanol Synthesis from Flue-Gas CO2 and Renewable Electricity: A Feasibility Study,” International Journal of Hydrogen Energy 28: 455-464.
Neiner, D. (Aug. 5, 2006). “Low-Temperature Solution Route to Macroscopic Amounts of Hydrogen Terminated Silicon Nanoparticles,” J. Am. Chem. Soc. 128:11016-11017.
Netzer, L. et al. (1983). “A New Approach to Construction of Artificial Monolayer Assemblies,” J. Am. Chem. Soc. 105(3):674-676.
Park, H.-Y. et al. (May 30, 2007). “Fabrication of Magnetic Core@Shell Fe Oxide@Au Nanoparticles for Interfacial Bioactivity and Bio-Separation,” Langmuir 23: 9050-9056.
Park, N.-G. et al. (Feb. 17, 2004). “Morphological and Photoelectrochemical Characterization of Core-Shell Nanoparticle Films for Dye-Sensitized Solar Cells: Zn—O Type Shell on SnO2 and TiO2 Cores,” Langmuir 20: 4246-4253.
“Plasma Spray and Wire Flame Spray Product Group,” located at http://www.processmaterials.com/spray.html, published by Process Materials, Inc., last accessed Aug. 5, 2013, 2 pages.
“Platinum Group Metals: Annual Review 1996” (Oct. 1997). Engineering and Mining Journal, p. 63.
Rahaman, R. A. et al. (1995). “Synthesis of Powders,” in Ceramic Processing and Sintering. Marcel Decker, Inc., New York, pp. 71-77.
Sailor, M. J. (1997). “Surface Chemistry of Luminescent Silicon Nanocrystallites,” Adv. Mater. 9(10):783-793.
Subramanian, S. et al. (1991). “Structure and Activity of Composite Oxide Supported Platinum—Iridium Catalysts,” Applied Catalysts 74: 65-81.
Tao, Y.-T. (May 1993). “Structural Comparison of Self-Assembled Monolayers of n-Alkanoic Acids on the surfaces of Silver, Copper, and Aluminum,” J. Am. Chem. Soc. 115(10):4350-4358.
Ünal, N. et al. (Nov. 2011). “Influence of WC Particles on the Microstructural and Mechanical Properties of 3 mol% Y2O3 Stabilized ZrO2 Matrix Composites Produced by Hot Pressing,” Journal of the European Ceramic Society (31)13: 2267-2275.
Zou, J. et al. (Jun. 4, 2004). “Solution Synthesis of Ultrastable Luminescent Siloxane-Coated Silicon Nanoparticles,” Nano Letters 4(7):1181-1186.
U.S. Appl. No. 13/291,983, filed Nov. 8, 2011, for Layman et al.
U.S. Appl. No. 12/152,084, filed May 9, 2008, for Biberger.
U.S. Appl. No. 13/028,693, filed Feb. 16, 2011, for Biberger.
U.S. Appl. No. 12/943,909, filed Nov. 10, 2010, for Layman.
U.S. Appl. No. 12/152,111, filed May 9, 2008, for Biberger et al.
U.S. Appl. No. 12/151,830, filed May 8, 2008, for Biberger et al.
U.S. Appl. No. 12/968,248, filed Dec. 14, 2010, for Biberger.
U.S. Appl. No. 12/968,245, filed Dec. 14, 2010, for Biberger.
U.S. Appl. No. 12/968,241, filed Dec. 14, 2010, for Biberger.
U.S. Appl. No. 12/968,239, filed Dec. 14, 2010, for Biberger.
U.S. Appl. No. 12/969,128, filed Dec. 15, 2010, for Biberger.
U.S. Appl. No. 12/962,463, filed Dec. 7, 2010, for Leamon.
U.S. Appl. No. 12/961,030, filed Dec. 6, 2010, for Lehman.
U.S. Appl. No. 12/961,108, filed Dec. 6, 2010, for Lehman.
U.S. Appl. No. 12/961,200, filed Dec. 6, 2010, for Lehman.
U.S. Appl. No. 12/968,253, filed Dec. 14, 2010, for Biberger.
U.S. Appl. No. 12/968,235, filed Dec. 14, 2010, for Biberger.
U.S. Appl. No. 12/969,306, filed Dec. 15, 2010, for Lehman et al.
U.S. Appl. No. 12/969,447, filed Dec. 15, 2010, for Biberger et al.
U.S. Appl. No. 12/969,087, filed Dec. 15, 2010, for Biberger.
U.S. Appl. No. 12/962,533, filed Dec. 7, 2010, for Yin et al.
U.S. Appl. No. 12/962,523, filed Dec. 7, 2010, for Yin et al.
U.S. Appl. No. 12/001,643, filed Dec. 11, 2007, for Biberger et al.
U.S. Appl. No. 12/474,081, filed May 28, 2009, for Biberger et al.
U.S. Appl. No. 12/001,602, filed Dec. 11, 2007, for Biberger et al.
U.S. Appl. No. 12/001,644, filed Dec. 11, 2007, for Biberger et al.
U.S. Appl. No. 12/954,813, filed Nov. 26, 2010, for Biberger.
U.S. Appl. No. 12/954,822, filed Nov. 26, 2010, for Biberger.
U.S. Appl. No. 13/033,514, filed Feb. 23, 2011, for Biberger et al.
U.S. Appl. No. 13/589,024, filed Aug. 17, 2012, for Yin et al.
U.S. Appl. No. 13/801,726, filed Mar. 13, 2013, for Qi et al.
Provisional Applications (1)
Number Date Country
61284329 Dec 2009 US