This disclosure relates to thermoelectric devices and fabrication methods of the said thermoelectric devices.
Thermoelectric generation is a technology for directly converting thermal energy into electric energy using the Seebeck effect, i.e. a phenomenon in which an electromotive force is generated in proportion to a temperature difference created between opposite ends of a substance. This technology has been described in United States Patent Publication Number 2008/0230107; United States Patent Publication Number 2008/0303375; United States Patent Publication Number 20110094556; United States Patent Publication Number 2011/0126874; United States Patent Publication Number 2014/0102501; U.S. Pat. No. 7,601,909. However, often times the device may not be flexible, which limits the possible applications or introduces complexities into manufacturing.
Thus, there is a need to enhance the utility of thermoelectric devices by reducing the thickness of the device, and/or increasing the flexibility of the device. In addition, since there are such multitudes of uses, there is a need for a manufacturing method to cheaply and rapidly manufacture flexible thermoelectric devices.
Methods for making thermoelectric devices may help to improve the flexibility of the thermoelectric device. Some embodiments include orienting alternating semiconductors orthogonally to the flow of electricity.
In some embodiments, a method for making a thermoelectric device is described, the method comprising (1) providing a sheet of alternating rows of parallel columns of p- or n-type thermoelectric materials; and (2) electrically communicating the parallel columns such that within each row the columns are connected in parallel but the rows are connected in series. In some embodiments, the p-type thermoelectric materials can comprise Bi0.5Sb1.5Te3. In some embodiments, the n-type thermoelectric materials can comprise Bi2Se0.3Te2.7. In some embodiments, both p-type and n-type thermoelectric materials also comprise poly(vinylidene fluoride co-hexafluoro-propylene) or P(VDF-HFP). In some embodiments, providing a sheet of alternating rows of parallel columns of p- or n-type thermoelectric materials comprises creating p- or n-type thermoelectric material strips by: (1) hot pressing either p- or n-type thermoelectric materials at 600 MPa to 1000 MPa, at 100° C. to 250° C., for 1 hour to 12 hours and (2) annealing the resulting materials at 275° C. to 400° C. for 30 minutes to 6 hours in a reducing atmosphere.
In some embodiments, providing a sheet of alternating rows of parallel columns of p- or n-type thermoelectric materials comprises placing alternate p- and n-type thermoelectric material strips in parallel and substantially equidistant from one another on a planar surface. In some embodiments, providing a sheet of alternating columns of parallel sheets of p- or n-type thermoelectric materials comprises affixing the alternative p- and n-type materials in parallel and substantially equidistant from one another relationship/position. In some embodiments, providing a sheet of alternating columns of parallel sheets of p- or n-type thermoelectric materials comprises stacking plural sheets to overlap like p- and n-type material on adjacent sheets. In some embodiments, providing a sheet of alternating columns of parallel sheets of p- or n-type thermoelectric materials comprises laminating the stack of plural sheets while retaining the alternative p- and n-type sheets spatial relationships at a temperature between 60° C. to 100° C. for 15 minutes to 45 minutes. In some embodiments, providing a sheet of alternating columns of parallel sheets of p- or n-type thermoelectric materials comprises subsequently curing the stack of plural sheets while retaining the alternative p- and n-type sheets spatial relationships at a temperature between 100° C. to 200° C. for 15 minutes to 45 minutes. In some embodiments, providing a sheet of alternating columns of parallel sheets of p- or n-type thermoelectric materials comprises slicing the stacked plural sheets in an orthogonal orientation to the stacked to create plural thermoelectric sheets.
In some embodiments a thermoelectric sheet device can be described, the device made according to the aforementioned processes. In some embodiments, the device made according to the aforementioned processes is flexible. In some embodiments, a thermoelectric sheet device can be described, the device comprising alternating rows of parallel columns of p- or n-type materials, where said columns within each row are connected electrically in parallel and alternating rows are electrically serially connected.
These and other embodiments are described in more detail herein.
An element may be described as ribbon-shaped if it has a shape that is reasonably recognizable as similar to the shape of a ribbon. This may include elements and/or articles that have a flat rectangular surface that is elongated in one dimension and thin in another dimension. The ribbon shape may also be curved or twisted, so that the element need not be substantially coplanar to be ribbon-shaped.
An element may also be described as pseudoplanar. The term “pseudoplanar” is a broad term that includes elements that are essentially planar. For example, a pseudoplanar article may have a z dimension that is relatively insignificant as compared to the x-y area of the particle that is substantially in the x-y plane.
An element may also be described as “rigid.” The term “rigid” is meant that the material cannot be significantly deformed without observing the formation of cracks or rupture in the monolithic material. In particular, this means that the monolithic material cannot be rolled.
An element may also be described as “flexible.” The term “flexible” is meant that the material can be deformed, in particular wound.
In some embodiments, a method for making a thermoelectric device can be described, the method comprising: providing a sheet of rows of parallel spaced apart columns, or ribbons, of thermoelectric materials, where the thermoelectric materials can comprise p- and/or n-type thermoelectric materials forming alternating rows of parallel spaced apart ribbons of thermoelectric p- and/or n-type materials, and electrically communicating the rows in series. In some embodiments, the method can also comprise electrically communicating the parallel columns such that within each row the columns are connected in parallel.
In some embodiments, the method can further comprise first making thermoelectric materials, where making comprises: (1) preparing a thermoelectric powder, creating a thermoelectric slurry, (2) forming the slurry to create a thermoelectric form, and then (3) sintering the form to create a thermoelectric material. In some embodiments, the method varies according to whether the material being made is p-type or n-type (i.e., p-type thermoelectric materials or n-type thermoelectric materials). In some embodiments, the method does not vary rather only the chemical ratios, or inputs into the process.
In some embodiments, the thermoelectric materials described herein can include p-type and/or n-type materials (i.e., p-type thermoelectric materials or n-type thermoelectric materials). In some embodiments the thermoelectric materials can comprise inorganic compounds. In some embodiments, the inorganic compounds may have a suitable crystallinity. In some embodiments, the thermoelectric material, compound or element can comprise bismuth (Bi), antimony (Sb), tellurium (Te), and/or selenium (Se). For example, a formula of the inorganic compound may be A2M3 (wherein, A is Bi and/or Sb, and M is Te and/or Se). For example, when a Bi—Te based thermoelectric material is used, thermoelectric performance at around room temperature may be excellent. In some embodiments the inorganic compound can be Bi—Te, Bi—Sb—Te, Bi—Se—Te, or Pb—Ge—Se. In some embodiments, the inorganic compound can be Bi2Te3, Bi0.5Sb1.5Te3 and/or Bi2Se0.3Te2.7. In some embodiments, the p-type material can comprise Bi0.5Sb1.5Te3. In some embodiments, the n-type material can comprise Bi2Se0.3Te2.7.
In some embodiments, preparing a thermoelectric powder can include mechanically alloying elemental powders to form an alloy. In some embodiments, the thermoelectric powder, or p-type and/or n-type material in powered form, can be synthesized starting from the respective elemental materials, e.g., Bi, Sb, Se and Te, using a mechanical alloying ball mill process that results in an ultra fine powder. In some embodiments, Bi, Sb and/or Te, can be ball-milled in molar fractions corresponding to either p-type or n-type materials. In some embodiments, the ball milling can last for at least about 16 hours to at least about 110 hours, or such that the materials have formed their requisite alloy (e.g. Bi0.5Sb1.5Te3 for p-type and/or Bi2Se0.3Te2.7 for n-type). In some embodiments, ball milling the elemental materials to form an alloy can be between about 500 rpm to about 5000 rpm, or about 1500 rpm. In some embodiments, for the p-type material, the ball milling can be done for at least about 80 hours, at least about 85 hours, at least about 90 hours, at least about 100 hours, at least about 110 hours or any value within that range, for example about 96 hours. The result is a p-type alloy. In some embodiments, for the n-type material, the ball milling can be done for at least about 16 hours, at least about 18 hours, at least about 20 hours, at least about 22 hours, at least about 24 hours or any value within that range, for example about 20 hours. The result is an n-type alloy. In some embodiments, the ball milling can be under a non-oxidizing atmosphere to reduce the oxidizing of the materials. In some embodiments, the non-oxidizing atmosphere can comprise between about 94% to about 100% inert gas and about 0% to about 6% reducing gas. In some embodiments, the inert gas can be argon, or nitrogen. In some embodiments, the reducing gas can be hydrogen and/or oxygen. In one illustrative embodiment, the ball milling process can be conducted in an argon environment with oxygen concentration under about 200 ppm. Associated with the ball milling process, chemical reactions between Bi, Sb and/or Te; Bi, Se, Te powders take place to form the alloys, e.g., Bi0.5Sb1.5Te3 and/or Bi2Se0.3Te2.7, in an ultra fine powder form with an average particle size of about 10 nm to about 100 μm, or about 10 nm to about 1 μm, for example about 100 nm. In one illustrative embodiment, the reacted powders are handled in a non-oxidizing environment to prevent oxidation of the semiconductor material prior to the sintering process.
In some embodiments, preparing a thermoelectric powder can further comprise ball milling the alloys to mechanically alloyed powders. In some embodiments, the elemental Bi, Sb, Se and/or Te semiconductor can be ball-milled a time and/or manner sufficient to effect the aforedescribed median size description. In some embodiments, preparing a thermoelectric powder further comprises reducing the semiconductor size population to the aforedescribed ranges, e.g., a median size of about 0.4 μm to about 0.6 μm. In some embodiments, the aforementioned ranges are achieved by ball milling the semiconductor between about 5 hours to about 25 hours, e.g., about 17 hours. In some embodiments, the aforementioned ranges are achieved by ball milling the semiconductor between about 500 rpm to about 5000 rpm, about 1500 rpm. In some embodiments, the aforementioned ranges are achieved by ball milling the semiconductor between about 500 rpm to about 5000 rpm, about 1500 rpm for between about 5 hours to about 25 hours, e.g., about 17 hours.
In some embodiments, the alloys can be acoustically mixed at any one or more intermediate process points before the coating step to average the molecular sizes to help uniformity where there are multiple batches being processed. In some embodiments, acoustic mixing can be for about 10 minutes to about 1 hour, or about 30 minutes. In some embodiments, acoustic mixing can be such that the variation between the mean particle sizes for different samples is less than 10%.
In some embodiments, making thermoelectric materials comprises creating a thermoelectric slurry. In some embodiments, forming the slurry comprises mixing the polymer with the alloy to create a thermoelectric composite. In some embodiments, the alloy can be a p-type material or an n-type material. In some embodiments, the slurry can comprise the aforementioned alloys dispersed within the polymer media. In some embodiments, the polymer can comprise a thermoplastic polymer. In some embodiments, the polymer can be a fluoroelastomer. In some embodiments, the fluoroelastomer can comprise polyvinylidene fluoride (PVDF). In some embodiments, the fluoroelastomer can be a copolymer system comprising vinylidene fluoride and hexapfluoropropylene (VDF/HFP), or poly(vinylidene fluoride co-hexafluoro-propylene) (P(VDF-HFP)). In some embodiments, the fluoroelastomer can comprise PVDF and poly(vinylidene fluoride co-hexafluoro-propylene) (P(VDF-HFP)). In some embodiments, the copolymer system of can comprise vinylidene fluoride and (at least 20%) hexafluoropropylene. In some embodiments, the fluoroelastomer can comprise tetrafluoroethylene (TFE)/propylene. In some embodiments, the fluorelasomer can be TFE/PMVE (perfluoromethylvinyl ether), which creates a perfluorinated fluoroelastomer. In some embodiments, the mass ratio of polymer to alloy can range from about 3:17 to about 3:7, or about 1:3. In some embodiments, the mixture can then be mixed acoustically for about 10 minutes to about 1 hour, or about 30 minutes. In some embodiments, the mixture can also be sonicated for a time ranging from about 30 minutes to about 4 hours, or about 2 hours, to help ensure a uniform mixture. In some embodiments, the slurry can comprise an organic solvent. In some embodiments, the organic solvent can be dimethylformamide (DMF). The result is a thermoelectric slurry.
In some embodiments, forming the slurry to create a thermoelectric form can comprise depositing the slurry on a substrate. In some embodiments, the substrate can comprise an elastomer. In some embodiments, the elastomer can comprise poly(ethylene-vinyl acetate) (PEVA). In some embodiments, the substrate only provides support for the slurry until curing. In other embodiments, the slurry is permanently bonded to the substrate. In some embodiments, depositing the slurry upon the substrate can be by blade coating, spray coating, dip coating, spin coating, tape casting, or other methods known by those skilled in the art. In some embodiments, the resulting coating can have a wet thickness ranging from about 100 μm to about 0.1 mm, or about 400 μm. In some embodiments, the resulting coating can have a dry coating of about 25 μm to about 500 μm, or about 50 μm. The result is a thermoelectric form.
In some embodiments the thermoelectric material can be created by sintering the thermoelectric form. In some embodiments, sintering can be accomplished in two steps: hot pressing and then annealing. In some embodiments, hot pressing the thermoelectric form comprises heating the form in an oven at a temperature ranging between 100° C. to 250° C. In some embodiments, hot pressing the thermoelectric form comprises heating the form at a pressure ranging from about 600 MPa to about 1000 MPa, or 850 MPa. In some embodiments, hot pressing the thermoelectric form can last for a time period between about 1 hour to about 12 hours, or about 2 hours to about 8 hours, or about 4 hours. The result is a pressed form. In some embodiments, the pressed form can then be annealed. In some embodiments, the annealing is performed under a reducing atmosphere. In some embodiments, the reducing atmosphere can be an atmosphere of mixed gas of nitrogen gas (N2) and hydrogen gas (H2). In some embodiments, the atmosphere can comprise a 97% N2/3% H2 atmosphere. In some embodiments, annealing can be done for a duration ranging from about 30 minutes to about 6 hours, or about 1 hour to about 4 hours, or about 2 hours. In some embodiments, annealing can be done at a temperature of between about 275° C. to about 400° C. In some embodiments, for p-type material, the annealing can be done at a temperature of about 275° C. to about 400° C., or about 375° C. For p-type materials chosen, although performance appears to increase as a function of temperature, higher temperatures result in a more brittle material. In some embodiments, for n-type material, the annealing can be done at a temperature of about 275° C. to about 400° C., or about 325° C. For n-type materials chosen, the thermoelectric form performance appears to peak around 325° C. The result is a thermoelectric material.
In some embodiments, the method can further comprise cutting the thermoelectric materials to create p- or n-type thermoelectric material strips. Cutting can be by any method known by those skilled in the art, including but not limited to: mechanical sawing (e.g. cutting by blade, saw, and the like), electrochemical sawing (e.g. etching, electrical discharge machining), or thermal (e.g. laser, flame cutting, plasma cutting). The result is p- or n-type thermoelectric material strips.
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In some embodiments, the variation in distance between adjacent ribbons can be sufficient to prevent short circuiting between adjacent ribbons. For example, in some embodiments, for a 5 mm wide ribbon, the distance between the adjacent ribbons can be 2.5 mm. In some embodiments, the distance between adjacent ribbons of similar material can be about 100 μm. In some embodiments, the variation in the distance between adjacent ribbons of differing materials, e.g., p-type and n-type materials can be less than 25% of the width of the ribbon element. In some embodiments, an additional planar surface can be optionally applied on top of the alternating rows of parallel spaced apart ribbons of p- or n-type materials.
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In some embodiments, a thermoelectric device for providing electricity from a thermal differential can be described. In some embodiments, the aforementioned device can be made from the aforedescribed methods. In some embodiments, the device can be in the form of a sheet. In some embodiments, the sheet can be a flexible sheet.
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In some embodiments, one of the first electrode and the second electrode may be electrically connected to a power supply, or electrically connected to the outside of a thermoelectric module, for example, to an electric device which consumes or stores electric power, e.g. a battery.
It has been discovered that embodiments of the thermoelectric devices and methods for making the same described herein improve the flexibility and/or thinness of the aforementioned thermoelectric devices. These benefits are further shown by the following examples, which are intended to be illustrative of the embodiments of the disclosure, but are not intended to limit the scope or underlying principles in any way.
Preparation of a thermoelectric metal tape can be carried out in at least two ways: (1) modifying a substrate by adding a thermoelectric coating and then cutting or slicing the resulting composite sheet to obtain a tape or (2) coating pre-sliced substrates. It may be better to coat a large substrate and then to cut the coating into the desired width because it is important that the tape edges are kept clean/bare for electrical communication.
Fabrication of the p-type Thermoelectric Compound (Bi0.5Sb1.5Te3): Elemental shots of Bi (1-12 mm, 99.999%, Aldrich, St. Louis, Mo. USA), Sb (6 mm, 99.999%, Alfa Aesar, Ward Hill, Mass. USA), and Te (4-5 mm, 99.999%, Aldrich) were selected as starting materials for mechanical alloying (MA). MA was carried out in a planetary ball mill machine (SFM-1, MTI Corp., Richmond, Calif. USA) at a rotation speed of 500 rpm. A stainless container (MTI Corp.) with a valve inlet, and stainless balls were utilized. About 15 g of the elemental shots (Bi: 2.34 g, Sb: 4.09 g and Te: 8.57 g) was put in the container with about 162 g stainless steel balls (3 of 20 mm ϕ (33.1 g), 3 of 15 mm ϕ (13.7 g), 6 of 8 mm ϕ (2.1 g) and 10 of 6 mm ϕ (0.9 g)), and then evacuation and argon purging were repeated 5 times to replace the air with argon (Airgas, San Marcos, Calif. USA). Finally, the container was filled with argon (Airgas), and the valve was tightly closed. Four sets of MA were simultaneously performed continuously for 96 hours without interruption. Recovery was greater than 99%. The obtained powder (about 4×15 g) was mixed for 10 minutes in an acoustic mixer (LabRAM, Resodyn Acoustic Mixer, Inc., MT, USA) to average the above 4 sets. The result was a p-type thermoelectric powder.
Fabrication of the n-type Thermoelectric Compound (Bi2Sb0.3Te2.7): Elemental shots of Bi (99.999%, Aldrich), Se (less than 5 mm, 99.999%, Aldrich) and Te (99.999%, Aldrich) were selected as starting materials for MA. MA was carried out in a planetary ball mill machine (SFM-1, MTI Corp.) at a rotation speed of 500 rpm. A stainless container with a valve inlet and stainless steel balls were utilized. About 15 g of the elemental shots (Bi: 7.97 g, Se: 0.45 g and Te: 6.58 g) was put in the container with about 162 g balls (3 of 20 mm ϕ (33.1 g), 3 of 15 mm ϕ (13.7 g), 6 of 8 mm ϕ (2.1 g) and 10 of 6 mm ϕ (0.9 g)), and then evacuation and argon purging were repeated 5 times to replace the air with argon (Airgas). Finally, the container was filled with argon (Airgas), and the valve was tightly closed. Four sets of MA were simultaneously performed continuously for 96 hours without interruption. Recovery was greater than 99%. The obtained powder (about 4×15 g) was acoustically mixed (LabRAM, Resodyn Acoustic Mixer, Inc.) for 10 minutes to average the above 4 sets. The result was an n-type thermoelectric powder.
Ball milling of the powder: The thermoelectric powders were further ball-milled in a sintered corundum container. Each powder was separated into four batches, all batches undergoing the process simultaneously. About 15 g of thermoelectric powder was put in the container with zirconia balls (˜165 pieces of 0.09 g balls and 5 pieces of 0.42 g balls) and 25 mL of 2-propanol (Aldrich), and then ball milling was carried out at a rotation speed of ˜300 rpm for 5 hours. After ball milling, the balls were separated with a strainer, and then dried at 110° C. overnight. The dried thermoelectric powder was then further dried at 100° C. under vacuum conditions for 1 hour. All four batches of 15 g ball-milled powder were then mixed acoustically (LabRAM, Resodyn Acoustic Mixer, Inc.) for 10 minutes to average the batches for each powder.
Creation of the Slurries: A slurry was prepared by mixing the appropriate amount of the thermoelectric powder (p-type or n-type) and the premade binder solution (10-20 wt % of poly(vinylidene fluoride-co-hexafluoropropylene), P-(VDF/HFP) (Aldrich) in dimethylformamid (DMF)) where the mass ratios were about 1:0.075:0.67 (thermoelectric powder:P(VDF-HFP):DMF) The resulting mixture was then placed in an acoustic mixer (LabRAM, Resodyn Acoustic Mixers) for 30 minutes. Then, the resulting mixture was sonicated in a water bath for 2 hours to separate amassed particles. The result was a thermoelectric slurry (p-type or n-type).
Creating a Coating: The thermoelectric slurry (p-type or n-type) was then cast on a releasing substrate, e.g., 0.003″ thick Kapton® HN film (3 mil, CS Hyde Company, Lake Villa, Ill. USA) using a square applicator (Paul N. Gardner Company, Inc., Pompano Beach, Fla. USA) with a gap of 4-15 mil (100-380 μm) at a cast rate of about 5 cm/second. After brief drying in air, the casted film was dried at 100° C. in vacuum for 1 hour. The result was a thermoelectric form (p-type or n-type).
Sintering the Coating to Create a Thermoelectric Form: The thermoelectric forms (p-type or n-type) were then sintered. First, the thermoelectric form was cut into 0.5 cm×2.5 cm, and then was hot-pressed at 150° C. at 800 MPa for 30 second. As a result, an approximately 50 μm thick thermoelectric film was obtained. The film was then annealed in a Pyrex tube in a tube furnace in 97% N2/3% H2 atmosphere at a ramp rate of 3° C./min to 375° C. and held for 2 hours for p-type materials. For n-type materials, the ramp rate was set to 3° C./min to 325° C. and held for 2 hours. The result was a thermoelectric material (p-type or n-type).
Creating a Stack of Plural Sheets: First, the two types of thermoelectric materials, p-type and n-type) were placed in parallel on a PEVA substrate (0.46 mm thick Photocap®, Specialized Technology Resources, Inc., Enfield, Conn. USA) at 75° C. such that they spanned the substrate, alternating material types, with a separation of about 2.5 mm. This process was repeated a total of four times to provide five identical sheets which were then stacked such that the individual strips of thermoelectric materials were stacked on top of each other. The result was a stack of plural sheets.
Laminating to Form one Thermoelectric Stack: Then, the stack of plural sheets was laminated to create one large continuous stack. The sheets were vacuum laminated using a module laminator (LM series, NPC Incorporated, Tokyo, Japan) set to an atmosphere of 0.002 atm at a temperature of 85° C. for 20 minutes. Then, the resulting stack was cured in situ at standard atmosphere at a temperature of about 150° C. for 15 minutes to harden the PEVA. The result was a thermoelectric stack.
Slicing the Stack to Create Multiple Thermoelectric Elements: The thermoelectric stack was then laser-cut in 1 mm thick layers using a laser engraving and cutting system (VLS 2.30, Universal Laser Systems) with a 25 W CO2 laser. The results were thermoelectric sheets.
Electrically Connecting the Thermoelectric Materials to Create Thermoelectric Devices: Then for each sheet, the exposed thermoelectric materials on the surface of the sheets were coated with silver paint (Ted Pella, Redding, Calif. USA) in a manner that connected stacked-like thermoelectric materials in parallel to create rows. Then, the silver paint was further applied between the rows to connect the alternating rows in series. The result was a thermoelectric device.
A thermoelectric device in a setup similar to the schematic depicted in
The following embodiments are specifically contemplated by the authors of the present disclosure:
Unless otherwise indicated, all numbers expressing quantities of ingredients, properties such as molecular weight, reaction conditions, and so forth used in the specification and claims are to be understood as being modified in all instances by the term “about.” Accordingly, unless indicated to the contrary, the numerical parameters set forth in the specification and attached claims are approximations that may vary depending upon the desired properties sought to be obtained. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques.
The terms “a,” “an,” “the” and similar referents used in the context of describing the invention (especially in the context of the following claims) are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., “such as”) provided herein is intended merely to better illuminate the invention and does not pose a limitation on the scope of any claim. No language in the specification should be construed as indicating any non-claimed element essential to the practice of the invention.
Groupings of alternative elements or embodiments disclosed herein are not to be construed as limitations. Each group member may be referred to and claimed individually or in any combination with other members of the group or other elements found herein. It is anticipated that one or more members of a group may be included in, or deleted from, a group for reasons of convenience and/or patentability. When any such inclusion or deletion occurs, the specification is deemed to contain the group as modified thus fulfilling the written description of all Markush groups used in the appended claims.
Certain embodiments are described herein, including the best mode known to the inventors for carrying out the invention. Of course, variations on these described embodiments will become apparent to those of ordinary skill in the art upon reading the foregoing description. The inventor expects skilled artisans to employ such variations as appropriate, and the inventors intend for the invention to be practiced otherwise than specifically described herein. Accordingly, the claims include all modifications and equivalents of the subject matter recited in the claims as permitted by applicable law. Moreover, any combination of the above-described elements in all possible variations thereof is contemplated unless otherwise indicated herein or otherwise clearly contradicted by context.
In closing, it is to be understood that the embodiments disclosed herein are illustrative of the principles of the claims. Other modifications that may be employed are within the scope of the claims. Thus, by way of example, but not of limitation, alternative embodiments may be utilized in accordance with the teachings herein. Accordingly, the claims are not limited to embodiments precisely as shown and described.
This application claims the benefit of U.S. Provisional Application No. 62/376,309, filed Aug. 17, 2016, the contents of which are incorporated herein by reference in their entirety.
Filing Document | Filing Date | Country | Kind |
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PCT/US2017/046986 | 8/15/2017 | WO | 00 |
Number | Date | Country | |
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62376309 | Aug 2016 | US |