Single and multiple-step electrochemical processes are useable to reduce metal-oxides to their corresponding metallic (unoxidized) state. Such processes are conventionally used to recover high purity metal, metals from an impure feed, and/or extract metals from their metal-oxide ores.
Multiple-step processes conventionally dissolve metal or ore into an electrolyte followed by an electrolytic decomposition or selective electro-transport step to recover unoxidized metal. For example, in the extraction of uranium from spent nuclear oxide fuels, a chemical reduction of the uranium oxide is performed at 650° C., using a reductant such as Li dissolved in molten LiCl, so as to produce uranium and Li2O. The solution is then subjected to electro-winning, where dissolved Li2O in the molten LiCl is electrolytically decomposed to regenerate Li. The uranium metal is prepared for further use, such as nuclear fuel in commercial nuclear reactors.
Single-step processes generally immerse a metal oxide in molten electrolyte, chosen to be compatible with the metal oxide, together with a cathode and anode. The cathode electrically contacts the metal oxide and, by charging the anode and cathode (and the metal oxide via the cathode), the metal oxide is reduced through electrolytic conversion and ion exchange through the molten electrolyte.
Single-step processes generally use fewer components and/or steps in handling and transfer of molten salts and metals, limit amounts of free-floating or excess reductant metal, have improved process control, and are compatible with a variety of metal oxides in various starting states/mixtures with higher-purity results compared to multi-step processes.
Example embodiments include modular cathode assemblies useable in electrolytic reduction systems. Example embodiment cathode assemblies include a basket that allows a fluid electrolyte to enter and exit the basket, while the basket is electrically conductive and may transfer electrons to or from an electrolyte in the basket. The basket extends down into an electrolyte from an assembly support having a basket electrical connector to provide electric power to the basket. The basket may be divided into an upper and lower section so as to provide a space where the material to be reduced may be inserted into the lower section and so as to prevent electrolyte or other material or thermal migration up the basket. Example embodiment cathode assemblies are disclosed with a rectangular shape that maximizes electrolyte surface area for reduction, while also permitting easy and modular placement of the assemblies at a variety of positions in reduction systems. Example embodiment modular cathode assemblies also include a cathode plate running down the middle of the basket. The cathode plate is electrically insulated from the basket but is also electrically conductive and provides a primary or reducing current to the material to be reduced in the basket. Thermal and electrical insulating bands or pads may also be placed along a length of the cathode plate to align and seal the basket upper portion with the cathode plate. Example embodiment modular cathode assemblies may have one or more standardized electrical connectors through which unique electrical power may be provided to the basket and plate. For example, the electrical connectors may have a same knife-edge shape that can electrically and mechanically connect modular cathode assemblies at several positions of electrical contacts having corresponding shapes.
Example embodiment modular cathode assemblies are useable in electrolytic oxide reduction systems where they may be placed at a variety of desired positions. Example embodiment modular cathode assembly may be supported by a top plate above an opening into the electrolyte container. Electrolytic oxide reduction systems may provide a series of standardized electrical contacts that may provide power to both baskets and cathode plates at several desired positions in the system. Example methods include operating an electrolytic oxide reduction system by positioning modular cathode and anode assemblies at desired positions, placing a material to be reduced in the basket, and charging the modular cathode and anode assemblies through the electrical connectors so as to reduce the metal oxide and free oxygen gas. The electrolyte may be fluidized in example methods so that the anodes, basket, and material to be reduced in the basket extend into the electrolyte. Additionally, unique levels and polarities of electrical power may be supplied to each of the modular cathode assembly baskets and cathode plates and modular anode assembly, in order to achieve a desired operational characteristic, such as reduction speed, material volume, off-gas rate, oxidizing or reducing potential, etc.
Hereinafter, example embodiments will be described in detail with reference to the attached drawings. However, specific structural and functional details disclosed herein are merely representative for purposes of describing example embodiments. The example embodiments may be embodied in many alternate forms and should not be construed as limited to only example embodiments set forth herein.
It will be understood that, although the terms first, second, etc. may be used herein to describe various elements, these elements should not be limited by these terms. These terms are only used to distinguish one element from another. For example, a first element could be termed a second element, and, similarly, a second element could be termed a first element, without departing from the scope of example embodiments. As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items.
It will be understood that when an element is referred to as being “connected,” “coupled,” “mated,” “attached,” or “fixed” to another element, it can be directly connected or coupled to the other element or intervening elements may be present. In contrast, when an element is referred to as being “directly connected” or “directly coupled” to another element, there are no intervening elements present. Other words used to describe the relationship between elements should be interpreted in a like fashion (e.g., “between” versus “directly between”, “adjacent” versus “directly adjacent”, etc.).
As used herein, the singular forms “a”, “an” and “the” are intended to include the plural forms as well, unless the language explicitly indicates otherwise. It will be further understood that the terms “comprises”, “comprising,”, “includes” and/or “including”, when used herein, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof.
It should also be noted that in some alternative implementations, the functions/acts noted may occur out of the order noted in the figures or described in the specification. For example, two figures or steps shown in succession may in fact be executed in series and concurrently or may sometimes be executed in the reverse order or repetitively, depending upon the functionality/acts involved.
The inventors have recognized a problem in existing single-step electrolytic reduction processes that the known processes cannot generate large amounts of reduced, metallic products on a commercial or flexible scale, at least in part because of limited, static cathode size and configuration. Single step electrolytic reduction processes may further lack flexibility in configuration, such as part regularity and replaceability, and in operating parameters, such as power level, operating temperature, working electrolyte, etc. Example systems and methods described below uniquely address these and other problems, discussed below or not.
Example Embodiment Electrolytic Oxide Reduction Systems
The disclosures of the above-listed co-pending applications are incorporated by reference herein in their entirety.
As shown in
EORS 1000 may include several supporting and structural members to contain, frame, and otherwise support and structure other components. For example, one or more lateral supports 1104 may extend up to and support a top plate 1108, which may include an opening (not shown) above electrolyte container 1050 so as to permit access to the same. Top plate 1108 may be further supported and/or isolated by a glove box (not shown) connecting to and around top plate 1108. Several standardized electrical contacts 1480 (
In
As shown in
The cathode assembly 1300 and anode assembly 1200 are connected to power sources so as to provide opposite charges or polarities, and a current-controlled electrochemical process occurs such that a desired electrochemically-generated reducing potential is established at the cathode by reductant electrons flowing into the metal oxide at the cathode. Because of the generated reducing potential, oxygen in the oxide material within the cathode assemblies 1300 is released and dissolves into the liquid electrolyte as an oxide ion. The reduced metal in the oxide material remains in the cathode assembly 1300. The electrolytic reaction at the cathode assemblies may be represented by equation (1):
(Metal Oxide)+2e−→(reduced Metal)+O2− (1)
where the 2e− is the current supplied by the cathode assembly 1300.
At the anode assembly 1200, negative oxygen ions dissolved in the electrolyte may transfer their negative charge to the anode assembly 1200 and convert to oxygen gas. The electrolysis reaction at the anode assemblies may be represented by equation (2):
2O2−→O2+4e− (2)
where the 4e− is the current passing into the anode assembly 1200.
If, for example, a molten Li-based salt is used as the electrolyte, cathode reactions above may be restated by equation (3):
(Metal Oxide)+2e−+2Li+→(Metal Oxide)+2Li→(reduced Metal)+2Li++O2− (3)
However, this specific reaction sequence may not occur, and intermediate electrode reactions are possible, such as if cathode assembly 1300 is maintained at a less negative potential than the one at which lithium deposition will occur. Potential intermediate electrode reactions include those represented by equations (4) and (5):
(Metal Oxide)+xe−+2Li+→Lix(Metal Oxide) (4)
Lix(Metal Oxide)+(2−x)e−+(2−x)Li+→(reduced Metal)+2Li++O2− (5)
Incorporation of lithium into the metal oxide crystal structure in the intermediate reactions shown in (4) and (5) may improve conductivity of the metal oxide, favoring reduction.
Reference electrodes and other chemical and electrical monitors may be used to control the electrode potentials and rate of reduction, and thus risk of anode or cathode damage/corrosion/overheating/etc. For example, reference electrodes may be placed near a cathode surface to monitor electrode potential and adjust voltage to anode assemblies 1200 and cathode assemblies 1300. Providing a steady potential sufficient only for reduction may avoid anode reactions such as chlorine evolution and cathode reactions such as free-floating droplets of electrolyte metal such as lithium or calcium.
Efficient transport of dissolved oxide-ion species in a liquid electrolyte, e.g. Li2O in molten LiCl used as an electrolyte, may improve reduction rate and unoxidized metal production in example embodiment EORS 1000. Alternating anode assemblies 1200 and cathode assemblies 1300 may improve dissolved oxide-ion saturation and evenness throughout the electrolyte, while increasing anode and cathode surface area for larger-scale production. Example embodiment EORS 1000 may further include a stirrer, mixer, vibrator, or the like to enhance diffusional transport of the dissolved oxide-ion species.
Chemical and/or electrical monitoring may indicate that the above-described reducing process has run to completion, such as when a voltage potential between anode assemblies 1200 and cathode assemblies 1300 increases or an amount of dissolved oxide ion decreases. Upon a desired degree of completion, the reduced metal created in the above-discussed reducing process may be harvested from cathode assemblies 1300, by lifting cathode assemblies 1300 containing the retained, reduced metal out of the electrolyte in container 1050. Oxygen gas collected at the anode assemblies 1200 during the process may be periodically or continually swept away by the assemblies and discharged or collected for further use.
Although the structure and operation of example embodiment EORS 1000 has been shown and described above, it is understood that several different components described in the incorporated documents and elsewhere are useable with example embodiments and may describe, in further detail, specific operations and features of EORS 1000. Similarly, components and functionality of example embodiment EORS 1000 is not limited to the specific details given above or in the incorporated documents, but may be varied according to the needs and limitations of those skilled in the art.
Example Embodiment Cathode Assemblies
As shown in
Lower portion 312 may form a basket or other enclosure that holds or otherwise retains the material to be reduced. As shown in
Permeable material 330 is placed along planar faces of lower portion 312 in the example embodiment of
Upper portion 311 may be hollow and enclosed, or any other desired shape and length to permit use in reduction systems. Upper portion 311 joins to an assembly support 340, such that upper portion 311 and lower portion 312 of basket 310 extend from and are supported by assembly support 340. Assembly support 340 may support example embodiment modular cathode assembly 300 above an electrolyte. For example, assembly support 340 may extend to overlap top plate 1108 in EORS 1000 so as to support modular cathode assembly extending into electrolyte container 1050 from above. Although lower portion 312 may extend into ionized, high-temperature electrolyte, the separation from upper portion 311 may reduce heat and/or caustic material transfer to upper portion 311 and the remaining portions of modular cathode assembly 300, reducing damage and wear. Although basket 310 is shown with a planar shape extending along assembly support 340 to provide a large surface area for permeable material 330 and electrolyte interaction therethrough, basket 310 may be shaped, positioned, and sized in any manner based on desired functionality and contents.
As shown in
Cathode plate 350 is electrically insulated from basket 310, except for indirect current flow from/into cathode plate 350 into/from an electrolyte or oxide material in basket 310 which plate 350 may contact. Such insulation may be achieved in several ways, including physically separating cathode plate 350 from basket 310. As shown in
Basket 310, including upper portion 311, sheet metal edge 315, and lower portion 312 dividers and bottom, and cathode plate 350 are fabricated from an electrically conductive material that is resilient against corrosive or thermal damage that may be caused by the operating electrolyte and will not substantially react with the material being reduced. For example, stainless steel or another nonreactive metallic alloy or material, including tungsten, molybdenum, tantalum, etc., may be used for basket 310 and cathode plate 350. Other components of example embodiment modular cathode assembly 300 may be equally conductive, with the exception of insulator 370, bands 355, and handling structures (discussed below). Materials in cathode plate 350 and basket 310 may further be fabricated and shaped to increase strength and rigidity. For example, stiffening hems or ribs 351 may be formed in cathode plate 350 or in sheet metal edge 315 to decrease the risk of bowing or other distortion and/or misalignment between cathode plate 350 and basket 310.
As shown in
Cathode assembly support 340 may further include a lift basket post 390 for removing/inserting or otherwise handling or moving cathode assembly 300, including basket 310 and potentially cathode plate 350. Lift basket posts 390 may be placed at either end of cathode assembly support 340 and/or be insulated from the remainder of example embodiment modular cathode assembly 300. When used in a larger reduction system, such as EORS 1000, individual modular cathode assemblies 300, and all subcomponents thereof including basket 310 and cathode plate 350, may be moved and handled, automatically or manually, at various positions through the lift basket post 390.
As shown in
Cathode assembly connectors 385 may electrically connect to, and provide appropriate reducing potential to, various components within example embodiment modular cathode assembly 300. For example, two separate pairs of cathode assembly connectors, 385a and 385b, may connect to different power sources and provide different electrical power, current, voltage, polarity, etc. to different parts of assembly 300. As shown in
Cathode assembly contacts 485b and 485a may provide different levels of electrical power, voltage, and/or current to connectors 385b and 385a and thus to basket 310 and cathode plate 350, respectively. For example, contact 485a may provide higher power to connectors 385a and cathode plate 350, near levels of opposite polarity provided through anode contacts 480. This may cause electrons to flow from cathode plate 350 into the electrolyte or material to be reduced and ultimately to anode assemblies and reduce oxides or other materials held in basket 310, in accordance with the reducing schemes discussed above.
Contact 485b may provide lower and/or opposite polarity secondary power to contact 385b and basket 310, compared to contact 485b. As an example, lower secondary power may be 2.3 V and 225 A, while primary level power may be 2.4 V and 950 A, or primary and secondary power levels may be of opposite polarity between cathode plate 350 and basket 310, for example. In this way, opposite and variable electrical power may be provided to example embodiment modular cathode assembly 300 contacting cathode assembly contacts 485a and 485b through connectors 385a and 385b. Additionally, both primary and secondary levels of power may be provided through contact 485a to connector 385a, or any other desired or variable level of power for operating example reduction systems. Table 1 below shows examples of power supplies for each contact and power line thereto.
Because basket 310 may act as a secondary anode when charged with opposite polarity from cathode plate 350, current may flow through the electrolyte or material to be reduced between cathode plate 350 and basket 310. This secondary internal current in example embodiment cathode assembly 300 may prevent metallic lithium or dissolved metallic alkali or alkaline earth atoms from exiting basket lower section 312 where it may not contact material to be reduced, such as a metal oxide feed. Operators may selectively charge basket 310 based on measured electrical characteristics of reduction systems, such as when operators determine electrolyte within basket contains dissolved metallic alkali or alkaline earth atoms.
As shown in
Example embodiments discussed above may be used in unique reduction processes and methods in connection with example systems and anode assembly embodiments. Example methods include determining a position or configuration of one or more modular cathode assemblies within a reduction system. Such determination may be based on an amount of material to be reduced, desired operating power levels or temperatures, anode assembly positions, and/or any other set or desired operating parameter of the system. Example methods may further connect cathode assemblies to a power source. Because example assemblies are modular, external connections may be made uniform as well, and a single type of connection may work with all example embodiment cathode assemblies. An electrolyte used in reduction systems may be made molten or fluid in order to position anode and/or cathode assemblies at the determined positions in contact with the electrolyte.
A desired power level or levels, measured in current or voltage or polarity, is applied to cathode assemblies through an electrical system so as to charge baskets and/or plates therein in example methods. This charging, while the basket and plate are contacted with a metal oxide and electrolyte in contact with nearby anodes, reduces the metal oxide in the baskets or in contact with the same in the electrolyte, while de-ionizing some oxygen dissolved into the electrolyte in the cathode assembly. Example methods may further swap modular parts of assemblies or entire assemblies within reduction systems based on repair or system configuration needs, providing a flexible system than can produce variable amounts of reduced metal and/or be operated at desired power levels, electrolyte temperatures, and/or any other system parameter based on modular configuration. Following reduction, the reduced metal may be removed and used in a variety of chemical processes based on the identity of the reduced metal. For example, reduced uranium metal may be reprocessed into nuclear fuel.
Example embodiments thus being described, it will be appreciated by one skilled in the art that example embodiments may be varied through routine experimentation and without further inventive activity. For example, although baskets in cathode assemblies containing three rectangular compartments are shown, it is of course understood that other numbers and shapes of compartments and overall configurations of baskets may be used based on expected cathode assembly placement, power lever, necessary oxidizing potential, etc. Variations are not to be regarded as departure from the spirit and scope of the example embodiments, and all such modifications as would be obvious to one skilled in the art are intended to be included within the scope of the following claims.
The present application is a divisional under 35 U.S.C. § 121 of U.S. application Ser. No. 12/978,005, filed Dec. 23, 2010, the entire contents of which is hereby incorporated herein by reference.
The invention was made with Government support under contract number DE-AC02-06CH11357, awarded by the U.S. Department of Energy. The Government has certain rights in the invention.
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Unofficial English translation of Japanese Office Action issued in connection with related JP Application No. 2014549039 dated Jun. 28, 2016. |
Unofficial English translation of Japanese Notice of Allowance issued in connection with related JP Application No. 2014549035 dated Aug. 23, 2016. |
Unofficial English translation of Japanese Notice of Allowance issued in connection with related JP Application No. 2014549037 dated Aug. 23, 2016. |
Unofficial English translation of Japanese Notice of Allowance issued in connection with related JP Application No. 2014549039 dated Aug. 23, 2016. |
Unofficial English translation of Japanese Office Action issued in connection with related JP Application No. 2014549036 dated Aug. 30, 2016. |
Japanese Search Report issued in connection with related JP Application No. 2014549038 dated Sep. 16, 2016. |
Unofficial English translation of Japanese Notice of Allowance issued in connection with related JP Application No. 2014549038 dated Oct. 18, 2016. |
Number | Date | Country | |
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20150053551 A1 | Feb 2015 | US |
Number | Date | Country | |
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Parent | 12978005 | Dec 2010 | US |
Child | 14528146 | US |