EP0096001B1

EP0096001B1 - Dimensionally stable drained aluminum electrowinning cathode method and apparatus

Info

Publication number: EP0096001B1
Application number: EP83810196A
Authority: EP
Inventors: Ajit Y. Sane; Douglas J. Wheeler; Charles S. Kuivila
Original assignee: Eltech Systems Corp
Current assignee: Moltech Invent SA
Priority date: 1982-05-10
Filing date: 1983-05-09
Publication date: 1987-01-14
Also published as: ATE24937T1; DE3369162D1; AU1438983A; JPS58207386A; NO159808C; NO831650L; NO159808B; AU571833B2; CA1218958A; EP0096001A1

Abstract

A method and apparatus for making a drained aluminum electrowinning cathode dimensionally stable. A thin, <1>/2 to 10 millimeter coating of substantially stagnant molten aluminum is maintained upon the cathode surface by an openly porous sheath or membrane closely conforming to contours of the electrowinning cathode. The sheath or membrane is made from a material substantially resistant to corrosives present in the aluminum electrowinning; it may be only slightly aluminum wettable, but should be relatively electrically nonconductive.

Description

Technical field

The present invention relates to an electrode for electrowinning aluminum in an electrolysis cell, presenting a drained electrically conductive electrowinning surface to contents of the cell.
The invention also relates to an electrolysis cell for electrowinning aluminum and to a method of electrowinning aluminum.

Background of the invention

Aluminum is commonly produced by the electrolysis of AI₂0₃ at about 900°C to 1000°C. Aluminum oxide being electrolyzed is generally dissolved in molten Na3AIF, (cryolite) that generally contains additives helpful to the electrolytic process such as CaF₂, AIF₃ and LiF.
In the electrolytic cell, reduction of the aluminum oxide occurs at a cathode generally positioned upon the bottom or floor of the electrolytic cell. Oxygen is liberated from electrochemically dissociating AI₂0₃, and in commercial cells, generally combines with carbonacious material comprising the cell anode and is emitted from the cell as CO or C0₂.
In many commercial cells, the cathode is comprised of a material relatively resistant to corrosive effects of contents of the cell such as cryolite. This cathode often covers substantially the entire floor of the cell which typically can be 6 feet wide by 18 or more feet in length.
Molten aluminum is a substance relatively. resistant to corrosive and solvating effects in an aluminum electrowinning cell. In utilizing aluminum for cathode purposes in a cell, typically the cathode is an assembly including a cathodic current feeder covered by a pool of aluminum ranging in depth, depending upon the cell, from a few inches to in excess of a foot. The aluminum pool functions effectively as a cathode and also serves to protect current feeders made from materials less than fully resistant to cell contents. For example, unprotected graphite used as a cathode can generate aluminum carbide an undesirable contaminant, while when used as a covered current feeder, no such contamination results.
These pool type cell cathode assemblies contain conductive current collectors. Where these conductive current collectors are utilized in some cell configurations, these collectors contribute to an electrical current flow within the cell that is not perpendicular to the cell bottom. These nonperpendicular electrical currents can interact with strong electromagnetic fields established around cells by current flow through busses and the like contributing to strong electromagnetic fluxes within the cell.
In cells employing a pool of aluminum covering the cathode floor of the cell, the cryolite, containing the A1₂0₃ to be electrolyzed, floats atop this aluminum pool. The cell anodes are immersed in this cryolite layer.
It is important that these anodes do not contact the aluminum pool, for such contact would result in a somewhat dysfunctional short circuit within the cell. The electromagnetic flux within the cell contributes to the formation of wave motion within the aluminum pool contained in the cell, making prediction of the exact depth of the aluminum pool, and therefore the minimum necessary spacing between the anode and cathode current collector and between the anode and the interface between aluminum and cryo|ite at any particular cell location somewhat imprecise. Therefore, cell anodes are positioned within the cryolite to be substantially above the normal or expected level of the interface between cryolite and aluminium within the cell.
The combination of a substantial aluminum pool depth and a posittoning of the anodes above the cryolite-aluminum normal interface position to forestall short circuits triggered, for example, by wave motion in the aluminum that would locally alter the aluminum pool depth, establishes a substantial gap between the anode and cathode in most conventional cells. A portion of the electrical power consumed in operation of the cell is somewhat proportional to the magnitude of this gap. Substantial reductions in the magnitude of this gap would result in considerable cost savings via reduced cell electrical power consumption during operation.
In one proposal, a packing or filler material is introduced into the cell, generally to a depth normally occupied by the aluminum pool. The packing tends to break up wave motion within the cell making prediction of the position of the interface between the aluminum pool and the cryolite more predictable. Where the interface position is more reliable, the anodes can be positioned somewhat closer to the interface, promoting incrementally reduced power consumption.
In such packed cells, however, the anode and cathode remain separated by a depth of cryolite, sufficient to forestall short circuits caused by localized disruptions in the aluminum pool depth existing notwithstanding the packing. This separation can lead to a large electrical power inefficiency in operating the aluminum electrowinning cell. Further, materials used for packing the cell must be substantially resistant to corrosive effects of cell contents. Such materials often are costly, and therefore packing the large numbers of these spacious electrolytic cells necessary for producing aluminum can be economically burdensome.
Another proposed solution has been to employ so-called drained cathodes in constructing aluminum electrolysis cells. In such cells, no pool of aluminum is maintained upon a cathode current feeder to function as a cathode, aluminum drains from the cathode as it forms to be recovered from a collection area. In drained cathode cells, without wave action problems attendant to the aluminum pool, the anode and the cathode may be quite closely arranged, realizing significant electrical power savings.
In these drained cathode cells, however, the cathode or vulnerable cathodic current feeder often is in generally continuous contact with molten cryolite. This aggressive material, in contact with a graphite or carbon cathode, contributes to material losses from the cathode as well as the formation of aluminum carbides, a dysfunctional impurity. Carbon or graphite for use as a drained cathode material of construction is therefore of quite limited utility due to service life constraints.
Other longer lived materials are, in theory, available for use in a drained cathode. Generally these materials are both conductive and aluminum wettable refractory materials such as TiB₂. It has been found that unless TiB₂ and similar materials are in essentially pure form, they too lose material or corrode at unacceptable rates in the aggressive cell environment. It is believed that the molten cryolite contributes to TiB₂ corrosion by fluxing reaction products of TiB₂ and aluminum generated near grain boundaries of the material. While it is known that essentially pure TiB₂ does not exhibit in aluminum electrowinning cells as substantial a corrosion susceptibility as does lower purity TiB₂, cost and availability factors seriously limit the use of TiB₂ sufficiently pure to withstand the aggressive cell environment.
International Patent application WO 83,01465 discloses a cathode for an aluminum production cell comprising a sloped surface covered by a felt e.g. of coated carbon fibers, within which felt aluminum may flow downwards to be collected in a lower part of the cell.
EP-A-0 069 502 discloses an electrolytic cell for the production of aluminum wherein one or several layers of shapes, such as spheres are arranged on the cathode floor.
In both of the above documents aluminum is allowed to move within the layers covering the cathode surface.
CH-A-362531 discloses cathode structures for electrowinning of aluminum, wherein the surface of the cathodes comprises either a carbon sponge to receive aluminum in its pores, or a saw-like surface forming recesses in which aluminum may collect. However, no indication is given in this Patent as to how the aluminum in the pores of the sponge may be retained or in the case of saw-like surface how the portions between the recesses may be protected.

Objects of the invention

It is an object of the present invention to provide an economical, improved cathode for aluminum electrolysis, which remains substantially dimensionally stable when used in an aluminum electrolysis cell.
It is another object of the present invention to provide a cathode configuration permitting relatively close anode-cathode spacing, thereby permitting substantial electrical power savings.
It is a further object of the present invention to provide a cathode configuration in which a film of molten metal is maintained on the cathode surface.

Disclosure of the invention

The above and other objects of the invention are achieved by an electrode as mentioned in the preamble, which is further characterized in that it comprises a sheath closely conforming to contours of the presented surface at least where the presented surface contacts aluminum being electrowon, the sheath having a plurality of apertures traversing the sheath from one surface thereof to the other, the apertures being of a size and configuration such that molten aluminum is retained therein in substantially stagnant manner in contact with the presented surface, the sheath being made of a material substantially resistant to corrosion by contents of the cell.
The pores of the sheath which extend through the thickness of the latter provide fluid pathways for the aluminum which enters and fills the sheath. The sheath or membrane is formed from a material substantially resistant to corrosion by contents of the aluminum electrolysis cell. It is preferred that the sheath or membrane be relatively nonelectrically conductive. It is desirable but not essential that the sheath or membrane be somewhat wettable by the molten aluminum being retained within the pores and thereby substantially coating the cathode with a film of aluminum.
A drained cathode used for aluminum electrowinning is therefore rendered relatively dimensionally stable by providing a substantially stagnant coating of molten aluminum upon the surface of such a cathode presented for the electrowinning process. In preferred embodiments, this coating or film retained upon the cathode electrowinning surface is not less than about 0.5 millimeter and not greater than about 10.0 millimeters. Aluminum depositing upon the cathode in a depth greater than the sheath thickness continues to drain from the cathode surface to be recovered.
A drained cathode structure results from the practice of the instant invention. Aluminum being electrolyzed fills the porous sheath thereby protecting the cathode substantially from contact with cryolite contained within the cell by providing a substantially stagnant aluminum coating upon the cathode. The cathode is rendered less subject to corrosion and therefore substantially dimensionally stable. Yet a narrow separation between anode and cathode within the cell can be maintained since substantial wave motion within the relatively thin aluminum coating provided upon the cathode by the sheath is unlikely.
In another aspect of the invention the drained electrowinning surface of a refractory hard metal boride, nitride, carbide or mixtures or combinations thereof has molten aluminum retained in substantially stagnant contact therewith by at least one piece of a substantially non-electrically conductive material selected from Si₃N₄, BN, AION, SiAION, AIN and AIB₁₂. This material can either be an apertured sheath, as described previously, or could be made up of several discrete pieces of any suitable shape which are so arranged as to leave spaces in which the molten aluminum is retained in stagnant contact with the electrowinning surface.
The above and other features and advantages of the invention will become apparent from the following detailed description of the invention along with the drawings of the invention and examples accompanying the detailed description, all forming a part of the specification.

Description of the drawings

Figure 1 is a cross-sectional view taken transversely of an aluminum electrolysis cell embodying the invention.
Figure 2 is an expanded view of a cathode shown in Figure 1.
Figure 3 is an elevational cross-section of a cell portion immediately adjacent the aluminum electrolysis surface of the cathode showing a sheath configuration.
Figure 4 is an elevational cross-section of a cell portion immediately adjacent the aluminum electrolysis surface of the cathode showing an alternate sheath configuration.

Best embodiment of the invention

The present invention provides a drained cathode structure for use in an aluminum electrolysis cell. The drained cathode is substantially dimensionally stable. Referring to the drawings, an aluminum electrolysis cell 10 is shown generally in Figure 1. The cell 10 includes an anode 12 and a cathode 14 contained within a housing 16 that includes a liner assembly 18.
The housing 16 includes a shell 25 usually made from a suitable or conventional substance like steel. Contained within the housing 16 is a liner assembly 18 that includes a layer 27 that generally resists aggressive attack upon the shell 25 by contents of the cell such as cryolite. In this best embodiment, the layer 27 functions also as a current conductor for supplying electrical current to the cathode 14. In equally preferred embodiments, this layer 27 can include embedded current conductors (not shown) for supplying electrical current to the cathode 14. Refractory materials and graphite are suitable for fabricating this layer 27, as are other suitable or conventional materials.
An insulating layer 29 is provided to resist heat flow from the cell 10. While a variety of well-known structures are available for making this insulating structure, commonly the insulating layer 29 is crystallized contents of the electrolytic cell.
The anode 12 is fabricated from any suitable or conventional material and immersed in a cryolite phase 30 contained in the cell. Since oxygen ions react at the anode, the material must be either resistant to attack by oxygen or should be made of a material that can be agreeably consumed by the oxygen. Typically carbon or graphite is utilized. The anode 12 should be arranged for vertical movement within the cell so that a desired spacing can be maintained between the anode and cathode notwithstanding the anode ₃eing consumed by evolved oxygen.
The cathode 14 is mounted in the cell in electrical contact with the conductive liner 27 or with conductors contained within the liner. Referring to Figures 2, 3 and 4, it may be seen that the cathode has a surface 31 for electrolyzing aluminum. This surface is covered by a sheath 33 or membrane having apertures 35 or being openly porous. The porosity should communicate through the thickness of the sheath 33 so that aluminum being formed by electrolysis fills the apertures 35 or pores. Once filled, the aluminum in the pores remains substantially stagnant with further electrolysis occurring not on the presented surface 31 but upon a surface 37 defined by the filled porous sheath 33. Aluminum forming at this surface drains away to recovery areas 40, 41 from which it is removed. Aluminum is maintained in the recovery areas 40, 41 to a depth necessary to insure immersion of edge portions 45 of the sheath 33.
By coating in this manner, the substance of the cathode is shielded from contact with cryolite. Once shielded from the cryolite, a variety of materials can be used in making the cathode that would otherwise be undesirable due to elevated material losses in the aggressive cell environment.
Desirably, refractory metal borides, carbides and nitrides are thereby rendered suitable for use in fabricating drained cathodes. For purposes of this invention, particularly of use are borides, carbides and nitrides of: titanium; zirconium; niobium; tungsten; tantalum; molybdenum; silicon; as well as mixtures thereof. Titanium boride of at least 97.5 percent purity and TiB₂ composited with other of the refractory metal boride carbides and nitrides are most preferred. While these materials can be prohibitively expensive where consumed or corroded at a significant rate in an aluminum cell, once under a thin protective aluminum coating, they may be employed for electrolyzing for extended periods with little material losses. Any cathode surface selected should be both electrically conductive and at least significantly aluminum wettable.
In an equally preferred alternate to the best embodiment, the cathode includes a refractory metal boride, nitride, or carbide layer 47 applied to a suitable or conventional electrically conductive substrate 49 such as graphite. Where the refractory layer 47 is TiB₂ and is protected by maintaining an aluminum film or coating on the TiB₂ surface using the sheath 33 or membrane, a particularly advantageous, substantially dimensionally stable cathode structure results.
Since when using a drained cathode structure, no pool of aluminum exists in which wave motion might cause a short between anode and cathode, the anode and cathode can be positioned closely opposing each other. This close positioning permits cell operation at a reduced cell voltage, the anode being positioned in molten cryolite only a short distance from the sheathed cathode upon which molten aluminum is being electrolytically generated.
The sheath 33 or membrane can be of any suitable or conventional construction having a plurality of pores or apertures traversing its thickness. The precise configuration can be an openly porous rigid foam 51, a single layer honeycomb structure, an interconnected cellular structure, or a bar and grid arrangement 53 to name a few, depending upon the material of construction. The pores or apertures form interstices in the sheath that fill with molten aluminum during electrolysis to coat the cathode surface 31.
The sheath 33 or membrane may be formed from any suitable or conventional material substantially inert to aggressive chemical attack in the cell environment. Electrical conductivity is not requisite. Preferably the material used for the sheath will be at least -slightly wettable by aluminum to assist in filling interstices in the sheath with molten aluminum. Particularly useful for making the sheath or membrane are: Si₃N₄, BN, AION, SiAION, AIB_12' AIN, TiB₂, and combinations thereof.
The sizing of pores 35 or apertures within the sheath 33 or membrane is critical to effective implementation of the instant invention. The sheath or membrane should substantially infiltrate with molten aluminum so that the molten aluminum forms a continuous electrical current pathway between the surface 31 of the cathode and cryolite phase 30 surrounding the sheath. Yet aluminum filling the sheath or membrane interstices should remain substantially stagnant avoiding circulation leading to significant contact between the molten cryolite phase 30 and the cathode surface 31. Since areas of the cathode 14, below the aluminum liquid and in the recovery areas 40, 41 do not contribute substantially to aluminum electrowinning, they are not sheathed.
The thickness of the sheath should preferably be such as to hold a thickness of between about 0.5 millimeter to about 10.0 millimeters of molten aluminum substantially stagnant upon the cathode surface 31. Most preferably, this thickness is between 1.0 and 2.5 millimeters.
Desirable cross-sectional dimensions of individual pores or apertures by necessity vary widely as a function of aluminum, cryolite and sheath material interfacial tensions. Generally the more aluminum wettable the sheath material, the smaller the pores may be made, and the less wettable by aluminum the sheath material, the larger the pores may be in cross-section. The wide variance in these traits from one sheath material to another requires individual determination of acceptable pore size for each sheath material of construction and cryolite phase formulation. Generally a suitable pore cross-sectional area will be found between about 25 microns and 5000 microns. It is to be expected that the thickness of the sheath 33 will impact upon the desirable pore or aperture 35 cross-sectional dimension.
The following examples are.offered to further illustrate the features and advantages of the invention.

Example 1

Two aluminum electrolysis cells are assembled in accordance with Figure 1 and the best embodiment of the invention. A TiB₂ tile of 99⁺ percent purity is used to form the refractory layer 47, adhered to a graphite substrate 49, thereby forming the cell cathode 14. A sheath of grid configuration as shown in Figure 4 is placed upon the electrolyzing surface 31- of the cathode in one of the cells. The sheath is a plate 34.9x12.4x2.3 millimeters drilled to include a plurality of 2.6 millimeter diameter apertures. The sheath or grid is formed from BN. The cells are filled with cryolite having the composition (percent by weight)
and electrolysis is commenced using a cell voltage of between about 2.98-3.27 volts D.C. at a current density of 0.5 amperes per square centimeter of cathode surface. Anode-cathode spacing is about 2.5 centimeters.
After 10 operating hours, the cells are shut down and the TiB₂ tiles checked for material losses. The tile from the cell having sheath protection providing a layer of aluminum on the refractory layer 47 surface 31 is found to have a layer of 175 micrometer (7 mils) or less in thickness in which grain boundary corrosion was observed, whereas the tile from the unprotected cathode is found to have suffered grain boundary type corrosion losses of between 25 and 30 micrometer in thickness. In the cell having a protected cathode current efficiency during aluminum electrolysis was found to be 66.8 percent, this efficiency customarily being substantially greater when applied to commercial scale cells. The aluminum produced in the cell was found to be contaminated with 65 parts per million titanium.

Example 2

Cells identical to those of Example 1 are assembled and operated for 100 hours before being shut down for evaluation of tile corrosion. The protected cathode is found to have suffered between 5 and 11 microns corrosion of the TiB₂ refractory layer 27, the unprotected cathode between 26 and 40 micrometer.
While a preferred embodiment has been described in detail, it will be apparent that various modifications and alterations may be made thereto without departing from the scope of the appended claims. Particularly a great variety of drained cathode cell configurations are conceivable deriving substantial benefit from sheathed configuration providing a protective layer of molten aluminum upon the electrolysis surface 31, the subject of the instant invention.

Claims

1. An electrode for electrowinning aluminum in an electrolysis cell, presenting a drained electrically conductive electrowinning surface to contents of the cell, and comprising a sheath closely conforming to contours of the presented surface at least where the presented surface contacts aluminum being electrowon, the sheath having a plurality of apertures traversing the sheath from one surface thereof to the other, the apertures being of a size and configuration such that molten aluminum is retained therein in substantially stagnant manner in contact with the presented surface, the sheath being made of a material substantially resistant to corrosion by contents of the cell.

2. The electrode of claim 1, wherein the electrically conductive electrowinning surface is made from a material selected from refractory metal borides, nitrides, carbides, carbon and mixtures thereof, the sheath being made of a material selected from Si₃N₄, BN, AION, SiAION, AIN, TiB₂, AIB₁₂ and mixtures thereof.

3. The electrode of claim 1 or 2, wherein the electrically conductive electrowinning surface is TiB2.

4. The electrode of any one of claims 1-3, wherein the cross sections of the apertures are within the range from 25-5000 micrometers.

5. The electrode of any one of claims 1-4, wherein the thickness of the sheath is between 0.5 and 10.0 mm.

6. The electrode of claim 5, wherein the thickness of the sheath is between 1.0 and 2.5 mm.

7. The electrode of any one of claims 1-6, wherein the sheath is made of individual pieces being arranged such as to leave spaces for receiving molten aluminum therein, the spaces being such that the aluminum is retained in stagnant manner in contact with the electrowinning surface.

8. An electrolysis cell for electrowinning aluminum, having at least one electrode according to any one of claims 1-7.

9. A method of producing aluminum by electrowinning in an electrolysis cell comprising at least one electrode according to any one of claims 1-7.