The present invention relates to deposition cathodes typically used in the refining or winning of metals. In particular, the present invention relates to a deposition cathode assembly comprising a deposition plate and a hanger bar sheathed in a protective cladding wherein the gap between the cladding and the internal welded joint of the deposition plate to the hanger bar is filled thereby encapsulating the weld in a corrosion resistant material and preventing the ingress of corrosive media.
Refining or winning of many non-ferrous metals can be achieved by electrolysis. For metals which are more readily oxidised and reduced than water, one electro-refining technique comprises placing an anode fabricated from the crude metal and a cathode together in suitable acid bath. Application of a voltage between the anode and the cathode cause the crude metal to oxidise and pure metal ions to migrate electrolytically through the acid bath to the cathode. The metal ions are deposited on the cathode as a refined metal of high purity, leaving the majority of impurities on the floor of the acid bath. Alternatively, in the electro-winning process the anode is fabricated from a material other than the metal being refined, for example for the electro-winning of copper one anode used is fabricated from an alloy of Lead, Tin and Calcium (Pb, Sn and Ca). The metal to be refined, copper in this case, is delivered to the electrolytic bath in soluble form, primarily from a leaching and solvent extraction process. Application of a voltage across the anode and cathode causes the copper to migrate from the solution and deposit on the cathode in a refined metallic state.
The cathodes are typically comprised of a flat, square deposition plate attached along an upper edge to an electrically conductive hanger bar. The hanger bar, which straddles the tank which houses the acid bath during refining, is in turn in electrical contact with an external power source, conventionally by means of a pair of electrically conductive bus bars which run in parallel along opposite edges of the tank and upon which the ends of the hanger bar rest. The hanger bar therefore serves a dual purpose: providing the means for suspending the deposition plate within the acid bath and providing a path for the flow of electrical current between the deposition plate and the power source.
After a suitable period of time when sufficient copper has migrated from the anode to the cathode, or from soluble (solution) form to the cathode, the cathode is removed from the acid bath. Alternatively, other metals can be used for the fabrication cathodes. In the event one of these metals is used, the refined metal can be extracted by a variety of well known stripping techniques, including scraping, hammering, the use of compressed air, etc. This has the benefit that the cathode can be reused with little or no preparatory work being required other than the removal of previously refined metal.
The prior art reveals a number of cathodes with deposition sheets and other elements fabricated from metals which are different from the metal being refined. Examples of such metals include aluminium, titanium and stainless steel. These metals exhibit a number of qualities which encourage their use as deposition plates, including a relatively high tensile strength and very good corrosion resistance. However, increase in tensile strength and corrosion resistance is typically offset by a decrease in conductivity and therefore a reduction in the efficiency of the process.
The prior art reveals cathode assemblies where the hanger bar is manufactured from the same or similar material as the deposition plate. The hanger bar and the deposition plate are welded together and the hanger bar, weld and a small portion of the deposition plate are then coated in a highly conductive cladding, such as copper, to improve conductivity between the conductive rails and the deposition plate. These prior art cathode assemblies suffer from the drawback that the current flow, and thereby the efficiency of the electrolytic process, is largely limited by the thickness of the conductive cladding. Additionally, the conductive cladding is exposed to the corrosive fluids of the acid bath due to splashing, etc., which can cause pitting and other corrosive effects further reducing the conductivity of the cladding as well as the electrolytic migration of the cladding to the surface of the deposition plate.
In order to address the above and other drawbacks, the prior art reveals alternative assemblies where the hanger bar is manufactured from a highly conductive material with very low internal resistance, such as solid copper, with the deposition plate being attached, typically via a weld, to the hanger bar. Due to the use of dissimilar metals, however, the weld is particularly susceptible to premature galvanic corrosion, and therefore the hanger bar, weld and a small portion of the deposition plate are sheathed in a suitably formed and snugly fitting cladding of the same or similar material as the deposition plate. The edges of the cladding are then welded to the deposition plate thereby protecting the hanger bar to some degree from the effects of the corrosive contents of the electrolytic bath. Additionally, as the hanger bar is used to haul the deposition plate out of acid bath on completion of the deposition process, which can leave a considerable mass of metal deposited on the deposition plate, the cladding also provides the added benefit of strengthening the assembly.
A major drawback, however, of the above prior art assembly is that corrosive liquid typically escapes from the acid bath, circumvents the weld between the shroud and the deposition plate and penetrates the joint between the hanger bar and the deposition plate. This leads to electrolytic migration of the metals and corrosion of the joint, thereby reducing the conductivity of the assembly and the efficiency of the unit as a whole. Additionally, as the joint is hidden behind the cladding, washing to remove the corrosive electrolyte is difficult if not impossible and therefore the effects of the corrosive liquid are difficult to arrest.
The present invention addresses the above and other drawbacks by providing a cathode for use in the refining of metals. The cathode comprises a substantially flat deposition plate fixedly attached along an upper edge thereof to an elongate hanger bar thereby defining a connection. A protective cladding abuts the deposition plate and at least partially surrounds the hanger bar such that a cavity is defined in the region of the connection. A corrosion resistant material is used to fill the cavity. The corrosion resistant material prevents corrosive substances from penetrating the connection.
There is also provided a method for fabricating a cathode assembly for use in the refining of metals. The cathode is of the type comprising a deposition plate for electrodepositing metals. The method comprises the steps of:
The illustrative embodiments of according to the present invention will now be described.
Referring to
In order to prevent creep of copper deposited on the surface of the deposition plate 12 around the edges, which can lead to the mechanical separation of the deposited copper (not shown) from the surface of the deposition plate 12, a pair of edge-strips as in 14 are attached along the edges 16 of the deposition plate 12 extending from the lower edge 18 to a point above the maximum level of the electrolyte 20 into which the deposition plate 12 is dipped. The edge-strips 14 are manufactured from a non-conductive material, for example polypropylene, and provide a seal against the ingress of electrolyte and copper onto the side edges 16. Prior to installation of the edge-strips 14 a self adhesive sealing gasket tape (not shown) is installed onto the side edges 16 to further improve the seal.
Referring to
In an alternative embodiment the upper edge 22 of the deposition plate is not inserted in a slot but rather butts against the lower surface 28 of the hanger bar 24.
The hanger bar 24 is manufactured from an unalloyed solid copper of a high purity, such as electrolytic tough pitch copper with the UNS (Unified Numbering System) designation C11000, and the first pair of seam welds 30 serve primarily to provide for good conduction of electrical current between the deposition plate 12 and the copper hanger bar 24.
Referring back to
Once positioned over the hanger bar 24 and deposition plate 12, the lower edges 34 of the cladding 32 are welded onto the surfaces of the deposition plate 12. The welding results in the deposition of a second pair of seam welds 36 along the entire breadth of the deposition plate 12 immediately below the first pair of seam welds 30. The cladding 32 and second pair of seam welds 36 provide the dual purpose of re-enforcing the hanger bar 24 as well as providing some protection against the ingress of corrosive electrolyte solution and other liquids onto the first pair of seam welds 30 and into the joint between the upper edge 22 of the deposition plate 12 and the lower surface 28 of the hanger bar 24. Additionally, the lower edges towards the ends 38 of the cladding 32 are joined and welded together.
Referring to
Referring back to
Typically, the corrosion resistant material 42 is injected by boring small holes as in 46 in the protective cladding 32. The corrosion resistant material 42 in a free flowing form is then injected into the space between the lower surface of the copper hanger bar 24 and the inside surface 44 of the cladding 32 along the entire length of the cladding 32. The corrosion resistant material 42 then hardens forming a hermetic seal around the first pair of seam welds 30.
Referring now to
Although the present invention has been described hereinabove by way of a preferred embodiment thereof, this embodiment can be modified at will, within the scope of the present invention, without departing from the spirit and nature of the subject of the present invention.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/CA03/00919 | 6/17/2003 | WO | 00 | 11/16/2005 |
Publishing Document | Publishing Date | Country | Kind |
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WO03/106738 | 12/24/2003 | WO | A |
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5172850 | Prengaman et al. | Dec 1992 | A |
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6131798 | Prengaman | Oct 2000 | A |
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2298264 | Nov 1998 | CN |
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63-57793 | Mar 1988 | JP |
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Number | Date | Country | |
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20060102470 A1 | May 2006 | US |
Number | Date | Country | |
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60389452 | Jun 2002 | US |