The recovery of metals from moving bed cells is known in the art as a very attractive technique, albeit still far from actual industrial practice. Moving bed metal deposition has been first described as an improvement of the more general concept of fluidised bed metal deposition (see for instance U.S. Pat. No. 4,141,804) by Scott et al. in U.S. Pat. No. 4,272,333. A bed of metallic beads is levitated by a liquid electrolyte jet until it passes the top edge of a metal cathode, overflowing in a chamber delimited by such cathode and a semi-permeable diaphragm, separating the falling bed from the anode. The falling bed is thus cathodically polarised, and the metal ions in the electrolyte can discharge on the beads causing their growth. The disclosed method allows to feed the beads as small seeds and to discharge them from the cell after reaching the required growth, but has the obvious drawback of being substantially a batch procedure. Moreover, the cell must be operated as a single cell and has no possibility of being effectively stacked in a laminar arrangement, and its productive capacity by unit volume or by unit installation surface is therefore very limited.
A significant improvement of this concept is offered by the disclosure of U.S. Pat. Nos. 5,635,051 and 5,958,210, directed to the electrowinning of zinc. In this case, the cathodic compartment contains a spouted bed generated by the ascending motion of the electrolyte supplied to a draft tube, and split in two annuli in the falling regions, disposed at the two sides of the tube. The cathodic and anodic compartments are separated by means of an ion-permeable barrier, such as an ion-exchange membrane or the like. The anolyte and the catholyte are therefore physically separated and the growing beads are again excluded from the anodic compartment, but the passage of the ion to be deposited from the anodic to the cathodic compartment is allowed. The cell is somehow better than the one disclosed in U.S. Pat. No. 4,272,333 in terms of productive capacity, being quite flat, and even foreseeing the possibility of a parallel arrangement of a plurality of draft tubes and relevant falling bead annuli to increase the size of at least one dimension thereof. Nevertheless, the deposition disclosed therein is still a typical batch process, the depletion of metal ions in the anolyte chamber having to be counteracted with a delicate restoring procedure, in order to maintain a certain stability of the cell conditions.
It is an object of the present invention to provide a spouted bed cell for the recovery of metal from metal solutions overcoming the drawbacks of the prior art.
Under a different aspect, it is an object of the present invention to provide a method for electrowinning metal from a metal ion bearing electrolyte overcoming the drawbacks of the prior art.
Under a first aspect, the invention consists in a spouted bed electrowinning cell element that can be laminated in an array of equivalent elements in a modular fashion.
Under another aspect, the invention consists in a spouted bed electrowinning cell element comprising a cathode shell delimited by a cathodic plate and provided with a draft tube capable of establishing a spouted bed of growing metallic beads, an anodic plate provided with protrusions for mechanically holding a metal anode and transmitting electric current thereto, and one insulating semi-permeable diaphragm separating the cathodic and the anodic compartments which allows the free passage of the electrolyte while hindering the passage of the metallic beads.
Under still another aspect, the invention consists in an array of stacked electrowinning spouted bed cell elements, each delimited by an anodic plate and a cathodic plate, each anodic plate put in contact with the cathodic plate of the adjacent cell, preferably by means of contact strips.
Under still another aspect, the invention consists in a method for electrowinning metals from metal solutions by controlled growth of spouted metal beads, carried out in an array of modular cell elements wherein the electrolyte is allowed to circulate freely between the anodic and the cathodic compartment upon flowing through an insulating semi-permeable diaphragm.
These and other aspects will be made apparent from the following description.
The invention will be described making reference to the appended exemplary drawings, however it is not intended to be limited thereto.
The cell of the invention is designed to act preferably as an element of a laminated array of equivalent cells, even though it can also be used as a single cell for metal electrowinning.
The cell of the invention is suited to carry out the electrowinning of many different metals, including, but not limited to, copper, tin, manganese, zinc, nickel, chromium and cobalt.
The cell element of the invention comprises a cathode shell and an anode shell, each delimited by a metallic plate. The anodic metallic plate of the cell is suited to be electrically coupled in a straightforward fashion to the cathodic plate of the adjacent cell in the laminated array; in a preferred embodiment, this electrical coupling is effected by clamping together a plurality of single cell elements in a stack, so that each single cell element can be removed and/or replaced at any time, for instance for maintenance purposes, upon releasing the clamping pressure and extracting the same. The cathode shell is preferably made of stainless steel, but for many applications other materials are suitable, such as nickel or titanium. In a preferred embodiment, the cathode shell is made of an array of rectangular stainless steel bars with a cathodic plate welded thereon. Making reference to
The anodic plate is preferably fabricated from a metal sheet; valve metals are normally used for this purpose, to withstand the aggressive conditions of the anodic environment, and titanium or titanium alloys are particularly preferred, also for considerations of cost and workability. As shown in
The preferred configuration for the anode shell (200) will be made clearer with the sketch of its back view in
The two shells (100) and (200) are first bolted or otherwise clamped together to form a single cell element, then the single cell elements are laminated in a stack array at a sufficient pressure so that the contact strips (10) can effectively transmit the electric current from the anodic compartment to the cathodic plate (3) of the adjacent cell; when contact strips (10) are not used, direct contact may be effected from the cathodic plate (3) to the anodic one (9), this being however a less preferred solution since the contact surface would be larger, thereby requiring a greater clamping force to apply the same pressure; moreover, if titanium or other valve metals are used for the anodic plate (9), the electric contact would be eventually spoiled in time due to oxide growth.
Metal electrowinning cells can be either of the divided or of the undivided type, according to the different technologies; in the cells of the divided type, such as those in accordance with the disclosure of U.S. Pat. Nos. 5,635,051 and 5,958,210, it would be more cumbersome to achieve a continuous type process. In the best mode for carrying out the invention, the cell is an undivided cell, in that there are no separate anolyte and catholyte, but rather a single electrolyte flowing from one compartment to the other. However, a mechanical separator is needed to exclude the cathodically polarised growing beads from the anodic compartment. This is achieved by means of a semi-permeable diaphragm, as illustrated in
In a preferred embodiment, the insulating diaphragm is simply obtained by applying an insulating coating to the surface of the anode (6) facing the spouted bed, while the anodic reaction takes place on the opposed surface. In this case, the anode (6) must be a foraminous structure with suitable perforations to exclude the beads from entering the anode shell (200) while allowing the free circulation of the electrolyte. The insulating coating is preferably a ceramic coating, such as a valve metal oxide (titanium or zirconium oxides being preferred) or silicon carbide. Plasma sprayed ceramic coatings are particularly preferred. According to an alternative embodiment, the insulating coating may be a polymeric coating, preferably obtained from a fluorinated polymer such as PTFE or ECTFE (Ethylene-chlorotrifluoro-ethylene).
In some cases, the fact that the perforations of the foraminous or porous region (12) of the diaphragm (11) are smaller than the tiniest beads fed in the cell, is not really sufficient to prevent a certain amount of metal from passing to the anodic compartment and dissolving therein. This is normally due to the fact that some tiny beads may stick in correspondence of the perforations and, due to the potential gradient, partially dissolve on one side while growing on the opposed side. Sometimes a spherical bead may even reshape in acicular form by means of this mechanism, until it is thin enough to pass to the anode side dissolving therein. In other cases, the friction of the falling bed is so high that the particles may experience some grinding effect. At least in the case of copper electrowinning, these phenomena are frequently experienced. It is therefore convenient to provide the insulating diaphragm (11) with particularly tortuous paths that prevent the easy escape of reshaped particles, without hindering too much the electrolyte circulation. For this purpose, fabrics, and particularly woven ones, are best suited. Woven polyester meets particularly well the requirements of bead exclusion, resistance to friction, insulating properties and cost. Plain weaves are suited to this scope; plain weaves are characterised by having warp and weft wires of the same diameter, the weft wire alternately passing above or below each subsequent warp wire. This is illustrated in the top section of
Another important parameter for the fabric is the ratio between the warp wire spacing (that is the mean distance between two adjacent warp wires) and the warp wire diameter, which must be preferably greater than 3.
The preferred thickness for a fabric-made diaphragm is comprised between 0.4 and 0.6 mm.
In the figure, it is shown how the beads (15) move upwardly in the draft tube (17), exit therefrom and form two annuli (15′) on either side of the same, moving then downward in falling region (16). This happens when the draft tube (17) is placed in the centre of the cathodic chamber, but it might as well be possible to place the draft tube (17) near one side wall of the cathodic chamber, so that the movement of the beads (15) would trace a single annulus. In another embodiment, a plurality of parallel draft tubes (17) is provided in the cathodic chamber, so that a plurality of bead annuli (15′) is formed. For the sake of simplicity, only the case of a single central draft tube will be discussed further. The electrolyte is supplied to the draft tube (17) by a nozzle (19), mounted on a support (20) connected to the pumping circuit (not shown). In one embodiment of the invention, the nozzle (19) has a porous top section (21) allowing the passage of the electrolyte but not of the beads (15). In this way, when scheduled or unforeseen shut-downs occur, the beads (15) are prevented from falling into the nozzle occluding the same, thereby hindering the restarting of the spouting action.
Other optional elements include a deflector (22) on top of the draft tube (17), which is used to limit the height of the spouted bed, a weir (23) connected to an over-flow system with a product collecting tank (not shown), providing for the withdrawal of a fraction of beads to allow the continuous operation of the cell, an electrolyte drain tube (24), provided with a filter element allowing the discharge of the electrolyte while preventing the concurrent discharge of beads, and a bead drain device (25) provided with a drainage tube and a Tee-shaped separation element, allowing the discharge of metal beads upon feeding electrolyte in the horizontal leg.
The over-flow system downstream of the weir (23) optionally comprises a tank with a cone shaped bottom where beads are collected, and means for withdrawing the beads from the tank bottom, as will be obvious for one skilled in the art. An electrolyte over-flow system, not shown, is also normally provided as obvious to one skilled in the art.
The lower corners of the cell could optionally be provided with triangle members, for instance plastic cones as known in the art, to facilitate the natural circulation of the beads. It has been found however that in the absence of such cones, beads tend to collect in the lower corner regions of the cell of the invention giving rise to self-forming moving cones of beads (15″), that in stationary conditions can act as efficiently as artificial cones. The natural formation of the cones is assisted by the correct dimensioning of the arrowhead shaped elements (18), and has the great advantage that cones can naturally reform changing their shape every time that the flow-rate is varied for any reason. The self-formation of moving cones of beads filling the lower corners of the cathode shell meanwhile allows the natural formation of bead flow channels into the vertical gap below the base of the draft tube.
The following two figures show alternative, preferred embodiments of some elements illustrated in
In
The invention can be practised, according to a less preferred embodiment, also with separate anodic and cathodic circulation in an array of stacked elements wherein the anodic plate of each cell, with the obvious exception of the terminal one, is put in contact with the cathodic plate of the adjacent cell. Preferably, each single cell element is constructed, by bolting or otherwise fastening each anode shell with the correspondent cathode shell, prior to stacking the elements. Preferably, the single cell elements are stacked interposing contact strips therebetween. The contact strips are preferably welded to the anodic plates. In the case of separate anodic and cathodic circulation, the cell elements may not include a semi-permeable diaphragm, an ion-exchange medium such as an ion-exchange membrane being sufficient. In this case, one still takes advantage of the cell lamination in terms of productivity per unit volume and per unit area of plant installation; this embodiment is however less preferred as a continuous process becomes more cumbersome to establish with separate anolyte and catholyte, each requiring ion concentration monitoring and restoring.
The above description shall not be understood as limiting the invention, which may be practised according to different embodiments without departing from the scopes thereof, and whose extent is solely defined by the appended claims.
In the description and claims of the present application, the word “comprise” and its variation such as “comprising” and “comprises” are not intended to exclude the presence of other elements or additional components.
Number | Date | Country | Kind |
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MI2002A001524 | Jul 2002 | IT | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP03/07541 | 7/11/2003 | WO | 2/11/2005 |