GB2536901A - Cathode block for electrolytic cell suitable for the Hall-Héroult process - Google Patents

Cathode block for electrolytic cell suitable for the Hall-Héroult process Download PDF

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Publication number
GB2536901A
GB2536901A GB1505435.6A GB201505435A GB2536901A GB 2536901 A GB2536901 A GB 2536901A GB 201505435 A GB201505435 A GB 201505435A GB 2536901 A GB2536901 A GB 2536901A
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United Kingdom
Prior art keywords
cathode
copper
bar
carbonaceous material
metallic
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GB1505435.6A
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GB201505435D0 (en
Inventor
Jonqua Bernard
Zarouni Abdalla
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Dubai Aluminium PJSC
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Dubai Aluminium PJSC
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Priority to GB1505435.6A priority Critical patent/GB2536901A/en
Publication of GB201505435D0 publication Critical patent/GB201505435D0/en
Priority to CA2980832A priority patent/CA2980832C/en
Priority to PL16771479T priority patent/PL3277864T3/en
Priority to EP16771479.9A priority patent/EP3277864B1/en
Priority to PCT/IB2016/051592 priority patent/WO2016157021A1/en
Publication of GB2536901A publication Critical patent/GB2536901A/en
Withdrawn legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25CPROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
    • C25C3/00Electrolytic production, recovery or refining of metals by electrolysis of melts
    • C25C3/06Electrolytic production, recovery or refining of metals by electrolysis of melts of aluminium
    • C25C3/08Cell construction, e.g. bottoms, walls, cathodes
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25CPROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
    • C25C3/00Electrolytic production, recovery or refining of metals by electrolysis of melts
    • C25C3/06Electrolytic production, recovery or refining of metals by electrolysis of melts of aluminium
    • C25C3/16Electric current supply devices, e.g. bus bars

Abstract

A cathode element suitable for use in a Hall-Héroult electrolysis cell is described. The element comprises: a cathode block 10 constructed of a carbonaceous material, one (or more) metallic connection bar (s) 13 made of copper or copper alloys. The metallic connection bar 13 is fitted into a groove or bore in direct contact with the carbonaceous material, and where the carbonaceous material can be the carbonaceous material of said cathode block 10, or an intermediate carbonaceous material 17 that is in direct contact with the carbonaceous material of said cathode block 10. The intermediate carbonaceous material may be compressed expanded graphite and/or a cured carbonaceous seal which comprises graphite particles.

Description

Intellectual Property Office Application No. GII1505435.6 RTM Date:25 January 2016 The following terms are registered trade marks and should be read as such wherever they occur in this document: Comalco -page 2 Pechiney -page 2, 3 Kaiser -page 3 Alcoa -page 3, 4 SGL -page 3, 4, 6 Rio Tinto Alcan -page 4 Papyex -page 6 Mersen and Sigraflex -page 6 (showing as TM on description but not on website) Carbone Savoie -page 6,11 Intellectual Property Office is an operating name of the Patent Office www.gov.uk /ipo Cathode block for electrolytic cell suitable for the Hall-Heroult process
Technical field of the invention
The invention relates to a cathode block for an electrolytic cell for producing aluminium by fused salt electrolysis using the Hall-Heroult-process. In particular, the invention relates to a cathode block in which the electrical contact between the cathode material and the busbar to which the cathode is connected involves a copper bar.
Prior art
The Hall-Fleroult process is the only continuous industrial process for producing metallic aluminium form aluminium oxide. Aluminium oxide (A1203) is dissolved in molten cryolite (Na3AIF6), and the resulting mixture (typically at a temperature comprised between 940°C and 970°C) acts as a liquid electrolyte in an electrolytic cell. An electrolytic cell (also called "pot") used for the Hall-Heroult process typically comprises a steel shell, a lining usually made from refractory bricks, a cathode usually covering the whole bottom of the pot (and which is usually made from graphite, anthracite or a mixture of both), and a plurality of anodes (usually made from carbon) that plunge into the liquid electrolyte. Anodes and cathodes are connected to external busbars. An electrical current is passed through the cell (typically at a voltage between 3.8 V to 5 V) which splits the aluminium oxide in aluminium ions and oxygen ions. The oxide ions are reduced to oxygen at the anode, said oxygen reacting with the carbon of the anode. The aluminium ions move to the cathode where they accept electrons supplied by the cathode; the resulting metallic aluminium is not miscible with the liquid electrolyte, has a higher density than the liquid electrolyte and will thus accumulate as a liquid metal pad on the cathode surface from where it needs to be removed from time to time, usually by suction.
The electrical energy is the main operational cost in the Hall-1-leroult process. Capital cost is an important issue, too. Ever since the invention of the process at the end of the 19th century much effort has been undertaken to improve the energy efficiency (expressed in kW/h per kg or ton of aluminium), and there has also be a trend to increase the size of the pots and the current intensity at which they are operated in order to increase the plant productivity and bring down the capital cost per unit of aluminium produced in the plant.
Electrolytic cells presently used for the Hall-1-leroult process are rectangular and have a length usually comprised between 8 and 20 meters and a width usually comprised between 3 and 5 meters. Most newly installed pots operate at a current intensity comprised between about 400 kA and 600 kA. They are always operated in series of several tens (up to more than a hundred) pots; within each series DC currents flow from one cell to the neighbouring cell. Much effort is still being made to optimise the process in order to increase its energy efficiency.
The passage of the enormous current intensities through the electrolytic cell leads to ohmic losses at various locations of the pot. Aluminium conductors are used for the busbar systems for both anodes and cathodes. However, aluminium cannot be used in direct contact with the cathode blocks due to its low melting point (about 660°C for pure aluminium). As a consequence, steel bars are conventionally used for ensuring electrical contact with the cathode blocks; these so-called cathode bars are connected to cathode busbars (made from aluminium) by welded and/or bolted connectors. Cathode bars are typically fitted into slots machined into the lower surface of the cathode block. Electrical contact between the steel bar and the carbon material of the cathode block can be direct, or the steel bar can be embedded in cast iron.
During the past decades, much effort has been devoted to the decrease of ohmic losses in cathode bars. Most inventions reported in prior art patents focus on the intrinsic conductivity of the steel cathode bar, or on the contact resistance between the cathode bar and the cathode block or between the cathode bar and the aluminium busbar.
The increase in the electrical conductivity of the cathode bars implies the use of a material having a higher electrical conductivity than steel bars. All reported solutions imply the use of inserts made from a material with a higher electrical conductivity into the cathode bar, which is usually made from steel. The material with a higher electrical conductivity is usually copper. Typical solutions comprise a copper rod or bar that is inserted into a groove or slot machined into the steel cathode bar, over all or part of the length of said cathode bar. The basic concept of a copper insert fitted into a slot or groove machined in a steel cathode bar is described in WO 2001/63014 (Comalco), WO 2005/098093 (Aluminium Pechiney) and WO 2009/055855 (BHB Billington).
FR 1 161 632 (Pechiney) discloses a copper insert fitted into a groove machined in a carbon cathode block using cast iron as a sealing material. The composition of cast iron used for sealing cathode bars into the grooves of carbon cathodes is known to be critical (see US 2,953,751 assigned to Pechiney), because the cast iron should not undergo any swelling due to structural transformations, as swelling could cause the carbon material to develop cracks.
A large number of more specific embodiments have been described for these copper inserts, such as: -A copper bar with circular cross section fitted into a steel bar with outer rectangular cross section and an inner "U" section, the "U" section being closed by a block, see US 3,551,319 (Kaiser).
-A copper bar welded to a lateral face of a steel bar, see US 3,846,388 (Pechiney).
-A copper bar with rectangular cross section inserted into a steel tube with rectangular cross sections, see US 5,976,333 (Alcoa).
-A copper bar with circular cross section inserted into a steel tube with rectangular external cross section and a bore with circular cross section, see WO 2005/098093 (Aluminium Pechiney).
Several documents disclose the use of a joint material present between the cathode material and the steel bar: WO 2013/039893 (Alcoa) describes the use of a copper insert as a joint, WO 2007/071392 (SGL Carbon) describes the use of sheets made from expanded graphite, and RU 2285764 describes the use of a carbonaceous paste. Such a joint material may improve the electrical contact between the carbon block and the steel bar.
RU 2285754 proposes to secure the copper bar inserted into the slot of the steel bar by welded-on steel plates while allowing for a narrow cavity between the copper insert and the steel bar, i.e. the section of the copper insert is somewhat smaller that that of the groove into which it is fitted.
The opposite approach is taken by WO 2009/055844 describing the use of roll bonding or explosion bonding in order to obtain an excellent contact between the copper insert and the steel bar over the whole length of the insert.
Another problem addressed by many inventions is the connection between the copper insert and the steel cathode bar. This contact is critical for at least three reasons: the electrical contact between the copper insert and the cathode bar should be as good as possible; the thermal expansion coefficients of steel and copper are rather different and may lead to dimensional variations during the start-up of the pot; and the thermal conductivity of copper and steel is rather different, which needs to be taken into account for designing (and minimising) the heat transfer between the pot and the aluminium busbar.
For this reason, in some prior art embodiments the copper inserts do not extend along the whole length of the steel cathode bar, but a spacer section is provided at each end of the cathode bar into which the copper insert does not extend. Also, the copper bar can be made in two pieces separated in the centre of the cathode by a steel plug and/or an air gap. Such a structure is described in US 6,387,237 and US 6,231,745 (Alcoa).
The opposite approach is proposed by WO 2002/42525 (Servico), namely a cathode bar comprising a steel bar into which at each end a copper bar is inserted, the copper insert extending beyond the end of the steel bar and ensuring the electrical contact with the connection to the the aluminium busbar.
The insertion of copper bars of complex shape into cathode bars has been used to fine-tune the current distribution over the length of the cathode bar; such an embodiment is described in WO 03/014434 (Alcoa). Other structures ensuring a variation of the electrical conductivity of the cathode bar along its length are described in WO 2004/059039 (SGL Carbon) and in WO 2008/062318 (Rio Tinto Alcan).
As can be seen, there has been a wealth of different designs of copper inserts in cathode bars. However, three potential problems with copper inserts have hardly ever been mentioned in the patent literature: Firstly, as all these copper inserts are inlaid into grooves machined into a steel bar, it should be noted that the machining of steel is a rather difficult and expensive process which adds to the cost of the copper material.
Secondly, the melting point of copper (about 1080°C for pure copper) is rather close to the temperature of the liquid phases in the pot (around 950°C to 1000°C). Knowing that cathode blocks have a lifetime between typically 4 to 7 years, and knowing that copper readily forms a dense oxide layer on its surface, and knowing that the melting point of steel is much higher than that of copper, and knowing that spent cathodes usually show a significant deformation of the steel cathode bars, there can be some concern about the long-term behaviour of copper-inserted cathode bars in relation with their dimensional stability (related to possible local melting or at least creep) and contact resistance.
Thirdly, it is desirable to be able to separate the copper insert from the steel bar in spent cathode blocks completely and easily (i.e. without intensive labour). There are two reasons for this: copper is much more expensive than steel, and it is therefore desirable to recover the copper insert from the steel bar for recycling. Furthermore, if the steel bar is recycled with the copper insert or with a significant amount of copper residues, not only the copper will be lost for separate recycling but also the copper may poison the steel batch into which the steel bar is recycled.
It is the objective of the present invention to come up with a new design of cathode bars that solves all of the abovementioned problems.
Figures Figures 1 illustrates the prior art. Figure la shows a schematic perspective view of a cathode block 1 according to prior art. The steel bar 2 is fitted into groove at the bottom surface 5 of the cathode block 1. A copper bar insert 3 is fitted into a groove machined into the higher surface 6 of the steel bar 2.
Figure lb shows a cross section of another prior art cathode block in which the steel bar 2 is fitted into the groove using cast iron 4; a copper bar 3 is fitted into the steel bar 2. Figure lc shows another variant of the prior art embodiment of figure la with two parallel cathode bars 2 made from steel with a copper insert 3.
Figures 2 to 5 illustrate embodiments of the cathode block according to the invention that will be discussed in more detail below.
Figures 6 and 7 show schematic perspective views of two examples of a connector (figure 6) or a connection plate (figure 7) used to connect the copper bar of the cathode block according to the invention to a busbar.
Description
The present invention applies to cathodes used in the Hall-Heroult process that form the bottom of an electrolytic cell, said cathodes being assembled from individual cathode blocks, each of which bears at least one cathode bar.
According to the invention the problem is solved by using a cathode bar comprising a full copper bar 13 over at least part of the length of said cathode block 10. That is to say that over at least part of the length of the cathode block the full section of said cathode bar is copper.
The present inventors have found that copper bars can be used directly as cathode bars, replacing the steel bars, instead of using them as inserts in steel bars. More precisely, the copper bar can be used in direct contact with a carbonaceous material. Said carbonaceous material can be the cathode block 10 itself, or an intermediate carbonaceous material 17 (shown on figure 4a) that is in direct contact with the metallic connection bar 13 made from copper or a copper alloy and also in direct contact with the carbon cathode block 10. No metallic seal (such as steel or cast iron) is used.
The intermediate carbonaceous material 17 in direct contact with the metallic connection bar 13 must be somewhat deformable, such as to accommodate the higher thermal expansion of the metallic connection bar 13, made from copper or a copper alloy, with respect to the material of the cathode block 10. As an intermediate carbonaceous material 17 in direct contact with the copper bar 13 and the cathode block 10, compressed expanded graphite (most conveniently in the form of a sheet) can be used, and/ or carbonaceous sealing paste.
Compressed expanded graphite is available in the form of sheet of different densities and thickness from several manufacturers and under different tradenames (such as PapyexTM manufactured by Mersen and Sigraflex TM manufactured by SGL).
Concerning the carbonaceous sealing paste, the sealing paste advantageously includes carbonaceous particles dispersed in a binder that has a high carbon yield after baking. Said carbonaceous particles can be graphite particles. Such sealing pastes are commercially available from different manufacturers and under various tradenames (Sealing paste HCF 80 from Carbone Savoie for example). The thickness of the sealing paste is calculated according to the width of the collector bar, taking into consideration the differential of thermal expansions between the copper and the graphitized cathode block; a thickness comprised between 15 and 25 mm can be used.
Considering the very different thermal expansion coefficients for the copper and the cathode block, if the copper bar 17 is sealed inside the cathode block groove, and for avoiding any mechanical stresses when starting the pot pre-heating, between the copper bar and the carbon material of the cathode block, the copper should be covered by a deformable intermediate carbonaceous material such as a sheet of compressed expanded graphite. It should be avoided to seal directly the copper bar inside the cathode block groove.
The cathode blocks 10 are usually graphitized carbon blocks.
The expression "direct contact" means that there is direct contact between the copper bar and the carbonaceous material (the carbonaceous material being the cathode block material itself, or an intermediate carbonaceous material such as graphite sheet or a carbonaceous sealing paste), without any intermediate metallic material (such as a steel bar or steel shell, or a metallic sealing material (for example cast iron)). The presence of the natural oxide layer on the copper bar is unavoidable and does not prevent "direct contact".
According to one embodiment of the invention shown schematically in figure 2a, the copper bar 13 is directly inserted into a groove machined in the lower surface 15 of the cathode block 10; this surface is advantageously the bottom surface of the cathode. The groove extends advantageously parallel to the length of the cathode block 10. In a first variant the groove extends over the whole length of the cathode block, and so does the cathode bar. In a second variant shown in figure 2d the groove is made on each end of the cathode block, and these two grooves are separated by a gap 16 centred at mid-length of the cathode block.
According to another embodiment of the invention shown on figures 2b and 2c, the copper bar is inserted into a hole drilled into the cathode block 10. The hole extends parallel to the length of the cathode block. In a first variant of this embodiment (shown on figure 2b) a continuous hole is made in the cathode block, a continuous copper bar 13 is inserted. In another variant of this embodiment (shown on figure 2c), the hole is discontinuous, and two half copper bars 13a,13b are inserted from each extremity of the cathode block 10; inside the cathode block they are separated by a gap 16 centred at mid-length of the cathode block 10.
The cathode bars 13, 13a, 13b can be made with full cylindrical copper bars inserted into a cylindrical hole of corresponding section. They can also be made with full rectangular copper bars inserted into a rectangular groove of corresponding section that has been machined at the bottom or at the sides of the cathode bar. In that case the rectangular copper bar can be either directly in contact with the cathode block or the copper bars can be sealed inside the grooves using a carbonaceous sealing paste, or there can be another intermediate carbonaceous material such as a sheet of compressed expanded graphite.
Other shapes of cross section of the copper bar and the corresponding groove or hole can be used, but are less preferred as a good surface contact between the cathode block and the copper bar is desirable. One cathode bar or two or more cathode bars can be used on each extremity of the cathode block. Figures 2d(1) and 2d(2) show embodiments with one rectangular bar 13a,13b at each end of the cathode block 10 that is inserted into a groove machined at the bottom face 15 of the cathode block 10; figure 2a(1) shows a continuous bar 13, figure 2d(1) a discontinuous bar 13a,13b. Figures 2a(3) and 2d(3) show corresponding embodiment with two rectangular bars at each end of the cathode block; figure 2a(3) shows continuous bars, figure 2d(3) discontinuous bars. Figures 2b(2) and 2c(2) show embodiments with one round bar inserted into a hole machined into the cathode block; figure 2b(2) shows a continuous bar, figure 2c(2) shows discontinuous bars. Figures 2b(3) and 2c(3) show embodiments with two round bars inserted into holes machined into the cathode block; figure 2b(3) shows continuous bars, figure 2c(3) shows discontinuous bars.
Figure 3 shows an example: two cylindrical copper bars 13a,13b having a diameter of 90 mm and a length e of 1850 mm each are inserted in a hole made on both sides of the lower part of the cathode block 10; the total length a of the cathode block was 3250 mm, the total height b was 425 mm, the total width c was 420 mm, and the cathode bar extends out of the block by a length f of about 525 mm; the gap d between the two embedded ends of the copper bars was about 600 mm. The axis of the collector bars made with full copper cylindrical rod was located at 70 mm from the bottom face of the cathode block. Figure 3 corresponds to the embodiment schematically represented by figure 2c(2).
As the electrical conductivity of the copper (1,68 x 10.8 0 m) is about 6 times higher than that of steel (10 x 10-8 4 m), a given conductivity value of the cathode bar can be obtained with a copper bar having a smaller diameter or section for rectangular copper bars than the steel bar. As an example, to replace a steel bar with a cross section of about 221 cm2 (width 170 mm, height 130 mm), a copper cross section of at least 37,14 cm2 is needed, corresponding to a cylindrical bar of 68.77 mm in diameter.
Using copper bars 13 with larger cross section will lead to an increase in electrical conductivity. In the above example, the increase of the cathode bar section for the copper bar beyond 37.14 cm2 will lead to a higher conductivity of the copper bar compared to the steel bar: the cylindrical copper bar with a diameter of 90 mm has a conductivity that has increased by about 71% compared to that of the steel bar (63.6 cm2 compared to 37.14 cm2 for the equivalent resistance using steel bars). This decrease in ohmic losses in the cell leads to a decrease in voltage drop across the cell. Such an embodiment is shown in figure 4b; this copper rod 13 is inserted into a hole drilled into the lower part of the cathode block 10, parallel to its length.
For replacing a rectangular steel bar with a cross section of 221 cm2 (width 170 mm, height 130 mm) by a rectangular copper bar, a copper cross section of 37.14 cm2 would be sufficient; such a rectangular copper bar could have a cross section of approximately 60 mm by 65 mm.
For the case of using rectangular copper bar and to obtain the same increase of conductivity of 71%, the copper section would have to be about 69 cm2, which could be achieved by a rectangular copper rod of 70 by 100 mm. Such a rectangular copper bar should be installed horizontally inside the cathode block groove, meaning that the groove must have between 120 to 125 mm of width and between 72.5 and 75 mm of depth if a carbonaceous sealing material (sheet of compressed expanded graphite and carbonaceous sealing paste) is used.
Another consequence of the higher electrical conductivity of copper (and the smaller diameter of the copper bar with respect to the steel bar) is the possibility to increase the depth of the copper bar in the cathode with respect of that of the steel bar, that is to say the spacing h between the upper surface 50 of the cathode block 10 that is in contact with the liquid aluminium and the upper surface 51 of the cathode bar 13. In the above example, the full copper bar (cylindrical rod of 90 mm diameter, i.e. a cross section of 63.6 cm2) replaces a rectangular steel bar of much greater height (130 mm, width 170 mm, i.e. a cross section of 221 cm2)), and the thickness of carbonaceous material in the cathode block is increased from h = 275 mm to h = 310 mm (see figure 4b), taking into account the additional thickness of the cast irons seal.
Figure 4b shows a cylindrical copper bar installed on the bottom of the cathode block. In this example, if cylindrical copper bars of 90 mm of diameter is used, the thickness h of carbonaceous material between the liquid aluminium and the upper surface of the copper bar can be increased from 275 mm to 310 mm. This increase of 35 mm (or 13 % more material) corresponds to about 8.4 months of wear for the cathode blocks, and therefore extends the life expectancy of the pot by 0.7 year.
In a variant of the rectangular copper rods, shown on figure 4a, a rectangular copper bar 13 with a width of 100 mm and an height of 70 mm (cross section = 70 cm2) has been inserted in a rectangular groove made in the bottom of the cathode block 10. The total height b of the cathode block is 425 mm. In this case the thickness h of carbon material above the copper bar (355 mm) is still higher than in the case of a cylindrical bar inserted into a hole: plus 45 mm. This increase of 80 mm (or 29 % more material) corresponds to about 1.6 years of wear for the cathode blocks, and therefore extends the life expectancy of the pot by 1.6 years. On the figure 4a, the intermediate carbonaceous material 17 is used between the rectangular copper bar 13 and the carbonaceous material of the cathode block 10. This carbonaceous material might be avoided on the horizontal faces of the copper bar as very small amount of current is going through this top surface.
In a variant of the rectangular copper rod shown in figure 4c, the rectangular copper bar can be inserted directly in contact inside the groove made on the bottom of the cathode block, providing that the right adjustment is made for the copper rod inside the groove.
As there is a temperature gradient across the thickness of the cathode block, the copper cathode bar will heat less than the steel cathode bar. Moreover, due to the higher thermal conductivity of copper compared to steel, the copper cathode bar will transport more heat than a steel cathode bar of identical design.
Figure 5 shows a cross section across a Hall-Heroult electrolysis pot 20 according to the invention with cylindrical copper bars; the cross section is parallel to the width of the pot. The copper cathode bars 23a, 23b are discontinuous, with a gap 26 in the centre of the length of the cathode block 21.
A possible problem related to the use of a full copper cathode bar is related to overheating of the cell. In modern Hall-Heroult cells the temperature of the liquid aluminium sheath 29 in contact with the upper surface 27 of the cathode blocks 21 is normally about 960°C to 965°C, and under these operating conditions the temperature in the centre of the cathode block can reach 950°C. However, in case of abnormal conditions the temperature of the aluminium sheath can increase to over 1000°C, typically up to 1080°C for short duration of up to 24 hours. Such overheating may occur especially when starting the pot. While modern potlines and sophisticated pot control can avoid and limit overheating (above 1080°C), this event cannot be fully excluded throughout the normal lifetime of an electrolysis pot (5 to 7 years).
Knowing that the melting point of pure copper is about 1084°C, it must be ruled out that in case of abnormal overheating the cathode bar 13 suffers irreversible damage. Increasing the carbon thickness 17 over the upper surface of the copper bar 13 will decrease the temperature seen by the copper bar 13 by a few degrees. Inserting the copper bar 13 in a groove at the bottom 15 of the cathode block 10 will further increase the carbon thickness h and gain a few degrees. In any case, using the cathode block according to the invention in a Hall-Heroult cell for the manufacture of aluminium requires a careful control of operating conditions in order to avoid overheating of the cell, or at least to limit it to small overheat and/or for short period periods of time.
In a preferred embodiment of the invention the copper cathode bars 13, 23 are made from 99.99% copper that is oxygen free (OFE Copper grade).
In another embodiment copper alloys are used that have a higher melting point (by about 15°C to 35°C) than pure copper; however, such alloys will have a lower electrical conductivity.
Another potential problem related to the use of unsealed copper bars is the copper carbon interface: copper oxidation or other changes in properties of the copper close to the carbon block may lead to higher electrical contact resistance. For this reason, and in case of rectangular copper bars, it is preferable to wrap the rectangular copper bars with graphite sheet (graphite "paper") before sealing it inside the cathode block groove shown in figure 4a. This graphite sheet separates the copper bar from the cathode block material, which is advantageous considering the very different thermal expansion coefficients of copper and of the cathode block material; the graphite foil can also act as a barrier preventing the oxidation of the copper surface.
When designing cathode blocks according to the invention in which steel cathode bars are replaced by copper cathode bars, another potential problem is related to the different thermal expansion coefficient of steel and copper: about 16.6 x 10.6 m/m/K for copper, about 12 x 10-6 m/m/K for average steel used in cathode bars and cast iron used for sealing steel cathode bars. The thermal expansion coefficient for typical graphite (such as D grade from Carbone Savoie) is about 5.3 x 10-6 m/m/K. The thermal expansion of copper is much higher than that of graphite, and higher than that of steel. This needs to be taken into account when determining the width of the hole or groove made in the cathode to insert the copper bar.
The invention has numerous advantages. A gain in voltage drop of more than 100 mV can be reached in industrial potlines.
The increase in capital cost over prior art embodiments is not very significant. Copper is more expensive than steel, but this difference is partially offset because less copper is needed. While copper does add to the initial cost of the cathode bar according to the invention, part of this initial cost is recovered by copper recycling. Since no cast iron is needed, the cost of cast iron and necessary man hours (and possibly the cost of the cast iron plant itself) is saved. On the other hand, the machining operation for the groove (and especially for the hole) is more expensive than for the groove according to prior art because the dimensional tolerance is a critical issue, while a steel bar can be sealed with cast iron into a groove with no special requirement of dimensional tolerance. Referring to the rectangular copper bars, the groove to machine is not expensive as a gap is needed to seal the copper bars, the groove machining tolerance can be the same as the genuine one for steel bars: +/-2 mm. Even for the cylindrical copper bars that need a very tight tolerance that may be difficult to achieve with some older machining equipment, the inventors have found that the total additional cost of the cathode block according to the invention is offset by the higher energy efficiency of such a cell.
The cathode block according to the invention needs to be connected to the cathode bus bar. Specific connectors 30 are needed to connect cylindrical copper bars 33 to the cathode bus bar.
For the cylindrical copper bars 33, an advantageous solution for connecting the copper bar extremities to the original cathode flex is shown in figure 6: to connect the copper tabs 34a, 34b welded to the aluminium flexes (not shown on the figure) to the cylindrical copper bar 33 extremities, two special copper plates 39a, 39b in contact with the copper cathode bar 33 are added: these copper plates 39a, 39b have a cylindrical recession on one side (in contact with the copper bar 33), the other side in contact with the genuine copper pads 34a, 34b being flat. A means of pressing the two copper tabs against the coper bar can be added (not shown on the figure). Advantageously the diameter of the cylindrical recess is about the same as that of the copper bar 33; as an example, for a copper bar of diameter 90 mm a recess of diameter 90 mm is used.
As shown in figure 7, another simple way to connect the cathode flexes (not shown) to the extremities 72 of the copper bar 33 is to add a metallic piece 70 to the extremities 72 of the copper bar 33, preferably by welding. Said metallic piece 70 comprises a steel plate providing a substantially vertical (preferably flat) contact surface 71 onto which tri-metallic dads (aluminium, titanium and steel parts, not shown) can be welded. This solution is far less expensive than to add extra copper plates between copper tabs and copper bars, and, more importantly, the short voltage drop, measured from the copper bar and the bus bar where the aluminium cathode flex is welded, will be very low.

Claims (15)

  1. CLAIMS1. Cathode element suitable for use in a Hall-Heroult electrolysis cell, comprising -a cathode block comprising a carbonaceous material, -at least one metallic connection bar made in copper or copper alloys, wherein said metallic connection bar is fitted into a groove or bore in direct contact with a carbonaceous material, and wherein said carbonaceous material can be the carbonaceous material of said cathode block, or an intermediate carbonaceous material that is in direct contact with the carbonaceous material of said cathode block.
  2. 2. Cathode element according to claim 1, wherein said cathode element does not comprise any other metallic connection bar in direct contact with the carbonaceous material than connection bars made in copper or copper alloys.
  3. Cathode element according to claim 1 or 2, wherein said intermediate carbonaceous material is compressed expanded graphite and/or a cured carbonaceous seal (and preferably a graphitized carbonaceous seal).
  4. 4. Cathode element according to claim 3, wherein said cured (and preferably graphitized) carbonaceous seal comprises graphite particles.
  5. 5. Cathode element according to claim 3 or 4, wherein the connection bar is in direct contact with compressed expanded graphite, and wherein said expanded compressed graphite is in direct contact with a cured (and preferably graphitized) carbonaceous seal, said cured carbonaceous seal being in direct contact with the carbonaceous material of the cathode block.
  6. 6. Cathode element according to any of claims 1 to 5, wherein said metallic connection bar has a round or a rectangular cross section.
  7. 7. Cathode element according to any of claims 1 to 6, wherein said metallic connection bar has a rectangular cross section, and an intermediate carbonaceous material is used in direct contact with the metallic connection bar, said intermediate carbonaceous material being preferably compressed expanded graphite.
  8. Cathode element according to any of claims 1 to 7, wherein a metallic piece is fixed to the extremities of the metallic connection bar, preferably by welding, said metallic piece comprising a steel plate providing a substantially vertical, preferably flat, contact surface.
  9. 9. Cathode element according to claim 8, wherein tri-metallic dads are welded onto said contact surface, which can be electrically connected to a cathode bus bar.
  10. 10. Cathode element according to any of claims 1 to 9, wherein said metallic connection bars extend from both extremities towards the centre length of the cathode block, leaving a gap in the centre of the cathode block.
  11. 11. Process for manufacturing a cathode element suitable for use in Hall-Heroult electrolysis cell comprising the steps of: -providing a cathode block comprising a carbonaceous material and at least one metallic contact bar made from copper or a copper alloy, -machining at least one groove or drilling at least one bore in a direction parallel to the length of said cathode block, -optionally covering at least part of the surface of said metallic bar with an intermediate carbonaceous material, -fitting said metallic connection bar into each of said grooves or said bores, wherein said metallic bar is fitted in such a way that direct contact between said carbonaceous material and the metallic bar is ensured, without the use of a metallic sealing material, said carbonaceous material in direct contact with said metallic contact bar being either the cathode block itself or said intermediate carbonaceous material.
  12. 12. Process according to claim 11, wherein said intermediate carbonaceous material comprises a sheet of compressed expanded graphite.
  13. 13. Process according to claim 11 or 12, wherein said intermediate carbonaceous material comprises a seal, preferable containing graphite particles, said seal being applied onto said metallic contact bar and/or onto at least one face of said sheet of compressed expanded graphite.
  14. 14. Process according to any of claims 11 to 13, wherein said intermediate carbonaceous material is used for rectangular metallic contact bars.
  15. 15. Process for producing aluminium in a Hall-Fleroult electrolysis cell, wherein said electrolysis cell comprises one or more cathode elements according to any of claims 1 to 10.
GB1505435.6A 2015-03-30 2015-03-30 Cathode block for electrolytic cell suitable for the Hall-Héroult process Withdrawn GB2536901A (en)

Priority Applications (5)

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GB1505435.6A GB2536901A (en) 2015-03-30 2015-03-30 Cathode block for electrolytic cell suitable for the Hall-Héroult process
CA2980832A CA2980832C (en) 2015-03-30 2016-03-22 Cathode block for electrolytic cell suitable for the hall-heroult process
PL16771479T PL3277864T3 (en) 2015-03-30 2016-03-22 Cathode block for electrolytic cell suitable for the hall-héroult process
EP16771479.9A EP3277864B1 (en) 2015-03-30 2016-03-22 Cathode block for electrolytic cell suitable for the hall-héroult process
PCT/IB2016/051592 WO2016157021A1 (en) 2015-03-30 2016-03-22 Cathode block for electrolytic cell suitable for the hall-héroult process

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GB1505435.6A GB2536901A (en) 2015-03-30 2015-03-30 Cathode block for electrolytic cell suitable for the Hall-Héroult process

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GB201505435D0 GB201505435D0 (en) 2015-05-13
GB2536901A true GB2536901A (en) 2016-10-05

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CA (1) CA2980832C (en)
GB (1) GB2536901A (en)
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GB2554702A (en) * 2016-10-05 2018-04-11 Dubai Aluminium Pjsc Cathode assembly for electrolytic cell suitable for the Hall-Héroult process
GB2558936A (en) * 2017-01-23 2018-07-25 Dubai Aluminium Pjsc Cathode assembly with metallic collector bar for electrolytic cell suitable for the Hall-Héroult process

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CN109082687A (en) * 2018-10-12 2018-12-25 三门三友科技股份有限公司 A kind of cupric electrolysis cathode collector bar
FR3090699B1 (en) * 2018-12-20 2021-04-09 Rio Tinto Alcan Int Ltd Anode assembly and associated manufacturing process
GB2595460A (en) * 2020-05-26 2021-12-01 Dubai Aluminium Pjsc Cathode assembly with metallic collector bar systems for electrolytic cell suitable for the Hall-Héroult process

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GB2554702A (en) * 2016-10-05 2018-04-11 Dubai Aluminium Pjsc Cathode assembly for electrolytic cell suitable for the Hall-Héroult process
GB2558936A (en) * 2017-01-23 2018-07-25 Dubai Aluminium Pjsc Cathode assembly with metallic collector bar for electrolytic cell suitable for the Hall-Héroult process

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CA2980832C (en) 2022-12-06
EP3277864A1 (en) 2018-02-07
CA2980832A1 (en) 2016-10-06
WO2016157021A1 (en) 2016-10-06
EP3277864A4 (en) 2018-09-05
GB201505435D0 (en) 2015-05-13
PL3277864T3 (en) 2020-10-19
EP3277864B1 (en) 2020-05-06

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