EP0353943A1 - Procédé pour la terminaison des effets anodiques au cours de la production de l'aluminium - Google Patents

Procédé pour la terminaison des effets anodiques au cours de la production de l'aluminium Download PDF

Info

Publication number
EP0353943A1
EP0353943A1 EP89307626A EP89307626A EP0353943A1 EP 0353943 A1 EP0353943 A1 EP 0353943A1 EP 89307626 A EP89307626 A EP 89307626A EP 89307626 A EP89307626 A EP 89307626A EP 0353943 A1 EP0353943 A1 EP 0353943A1
Authority
EP
European Patent Office
Prior art keywords
anodes
groups
cell
anode
moved
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP89307626A
Other languages
German (de)
English (en)
Inventor
Vinko Potocnik
Jean-Eudes Gagne
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Rio Tinto Alcan International Ltd
Original Assignee
Alcan International Ltd Canada
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Alcan International Ltd Canada filed Critical Alcan International Ltd Canada
Publication of EP0353943A1 publication Critical patent/EP0353943A1/fr
Withdrawn legal-status Critical Current

Links

Images

Classifications

    • 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

Definitions

  • This invention relates to a process for quenching or terminating so-called “anode effects" which occur when aluminum is produced from alumina by electrolysis.
  • the electrolytic reduction of alumina is normally carried out in a Hall-Heroult cell which comprises an elongated shallow container lined with a conductive material., such as carbon, used to form a cathode.
  • the container holds a molten electrolyte, normally cryolite containing about 2-6% by weight of dissolved alumina, and a number of carbon anodes dip into the electrolyte from above.
  • molten aluminum is formed and descends to the bottom of the cell where it forms a pool acting as the cell cathode.
  • Oxygen gas is also liberated and this tends to oxidize the carbon anodes and thereby forms carbon dioxide and/or carbon monoxide. Since the anodes are gradually consumed and since a generally constant anode-cathode spacing must be main­tained, lifting apparatus is provided above the cell to enable the anodes to be raised, lowered and eventually replaced.
  • anode panel In one type of cell, namely the Soderberg cell, only one large carbon anode is provided which almost completely covers the upper surface of the cell.
  • a large number of smaller anodes are provided and arranged in longitudinal and trans­verse rows referred to as the anode panel. Normally there are two longitudinal rows of anodes arranged symmetrically on each side of the longitudinal cell axis. The spacing between the two rows along the cell axis is referred to as the centre channel. The number of tranverse rows is variable according to the size of the cell, but there are normally up to fifteen, usually 8 to 15, such rows, all of which are normally equally spaced from each other.
  • the elec­trolyte is held at a temperature in the range of 950-980°C in order to keep the electrolyte and aluminum in a molten state.
  • the temperature is lower at the electrolyte surface which solidifies to form a solid crust.
  • the electrolyte may also solidify adjacent to the cell walls where the tempera­ture also tends to be lower.
  • the concentration of alumina in the electrolyte falls and more is added by periodically breaking the crust in limited places and adding the alumina from above.
  • the concentration of alumina declines most rapidly in the region of the electrolyte immediately beneath the anodes. When the concentration in these regions falls to about 2% by weight or less, the so-called anode effect is observed. This manifests itself as a high voltage (up to around 40 volts) and the appearance of fluorocarbons in the anode gas.
  • the anode effect is explained in detail in such publications as Aluminum Electrolysis Fundamentals of the Hall-Heroult Process, 2nd Edition, by K. Grjotheim et al, Aluminum Verlag, 1982, pp 264-283; and Aluminum Smelter Technology, 2nd Edition, by K. Grjotheim and B. J.
  • Quenching is conventionally carried out by (a) break­ing the crust and adding alumina to the cell, and (b) sweeping the gas from beneath the affected anodes by vigorous stirring of the electrolyte, which also helps to distribute the alumina from the feeding points into the whole volume of the cell.
  • Wooden poles or gas lances were traditionally used to stir the electrolyte under the anodes, but attempts have been made in the last few years to develop more effective and automated techniques.
  • Canadian Patent 1,148,892 issued on June 28, 1983 to Saksvikr ⁇ nning et al . (which relates to a Soderberg type of cell) discloses the idea of tilting and rocking the single anode to sweep away the unwanted gases and to mix the cell contents.
  • this is not really suitable for use in prebake cells because the numerous anodes of the latter type of cell are spaced too closely for individual tilting and because complex equipment would be required.
  • Spence suggests that all anodes on one longitudinal side of the cell could be raised while all anodes on the other longitudinal side could be lowered (pivoting around the longitudinal axis of the cell), or that all anodes at one end of the cell could be raised while all those at the opposite side could be lowered (pivoting around the transverse axis of the cell), or further that one quarter of the anodes in one corner could be raised while those in the diagonally opposed quarter could be lowered (a so-called "kitty corner” action). While these procedures are effective, the efficiency with which anode effect quenching can be achieved is not as high as we would have hoped and is usually in the range of 80-90%.
  • an object of the present invention is to provide a process for quenching or terminating the anode effect which can be carried out with improved efficiency.
  • a method of terminating an anode effect occurring during the produc­tion of aluminum in an electrolytic cell containing a molten electrolyte including alumina and having a plurality of carbon-containing anodes arranged in at least two longitu­dinal rows and at least three transverse rows forming an anode panel comprising: adding alumina to the electrolyte; dividing at least 25% of the total number of anodes into groups of adjacent anodes located at different positions in the longitudinal direction of the cell, each group containing at least two anodes but no more than one third of the total number of anodes; initially moving at least one of said groups in a first vertical direction from an original operating position, moving the remaining groups in an opposite vertical direction from an original operating position, wherein said group(s) moved in said first vertical direction and said group(s) moved in said opposite vertical direction alternate with each other in the longitudinal direction of the cell; returning said anodes to their original operating positions; and repeating or reversing said movements of the
  • the pattern of movement required by the present invention ensures that only a relatively small number of adjacent anodes forming a group moves in the same direction at the same time within a particular area of the cell while anodes neighboring the group either do not move at all or move in the opposite direction.
  • This has the advantage that, breakage of the crust is minimized since widespread up and down forces are not exerted on the crust.
  • the invention ensures that the pumping action is maximized because anode movement takes place at various positions along the cell and the opposed direction of movement of longitudin­ally neighboring groups causes efficient mixing of the added alumina with the electrolyte. There may also be some electromagnetic stirring of the cell contents as a result of the anode movements.
  • the invention at least in its preferred forms, can provide a quenching efficiency of up to 99% and can quench anode effects in short periods of time, e.g. less than one minute.
  • Other advantages are that there is a low loss of energy (e.g. 10-20 millivolts equivalent per anode effect day), and variations in the bath level can be minimized or eliminated altogether.
  • each group must contain at least two adjacent anodes and preferably contains no more than six adjacent anodes.
  • the adjacent anodes of each group preferably form one or more entire transverse rows although this is not essential.
  • adjacent anodes on each side of the longitudinal centreline of the cell always move in the same direction and this tends to minimize breakage of the crust over the centre channel, which breakage can result in pieces of the crust falling into the electrolyte causing sludging of the cathode floor and an unnecessary loss of heat.
  • the alternating arrangement of the groups means that each group of anodes which initially moves up is positioned between two groups that initially move down, and vice versa, except at the extreme ends of the cell.
  • immobile anodes may separate "up" groups from “down” groups, at least in some parts of the cell.
  • While as few as 25% of the anodes may be caused to move, either up or down, preferably at least 40% are caused to move and, most desirably, all of the anodes are caused to move.
  • the groups of anodes may be moved simultaneously or sequentially in a continuous or stepwise manner.
  • the number of anodes raised at a given time may equal the number of anodes lowered, with the distance of travel being the same, so that there is no change of electrolyte level in the cell. This, however, is by no means essential because small variations in the electrolyte level, either up or down, can normally be tolerated and may even be beneficial in some cases.
  • the pattern of anode movement clearly should not be such as to cause unacceptable degrees of movement of the electrolyte level.
  • the group(s) of anodes designated to move upwardly should preferably be moved first in order to prevent electrolyte overflow.
  • All of the "up” groups may be raised at the same time and simultaneously or subsequently all of the “down” groups may be lowered.
  • the different “up” groups may be raised at different times (e.g. producing a "ripple” effect along the cell) and the different “down” groups may be lowered in the same way.
  • the anodes may be moved either up or down continuously or in steps (i.e. short rapid movements with pauses between them). If the movement is stepwise, the stepwise motions of all of the anodes may be simultaneous or alternatively may be completely independent.
  • the anodes should not be moved.
  • the maximum down travel might be beyond the short-out point because shorting may be desired in some cases (e.g. it is a radical way to quench an anode effect that does not respond to the method of the invention).
  • the upward movement should not remove the anode from the electrolyte and, particularly, should not let the anode break free of the crust. This causes a greater amount of current to flow through the other anodes and can result in catastrophic heating and even explosion.
  • the anodes After the anodes have been moved through their maxi­mum distance of travel in either the up or down directions, the anodes are returned to their original operating positions (i.e. their positions prior to the appearance of the anode effect).
  • the anodes may be returned with the same, but opposite, pattern of motion and at the same speed that they were moved away from the original operating position (e.g. if they were initially moved in a stepwise fashion, they may be returned in a stepwise fashion).
  • the anodes may be returned with a different pattern of motion and/or at a different speed.
  • one or more other cycles may be carried out until quenching results.
  • the pattern of motion of the anodes in the subsequent cycle(s) may be the same as, or opposite to, the pattern in the first cycle. That is, the "up" anodes and the “down" anodes of the first cycle may move in the same, or alternatively in the opposite, initial directions.
  • the pattern of motion of the electrodes is often reversible as described above (i.e. the groups which initially move upwardly from the original operating position, may instead be moved downwardly and vice versa ), it may some­times be desirable to ensure that the electrodes at the extreme longitudinal ends of the cell never move downwardly from the original operation position. This is because the electrolyte may "freeze" adjacent to the end walls and the resulting solid electrolyte may extend partially beneath the end electrodes so that downward movement of the electrodes might result in damage either to the electrodes themselves or to the electrode supporting structure.
  • the alumina may be added to the cell in the conven­tional manner, e.g. by breaking the crust (normally at the centreline of the cell) and adding the alumina to the liquid electrolyte.
  • the pumping effect of the anodes quickly distributes the added alumina throughout the cell.
  • the quantity of alumina added may again be the amount conventionally used.
  • the alumina addition does not have to be simultaneous with the commencement of the anode movement.
  • the alumina may be added shortly before the anodes are moved or alternatively there may be a delay of 10 to 20 seconds, or even more, before the alumina is added. Naturally, the sooner the alumina is added, the sooner quenching is likely to begin.
  • the speed with which the anodes are moved is not particularly critical to the success of the invention.
  • a slow speed requires more time for the quenching effect to take place and therefore faster speeds are preferable.
  • the movement should not be so fast as to produce damage to the crust or spillage of the electrolyte.
  • the method of the invention requires an anode support­ing structure capable of moving different groups of anodes in different directions either simultaneously or sequen­tially.
  • the apparatus described in our U.S. Patent 4,414,070 to Spence is suitable for this purpose because it provides individual up and down movement of the anodes for all of the anodes of the anode panel.
  • a less complex apparatus could physically interconnect the electrodes of individual groups or of all the "up” groups and all the "down" groups for simultaneous movement.
  • the pattern of anode movement, as well as the maximum distances of anode travel may be computer controlled, which is particularly easy to arrange when using the apparatus described in the patent referred to above.
  • the anodes of a cell having two longitudinal rows and 12 transverse rows are divided into groups consisting of four and six anodes (the drawing shows individual anode blocks, two of which in the transverse direction form a single anode as will be apprec­iated by persons skilled in the art).
  • the groups consisting of four anodes are initially moved upwardly from their original operating positions and the groups consisting of six anodes are initially moved downwardly, as shown.
  • the direction of movement is reversed and the anodes are returned to their original operating positions.
  • alumina is added to the cell through a hole made in the crust along the centre channel.
  • the procedure may be repeated, with the anodes moving in the same initial directions indicated in the Figure or in the opposite directions, and the anodes again returned to their original operating positions.
  • the procedure may be repeated any number of times until the anode effect is suitably quenched.
  • the anodes of the three "up” groups may all be moved simultaneously or they may alternatively be moved sequentially (to produce a "ripple” effect along the cell).
  • the movement may be continuous or step wise, i.e. in small increments.
  • the same is true of the movement of the "down” groups (i.e. the anodes in rows 3-4-5 and 8-9-10).
  • the "up” and “down” groups may be moved simultaneously or sequentially.
  • the number of anodes moving up equals the number of anodes moving down at any particular time so that the electrolyte level remains the same as it was when the electrodes were in the original positions.
  • small variations in the electrolyte level are permissible, and so virtually any continuous or sequential anode movement pattern can be adopted, provided the anodes initially move in the directions indicated.
  • Fig. 1 The pattern shown in Fig. 1 can be reversed, i.e. the "up” groups can be made “down” groups and vice versa .
  • Fig. 2 shows an alternative movement pattern for the cell of Fig. 1 and Fig. 3 shows a preferred movement pattern for a cell having 9 transverse rows.
  • the movement can be continuous or stepwise, simultaneous or sequential and the direction of initial movement can be reversed.
  • a Hall-Heroult cell (Apex cell) having two longitudinal rows of anodes and twelve transverse rows was equipped with a superstructure capable of producing individual anode movements, and the cell was operated in the normal way until anode effects developed. Attempts were then made to quench the anode effects by particular anode movement patterns coupled with the addition of alumina.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electrolytic Production Of Metals (AREA)
EP89307626A 1988-08-04 1989-07-27 Procédé pour la terminaison des effets anodiques au cours de la production de l'aluminium Withdrawn EP0353943A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CA573886 1988-08-04
CA573886 1988-08-04

Publications (1)

Publication Number Publication Date
EP0353943A1 true EP0353943A1 (fr) 1990-02-07

Family

ID=4138492

Family Applications (1)

Application Number Title Priority Date Filing Date
EP89307626A Withdrawn EP0353943A1 (fr) 1988-08-04 1989-07-27 Procédé pour la terminaison des effets anodiques au cours de la production de l'aluminium

Country Status (5)

Country Link
EP (1) EP0353943A1 (fr)
CN (1) CN1040065A (fr)
AU (1) AU3926089A (fr)
BR (1) BR8903916A (fr)
NO (1) NO893153L (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004038069A1 (fr) * 2002-10-23 2004-05-06 Alcan International Limited Procede de regulation d'effets d'anode pendant la production d'aluminium

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102758224B (zh) * 2011-04-29 2015-02-25 沈阳铝镁设计研究院有限公司 阳极效应抑制与熄灭的方法
CN103668328A (zh) * 2013-12-14 2014-03-26 云南云铝润鑫铝业有限公司 一种消除铝电解槽阳极效应的装置及方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2083362A1 (en) * 1970-03-18 1971-12-17 Inst Politehnic Ti Electrolysis of aluminium - with suppressed anodic effect
US4039419A (en) * 1976-07-23 1977-08-02 Aluminum Company Of America Anode positioning device
EP0086593A1 (fr) * 1982-02-12 1983-08-24 Alcan International Limited Dispositif de positionnement d'anodes

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2083362A1 (en) * 1970-03-18 1971-12-17 Inst Politehnic Ti Electrolysis of aluminium - with suppressed anodic effect
US4039419A (en) * 1976-07-23 1977-08-02 Aluminum Company Of America Anode positioning device
EP0086593A1 (fr) * 1982-02-12 1983-08-24 Alcan International Limited Dispositif de positionnement d'anodes

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004038069A1 (fr) * 2002-10-23 2004-05-06 Alcan International Limited Procede de regulation d'effets d'anode pendant la production d'aluminium
US6866767B2 (en) 2002-10-23 2005-03-15 Alcan International Limited Process for controlling anode effects during the production of aluminum

Also Published As

Publication number Publication date
NO893153D0 (no) 1989-08-03
AU3926089A (en) 1990-02-08
BR8903916A (pt) 1990-03-27
NO893153L (no) 1990-02-05
CN1040065A (zh) 1990-02-28

Similar Documents

Publication Publication Date Title
EP0560814B1 (fr) Ensembles d'electrodes et cellules multimonopolaires pour l'extraction electrolytique d'aluminium
DE60013886T2 (de) Bei niedriger temperatur betriebene elektrolysezelle zur herstellung von aluminium
CA1072055A (fr) Pile electrolytique, et procede de circulation de l'electrolyte
RU2006114034A (ru) Электрохимическое восстановление оксидов металлов
EP0353943A1 (fr) Procédé pour la terminaison des effets anodiques au cours de la production de l'aluminium
US4110179A (en) Process and device for the production of aluminium by the electrolysis of a molten charge
AU2008327757B2 (en) Grooved anode for an electrolysis tank
CA2496533A1 (fr) Anode a emission d'oxygene dans des cellules hall-heroult : utilisation et fabrication
US4230540A (en) Technique for automatic quenching of anode effects in aluminium reduction cells
DE69837966T2 (de) Zelle für aluminium-herstellung mit drainierfähiger kathode
CA3030330C (fr) Cellule perfectionnee d'electrolyse d'aluminium
CA1126684A (fr) Traitement electrolytique du plomb
US3178363A (en) Apparatus and process for production of aluminum and other metals by fused bath electrolysis
US20240003031A1 (en) Controlling electrode current density of an electrolytic cell
DE60019782T2 (de) Aluminium elektrogewinnungszelle mit drainierter kathode und verbesserter elektrolytumwälzung
SU828979A3 (ru) Электролизер дл получени АлюМиНи
US3501386A (en) Apparatus and process for the reduction of aluminum
EP0393816A1 (fr) Cuve pour la production électrolytique d'aluminium en bain fondu
CA2123417A1 (fr) Pile pour l'electrolyse d'alumine preferablement a basses temperatures
EP1062382B1 (fr) Distribution d'un electrolyte riche en alumine dans des cellules d'extraction electrolytique a l'aluminium
US20040178079A1 (en) Arrangement of anode for utilisation in an electrolysis cell
CA2458984A1 (fr) Cellule d'electro-extraction avec anode a emission d'oxygene foraminulee inclinee
CA1148892A (fr) Reduction de l'effet anodique, par inclinaison de l'anode
US4673478A (en) Alumina reduction cell
RU1772219C (ru) Способ получени алюмини

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): CH DE ES FR GB LI NL

17P Request for examination filed

Effective date: 19900424

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 19920201