Conditioning of cell components for aluminum production

Chemistry: electrical and wave energy – Apparatus – Electrolytic

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204291, 204290R, 204279, 427113, 4271263, 4271264, 427294, 427314, 4273722, 205384, 205385, C25C 308

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055781748

DESCRIPTION:

BRIEF SUMMARY
This application is a 371 of PCT/IB94/00071 filed Apr. 15, 1994.


FIELD OF THE INVENTION

This invention relates to a method of conditioning components of electrolytic cells for the production of aluminium in particular by the electrolysis of alumina in a molten fluoride electrolyte.


BACKGROUND ART

Aluminium is produced conventionally by the Hall-Heroult process, by the electrolysis of alumina dissolved in cryolite-based molten electrolytes at temperatures up to around 950.degree. C. A Hall-Heroult reduction cell typically has a steel shell provided with an insulating lining of refractory material, which in turn has a lining of carbon which contacts the molten constituents. Conductor bars connected to the negative pole of a direct current source are embedded in the carbon cathode substrate forming the cell bottom floor. The cathode substrate is usually an anthracite based carbon lining made of prebaked cathode blocks, joined with a ramming mixture of anthracite, coke, and coal tar.
In Hall-Heroult cells, a molten aluminium pool acts as the cathode. The carbon lining or cathode material has a useful life of three to eight years, or even less under adverse conditions. The deterioration of the cathode bottom is due to erosion and penetration of electrolyte and liquid aluminium as well as intercalation of sodium, which causes swelling and deformation of the cathode carbon blocks and ramming mix. In addition, the penetration of sodium species and other ingredients of cryolite or air leads to the formation of toxic compounds including cyanides.
The anodes are usually prebaked carbon blocks that are consumed by the electrochemical reaction, corroded by contact with the electrolyte and eroded by the evolved oxidizing gases. Attempts to replace these consumable carbon anodes by non-consumable oxygen evolving anodes have encountered difficulties linked to the inherent porosity of the ceramic and metal ceramic materials proposed for this purpose, and because of the imperfect impermeability of protective coatings, e.g. based on cerium oxyfluoride, whereby unwanted species penetrate into the bulk of the anode material and cause damage.
The problems associated with penetration of sodium into the carbon cathode have been extensively studied and discussed in the literature.
Several papers in Light Metals 1992 published by the The Minerals, Metals and Materials Society discuss these problems. A paper "Sodium, Its Influence on Cathode Life in Theory and Practice" by Mirtag et al, page 789, emphasises the advantages of using graphitic carbon over anthracite. Reasons for the superiority of graphitic carbon were also set out in a paper "Change of the Physical Properties and The Structure in Carbon Materials under Electrolysis Test" by Ozaki et al, page 759. Another paper "Sodium and Bath Penetration into TiB.sub.2 Carbon Cathodes During Laboratory Aluminium Electrolysis" by Xue et al, page 773, presented results showing that the velocity of sodium penetration increased with increasing TiB.sub.2 content. Another paper "Laboratory Testing of the Expansion Under Pressure due to Sodium Intercalation in Carbon Cathode Materials for Aluminium Smelters" by Peyneau et al, page 801, also discusses these problems and describes methods of measuring the carbon expansion due to intercalation.
There have been several attempts to avoid or reduce the problems associated with the intercalation of sodium in carbon cathodes in aluminum production.
Some proposals have been made to dispense with carbon and instead use a cell bottom made entirely of alumina or a similar refractory material, with a cathode current supply arrangement employing composite current feeders using metals and refractory hard materials. See for example, EP-B-0 145 412, EP-A-0 215 555, EP-B-0 145 411, and EP-A-0 215 590. So far, commercialization of these promising designs has been hindered due to the high cost of the refractory hard materials and difficulties in producing large pieces of such materials.
Other proposals have been made to re-design the cell bottom making u

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Laboratory Testing of the Expansion Under Pressure Due to Sodium Intercalation in Carbon Cathode Materials for Aluminium Smelters, Jm. Peyneau, Jr., et al., Light Metals 1992, pp. 801-808 no month available.
Sodium, Its Influence on Cathode Life in Theory and Practice, Jorg Mittag, et al., Light Metals 1992, pp. 789-793 no month available.
Sodium and Bath Penetration into TIB.sub.2 -Carbon Cathodes during Laboratory Aluminium Electrolysis, Jilai Xue, et al., Light Metals 1992, pp. 773-778 no month available.
Change of the Physical Properties and the Structure in Carbon Materials Under Electrolysis Test, C. Ozaki, et al., Light Metals 1992, pp. 759-764 no month available.

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