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RESEARCH<br />

Cathode wear in Hall-Héroult cells<br />

K. Tschöpe, E. Skybakmoen, A. Solheim, SINTEF Materials and Chemistry; T. Grande, NTNU<br />

Laboratory tests for cathode wear identify<br />

some variables as important, and eliminate<br />

others. These results are compared<br />

with models and with industrial potline<br />

experience.<br />

Introduction<br />

The research team Electrolysis in SINTEF<br />

Materials and Chemistry offers a high level of<br />

competence in the field of light metals production,<br />

molten salt chemistry, and particularly,<br />

the process of aluminium electrolysis. The<br />

activities cover fundamental as well as applied<br />

research in close collaboration with the<br />

industry and NTNU (Norwegian University of<br />

Science and Technology). This paper reviews<br />

the recent activities in the Durable Materials<br />

in Primary Aluminium Production (DuraMat)<br />

project on cathode wear, a phenomenon that<br />

is of great interest for all primary aluminium<br />

producers.<br />

The Hall-Héroult process has for more than<br />

125 years been the only commercial method<br />

for primary aluminium production. To date,<br />

this process has survived the attempts to replace<br />

it by alternative methods such as carbothermal<br />

reduction, electrochemical reduction<br />

of anhydrous aluminium chloride, and electrolysis<br />

based on inert electrodes.<br />

Tremendous scientific and technological<br />

efforts have been made to improve the efficiency<br />

of the process; e. g. the potline amperage<br />

has been increased from 50 kA in 1940<br />

to currently 400-500 kA [1]. Modern cells<br />

may operate at specific energy consumptions<br />

as low as 12.5 kWh/kg Al, and the current efficiency<br />

is typically in the range of 92-96%.<br />

Careful choice of new lining materials, and in<br />

particular, the increase of the graphite content<br />

in cathode blocks, is one of the factors that<br />

made this possible. Anthracitic carbon has<br />

been gradually replaced by the now state-ofthe-art<br />

graphitised cathode blocks. While this<br />

has allowed additional energy savings and<br />

increased productivity through the increased<br />

electrical conductivity, these benefits need to<br />

be weighed against higher material costs and<br />

lower wear resistance.<br />

eventually leads to direct<br />

contact between<br />

the metal and the<br />

collector bar. Consequently,<br />

cathode wear<br />

is usually the limiting<br />

factor for the service<br />

life of aluminium reduction<br />

cells. The cross<br />

sectional view of cathode<br />

blocks often reveals<br />

a W-shaped wear<br />

pattern, and even a<br />

WW-pattern has been<br />

observed, as shown in<br />

Fig. 1 [3]. Typical wear<br />

rates are in the range<br />

of 2-6 cm/year [4].<br />

The cell service life is<br />

a crucial economic<br />

parameter, which<br />

makes it important to<br />

understand the wear<br />

mechanism(s).<br />

It is generally agreed<br />

that formation, dissolution<br />

and transport<br />

of aluminium carbide are important factors<br />

that influence the cathode wear. Aluminium<br />

carbide can be formed chemically as well as<br />

electrochemically, according to reaction (1)<br />

Fig. 1: Visualisation of the wear profile. Cathode surface of a shutdown<br />

cell after 2,088 days in operation (a); plotted image using the laser scanning<br />

method, the blue colour corresponds to less wear and the red colour<br />

indicates the highest wear (b); longitudinal wear profile of all 19 cathodes<br />

showing the WW-shaped wear pattern (c) [3].<br />

and (2), respectively. However, the underlying<br />

mechanism(s) suggested are mainly based<br />

on theoretical considerations and are still a<br />

matter of discussion [5-10].<br />

<br />

Characteristics of cathode wear<br />

Wear is generally defined as net removal of<br />

material from a surface [2]. Carbon blocks<br />

wear excessively along their periphery, which<br />

a) b)<br />

Fig. 2: Schematic drawing of the experimental set-up with a quartz glass tube and position of the sample<br />

(a) as well as the sample appearance and its exposed cross section after embedding and polishing (b)<br />

<strong><strong>ALU</strong>MINIUM</strong> · 1-2/2013 95

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