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e s e a r c h<br />
the mass has particle diameter less<br />
than d 0.5 ).<br />
The results showed that there was<br />
a marked difference in dissolution<br />
time of the various aluminas; in fact<br />
more than one or<strong>de</strong>r of magnitu<strong>de</strong>.<br />
The best dissolution behaviour was<br />
observed for the ‘normal’ metal gra<strong>de</strong><br />
alumina, as shown in Figure 9. In this<br />
case relatively short dissolution times<br />
were observed, similar to those previously<br />
observed for commercial aluminas<br />
in cryolite. The longest dissolution<br />
times were observed for crushed<br />
MG alumina, calcined at 1,600°C,<br />
where the dissolution time was of<br />
the or<strong>de</strong>r of 5 to 20 minutes in the<br />
alumina concentration range of 1 to 2<br />
wt-% (see. Fig. 9). Even crushed MG<br />
alumina pre-dried to 300°C, showed<br />
dissolution times 4 to 10 times higher<br />
than the ‘normal’ gra<strong>de</strong> alumina in<br />
this concentration range.<br />
In view of the observations ma<strong>de</strong><br />
in these experiments it appears that<br />
the fineness of the alumina is a <strong>de</strong>termining<br />
factor for the dissolution<br />
process. A high content of the alpha<br />
phase seem to have an additional<br />
<strong>de</strong>trimental effect, i. e. it increases the<br />
time of dissolution. It has previously<br />
been found that high alpha alumina<br />
dissolves somewhat more slowly than<br />
the gamma phase alumina in cryolitic<br />
melts at 1,030°C [2] and it is possible<br />
that this difference is enhanced in lowmelting<br />
baths, where the solubility of<br />
alumina is lower. However, no simple<br />
relationship could be found between<br />
Type, <strong>de</strong>scription Term d 0.5 /µm<br />
Metal gra<strong>de</strong>, commercial alumina MG 82.95<br />
A-152, fine, 1 µm, highly calcined alumina, from Alcoa A152 1.86<br />
Crushed MG * alumina, calcined at 1600°C CMG 1600 4.51<br />
Crushed MG alumina, pre-dried at 300°C<br />
* MG – Metal Gra<strong>de</strong><br />
CMG 300 5.45<br />
Table 3: Materials tested and cut sizes (see text)<br />
these parameters and the time of dissolution.<br />
For example, the slowest dissolving<br />
alumina in these experiments<br />
was the CMG 1600 material. Table 3<br />
shows that 50% of the mass of this material<br />
has particles with diameter 4.5<br />
µm or less (d 0.5 =4.507 µm), compared<br />
to 1.86 µm for the A152 material.<br />
These materials have both been calcined<br />
at 1,600°C and have thus been<br />
converted to 100% α-alumina, but the<br />
finer A152 (d 0.5 =1.86) dissolves more<br />
rapidly than the coarser CMG 1600<br />
(d 0.5 =4.5 µm).<br />
conclusion<br />
It can be conclu<strong>de</strong>d from this investigation<br />
that if the only selection<br />
criterion is the rate of dissolution in<br />
low-melting baths, the normal industrial<br />
gra<strong>de</strong> alumina is the best choice.<br />
The main concern will probably be<br />
the ability to operate the bath at near<br />
saturation concentration with respect<br />
to alumina. Hence, the problem of<br />
maintaining slurry and avoiding forming<br />
sludge, i. e. alumina <strong>de</strong>posits, must<br />
be given high priority, and operating<br />
with fine-grained alumina might be<br />
Fig. 9: Results from three parallel runs with ‘normal’ MG alumina in low-melting bath.<br />
Time observed to obtain transparent melt after addition of batches of 0.5 wt-% alumina.<br />
Time plotted as a function of the concentration of alumina dissolved in the bath, <strong>de</strong>termined<br />
from bath samples taken before the addition<br />
the only option. In that case finely<br />
ground low-calcined alumina appears<br />
to be the best choice.<br />
acknowledgement<br />
Permission to publish given by Gol<strong>de</strong>n<br />
Northwest <strong>Alu</strong>munum Holding Company,<br />
is gratefully acknowledged.<br />
references<br />
[1] E.J. Frazer and J. Thonstad, “<strong>Alu</strong>mina<br />
solubility and diffusion coefficient in lowtemperature<br />
fluori<strong>de</strong> electrolytes”, to be<br />
published.<br />
[2] J. Thonstad, F. Nordmo, J. B. Paulsen,<br />
“Dissolution of <strong>Alu</strong>mina in Molten Cryolite”.<br />
Met Trans. 1972, pp. 403-408.<br />
[3] J. Thonstad, A. Solheim, S. Rolseth,<br />
O. Skaar, “The Dissolution of <strong>Alu</strong>mina in<br />
Cryolite Melts”, Light Metals 1988, pp.<br />
655-661.<br />
[4] T. Beck and R. J. Brooks. “Non-Consumable<br />
Ano<strong>de</strong> and Lining for <strong>Alu</strong>minum<br />
Electrolytic Reduction Cell”, United States<br />
Patent No. 5,284,562, 1994.<br />
[5] S. Rolseth, R. Hovland, O. Kobbeltvedt,<br />
”<strong>Alu</strong>mina Agglomeration and Dissolution<br />
in Cryolitic melts”, Light Metals 1994,<br />
pp.351-357.<br />
[6] O. Kobbeltvedt, S. Rolseth and<br />
J. Thonstad, “On the Mechanism of <strong>Alu</strong>mina<br />
Dissolution with Relevance to Point<br />
Feeding <strong>Alu</strong>minium Cells”, Light Metals<br />
1996, pp. 421-427.<br />
[7] R. G. Haverkamp, B. J. Welch and<br />
J. B. Metson, ”An Electrochemical Method<br />
for Measuring the Dissolution Rate of<br />
<strong>Alu</strong>mina in Molten Cryolite”, Bulletin<br />
of Electrochemistry, Vol.8, pp.334-340,<br />
1992.<br />
authors<br />
S. Rolseth, H. Gudbrandsen, K.S. Osen and<br />
J. Kvello are from SINTEF Materials and<br />
Chemistry, Trondheim, Norway.<br />
J. Thonstad is from Department of Materials<br />
Technology and Electrochemistry,<br />
Norwegian University of Science and<br />
Technology, Trondheim, Norway.<br />
56 ALUMINIUM · 9/2009