Scaling of Fold, bronze, and stainless steel was investigated in synthetic
fresh and seawater. It is shown that the calcium carbonate precipitation ra
te increased from stainless steel, to bronze and then to gold whatever the
composition of the scaling water. The morphology of the deposited scale dep
ended on the substrate and on its surface state. For fast scaling, as with
200 mg dm(-3) Ca2+ carbonically pure water, calcite was mainly deposited: f
or slower scaling vaterite was also observed. When foreign ions were added
in the scaling water, aragonite appeared. In particular, for synthetic seaw
ater, cc-here magnesium ions are highly concentrated, aragonite is preferen
tially selected, so at the end of scaling aragonite covered the whole elect
rode surface. The kinetic parameters, which characterize a precipitation mo
del, were extracted from impedance measurements through a fitting procedure
. The morphology of the precipitated calcium carbonate was examined by mean
s of a scanning electron microscope. (C) 2000 The Electrochemical Society.
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