© 2006 by Taylor & Francis Group, LLC
© 2006 by Taylor & Francis Group, LLC
© 2006 by Taylor & Francis Group, LLC
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120 Corrosion Control Through Organic Coatings<br />
It should be noted that the 90 g/m 2 zinc coating in this study is hot-dipped<br />
galvanized, and the two thinner coatings are electrogalvanized. It may be that differences<br />
other than zinc thickness — for example, structure and morphology of the<br />
zinc coating — play a not yet understood role. Further research is needed in this<br />
area, to understand the role played <strong>by</strong> zinc layer structure and morphology in<br />
under–cutting.<br />
7.2.3.3 Differences in Absorption and Desorption Rates<br />
The rate at which a coating absorbs water is not necessarily the same as the rate at<br />
which it dries out. Some coatings have nearly the same absorption and desorption<br />
rates, whereas others show slower drying than wetting, or vice versa.<br />
In constant stress testing, in which samples are always wet or always dry, this<br />
difference does not become a factor. However, as soon as wet-dry cycles are introduced,<br />
the implications of a difference between absorption and desorption rates<br />
becomes highly important. Two coatings with roughly similar absorption rates can<br />
have vastly different desorption rates. The duration of wet and dry periods in modern<br />
accelerated tests is measured in hours, not days, and it is quite possible that, for a<br />
coating with a slower desorption rate, the drying time in each cycle is shorter than<br />
the time needed <strong>by</strong> the coating for complete desorption. In such cases, the coating<br />
that desorbs more slowly than it absorbs can accumulate water.<br />
The problem is not academic. Lindqvist [22] has studied absorption and<br />
desorption rates for epoxy, chlorinated rubber, linseed oil, and alkyd binders, using<br />
a cycle of 6 hours of wet followed <strong>by</strong> 6 hours of drying. An epoxy coating took up<br />
100% of its possible water content in the wet periods but never dried out in the<br />
drying periods. Conversely, a linseed oil coating in this study never reached its full<br />
saturation during the 6-hour wet periods but dried out completely during the drying<br />
periods.<br />
Lindqvist has pointed out that the difference in the absorption and desorption rates<br />
of a single paint, or of different types of paint, could go far in explaining why cyclic<br />
accelerated tests often do not produce the same ranking of coatings as does field<br />
exposure. There is a certain risk to subjecting different types of coatings with unknown<br />
absorption and desorption characteristics to a cyclic wet-dry accelerated regime. The<br />
risk is that the accelerated test will produce a different ranking from that seen in reality.<br />
It could perhaps be reduced <strong>by</strong> some preliminary measurements of water uptake and<br />
desorption; an accelerated test can then be chosen with both wet times and drying<br />
times long enough to let all the paints completely absorb and desorb.<br />
7.2.4 TEMPERATURE<br />
Temperature is a crucial variable in any accelerated corrosion testing. Higher temperature<br />
means more energy available, and thus faster rates, for the chemical processes<br />
that cause both corrosion and degradation of cured films. Increasing the<br />
temperature — within limits — does not alter the corrosion reaction at the metal<br />
surface; it merely speeds it up. A potential problem, however, is what the higher<br />
<strong>©</strong> <strong>2006</strong> <strong>by</strong> <strong>Taylor</strong> & <strong>Francis</strong> <strong>Group</strong>, <strong>LLC</strong>