© 2006 by Taylor & Francis Group, LLC
© 2006 by Taylor & Francis Group, LLC
© 2006 by Taylor & Francis Group, LLC
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114 Corrosion Control Through Organic Coatings<br />
The difference may seem unimportant; however, there are advantages to separating<br />
the two questions. Testing a coating for initial corrosion protection is relatively<br />
inexpensive and straightforward. The stresses — water, heat, electrolyte — that<br />
cause corrosion of the underlying metal are exaggerated and then the metal under<br />
the coating is observed for corrosion. However, trying to replicate the aging process<br />
of a coating is expensive and difficult for several reasons:<br />
1. Coatings of differing type cannot be expected to have a similar response<br />
to an accentuated stress.<br />
2. Scaling down wet-dry cycles changes mass transport phenomena.<br />
3. Climate variability means that the balance of stresses, and subsequent<br />
aging, is different from site to site.<br />
7.2 WHAT FACTORS SHOULD BE ACCELERATED?<br />
The major weathering stresses that cause degradation of organic coatings are:<br />
• UV radiation<br />
• Water and moisture<br />
• Temperature<br />
• Ions (salts such as sodium chloride and calcium chloride) and chemicals<br />
The first of these weathering factors is unique to organic coatings; the latter three<br />
are also major causes of corrosion of bare metals. Most testing tries to reproduce<br />
natural weathering and accelerate it <strong>by</strong> accentuating these stresses. However, it is<br />
critically important to not overaccentuate them. To accelerate corrosion, we scale<br />
up temperature, salt loads, and frequency of wet-dry transitions; therefore, we must<br />
scale down the duration of each temperature–humidity step. The balances of mass<br />
transport phenomena, electrochemical processes, and the like necessarily change<br />
with every accentuation of a stress. The more we scale, the more we change the<br />
balances of transport and chemical processes from that seen in the field and the<br />
farther we step from real service performance. The more we force corrosion in the<br />
laboratory, the less able are we to accurately predict field performance.<br />
For example, a common method of increasing the rate of corrosion testing is to<br />
increase the temperature. For certain coatings, the transport of water and oxygen<br />
increase markedly at elevated temperature. Even a relatively small increase in temperature<br />
above the service range results in large changes in these coating properties.<br />
Such coatings are especially sensitive to artificially elevated temperatures in accelerated<br />
testing, which may never be seen in service. Other coatings, however, do not<br />
see strongly increased oxygen and water transport at the same elevated temperature.<br />
An accelerated test at elevated temperatures of these two coatings may falsely show<br />
that one was inferior to the other, when in reality both give excellent service for the<br />
intended application.<br />
And, of course, interactions between stresses are to be expected. Some major<br />
interactions that the coatings tester should be aware of include:<br />
• Frequency of temperature/humidity cycling. Because the corrosion reaction<br />
depends on supplies of oxygen and water, the accelerated test must<br />
<strong>©</strong> <strong>2006</strong> <strong>by</strong> <strong>Taylor</strong> & <strong>Francis</strong> <strong>Group</strong>, <strong>LLC</strong>