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© 2006 by Taylor & Francis Group, LLC

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Blast Cleaning and Other Heavy Surface Pretreatments 79<br />

rusted steel, the meter cannot distinguish how much of the conductivity is due to<br />

chlorides and how much is due simply to ferrous ions in the test water.<br />

The Bresle method is robust; it can be used on very uneven or curved surfaces.<br />

The technique is easy to perform, and the equipment inexpensive. Its major drawback<br />

is the time it requires; 10 minutes for a test is commonly believed to be too long,<br />

and there is a strong desire for something as robust and reliable — but faster.<br />

The filter-paper technique is much faster. A piece of filter paper is placed on the<br />

surface to be tested, and deionized water is squirted on it until it is saturated. The<br />

wet paper is then placed on an instrument (such as the SCM-400 from Elcometer)<br />

that measures its resistivity. As in the conductivity measurements discussed above,<br />

when this is used for repainting applications, it is not certain how much of the<br />

resistivity of the paper is due to chlorides and how much is due simply to rust in<br />

the test water. In all, the technique is reliable and simple to implement, although<br />

initial equipment costs are rather high.<br />

Neither technique measures all the chlorides present in steel. The Bresle technique<br />

is estimated to have around 50% leaching efficiency; the filter paper technique<br />

is somewhat higher. One could argue, however, that absolute values are of very<br />

limited use; if chlorides are present in any quantity, they will cause problems for<br />

the paint. It does not perhaps matter at all that a measurement technique reports<br />

200 mg/m 2 , when the correct number was 300 mg/m 2 . Both are far too high. This,<br />

indeed, is a weakness in the field of pretreatment quality control; it is not known<br />

how much chlorides is too much. Although there is some consensus that the acceptable<br />

amount is very low, there is no consensus on what the cut-off value is [18–20].<br />

4.5.2 HYDROCARBONS<br />

Like salts, hydrocarbons in the form of oils and grease also come from a variety of<br />

sources: diesel fumes, either from passing traffic or stationary equipment motors;<br />

lubricating oils from compressors and power tools; grease or oil in contaminated<br />

blasting abrasive; oil on operators’ hands; and so on. As mentioned above, the<br />

presence of oils and grease on the surface to be painted prevents good adhesion.<br />

Testing for hydrocarbons is more complex than is testing for salts for two<br />

reasons. First, hydrocarbons are organic, and organic chemistry in general is much<br />

more complex than the inorganic chemistry of salts. A simple indicator kit of reagents<br />

is quite tricky to develop when organic chemistry is involved. Second, a vast range<br />

of hydrocarbons can contaminate a surface, and a test that checks for just a few of<br />

them would be fairly useless. What is needed, then, is a test simple enough to be<br />

done in the field and powerful enough to detect a broad range of hydrocarbons.<br />

Ever game, scientists have developed a number of approaches for testing for<br />

hydrocarbons. One approach is ultraviolet (UV) light, or black lights. Most hydrocarbons<br />

show up as an unappetizing yellow or green under a UV lamp. This only<br />

works, of course, in the dark and, therefore, testing is done under a black hood,<br />

rather like turn-of-the-century photography. Drawbacks are that lint and possibly<br />

dust show up as hydrocarbon contaminations. In addition, some oils are not detected<br />

<strong>by</strong> black lights [21]. In general, however, this method is easier to use than other<br />

methods.<br />

<strong>©</strong> <strong>2006</strong> <strong>by</strong> <strong>Taylor</strong> & <strong>Francis</strong> <strong>Group</strong>, <strong>LLC</strong>

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