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© 2006 by Taylor & Francis Group, LLC

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Composition of the Anticorrosion Coating 19<br />

FIGURE 2.6 Some typical isocyanate reactions. A-hydroxyl reaction; B-amino reaction;<br />

C-moisture core reaction.<br />

2.2.3 POLYURETHANES<br />

A. R NCO + HO R′ R N<br />

H<br />

O<br />

C OR′<br />

(Urethane)<br />

B. R NCO + H2N R′ R N<br />

O<br />

C NR′<br />

H H<br />

(Urea)<br />

C. R NCO + HOH R N<br />

H<br />

O<br />

C OH R NH2 + CO2 (Carbamic acid)<br />

Polyurethanes as a class have the following characteristics:<br />

• Excellent water resistance [1]<br />

• Good resistance to acids and solvents<br />

• Better alkali resistance than most other polymers<br />

• Good abrasion resistance and, in general, good mechanical properties<br />

They are formed <strong>by</strong> isocyanate (R–N=C=O) reactions, typically with hydroxyl<br />

groups, amines, or water. Some typical reactions are shown in Figure 2.6. Polyurethanes<br />

are classified into two types, depending on their curing mechanisms: moisturecure<br />

urethanes and chemical-cure urethanes [1]. These are described in more detail<br />

in subsequent sections. Both moisture-cure and chemical-cure polyurethanes can be<br />

made from either aliphatic or aromatic isocyanates.<br />

Aromatic polyurethanes are made from isocyanates that contain unsaturated<br />

carbon rings, for example, toluene diisocyanate. Aromatic polyurethanes cure faster<br />

due to inherently higher chemical reactivity of the polyisocyanates [8], have more<br />

chemical and solvent resistance, and are less expensive than aliphatics but are more<br />

susceptible to UV radiation [1,9,10]. They are mostly used, therefore, as primers or<br />

intermediate coats in conjunction with nonaromatic topcoats that provide UV protection.<br />

The UV susceptibility of aromatic polyurethane primers means that the time<br />

that elapses between applying coats is very important. The manufacturer’s recommendations<br />

for maximum recoat time should be carefully followed.<br />

Aliphatic polyurethanes are made from isocyanates that do not contain unsaturated<br />

carbon rings. They may have linear or cyclic structures; in cyclic structures, the ring<br />

is saturated [11]. The UV resistance of aliphatic polyurethanes is higher than that of<br />

aromatic polyurethanes, which results in better weathering characteristics, such as<br />

gloss and color retention. For outdoor applications in which good weatherability is<br />

necessary, aliphatic topcoats are preferable [1,9]. In aromatic-aliphatic blends, even<br />

small amounts of an aromatic component can significantly affect gloss retention [12].<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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