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© 2006 by Taylor & Francis Group, LLC

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Waterborne Coatings 57<br />

blocks and then undergo polymerization. Polyurethane dispersions, on the other<br />

hand, are produced <strong>by</strong> polycondensation of aqueous building blocks [3].<br />

3.2 WATER VS. ORGANIC SOLVENTS<br />

The difference between solvent-borne and waterborne paints is due to the unique<br />

character of water. In most properties that matter, water differs significant from<br />

organic solvents. In creating a waterborne paint, the paint chemist must start from<br />

scratch, reinventing almost everything from the resin to the last stabilizer added.<br />

Water differs from organic solvents in many aspects. For example, its dielectric<br />

constant is more than an order of magnitude greater than those of most organic<br />

solvents. Its density, surface tension, and thermal conductivity are greater than those<br />

of most of the commonly used solvents. For its use in paint, however, the following<br />

differences between water and organic solvents are most important:<br />

• Water does not dissolve the polymers that are used as resins in many<br />

paints. Consequently the polymers have to be chemically altered so that<br />

they can be used as the backbones of paints. Functional groups, such as<br />

amines, sulphonic groups, and carboxylic groups, are added to the resins<br />

to make them soluble or dispersible in water.<br />

• The latent heat of evaporation is much higher for water, than for<br />

organic solvents. Thermodynamically driven evaporation of water occurs<br />

more slowly at room temperature.<br />

• The surface tension of water is higher than those of the solvents<br />

commonly used in paints. This high surface tension plays an important<br />

part in the film formation of latexes (see Section 3.3).<br />

3.3 LATEX FILM FORMATION<br />

Waterborne dispersions form films through a fascinating process. In order for<br />

crosslinking to occur and a coherent film to be built, the solid particles in dispersion<br />

must spread out as the water evaporates. They will do so because coalescence is<br />

thermodynamically favored over individual polymer spheres: the minimization of<br />

total surface allows for a decrease in free energy [5].<br />

Film formation can be described as a three-stage process. The stages are<br />

described below; stages 1 and 2 are depicted in Figure 3.1.<br />

1. Colloid concentration. The bulk of the water in the newly applied paint<br />

evaporates. As the distance between the spherical polymer particles<br />

shrinks, the particles move and slide past each other until they are densely<br />

packed. The particles are drawn closer together <strong>by</strong> the evaporation of the<br />

water but are themselves unaffected; their shape does not change.<br />

2. Coalescence. This stage begins when the only water remaining is inbetween<br />

the particles. In this second stage, also called the ‘‘capillary’<br />

stage,” the high surface tension of the interstitial water becames a factor.<br />

The water tries to reduce its surface at both the water-air and water-particle<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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