Coatings Clinic By Clifford K. Schoff, Schoff Associates Sagging Sagging is a defect caused by gravity-driven flow on vertical surfaces. Sags can be subtle or very obvious, such as the ones in Figure 1. Occasionally, the defect is not noticeable except for fine pops or pinholes that occur in the thick area. Sag is caused by excess flow where a thick section flows faster than other parts of the wet film. This does not happen if the film thickness is exactly the same across the entire area. Downward flow would occur, but it would be the same everywhere and there would not be noticeable sag. This actually happens occasionally on lab panels hung vertically during application. A known sag-prone coating will look better than a normally superior one. Sag in customer plants or in the field is more apt to happen where there is a hole, bracket, corner, edge, style line or other place that catches more paint. In addition, spray application of paint often produces a pattern of droplets and the “bumps” may form very small sags (microsags) on vertical surfaces, but will flow out on horizontal surfaces. This is one reason why verticals on automobiles, such as doors and verticals on deck lids (“waterfalls”), look rough in comparison to hoods, roofs, and deck lid horizontals. Another reason is that auto companies are so concerned about sagging that paint applied to verticals often has a higher viscosity, which prevents sag, but also interferes with leveling. When sagging occurs on application, it is called cold sag. When it occurs in the oven, not surprisingly, we call it hot sag. The latter problem has become a lot more common as the industry has gone to high solids coatings with low molecular weight polymers and oligomers that flow and flow and flow at elevated temperatures even after all the solvent has gone. Sag velocity and sag volume are given by the following equations: v = ρgT2/2η v = ρgT3/3η where ρ is the density of the coating, g is the force due to gravity, T is the film thickness, and η is the viscosity. These equations really work only for Newtonian coatings (of which there are very few these days), but still can provide valuable information. For example, they show the great importance of film thickness. Doubling the film thickness increases the sag velocity by a factor of four and sag volume by a factor of eight. In preventing sag, it is not necessary to stop downward flow completely. In fact, some flow is 52 October 2014 COATINGSTECH Figure 1—Sags in an architectural coating (plus a few seeds). needed for leveling. If the sagging velocity is low enough, the paint will dry or cure before noticeable sag will occur. S.Wu [J. Appl. Polym. Sci, 22, 2769, 2783 (1978) (two excellent papers)] estimated that 0.1 cm sag was acceptable and that sag time for most high solids coatings was about 10 min. This works out to a low enough velocity, being about 10-2 cm/min. According to Wu, a viscosity of 25–50 Ps at low shear after application is sufficient. (Such measurements are done by spraying and scraping or drawing down, flashing, and scraping to produce specimens.) In addition, coatings with yield stresses (which includes most architectural paints) are sagresistant. Unless the gravitational shear stress exceeds the yield stress, no sagging will occur. Sagging can be reduced or prevented by raising the viscosity of the paint at low shear stress or rate and/or by applying thinner coats of paint. The exact viscosity needed depends on the paint and the conditions. The film viscosity can be raised by using faster solvents or by introducing thickeners or thixotropes. The latter are additives such as fumed silica, treated clays, microgels, and castor oil derivatives that form physical networks, which produce yield stresses. Associative thickeners in waterborne paints serve a similar purpose. Structures form after application to reduce flow and prevent sag. Unfortunately, they also can prevent flow-out and leveling on horizontal surfaces, so amounts of the additives must be chosen carefully. Ideally, there will be initial flow to allow leveling, followed by viscosity build to prevent sagging. Thickeners that produce networks also reduce hot sag, as do materials such as waxes and certain castor oil derivatives that melt in to raise dissolved solids. All of these change viscosity–temperature behavior to prevent or reduce the initial sharp viscosity drop that usually occurs on the heating of a coating. CT
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