Page 166 - Fundamentals of Air Pollution
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V. Effects on Rubber                   133

       to blacken white and light-tinted paints. Wohlers and Feldstein (12) con-
       cluded that lead base paints could discolor surfaces in several hours at a
                               3
       concentration of 70 ftg/m  H 2S (0.05 ppm). In time the black lead sulfide
       oxidizes to the original color. Paints pigmented with titanium or zinc do
       not form a black precipitate. Alkyd or vinyl vehicles and pigments contain
       no heavy metal salts for reaction with H 2S. Painted surfaces are also dirtied
       by participate matter. Contaminating dirt can readily become attached to
       wet or tacky paint, where it is held tenaciously and forms focal points for
       gaseous sorption for further attack. Dirt that collects on roofs or in gutters,
       blinds, screens, windowsills, or other protuberances is eventually washed
       over external surfaces to mar decorative effects.
         Paints and coatings for automobiles have not been immune to damage
       by air pollution. Wolff and co-workers (13) found that damage to automobile
       finishes was the result of scarring by calcium sulfate crystals formed when
        sulfuric acid in rain or dew reacted with dry deposited calcium.
         Glass is normally considered a very stable material. However, there is
        growing evidence that SO 2 air pollution may be accelerating the deteriora-
        tion of medieval glass. A corrosion surface forms on these glass surfaces
        and the sulfate present helps prolong surface wetness. This condition is
       conducive to further attack and degradation of the glass surface (14).



                             V. EFFECTS ON RUBBER

         Although it was known for some time that ozone cracks rubber products
        under tension, the problem was not related to air pollution. During the
        early 1940s, it was discovered that rubber tires stored in warehouses in Los
       Angeles, California, developed serious cracks. Intensified research soon
       identified the causative agent as ozone that resulted from atmospheric
        reaction between sunlight (3000-4600 A), oxides of nitrogen, and specific
        types of organic compounds, i.e., photochemical air pollution.
         Natural rubber is composed of polymerized isoprene units. When rubber
       is under tension, ozone attacks the carbon-carbon double bond, breaking
        the bond, The broken bond leaves adjacent C = C bonds under additional
        stress, eventually breaking and placing still more stress on surrounding
       C = C bonds. This "domino" effect can be discerned from the structural
       formulas in Fig. 9-4. The number of cracks and the depth of the cracks in
       rubber under tension are related to ambient concentrations of ozone.
          Rubber products may be protected against ozone attack by the use of a
       highly saturated rubber molecule, the use of a wax inhibitor which will
        "bloom" to the surface, and the use of paper or plastic wrappings to protect
        the surface. Despite these efforts, rubber products still crack more on the
       West Coast than on the East Coast of the United States.
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