Structure-dependent mechanisms for plastic degradation in the marine environment
Maciulis, N.A.; Bingaman, J.M.; Scott, S.L. (2025). Structure-dependent mechanisms for plastic degradation in the marine environment, in: Shumway, S.E. et al. Plastics in the sea: occurrence and impacts. pp. 87-136. https://dx.doi.org/10.1016/b978-0-12-822324-6.00007-4
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| Keywords |
Chemical reactions > Hydrolysis
Environmental effects > Temperature effects
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| Author keywords |
Photo-oxidation; Radical mechanism; Degradation rate; Autocatalysis; Crystallinity; pH effect; Reactive oxygen species |
| Authors | | Top |
- Maciulis, N.A.
- Bingaman, J.M.
- Scott, S.L.
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| Abstract |
The visible and invisible accumulation of waste plastic in our oceans is a consequence of rapidly increasing inputs and very slow degradation rates. In general, this combination of effects results in long residence times. Nevertheless, the abiological degradation rate of a specific synthetic plastic varies widely, depending on its structural characteristics at the molecular, mesoscopic, and macroscopic levels. This chapter summarizes factors that determine these rates of degradation, and describes their principal mechanisms, for several of the major types of waste plastic found in the oceans. Mechanical forces cause cracking and flaking that break macroplastics into microplastics and even smaller fragments with increasing surface-to-volume ratios. Chemical degradation rates increase with surface area, influenced by intrinsic variations in crystallinity and the presence of additives, as well as extrinsic factors such as temperature, pH, and UV light intensity. Since polyolefin-based plastics are less dense than seawater and lack hydrolysable bonds in their polymer backbones, they accumulate close to the surface of the ocean where photo-oxidation is the principal cause of C–C bond cleavage in the polymer backbone. In contrast, polyesters and polyamides are denser than seawater and they sink, experiencing less exposure to solar irradiation. However, they can also degrade by slow hydrolysis of the C–O or C–N bonds intrinsic to the polymer structures. |
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