Polypropylene (PP) and polyethylene (PE) are commonly used polyolefins in a variety of applications, which have resulted in their accumulation in the environment. Once in the environment, these polymers undergo various chemical and physical transformations as the result of environmental stressors including sunlight. During photodegradation, PP and PE undergo reactions such as oxidation, crosslinking, and chain scission that are induced from UV light; yet, there are key gaps in knowledge on the phototransformations that occur under aqueous conditions. Therefore, it is the goal of this project to characterize the phototransformations of PP and PE in simulated natural water conditions. This work focuses on PP and PE thin films with 25 and 30 mm thicknesses, respectively. The polymer films were irradiated with 254 nm and 350 nm UV light in air, ultra-pure water, and solutions of dissolved organic matter (DOM) (10 mgC/L Suwanee River natural organic matter) to simulate natural systems. For comparison, the films were subjected to natural weathering over the course of Summer 2019 in Duluth, Minnesota. Irradiated plastics were then evaluated for a variety of chemical transformations. It was observed using Fourier Transform Infrared Spectroscopy (FTIR) that oxidation occurred both in air and aqueous environments, with oxidation in aqueous environments happening at a slower rate. Using gel fraction analysis crosslinking was observed to occur in both air and aqueous environments with a higher crosslinking fraction occurring in aqueous environments. Through this work, we have gained a more clear perspective on the chemical weathering of materials found in aquatic plastic debris, which will allow us to predict the behavior of these materials, including the breakdown into microplastics.

Aqueous photochemistry of polyolefins

Macromolecular Chemistry: The Second Century

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ACS Spring 2020 National Meeting & Expo

The official archive and repository for all ACS Meetings & Expositions abstracts and select posters or presentations.