Significant contribution of different sources of particulate organic matter to the photoaging of microplastics.

ABSTRACT

Particulate organic matter (POM), as an important component of organic matter, can act as a redox mediator and thus intervene in the environmental behavior of microplastics (MPs). However, quantitative information on the role of POM in the photoaging of MPs under ultraviolet (UV) light is still lacking. To raise the knowledge gap, through environmental simulation experiments and qualitative/quantitative experiments of active substances, we found that POM from peat soil has stronger oxidation capacity than POM from sediment, and the involvement of POM at high water content makes the aging of MPs more obvious. This is because the persistent radicals and electron-absorbing groups on the surface of POM indirectly generate reactive oxygen species (ROS) by promoting electron transfer, and the dissolved organic matter (DOM) released from POM under UV light (POM-DOM) is further excited to generate triplet-state photochemistry of DOM (3DOM*) to promote the aging of MPs. Theoretical calculations revealed that the benzene ring, mainly C = C, and C = O in the main chain in the plastic macromolecule structure are more susceptible to ROS attack, and the differences in the vulnerable sites contained in different plastic structures as well as the differences in the energy band gaps lead to differences in their aging processes. This study firstly elucidates the key role and intrinsic mechanism of POM in the photoaging of MPs, providing a theoretical basis for a comprehensive assessment of the effect of POM on MPs in the environment.