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Once plastics enter the environment, exposure to sunlight and waves can cause degradation and fragmentation. Larger plastic debris may break down into microplastics, generally defined as plastic particles smaller than 5 millimeters (0.2 inches). These smaller particles can disperse more widely in the marine environment. Fragmentation also increases the surface area of plastics relative to their mass, potentially affecting both the leaching of chemicals from plastics and the sorption of chemicals from surrounding water and particles.
A research team led by Go Suzuki of the National Institute for Environmental Studies, Japan, in collaboration with the Tokyo University of Marine Science and Technology and Nagasaki University, analyzed additive-derived chemicals in floating microplastics and larger plastic debris collected from coastal, offshore, riverine and seafloor environments around Japan.
Floating microplastics were collected from five marine areas: Tokyo Bay, the Genkai Sea, Pacific coastal waters, waters off Hokkaido and Sea of Japan coastal waters. Larger plastic debris, including bags, ropes, nets and hard fragments, was recovered from offshore and coastal areas across Japan, as well as from a river drainage pump station in Tokyo. The researchers identified the polymer types of the samples and analyzed extracted chemicals using gas chromatography–mass spectrometry.
A wide range of chemicals were detected in both microplastics and larger plastic debris, including antioxidants, plasticizers, ultraviolet stabilizers, flame retardants and polycyclic aromatic hydrocarbons. Based on detection frequency, concentration and regulatory or management relevance, the researchers focused on three groups of chemicals: Irgafos 168-related compounds, di(2-ethylhexyl) phthalate (DEHP) and hexabromocyclododecane (HBCD).
Irgafos 168 is an antioxidant used to reduce oxidative degradation in plastics such as polyethylene and polypropylene. The distribution of Irgafos 168 and its oxidation products differed by polymer type and particle size. The observed patterns were consistent with leaching and transformation from within the plastic matrix.
DEHP is a plasticizer historically used primarily in flexible polyvinyl chloride products. It was widely detected in both microplastics and larger plastic debris. In some samples, concentrations exceeded 1,000 micrograms per gram (equivalent to 0.1% by weight). DEHP concentrations were higher in floating microplastics than in larger plastic debris recovered from the seafloor in both polyethylene and polypropylene samples. The results suggest that, in addition to chemicals remaining within plastics, DEHP present in surrounding water, suspended particles and organic matter may be sorbed to microplastics from the surrounding environment.
HBCD is a brominated flame retardant that has been used in materials such as expanded polystyrene. Because it is persistent, bioaccumulative and capable of long-range environmental transport, HBCD is regulated as a persistent organic pollutant. The researchers detected HBCD at concentrations of 110–590 micrograms per gram in microplastics collected from the Genkai Sea, Pacific coastal waters and Sea of Japan coastal waters. The findings indicate that fragmented plastic particles containing HBCD can remain mobile in the marine environment and may act as secondary sources of exposure.
The study shows that fragmentation does not necessarily remove chemical concerns associated with plastics that have entered the marine environment. Chemicals may leach from plastic matrices, be sorbed to fragmented particles from the surrounding environment or remain in those particles during transport. Product-based chemical controls alone may not fully capture these processes after plastics enter the environment.
The findings are published in the journal Environmental Science & Technology.
Further research is needed to determine how much of the chemicals associated with microplastics are taken up by organisms and whether they contribute to ecological effects. It is also important to identify the sources and release pathways of plastics containing chemicals of concern and to apply this knowledge to leakage prevention, selective collection and appropriate treatment.
These findings provide a scientific basis for connecting measures to address marine plastic pollution with chemical management. They may also contribute to discussions on the international legally binding instrument on plastic pollution currently under negotiation.
Publication details
Go Suzuki et al, Priority Plastic Additives of Environmental Concern in Marine-Leaked Micro- and Macroplastics: Occurrence, Distribution, and Management Implications, Environmental Science & Technology (2026). DOI: 10.1021/acs.est.6c03000
Provided by National Institute for Environmental Studies
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Citation: Microplastics may transport hazardous plastic additives through marine environments (2026, August 10) retrieved 10 August 2026 from https://phys.org/news/2026-08-microplastics-hazardous-plastic-additives-marine.html
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