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Combined Effects of UV Exposure Duration and Mechanical Abrasion on Microplastic Fragmentation by Polymer Type
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Researchers studied how UV exposure duration and mechanical abrasion combine to fragment different plastic types under simulated beach conditions. They found that polypropylene was far more susceptible to fragmentation than polyethylene after UV weathering, while expanded polystyrene broke apart readily even without UV exposure. The experiments showed that a large fraction of fragmented particles were too small to recover, suggesting that significant amounts of nanoplastic are being generated on beaches.
It is important to understand the fragmentation processes and mechanisms of plastic litter to predict microplastic production in the marine environment. In this study, accelerated weathering experiments were performed in the laboratory, with ultraviolet (UV) exposure for up to 12 months followed by mechanical abrasion (MA) with sand for 2 months. Fragmentation of low-density polyethylene (PE), polypropylene (PP), and expanded polystyrene (EPS) was evaluated under conditions that simulated a beach environment. PE and PP were minimally fragmented by MA without photooxidation by UV (8.7 ± 2.5 and 10.7 ± 0.7 particles/pellet, respectively). The rate of fragmentation by UV exposure duration increased more for PP than PE. A 12-month UV exposure and 2-month MA of PP and PE produced 6084 ± 1061 and 20 ± 8.3 particles/pellet, respectively. EPS pellets were susceptible to MA alone (4220 ± 33 particles/pellet), while the combination of 6 months of UV exposure followed by 2 months of MA produced 12,152 ± 3276 particles/pellet. The number of fragmented polymer particles produced by UV exposure and mechanical abrasion increased with decreasing size in all polymer types. The size-normalized abundance of the fragmented PE, PP, and EPS particles according to particle size after UV exposure and MA was predictable. Up to 76.5% of the initial EPS volume was unaccounted for in the final volume of pellet produced particle fragments, indicating that a large proportion of the particles had fragmented into undetectable submicron particles.
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A systematic study of UV dose, humidity, and temperature effects on six polymer types found that photo-oxidation is the primary driver of microplastic fragmentation and release of secondary nano-sized particles, with the relationship between weathering conditions and fragmentation rates varying by polymer type.
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Researchers simulated UV weathering of polypropylene plastic and tracked how exposure progressively degraded the polymer, causing surface cracking and changes in mechanical properties that facilitate breakdown into microplastics. The results help explain how environmental weathering of plastic waste accelerates microplastic formation.
Environmental degradation and fragmentation of microplastics: dependence on polymer type, humidity, UV dose and temperature
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Researchers systematically tested how UV light, temperature, and humidity cause five common plastic types to break apart into secondary microplastics and nanoplastics. They found that the type of plastic — not the aging conditions — was the main factor determining how quickly it fragmented and what byproducts it released, data that can improve models predicting how plastics break down in the environment.
Analysis of ultraviolet and thermal degradations of four common microplastics and evidence of nanoparticle release
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Researchers studied how UV light and elevated temperature break down four common plastics and found that weathering releases nanoscale plastic particles. Polystyrene and polypropylene were particularly susceptible to UV degradation, generating significant numbers of nanoparticles. The findings confirm that environmental conditions actively fragment microplastics into even smaller, potentially more harmful nanoplastics.
Nanofragmentation of Expanded Polystyrene Under Simulated Environmental Weathering (Thermooxidative Degradation and Hydrodynamic Turbulence)
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