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Exploring the mechanisms of humic acid mediated degradation of polystyrene microplastics under ultraviolet light conditions
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Humic acid in water promoted the photodegradation of polystyrene microplastics under UV light by generating higher levels of hydroxyl radicals (0.631 mM), resulting in 4.3% greater weight loss, smaller average particle size (89.5 microns), and more oxygen-containing products compared to UV alone.
Microplastics (MPs) are emerging pollutants that interact extensively with dissolved organic matter (DOM) and this influences the environmental behavior of MPs in aqueous ecosystems. However, the effect of DOM on the photodegradation of MPs in aqueous systems is still unclear. The photodegradation characteristics of polystyrene microplastics (PS-MPs) in an aqueous system in the presence of humic acid (HA, a signature compound of DOM) under ultraviolet light conditions were investigated in this study through Fourier transform infrared spectroscopy coupled with two-dimensional correlation analysis, electron paramagnetic resonance, and gas chromatography-mass spectrometry (GC/MS). HA was found to promote higher levels of reactive oxygen species (0.631 mM of ▪OH), which accelerated the photodegradation of PS-MPs, with a higher degree of weight loss (4.3%), higher level of oxygen-containing functional groups, and lower average particle size (89.5 μm). Likewise, GC/MS analysis showed that HA contributed to a higher content of oxygen-containing compounds (42.62%) in the photodegradation of PS-MPs. Moreover, the intermediates and final degradation products of PS-MPs with HA were significantly different in the absence of HA during 40 days of irradiation. These results provide an insight into the co-existing compounds on the degradation and migration processes of MP and also support further research toward the remediation of MPs pollution in aqueous ecosystems.
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Researchers found that high salinity seawater significantly accelerates the photoaging of polystyrene microplastics in the presence of humic acid, producing more hydroxyl radicals that promote fragmentation and oxidation of the plastic particles.
Dissolved Organic Matter Promotes the Aging Process of Polystyrene Microplastics under Dark and Ultraviolet Light Conditions: The Crucial Role of Reactive Oxygen Species
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Researchers found that dissolved organic matter commonly present in natural water environments accelerates the aging and degradation of polystyrene microplastics under both dark and ultraviolet light conditions. The study identified reactive oxygen species as the crucial driver of this aging process, with fulvic acid showing a stronger effect than humic acid due to its greater ability to generate semiquinone radicals.
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This study examined how sunlight breaks down polystyrene microplastics in water with different salt levels and dissolved organic matter. The combination of salt and humic acid accelerated the aging of microplastics, making them smaller and more chemically reactive. This matters because aged microplastics can more easily absorb toxic pollutants and are small enough to be taken up by organisms, increasing potential health risks.
Investigation of Surface Alteration of Microplastics by Using UV Irradiation
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UV radiation causes polystyrene and other plastic microparticles to undergo photooxidative degradation, changing their surface chemistry and potentially making them more likely to adsorb or release chemical pollutants. Understanding these weathering processes is important for predicting the environmental behavior and toxicity of microplastics.
Humic substance mitigated the microplastic-induced inhibition of hydroxyl radical production in riparian sediment
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Researchers investigated how humic substances mitigate the inhibitory effects of microplastics on hydroxyl radical production during photochemical reactions in water, finding that humic matter partially restored radical generation suppressed by plastic particles. The results suggest natural organic matter plays a protective role in environments where microplastics otherwise dampen oxidative water chemistry.
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