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Phthalate acid ester release from microplastics in water environment and their comparison between single and competitive adsorption
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Microplastics release phthalate plasticizers (PAEs) into water, and this study found that release rates and adsorption behavior differ significantly between polyethylene, polypropylene, and polystyrene particles, with temperature, pH, and salinity all affecting how much chemical leaches out. When multiple PAEs were present simultaneously, competitive adsorption reduced the uptake of individual chemicals — important context for understanding the real-world chemical exposure that aquatic organisms and humans face from microplastic-contaminated water.
The ability of microplastics (MPs) to adsorb environmental pollutants has been extensively studied. However, little is known about the ability of MPs to release inherent additives and the interaction between them. This paper explored the effects of environmental factors on the release of phthalic acid esters (PAEs) from three different types of microplastics (polyethylene microplastics (PE-MPs), polypropylene microplastics (PP-MPs), and polystyrene microplastics (PS-MPs)) by simulating water environments, as well as the differences in the adsorption of one or more PAEs by MPs. The results showed that the types of MPs, single environmental factors, and combined environmental factors had a great influence on the release of di(2-ethylhexyl) phthalate (DEHP). In the influence of a single environmental factor, the releasing amount of DEHP increased significantly. When the pH value increased from 5 to 9, the release of three PAEs from all MPs decreased. Moreover, under the combined influence of three environmental factors, the DEHP release from PP-MPs was most affected by environmental factors, and the order of influence of the three environmental factors was ionic strength > organic matter > pH. The DEHP release of PS-MPs was the highest (0.058 ± 0.023 μg/L), followed by PP-MPs (0.038 ± 0.010 μg/L) and PE-MPs (0.035 ± 0.008 μg/L). Adsorption kinetics and isotherm fitting showed that the adsorption process of the three MPs was suitable for the pseudo-second-order kinetic model, and the Freundlich adsorption isotherm had a higher fitting degree. Compared with single adsorption, the competitive adsorption of three PAEs increased the adsorption capacity of DEHP and decreased the adsorption capacity of dibutyl phthalate (DBP) and diisobutyl phthalate (DIBP). These findings help predict the potential of MPs to release toxic additives under different environmental conditions.
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