Adsorption mechanism of cadmium on microplastics and their desorption behavior in sediment and gut environments: The roles of water pH, lead ions, natural organic matter and phenanthrene

Abstract

Microplastics (MPs) in aquatic systems can act as a vector for various toxic contaminants, such as metal ions. Although some studies have investigated the adsorption characteristics of metal ions on MPs, the desorption behaviors of metal ions from MPs in different environments are largely unknown. Here, the adsorption of cadmium (Cd(II)) onto five different types of MPs were compared to examine the relationship between the surface characteristics and the adsorption properties of MPs. Our results showed that polyamide had the highest Cd(II) adsorption capability with a value of 1.70 ± 0.04 mg/g, followed by polyvinyl chloride (1.04 ± 0.03 mg/g), polystyrene (0.76 ± 0.02 mg/g), acrylonitrile butadiene styrene (0.65 ± 0.02 mg/g) and polyethylene terephthalate (0.25 ± 0.01 mg/g). The specific surface area and total pore volume were closely correlated with the adsorption capacity of the MPs, and the π–π interaction, electrostatic interaction and oxygen-containing functional groups played crucial roles in the adsorption of Cd(II) onto the MPs. The sorption capabilities of Cd(II) onto the MPs first increased and then decreased with increasing solution pH from 2.0 to 9.0. In addition, the adsorption capacities were suppressed with the presence of lead ions (20–80 mg/L), while the coexistence of phenanthrene had a minor impact. Interestingly, the presence of humic acid promoted the desorption of Cd(II) from the MPs both in the synthetic earthworm gut and in the sediment system. A higher desorption rate was observed in the simulated gut environment, suggesting that metal-contaminated MPs would pose higher ecological risks to macroinvertebrates. Overall, our findings provide a better understanding of the sorption mechanism of Cd(II) onto MPs and the desorption behavior under different environmental conditions in aquatic ecosystems.