Behavior and mechanisms of ciprofloxacin adsorption on aged polylactic acid and polyethlene microplastics.

Microplastics (MPs) and antibiotics are emerging pollutants in aquatic environments. MPs can absorb antibiotics, resulting in compound pollution. Batch adsorption experiments were used to investigate the adsorption behavior of CIP on polylactic (PLA) and polyethlene (PE) under various environmental conditions. After a lengthy aging process, both MPs underwent significant physicochemical changes. The equilibrium adsorption capacities of aged PLA and PE were 0.382 mg/g and 0.28 mg/g, respectively, which increased by 18.06% and 75% compared to pristine PLA and PE. The sorption capacity of MPs increased when the pH of the solution approached the dissociation constant (6.09, 8.74) of CIP. When the salinity of the solution was 3.5%, the adsorption capacity of MPs was reduced by more than 65%. The adsorption capacity of MPs rapidly decreased when 20 mg/L fulvic acid was added. Because norfloxacin (NOR) competes for adsorption sites on the microplastic, CIP adsorption is inhibited. Based on the adsorption models, FTIR, and XPS spectra, we demonstrated that the process was monolayer adsorption, with chemical and physical mechanisms including hydrogen bonding, π-π conjugation, ion exchange, and electrostatic interactions controlling it. Thus, PLA and PE microplastics may be a potential vector for CIP in water, and their interaction is mainly influenced by the physicochemical properties of the MPs and environmental factors.

Adsorption of perfluoroalkyl substances on polyamide microplastics: Effect of sorbent and influence of environmental factors.

Microplastics (MPs) and perfluoroalkyl substances (PFASs) are two types of pollutants coexisting in the environment. Their co-exposure is a source of increasing concern. MPs present in the natural environment suppose an ideal surface for the sorption of hazardous contaminants. This study investigates the adsorption behaviour of six PFASs on polyamide (PA) MPs. Adsorption experiments under various internal (PA and PFASs dosage, PA particle size) and environmental (pH, ionic strength, dissolved organic matter) factors were carried out. Isotherm results (from 0.1 to 25 mg/L of PFASs) showed that the maximum adsorption capacity of the selected PFASs on the PA was as follows: perfluorooctanesulfonic acid (PFOS, 0.873 mg/g) > perfluorooctanoic acid (0.235 mg/g) > perfluoroheptanoic acid (0.231 mg/g) > perfluorohexanoic acid (0.201 mg/g) > perfluoropentanoic acid (0.192 mg/g) > perfluorobutanoic acid (0.188 mg/g) (pH 5.88, 0% salinity and 0% of dissolved organic matter). The PFOS has more tendency to be sorbed onto PA than perfluorocarboxilic acids. The MP characterization by scanning electron microscopy, X ray diffraction and Fourier transform infrared spectroscopy showed changes in the PA surface after adsorption assays. Pore filling, hydrophobic interactions and hydrogen bonds governed sorption process. The sorption capacity of PFASs was crucially affected by the PA size (from 19.6% to 99.9% for 3 mm and 50 µm particle size, respectively). The process was not significantly influenced by salinity while the dissolved organic matter exerted a negative effect (decrease from 100% to 26% for PFOS in presence of 25 mg/L of humic acid). Finally, adsorption rates of PFASs were quantified in real water matrices (influent and effluent wastewater, surface and tap water samples). The results revealed interactions between PA and PFASs and evidenced the role of PA as a vector to transport PFASs in the aquatic environment.