RESUMEN

To evaluate the co-migration potential between heavy metal ions and road runoff colloids, the influence of contact time, temperature, initial concentration of metal ions, pH, humic acid (HA), and polymetallic coexistence on the binding capacity of heavy metals onto runoff colloids were investigated. The adsorption of heavy metals by runoff colloids was extremely rapid, approximately 80% of the equilibrium adsorption capacity was achieved in the first 30 min. The binding capacity exhibited an increasing trend with the initial concentration of metal ions increasing, and the maximum adsorption capacities of Pb(II), Cu(II), and Cd(II) achieved 159.13, 56.06, and 78.35 mg/g at 298 K, respectively. The adsorption capacity of Cu(II) and Cd(II) by runoff colloids increased with temperature increasing, while it displayed a converse trend for Pb(II). Neutral pH facilitated the combination of metal ions and runoff colloids. The presence of humic acid increased the binding capacity of Pb(II), Cu(II), and Cd(II) onto runoff colloids by 72.19, 63.31, and 13.83mg/g, respectively. Compared to the monometallic systems, the binding capacity of Pb(II), Cu(II), and Cd(II) by runoff colloids decreased by 18.44%, 22.35%, and 56.06% in polymetallic systems, respectively. Pb(II) bounded with colloids in the road runoff should be controlled preferentially to avoid their migrations to aquatic environments.

RESUMEN

The characteristics of dissolved organic matter (DOM) in road runoff under different traffic densities were compared using resin fractionation, molecular weight distribution analysis, three-dimensional excitation-emission matrix fluorescence spectroscopy, and UV-visible spectroscopy. Heavy traffic density strongly increased the concentration of DOM in road runoff, resulting in higher dissolved organic carbon. The distribution of molecular weights in DOM was not influenced by the traffic. DOM was dominated by colloidal organic matter with molecular weight in the 1 kDa to 0.45 µm size range. Hydrophobic fractions accounted for a large proportion than hydrophilic fractions in DOM, and hydrophobic acids increased with higher traffic density. Traffic density did not alter the fluorescent substances in DOM, including fulvic-like UV fluorescent substances and protein-like substances. However, more tryptophan-like protein substances were found in DOM from road runoff with heavy traffic. Moreover, the aromatization degree of DOM was not affected by heavy traffic, while the degree of humification decreased.

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RESUMEN

In this study, the effect of Chlamydomonas reinhardtii on the fate of CuO nanoparticles (CuO-NPs) in aquatic environment were investigated in terms of the colloidal stability, the free Cu2+ releasing, extracellular adsorption Cu (Cuex) and intracellular assimilation Cu (Cuin). The results showed that, with the increasing microalgal density, the absolute value of zeta potential of CuO-NPs decreased and the mean hydrodynamic diameter (MHD) became larger, leading to a better aggregation and settling behavior of CuO-NPs. The microalgae also promoted the free Cu2+ releasing, however, inhibited adsorption and assimilation of metal nanoparticles (MNPs) into microalgal cells, resulting in the reduction of the Cuex and Cuin per microalgal cell. The phenomenon was probably due to the reduced chance of contact between microalgae and MNPs. The internalization of CuO-NPs was also observed in microalgal cells by high resolution transmission electron microscope (HRTEM). Furthermore, the results of fast fourier transform (FFT)/inversed FFT (IFFT) analysis indicated that the CuO-NPs was reduced to Cu2O-NPs in the microalgae cells. The above results suggested that the microalgae can significantly affect the fate of MNPs, and subsequently, influencing the bioavailability and toxicity of MNPs in the aquatic environment.

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