The large-scale production and usage of zinc oxide nanoparticles (ZnO NPs) may lead to their post-release into the aquatic environment. In this study, the effect of hydrophobic/hydrophilic organic ligands on sorption and sedimentation of ZnO NPs has been systematically investigated. In addition, the coagulation efficiency of ZnO NPs, Zn2+, dissolved organic carbon (DOC), and UV254 with varying ferric chloride (FC) dosages in synthetic waters were also evaluated. The results showed that the higher concentration of organic ligands, i.e., humic acid (HA), salicylic acid (SA), and L-cysteine (L-cys) reduced the ζ-potential and hydrodynamic diameter (HDD) of particles, which enhanced the NPs stability. The adsorption of organic ligands onto ZnO NPs was fitted with the Langmuir model, with maximum adsorption capacities of 143, 40.47, and 66.05 mg/g for HA, SA and L-cys respectively. Removal of up to 95% of ZnO NPs and Zn2+ was achieved in studied waters at the effective coagulation zone (ECR), above which excess charge induced by coagulant restabilized the NPs in suspension. Moreover, the removal rate of DOC and UV254 were found to be higher in hydrophobic waters than hydrophilic waters. The width of ECR strongly depends on the characteristics of source water. The waters with hydrophobic ligand and higher UV254 values require more coagulant than hydrophilic waters to achieve the similar ZnO NPs and Zn2+ removal. The results of Fourier transform infrared (FT-IR) analysis of ZnO NPs composite contaminant flocs indicated that the combined effect of enmeshment and charge neutralization might be a possible removal mechanism. These findings may facilitate the prediction of fate, transport, and removal of ZnO NPs in the natural waters, and might contribute to risk assessment, as well as decision making about engineered nanoparticles (ENPs) in aquatic systems.
Zinc oxide nanoparticles (ZnO NPs) are among the most widely used engineered nanoparticles (ENPs) in various commercial sectors to achieve both social and economic benefits. The post-use release of these NPs to the environment is inevitable, and may pose threat to the human and eco-system. In the present study, we investigated the influence of single and multiple environmental factors on sedimentation behavior of ZnO NPs. The fractional-factorial method based on Taguchi orthogonal array (OA) L 27 (3 13 ) design matrix was used for systematic investigation on the contribution and significance of multiple factors and their interactions. The result of single-factor showed that the ZnO NPs were unstable at or near pH zpc , with high electrolyte concentration; however, the adsorption of natural organic matter (NOM) i.e., humic acid, salicylic acid, and citric acid reverses the surface charge and enhanced NP stability. The Fourier transform infrared (FT-IR) analysis confirms the organic capping ligands on the NP surface. Moreover, the matrix result of analysis of variance (ANOVA) showed that electrolyte concentration and type, and NOM concentration were the most significant factors (p < 0.001) in promoting and influencing aggregation, while the interaction between the factors was also found insignificant. In addition, the result of aggregation kinetics and environmental water samples indicated that the mobility of ENPs may vary substantially in an environment with complex and heterogeneous matrices. This study may contribute to better understanding and prediction of the sedimentation behavior and fate of ZnO NPs in aqueous environments, to facilitate their sustainable use in products and process.
The increased use of copper oxide nanoparticles (CuO NPs) in commercial products and industrial applications raises concerns about their adverse effects on aquatic life and human health. Therefore, the current study explored the removal of CuO NPs from water via coagulation by measuring solubility under various pH values and humic acid (HA) concentrations. The results showed that the media pH significantly affected the coagulation efficiency of CuO NPs (30 mg/L) under various (0–0.30 mM) ferric chloride (FC) dosages. The concentration of dissolved Cu2+ ions at pH 3–6 was (16.5–4.8 mg/L), which was higher than at other studied pH (7–11). Moreover, the simultaneous effect of coagulants and charge neutralization at pH 6–8 enhanced the removal of CuO NPs. At a lower FC (0–0.05 mM) dosage, the higher HA concentration inhibited the aggregation of CuO NPs. However, at the optimum dose of (0.2 mM) FC, the efficiency of turbidity removal and solubility of CuO NPs between pH 8 and 11 was above 98% and 5%, respectively, probably due to coagulant enmeshment. Our study suggested that coagulation was effective in removing the CuO NPs from the complex matrices with pH values ranging from 8–11. The findings of the present study provide insight into the coagulation and dissolution behavior of CuO NPs during the water treatment process.
The dynamic nature of engineered nanoparticle (ENP) aggregation behavior and kinetics are of paramount importance in the field of toxicological and environmental nanotechnology. The Taguchi orthogonal array (OA) L 27 (3 13) matrix based on a fractional factorials design was applied to systematically evaluate the contribution and significance of water chemistry parameters (pH, temperature, electrolyte, natural organic matter (NOM), content and type) and their interactions in the aggregation behavior of zinc oxide nanoparticles (ZnO NPs). The NPs were dispersed into the solution using a probe-sonicator cell crusher (Bio-safer, 1200-90, Nanjing, China). The data were obtained from UV-Vis spectroscopy (Optizen 2120 UV, Mecasys, Daejeon, Korea), Fourier Transform Infrared Spectrometery (FT-IR 4700, spectroscopy, a JASCO Analytical Instruments, Easton, Pennsylvania, USA) and particle electrophoresis (NanoZS, Zetasizer, Malvern Instruments Ltd., Worcestershire, UK). The dataset revealed that Taguchi OA matrix is an efficient approach to study the main and interactive effects of environmental parameters on the aggregation of ZnO NPs. In addition, the aggregation profile of ZnO NPs was significantly influenced by divalent cations and NOM. The result of the FT-IR data presents a possible mechanism of ZnO NP stabilization in the presence of different NOM. This data may be helpful to predict the aggregation behavior of ZnO NPs in environmental and ecotoxicological contexts.
The extensive use of engineered nanoparticles (ENPs) such as zinc oxide nanoparticles (ZnO NPs) in various commercial fields has spurred significant concern about its possible toxicological effects of ZnO NPs on human health and eco-system. Therefore, it is substantial to understand the aggregation phenomena which could attenuate this effect. This data article provides information on aggregation of ZnO NPs under the influence of various parameters of water chemistry. Moreover, Taguchi orthogonal array L27(313) design matrix was used to evaluate the effect of multiple parameters in aqueous solution. The data were obtained from single beam UV-Vis spectrophotometer (Optizen 2120 UV, Mecasys, Korea) using Optizenview 4.2.5 PC interference software, Fourier transform infrared spectrometer (FT/IR-4700, spectroscopy, JASCO Analytical Instruments, Easton, USA) and particle electrophoresis (NanoZS, Zetasizer, Malvern Instruments Ltd, Worcestershire, UK). The dataset draws attention on dominant parameters influencing aggregation of ZnO NPs in water. The analysis of variance (ANOVA) data revealed that electrolyte concentration, type and natural organic matter (NOM) concentration were the most significant parameters. Furthermore, FT-IR data presents a possible mechanism of ZnO NPs stabilization in the presence of different NOM. This data will be helpful for the development of environmental risk assessment strategies and prediction of fate and mobility of other ENPs in the aquatic environment.
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