Although recent studies have been conducted on the pollution and toxicity of microplastics with heavy metals or antibiotics, it is necessary to further investigate the coexistence of antibiotics and heavy metals on the surface of microplastics. In this study, the mechanisms of As(III) adsorption by polystyrene (PS) and polyamide (PA) microplastics in the presence of antibiotics (ciprofloxacin, CIP) were investigated. Adsorption behavior was investigated using kinetic and isotherm models, and the effects of microplastic particle size, aging, ion concentration, pH, xanthic acid (FA), and tannic acid (TA) were considered. Adsorption kinetics and isotherm models showed that the kinetics of As(III) adsorption on PS were consistent with a pseudo-first-order model; the kinetics of adsorption on PA were more consistent with segmented linear regression. The Freundlich model is consistent with the adsorption isotherms of As(III) on PS and PA. The smaller the microplastic particle size and the longer the aging time, the better the adsorption of As(III). Increasing NOsignificantly inhibited the adsorption of As(III) by PS, while it first promoted and then inhibited the adsorption by PA. The effect of pH was similar to that ofNO. The adsorption of As(III) by PS was significantly promoted by FA and TA, regardless of the presence of CIP; the adsorption of As(III) by PA was inhibited. Scanning electron microscopy (SEM) was used to characterize microscopic morphology of pristine and aged PS and PA microplastics; Fourier transform infrared (FTIR) and X-ray absorption spectroscopy (XPS) revealed changes in surface functional groups of PS and PA, while demonstrating the importance of different functional groups in exogenous additives (CIP and dissolved organic matter, DOM) in the adsorption of As(III). This study provides new insight into adsorption behaviors and interaction mechanisms between ternary pollutants.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.scitotenv.2023.167857 | DOI Listing |
Nanomaterials (Basel)
December 2024
Unidad Departamental de Química Analítica, Departamento de Química, Facultad de Ciencias, Universidad de La Laguna, Avda. Astrofísico Fco. Sánchez, s/n, 38206 La Laguna, Spain.
Arsenic contamination of water endangers the health of millions of people worldwide, affecting certain countries and regions with especial severity. Interest in the use of Fe-based metal organic frameworks (MOFs) to remove inorganic arsenic species has increased due to their stability and adsorptive properties. In this study, the performance of a synthesized Nano-{Fe-BTC} MOF, containing iron oxide octahedral chains connected by trimesic acid linkers, in adsorbing As(III) and As(V) species was investigated and compared with commercial BasoliteF300 MOF.
View Article and Find Full Text PDFWater Res
December 2024
Department of Sanitation and Environmental Engineering, School of Engineering, Federal University of Minas Gerais, Avenue Antônio Carlos, 6627, Campus Pampulha, Belo Horizonte, MG, Brazil. Electronic address:
Arsenic (As) enrichment in groundwater stems from natural and hydrogeochemical factors, leading to geological contamination. Groundwater and surface water are interconnected, allowing As migration and surface water contamination. The As contamination poses health risks through contaminated water consumption.
View Article and Find Full Text PDFHuan Jing Ke Xue
January 2025
College of Environmental and Resource Sciences, Zhejiang A&F University, Lin'an 311300, China.
Cadmium (Cd) and arsenic (As) often coexist in water and agricultural soils around mining areas, and it is difficult to remove them at the same time due to their opposite chemical behaviors. Therefore, this study employed a co-precipitation-pyrolysis method to synthesize silica-based magnetic biochar (SMB) materials for the remediation of water contaminated with both Cd and As. The optimization of preparation conditions involved introducing three different types of silicates (NaSiO, CaSiO,and SiO) into the biomass-magnetite mixture, followed by pyrolysis at various temperatures (300℃, 500℃, and 700℃), and the optimal preparation conditions were determined based on the composite batch experiments.
View Article and Find Full Text PDFJ Hazard Mater
December 2024
School of Environmental and Municipal Engineering, Xi'an University of Architecture and Technology, No.13, Yanta Road, Beilin District, Xi'an 710055, Shaanxi, PR China.
Combining chemical oxidation and adsorption is highly desirable but challenging to remove organoarsenic compounds for water purification. Herein, we prepared a Zn-doped CuO (CuZnO-2) catalyst by incorporating Zn atoms into the CuO lattice, which results in abundant surface oxygen vacancies (OVs) and modulates the electronic structure of Cu-OVs-Zn sites for PMS activation to degrade p-arsanilic acid (p-ASA) and adsorb the secondary arsenic species simultaneously. The elevated d-band centers for Cu upward to the Fermi level can significantly strengthen the adsorption of PMS, p-ASA, and the generated arsenic species.
View Article and Find Full Text PDFJ Environ Manage
December 2024
Korea Biochar Research Center, Division of Environmental Science and Ecological Engineering, Korea University, Seoul, 02841, Korea.
Pristine or modified nanoscale zero-valent iron (nZVI) synthesized though conventional chemical reduction have been widely recommended for remediating metal(loid)-contaminated water. However, their eco-friendliness is often challenged with the concomitant bio-toxicity and secondary environmental risks. Alternatively, this study utilized waste tea leaves extract and remaining residue as the reducing agent and pyrolytic matrix to innovatively fabricate a green synthesized nZVI impregnated tea residue biochar (G-nZVI/TB).
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!