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Natural organic matters (NOMs) are ubiquitous in the environment, but few systematic studies have examined the influence of NOMs on the sorption ability of magnetic sludge biochar. In this study, magnetic sludge biochar was synthesized, characterized, and used as a sorbent to remove tetracycline (TC) from aqueous solutions. The effects of pH, humic acid (HA), and fulvic acid (FA) on TC adsorption by magnetic sludge biochar were studied using batch experiments. Adding HA and FA can alter the adsorption behavior of TC, except for its pH dependency. The results of this study show that relatively low concentrations of dissolved HA (≤8 ppm) and FA (≤5 ppm) promote the adsorption capacity of TC, but higher concentrations compete against TC for sorption sites on the surface of magnetic sludge biochar. The results of this study promote a better understanding of the application of magnetic sludge biochar in real antibiotic wastewater.

Owing to its ubiquity in natural water systems and the high toxicity of its accumulation in the human body, it is essential to develop simple and low-cost electrochemical sensors for the determination of 3,3′,5,5′-tetrabromobisphenol A (TBBPA). In this work, Fe3O4–activated biochar, which is based on excess sludge, was prepared and characterized using scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR) and BET analysis to analyze its basic features. Subsequently, it was used to fabricate an electrochemical sensor for the detection of TBBPA. The electrochemical test results revealed that the Fe3O4–activated biochar film exhibited a larger active surface area, a lower charge transfer resistance and a higher accumulation efficiency toward TBBPA. Consequently, the peak current of TBBPA was significantly enhanced on the surface of the Fe3O4–activated biochar. The TBBPA sensing platform developed using the Fe3O4–activated biochar composite film, with relatively a lower detection limit (3.2 nM) and a wider linear range (5–1000 nM), was successfully utilized to determine TBBPA levels in water samples. In summary, the effective application of Fe3O4–activated biochar provided eco-friendly and sustainable materials for the development of a desirable high-sensitivity sensor for TBBPA detection.

Nanocubic pyrite (FeS2) crystals with exposed (100) crystal faces and sizes of 100−200 nm were successfully synthesized via a facile hydrothermal method using greigite (Fe3S4) as the iron precursor and thiourea (NH2CSNH2) as the sulfur source. When the concentration of thiourea was 40 mmol/L, both pyrite and hematite were observed in the as-prepared sample, indicating incomplete conversion of greigite into pyrite. With an increased thiourea concentration to 80 mmol/L, pyrite was found to be the only crystalline phase in the synthesized samples. All greigite could be transformed to pyrite within 24 h via the hydrothermal method, while further prolonging the hydrothermal time had insignificant effect on the crystal phase composition, crystallinity, and morphologies of the prepared nanocubic pyrite crystals. In contrast, when a mixture of Na2S and S powder was used to replace the thiourea as the sulfur source, tetragonal, orthorhombic, cubic, and irregular pyrite crystal particles with sizes of 100 nm−1 μm were found to co-exist in the prepared samples. These results demonstrate the critical influence of sulfur source on pyrite morphology. Furthermore, our hydrothermal process, using a combination of greigite and thiourea, is proved to be effective in preparing nanocubic pyrite crystals. Our findings can also provide new insight into the formation environments and pathways of nanocubic pyrite under hydrothermal conditions.

Sorption of nanoparticles on mineral surfaces has been well recognized for its environmental implication. For certain gold ore deposits, sorption of gold nanoparticles (AuNPs) on pyrite may constitute a critical step in the metallogenesis process, yet it has not been adequately investigated. In this work, we synthesized negatively charged, positively charged AuNPs and pyrite respectively, and experimentally studied sorption of AuNPs on pyrite in an anaerobic environment. The effects of AuNPs charge characteristics, pH, hexadecyl trimethyl ammonium bromide (CTAB) concentration, and ionic strength were evaluated. For the negatively charged AuNPs, almost no sorption was observed owing to the electrostatic repulsion between the AuNPs and pyrite surface (with a measured isoelectric point of 2.0). In contrast, positively charged AuNPs could be significantly adsorbed on pyrite through electrostatic attraction, with the sorption extent decreasing with the increase of pH (2.2–9.1). However, the adsorption of CTAB from the solution was found to increase with the increase of pH. Furthermore, deliberately added CTAB seemed to inhibit the sorption of AuNPs. Our study not only demonstrates that the electrostatic interaction is the dominant mechanism in the sorption of AuNPs on pristine pyrite, but also reveals the important competitive relation between AuNPs and CTAB in the sorption process.