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[Display omitted] The rapid development of process technology has led to rapid daily industrial production, which also produced a large amount of waste liquid. At the same time, the existing treatment technology cannot keep up with the demand, resulting in the malicious destruction of the environment by wastewater, especially mercury-containing wastewater was very harmful. Effective means of removing mercury ions need to be found. With magnetic ferric oxide as the core and titanium-based metal–organic frameworks as the shell, a new type of magnetic adsorbent (BTA-MIL-125(Ti)@Fe 3 O 4) was synthesized. Materials were tested by multiple characterization methods and multiple sets of experiments. At optimal pH 6, the removal rate in 100 ppm Hg(Ⅱ) was as high as 95.8%. The theoretical adsorption capacity was 615 mg/L. Isothermal experiments, kinetic experiments and thermodynamic experiments have respectively verified that the material was a kind of adsorption material with self-emission heat based on chemical action and synergistic adsorption with Hill model. By simulating the immunity of a variety of ions (Cu, Zn, Mg, Ni, Cd), the material itself also exhibited a very high affinity for Hg(Ⅱ). The results of five high-cycle stable adsorption proved the repeatable stability of the material itself. Various characterization methods have also shown that nitrogen and sulfur-containing groups chelated with Hg(Ⅱ). All of the above was enough to show that the BTA-MIL-125(Ti)@Fe 3 O 4 was a magnetic adsorption material with excellent performance and great prospects. [ABSTRACT FROM AUTHOR]

Microplastics (MPs) are emerging pollutants that act as a carrier of toxic pollutants, release toxic substances, and aggregate in biota. The adsorption behavior of MPs has recently become a research hot spot. The objective of this study was to summarize the main mechanisms by which MPs adsorb organic pollutants, introduce some mathematical models commonly used to study the adsorption behavior of MPs, and discuss the factors affecting the adsorption capacity from three perspectives, i.e., the properties of MPs and organic pollutants, and environmental factors. Adsorption kinetics and isothermal adsorption models are commonly used to study the adsorption of organic pollutants on MPs. We observed that hydrophobic interaction is the most common mechanism by which MPs adsorb organic pollutants, and also reportedly controls the portion of organic pollutants. Additionally, electrostatic interaction and other non-covalent forces, such as hydrogen bonds, halogen bonds, and π–π interactions, are also mechanisms of organic pollutant adsorption on MPs. The particle size, specific surface area, aging degree, crystallinity, and polarity of MPs, and organic pollutant properties (hydrophobicity and dissociated forms) are key factors affecting adsorption capacity. Changes in the pH, temperature, and ionic strength also affect the adsorption capacity. Current research on the adsorption behavior of MPs has mainly been conducted in laboratories, and in-depth studies on the adsorption mechanism and influencing factors are limited. Therefore, studies on the adsorption behavior of MPs in the environment are required, and this study will contribute to a better understanding of this topic. [Display omitted] • This study reviews the mechanisms by which microplastics adsorb organic pollutants. • Factors affecting the adsorption capacity of microplastics are determined. • Microplastics adsorb organic pollutants mainly through hydrophobic interactions. • Microplastic and environmental properties affect adsorption of organic pollutants. [ABSTRACT FROM AUTHOR]

[Display omitted] • CAL and PPy-CAL were prepared using hydrothermal and in situ polymerization methods. • The theoretical adsorption capacity of CAL-PPy for Cr(VI) was nearly twice than that of CAL. • CAL-PPy removed 100 mg/L of aqueous Cr(VI) efficiently and quickly. • Mechanisms included electrostatic attraction, anion exchange, complexation, and reduction. To efficiently remove high concentrations of hexavalent chromium (Cr(VI)), calcium–aluminum-layered double hydroxide (CaAl-LDH, denoted as CAL), and polypyrrole-modified CAL (CAL-PPy) were prepared by hydrothermal and in situ polymerization methods, respectively. The chemical structure, morphology, and elemental results indicated that the chain-like polypyrrole was decorated with hexagonal CAL. The specific surface area of CAL-PPy increased from 8.746 m2/g to 24.24 m2/g. The adsorption performances of CAL and CAL-PPy for aqueous Cr(VI) were investigated using batch equilibrium experiments. The decontamination process of aqueous Cr(VI) (100 mg/L) reached the equilibrium state within 50 min, and the kinetic data met the pseudo-second-order kinetic equation. The Langmuir model described the isothermal data properly, and the obtained theoretical adsorption capacity of CAL for Cr(VI) at 318 K was 34.06 mg/g, while that of CAL-PPy was 66.14 mg/g. The removal mechanisms involved electrostatic attraction, surface complexation, anion exchange, and reduction to low-toxicity Cr(III). Therefore, CAL and CAL-PPy have underlying applications in treating real wastewater containing Cr(VI). [ABSTRACT FROM AUTHOR]