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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]

[Display omitted] In the context of industrialization and severe wastewater pollution, mercury ions pose a major threat due to their high toxicity. However, traditional adsorbents and common metal-organic framework (MOF) materials have limited effectiveness. This study focuses on combining magnetic materials with functionalized titanium-based MOF composite (SNN-MIL-125(Ti)@Fe 3 O 4) to improve mercury ion adsorption. Through comprehensive characterization and analysis, the adsorption performance and mechanism of the material were studied. The optimal adsorption of the material was achieved at pH 5, exhibiting a pseudo-second-order adsorption model and the Hill theoretical capacity of 668.98 mg/g. Hill and Tempkin models confirmed the presence of chemical and physical adsorption sites on the material surface. Thermodynamic experiments showed a spontaneous endothermic process. Despite the presence of interfering ions, the material exhibited high selectivity for mercury ions. After four cycles, adsorption performance decreased by only 8%, indicating excellent reusability. Nitrogen- and sulfur-containing functional groups played a key role in mercury ion adsorption. In conclusion, SNN-MIL-125(Ti)@Fe 3 O 4 , as a magnetic MOF adsorption material, showed potential for effective remediation of mercury-contaminated wastewater. This study contributes to the development of efficient adsorption materials and enhances the understanding of their mechanism. [ABSTRACT FROM AUTHOR]

The urgent concerns of controlling water body eutrophication and the alleviating phosphorus shortage have led to an urgent need for action. The removal of phosphate from polluted waters and its reuse are essential for the prevention of eutrophication and for the sustainable utilization of phosphate resources. In this study, modified attapulgite with different Ca:Mg molar ratios was synthesized to facilitate the recovery of phosphate, with subsequent use of soil fertilizer. Ca–Mg modified attapulgite with the optimal ratio (ACM-5:3) exhibited an exceptional adsorption quality, achieving a maximum adsorption capacity of 63.2 mg/g. The pseudo-second-order model and Langmuir model could well describe the adsorption kinetics and isotherms, respectively. The adsorption mechanism analyses suggested that the interaction between ACM-5:3 and phosphate depended mainly on ion exchange and electrostatic attraction. Moreover, phosphate-laden-ACM-5:3 demonstrated a significant potential as a phosphorus-releasing fertilizer. It could promote corn growth by ensuring a continuous supply of phosphorus and minimizing phosphorus runoff losses. The above results suggested that ACM-5:3 was a potential adsorbent for efficient phosphate removal and recovery. [Display omitted] • Ca–Mg modified attapulgite was prepared using the co-precipitation method. • The maximum adsorption capacity of ACM-5:3 was 63.2 mg/g. • Phosphate-laden-ACM-5:3 was directly used as a slow-release phosphorus fertilizer. • Efficient recovery and reuse of phosphates was achieved. [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]