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Industrial solid waste has a wide range of impacts, and it is directly or indirectly related to land, atmosphere, water, and other resources. Industrial solid waste has a large amount of production, complex and diverse components and contains a variety of harmful substances. However, as industrial by-products, it also has a lot of available value. Industrial solid waste has been continuously studied in water treatment due to its special composition and porous and loose structure. It is known that there are few reviews of various industrial solid wastes in the field of wastewater treatment, and most of them only discuss single industrial solid waste. This paper aims to sort out the different studies on various solid wastes such as fly ash, red mud, wastewater sludge, blast furnace slag and steel slag in dyeing, heavy metal, and phosphorus-containing wastewater. Based on the modification of industrial solid waste and the preparation of composite materials, adsorbents, coagulants, catalysts, filtration membranes, geological polymers, and other materials with high adsorption properties for pollutants in wastewater were formed; the prospect and development of these materials in the field of wastewater were discussed, which provides some ideas for the mutual balance of environment and society. Meanwhile, some limitations of solid waste applications for wastewater treatment have been put forward, such as a lack of further researches about environment-friendly modification methods, application costs, the heavy metal leaching, and toxicity assessment of industrial solid waste., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Utilising waste amine-oxime (WAO) resin through microwave semi-carbonization, a carbon adsorbent (CA) was obtained to remove Pb(II). After microwave treatment, the pore size of the skeleton structure, three-dimensional porous network, and lamellar pore structure of WAO was improved. The distribution coefficient (Kd) of Pb(II) onto CA is 620 mL/g, and the maximum adsorption capacity of Pb(II) is 82.67 mg/g after 20 min of WAO microwave treatment. The adsorption kinetics and adsorption isotherms conform to the quasi-second-order kinetic equation and Langmuir adsorption isotherm model, respectively. The surface of MT-WAO is negatively charged and the adsorption mechanism is mainly electrostatic interaction. Pb(II) elution in hydrochloric acid solution is more than 98%, and its recovery is high at 318 K and for 1 h.

Herein, a chemical-vapor deposition-like strategy was developed for the synthesis of versatile core-shell transition metal sulfide (TMS)@carbon nanowires with chemically-bonded heterostructures and significantly improved electrochemical performance. The morphological evolution observations revealed the simultaneous growth of TMS nanowires and their bonding with an ultrathin carbon layer. The resulting core-shell heterostructured nanowires possessed notable advantages, including fast ion/electron diffusion rates, improved conductivity, and chemical/mechanical stability, thereby leading to remarkable reversible capacity, rate capability, and cycling stability for Na-ion storage applications. The in situ transmission electron microscopy and in situ X-ray diffraction studies for FeS@C demonstrated the crystalline phase evolution between hexagonal and tetragonal FeS species during the electrochemical charging/discharging process, clearly indicating the excellent Na-ion storage performance of FeS@C nanowires. This work provides a new methodology for achieving 1D core-shell nanoarchitectures, while elucidating the electrochemical reaction mechanism underlying Na-ion storage in TMS materials., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Three types of alkyl-ammonium with different branching chains and three complexants with different functional groups were used to prepare alkyl-ammonium or complexant intercalated montmorillonite nanocomposite (A-Mt or C-Mt). In addition, synergistic intercalated montmorillonite nanocomposites (A/C-Mt) with alkyl-ammonium along with complexant were also prepared. The adsorption performance of the various nanocomposites toward Zn 2+ and p-nitrophenol (PNP) from simulated binary wastewater containing both Zn 2+ and PNP were systematically investigated. Characterization of Mt nanocomposites showed that both alkyl-ammoniums and complexants were successfully intercalated into the interlayers of Mt. The surfactant loading amounts of the various nanocomposites were also determined and correlated with the resulting expansion of the interlayer spacing. It was found that intercalation of alkane (OTAC) and -SH (CSH) were conducive to the adsorption of Zn 2+ while -C 2 H 4 NH (TETA) and all alkyl-ammoniums were beneficial for PNP adsorption. The extent of adsorption was found to be controlled primarily by pH, i.e., the higher pH had a good effect on the adsorption of both Zn 2+ and PNP. The adsorption process of Zn 2+ onto Mt nanocomposites was more in line with the Freundlich model (R 2  = 0.99), while the Langmuir model described the adsorption of PNP well (R 2  = 0.99). The adsorption kinetics could be well described by the Elovich equation (R 2  = 0.98) and the double-constant model (R 2  = 0.89). Chemical adsorption was determined to be the dominant process between the contaminant and Mt nanocomposite surfaces., (Copyright © 2021 Elsevier Inc. All rights reserved.)

Rational structure and morphology design are of great significance to realize excellent Na storage for advanced electrode materials in sodium-ion batteries (SIBs). Herein, a cube-like core/shell composite of single MnS nanocubes (≈50 nm) encapsulated in N, S co-doped carbon (MnS@NSC) with strong CSMn bond interactions is successfully prepared as outstanding anode material for SIBs. The carbon shell significantly restricts the expansion of the MnS volume in successive sodiation/desodiation processes, as demonstrated by in situ transmission electron microscopy (TEM) of one single MnS@NSC nanocube. Moreover, the in situ generated CSMn bonds between the MnS core and carbon shell play a significant role in improving the Na-storage stability and reversibility of MnS@NSC, as revealed by in situ Raman and TEM. As a result, MnS@NSC exhibits a high reversible specific capacity of 594.2 mAh g -1 at a current density of 100 mA g -1 and an excellent rate performance. It also achieves a remarkable cycling stability of 329.1 mAh g -1 after 3000 charge/discharge cycles at 1 A g -1 corresponding to a low capacity attenuation rate of 0.0068% per cycle, which is superior to that of pristine MnS and most of the reported Mn-based anode materials in SIBs., (© 2020 Wiley-VCH GmbH.)

In this study, a novel dual-cation organomontmorillonites (OMt) nanocomposite was synthesized by two kinds of modifiers cetyltrimethylammonium chloride and cysteamine hydrochloride, and the adsorption behavior of modifiers into montmorillonite (Mt) has been investigated. The OMt were characterized by techniques, such as X-ray diffraction (XRD), Fourier Transform Infrared (FTIR) spectroscopy, and thermogravimetric and differential thermal (TG-DTA) analyses. The effects of temperature, contact time, the order of addition and the concentration of organic modifiers on the amounts of organics adsorbed were investigated. The adsorption amount of cetyltrimethylammonium chloride (CTAC) and cysteamine hydrochloride (CSH) increased with the increase of the added CTAC amount and contact time, while the addition order of modifiers and modification temperature had no significant effect on the actual adsorption amount of CTAC and CSH on Mt, as confirmed by the XRD patterns. The experimentally determined isotherms showed a good fit with the Langmuir adsorption models. The adsorption kinetics demonstrated that the adsorption of CTAC and CSH by Mt followed the pseudo-second-order model, and CTAC adsorption rate on Mt was faster than that of CSH. FTIR spectrum clearly revealed the incorporation of surfactant ions into the interlayer region. The TG-DTA analyses showed that the total mass losses of OMt strongly depended on the molecular volume of modifiers.