Synthesis and evaluation of a novel cross-linked biochar/ferric chloride hybrid material for integrated coagulation and adsorption of turbidity and humic acid from synthetic wastewater: Implications for sludge valorisation.

The deep removal of organic pollutants is challenging for coagulation technology in drinking water and wastewater treatment plants to satisfy the rising water standards. Iron (III) chloride (FeCl3) is a popular inorganic coagulant; although it has good performance in removing the turbidity (TB) in water at an alkaline medium, it cannot remove dissolved pollutants and natural organic matter such as humic acid water solution. Additionally, its hygroscopic nature complicates determining the optimal dosage for effective coagulation. Biochar (BC), a popular adsorbent with abundant functional groups, porous structure, and relatively high surface area, can adsorb adsorbates from water matrices. Therefore, combining BC with FeCl3 presents a potential solution to address the challenges associated with iron chloride. Consequently, this study focused on preparing and characterizing a novel biochar/ferric chloride-based coagulant (BC-FeCl3) for efficient removal of turbidity (TB) and natural organic matter, specifically humic acid (HA), from synthetic wastewater. The potential solution for the disposal of produced sludge was achieved by its recovering and recycling, then used in adsorption of HA from aqueous solution. The novel coagulant presented high TB and HA removal within 10 min of settling period at pH solution of 7.5. Furthermore, the recovered sludge presented a good performance in the adsorption of HA from aqueous solution. Adsorption isotherm and kinetics studies revealed that the Pseudo-second-order model best described kinetic adsorption, while the Freundlich model dominated the adsorption isotherm.

Chemical methods to remove microplastics from wastewater: A review.

Microplastics (Mps) have emerged as a pervasive environmental concern, with their presence detected not only in freshwater ecosystems but also in drinking and bottled water sources. While extensive research has centered on understanding the origins, migration patterns, detection techniques, and ecotoxicological impacts of these contaminants, there remains a notable research gap about the strategies for Mps removal. This study reviews existing literature on chemical approaches for mitigating microplastic contamination within wastewater systems, focusing on coagulation precipitation, electrocoagulation, and advanced oxidation methods. Each approach is systematically explored, encompassing their respective mechanisms and operational dynamics. Furthermore, the comparative analysis of these three techniques elucidates their strengths and limitations in the context of MPs removal. By shedding light on the intricate mechanisms underlying these removal methods, this review contributes to the theoretical foundation of microplastic elimination from wastewater and identifies future research trajectories and potential challenges.

Spatiotemporal profile and ecological impacts of major and trace elements in surface sediments of marginal seas of the Arctic and Northern Pacific Oceans.

The status and ecological impacts of sedimentary elements of the marginal seas of Arctic and Northern Pacific Oceans was investigated during 2016 to 2018 by using inductively coupled plasma mass spectrometry. Industrial (0.006 mg kg-1-64.6 g kg-1), precious (0.003-43.8 mg kg-1), rare earth (0.006-112.9 mg kg-1), and heavy metal (0.009-398.9 mg kg-1) elements showed spatial variation, and temporal uniformity. The results indicated ΣREEs and light REEs enrichment compared to chondrite and heavy REEs, respectively, while nonsignificant positive and negative δCe and δEu anomalies existed, respectively. High contamination and extreme enrichment of priority control, industrial (As, Mo, Re, Sb), precious (Au, Ir, Pd, Pt, and Ru) and RE elements indicated potential moderate to high ecological and biological risks. The study highlighted the ecological importance and fragile nature of these ecosystems and calls for an urgent action to ensure sustainability of these ecosystems.

Effect of montmorillonite biochar composite amendment on thallium bioavailability in contaminated agricultural soils and its mitigated health risk.

Little information is available on the effect of clay minerals and biochar composite on the remediation and bioavailability of thallium in agricultural soils. This study thus investigated the influence of montmorillonite biochar composite (Mnt-BC) amendment on the remediation of agricultural soil contaminated artificially by Tl and its potential health risks. Herein, bok choi was cultured to estimate the efficiency of soil Mnt-BC amendments through the bioavailability of Tl of the vegetable. Results showed that Tl bioavailability was significantly reduced in Mnt-BC-amended soils, mainly ascribed to the elevated soil pH and other improved soil properties of high functional groups (-OH, -COOH), negative charges, and exchangeable cations after amendment. Specifically, the highest immobilization efficiency of Tl in soils was observed in 2.5% treated soils with 79.11%, while in plant leaves the highest reduction of Tl was estimated to be 75.1% compared to the control treatment. Hence, the amendment dosage improved the immobilization of Tl in soil and subsequently reduced Tl uptake by the vegetable. Furthermore, from target hazard quotient (THQ) estimation, Mnt-BC amendment can lower the potential health risk while consuming such cultured bok choi in Tl-contaminated soils. Considering the environmental friendliness and high efficiency of Mnt-BC, it could be used as a potential soil amendment to remediate agricultural soils contaminated by Tl.

Current Progress on Methods and Technologies for Catalytic Methane Activation at Low Temperatures.

Methane (CH4 ) is an attractive energy source and important greenhouse gas. Therefore, from the economic and environmental point of view, scientists are working hard to activate and convert CH4 into various products or less harmful gas at low-temperature. Although the inert nature of CH bonds requires high dissociation energy at high temperatures, the efforts of researchers have demonstrated the feasibility of catalysts to activate CH4 at low temperatures. In this review, the efficient catalysts designed to reduce the CH4 oxidation temperature and improve conversion efficiencies are described. First, noble metals and transition metal-based catalysts are summarized for activating CH4 in temperatures ranging from 50 to 500 °C. After that, the partial oxidation of CH4 at relatively low temperatures, including thermocatalysis in the liquid phase, photocatalysis, electrocatalysis, and nonthermal plasma technologies, is briefly discussed. Finally, the challenges and perspectives are presented to provide a systematic guideline for designing and synthesizing the highly efficient catalysts in the complete/partial oxidation of CH4 at low temperatures.

Evaluation and optimization of the influence of silver cluster ions on the MALDI-TOF-MS analysis of polystyrene nanoplastic polymers.

In the analysis of polystyrene nanoplastics (PSNs), a nonpolar polymer (NP), using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS), silver salts were used as cationization reagents and simultaneously brought the potential problems of silver clusters that interfered with the PSN signal of MS. To detect PSNs, silver trifluoroacetate (AgTFA) and silver nitrate (AgNO3) were mixed with five polar matrices, namely 2-(4-hydroxyphenylazo) benzoic acid (HABA), dithranol (DI), sinapic acid (SA), trans-3-indoleacrylic acid (IAA), and 2,5-dihydroxybenzoic acid (DHB), and three nonpolar matrices, namely pyrene (PRN), anthracene (ATH) and acenaphthene (ACTH). The results showed that silver salt cluster ions were detected in the range of m/z 1000-4000. Five polar matrices with silver salts produced silver clusters, which interfered with the signals in the mass spectrum of PSNs, but the combination of these matrices with copper II chloride (CuCl2) salt did not produce copper-related clusters. However, the use of nonpolar matrices such as PRN, ATH or ACTH significantly decreased the signals of silver salt cluster ions, and this alteration of matrix types is considered a promising optimization approach for silver cluster ions. The nonpolar matrix conditions were optimized without producing silver cluster ions and the optimal detection conditions were found to be under nonpolar matrices (e.g., pyrene) with silver salts (e.g., AgTFA). The results suggest that when polar matrices, such as HABA, DI, SA, IAA, and DHB, are combined with silver salts in MALDI-TOF-MS analysis, silver-related clusters are detected in the range of m/z 1000-4000. Inhibition of the production of silver cluster ions can be achieved by the use of a nonpolar matrix (e.g., PRN) or polar matrix (e.g., DHB) with copper salts.

Integrated assessment of major and trace elements in surface and core sediments from an urban lagoon, China: Potential ecological risks and influencing factors.

Marine sediments serve as a sink for contaminants of anthropogenic origin. Here, 25 major and trace elements were determined in surface and core sediments from an urban lagoon (Yundang Lagoon), China. The median concentrations of Pb, Cd, Cu, and Zn in both surface and core sediments exceeded global and crustal averages. Principal component analysis for the elements and ecological impact of the heavy metals indicated spatial heterogeneity in core sediments from different lagoon areas; however, no such pattern was observed in surface sediments. Geodetector analysis indicated spatial locations of lakes, pH, N%, C%, and S% as the major factors influencing the heterogeneity of potential ecological risk index, a cumulative measure of the ecological impact of heavy metal. The interaction detector indicated nonlinear and bivariate enhancement between different physicochemical parameters. Besides, a depth profile of the elements in different samples was also elucidated.

Determination of 38 pharmaceuticals and personal care products in water by lyophilization combined with liquid chromatography-tandem mass spectrometry.

A convenient, effective, and low-cost method was developed for the determination of 38 pharmaceuticals and personal care products (PPCPs), including 19 antibiotics in surface water samples by lyophilization combined with liquid chromatography-tandem quadrupole mass spectrometry (LC-MS/MS). The components of the extraction solvent, the volume of the water sample, and the volume of extraction solvent were successively optimized. The analytes in 80 mL water samples were concentrated by lyophilization, eluted effectively by the solvent of 2 mL acetonitrile, 2 mL acetone, and 2 mL ultrapure water. The method detection limits ranged from 0.02 ng L-1 (caffeine) to 0.17 µg L-1 (glibenclamide). The recoveries of 30 analytes ranged from 40.0% (sulfaguanidine) to 124.4% (flumequine). The relative standard deviations of all analytes were below 21% except ciprofloxacin (29%). The performance of the optimized method was comparable to the solid phase extraction and ultrasonic extraction method with much less consumption of labor, organic solvent, and consumables. The developed method was successfully applied to surface river water, reservoir water, and effluent of the wastewater treatment plant.

Selective and fast recovery of rare earth elements from industrial wastewater by porous ß-cyclodextrin and magnetic ß-cyclodextrin polymers.

Recovery of rare earth elements (REEs) from industrial wastewater has drawn great attention due to their potential environmental toxicity, as well as their high demand in modern technologies. In this study, we developed a magnetic composite based on the high surface area porous ß-cyclodextrin polymer (P-CDP), namely P-CDP@Fe3O4. Both P-CDP and P-CDP@Fe3O4 rapidly sequester REEs such as Nd, Gd, Eu, and Y, reaching equilibrium in less than 10 min and fitting the Langmuir isotherm model with maximum adsorption capacities ranging from 7.76 to 9.59 mg/g at 25 °C when the highest initial concentration was 100 mg/L. Besides, the recovery of these REEs was not affected by competitive alkali, alkaline earth, and transition metal ions in model studies and industrial wastewater as revealed by the recovery efficiencies, which ranged from 62% to 100% indicating an excellent selectivity on both adsorbents. In addition, both adsorbents can be fully regenerated under mildly acidic conditions for at least five consecutive cycles. Moreover, P-CDP@Fe3O4 can be easily isolated by an external magnetic field which simplifies its synthesis and usability. It also overcomes the clogging and high backpressure issues of P-CDP, which facilitates its application for REEs recovery as compared with P-CDP. These characteristics demonstrate the promise of P-CDP and P-CDP@Fe3O4 for the pollution control and recovery of REEs.

Occurrence, geochemical fractionation, and environmental risk assessment of major and trace elements in sewage sludge.

Industrialization and accelerated population growth have created a huge amount of sewage sludge. Many studies have reported the sewage sludge as a sink of major and trace elements, but less is known about their geochemical fractionations. In order to assess the mobility, the distribution, bioavailability, and toxicity of those elements in sludge, we collected the sewage sludge samples from all the seven wastewater treatment plants in Xiamen City, China. Results revealed a strong spatial variation and the occurrence of 48 elements with concentrations ranging from 1.00×10-2 mg kg-1 (Re) to 9.03×101 g kg-1 (Fe) on the basis of dry sludge weight. Sequential extraction procedure showed that residual and oxidizable fractions were the main geochemical fractions of most studied elements. However, Ca, Mn, Sr, and Ni were mainly bound to acid-exchangeable fractions, while Fe, Zn, Cd, Cr, Co, and V were mainly distributed in the reducible fractions. The contamination factor and risk assessment code indicated that Ni, Cu, Zn, Cd, Cr, Co, Sr, Ca, Mn, Mo, Re, and W were highly mobile with less retention time and exerted high environmental risks through sludge land application. The sludge disposal strategy should consider not only the total concentrations of a broad range of elements but also their bioavailability.