Plant-substrate biochar properties critical for mediating reductive debromination of 1,2-dibromoethane.

Dibromoethane is a widespread, persistent organic pollutant. Biochars are known mediators of reductive dehalogenation by layered FeII-FeIII hydroxides (green rust), which can reduce 1,2-dibromoethane to innocuous bromide and ethylene. However, the critical characteristics that determine mediator functionality are lesser known. Fifteen biochar substrates were pyrolyzed at 600 °C and 800 °C, characterized by elemental analysis, X-ray photo spectrometry C and N surface speciation, X-ray powder diffraction, specific surface area analysis, and tested for mediation of reductive debromination of 1,2-dibromoethane by a green rust reductant under anoxic conditions. A statistical analysis was performed to determine the biochar properties, critical for debromination kinetics and total debromination extent. It was shown that selected plant based biochars can mediate debromination of 1,2-dibromoethane, that the highest first order rate constant was 0.082/hr, and the highest debromination extent was 27% in reactivity experiments with 0.1 µmol (20 µmol/L) 1,2-dibromoethane, ≈ 22 mmol/L FeIIGR, and 0.12 g/L soybean meal biochar (7 days). Contents of Ni, Zn, N, and P, and the relative contribution of quinone surface functional groups were significantly (p < 0.05) positively correlated with 1,2-dibromoethane debromination, while adsorption, specific surface area, and the relative contribution of pyridinic N oxide surface groups were significantly negatively correlated with debromination.

Remediation mechanism of high concentrations of multiple heavy metals in contaminated soil by Sedum alfredii and native microorganisms.

Pollution accident of nonferrous metallurgy industry often lead to serious heavy metal pollution of the surrounding soil. Phytoremediation of contaminated soil is an environmental and sustainable technology, and soil native microorganisms in the process of phytoremediation also participate in the remediation of heavy metals. However, the effects of high concentrations of multiple heavy metals (HCMHMs) on plants and native soil microorganisms remain uncertain. Thus, further clarification of the mechanism of phytoremediation of HCMHMs soil by plants and native soil microorganisms is required. Using the plant Sedum alfredii (S. alfredii) to restore HCMHM-contaminated soil, we further explored the mechanism of S. alfredii and native soil microorganisms in the remediation of HCMHM soils. The results showed that (i) S. alfredii can promote heavy metals from non-rhizosphere soil to rhizosphere soil, which is conducive to the effect of plants on heavy metals. In addition, it can also enrich the absorbed heavy metals in its roots and leaves; (ii) native soil bacteria can increase the abundance of signal molecule-synthesizing enzymes, such as trpE, trpG, bjaI, rpfF, ACSL, and yidC, and promote the expression of the pathway that converts serine to cysteine, then synthesize substances to chelate heavy metals. In addition, we speculated that genes such as K19703, K07891, K09711, K19703, K07891, and K09711 in native bacteria may be involved in the stabilization or absorption of heavy metals. The results provide scientific basis for S. alfredii to remediate heavy metals contaminated soils, and confirm the potential of phytoremediation of HCMHM contaminated soil.

A review of functions and mechanisms of clay soil conditioners and catalysts in thermal remediation compared to emerging photo-thermal catalysis.

High temperatures and providing sufficient time for the thermal desorption of persistent organic pollutants (POPs) from contaminated clay soils can lead to intensive energy consumption. Therefore, this article provides a critical review of the potential additives which can improve soil texture and increase the volatility of POPs, and then discusses their enhanced mechanisms for contributing to a green economy. Ca-based additives have been used to reduce plasticity of bentonite clay, absorb water and replenish system heat. In contrast, non-Ca-based additives have been used to decrease the plasticity of kaolin clay. The soil structure and soil plasticity can be changed through cation exchange and flocculation processes. The transition metal oxides and alkali metal oxides can be applied to catalyze and oxidize polycyclic aromatic hydrocarbons, petroleum and emerging contaminants. In this system, reactive oxygen species (•O2- and •OH) are generated from thermal excitation without strong chemical oxidants. Moreover, multiple active ingredients in recycled solid wastes can be controlled to reduce soil plasticity and enhance thermal catalysis. Alternatively, the alkali, nano zero-valent iron and nano-TiN can catalyze hydrodechlorination of POPs under reductive conditions. Especially, photo and photo-thermal catalysis are discussed to accelerate replacement of fossil fuels by renewable energy in thermal remediation.

Hybrid and enhanced electrokinetic system for soil remediation from heavy metals and organic matter.

The electrokinetic (EK) process has been proposed for soil decontamination from heavy metals and organic matter. The advantages of the EK process include the low operating energy, suitability for fine-grained soil decontamination, and no need for excavation. During the last three decades, enhanced and hybrid EK systems were developed and tested for improving the efficiency of contaminants removal from soils. Chemically enhanced-EK processes exhibited excellent efficiency in removing contaminants by controlling the soil pH or the chemical reaction of contaminants. EK hybrid systems were tested to overcome environmental hurdles or technical drawbacks of decontamination technologies. Hybridization of the EK process with phytoremediation, bioremediation, or reactive filter media (RFM) improved the remediation process performance by capturing contaminants or facilitating biological agents' movement in the soil. Also, EK process coupling with solar energy was proposed to treat off-grid contaminated soils or reduce the EK energy requirements. This study reviews recent advancements in the enhancement and hybrid EK systems for soil remediation and the type of contaminants targeted by the process. The study also covered the impact of operating parameters, imperfect pollution separation, and differences in the physicochemical characteristics and microstructure of soil/sediment on the EK performance. Finally, a comparison between various remediation processes was presented to highlight the pros and cons of these technologies.

Enhanced efficiency and stability in the degradation of triazophosphorus pesticides by Al6Si2O13/WO2.72 nanocomposites through synergistic action of S-scheme heterojunction and oxygen vacancies.

The environmental contamination caused by organophosphorus pesticides (for example, triazophos) is an escalating concern. To mitigate this issue, this study introduces a novel Al6Si2O13/WO2.72 (ASO/WO) nanocomposite photocatalyst, which markedly enhances the photocatalytic degradation of triazophos. The optimized nanocomposite material with a 60.0 % ASO loading (60-ASO/WO) achieves a degradation rate of 86.3 % for triazophos within 140.0 min, marginally exceeding 60-ASO/WO3 (72.6 %) and significantly outperforming individual ASO (65.0 %), WO (59.5 %), and WO3 (56.2 %). This catalyst retains 88.9 % of its activity after five cycles, showcasing exceptional efficiency and stability. Additionally, its electrochemical surface area (ECSA, 310.0 cm2), total organic carbon (TOC, removal rate of 73.7 %), photocurrent, and electrochemical impedance are all optimal. X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance (EPR), and theoretical calculations elucidate the critical role of oxygen vacancies and the S-scheme heterojunction in augmenting charge separation and photocatalytic performance, corroborating the synergistic effect of oxygen defects and the S-scheme. While individual factors can enhance photocatalytic activity, their combination results in a more pronounced effect. Liquid chromatography-mass spectrometry (LCMS) identifies the principal degradation intermediates, including 1-phenyl-3-hydroxy-1, 2, 4-triazole, diethyl thiophosphate, and 3, 5, 6-trichloro-2-pyridinol, underscoring the material's potential in environmental remediation.

Research progress on the environmental risk assessment and remediation technologies of heavy metal pollution in agricultural soil.

Controlling heavy metal pollution in agricultural soil has been a significant challenge. These heavy metals seriously threaten the surrounding ecological environment and human health. The effective assessment and remediation of heavy metals in agricultural soils are crucial. These two aspects support each other, forming a close and complete decision-making chain. Therefore, this review systematically summarizes the distribution characteristics of soil heavy metal pollution, the correlation between soil and crop heavy metal contents, the presence pattern and migration and transformation mode of heavy metals in the soil-crop system. The advantages and disadvantages of the risk evaluation tools and models of heavy metal pollution in farmland are further outlined, which provides important guidance for an in-depth understanding of the characteristics of heavy metal pollution in farmland soils and the assessment of the environmental risk. Soil remediation strategies involve multiple physical, chemical, biological and even combined technologies, and this paper compares the potential and effect of the above current remediation technologies in heavy metal polluted farmland soils. Finally, the main problems and possible research directions of future heavy metal risk assessment and remediation technologies in agricultural soils are prospected. This review provides new ideas for effective assessment and selection of remediation technologies based on the characterization of soil heavy metals.

Combination of electrochemical advanced oxidation and biotreatment for wastewater treatment and soil remediation.

The global concern surrounding the advancement of methods for treating wastewater and polluted soil has markedly increased over time. While electrochemical advanced oxidation processes (EAOPs) and biotreatments are commonly employed technologies for remediating wastewater and polluted soil, their widespread adoption is hindered by their limitations, which include high costs associated with EAOPs and prolonged remediation time of biotreatments. In the review, we provided an overview of EAOP technology and biotreatment, emphasizing the critical aspects involved in building a combined system. This review systematically evaluates recent research that combines EAOPs with bioremediation for treating wastewater or contaminated soil as pretreatment or post-treatment process. Research findings suggest that the combined treatment method represents a promising and competitive technology that can overcome some of the limitations of individual treatments. Additionally, we discussed the potential applications of this technology in varying levels of wastewater and soil pollution, as well as the underlying combination mechanisms.

Bacterial biofilm-mediated environmental remediation: Navigating strategies to attain Sustainable Development Goals.

Bacterial biofilm is a structured bacterial community enclosed within a three-dimensional polymeric matrix, governed by complex signaling pathways, including two-component systems, quorum sensing, and c-di-GMP, which regulate its development and resistance in challenging environments. The genetic configurations within biofilm empower bacteria to exhibit significant pollutant remediation abilities, offering a promising strategy to tackle diverse ecological challenges and expedite progress toward Sustainable Development Goals (SDGs). Biofilm-based technologies offer advantages such as high treatment efficiency, cost-effectiveness, and sustainability compared to conventional methods. They significantly contribute to agricultural improvement, soil fertility, nutrient cycling, and carbon sequestration, thereby supporting SDG 1 (No poverty), SDG 2 (Zero hunger), SDG 13 (Climate action), and SDG 15 (Life on land). In addition, biofilm facilitates the degradation of organic-inorganic pollutants from contaminated environments, aligning with SDG 6 (Clean water and sanitation) and SDG 14 (Life below water). Bacterial biofilm also has potential applications in industrial innovation, aligning SDG 7 (Affordable and clean energy), SDG 8 (Decent work and economic growth), and SDG 9 (Industry, innovation, and infrastructure). Besides, bacterial biofilm prevents several diseases, aligning with SDG 3 (Good health and well-being). Thus, bacterial biofilm-mediated remediation provides advanced opportunities for addressing environmental issues and progressing toward achieving the SDGs. This review explores the potential of bacterial biofilms in addressing soil pollution, wastewater, air quality improvement, and biodiversity conservation, emphasizing their critical role in promoting sustainable development.

Application of electrospun N-doped carbon dots loaded cellulose acetate membranes as cationic dyes adsorbent.

This work aims to apply carbon quantum dots (CQDs) from agriculture cellulosic waste (agro wastes), produced via an economically and eco-friendly single-step method, to be used into cellulose acetate composite microfibrous membranes as an innovative solution specifically designed to adsorb methylene blue (MB) and other cationic dyes that are present in various water effluents. Batch adsorption tests were conducted, with variations in contact time (1-24 h), initial MB concentration (25-300 ppm), and adsorbent doses (1-20 g/L). The maximum adsorption capacity of the membrane was 198 mg/g with an initial concentration of 300 ppm at 298 K. Thermodynamic parameters showed that the process is endothermic. Equilibrium experimental data for MB adsorption onto electrospun adsorbent were fitted using different isothermal models, with the Freundlich model showing the best fit. The pseudo-second-order model accurately described the kinetic data with high reliability (R2 > 0.99), and the calculated adsorption capacity was very close to the experimental data. N-CQDs loaded membranes were also tested for removing methyl violet and rhodamine B, demonstrating remarkably high dye removal efficiency. The underlying adsorption mechanism was also reported. Finally, it is worth mentioning that composite adsorbents can be efficiently applied to actual industrial cases because of the possibility of reusing them, opening the route to the fabrication of novel and highly performant adsorbents. These findings underscore N-CQDs' effectiveness in enhancing pollutant removal efficiency from wastewater, highlighting their environmental benefits and promoting a more sustainable approach to water treatment. Therefore, the prepared adsorbent, showing excellent adsorption performance, places them among adsorbents for practical applications in wastewater purification.

Crucial role of humic substance type in Cr(VI) reduction by humic substance-Fe(III) coprecipitates but not in adsorption.

Wetlands exhibit a self-purification effect on Cr(VI) owing to the adsorption and reduction capabilities of their humic substance (HS)-Fe(III) coprecipitates. However, the similarities and differences in the adsorption and reduction of Cr(VI) by different types of HS-Fe(III) coprecipitates remains unknown. In this study, fulvic acid (FA)- and humic acid (HA)-Fe(III) coprecipitates were synthesized with initial C/Fe ratios ranging from 0.25 to 15, and a comparative analysis of their adsorption and reduction effects was conducted. The results showed that FA- and HA-Fe(III) coprecipitates exhibit similar abilities to adsorb Cr(VI) by forming inner-sphere complexes with ferrihydrite (Fh), as well as with FA/HA. The association between FA/HA and Fe(III) not only blocked certain FeOH adsorption sites, but also enhanced the electrostatic repulsion towards Cr(VI), resulting in a proportionate decrease in their adsorption ability. For reduction, inductive and intrinsic reduction were involved in both FA- and HA-Fe(III) coprecipitates. However, the synergism/antagonism differed with the inherent sites (e.g., phenolic hydroxyl, ArOH) and activated sites (e.g., alcoholic hydroxyl, AlOH). Based on the size differences between FA and HA, the AlOH contained in FA was more easily activated by Fe(III) than that in HA, owing to the shorter induction path required. Thus, consistent synergism was observed in FA-Fe(III) coprecipitates regardless of Fe(III) species. In contrast, synergism was only observed in HA-Fe(III) coprecipitates containing Fh, because the inductive ability of Fe(III) cations was too weak to activate AlOH through the longer path. Moreover, with irreversible consumption of AlOH, intrinsic reduction became the dominant pathway at concentrations >1 mM Cr(VI). The preferential elimination of ArOH subsequently led to a transition to antagonism. These outcomes deepen our scientifical understanding of the environmental effects of HS-Fe(III) coprecipitates and offer new perspectives for exploring their potential applications in the remediation of Cr-contaminated sites.

Advancements in microbial-mediated radioactive waste bioremediation: A review.

The global production of radioactive wastes is expected to increase in the coming years as more countries have resorted to adopting nuclear power to decrease their reliance on fossil-fuel-generated energy. Discoveries of remediation methods that can remove radionuclides from radioactive wastes, including those discharged to the environment, are therefore vital to reduce risks-upon-exposure radionuclides posed to humans and wildlife. Among various remediation approaches available, microbe-mediated radionuclide remediation have limited reviews regarding their advances. This review provides an overview of the sources and existing classification of radioactive wastes, followed by a brief introduction to existing radionuclide remediation (physical, chemical, and electrochemical) approaches. Microbe-mediated radionuclide remediation (bacterial, myco-, and phycoremediation) is then extensively discussed. Bacterial remediation involves biological processes like bioreduction, biosorption, and bioprecipitation. Bioreduction involves the reduction of water-soluble, mobile radionuclides to water-insoluble, immobile lower oxidation states by ferric iron-reducing, sulfate-reducing, and certain extremophilic bacteria, and in situ remediation has become possible by adding electron donors to contaminated waters to enrich indigenous iron- and sulfate-reducing bacteria populations. In biosorption, radionuclides are associated with functional groups on the microbial cell surface, followed by getting reduced to immobilized forms or precipitated intracellularly or extracellularly. Myco- and phycoremediation often involve processes like biosorption and bioaccumulation, where the former is influenced by pH and cell concentration. A Strengths, Weaknesses, Opportunities, and Threats (SWOT) analysis on microbial remediation is also performed. It is suggested that two research directions: genetic engineering of radiation-resistant microorganisms and co-application of microbe-mediated remediation with other remediation methods could potentially result in the discovery of in situ or ex situ microbe-involving radioactive waste remediation applications with high practicability. Finally, a comparison between the strengths and weaknesses of each approach is provided.

Unveiling trends in migration of iron-based nanoparticles in saturated porous media.

Nanoscale zero-valent iron (nZVI) particles are routinely used for environmental remediation, but their transport dynamics in different settings remain unclear, hindering optimization. This study introduces a novel approach to predicting nZVI transport in saturated porous model environment. The method employs advanced long column devices for real-time monitoring via controlled magnetic susceptibility measurements. Numerical modeling with a modified version of the MNMs 2023 software was then used to predict nZVI and its derivatives mobility in field-like conditions, offering insights into the radius of influence (ROI) and shape factor (SF) of their distribution. A standard nZVI precursor was compared with its four major commercial derivatives: nitrided, polyacrylic acid-coated, oxide-passivated, and sulfidated nZVI. All these iron-based nanoparticles exhibited identical particle sizes, morphologies, surface areas, and phase compositions, isolating surface properties, dominated by charge, as the sole variable affecting their mobility. The study revealed optimal transport when the surface charge of nZVI and its derivatives was strongly negative, while rapid aggregation of nZVI derivatives due magnetic attraction reduced their mobility. Modeling predictions based on column scale-up, indicated that detectable concentrations of 20 g L⁻1 were found at distances ranging from 0.4 to 1.1 m from the injection well. Slightly sulfidated nZVI traveled farther than the nZVI precursor and ensured more homogenous particle distribution around the well. Organically modified nZVI migrated the longest distances but showed particle accumulation close to the injection point. The findings suggest that minimal sulfidation combined with organic modification of nZVI surfaces may effectively enhance radial and vertical nZVI distribution in aquifers. Such improvements increase the commercial viability of modified nZVI, reduce their adverse impacts, and boosts their practical applications in real-world scenarios.

Evaluation of intensive remediation using simulation-optimization modeling based on long-term monitoring at a DNAPL contaminated site.

Simulation-optimization modeling is extensively used to identify optimal remediation designs. However, verifying these optimal solutions often remains unclear. In this study, we determine optimal groundwater remediation strategies using simulation-optimization modeling and assess the effectiveness of previous remediation efforts by validating optimized results through 14 years of long-term monitoring of trichloroethylene (TCE) contamination. The study site is the Road Administrative Office (RAO) in Wonju, Korea, where significant TCE contamination has occurred, and long-term in-situ remediation and monitoring have been conducted. We employ MODFLOW for simulating groundwater flow and MT3D for modeling dissolved TCE concentration distribution. The Non-dominated Sorting Genetic Algorithm-II (NSGA-II) is applied to derive optimal groundwater remediation designs. Initial simulation results effectively predicted long-term TCE contamination trends and the impact of short-term in-situ remediation. Our evaluation involved comparing these optimal designs with field test outcomes, leading to the integration of continuous intensive pump-and-treat with in-situ remediation strategies. By comparing various modeling scenarios against long-term TCE contamination trends, we confirmed the effectiveness of previous remediation efforts and demonstrated that the optimal remediation design substantially minimized TCE concentrations at the main source zone. This study highlights successful strategies in historical contamination and remediation trend assessments, proposing an optimal design for pump-and-treat with reduced pumping stress to manage remaining TCE contamination at the site effectively.

A slow-release reduction material of Escherichia sp. F1 coupled with micron iron powder achieves the remediation of trichloroethylene-contaminated soil.

Trichloroethylene (TCE) is a prevalent organic pollutant found in soil. The oxide passivation layer on the surface of micron iron powder inhibits the release of its reducing components, leading to ineffective reduction and purification of TCE in soil. To enhance TCE degradation, a slow-release reduction material "Escherichia sp. F1-micron iron powder" was developed. A novel iron-reducing bacterium, Escherichia sp. F1, was isolated from soil contaminated with chlorinated hydrocarbons. This bacterium demonstrated a sustained iron reduction capability, achieving a reduction rate of 38.7% for Fe(Ⅲ) within 15 days. Genome sequencing revealed that strain F1 harbors 53 functional iron reduction genes and 2 dehalogenation genes. Single-factor experiments identified the optimal conditions for TCE degradation in soil using the coupling material: glucose concentration at 40 mmol/kg, soil water content at 50%, and bacterial inoculum at 1% (v:w). Under these optimal conditions, the coupled material achieved 86.86% degradation of TCE in soil within 28 days. Further analysis using X-ray photoelectron spectroscopy of micron iron powder, soil Fe(Ⅱ) concentration, and soil physicochemical properties demonstrated that the addition of strain F1 to the soil could disrupt the passivation layer of iron oxide on the surface of micron iron powder, promoting the exposure of its reactive sites and internal reducing active components. This resulted in an in situ self-actuated activation of passivated micron iron powder, leading to an improved removal rate and complete dechlorination of TCE in the soil. Soil microbial high-throughput sequencing revealed that the addition of strain F1 regulated the soil bacterial community, significantly enriching of Escherichia-Shigella species associated with iron-reducing functions. This enrichment facilitated the degradation of TCE in the soil through coupling materials. The functional material plays a crucial role in achieving green treatment and risk control of sites contaminated with chlorinated organic pollutants.

Versatile Keratin Fibrous Adsorbents with Rapid-Response Shape-Memory Features for Sustainable Water Remediation.

Biodegradable shape-memory polymers derived from protein substrates are attractive alternatives with strong potential for valorization, although their reconstruction remains a challenge due to the poor processability and inherent instability. Herein, based on Maillard reaction and immobilization, a feather keratin fibrous adsorbent featuring dual-response shape-memory is fabricated by co-spinning with pullulan, heating, and air-assisted spraying ZIF-8-NH2. Maillard reaction between the amino group of keratin and the carbonyl group of pullulan improves the mechanics and thermal performance of the adsorbent. ZIF-8-NH2 immobilization endows the adsorbent with outstanding multipollutant removal efficiency (over 90%), water stability, and photocatalytic degradation and sterilization performance. Furthermore, the adsorbent can be folded to 1/12 of its original size to save space for transportation and allow for rapid on-demand unfolding (12 s) upon exposure to water and ultraviolet irradiation to facilitate the adsorption and photocatalytic activity with a larger water contact area. This research provides new insight for further applications of keratin-based materials with rapid shape-memory features.

Electrokinetic remediation of cadmium-contaminated soil using polarity reversal method: Optimization analysis and mechanism exploration.

Electrokinetic remediation (EKR) has been applied for in-situ removal of Cd from contaminated soil, and the EKR enhanced with polarity reversal has achieved a higher Cd removal efficiency. However, the migration and accumulation mechanisms of Cd in the EKR process have not been investigated. In this paper, the cross-impacts of the voltage gradient, citric acid concentration in the electrolyte, and polarity reversal frequency on the removal efficiency by EKR of Cd and the optimization conditions were investigated. The migration and accumulation mechanisms of Cd were explored by analyzing the changes in electrokinetic process parameters, experimental phenomena, and X-ray diffraction (XRD) analysis. The results showed that the maximum removal efficiency of Cd reached 82.26%. The optimal conditions were determined by fitting the RSM model using the BBD design. In the EKR experiment with polarity reversal, Cd accumulated mainly in the middle part of the soil, attributed to the formation of chemical precipitation focusing area caused by soil pH transition, ion-induced potential gradient well trapping effect (IIPGWTE), or soil compaction induced by water loss. In conclusion, the various parameters have cross-impacts on the EKR of Cd-contaminated soil, and efficient in-situ removal of Cd from the contaminated soil can be achieved by adjusting the parameter conditions.

Ionic and nano calcium to reduce cadmium and arsenic toxicity in plants: Review of mechanisms and potentials.

Contamination of agricultural soils with heavy metal(loid)s like arsenic (As) and cadmium (Cd) is an ever increasing concern for crop production, quality, and global food security. Numerous in-situ and ex-situ remediation approaches have been developed to reduce As and Cd contamination in soils. However, field-scale applications of conventional remediation techniques are limited due to the associated environmental risks, low efficacy, and large capital investments. Recently, calcium (Ca) and Ca-based nano-formulations have emerged as promising solutions with the large potential to mitigate As and Cd toxicity in soil for plants. This review provides comprehensive insights into the phytotoxic effects of As and Cd stress/toxicity and discusses the applications of Ca-based ionic and nano-agrochemicals to alleviate As and Cd toxicity in important crops such as rice, wheat, maize, and barley. Further, various molecular and physiological mechanisms induced by ionic and nano Ca to mitigate As and Cd stress/toxicity in plants are discussed. This review also critically analyzes the efficiency of these emerging Ca-based approaches, both ionic and nano-formulations, in mitigating As and Cd toxicity in comparison to conventional remediation techniques. Additionally, future perspectives and ecological concerns of the remediation approaches encompassing ionic and nano Ca have been discussed. Overall, the review provides an updated and in-depth knowledge for developing sustainable and effective strategies to address the challenges posed by As and Cd contamination in agricultural crops.

Investigating the Effect of UV Irradiation and TiO2 Addition on Heavy Metal Adsorption by Inverse Vulcanized Sulfur Polymers.

Organomercury contamination in wastewater is a longstanding global concern, prompting the establishment of the Mi-namata Convention in 2013, following the tragic Minamata Bay incident in Japan. Despite numerous proposed solutions, the development of an affordable and convenient adsorbent remains a challenge. Sulfur, being one of the most abundant elements globally, has shown promise in mercury adsorption in previous research. This study delves into the influence of light exposure on the process of mercury adsorption. Our findings reveal that exposure to UV-A wavelengths (315 nm - 400 nm), in combination with the addition of titanium dioxide (TiO2), enhances the adsorption capacity of a sulfur-rich polymer. The maximum observed adsorption capacity reached 47 mg/g under these conditions. Notably, the presence of TiO2 and UV exposure did not significantly impact the adsorption of inorganic mercury and gold.

Putting advanced materials to the test: Ti3C2 MXenes alleviate the hazardous effects of the environmental pollutant benzo[a]pyrene.

Advanced materials are materials that have been engineered to exhibit novel or enhanced properties that confer superior performance when compared to conventional materials. Here, we evaluated the impact of Ti3C2 MXenes, a two-dimensional (2D) material, on the adverse effects caused by polycyclic aromatic hydrocarbons. To this end, we studied benzo[a]pyrene denoted here as B[a]P as a model compound. B[a]P was found to adsorb to MXenes as evidenced by UV-Vis spectroscopy. MXenes in the presence or absence of natural organic matter (NOM) were well tolerated by zebrafish embryos. The uptake (ingestion) of MXenes by zebrafish was determined by quantifying the Ti content using inductively coupled plasma mass spectrometry (ICP-MS) while Raman confocal mapping was applied for the label-free identification of MXenes in situ in exposed zebrafish. The body burden of B[a]P was determined by gas chromatography-mass spectrometry (GC-MS). The potential impact of MXenes on B[a]P triggered aryl hydrocarbon receptor (AhR) induction was assessed by evaluating the induction of downstream genes including cyp1a, and results were validated by using the transgenic zebrafish reporter tg(cyp1a-eGFP). The potential impact of MXenes on the genotoxicity caused by B[a]P was also assessed. MXenes were shown to ameliorate AhR induction and DNA damage caused by B[a]P. This was corroborated by using the human colon-derived cell line HT-29. Taken together, MXenes were found to be non-hazardous and alleviated the adverse effects caused by B[a]P in vitro and in vivo.

Interaction of biochar with extracellular polymers of resistant bacteria restrains Pb(II) adsorption onto their composite: Macro and micro scale investigations.

Pb(II) sequestration in extracellular polymers-biochar composites (EPS-BC) was explored using macroscopic models and microscopic technology. The results showed that the actual adsorption capacity of EPS-BC was 52.2% lower than the calculated capacity based on adsorption onto pure components due to the interaction of polysaccharide and amide group in extracellular polymers with biochar, which masked the reactive sites related to Pb(II) in EPS-BC. The bond of Pb-O (40.8%) and Pb-OOC (31.5%) mainly contributed to Pb(II) speciation on the EPS-BC surfaces. Furthermore, each Pb atom coordinated with 6O atoms in the first shell and with 0.5C atoms in the second shell, indicating that the carboxyl group in composite was complexed with Pb(II) as a monodentate inner-sphere structure. The findings provide an in-depth understanding of the adsorption mechanism of heavy metals by extracellular polymers coupled with biochar at molecular scale, guiding bioremediation with respect to heavy metal contamination.