Chemosphere最新文献

Magnetite has been proved to facilitate direct interspecies electron transfer (DIET)-based syntrophys and might alleviate inhibitory effects of antibiotics in anaerobic digestion (AD), while feeding ethanol was an effective approach to enrich the DIET partners. However, most of the existing studies were conducted at fixed ethanol concentration, few attentions were paid on the effects of differential ethanol proportion on AD, the underlying roles and mechanisms of ethanol stimulation remains unclear. This study systematically investigated the impact of ethanol stimulation on anaerobic processes treating oxytetracycline (OTC)-contaminated wastewater at varying proportions (20%, 50%, and 80%, based on equivalent COD value). In the presence of magnetite, ethanol stimulation promoted the methane production from 244.9 mL/g COD to a maximum 434.2 mL/g COD, with the most pronounced enhancement observed at high ethanol proportions. In particular, the average methane production obtained at 50% and 80% ethanol was 328.5 and 297.7 mL/g COD, respectively, whereas the enhancement of 20% ethanol stimulation was relatively limited. Concurrently, more stable COD removal and OTC reduction was noted in the existence of both magnetite and high ethanol proportions. Microbial analysis revealed the pivotal roles of Methanosaeta, alongside the predominance of Methanobacterium, in regulating COD conversion and driving methanogenesis through the CO₂ reduction pathway. Notably, high ethanol proportions fostered the enrichment of exoelectrogens (Geobacter, Desulfovibrio) in the magnetite-amended system, accompanied by the up-regulation of genes involved in organic metabolism pathways. Further investigation of functional genes highlighted the prevalence of pilA enrichment in the magnetite-amended system at low ethanol proportions, whereas omcS became more abundant at high ethanol proportions.

This research aimed to assess the potential of Cu₅₀PANI@UG composite for sunlight drive photocatalytic dye degradation, targeting specifically Thymol Blue (TB) and Black NT (BNT) dyes and their mixture (DM). The Cu₅₀PANI@UG composite was successfully synthesized via electropolymerization in acetonitrile/sulfuric acid mixture under atmospheric conditions. Photocatalytic experiments were conducted by exposing aqueous dye solutions to sunlight. N,N-dimethyl-p-nitrosoaniline (RNO) served as a molecular probe for detecting hydroxyl radicals (^•OH). Additionally, experiments capturing free radicals were performed to identify active components, with a concomitant proposal of plausible degradation reaction mechanism for the Photo-Fenton-Like degradation into the Cu₅₀PANI@UG composite + H₂O₂ + hv reaction system. Various operating parameters affecting dye degradation were evaluated, including catalyst dosage (from 0.27 to 0.67 g L^-1), H₂O₂ concentration (from 16 to 64 mM), pH (from 3.0 to 9.0), and dye concentration (from 25 to 100 mg L^-1). Optimization of key parameters such as pH, catalyst dosage, and H₂O₂ concentration was conducted. The highest degradation efficiency, ca. 100% of DM dye, was achieved within 35 min under optimized conditions, using Cu₅₀PANI@UG composite as a catalytic precursor. These conditions were determined as follows: Catalyst dosage = 0.67 g L^-1, pH = 3.0-6.0, H₂O₂ = 32-64 mM, and irradiation time of 35 min. The degradation percentage under the Response Surface Methodology (RSM) was utilized as a statistical tool to correlate influential parameters. Four consecutive reusability trials were performed to assess catalyst stability.

The presence of herbicides, including simazine (SIM), in aquatic environments pose significant threats to these ecosystems, necessitating a method for their removal. In this study, a hemin-doped rice husk-derived biochar (RBC@Hemin_20%) was synthesized using a simple, one-step pyrolysis, and its degradation efficiency towards SIM via peroxymonosulfate (PMS) was assessed. Under optimized conditions (hemin loading = 20 wt%, SIM = 0.5 ppm, RBC@Hemin_20% catalyst = 0.2 g L^-1, PMS = 2.0 mM, and pH = 5.84 [unadjusted]), RBC@Hemin_20%, as an Fe/N-C catalyst, could activate PMS to achieve >99% degradation of SIM. Based on radical scavenger and electron spin resonance spectroscopy (ESR) experiments, both radical (^•OH and SO₄^•-) and non-radical (such as singlet oxygen, ¹O₂) mechanisms and electron transfer were involved in the degradation system. Significant mineralization (97.3%) and reusability efficiency (∼74.1% SIM degradation after 4 applications) were exhibited by the RBC@Hemin_20%/PMS system, which also maintained a remarkable degradation efficiency in tap-, river-, and ground-water. Additionally, the RBC@Hemin_20%/PMS system exhibited rapid degradation of tetracycline (TC) and diclofenac (DCF), indicating its prospects in the degradation of other organic pollutants of aquatic environments. The plausible degradation mechanism pathways of SIM are proposed based on identified intermediates. Finally, the toxicity of these intermediate products is analysed using the Ecological Structure Activity Relationship (ECOSAR) software. It is expected that this study will expand the current knowledge on the synthesis of efficient biomass-based Fe/N-C composites for the removal of organic pollutants in water.

Contamination of water sources is a major environmental problem with far-reaching consequences for humanity. Organic substances are among the most widespread and persistent pollutants. Advanced oxidation processes, especially photocatalysis, have been considered as one of the most promising technologies for organic pollution control. In this study, hybrid photocatalysts based on N-doped TiO₂, which exhibits activity in the visible region of the spectrum, and different content of octahedral Mo₆ bromide and iodide cluster complexes were synthesized to achieve the highest efficiency of the formed S-scheme photocatalytic system under white light irradiation. According to the data obtained, the resulting materials are nanoparticles with a diameter of ∼10 nm exhibiting absorption up to ∼550 nm. Photocatalytic studies were performed using model organic molecules - the more colored rhodamine B (RhB) and the less colored antibiotic tetracycline (TET). The most active samples showed high efficiencies against both pollutants with k_eff ∼0.3-0.4 and 0.4-0.5 min^-1, respectively, while the activity of iodide complexes was ∼1.3 times higher than that of bromide complexes. The stability of the catalysts is preserved for up to 5 cycles of TET photodegradation.

Herein, effort was made to construct innovative adsorbent for the removal of polar organic micropollutants (OMPs) from water. Tetra-meso resorcinol-functionalized calix[4]pyrrole (CP) featured with endo-functionalized attribute and polyphenol hydroxyl structure was crosslinked by π-electron-rich 4,4'-bis(chloromethyl)biphenyl (BCMBP) through Friedel-Crafts reaction to generate porous calix[4]pyrrole-based polymers (PCPPs) with high surface area. The porosity of the PCPPs could be tuned by adjusting the molar ratio of hydrophilic CP to hydrophobic BCMBP, and diversified binding sites were integrated together. Based on adsorption kinetics and isotherm studies, PCPP(1-16) showed rapid adsorption rate and high removal efficiency (RE) as well as advanced adsorption capacity. The REs towards the tested polar OMPs by PCPP(1-16) were all above 95% in 30 min. Compared with granular activated carbon (GAC), the rate constant of pseudo-second-order model (k₂) and adsorption capacity upon PCPP(1-16) were 8-230 times and 1.3-3.1 times greater than those by GAC. Adsorption mechanism studies confirmed the presence of multiple interactions and thermodynamic investigation revealed the spontaneous and physical adsorption nature. Besides, PCPP(1-16) showed excellent adsorption performance in real water samples at environmental levels and exhibited advanced absorption ability in flow-through mode. Accompanied by facile regeneration under eluting with methanol and cost-effective preparation, PCPP(1-16) demonstrated great potential as promising adsorbent for water treatment.

The rapid growth of population and the effects of climate change have placed unprecedented pressure on urban water supplies and pollution control. Consequently, it is essential to explore new local water resources in water-strained areas. To this end, this work focuses on evaluating pollutant removal effectiveness of decentralized treatment systems for groundwater reclamation. Two pilot-scale treatment trains, Treatment Line 1 (L1) and Treatment Line 2 (L2), which use membrane-free (with granulated activated carbon as the main process) or membrane-based (with reverse osmosis as the primary technology), were compared for their effectiveness in reducing concentrations of organic contaminants of emerging concern (CECs). Additionally, the effect of sodium hypochlorite addition for biofilm control on the contaminant removal performance was also examined. Results from the analysis of nearly 120 trace organic compounds (only 21 were detected in the raw water) showed that L2 significantly overperformed L1. Furthermore, the addition of a pre-chlorination step did not improve the removal performance. Regarding trace organic compounds, L1 without pre-chlorination averaged an overall good removal performance (94 ± 12%). However, Irbesartan, gemfibrozil and gabapentin showed moderate removals (50-90%) and Valsartan was poorly removed (<50%). After pre-chlorinating L1, the overall removal performance decreased (86 ± 20%). Nearly one third of the target contaminants showed moderate removal (50-90%), with Irbesartan and Valsartan exhibiting poor attenuations (<50%), highlighting that negatively-charged compounds were challenging to eliminate. In contrast, L2 exhibited very high removals (>99%) on all studied trace organic contaminants regardless of pre-chlorination. Our study also identified several indicator compounds to monitor CEC removal. Finally, considering the trade-offs between cost and final water use (non-potable), L1-based schemes with intermittent pre-chlorination could be the preferred implementation option. The results of this work will offer valuable insights into decentralized treatment systems, assisting decision-makers in choosing suitable approaches for sustainable urban water management.

β-N-Methylamino-L-alanine (BMAA), a neurotoxin produced by various microalgal groups, is associated with neurodegenerative diseases and is considered a major environmental factor potentially linked to sporadic amyotrophic lateral sclerosis. This study systematically reviews the analytical methods used to study BMAA in publications from 2019 to the present. It also investigates the causative microalgae of BMAA and its geographical distributions in aquatic ecosystems based on studies conducted since 2003. A comprehensive search using the Web of Science database revealed that hydrolysis for extraction (67%), followed by quantification using LC-MS/MS (LC: 84%; MS/MS: 88%), is the most commonly employed method in BMAA analysis. Among analytical methods, RPLC-MS/MS had the highest percentage (88%) of BMAA-positive results and included a high number of quality control (QC) assessments. Various genera of cyanobacteria and diatoms have been reported to produce BMAA. The widespread geographical distribution of BMAA across diverse ecosystems highlights significant environmental and public health concerns. Notably, BMAA accumulation and biomagnification are likely more potent in marine or brackish water ecosystems than in freshwater ecosystems, potentially amplifying its ecological impacts. Future research should prioritize advanced, sensitive methods, particularly LC-MS/MS with as many QC assessments as possible, and should expand investigations to identify novel microalgal producers and previously uncharted geographical areas, with a special focus on marine or brackish water ecosystems. This effort will enhance our understanding of the environmental distribution and impacts of BMAA.

Vertical flow-constructed wetlands (VFCWs) are treatment systems that can be used for the phytoremediation of highly polluted textile wastewater. Using plant-derived biochar to simultaneously improve the contaminant removal performance of CWs and sustainable utilization of harvested plant biomass is an interesting proposition. The present study explored the phytoremediation potential of Phragmites karka and verified the impact of using P. karka-derived biochar as a substrate in VFCWs for the treatment of textile wastewater. For this, three types of VFCWs were designed; (i) non-vegetated (VFCW), (ii) vegetated with P. karka (VFCW-P), and (iii) vegetated with P. karka and amended with P. karka-derived biochar (VFCW-BP) and semi-batch experiments were conducted. The investigation confirmed that wetlands using biochar as substrate were more efficient than other wetlands in pollutant load reduction. The maximum pollutant removal efficiencies were recorded for VFCW-BP vis-à-vis COD (83.61%), color (77.87%), chloride (73.22%), calcium (73.52%), sodium (67.18%), and potassium (75.72%) after five days. Furthermore, biochar addition enhanced the growth conditions for wetland plants by alleviating osmotic and oxidative stresses and hence helped them to perform better while removing pollutants. The maximum reduction of various pollutant parameters was reached within 72 h, after which remediation efficiency was slowed down. The study suggests that VFCW with biochar amendment is a useful strategy for textile wastewater treatment. Because the experimental design satisfies the needs for low-cost wastewater treatment, it may find widespread applications.

Drought stress (DS) is a hazardous abiotic prerequisite that is becoming increasingly severe around the world. As a result, new management measures to reduce the negative effects of DS are desperately needed to ensure improved agricultural productivity. This review focuses primarily on various DS mitigation strategies that can be utilized to overcome DS. In recent years, the application of biochar, plant growth promoting rhizobacteria (PGPR), and arbuscular mycorrhizal fungi (AMF) have emerged as major strategies for improving crop yields under DS conditions. PGPR increases osmolyte buildup, increases the aminocyclopropane-1-carboxylate (ACC) deaminase enzyme, and provides inaccessible nutrients to plants, hence boosting drought tolerance. Different genetic approaches, including as transcriptional engineering, miRNA engineering, and quantitative trait loci (QTL) mapping, have emerged as an incredibly efficient method for making drought-resistant plants. Drought-related phytohormones, signaling molecules, transcription factors, and transcriptional and translational changes are all affected by genomic intervention. It is critical for enhancing tolerance response to identify prospective transcription factors and target them for engineering the abiotic stress tolerance response in crop plants. Investigating novel QTLs for drought tolerance features using a fresh genetic resource would also be beneficial in dissecting the mechanisms governing the trait's diversity. This review aims to provide information to readers about drought mitigation measures including the usage of PGPR, AMF, biochar, phytohormones, chemicals, and genetic approaches.

Lead (Pb), a persistent and bio-accumulative contaminant, poses threats to the environment and human health. The effective removal of Pb from contaminated soil proves challenging due to its tendency to form stable complexes with soil components. Chelators have been extensively studied for their ability to extract metal contaminants, including Pb, from soil environment. However, the prolonged environmental persistence of traditional chelators and the high cost of biodegradable alternatives have hindered their practical application in remediation efforts. This study investigated a novel synergistic approach that combined a biodegradable chelator, [S,S]-ethylenediamine succinic acid (EDDS), with cationic and anionic surfactants to enhance Pb extraction efficiency. The study revealed that cationic surfactants, such as cetylpyridinium chloride (CPC) and cetyltrimethylammonium bromide (CTAB), significantly enhanced Pb extraction efficiency when combined with EDDS, whereas anionic surfactants, like sodium N-dodecanoyl-taurinate (SDT) and sodium dodecyl sulfate (SDS), inhibited the extraction process. Specifically, blending 5 mmol L^-1 EDDS with 20 mmol L^-1 CPC resulted in a 72.6% enhancement in Pb extraction efficiency. The proposed synergistic strategy offers a promising avenue for soil remediation, mitigating Pb contamination while preserving essential soil minerals. By addressing chelator limitations and improving efficiency, this approach presents a viable solution for enhancing soil remediation practices.