Toxic Removal Research Articles

Ozonation combined to BAC filtration for secondary effluent treatment containing moderate concentration of heavy metals

The treatment of industrial and urban effluents is a recognized strategy for environmental preservation, which brings benefits not only to fauna and flora but also to human health. In this paper, the combination effect of ozonation (O3) and biological activated carbon (BAC) filtration treatments on the inorganic contaminants removal, disinfection, and mitigation of toxicity in secondary effluent from wastewater treatment plants (WWTP) were evaluated. Disinfection efficiency was evaluated using total coliforms and Escherichia coli inactivation, and toxicity was investigated by Eruca sativa germination, Artemia salina larvae and Daphnia similis. The O3-BAC system was efficient to remove metals, disinfect the samples and reduce toxicity. The combined treatment reduced 99.9 % of the assessed metal concentration and ≥ 96 % on samples enriched with 2x the concentration allowed by Brazilian legislation. O3-BAC also demonstrated superior bactericidal performance compared to BAC and O3 alone, exhibiting a 5-log reduction within 24 h against total coliforms and 4-log reduction in E. coli, whereas BAC and O3 achieved ≤ 3-log inactivation. Regarding toxicity, the bioassays demonstrated that the combined treatment effect improved the relative germination of E. sativa (∼97 %), and the relative root elongation showed no differences compared to the control group (∼100 %). Similar behavior was also observed in the analysis with wheat and radish seeds, with no differences noted between the treated samples and the positive control. In relation to A. salina, no toxic results were observed even at high metals concentration. Additionally, BAC treatment reduced D. similis immobilization from 97 ± 6 % to a level with no observed effect. The observed synergy suggests that the O3-BAC combination may address a variety of pollutants and improve treatment efficacy.

Neural network cognitive analysis of accumulation metals by marigold

The article presents the results of studies to assess the effect of humic acids, taken at a concentration of 250 ppm, on the process of induced phytoextraction of heavy metals from soils selected near Norilsk. Phytoxtraction was carried out by different types of marigold plants: Tagetes patula and Tagetes erecta. The studies were carried out in greenhouse conditions under controlled spectral illumination (light culture). The duration of the experiment was 21 days. A short vegetation period was chosen based on the conditions of a short summer period typical for this region, where it is more rational to keep records of the systemic removal of toxicants from contaminated soils by several cycles of their sowing/cutting per season, already at the juvenile phase of ontogenesis. For elemental analysis, the method of atomic emission spectrometry with inductively coupled plasma was used. To assess the level of efficiency of metal accumulation, the authors developed and used the original computing neural network CompNN, which allows calculating the cognitive significance index (CSI) based on empirical data on the accumulation of toxicants, both in shoots and roots of plants. The results of the study showed that the introduction of an organic additive in the form of humic acids into the soil led to inhibition of the growth of the above-ground part of T. patula. As for T. erecta, the rate of accumulation of green plant biomass did not change when humic acids were added. The decrease in the biomass of shoots of T. patula plants is explained by an increase in the accumulation of metals in them by an average of 91.6% for the variants. The content of metals in the shoots of T. erecta under the influence of humic acids, on the contrary, decreased by 17.3% on average. A similar result was observed in relation to the root zone: the trend of change in the fixation of metals for both plant species here was 40.8 and 10.8%, respectively. Calculation of CSI indices also showed that the addition of humic acids in T. patula increases the intensity of metal accumulation from the soil in its biomass in all variants, while in T. erecta, on the contrary, it decreases. The performed cluster analysis demonstrated the fixation of metals in the main buffer zone of plants, and also made it possible to isolate nickel into a separate homogeneous series. With regard to the distribution of this element in the shoots by variants, experience has shown that it has demonstrated here the proximity of convergence with copper. The correlation coefficients of their accumulation with the CSI index in the shoots of both plants were r = 0.82; 0.87 for Cu and r = 0.87; 0.83 for Ni. The proximity of these values indicates the priority nature of the accumulation of these metals in the plant biomass of marigolds, and also characterizes the manifestation of certain interactions between them in contaminated soil by the type of antagonism or synergism.

Advancing the Effect-Directed Identification in Combined Pollution: Using Pathways to Link Effects and Toxicants.

The difficulty in associating diverse pollutants with mixture effects has led to significant challenges in identifying toxicants in combined pollution. In this study, pathways were used to link effects and toxicants. By pathways evaluated by the concentration-dependent transcriptome, individual effects were extended to molecular mechanisms encompassing 135 pathways corresponding to 6 biological processes. Accordingly, mechanism-based identification of toxicants was achieved by constructing a pathway toxicant database containing 2413 chemical-pathway interactions and identifying pathway active fragments of 72 pathways. The developed method was applied to two different wastewaters, industrial wastewater OB and municipal wastewater HL. Although lethality and teratogenesis were both observed at the individual level, different molecular mechanisms were revealed by pathways, with cardiotoxicity- and genotoxicity-related pathways significantly enriched in OB, and neurotoxicity- and environmental information processing-related pathways significantly enriched in HL. Further suspect and nontargeted screening generated 59 and 86 causative toxicants in OB and HL, respectively, among which 29 toxicants were confirmed, that interacted with over 90% of enriched pathways and contributed over 50% of individual effects. After upgrading treatments based on causative toxicants, consistent removal of toxicants, pathway effects, and individual effects were observed. Mediation by pathways enables mechanism-based identification, supporting the assessment and management of combined pollution.

A novel polymer nanocomposite system for rapid dimethyl phthalate toxicity removal

A novel polymer nanocomposite system for rapid dimethyl phthalate toxicity removal

New insights into mechanism of ellagic acid alleviating arsenic-induced oxidative stress through MAPK/keap1-Nrf2 signaling pathway response, molecular docking and metabolomics analysis in HepG2 cells

The increase of oxidative stress level is one of the vital mechanisms of liver toxicity induced by arsenic (As). Ellagic acid (EA) is widely known due to its excellent antioxidation. Nevertheless, whether EA could alleviate As-induced oxidative stress and the underlying mechanisms remain unknown. Herein, As (2 and 4 μM) and EA (25 and 50 μM) were selected for alone and combined exposure of HepG2 cells to investigate the effects of EA on As-induced oxidative stress. Results indicated that EA could alleviate the oxidative stress caused by As via decreasing intracellular ROS level and MDA content, as well as improving SOD, CAT and GSH-PX activities. qRT-PCR showed that EA might enhance the expression levels of antioxidant enzymes NQO1, CAT and GPX1 by activating MAPK (JNK, p38 and ERK)/keap1-Nrf2 signaling pathway. EA was found to promote dissociation from keap1 and nuclear translocation of Nrf2 by competing with Nrf2 at ARG-380 and ARG-415 sites on keap1 to exert antioxidation using molecular docking. Moreover, metabolomics revealed that EA might maintain the redox balance of HepG2 cells by modulating or reversing disorders of carbon, amino acid, lipid and other metabolisms caused by As. This study provides diversified new insights for the removal of liver toxicity of As and the application of EA.

Heavy metals altered the xenobiotic metabolism of rats by targeting the GST enzyme: An in vitro and in silico study

Among all the heavy metals, Pb, Cd, and As are the most harmful pollutants in the environment. They reach into the organisms via various levels of food chains i.e. air and water. Glutathione-s-transferase (GST, E.C. 2.5.1.18), a key enzyme of xenobiotics metabolism, plays an important role in the removal of several toxicants. The present study aimed to evaluate any inhibitory action of these heavy metals on the GST enzyme isolated from the hepatic tissues of rats. A 10 % (w/v) homogenate of rat liver was prepared in cold and centrifuged at 4 °C at 9000xg for 30 min. The supernatant was collected and kept frozen at −20 °C or used fresh for carrying out different experiments. The activity of GST was monitored spectrophotometrically at 340 nm using 220 μg of soluble protein with varying equal substrate concentrations (0.125–2 mM) in phosphate buffer (50 mM, pH 6.5). To assess the impact of heavy metals on the enzyme activity, different concentrations of Cd (0–0.6 mM) and Pb (0–2 mM) were added to the reaction mixture followed by monitoring the residual activity. The optimum temperature and pH of rat liver GST were found to be 37 °C and 6.5, respectively. The Km value for GST was 0.69 mM and the Vmax was found to be 78.67 U/mg. The Cd and Pb significantly altered the kinetic behaviour of the enzyme. The Vmax and Kcat/Km parameters of GST were recorded to be decreased after interaction with Cd and Pb individually and showed a mixed type of inhibition pattern suggesting that these inhibitors may have a greater binding affinity either for the free enzyme or the substrate-enzyme complex. These metals showed a time-dependent enzyme inhibition profile. Cd was found to be the most potent inhibitor when compared to other treated metals; the order of inhibitory effect of metal ions was Cd>Pb>As. The in silico ion docking analysis for determining the probable interactions of Cd and Pb with fragmented GST validated that Cd exhibited higher inhibition potential for the enzyme as compared to Pb. The results of the present study indicated that exposure of both the Cd and Pb may cause significant inhibition of hepatic GST; the former with higher inhibitory potential than the later. However, As proved to be least effective against the enzyme under the aforesaid experimental conditions.

Reconstructing Electrically Conductive Nanofiltration Membranes with an Aniline-Functionalized Carbon Nanotubes Interlayer for Highly Effective Toxic Organic Treatment.

Conductive nanofiltration (CNF) membranes hold great promise for removing small organic pollutants from water through enhanced Donnan exclusion and electrocatalytic degradation. However, current CNF membranes face limitations in conductivity, structural stability, and nanochannel control strategies. This work addresses these challenges by introducing aniline-functionalized carbon nanotubes (NH2-CNTs) as an interlayer. NH2-CNTs enhance the dispersibility and adhesion of pristine carbon nanotubes, leading to a more conductive and stable composite nanofiltration membrane. The redesigned NH2-CNTs interlayered conductive nanofiltration (NICNF) membrane exhibits a 10-fold increase in conductivity and a high response degree (80%) with excellent cyclic stability, surpassing existing CNF membranes. The synergistic effects of enhanced Donnan exclusion, voltage switching, and electrocatalysis enable the NICNF membrane to achieve selective recovery of mixed dyes, 98.97% removal of residual wastewater toxicity, and a 5.2-fold increase in permeance compared to the commercial NF270 membrane. This research paves the way for next-generation multifunctional membranes capable of the efficient recovery and degradation of toxic organic pollutants in wastewater.

A review on algae-mediated adsorption and catalytic processes for organic water pollution remediation

Wastewaters consist of organic pollutants that have environmental concerns. Wastewaters are treated by different methods, but efficient, low-cost, and sustainable techniques still need to be developed. Algae-based water pollution remediation techniques are considered to be sustainable approaches. This review exclusively discusses the facets of macro and microalgae in the treatment of organic toxicants. The current trends of algae-mediated water treatments have been discussed under adsorption and degradation methods. A focus on algae fuel cell, algae mediated activation of oxidizing agents, Fenton-like reactions, and photocatalysis was given. The need of algae-based adsorptive and catalytic materials was mentioned. The role of algae in the synthesis of catalysts which were employed in pollutant removal methods was also explained. The integrated algae-mediated water treatment techniques were also highlighted. The toxicant removal performances of different algae-based materials in the water medium were summarized. The conclusion and future prospects derived from the literature survey were described. This review will be helpful for researchers who are working in the field of sustainable water pollution remediation.

Micro-particle-clay aided microporous support for removal of hydrocarbon toxicity from petroleum refinery wastewater in single-slope solar distillation

The removal of toxic hydrocarbon pollutants is not sustainable via conventional treatment technology. This research investigates the feasibility of a solar distillation (SSD) system to eliminate soluble hydrocarbon salts, stubborn organics, and separation of oil emulsion from petroleum refinery wastewater (PRW). The PRW collected from the petroleum refinery facility and hydrophilic micro-particle clay (MP-clay) samples were characterized following the ASTM and SEM techniques. The treatment process for the removal of total dissolved salts (TDS), biological oxygen demand (BOD), and separation of oil emulsion was monitored in the SSD still using MP-clay aided microporous filter support, at varying MP-clay concentrations (0.5–3.5 mg/L), pH (6.6–7.3), temperature (27–80 0C), and exposure time (1–18hrs) respectively. The results showed MP-clay as self-assembled monolayers on microporous support with a 98 % reduction in BOD concentration under optimum conditions: pH of 7.3, contact time of 9 hours, and MP-clay concentration of 3.2 mg/L. The TDS concentration decreased by 94 % at the optimal exposure time (15hrs) and temperature (48 0C) in SSD still. The investigation also examined the recyclability of MP-clay for oil content accumulation and water separation. The findings demonstrated MP-clay on reuse retained 90.5 % of its activity in water separation and established MP-clay can be operated to the optimum of 3 cycles, each lasting 60 minutes. After this period, reactivity loss becomes severe owing to lipase leakage and substrate obstruction. The research findings will help harness solar energy for environmentally friendly and cost-effective PRW remediation.

Proteomics of Penicillium chrysogenum for a Deeper Understanding of Lead (Pb) Metal Bioremediation.

Penicillium chrysogenum (P. chrysogenum), a ubiquitous filamentous fungus, has demonstrated remarkable potential in the bioremediation of lead-contaminated environments. Its inherent tolerance and bioaccumulation capacity for lead (Pb), coupled with its relatively rapid growth rate, make it an attractive candidate for bioremediation applications. This study aims to identify the proteomic changes in P. chrysogenuminduced by Pb metal stress and unravel the roles of identified proteins in molecular mechanisms and cellular responses. Untargeted proteomic analysis was carried out using a two-dimensional difference in gel electrophoresis (2D-DIGE) coupled with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS). This study reported the identification of 43 statistically significant proteins (24 upregulated and 19 downregulated, ANOVA, p ≤ 0.05; fold change ≥1.5) in P. chrysogenum as a consequence of Pb treatment. Proteins were grouped according to their function into 18 groups from which 13 proteins were related to metabolism, 11 were related to cellular process and signaling, and 19 proteins were related to information storage and processing. The current study is considered the first report about the proteomics study of P. chrysogenum under Pb stress conditions, where upregulated proteins could better explain the mechanism of tolerance and Pb toxicity removal. Our research has provided a thorough understanding of the molecular and cellular processes involved in fungal-metal interactions, paving the way for the development of innovative molecular markers for heavy metal myco-remediation. To the best of our knowledge, this study of P. chrysogenum provides valuable insights toward growing research in comprehending the metal-microbe interactions. This will facilitate development of novel molecular markers for metal bioremediation.

Biodecolorization and biodegradation of Reactive Green 12 textile industry dye and their post-degradation phytotoxicity-genotoxicity assessments.

The employment of versatile bacterial strains for the efficient degradation of carcinogenic textile dyes is a sustainable technology of bioremediation for a neat, clean, and evergreen globe. The present study has explored the eco-friendly degradation of complex Reactive Green 12 azo dye to its non-toxic metabolites for safe disposal in an open environment. The bacterial degradation was performed with the variable concentrations (50, 100, 200, 400, and 500mg/L) of Reactive Green 12 dye. The degradation and toxicity of the dye were validated by high-performance liquid chromatography, Fourier infrared spectroscopy analysis, and phytotoxicity and genotoxicity assay, respectively. The highest 97.8% decolorization was achieved within 12h. Alternations in the peaks and retentions, thus, along with modifications in the functional groups and chemical bonds, confirmed the degradation of Reactive Green 12. The disappearance of a major peak at 1450cm-1 corresponding to the -N=N- azo link validated the breaking of azo bonds and degradation of the parent dye. The 100% germination of Triticum aestivum seed and healthy growth of plants verified the lost toxicity of degraded dye. Moreover, the chromosomal aberration of Allium cepa root cell treatment also validated the removal of toxicity through bacterial degradation. Thereafter, for efficient degradation of textile dye, the bacterium is recommended for adaptation to the sustainable degradation of dye and wastewater for further application of degraded metabolites in crop irrigation for sustainable agriculture.

A sustainable electrochemical strategy utilizing pulsed alternating current and dual carbon felt electrodes for enhanced degradation of organic pollutants: Oxidation performance and mechanisms

In this work, a novel electrochemical (EC) oxidation system utilizing pulsed alternating current (PAC) and dual carbon felt (CF) electrodes has been established for sustainable degradation of sulfamethoxazole (SMX) with no addition of extra oxidant. The EC/PAC system showed high degradation efficiency and energy efficiency compared to the pulsed direct current (PDC) and direct current (DC) systems. The EC/PAC process was effective across a wide pH range of 3–11 for SMX removal. The results showed that the 1O2 confined to the CF electrode surface was the dominant oxidative specie that was generated from dissolved oxygen in the system. Under PAC conditions, the cathode and anode were rapidly switched on the same CF electrode, increasing the generation of 1O2 for enhanced SMX oxidation. Furthermore, the EC/PAC system demonstrated resistance to interference from various anions of different concentration levels found in natural environment. In contrast to the EC/PDC system, the EC/PAC system emerged as a promising option for more efficient H2O2 production. High-resolution mass spectrometry results revealed the SMX degradation pathways and byproducts, which were then evaluated for toxicity removal. Overall, the EC/PAC system offers a green and sustainable solution to future wastewater treatment, with high degradation rates, energy efficiency, and sustainability.

Cinnamic Acid: A Low-Toxicity Natural Bidentate Ligand for Uranium Decorporation.

Uranium accumulation in the kidneys and bones following internal contamination results in severe damage, emphasizing the pressing need for the discovery of actinide decorporation agents with efficient removal of uranium and low toxicity. In this work, cinnamic acid (3-phenyl-2-propenoic acid, CD), a natural aromatic carboxylic acid, is investigated as a potential uranium decorporation ligand. CD demonstrates markedly lower cytotoxicity than that of diethylenetriaminepentaacetic acid (DTPA), an actinide decorporation agent approved by the FDA, and effectively removes approximately 44.5% of uranyl from NRK-52E cells. More importantly, the results of the prompt administration of the CD solution remove 48.2 and 27.3% of uranyl from the kidneys and femurs of mice, respectively. Assessments of serum renal function reveal the potential of CD to ameliorate uranyl-induced renal injury. Furthermore, the single crystal of CD and uranyl compound (C9H7O2)2·UO2 (denoted as UO2-CD) reveals the formation of uranyl dimers as secondary building units. Thermodynamic analysis of the solution shows that CD coordinates with uranyl to form a 2:1 molar ratio complex at a physiological pH of 7.4. Density functional theory (DFT) calculations further show that CD exhibits a significant 7-fold heightened affinity for uranyl binding in comparison to DTPA.

Removal of antibiotics, bacterial toxicity, and occurrence of antibiotic resistance genes in secondary hospital effluents treated with granular activated carbon and the impact of preceding chlorination

This comprehensive investigation highlighted the complex adsorption behaviors of antibiotics onto granular activated carbon (GAC), the effectiveness of this adsorption in reducing bacterial toxicity, and the reduction of antibiotic resistance genes (ARGs) and antibiotic resistant bacteria (ARB) in hospital wastewater (HWW) effluents. Six GACs were characterized for their physicochemical properties, and their ability to adsorb six antibiotics in the background matrix of actual HWW was evaluated. Coconut shell-derived GAC (Co-U), which had the highest hydrophobicity and lowest content of oxygen-containing acidic functional groups, demonstrated the highest adsorption capacities for the tested antibiotics. Bacterial toxicity tests revealed that GACs could eliminate the bacterial toxicity from antibiotic intermediates present in chlorinated HWW. By contrast, the bacterial toxicity could not be removed by GACs in non-chlorinated HWW due to the greater presence of intermediate components identified by LC-MS/MS. The intraparticle diffusion coefficient of antibiotics adsorbed onto Co-U could be calculated by adsorption kinetics derived from the linear driving force model and the homogenous intraparticle diffusion model associated with the linear adsorption isotherms (0–150 μg/L). Meropenem and sulfamethoxazole exhibited the highest adsorption capacities in a single-solute solution compared to penicillin G, ampicillin, cetazidime, and ciprofloxacin. However, the greater adsorption capacities of meropenem and sulfamethoxazole disappeared in mixed-solute solutions, indicating the lowest adsorption competition. GAC can eliminate most ARGs while also promoting the growth of some ARB. Chlorination (free chlorine residues at 0.5 mg Cl2/L) did not significantly affect the overall composition of ARGs and ARB in HWW. However, the accumulation of ARGs and ARB on GAC in fixed bed columns was lower in chlorinated HWW than in non-chlorinated HWW due to an increase in the adsorption of intermediates.

Toxicity removal from contaminated water by constructed wetlands assessed using multiple biomarkers in human stem cell assays

Constructed wetlands (CWs) have been developed rapidly as a sustainable water treatment technique. However, the capability of CWs for remediating the contaminated water based on toxicity assessment remains largely unknown. Four surface flow CWs and two integrated surface-subsurface flow CWs, from five cities in central and eastern region of China were evaluated, concerning the adverse effects of effluents and the toxicity reduction efficiency. Human bone marrow mesenchymal stem cells (hBMSCs) were employed as a human relevant in vitro model. The influent extractions caused cytotoxicity in a dose-dependent manner. The non-cytotoxic dilutions of the influents enhanced the genotoxicity marker γ-H2AX and reactive oxygen species levels. In addition, the influent repressed the osteogenic and neurogenic differentiation, and stimulated the adipogenic differentiation. Cytotoxicity of the contaminated water was reduced by 54 %–86 % after treatment with CWs. CWs were effective to remove part of the sub-lethal effects, with lower reduction than cytotoxicity. The integrated biomarker response (IBR) value of the effluents from the six CWs is lower than that of four secondary and one tertiary wastewater treatment plants. The IBR of the six CWs influents were in the range of 8.6–10.6, with a reduction of 15–50 % after the pollution restoration in CWs. The two integrated surface-subsurface flow CWs achieved higher IBR removal than the four surface flow CWs, possibly due to improved treatment effects by the combined systems. Cytotoxic and genotoxic effects of polar fractions in the CW effluents were stronger than the medium-polar and the non-polar fractions. Besides, PPARγ agonists present in the effluents played crucial roles and ERα agonists may make modest contributions. The present study enhances understanding of the role of CWs in achieving safe wastewater reclamation and provides evidence for further improving toxicity reduction in CWs performance.

Remediation of phenanthrene-contaminated soil by iron oxide/carboxylate-rich porous carbon composites from vinegar residue

Conversion of solid wastes into useful remediation materials is an encouraging strategy in resource recovery. Iron oxide/carboxylate-rich porous carbon composites (IOCRPC) can be synthesized by using vinegar residue (VR) and ferrous sulfate heptahydrate (FeSO4∙7 H2O) recovered from a waste acid of a titanium dioxide factory. Characterization of FeSO4-impregnated VR exhibited a high proportion of ferricarboxylate complexes [i.e. FeII(R-COO)n2-n]. Pyrolysis temperature was the most important reaction parameter to define IOCRPC phase composition. Thermal decomposition of FeII(R-COO)n2-n produced Fe3O4 nanoparticles partly at a relatively lower pyrolysis temperature (350 ºC), while successful carbonization of VR formed the porous structures of carbon. Both Fe3O4 and ferricarboxylate complexes were the components of IOCRPC responsible for its excellent visible light absorption ability. Under visible light, phenanthrene in contaminated soil was efficiently degraded (90.1%) by IOCRPC at circumneutral pH. Phytotoxicity bioassays demonstrated significant removal of toxicity after treatment with IOCRPC, highlighting its application potential in revegetation strategies.

Calcium peroxide orchestrates virus-induced heavy metal resistome via shaping humeomics in sludge composting

This study aims to investigate the impact of calcium peroxide (CaO2) on compost humeomics and its effect on the toxicity removal of heavy metals (HMs), viral communities, and heavy metal resistance genes (HMRGs) during composting. The results indicate that CaO2 reduced the concentrations of toxic HMs As and Ni by 2.08 mg/kg and 10.41 mg/kg, respectively, compared to the control group (CK). Furthermore, it led to an increase in the stable fractions of As, Cu, Fe, and Ni by 6.32 %, 13.23 %, 3.09 %, and 3.01 % in the treatment group (T), respectively. CaO2 facilitated the transformation of heavy metal components, mitigated their harmful effects, induced their stabilization, and enhanced the humic quality. Metagenomic analysis shows that CaO2 effectively reduces the abundance of viruses (VRs) associated with HMRGs, leading to the inhibition and removal of HMRGs. Network analysis reveals that VRs, such as g__unclassified_f__Pithoviridae and g__unclassified_d__Viruses, which are related to toxic HMs, play a key role in regulating the hazardousness of pollutants in compost, and their abundance is effectively reduced by CaO2. Finally, mantel test analysis confirms that the Fenton-like reactions triggered by CaO2 and the succession of viral communities are crucial factors in pollutant removal. These results collectively indicate that under the influence of CaO2, the hazardousness of HMs, VRs, and HMRGs in the composting process is reduced, and they are effectively inhibited and removed.

In-co-doped Bi1-xVO4 drenched sulfur–doped g-C3N4 nanocomposite: A type-II photo(electro)catalytic system for visible-light–driven water-splitting and toxic removal applications

In-co-doped Bi1-xVO4 drenched sulfur–doped g-C3N4 nanocomposite: A type-II photo(electro)catalytic system for visible-light–driven water-splitting and toxic removal applications

Effect of Nickel-Aluminum Trioxide/Titanium Dioxide Nanocomposites on Photo-oxidation of Olive Mill Wastewater

In this study, the magnetic nickel (Ni) doped aluminium trioxide (aluminium oxide or alumina, Al2 O3 ) based titanium dioxide (TiO2 ) [Ni-Al2 O3 /TiO2 ] nanocomposites (NCs) was used for the photocatalytic oxidation (photo-oxidation) of pollutant parameters {chemical oxygen demand (COD) components [CODtotal, CODdis, CODinert]}, toxic polyphenols [catechol, 3-hydroxybenzoic acid, tyrosol, 4-hydroxybenzoic acid, 4-hydroxyphenylacetic acid, 3-hydroxyphenylpropionic acid, 4-hydroxyphenylpropionic acid, 3,4-dihydroxyphenylethanol, 3,4-dihydroxyphenylacetic acid], and toxic polyaromatics [aniline, 4–nitroaniline, o–toluidine, o-anisidine, benzene, nitrobenzene, ethylbenzene, 3,6-bis(dimethylamino)durene, benzidine, dimethylaniline, 3,3–dichlorobenzidine]} from the olive mill effluent wastewaters (OMW), at different mass ratios of Al2 O3 , TiO2 and Ni (1%/5%/10%; 10%/1%/5% and 1%/10%/5%), at increasing photooxidation times (10, 30, 60, 100 and 120 min), at different Ni/Al2 O3 /TiO2 photocatalyst concentrations (50, 250, 500 and 1000 mg/l), pH values (4.0-7.0-9.0 and 10.0) and temperatures (15°C, 25°C, 50°C and 80°C), under 500 W ultraviolet visible (UV-vis) and 50 W sun lights irradiations, respectively. The acute toxicity assays were operated with Microtox (Aliivibrio fischeri also called Vibrio fischeri) and Daphnia magna acute toxicity tests. The significance of the correlations between data of all experimental samples were determined using the Analysis of Variance (ANOVA) test statistics. Under the optimized conditions, the maximum CODdis, total phenol and total aromatic amines (TAAs) photooxidation yields were 98%, 88%, 94%, respectively, at pH=9.0, at 500 mg/l Ni/Al2 O3 / TiO2 NCs, under 500 W UV-vis light, after 100 min photooxidation time, at 50°C, respectively. The photooxidation yields in OMW under sun light was lower than the photooxidation yields in the OMW under UV-vis light. 94.44% maximum Microtox acute toxicity yield was found in Ni/Al2 O3 /TiO2 NCs=500 mg/l after 150 min photooxidation time, at 60°C. 90% maximum Daphnia magna acute toxicity removal was obtained in Ni/Al2 O3 /TiO2 NCs=500 mg/l after 150 min photooxidation time, at 60o C. Microtox acute toxicity test was more sensitive than Daphnia magna acute toxicity assay

Efficient removal of toxicity associated to wastewater treatment plant effluents by enhanced Soil Aquifer Treatment

The regeneration of wastewater has been recognized as an effective strategy to counter water scarcity. Nonetheless, Wastewater Treatment Plant (WWTP) effluents still contain a wide range of contaminants of emerging concern (CECs) even after water depuration. Filtration through Soil Aquifer Treatment (SAT) systems has proven efficient for CECs removal although the attenuation of their associated biological effects still remains poorly understood. To evaluate this, three pilot SAT systems were monitored, two of them enhanced with different reactive barriers. SATs were fed with secondary effluents during two consecutive campaigns. Fifteen water samples were collected from the WWTP effluent, below the barriers and 15 m into the aquifer. The potential attenuation of effluent-associated biological effects by SATs was evaluated through toxicogenomic bioassays using zebrafish eleutheroembryos and human hepatic cells. Transcriptomic analyses revealed a wide range of toxic activities exerted by the WWTP effluents that were reduced by more than 70% by SAT. Similar results were observed when HepG2 hepatic cells were tested for cytotoxic and dioxin-like responses. Toxicity reduction appeared partially determined by the barrier composition and/or SAT managing and correlated with CECs removal. SAT appears as a promising approach to efficiently reduce effluent-associated toxicity contributing to environmental and human health preservation.