Mixed Pollutants Research Articles

Fluorescent nanoplastics increase the toxic effects of Graphene oxide nanoparticles in freshwater algae Scenedesmus obliquus

The increased usage of Graphene oxide (GO) in various industrial applications led to their entry into freshwater systems. Other secondary contaminants like nanoplastics (NPs) often co-exist with GO in the environment. This study examines the possible role of fluorescent nanoplastics (FNPs) in modifying the toxic effects of GO on freshwater algae Scenedesmus obliquus. Selected concentrations of GO (0.1, 1, and 10 mg L−1) were combined with a fixed concentration of FNPs (1 mg L−1) to perform combinational toxicity tests on algae. FNPs significantly enhanced the toxic effects of GO in the mixtures in comparison with the pristine GO. In addition to the cytotoxic effects, oxidative stress parameters like total ROS generation and malondialdehyde (MDA) production also increased in the case of the combined pollutants. The antioxidant enzymatic activities like catalase (CAT) and superoxide dismutase (SOD) in the cells were also assessed. Algal exposure to the pristine pollutants and their mixture led to a notable decrease in photosynthetic activities in the cells, with the mixed pollutants aggravating the loss of activity. The interactive toxic effects of the contaminants when present in mixtures were evaluated using Abbotts' Independent action modelling. Furthermore, optical microscopic images revealed the morphological changes in the algal cells after exposure to the contaminants both in the pristine and combined forms.

A comparative study on the toxic effects of lead pollution and nanoplastic-lead mixed pollution on red drum and their detoxification strategies

Nanoplastics and heavy metals pose various adverse effects on marine organisms. However, the combined toxicity of nanoplastics and lead pollution to marine fish is not fully understood. This study investigates the toxic effects and detoxification strategies of lead pollution (p07) compared to nanoplastic-lead mixed pollution (m07) in red drum during exposure and recovery phases. Under m07 pollution, the maximum lead content in muscle was 22.61 mg/kg, which was significantly higher than the 15.82 mg/kg observed under p07 pollution. This finding demonstrated that nanoplastics significantly enhance lead accumulation, leading to more severe toxic effects on red drum. Histological analyses revealed that lipid droplets in the liver and epithelial lifting in the gills were the primary lesion types. During the exposure periods, red drum primarily detoxified lead through cellular renewal and the removal of damaged proteins under p07 pollution. Conversely, under m07 pollution, detoxification relied on cellular senescence, apoptosis, endocytosis, and the removal of damaged proteins. In the recovery phases, red drum predominantly recovered through cell proliferation and antioxidant responses under p07 pollution. Under m07 pollution, the focus shifted to functional protein synthesis, apoptosis, endocytosis, and lipid metabolism. This study offers valuable insights into the monitoring and management of combined environmental pollution.

Controlled synthesis of CeNbZrO solid solution with high thermal stability and application in catalytic degradation of C6H5CH3 and C6H5Cl

A series of CeNbZrO composite oxides with different (CeNb)/Zr molar ratios were prepared by urea homogeneous precipitation method and systematically characterized. The thermal stability, degradation performance and structure-activity relationship of these catalysts for eliminating C6H5CH3 and C6H5Cl mixed pollutants were evaluated. The results indicated that with the increase of ZrO2 content, the catalytic activity of CeNbxZrO increased first and then decreased. Among them, the CeNb3.3ZrO catalyst (Ce/Nb/Zr=2/1/3.3, molar ratio) exhibited the highest catalytic activity (C6H5CH3: T90%=310oC, C6H5Cl: T90%=344oC) and thermal stability. Compared with the traditional CeO2-MnO2 catalyst, the T90% of the CeNb3.3ZrO catalyst in the degradation of C6H5Cl was reduced by 100oC. CeNb3.3ZrO exhibited high specific surface area and strong oxidation ability, which enhanced the redox cycles and promoted the interactions between metal ions. In addition, the formation of Ce2Zr3O10 solid solution made its structure stable even at high temperature. Overall, the optimized CeNb3.3ZrO has broad prospects in the catalytic treatment of volatile organic compounds and some other related fields in thermal catalysis. Environmental implicationC6H5CH3 and C6H5Cl are typical VOCs with certain toxicity, which pollute air environment and cause harm to human health. In this paper, CeNbZrO composite oxides with different (CeNb)/Zr molar ratios were prepared by urea homogeneous precipitation method. It was found that the CeNb3.3ZrO catalyst had higher specific surface area and stronger oxidation ability, and promoted the complete degradation of C6H5CH3 and C6H5Cl at lower temperatures by destroying the C-C, C-H and C-Cl bonds of the reactants.

One stone two birds: Simultaneous control of eutrophication and microplastic pollution via surface functionalized nano-Fe3O4

Microplastics (MPs) aggregate with phytoplankton to form aggregates that impede light and oxygen penetration, and the adsorbed nitrogen and phosphorus are either taken up by algae or released into the water column, thereby exacerbating water eutrophication. Therefore, it is imperative to simultaneously control nutrients (N and P) and MPs pollution in water. To address this, nano-Fe3O4 with different surface modifications (–COOH, –NH2, and –OH) was developed to control these mixed pollutants. The results showed that the surface modification can enhance the affinity for NH4+, PO43- and polyethylene microplastic (PE-MP), which can achieve exceptional adsorption capacities for NH4+-N (18.45 mg/g), PO43--P (30.04 mg/g), and PE-MP (1611 mg/g). OH-Fe3O4 efficiently removed NH4+-N (2 mg/L), PO43--P (5 mg/L), and PE-MP (1 g/L, 13 μm) from two types of water, achieving removal rates of 80 %, 95 %, and 62 % in freshwater, and 78 %, 94 %, and 70 % in seawater, respectively. FTIR, XPS, kinetic analysis, and density functional theory (DFT) calculations revealed that nano-Fe3O4 provides abundant active sites for MPs and PO43- through electrostatic adsorption and hydrogen bonding, while there is a Fe-O-P bond with PO43-. The NH4+ can be adsorbed on MPs via ion exchange. In addition, –COOH enhances affinity for NH4+, –NH2 increases the holding capacity for PO43-, and –OH strengthens PE-MP adsorption. The environmental impact of the production of nano-Fe3O4 demonstrates the economic feasibility and environmental friendliness of this process. The findings of this study offer promising data that can inform the future development of sustainable and cost-effective materials to combat eutrophication and MPs pollution.

A mechanistic study on the interaction effects between legacy and pollutants of emerging concern: A case study with B[a]P and diclofenac

To study the intricate toxicological mechanisms triggered by exposure to mixed pollutants, we exposed zebrafish embryos to legacy and emerging pollutants through binary mixtures of benzo[a]pyrene (B[a]P) and diclofenac (DFC). The combination of next-generation transcriptomics and toxicopathology disclosed instances where exposure to mixtures did not attain the expected sum of acute effects of individual toxicants, indicating potential antagonism. Despite overall higher mortality in DFC treatments, the same antagonistic trend was noted in genotoxicity and molecular pathways related to RNA turnover, cell proliferation, apoptosis and cell-cycle control. The formation of oedemas in the heart cavity and yolk sac can be an adverse outcome (AO) resulting from exposure to DFC isolated or combined, whose potential key events (KEs) may involve cell cycle arrest and apoptosis via p53 and MAPK pathways. From the findings it can be hypothesised that, rather than genotoxicity, the molecular initiating event (MIE) maybe inflammation triggered by oxidative stress. Nonetheless, the exact role of ROS in the process needs further clarification. Impaired eye function by action of DFC and B[a]P combined may be another AO, in the case caused by ocular degeneration following the suppression of biologic processes and molecular functions involved in eye development and its functionalities, possibly linked to hindered regulation of the expression of hsf4 and cryaa. Altogether, toxicopathology suggests predominance of antagonistic effects, but its integration with mechanism suggests that interactions between DFC and B[a]P in environmentally-relevant concentrations that may lead to hindrance of key functions such as the control of inflammation and cell cycle. These outcomes suggest potentially severe implications for health and survival, in case of prolonged chronic exposure to combined toxicants.

Unveiling electron transfer and radical transformation pathways in coupled electrocatalysis and persulfate oxidation reactions for complex pollutant removal

The degradation of multiple organic pollutants in wastewater via advanced oxidation processes might involve different radicals, of which the types and concentrations vary upon interacting with different pollutants. In this study, electrochemical activation of peroxymonosulfate (E/PMS) using advanced activated carbon cloth (ACC) as electrode was applied for simultaneous degradation of mixed pollutants, e.g., metronidazole (MNZ) and p-chloroaniline (PCA). 92.5 % of MNZ and 91.4 % of PCA can be degraded at the cathode and anode at a low current density and PMS concentration, respectively. The rate constants for the simultaneous removal of MNZ and PCA in the E/PMS/MNZ(PCA) system were 118 times and 6 times higher than those in the sole PMS system, and 2.5 times and 1.6 times higher than those in the E/Na2SO4/MNZ(PCA) system, respectively. Different electrochemical characteristics, EPR spectra and radical quenching tests verified that the degradation of MNZ and PCA in the optimal system proceeded primarily through non-radical-dominated oxidation, involving electron transfer and 1O2 effect. The system also exhibited low energy consumption (0.215 kWh/m−3·order−1), broad operational pH range, excellent removal efficiency for water matrix, and low by-products toxicity, indicating its strong potential for practical applications. The ACC, with its super stable, low cost, and electrochemical activity, make it as a promising materials applicable in the E/PMS system for degradation of multiple pollutants. The study further elucidated the mechanism of pollutant interaction with electrode materials in terms of radical and non-radical transformation, providing fundamental insight into the application of this system for treatment of complex wastewater.

Watershed landscape characteristics and connectivity drive river water quality under seasonal dynamics

Landscape characteristics and connectivity are pivotal determinants of river water quality within the context of water quality management. They play particularly important roles in the spread of non-point source pollution. However, previous research has not investigated their combined effects, especially in the topographically and ecologically volatile Loess Plateau, China. This study applied machine learning and positive matrix factorization techniques to water quality monitoring data for the Wuding River basin, China, from 2017 to 2021 to assess the seasonal impacts of environmental factors on river water quality. The results showed that there were spatial and seasonal variations in pollution sources, and specific thresholds for the key landscape indices that influence water quality were identified. Landscape composition and configuration have the greatest influence on the water quality parameters during the dry season, whereas connectivity and landscape configuration are more critical during the wet season. The connectivity contributions to chemical oxygen demand, the potassium permanganate index, and total phosphorus in the wet season were 19.07%, 27.47%, and 5.08% greater than in the dry season, respectively. Connectivity also made a significant contribution to the composite water quality index, accounting for 33.46% in the dry season and 36.22% in the wet season. The positive matrix factorization model identified agricultural non-point sources and mixed pollutants as the main factors affecting water quality during the dry season, whereas erosion and mixed pollution sources dominated the wet season. Critical thresholds were established for the landscape indices that affected water quality, such as a landscape shape index below 18.5 and a grassland proportion above 65%. The results can be used to develop more effective water quality management strategies and illustrate the essential role played by connectivity when tailoring water quality management strategies to seasonal variations.

Precise management and control around the landfill integrating artificial intelligence and groundwater pollution risks

The Landfill plays an important role in urban development and waste disposal. However, landfill leachate may also bring more serious pollution and health risks to the surrounding groundwater environment. Compared with other areas, the area around the landfill needs more precise management. To solve this problem, based on the “pressure-state-response” framework, a method for the identification and evaluation of groundwater pollution around the landfill was constructed. The LPI method was used to assess the contamination potential of the leachate. The comprehensive quality of groundwater was evaluated by the entropy-AHP water quality assessment method, sodium adsorption ratio and sodium percentage. The probabilistic health risks of groundwater were assessed based on a Monte Carlo algorithm. The sources of pollutants were identified by comprehensively using the PCA-APCS-MLR model and the PMF model. Finally, the self-organizing map algorithm and the Kmeans algorithm were integrated to enhance the precision of groundwater management and control measures. The results showed that the leachate of the landfill was in the mature stage, and the concentration of inorganic substances was relatively high. Leachate had the potential to contaminate surrounding groundwater. The groundwater quality of 68.14% of the study area was in the poor or lower level. The groundwater near the landfill was unsuitable not only for drinking but also for irrigation purposes. Cl− was the main non-carcinogenic risk factor. Reducing pollutant concentration and controlling exposure time are effective strategies for mitigating health risks caused by high-concentration pollutants (Cl−, NO3−) and low-concentration pollutants (F−), respectively. The groundwater around the landfill was jointly affected by six pollution sources. The PMF model has better analytical ability in mixed pollution areas. The groundwater in the study area was divided into five clusters, of which cluster Ⅰ was significantly affected by leachate, and cluster Ⅴ had the lowest pollution and health risk.

Inhibitory Effect of Combined Exposure to Copper Ions and Polystyrene Microplastics on the Growth of Skeletonema costatum

As two significant pollutants, the increased concentrations of copper ions and microplastics in coastal waters pose a substantial threat to the health of marine ecosystems. This study explored the individual and combined toxic effects of copper ions and microplastics on the marine diatom Skeletonema costatum. The results indicated that copper ions at a concentration of 0.05 mg/L exerted a negative impact on the growth of S. costatum; however, the influence of microplastics on algal cell growth was more complex: there was no significant inhibition of algal cell growth observed within the first 72 h of cultivation, but a pronounced negative effect on cell growth was noted between 72 and 96 h, with high concentrations (10.00 mg/L) of microplastics even causing a premature stagnation phase in algal cell growth. When both pollutants were present simultaneously, their impact on cell growth was similar to that of the microplastic pollution group, yet the growth condition was better than that of the copper ion pollution group. Through investigation of adsorption rates and toxicity mitigation rates, it was found that the adsorption of copper ions by microplastics was a significant reason for the improved growth condition of algal cells in the mixed pollution group compared to the copper ion pollution group. However, in the later stages of cultivation, the inhibitory effect of microspheres on algal cell growth counteracted their mitigating effect on copper ion toxicity. This study provides a reference for evaluating the impact of microplastics and heavy metals on coastal ecosystem health and for revealing the interactions between different pollutants.

Efficient adsorption of cationic dyes by a novel honeycomb-like porous hydrogel with ultrahigh mechanical property

The optimization of hydrogel structure is crucial for adsorption capacity, mechanical stability, and reusability. Herein, a chitosan and laponite-XLS co-doped poly(acrylic acid-co-acrylamide) hydrogel (CXAA) with honeycomb-like porous structures is synthesized by cooperative cross-linking of 2-hydroxypropyltrimethyl ammonium chloride chitosan (HACC) and laponite-XLS in reticular frameworks of acrylic acid (AAc) and acrylamide (AM). The CXAA exhibits extraordinary mechanical performances including tough tensile strength (3.36 MPa) and elasticity (2756 %), which facilitates recycling in practical adsorption treatment and broadens potential applications. Since the regular porous structures can fully expose numerous adsorption sites and electronegative natures within polymer materials, CXAA displays efficient and selective adsorption properties for cationic dyes like methylene blue (MB) and malachite green (MG) from mixed pollutants and can reach record-high values (MB = 6886 mg g−1, MG = 11,381 mg g−1) compared with previously reported adsorbents. Therefore, CXAA exhibits promising potential for separating cationic and anionic dyes by their charge disparities. Mechanism studies show that the synergistic effects of HACC, laponite-XLS, and functional groups in monomers promote highly efficient adsorption. Besides, the adsorption capacity of CXAA remains stable even after undergoing five cycles of regeneration. The results confirm that CXAA is a promising adsorbent for effectively removing organic dyes in wastewater.

Development of a multiple-biomarker approach using the green-lipped mussel Perna viridis for marine pollution monitoring: a case study in Victoria Harbour, Hong Kong

Pollutants often exist as mixtures in environmental settings, creating a challenge in selecting the most effective combination of biomarkers for routine monitoring. This study was conducted seasonally in Victoria Harbour, Hong Kong, to compare the responses of nine biomarkers in the green-lipped mussel Perna viridis with respect to its tissue levels of persistent organic pollutants and heavy metals. Multivariate statistical techniques were utilised to determine the single best predictor and optimal subset of biomarkers in P. viridis for each of the four scenarios: representing overall biomarker responses in the dry season, and wet season, as well as correlating tissue levels of mixed pollutants in the dry season, and wet season. Our findings recommend lysosomal destabilisation, and the nucleic acid ratio of RNA to DNA, as the core biomarkers in P. viridis for marine pollution monitoring. The non-specificity of these biomarkers allows effective identification of pollution hotspots and guides further detailed assessment.

Removal of mixed pollutants of perfluorooctanoic acid and 2,4,6-trichlorophenol via adsorption-photocatalysis using Ga2O3-Bi4O7 combining with fluorine-doped covalent triazine framework: Role of different active species

Perfluorooctanoic acid (PFOA) and 2,4,6-trichlorophenol (2,4,6-TCP) are significant pollutants found in textile wastewater, posing severe threats to ecological environments. The construction of an adsorption-photocatalytic system enables the efficient removal of mixed pollutants by harnessing their synergistic effect, thereby overcoming the limitations of removing mixed pollutants with single water treatment technologies. Herein, fluorine-doped covalent triazine framework (F-CTF) was combined with Ga2O3-Bi4O7 heterojunction to obtain Ga2O3-Bi4O7/F-CTF (GaBi/CTF). F-CTF greatly facilitates the adsorption process and provides convenience for photocatalysis. Simultaneously, the excellent conductivity of F-CTF promoted the separation of photoinduced charge carriers in Ga2O3-Bi4O7. GaBi/CTF5 (5 is the mass percentage of F-CTF) showed excellent degradation performance, and the removal rates of PFOA and 2,4,6-TCP reached 93.0 % and 100.0 % within 90 min, respectively. Mechanistic analysis revealed that 2,4,6-TCP and PFOA were attacked by distinct active species because of the disparate characteristics. The presence of phenolic hydroxyl groups makes 2,4,6-TCP more vulnerable to superoxide radicals (·O2–) and hydroxyl radicals (·OH), whereas PFOA is oxidized by holes (h+). The coexistence of mixed pollutants with diverse characteristics enables optimal utilization of active species generated within photocatalytic system. Moreover, the good stability of GaBi/CTF5 provides a feasible solution for efficient treatment of mixed pollutants in textile wastewater.

Comparative effects of ammonium nitrogen on perchlorate degradation performance under heterotrophic condition with different carbon sources

Perchlorate (ClO4-) mainly exists in the form of ammonium perchlorate in industrial production. However, the degradation mechanisms of different concentrations of ammonium nitrogen (NH4+-N) and ClO4- mixed pollutants in the environment are not well understood. This study aims to explore the potential of different types of carbon sources for ClO4- and NH4+-N biodegradation. Experimental results showed that the concentration and type of carbon sources are decisive to simultaneous removal of NH4+-N and ClO4-. Under condition of C(COD)/C(ClO4-) ratio of 21.15 ± 4.40, the simultaneously removal efficiency of ClO4- and NH4+-N in acetate (Ace) was relatively higher than that in methanol (Met). C(NH4+-N)/C(ClO4-) ratio of 9.66 ± 0.51 and C(COD)/C(ClO4-) ratio of 2.51 ± 0.87 promoted ClO4- reduction in glucose-C (Glu-C). However, high concentration of Glu could cause pH decrease (from 7.57 to 4.59), thereby inhibiting ClO4- reduction. High-throughput sequencing results indicated that Proteobacteria and Bacteroidetes have made a major contribution to the simultaneous removal of NH4+-N and ClO4-. They are two representative bacterial phyla for participating in both ClO4- reduction and denitrification. Notably, the abundance of main ClO4- degrading bacteria (such as Proteobacteria, Chloroflexi, and Firmicutes) significantly increased by 528.57 % in Glu-C. It can be inferred that the concentration of carbon source and NH4+-N were the most important factors determining the removal efficiency of ClO4- by influencing changes in the core microbial community. This study will provide new techniques and mechanistic insights for the simultaneous removal of mixed ClO4- and nitrogen pollutants, which can also provide theoretical support for innovation in future biological treatment processes.

Combined Effects of Tetracycline and Copper Ion on Microorganisms During the Biological Phosphorus Removal.

Tetracycline and copper ion are common pollutants in wastewater, and the effects of mixed pollutants on microorganisms in wastewater biological treatment have been less studied. In order to reveal the effects of mixed pollutants of tetracycline and copper ion on the microorganisms during the biological phosphorus removal, three ratios of tetracycline and copper ions were designed by the direct equipartition ray method. The relative abundance and diversity of microbial community were investigated, and the microbial interactions were revealed through microbiological methods. The results demonstrated that, for three different ratios, the inhibitory effect of specific phosphorus uptake rate became more significant with the increase of the tetracycline-copper ions concentration and the reaction time. The microbial community decreased with the increase of the proportion of tetracycline in different ratios. The relative abundance of Acinetobacter decreased with the increase of the proportion of tetracycline, while the relative abundance of Ca.Competibacter was higher under the conditions of low mixtures concentrations. Positive interactions and symbiotic relationships among microorganisms were predominant for three different ratios. However, as the proportion of tetracycline increased, the community structure of microorganisms shifted from phosphate-accumulating organisms to glycogen accumulating organisms and denitrifying bacteria. This study can provide a reference for the effect of mixed pollutants on microorganisms and the mechanism of wastewater treatment.

Facile fabrication of chitosan/bone/bamboo biochar beads for simultaneous removal of co-existing Cr(VI) and bisphenol a from water

Heavy metal Cr(VI) and organic BPA have posed harmful risks to human health, aquatic organisms and the ecosystem. In this work, Chitosan/bone/bamboo biochar beads (CS-AMCM) were synthesized by co-pyrolysis and in situ precipitation method. These microbeads featured a particle size of approximately 1 ± 0.2 mm and were rich in oxygen/nitrogen functional groups. CS-AMCM was characterized using XRD, Zeta potential, FTIR, etc. Experiments showed that adsorption processes of CS-AMCM on Cr(VI) and BPA fitted well to Langmuir model, with theoretical maximum capacities of 343.61 mg/g and 140.30 mg/g, respectively. Pore filling, electrostatic attraction, redox, complexation and ion exchange were the main mechanisms for Cr(VI), whereas for BPA, the intermolecular force (hydrogen bond) and pore filling were involved. CS-AMCM with adsorbed Cr(VI) demonstrated effective activation in producing ·OH and ·O2 from H2O2, which degraded BPA and Cr(VI) with the removal rates of 99.2% and 98.2%, respectively. CS-AMCM offers the advantages of low-cost, large adsorption capacity, high catalytic degradation efficiency, and favorable recycling in treating Cr(VI) and BPA mixed wastewater, which shows great potential in treating heavy metal and organic matter mixed pollution wastewater.

Novel multineedle-to-cylinder plasma coupled with bimetallic catalysts for efficient removal of sulfides and ammonia in odor gases

Dielectric barrier discharge (DBD) plasma is a promising technology for treating odor gases. This study developed an innovative multineedle-to-cylinder (MC) configuration DBD plasma reactor and investigated its synergistic effect with bimetallic catalysts. The results demonstrated that MC-DBD plasma achieved complete elimination of ammonia and organic sulfides, while the removal efficiencies of inorganic H2S and CS2 reached 44.0 % and 53.0 % respectively. Compared with conventional plasma, the specific energy input (SEI) of MC-DBD was significantly reduced to 4.44 J/L. Furthermore, with the incorporation of Mn-Ce/ZSM-5 catalyst, optimal removal efficiencies of H2S and CS2 were significantly improved to 82.6 % and 90.7 %, and the SEI was reduced by 18 %. The electrical performance revealed that the low energy consumption was mainly attributed to stable fast-pulse micro-discharge channels and significantly enhanced inhomogeneous electric fields achieved by the filament discharge mode. Catalyst characterization (X-ray photoelectron spectroscopy and O2-temperature programming desorption) confirmed that surface catalytic reaction mainly follows the Mars-van Krevelen mechanism, where increased lattice oxygen content and the electron transfer between Mn and Ce play crucial roles in enhancing malodor degradation performance. This work proposes an efficient solution for degrading mixed malodors and provides an experimental and theoretical basis for optimizing plasma structure as well as researching treatment of mixed pollutants.

Optimization, kinetics, and pathways of pharmaceutical pollutant degradation using solar Fenton technique.

Solar Fenton is an important and extensively used advanced oxidation process (AOP) to degrade pharmaceutical pollutants. The objective of this study was to evaluate the performance of simultaneous degradation of the mixed pollutants (amoxicillin, acetaminophen, and ciprofloxacin) for an aqueous solution using the solar Fenton process. Operating parameters such as pH, iron doses, H2O2 doses, pollutant concentrations, and time were studied. From the experimental results, the ideal conditions were obtained for the removal of mixed pollutants such as pH 3, Fe2+ 0.04mM, H2O2 4mM, the concentration of the mixed pollutants 5mg/L, solar radiation 400 W/m2, and time 10min, respectively. The pseudo-first-order kinetics were utilized to investigate the degradation efficacy of the mixed pollutants. The result of the study indicates that the degradation efficiency was > 99% for the mixed pollutants. A maximum of 63% mineralization was observed, and hydroxyl radical scavenger effects were studied. The best optimal conditions were applied to assess the spiked wastewater (municipal wastewater (MWW) and hospital wastewater (HWW)). The highest elimination rates for AMX, ACET, and CIP were observed as 65%, 89%, and 85% for MWW and 76%, 92%, and 80% for HWW, respectively. The degraded by-products were detected by LC-ESI-MS in the water matrix (aqueous solution and spiked wastewater), and ECOSAR analysis was performed for the transformed products. The study concluded that the solar Fenton technique is promising and effective for the removal of mixed pollutants from the water matrix.

Corona discharge plasma-excited activation of MnZrLaCe/γ-Al2O3 catalyst for simultaneous degradation of meta-xylene and ethyl acetate: Effects and mechanism

The effects for the simultaneous degradation of meta-xylene (MX) and ethyl acetate (EA) by corona discharge plasma (CDP) combined with MnZrLaCe/γ-Al2O3 were investigated. The MnZrLaCe/γ-Al2O3 were characterized by SEM-EDS, XRD, BET, XPS, FT-IR and O2-TPD. The simultaneous degradation mechanism of the CDP combined catalyst for the mixed VOCs was discussed. Compared with degradation the single component, the degradation efficiency of MX and EA simultaneously is greatly higher than that of the CDP alone. The degradation efficiency of EA, MX and the mixture by the CDP combined with catalyst is up to 93.6 %, 94.5 % and 83.5 % at supply voltage 40 kV, and is 61.2 %, 43.3 % and 33.4 % higher than that of the NTP alone, respectively. The simultaneous degradation efficiency of MA and EA mixed pollutants is significantly improved after the addition of catalysts at the same supply voltage. The EY of all CDP combined with catalysis generally have a down ward trend with increasing of the supply voltage. The best EY for degrading MA and EA mixed pollutants simultaneously by the CDP combined with MnZrLaCe/γ-Al2O3 are up to 7.45 g/kWh at supply voltage 24 kV. The O3 concentration in the outlet gas of the CDP reactor is relatively low, and the NOx in the outlet gas is essentially absent. The main intermediate products of simultaneous degradation MX and EA by the CDP combined with MnZrLaCe/γ-Al2O3 are n-heptane, toluene and paraxylene, etc. Finally, the degradation mechanism for the MX and EA simultaneously by the CDP over the MnZrLaCe/γ-Al2O3 catalyst are proposed.

Research Progress on Toxicity Assessment Methods of Mixed Pollutants

Since the 1930s, the field has used the following three models to evaluate the toxic effects of mixed pollutants: concentration addition model, independent action model and interaction model. The first two are applicable to the case that there is no interaction between the mixed components and do not affect each other, and the third is mainly applied to the case that there is an interaction between the components, which may lead to the enhancement or reduction of toxicity. In the environment, mixtures are not always simply composed of chemicals with similar or different effects, and it may be necessary to consider multiple models applied together during the toxicity assessment process, especially for mixture contamination in complex environments.

Full solar spectrum available hierarchical porous ZIF/Fe-DCA (70) co-assisted by isolated Fe and rich defects for boosted environmental remediation efficiency

The cationic defects engineering and molecular-scale cages effect work together to harvest rich defects and high-density isolated Fe on ZIF, endowing ZIF/Fe-DCA (70) with exposed active sites, facilitating photogenerated carrier separation and optimizing electronic structure. The LSPR effect, intermediated energy band and photothermal transition broaden the light absorption to NIR range with Eg = 2.15 eV. Removal rates for TC (60 mg/L), MB (10 mg/L), MO (10 mg/L) and GV (10 mg/L) are 93 %/86.3 %, 98.2 %/85.1 %, 83.7 %/70.2 % and 82 %/68 % after Vis/NIR irradiation, respectively. A satisfactory purifying efficiency was also detected on the mixed pollutants solution under real sunlight. Besides, the infrared thermography was employed to verify the photothermal conversion visually. The ‧O2−, 1O2, and triplet state are the most effective active species, and the ‧OH and h+ both apparently participate in the photodegradation. This study provides effective design ideas involving single atomic co-catalyst and defects into MOFs as full-spectrum photocatalysts to repair environment.