Pollution Abatement Research Articles

Efficient Electrosynthesis of Valuable para‐Benzoquinone from Aqueous Phenol on NiRu Hybrid Catalysts

AbstractElectrocatalytic oxidation of aqueous phenol to para‐benzoquinone (p‐BQ) offers a sustainable approach for both pollutant abatement and value‐added chemicals production. However, achieving high phenol conversion and p‐BQ yield under neutral conditions remains challenging. Herein, we report a Ni(OH)2‐supported Ru nanoparticles (NiRu) hybrid electrocatalyst, which exhibits a superior phenol conversion of 96.5 % and an excellent p‐BQ yield of 83.4 % at pH 7.0, significantly outperforming previously reported electrocatalysts. This exceptional performance benefits from the triple synergistic modulation of the NiRu catalyst, including enhanced phenol adsorption, increased p‐BQ desorption, and suppressed oxygen evolution. By coupling a flow electrolyzer with an extraction‐distillation separation unit, the simultaneous phenol removal and p‐BQ recovery are realized. Additionally, the developed electrocatalytic system with the NiRu/C anode displays good stability, favorable energy consumption, and reduced greenhouse gas emissions for phenol‐containing wastewater treatment, demonstrating its potential for practical applications. This work offers a promising strategy for achieving low‐carbon emissions in phenol wastewater treatment.

Protecting Lucid Waters and Lush Mountains of Hometown: Local-Born Mayors and Pollution Reduction

ABSTRACT Pollution prevention and control have garnered significant attention globally. Existing literature indicates that local officials play an important role in pollution abatement in China. We used unique firm-level data to investigate the impact of local-born mayors on pollution emissions. The results showed that local-born mayors could bring approximately a 4.41% reduction in pollution emissions; the pollution reduction is more pronounced in high-polluting cities, mayors with weaker promotion incentives, state-owned firms, and small firms. The potential mechanisms are encouraging high-polluting firms to install waste gas facilities and reducing government subsidies. Finally, we provided suggestive evidence supporting the information advantage and reputation effect of local-born mayors.

Understanding the relationship between land use/land cover changes and air quality: A GIS-based fuzzy inference system approach.

Air pollution is a global issue that demands urgent attention due to its detrimental effects on human health and the environment. Land Use and Land Cover (LULC) change is an essential factor that significantly impacts ambient air quality through alterations in emission sources, vegetation cover, natural processes, and urban design. This study investigates the spatio-temporal variation of key air pollutants resulting from urban LULC changes in the Delhi region. Findings reveal a notable increase in pollutant concentrations, particularly particulate matter, in 2019 (PM10: 318.65 ± 45.80 µg/m3) and 2023 (PM10: 383.70 ± 61.49 µg/m3), compared to 2008 (PM10: 246.76 ± 30.66). LULC change analysis demonstrates a rise in built-up areas 24.59%(2008 to 2019), 33.62% (2008 to 2023) and a decline in vegetation cover 27.49% (2008 to 2019),32.37% (2008 to 2023). Correlation analysis indicates a positive correlation between PM10 and urban indices (+ 0.63) and a negative correlation between PM10 and vegetation indices (- 0.61), highlighting the impact of LULC on air quality deterioration. Subsequently, a fuzzy inference system model integrates LULC information to develop an air quality index (AQI). Incorporating LULC changes in AQI assessment offers a realistic approach to address the complexity arising from combined air pollutant effects, surpassing conventional AQI calculation methods. The findings underscore the significance of understanding the impact of Land Use and Land Cover (LULC) change on ambient air quality in formulating effective air quality management programs and policies. Integrating this knowledge into policymaking is crucial for the successful abatement of air pollution in urbanized areas.

PM2.5 Induces Developmental Neurotoxicity in Cortical Organoids

There is mounting evidence implicating the potential neurotoxic effects of PM2.5 during brain development, as it has been observed to traverse both the placental barrier and the fetal blood-brain barrier. However, the current utilization of 2D cell culture and animal models falls short in providing an accurate representation of human brain development. Consequently, the precise mechanisms underlying PM2.5-induced developmental neurotoxicity in humans remain obscure. To address this research gap, we constructed three-dimensional (3D) cortical organoids that faithfully recapitulate the initial stages of human cerebral cortex development. Our goal is to investigate the mechanisms of PM2.5-induced neurotoxicity using 3D brain organoids that express cortical layer proteins. Our findings demonstrate that exposure to PM2.5 concentrations of 5 μg/mL and 50 μg/mL induces neuronal apoptosis and disrupts normal neural differentiation, thereby suggesting a detrimental impact on neurodevelopment. Furthermore, transcriptomic analysis revealed PM2.5 exposure induced aberrations in mitochondrial complex I functionality, which is reminiscent of Parkinson's syndrome, potentially mediated by misguided axon guidance and compromised synaptic maintenance. This study is a pioneering assessment of the neurotoxicity of PM2.5 pollution on human brain tissues based on 3D cortical organoids, and the results are of great significance in guiding the formulation of the next air pollution prevention and control policies in China to achieve the sustainable improvement of air quality and to formulate pollution abatement strategies that can maximize the benefits to public health.

Tolerance and performance assessment of common subtropical vegetation growing along a highway for bio-monitoring and abatement of air pollution

Tolerance and performance assessment of common subtropical vegetation growing along a highway for bio-monitoring and abatement of air pollution

Symmetry-Engineered BINOL-Based Porous Aromatic Frameworks for H2O2 Production via Artificial Photosynthesis and In Situ Degradation of Pharmaceutical Pollutants.

Accomplishing visible light-driven H2O2 production at millimolar concentrations is practically challenging, particularly for organic semiconductors. In this context, achieving a maximum H2O2 production rate of 31.60 mmol·g-1·h-1 by using porous aromatic frameworks (PAFs) represents a significant accomplishment. We report the unusual photoactivity of tetraphenylmethane-BINOL-linked PAFs in triplet oxygen activation to facilitate the generation of reactive oxygen species (ROS), as confirmed by their optical and electrochemical responses, despite the absence of a conventional chromophoric moiety. Moreover, an in situ BINOL formation strategy was used to synthesize these PAFs during polymerization in contrast to the reported protocols involving chiral BINOLs as precursors. The as-synthesized polymers had a capsule-like morphology (for TPM-BINOL-6), high thermal stability up to 348 °C, and a high Brunauer-Emmett-Teller (BET) surface area of up to 1382 m2/g (for TPM-BINOL-4). Interestingly, they showed sunlight-driven production of H2O2 via an oxygen reduction reaction of up to 17.05 mmol·g-1·h-1 in 1:10 isopropanol in water for TPM-BINOL-6, which was quantified by titration with ceric sulfate. It also exhibited exemplary photocatalytic efficiency with an H2O2 production rate of 6.65 mmol·g-1·h-1 in seawater. Interestingly, the H2O2 production rate reached a maximum of 18.03 mmol·g-1·h-1 with an SCC efficiency of 4.5% under an AM 1.5G solar simulator and apparent quantum yield (AQY) of 15.8% (at λ = 456 nm) for TPM-BINOL-6 in ethanol:water = 1:10. Moreover, the exceptionally high H2O2 production rate of 31.60 mmol·g-1·h-1 was achieved in 1:1 ethanol in water under 50 W blue LED light. Furthermore, these PAFs generated adequate ROS, which were utilized in the photocatalytic degradation of tetracycline via the superoxide intermediate. Additionally, the as-formed H2O2 was further channelized in the pollution abatement catalytic system for the fast degradation of ciprofloxacin (within 4 h) and the reduction of toxic oxometallate Cr(VI) within 10 min, which is one of the earliest reports of utilizing photosynthesized H2O2 for environmental detoxification.

Efficient Electrosynthesis of Valuable para-Benzoquinone from Aqueous Phenol on NiRu Hybrid Catalysts.

Electrocatalytic oxidation of aqueous phenol to para-benzoquinone (p-BQ) offers a sustainable approach for both pollutant abatement and value-added chemicals production. However, achieving high phenol conversion and p-BQ yield under neutral conditions remains challenging. Herein, we report a Ni(OH)2-supported Ru nanoparticles (NiRu) hybrid electrocatalyst, which exhibits a superior phenol conversion of 96.5% and an excellent p-BQ yield of 83.4% at pH 7.0, significantly outperforming previously reported electrocatalysts. This exceptional performance benefits from the triple synergistic modulation of the NiRu catalyst, including enhanced phenol adsorption, increased p-BQ desorption, and suppressed oxygen evolution. By coupling a flow electrolyzer with an extraction-distillation separation unit, the simultaneous phenol removal and p-BQ recovery are realized. Additionally, the developed electrocatalytic system with the NiRu/C anode displays good stability, favorable energy consumption, and reduced greenhouse gas emissions for phenol-containing wastewater treatment, demonstrating its potential for practical applications. This work offers a promising strategy for achieving low-carbon emissions in phenol wastewater treatment.

Sustainable Wastewater Treatment Strategies in Effective Abatement of Emerging Pollutants

The fundamental existence of any living organism necessitates the availability of pure and safe water. The ever-increasing population has led to extensive industrialization and urbanization, which have subsequently escalated micropollutants and water contamination. The environmental impact on various life forms poses a dire need for research in effective environmental management. Versatile technologies involving multiple approaches, including physiochemical and biological bioremediation strategies, draw insights from environmental biology. Metabolic annihilation mediated by microbes shows significant potential in the bioconversion of toxic micropollutants to tolerable limits. Environmentally friendly, cost-effective, and sustainable strategies are envisaged for efficient environmental protection. Phytoremediation technology, especially floating wetland treatments, facilitates micropollutant elimination, landscape management, ecosystem conservation, and aesthetic enhancement in diverse environments. The incorporation of nanomaterials in the bioremediation of toxic micropollutants augments novel and innovative strategies for water pollution abatement. This paper offers a novel strategy that combines nanomaterials to improve micropollutant degradation with bioremediation techniques, particularly the creative application of phytoremediation technologies like floating wetlands. Combining these techniques offers a novel viewpoint on long-term, affordable approaches to reducing water pollution. Additionally, the review proposes a forward-looking strategic framework that addresses the accumulation and refractory nature of micropollutants, which has not been thoroughly explored in previous literature.

Quantification of the Contribution of Heterogeneous Surface Processes to Pollutant Abatement during Heterogeneous Catalytic Ozonation.

Heterogeneous surface processes such as adsorption and oxidation with surface-adsorbed reactive oxygen species (ROSad, e.g., adsorbed oxygen atom (*Oad) and hydroxyl radicals (•OHad)) have been suggested to play an important role in pollutant abatement during heterogeneous catalytic ozonation (HCO). However, to date, there is no reliable method to quantitatively evaluate the contribution of heterogeneous surface processes to pollutant abatement (fS) during HCO. In this study, we developed a method by combining probe compound-based experiments with kinetic modeling to distinguish heterogeneous surface processes from homogeneous bulk reactions with aqueous O3 and ROS (•OH and superoxide radicals (O2•-) in the abatement of various pollutants (e.g., atrazine, ibuprofen, tetrachloroethylene, and perfluorooctanoic acid) during HCO with reduced graphene oxide. The results show that the pollutants that have a low affinity for the rGO surface (e.g., ibuprofen and tetrachloroethylene) were essentially abated by homogeneous bulk reactions, while the contribution of heterogeneous surface processes was negligible (fS < 5%). In contrast, heterogeneous surface processes played an important or even dominant role in the abatement of pollutants that have a high surface affinity (e.g., fS = 32-82% for atrazine and perfluorooctanoic acid). This study is a critical first step in quantitatively evaluating the role of heterogeneous surface processes for pollutant abatement during HCO, which is crucial to understanding the mechanism of HCO and designing catalysts for effective pollutant abatement.

Bluer skies and clearer rivers? Returnees as silver bullets for pollution abatement in an emerging economy

Emerging economies are burdened with multiple tasks related to economic development and environmental protection. Based on the phenomenon of “brain gain,” we examine whether overseas-returned executives (“returnees”) help emerging economies better cope with this multitasking. Drawing insights from a Chinese listed firm dataset for the period 2010–2020, this study provides significant observations regarding returnees' influence on firms' environmental performance. The findings show that hiring returnees makes firms greener for three main reasons. First, returnees enjoy favorable treatment provided by the worksite, and the mood of giving back makes them inclined toward low-pollution development. Second, returnees have more green skills. Third, returnees alleviate the principal–agent problem of firms in green development. There are also some extended findings from this study. As inferred from the firms' environmental performance, returnees' overseas study experience may be more important than pure overseas work experience. Additionally, firms that green up by hiring returnees are not biased by firm seniority. Finally, if returnees are viewed as a scarce resource, conditional talent wars will emerge among firms. These findings provide insight into how emerging economies can balance economic development with environmental protection.

WITHDRAWN: Studies on decontamination of cadmium rich water by a novel nano Iron oxide adsorbent

Synthesizing non-toxic adsorbent for abatement of hazardous pollutants from water is important to develop safe environment. In this study, nanocrystalline iron oxide particles were synthesized and utilized as effective nanoadsorbent for removing cadmium through adsorption. The as-prepared nanoadsorbent was characterized using sophisticated techniques. The objective of this study was to improve cadmium adsorption from aqueous solutions under a variety of conditions. With the help of Box-Behnken design, adsorption parameter settings were improved. Response Surface Methodology analysis was conducted to optimize the adsorption conditions, including pH, initial concentration of metal ions, and adsorbent dose. Comparisons were made between the optimal equations for linear and non-linear kinetics, along with isotherm models. Origin's curve fitting tool and the Solver add-in of Microsoft Excel are two non-linear analytical tools. The obtained results showed that the Origin curve fitting tool is superior to solver add in's error analysis method for determining isotherm parameters. The equilibrium data for cadmium removal using nano iron oxide/hydroxide adsorbent was best fitted to Langmuir isotherm model. The adsorption of cadmium was well described by the pseudo-second-order model. The study shows that the system appears to be spontaneous according to the Langmuir constant method and thermodynamic parameter via partition.

Selective oxidation of electron-rich pollutants in peroxymonosulfate-activated electro-Fenton system: the role of microenvironment-regulated cathode

Electro-Fenton technologies driven by peroxymonosulfate (PMS) activation have been extensively explored for abatement of organic pollutants from water. Unfortunately, a great diversity of matrix components in contaminated water scenarios inevitably and significantly compromises the efficiency of the generated radicals toward target pollutants. Thus, selective oxidation of the electro-Fenton technologies is urgently desired for cost effective and sustainable water treatment, but challenged by the traditional electron transfer pathway from cathode to PMS to mainly form SO4•− and HO• radicals. In this study, we successfully realized selective generation of 1O2, a non-radical species specific for electron-rich pollutants, by regulating the second-shell coordination environment of single-atom Fe in carbonaceous cathode. The doped electron-accepting B drives directional electron transfer from PMS to electrode and inhibiting the undesirable radical pathways. Besides, the electrochemical reduction of H+ in-situ generated from the dissociation of H-O in PMS is favourable for the formation of 1O2 as high as 163.4 μmol.L−1min−1. Fast and preferential removal of sulfonamides pollutants in different water matrices demonstrated the excellent matrix tolerance of the newly developed electro-Fenton process. A pilot electrochemical device was designed to further selective remove phenols in real-scenario application. No residual phenol was detected (<0.01 mg/L) with TOC removal around 50% (down to 23.9±0.3 mg L−1) during the continuous 24-h operation. This study is also believed to shed new light on how to achieve desirable electrochemical reactions via microenvironmental regulation in response to sustainable water decontamination and beyond.

Transforming waste into multifunctional nanomaterials: Mg-doped carbon dots from cow dung for Y(III) detection and biomedical applications

Rare earth metal Yttrium (Y3+) plays a vital role in many electronic devices however, discarding these devices eventually contaminates the environmental sources. Herein, we have developed a Mg-doped carbon dots (M-CDs) as a fluorescent probe for selective and sensitive determination of Y3+ in water bodies. The M-CDs having maximum emission at 420 nm upon 310 nm excitation with 20 % quantum yield and which was synthesized from upcycling of agricultural waste i.e., cow dung by simple carbonization followed by hydrothermal method. M-CDs were confirmed using different analytical and characterization techniques as well as stable in different pH and ionic strength solutions. The M-CDs was highly selective towards Y3+ ions over different metal ions with significant blue shift. This fluorescent probe performs a good linear relationship between the different concentrations of Y3+ ion and fluorescence intensity (R2 = 0.99) within the range of 0.2 to 20 μg/mL with a detection limit of 0.019 µg/mL. The study indicates quenching of Y3+ was result of dynamic quenching and the Inner Filter Effect (IFE) effect. Also, the cytotoxicity of M-CDs was checked via CAM assay and significant growth in blood vascularization with healthy growth of chick embryo confirmed the M-CDs were biocompatible. The nontoxic M-CDs was employed for MCF-7 breast cancer cell imaging which gives bright blue fluoresce under UV light excitation. Further, aiming to a circular economy approach the residual carbon remaining after hydrothermal was used as reactivated carbon for the abatement of environmental pollutants. The sustainable, cost-effective and agricultural waste-derived Mg-doped CDs have potential applications in analytical, environmental, forensic as well as biomedical fields.

Sustainable waste management practices in the informal sector: Towards industrial symbiosis

Industrial pollution is considered to be routed in the waste and byproducts of the production process. Traditional pollution control approaches try to eliminate and/or treat the pollutants which are often technically complicated and expensive. In this regard, industrial ecology and industrial symbiosis have emerged as effective strategy to eliminate industrial pollution. This principle requires the generated waste/by-products absorbed in the same or other industrial process cycles and thus the material cycle remains closed. Industrial pollution appears as a big problem in the global south countries, where industrialization is considered as the main thrust of economic development. Usually, in such countries formal pollution control approaches are primarily directed to the formal sectors (such as state owned and legally registered industries), informal sectors are often left behind. Although the role of informal sector is increasingly being recognized for sustainable development, their significance in pollution abatement is a less discussed topic. This article attempts to investigate the informal industrial sector in Dhaka, Bangladesh with empirical evidence. Adopting a qualitative approach with field investigation of the informal industries and detail interviews, this study identified that the informal industries are closely linked in clusters according to the manufacturing process and continue material/byproduct/waster exchange primarily from the need to minimize cost. The studied patterns of waste management practice indicate existence of industrial symbiosis without adequate academic/technical knowledge and designed efforts. This suggests that the informal sector can meaningfully contribute to sustainable development offering insights for the application of similar approaches in the formal sector.

Experimental Analysis of Noise Characteristics on Different Types of Pavements inside and outside Highway Tunnels

Aiming to reduce noise pollution and optimize the acoustic quality in highway tunnels, the noise characteristics on different types of pavements were analyzed and compared in this research, based on the on-site noise measurement in two tunnels with the free fields as a control group. Specifically, the noise characteristics include two aspects: various noise and noise time attenuation performance. Various noise includes on-board sound intensity (OBSI) noise and cabin noise. The noise time attenuation performance uses the indicator of reverberation time. Three types of pavements were measured, including dense-graded asphalt concrete (DAC) and single-layered and double-layered porous asphalt (PA) pavement. The results showed that, for the same type of pavement, compared with the free fields, the difference in OBSI noise in tunnels was within a range of less than 1 dBA; the cabin noise increased by 3.4 dBA~6.6 dBA. The noise level in tunnels was greater than that outside tunnels, and the longer tunnel exhibited higher traffic noise and worse noise time attenuation performances. For the same tunnel, PA pavement could reduce the cabin noise by 3.8 dBA~6.7 dBA. PA pavement also exhibited shorter reverberation time. The application of PA pavement could effectively improve the acoustic quality in the tunnel. This research contributes to noise pollution abatement and the improvement of the comfort and safety of drivers in tunnels.

Tempo-spatial Variations in Nitrogen and Phosphorus Loads in Jianli-Hankou Reach of the Middle Yangtze River During the Past 20 Years

Ammonia nitrogen （NH4+-N） and total phosphorus （TP） were the major control pollutants in the Yangtze River Basin. Based on measured data from 2003 to 2020, the temporal and spatial variations in concentrations and fluxes of NH4+-N and TP in the Jianli to Hankou （JL-HK） reach of the Middle Yangtze River were studied, and the impacts of flow-sediment factors, tributary inflows, and others on variations in NH4+-N and TP fluxes were discussed. The results showed that： ① In recent years, NH4+-N and TP concentrations in the mainstream have declined significantly, with annual NH4+-N and TP concentrations at each monitoring station in 2020 averagely decreasing by 41% and 34% compared to those in 2003, respectively. Spatially, NH4+-N and TP concentrations decreased and then increased along the mainstream. NH4+-N and TP concentrations of tributary inflows, which include the Dongting Lake and Han River, were generally lower than that of the mainstream. The multi-year average values of NH4+-N and TP concentrations were both averaged at 0.12 mg·L-1 in the mainstream and were averaged at 0.11 mg·L-1 and 0.09 mg·L-1 in the tributary inflows. ② The flux differences between the upper and lower sections net of tributary confluences showed that NH4+-N and TP fluxes were lost in the Jianli to Luoshan （JL-LS） sub-reach and increased in the Luoshan to Hankou （LS-HK） sub-reach in most years. NH4+-N and TP fluxes decreased in the JL-LS sub-reach, which was related to the lower NH4+-N and TP concentrations in lateral inflows, such as Dongting Lake, and thus lowered the NH4+-N and TP concentrations in the mainstream. The LS-HK sub-reach showed the opposite trends, and the water and sediment loads increased in this sub-reach. Across the whole JL-HK reach, TP flux as well as water and sediment loads were recharged along the reach, whereas NH4+-N flux was reduced greatly, which could be attributed to the pollution abatement conducted in the Yangtze River Basin, which mainly focused on NH4+-N. ③ The correlation analysis results showed that NH4+-N fluxes had the strongest correlation with NH4+-N concentrations but not significantly correlated with discharges and sediment transport rates, indicating that NH4+-N was mainly controlled by point source pollution in the study reach. TP fluxes had higher correlations with discharges and sediment transport rates in high flow level periods, and the correlations between TP fluxes and TP concentrations were better in low flow level periods, reflecting that point source pollution contributed more to TP in dry seasons compared to flood seasons.

Synergistic Coordination in Cu Single-Atom Catalysts Enhances High-Valent Copper-Oxo Species for Efficient PMS Activation.

In the domain of heterogeneous catalytic activation of peroxymonosulfate (PMS), high-valent metal-oxo (HVMO) species are widely recognized as potent oxidants for the abatement of organic pollutants. However, the generation selectivity and efficiency of HVMO are often constrained by stringent requirements for catalyst adsorption sites and electron transfer efficiency. In this study, a single-atom catalyst, CuSA/CNP&S, is synthesized featuring multiple types (planar/axial) of heteroatom coordination via an H-bond-assisted self-assembly strategy. It isconfirmed that CuN3 active centers with axial S coordination are uniformly distributed in a carbon matrix modified by planar P atoms. CuSA/CNP&S activated PMS to selectively generate Cu(III)═OH species as the primary reactive oxygen species (ROS). The pseudo-first-order kinetic rate for bisphenol A degradation reached 1.51min-1, a 17.57-fold increase compared to the unmodified CuSA/CN catalyst. Additionally, the CuSA/CNP&S catalyst demonstrates high efficiency and durability in removing contaminants from various aqueous matrices. Theoretical calculations and experimental results indicate that the intrinsic electric field generated by distal planar P atoms enhances electron transfer efficiency within the carbon matrix. Meanwhile, axial S coordination elevates the d-band center and tunes the eg * band broadening of Cu, thereby enhancing the adsorption selectivity for the terminal oxygen of PMS. This multitype coordination synergistically mitigates the issues of low selectivity and yield of HVMO species.

Exploration of radical chemistry, precursor sensitivity and O3 control strategies in a provincial capital city, northwestern China

As the core city in northwestern China, Xi'an has suffered from serious O3 pollution in recent years. An observational model, coupled with the Master Chemical Mechanism (V3.3.1) and comprehensive data, analyzed atmospheric oxidation capacity (AOC), O3 formation mechanism, precursor sensitivity and control strategies in Xi'an. The study examined two periods (period I and II), with notable temperature and humidity differences. Despite lower precursor levels in period I, an O3 episode (peak value: 102.68 ppb) occurred only in period I, highlighting the crucial influence of meteorological conditions. Higher removal rate of primary pollutants occurs in period I, but meteorological conditions may not alter the dominant factor of AOC. Period I exhibited markedly high OH reactivity, with aromatics, alkenes, and NOx being the main contributors. HONO photolysis (50.78%) in the morning and O3 photolysis (34.13%) in the afternoon were the main HOx sources in period I, while HONO photolysis (62.86–80.68%) was significant at daytime for period II. Higher temperatures in period I accelerated all reaction rates involved in radical cycling, especially emphasizing RO2 + NO → RO + NO2. The results of sensitivity analysis showed that O3 sensitivity regime is VOC-limited in Xi'an, but the specific reactive species target VOC reductions emissions exhibited discrepancies for two distinct periods. A 20% decrease in VOCs and a 50% decrease in NOx (VOCs/NOx = 0.4) was proposed to be the optimal solution to achieve the O3 control target in period I. This study enhances our understanding of O3 formation under different meteorological conditions and provides scientific evidence for O3 pollution abatement policies in northwestern China, with potential applicability to other cities in this region and similar countries.

Recent advancement in microplastic removal process from wastewater - A critical review

Microplastics, small sized plastic particles having size <5 mm are formed through primary process including production of beauty products, microbeads and microfibres as well as secondary process including mechanical weathering, friction, aberration and fragmentation of large plastics. The major sources of microplastics are land-based and ocean-based sources. Microplastic pollution is a serious concern due to the persistent, low biodegradability and bio-accumulative behaviour. Microplastics can bioaccumulate in the food chain and can cause ecological and human health risk. Hence, it is important to remove from the aquatic ecosystems. Microplastics are removed from aquatic systems and wastewater through a series of processes such as physical, chemical and biological treatments. In the present articles, >250 articles are reviewed to collect the information regarding the various physical, chemical and biological methods for the removal of microplastics. Also, the probable control strategies to combat with plastic pollution were assessed. It was concluded that recent water treatment methods are efficient in removing microplastic pollution. The efficiencies to remove microplastic from the water ranged between 74 %-99.2 %, 65 %-99.20 % and 77 %-100 % for physical, chemical and biological treatment methods, respectively. Among the three treatment methods, physical methods especially the filtration of water from biochar is the most efficient way (efficiency up to 100 %) to remove microplastics. It was also concluded that creating public awareness, promoting reusing, recycling and reducing, and application of bioplastics can control the production of microplastics from plastic wastes. This review will be useful to add current knowledge regarding the abatement of microplastic pollution, and finding novel solution to control microplastics. This review will also help the policymakers to implement most effective and cost-efficient method to remove microplastics, and to find out new methods to reduce, reuse and recycle plastic wastes.

Occurrence, source identification and risk assessment of polybrominated diphenyl ethers in water and sediments of Osun River, Nigeria

BackgroundIn the present study, the concentrations of polybrominated diphenyl ethers (PBDEs) in water and sediments of Osun River, Nigeria were determined.MethodsThe obtained water samples were subjected to liquid-liquid extraction while the sediment samples were subjected to extraction using n-hexane and acetone. The extracts were quantified using a Gas Chromatography-Mass Spectrometer to assess their distribution, source identification, and ecological risk assessments.ResultsThe results of the study indicated that BDE-99, BDE-183, and BDE-209 were not detected in the water samples while BDE-28 had the most significant mean contribution (0.057 mg/L w.w) to the total PBDEs in the water samples. The sediment samples were dominated by enhanced concentrations of BDE-100 congener (mean concentration 0.184 mg/kg d.w). The compositional profiles of the PBDE congeners indicated the abundance of higher BDEs in the sediment samples compared to the water samples, a phenomenon attributed to the lower reduction rate and lower water solubility of the higher BDEs. Source identification indicated that commercial deca-BDE mixtures might represent the major source of PBDEs in the studied river. Risk assessment of PBDEs in water samples showed that the mean concentrations of tri-BDE, tetra-BDE, penta-BDE, and hexa-BDE exceeded the acceptable limits, suggesting adverse health risks to the public. Ecological risk assessment of PBDEs in sediment samples showed medium ecological risk by hexa-BDE (0.1 ≤ RQ ≤ 1) and high ecological risks due to tri-, tetra-, penta-, and deca-BDEs (RQ > 1).ConclusionThe study concludes that efficient and cost-effective remediation strategies should be developed and employed in the abatement of these persistent organic pollutants from the environment.