On the potential of iPhone significant location data to characterize individual mobility for air pollution health studies

● We evaluated the accuracy of iPhone data in capturing time-activity patterns. ● iPhone data captured the most important microenvironments and time spent in them. ● iPhone data also accurately captured daily exposure to ambient PM pollution. ● A considerable fraction of the population in the USA may have iPhone data available. ● iPhone data has great potential in air pollution health studies. In many air pollution health studies, the time-activity pattern of individuals is often ignored largely due to lack of data. However, a better understanding of this location-based information is expected to decrease uncertainties in exposure estimation. Here, we showcase the potential of iPhone’s Significant Location (iSL) data in capturing the user’s historical time-activity patterns in order to estimate exposure to ambient air pollutants. In this study, one subject carried an iPhone in tandem with a reference GPS tracking device for one month. The GPS device recorded locations in 10 second intervals while the iSL recorded the time spent in locations the subject visited frequently. Using GPS data as a reference, we then evaluated the accuracy of iSL data in capturing the subject’s time-activity patterns and time-weighted air pollution concentration within the study time period. We found the iSL data accurately captured the time the subject spent in 16 microenvironments (i.e. locations the subject visited more than once), which was 93% of the time during the study period. The average error of time-weighted aerosol optical depth value, a surrogate of particle pollution, is only 0.012%. To explore the availability of iSL data among iPhone users, an online survey was conducted. Among the 349 surveyed participants, 72% of them have iSL data available. Considering the popularity of iPhones, iSL data may be available for a significant portion of the general population. Our results suggest iSL data have great potential for characterizing historical time-activity patterns to improve air pollution exposure estimation.     

Long-term exposure to air pollution and cerebrovascular disease: findings from Beijing Health Management Cohort study

● This study explored the long-term association by double robust additive models. ● Individual exposure concentrations were assessed by integrating GAM, LUR and BPNN. ● PM_2.5, SO₂ and NO₂ are positively associated with cerebrovascular disease. ● CO could reduce the risk of cerebrovascular disease with the highest robustness. ● The elderly, women and people with normal BMI are at higher risk for air pollution. The relationship between air pollution and cerebrovascular disease has become a popular topic, yet research findings are highly heterogeneous. This study aims to investigate this association based on detailed individual health data and a precise evaluation of their exposure levels. The integrated models of generalized additive model, land use regression model and back propagation neural network were used to evaluate the exposure concentrations. And doubly robust additive model was conducted to explore the association between cerebrovascular disease and air pollution after adjusted for demographic characteristics, physical examination, disease information, geographic and socioeconomic status. A total of 25097 subjects were included in the Beijing Health Management Cohort from 2013 to 2018. With a 1 μg/m³ increase in the concentrations of PM_2.5, SO₂ and NO₂, the incidence risk of cerebrovascular disease increased by 1.02 (95% CI: 1.008–1.034), 1.06 (95% CI: 1.034–1.095) and 1.02 (95% CI: 1.010–1.029) respectively. Whereas CO exposure could decrease the risk, with an odds ratio of 0.38 (95% CI: 0.212–0.626). In the subgroup analysis, individuals under the age of 50 with normal BMI were at higher risk caused by PM_2.5, and SO₂ was considered more hazardous to women. Meanwhile, the protective effect of CO on women and those with normal BMI was stronger. Successful reduction of long-term exposure to PM_2.5, SO₂ and NO₂ would lead to substantial benefits for decrease the risk of cerebrovascular disease especially for the health of the susceptible individuals.     

Electroconductive RGO-MXene membranes with wettability-regulated channels: improved water permeability and electro-enhanced rejection performance

● Electroconductive RGO-MXene membranes were fabricated. ● Wettable membrane channels were established between RGO and MXene nanosheets. ● Hydrophilic MXene reduces the resistance of water entering the membrane channels. ● Water permeance of RGO-MXene membrane is 16.8 times higher than that of RGO membrane. ● Electro-assistance can enhance the dye rejection performance of RGO-MXene membrane. Reduced graphene oxide (RGO) membranes are theoretically more conducive to the rapid transport of water molecules in their channels compared with graphene oxide (GO) membranes, as they have fewer oxygen-containing functional groups and more non-oxidized regions. However, the weak hydrophilicity of RGO membranes inhibits water entry into their channels, resulting in their low water permeability. In this work, we constructed wettable RGO-MXene channels by intercalating hydrophilic MXene nanosheets into the RGO membrane for improving the water permeance. The RGO-MXene composite membrane exhibits high pure water permeance of 62.1 L/(m²·h·bar), approximately 16.8 times that of the RGO membrane (3.7 L/(m²·h·bar)). Wettability test results and molecular dynamics simulations suggest that the improved water permeance results from the enhanced wettability of RGO-MXene membrane and increased rate of water molecules entering the RGO-MXene channels. Benefiting from good conductivity, the RGO-MXene membrane with electro-assistance exhibits significantly increased rejection rates for negatively charged dyes (from 56.0% at 0 V to 91.4% at 2.0 V for Orange G) without decreasing the permeate flux, which could be attributed to enhanced electrostatic repulsion under electro-assistance.     

Microplastics in municipal wastewater treatment plants: a case study of Denizli/Turkey

● High amounts of microplastics are released to receiving media from WWTPs. ● The effect of classical treatment processes on MP removal is important. ● MP load in the effluent of WWTPs is important for developing treatment technology. ● Additional physical treatment could help further reduce MP discharge. Plastic particles smaller than 5 mm are microplastics. They are among the significant pollutants that recently attracted attention. Great quantities of microplastics enter the sewage system daily and reach wastewater treatment plants (WWTPs). As a result, WWTPs are potential microplastic sources. Hence, they create a pathway for microplastics to reach aquatic environments with treated wastewater discharge. Studies on microplastic characterization in WWTPs have gained momentum in academia. This study investigates the abundance, size, shape, color, polymer type, and removal efficiencies of microplastics in a municipal wastewater treatment plant (WWTP) in Denizli/Turkey. The results showed that the dominant microplastic shape in wastewater samples was fibers (41.78%–60.77%) in the 100–500 µm (58.57%–80.07%) size range. Most of the microplastics were transparent-white (32.86%–58.93%). The dominant polymer types were polyethylene (54.05%) and polyethylene vinyl acetate (37.84%) in raw wastewater. Furthermore, the microplastic removal efficiencies of the Denizli Central WWTP as a whole and for individual treatment units were evaluated. Although the microplastic pollution removal efficiency of the Denizli Central WWTP was over 95%, the microplastic concentration discharged daily into the receiving environment was considerably high (1.28 × 10¹⁰ MP/d). Thus, Denizli Central WWTP effluents result in a high volume of emissions in terms of microplastic pollution with a significant daily discharge to the Çürüksu Stream.     

Identification of pollution sources in rivers using a hydrodynamic diffusion wave model and improved Bayesian-Markov chain Monte Carlo algorithm

● A hydrodynamic-Bayesian inference model was developed for water pollution tracking. ● Model is not stuck in local optimal solutions for high-dimensional problem. ● Model can estimate source parameters accurately with known river water levels. ● Both sudden spill incident and normal sewage inputs into the river can be tracked. ● Model is superior to the traditional approaches based on the test cases. Water quality restoration in rivers requires identification of the locations and discharges of pollution sources, and a reliable mathematical model to accomplish this identification is essential. In this paper, an innovative framework is presented to inversely estimate pollution sources for both accident preparedness and normal management of the allowable pollutant discharge. The proposed model integrates the concepts of the hydrodynamic diffusion wave equation and an improved Bayesian-Markov chain Monte Carlo method (MCMC). The methodological framework is tested using a designed case of a sudden wastewater spill incident (i.e., source location, flow rate, and starting and ending times of the discharge) and a real case of multiple sewage inputs into a river (i.e., locations and daily flows of sewage sources). The proposed modeling based on the improved Bayesian-MCMC method can effectively solve high-dimensional search and optimization problems according to known river water levels at pre-set monitoring sites. It can adequately provide accurate source estimation parameters using only one simulation through exploration of the full parameter space. In comparison, the inverse models based on the popular random walk Metropolis (RWM) algorithm and microbial genetic algorithm (MGA) do not produce reliable estimates for the two scenarios even after multiple simulation runs, and they fall into locally optimal solutions. Since much more water level data are available than water quality data, the proposed approach also provides a cost-effective solution for identifying pollution sources in rivers with the support of high-frequency water level data, especially for rivers receiving significant sewage discharges.     

Mechanism and characterization of microplastic aging process: A review

● Methods for estimating the aging of environmental micro-plastics were highlighted. ● Aging pathways & characterization methods of microplastics were related and reviewed. ● Possible approaches to reduce the contamination of microplastics were proposed. ● The prospect and deficiency of degradable plastics were analyzed. With the increasing production of petroleum-based plastics, the problem of environmental pollution caused by plastics has aroused widespread concern. Microplastics, which are formed by the fragmentation of macro plastics, are bio-accumulate easily due to their small size and slow degradation under natural conditions. The aging of plastics is an inevitable process for their degradation and enhancement of adsorption performance toward pollutants due to a series of changes in their physiochemical properties, which significantly increase the toxicity and harm of plastics. Therefore, studies should focus on the aging process of microplastics through reasonable characterization methods to promote the aging process and prevent white pollution. This review summarizes the latest progress in natural aging process and characterization methods to determine the natural aging mechanism of microplastics. In addition, recent advances in the artificial aging of microplastic pollutants are reviewed. The degradation status and by-products of biodegradable plastics in the natural environment and whether they can truly solve the plastic pollution problem have been discussed. Findings from the literature pointed out that the aging process of microplastics lacks professional and exclusive characterization methods, which include qualitative and quantitative analyses. To lessen the toxicity of microplastics in the environment, future research directions have been suggested based on existing problems in the current research. This review could provide a systematic reference for in-depth exploration of the aging mechanism and behavior of microplastics in natural and artificial systems.     

New insights into the formation of ammonium nitrate from a physical and chemical level perspective

● Factor analysis of ammonium nitrate formation based on thermodynamic theory. ● Aerosol liquid water content has important role on the ammonium nitrate formation. ● Contribution of coal combustion and vehicle exhaust is significant in haze periods. High levels of fine particulate matter (PM_2.5) is linked to poor air quality and premature deaths, so haze pollution deserves the attention of the world. As abundant inorganic components in PM_2.5, ammonium nitrate (NH₄NO₃) formation includes two processes, the diffusion process (molecule of ammonia and nitric acid move from gas phase to liquid phase) and the ionization process (subsequent dissociation to form ions). In this study, we discuss the impact of meteorological factors, emission sources, and gaseous precursors on NH₄NO₃ formation based on thermodynamic theory, and identify the dominant factors during clean periods and haze periods. Results show that aerosol liquid water content has a more significant effect on ammonium nitrate formation regardless of the severity of pollution. The dust source is dominant emission source in clean periods; while a combination of coal combustion and vehicle exhaust sources is more important in haze periods. And the control of ammonia emission is more effective in reducing the formation of ammonium nitrate. The findings of this work inform the design of effective strategies to control particulate matter pollution.     

Preliminary techno-economic analysis of three typical decentralized composting technologies treating rural kitchen waste: a case study in China

● Decentralized composting (DC) is a profitable KW treating technology. ● SAC and BEC were economically attractive in rural area, while HDC was unprofitable. ● KW handling subsidy plays a vital role in making DC profitable. ● SAC and BEC have great potential in promoting rural KW treatment. This study was designed to evaluate whether the decentralized rural kitchen waste (KW) composting technologies used in China can be widely applied. To this end, we completed a techno-economic analysis of three typical types of KW compositing, namely solar-assisted (SAC), bio-enhanced (BEC), and heat-dewatering composting (HDC). These evaluations revealed that all three technologies produce composting products that meet China’s organic fertilizer standard and that both SAC and BEC are economically self-sustaining and generate net profits (18824.94 and 17791.52 US$/a) and positive net present values (32133.11 and 25035.93 US$). Subsequent sensitivity analysis demonstrated that the KW-handling subsidy plays a critical role in making decentralized composting economically attractive. Based on these analyses, we believe that reducing the coverage area of SAC, reducing the operating cost of BEC and HDC, upgrading composting products, and strengthening secondary pollution control would aid in supporting the technological improvement of these processes. Moreover, providing appropriate subsidies and promulgating specific standards and policies for KW fertilizer are key strategies for decentralized rural KW composting management.     

Electrocatalytic reduction of nitrate using Pd-Cu modified carbon nanotube membranes

● Pd-Cu modified CNT membranes were prepared successfully by electrodeposition method. ● The deposition voltage and deposition time were optimized for Pd-Cu co-deposition. ● NO₃⁻-N was removed efficiently from water by Pd-Cu modified CNT membranes. ● The presence of dissolved oxygen did not affect the nitrate reduction performance. ● Mass transfer rate was promoted significantly with the increase in membrane flux. Excessive nitrate in water is harmful to the ecological environment and human health. Electrocatalytic reduction is a promising technology for nitrate removal. Herein, a Pd-Cu modified carbon nanotube membrane was fabricated with an electrodeposition method and used to reduce nitrate in a flow-through electrochemical reactor. The optimal potential and duration for codeposition of Pd and Cu were −0.7 V and 5 min, respectively, according to linear scan voltammetry results. The membrane obtained with a Pd:Cu ratio of 1:1 exhibited a relatively high nitrate removal efficiency and N₂ selectivity. Nitrate was almost completely reduced (~99 %) by the membrane at potentials lower than −1.2 V. However, −0.8 V was the optimal potential for nitrate reduction in terms of both nitrate removal efficiency and product selectivity. The nitrate removal efficiency was 56.2 %, and the N₂ selectivity was 23.8 % for the Pd:Cu=1:1 membrane operated at −0.8 V. Nitrate removal was enhanced under acidic conditions, while N₂ selectivity was decreased. The concentrations of Cl⁻ ions and dissolved oxygen showed little effect on nitrate reduction. The mass transfer rate constant was greatly improved by 6.6 times from 1.14 × 10⁻³ m/h at a membrane flux of 1 L/(m²·h) to 8.71 × 10⁻³ m/h at a membrane flux of 15 L/(m²·h), which resulted in a significant increase in the nitrate removal rate from 13.6 to 133.5 mg/(m²·h). These findings show that the Pd-Cu modified CNT membrane is an efficient material for nitrate reduction.     

Effects of manufactured nanomaterials on algae: Implications and applications

● Summary of positive and negative effects of MNMs on algae. ● MNMs adversely affect algal gene expression, metabolite, and growth. ● MNMs induce oxidative stress, mechanical damage and light-shielding effects on algae. ● MNMs can promote production of bioactive substances and environmental remediation. The wide application of manufactured nanomaterials (MNMs) has resulted in the inevitable release of MNMs into the aquatic environment along their life cycle. As the primary producer in aquatic ecosystems, algae play a critical role in maintaining the balance of ecosystems’ energy flow, material circulation and information transmission. Thus, thoroughly understanding the biological effects of MNMs on algae as well as the underlying mechanisms is of vital importance. We conducted a comprehensive review on both positive and negative effects of MNMs on algae and thoroughly discussed the underlying mechanisms. In general, exposure to MNMs may adversely affect algae’s gene expression, metabolites, photosynthesis, nitrogen fixation and growth rate. The major mechanisms of MNMs-induced inhibition are attributed to oxidative stress, mechanical damages, released metal ions and light-shielding effects. Meanwhile, the rational application of MNMs-algae interactions would promote valuable bioactive substances production as well as control biological and chemical pollutants. Our review could provide a better understanding of the biological effects of MNMs on algae and narrow the knowledge gaps on the underlying mechanisms. It would shed light on the investigation of environmental implications and applications of MNMs-algae interactions and meet the increasing demand for sustainable nanotechnology development.     

Stress response to nanoplastics with different charges in Brassica napus L. during seed germination and seedling growth stages

● Higher concentrations of PS, PS-NH₂ and PS-SO₃H inhibited seed germination. ● PS, PS-NH₂ and PS-SO₃H influenced seedling growth in a dose-dependent manner. ● PS, PS-NH₂ and PS-SO₃H reduced essential nutrients uptake and plant quality. ● PS, PS-NH₂ and PS-SO₃H increased antioxidant enzyme activities and MDA content. ● Nanoplastic toxicity was related to surface charges. Nanoplastic pollution has become a significant problem in farmland systems worldwide. However, research on the effects of nanoplastics (NPs) with different charges on field crops is still limited. In our study, NPs with different charges, including unmodified polystyrene nanoplastics (PS), positively charged polystyrene nanoplastics (PS-NH₂), and negatively charged polystyrene nanoplastics (PS-SO₃H), were investigated for their impacts on seed germination and seedling growth of rape. The results showed that seed water uptake (after 12 h), seed germination, seed vigour, and relative root elongation were all significantly reduced under exposure to NPs (200 mg/L). Similarly, remarkable decreases in plant biomass (root weight, shoot weight), growth (root length, plant height), photosynthesis ability (chlorophyll a, chlorophyll b, carotenoids), essential nutrient uptake (Fe, Mn, Zn, Cu), and plant quality (soluble protein, soluble sugar, crude fibre content) of rape seedlings were also observed after exposure to NPs. Among the three kinds of NPs, PS-NH₂ showed stronger effects. Moreover, superoxide dismutase, peroxidase, and catalase activities of rape seedlings were changed, and the content of malondialdehyde was significantly increased under exposure to NPs. Furthermore, positively charged PS-NH₂ showed stronger effects on the phenotype, physiology, biochemistry, nutrient uptake, and plant quality of rape. Notably, a comprehensive toxicity evaluation revealed that PS-NH₂ had the strongest toxicity to rape. The present study provides important implications for the interaction and risk assessment of NPs and crops in soil-plant systems.     

Distribution,enrichment mechanism and risk assessment for fluoride in groundwater: a case study of Mihe-Weihe River Basin,China

● High fluorine is mainly HCO₃·Cl-Na and HCO₃-Na type. ● F⁻ decreases with the increase of depth to water table. ● High fluoride is mainly affected by fluorine-containing minerals and weak alkaline. ● Fluorine pollution is mainly in the north near Laizhou Bay (wet season > dry season). ● Groundwater samples have a high F⁻ health risk (children > adults). Due to the unclear distribution characteristics and causes of fluoride in groundwater of Mihe-Weihe River Basin (China), there is a higher risk for the future development and utilization of groundwater. Therefore, based on the systematic sampling and analysis, the distribution features and enrichment mechanism for fluoride in groundwater were studied by the graphic method, hydrogeochemical modeling, the proportionality factor between conventional ions and factor analysis. The results show that the fluorine content in groundwater is generally on the high side, with a large area of medium-fluorine water (0.5–1.0 mg/L), and high-fluorine water is chiefly in the interfluvial lowlands and alluvial-marine plain, which mainly contains HCO₃·Cl-Na- and HCO₃-Na-type water. The vertical zonation characteristics of the fluorine content decrease with increasing depth to the water table. The high flouride groundwater during the wet season is chiefly controlled by the weathering and dissolution of fluorine-containing minerals, as well as the influence of rock weathering, evaporation and concentration. The weak alkaline environment that is rich in sodium and poor in calcium during the dry season is the main reason for the enrichment of fluorine. Finally, an integrated assessment model is established using rough set theory and an improved matter element extension model, and the level of groundwater pollution caused by fluoride in the Mihe-Weihe River Basin during the wet and dry seasons in the Shandong Peninsula is defined to show the necessity for local management measures to reduce the potential risks caused by groundwater quality.     

Revealing the GHG reduction potential of emerging biomass-based CO2 utilization with an iron cycle system

● Greenhouse gas mitigation by biomass-based CO₂ utilization with a Fe cycle system. ● The system including hydrothermal CO₂ reduction with Fe and Fe recovery by biomass. ● The reduction potential quantified by experiments, simulations, and an ex-ante LCA. ● The greatest GHG reduction potential is −34.03 kg CO₂-eq/kg absorbed CO₂. ● Ex-ante LCA supports process optimization to maximize GHG reduction potential. CO₂ utilization becomes a promising solution for reducing anthropogenic greenhouse gas (GHG) emissions. Biomass-based CO₂ utilization (BCU) even has the potential to generate negative emissions, but the corresponding quantitative evaluation is limited. Herein, the biomass-based CO₂ utilization with an iron cycle (BCU-Fe) system, which converts CO₂ into formate by Fe under hydrothermal conditions and recovers Fe with biomass-derived glycerin, was investigated. The GHG reduction potential under various process designs was quantified by a multidisciplinary method, including experiments, simulations, and an ex-ante life-cycle assessment. The results reveal that the BCU-Fe system could bring considerable GHG emission reduction. Significantly, the lowest value is −34.03 kg CO₂-eq/kg absorbed CO₂ (−2.44 kg CO₂-eq/kg circulated Fe) with the optimal yield of formate (66%) and Fe (80%). The proposed ex-ante evaluation approach not only reveals the benefits of mitigating climate change by applying the BCU-Fe system, but also serves as a generic tool to guide the industrialization of emerging carbon-neutral technologies.     

Insights into the electron transfer mechanisms of permanganate activation by carbon nanotube membrane for enhanced micropollutants degradation

● A CNT filter enabled effective KMnO₄ activation via facilitated electron transfer. ● Ultra-fast degradation of micropollutants were achieved in KMnO₄/CNT system. ● CNT mediated electron transfer process from electron-rich molecules to KMnO₄. ● Electron transfer dominated organic degradation. Numerous reagents have been proposed as electron sacrificers to induce the decomposition of permanganate (KMnO₄) by producing highly reactive Mn species for micropollutants degradation. However, this strategy can lead to low KMnO₄ utilization efficiency due to limitations associated with poor mass transport and high energy consumption. In the present study, we rationally designed a catalytic carbon nanotube (CNT) membrane for KMnO₄ activation toward enhanced degradation of micropollutants. The proposed flow-through system outperformed conventional batch reactor owing to the improved mass transfer via convection. Under optimal conditionals, a > 70% removal (equivalent to an oxidation flux of 2.43 mmol/(h·m²)) of 80 μmol/L sulfamethoxazole (SMX) solution can be achieved at single-pass mode. The experimental analysis and DFT studies verified that CNT could mediate direct electron transfer from organic molecules to KMnO₄, resulting in a high utilization efficiency of KMnO₄. Furthermore, the KMnO₄/CNT system had outstanding reusability and CNT could maintain a long-lasting reactivity, which served as a green strategy for the remediation of micropollutants in a sustainable manner. This study provides new insights into the electron transfer mechanisms and unveils the advantages of effective KMnO₄ utilization in the KMnO₄/CNT system for environmental remediation.     

Efficient production of hydrogen peroxide in microbial reverse-electrodialysis cells coupled with thermolytic solutions

● Appreciable H₂O₂ production rate was achieved in MRCs utilizing NH₄HCO₃ solutions. ● Carbon black outperformed activated carbon as the catalyst for H₂O₂ production. ● The optimum carbon black loading for H₂O₂ production on air-cathode was 10 mg/cm². ● The optimum number of cell pairs was determined to be three. ● A maximum power density of 980 mW/m² was produced by MRCs with 5 cell pairs. H₂O₂ was produced at an appreciable rate in microbial reverse-electrodialysis cells (MRCs) coupled with thermolytic solutions, which can simultaneously capture waste heat as electrical energy. To determine the optimal cathode and membrane stack configurations for H₂O₂ production, different catalysts, catalyst loadings and numbers of membrane cell pairs were tested. Carbon black (CB) outperformed activated carbon (AC) for H₂O₂ production, although AC showed higher catalytic activity for oxygen reduction. The optimum CB loading was 10 mg/cm² in terms of both the H₂O₂ production rate and power production. The optimum number of cell pairs was determined to be three based on a tradeoff between H₂O₂ production and capital costs. A H₂O₂ production rate as high as 0.99 ± 0.10 mmol/(L·h) was achieved with 10 mg/cm² CB loading and 3 cell pairs, where the H₂O₂ recovery efficiency was 52 ± 2% and the maximum power density was 780 ± 37 mW/m². Increasing the number of cell pairs to five resulted in an increase in maximum power density (980 ± 21 mW/m²) but showed limited effects on H₂O₂ production. These results indicated that MRCs can be an efficient method for sustainable H₂O₂ production.     

Recent advances in electrochemical decontamination of perfluorinated compounds from water: a review

● Recent advances in the electrochemical decontamination of PFAS are reviewed. ● Underlying mechanisms and impacting factors of these processes are discussed. ● Several novel couped systems and electrode materials are emphasized. ● Major knowledge gaps and research prospects on PFAS removal are identified. Per- and polyfluoroalkyl substances (PFAS) pose serious human health and environmental risks due to their persistence and toxicity. Among the available PFAS remediation options, the electrochemical approach is promising with better control. In this review, recent advances in the decontamination of PFAS from water using several state-of-the-art electrochemical strategies, including electro-oxidation, electro-adsorption, and electro-coagulation, were systematically reviewed. We aimed to elucidate their design principles, underlying working mechanisms, and the effects of operation factors (e.g., solution pH, applied voltage, and reactor configuration). The recent developments of innovative electrochemical systems and novel electrode materials were highlighted. In addition, the development of coupled processes that could overcome the shortcomings of low efficiency and high energy consumption of conventional electrochemical systems was also emphasized. This review identified several major knowledge gaps and challenges in the scalability and adaptability of efficient electrochemical systems for PFAS remediation. Materials science and system design developments are forging a path toward sustainable treatment of PFAS-contaminated water through electrochemical technologies.     

Functional flax fiber with UV-induced switchable wettability for multipurpose oil-water separation

● A PAA-ZnO-HDTMS flax fiber with UV-induced switchable wettability was developed. ● The property of flax fiber could be switched from hydrophobicity to hydrophilicity. ● The mechanism of the acquired UV-induced switchable wettability was discussed. ● The developed flax fiber was successfully used for multipurpose oil-water separation. The large number of oily wastewater discharges and oil spills are bringing about severe threats to environment and human health. Corresponding to this challenge, a functional PAA-ZnO-HDTMS flax fiber with UV-induced switchable wettability was developed for efficient oil-water separation in this study. The developed flax fiber was obtained through PAA grafted polymerization and then ZnO-HDTMS nanocomposite immobilization. The as-prepared PAA-ZnO-HDTMS flax fiber was hydrophobic initially and could be switched to hydrophilic through UV irradiation. Its hydrophobicity could be easily recovered through being stored in dark environment for several days. To optimize the performance of the PAA-ZnO-HDTMS flax fiber, the effects of ZnO and HDTMS concentrations on its switchable wettability were investigated. The optimized PAA-ZnO-HDTMS flax fiber had a large water contact angle (~130°) in air and an extremely small oil contact angle (~0°) underwater initially. After UV treatment, the water contact angle was decreased to 30°, while the underwater oil contact angle was increased to more than 150°. Based on this UV-induced switchable wettability, the developed PAA-ZnO-HDTMS flax fiber was applied to remove oil from immiscible oil-water mixtures and oil-in-water emulsion with great reusability for multiple cycles. Thus, the developed flax fiber could be further fabricated into oil barrier or oil sorbent for oil-water separation, which could be an environmentally-friendly alternative in oil spill response and oily wastewater treatment.     

Removal of virus aerosols by the combination of filtration and UV-C irradiation

● The removal of virus aerosols by filtration and UV-C irradiation was proposed. ● The filtration efficiency for virus aerosols was affected by the filtration rate. ● The inactivation rate by UV-C was not linear with irradiation intensity or time. ● The virus trapped by filter material had a shielding effect on UV-C irradiation. The COVID-19 pandemic remains ever prevalent and afflicting—partially because one of its transmission pathways is aerosol. With the widely used central air conditioning systems worldwide, indoor virus aerosols can rapidly migrate, thus resulting in rapid infection transmission. It is therefore important to install microbial aerosol treatment units in the air conditioning systems, and we herein investigated the possibility of combining such filtration with UV irradiation to address virus aerosols. Results showed that the removal efficiency of filtration towards f2 and MS2 phages depended on the type of commercial filter material and the filtration speed, with an optimal velocity of 5 cm/s for virus removal. Additionally, it was found that UV irradiation had a significant effect on inactivating viruses enriched on the surfaces of filter materials; MS2 phages had greater resistance to UV-C irradiation than f2 phages. The optimal inactivation time for UV-C irradiation was 30 min, with higher irradiation times presenting no substantial increase in inactivation rate. Moreover, excessive virus enrichment on the filters decreased the inactivation effect. Timely inactivation is therefore recommended. In general, the combined system involving filtration with UV-C irradiation demonstrated a significant removal effect on virus aerosols. Moreover, the system is simple and economical, making it convenient for widespread implementation in air-conditioning systems.     

Impacts of methanol fuel on vehicular emissions: A review

● Methanol effectively reduces CO, HC, CO₂, PM, and PN emissions of gasoline vehicles. ● Elemental composition of methanol directly affects the reduction of emissions. ● Several physicochemical properties of methanol help reduce vehicle emissions. The transport sector is a significant energy consumer and a major contributor to urban air pollution. At present, the substitution of cleaner fuel is one feasible way to deal with the growing energy demand and environmental pollution. Methanol has been recognized as a good alternative to gasoline due to its good combustion performance. In the past decades, many studies have investigated exhaust emissions using methanol-gasoline blends. However, the conclusions derived from different studies vary significantly, and the explanations for the effects of methanol blending on exhaust emissions are also inconsistent. This review summarizes the characteristics of CO, HC, NO_x, CO₂, and particulate emissions from methanol-gasoline blended fuels and pure methanol fuel. CO, HC, CO₂, particle mass (PM), and particle number (PN) emissions decrease when methanol-blended fuel is used in place of gasoline fuel. NO_x emission either decreases or increases depending on the test conditions, i.e., methanol content. Furthermore, this review synthesizes the mechanisms by which methanol-blended fuel influences pollutant emissions. This review provides insight into the pollutant emissions from methanol-blended fuel, which will aid policymakers in making energy strategy decisions that take urban air pollution, climate change, and energy security into account.     

Porous silica synthesis out of coal fly ash with no residue generation and complete silicon separation

● Both amorphous and crystalline silicon are completely separated from coal fly ash. ● Porous silica is synthesized out of coal fly ash. ● No residues is produced during the whole synthesis process. ● The one-step method to synthesize silica don’t need long-time reaction and aging. Ordered mesoporous silica materials exhibit enormous potential in industrial production. Since coal fly ash (CFA) is abundant in Si, it has become a green and promising way to utilize CFA by synthesizing porous silica materials. However, the stable crystalline structure of CFA limits the extraction of Si, and the residue is generated during the process of extracting Si. In this work, we proposed a no-residue method to synthesize ordered mesoporous silica out of CFA. Sodium carbonate (Na₂CO₃) was used to reconstruct the crystals of the CFA, and the calcined mixture then directly reacted with the precipitators. This method combined the process of Si extraction and porous material synthesis. In this method, no residue was generated and the silicon in both amorphous and crystalline phases of CFA was fully utilized. By this method, the extraction efficiency of Si was increased from 31.75% to nearly 100%. The as-synthesized mesoporous silica had a highly-ordered pore structure with a space group of la-3d, a surface area of 663.87 m²/g, a pore volume of 0.41 cm³/g, and an average pore diameter of 2.73 nm. The mechanism of crystalline transformation and material structure formation were systematically studied. This method provides a new idea to dispose of CFA and synthesize porous silica materials.