Potential toxic metal(loid)s (PTMs) in road dust are a major concern in relation to urban environmental quality. Identifying pollution hotspots and sources of PTMs is an essential prerequisite for pollution control and management. Herein, the concentrations, pollution and potential health risks of 8 PTMs (As, Cd, Co, Cu, Hg, Mo, Pb and Zn) in road dust from the highly urbanized areas of Nanjing were studied. Spatial occurrences and sources of PTMs were explored using geostatistics, principal component analysis (PCA) and local Moran’s index. The contamination factor (CF) results showed that Co was mainly natural in origin, while the other PTMs were polluted, with average CFs ranging from 1.4 to 11.0 as follows: Hg > Mo > Cd > Cu > Pb > Zn > As, indicating moderate to very high contamination. Except for Co and Hg, the other PTMs were heavily loaded on PC1, which explained 44.72% of the total variance. Combining the statistical results and distributions of potential sources, we deduced that industrial emissions dominated the spatial patterns of all polluted PTMs in road dust, which showed high levels in the northern parts of the study region and generally decreasing levels southwards. Moreover, Pb and Zn in the south-central area and Cd in the north-central area displayed hotspots, with maximum CFs of 5.5 (Pb), 4.2 (Zn) and 16.2 (Cd), which were related to additional automotive and railway braking emissions, respectively. The resuspension of legacy pesticides in soil is likely responsible for the As pollution hotspot in the southwestern part. Despite the high anthropogenic contributions (27% for As and 68–88% for the other metals) to the PTMs in road dust, their noncarcinogenic and carcinogenic health risks were rarely found for children and adults based on the values of the hazard index and carcinogenic risk index. However, attention still should be paid to the pollution hotspots in the northern region.

The active use of solid fossil fuels (coal) in the production of heat and electricity has led to significant pollution, climate change, environmental degradation, and an increase in morbidity and mortality. Many countries (in particular, European ones, China, Japan, the USA, Canada, etc.) have launched programs for using plant and agricultural raw materials to produce heat and electricity by burning them instead of or together with traditional fuels. It is a promising solution to produce slurry fuels, based on a mixture of coal processing, oil refining and agricultural waste. This paper presents the results of experimental research into the formation and assessment of the most hazardous emissions (sulfur and nitrogen oxides) from the combustion of promising coal slurry fuels with straw, sunflower and algae additives, i.e. the most common agricultural waste. A comparative analysis has been carried out to identify the differences in the concentrations of sulfur and nitrogen oxides from the combustion of typical coal, coal processing waste, as well as fuel slurries with and without plant additives. It has been shown that the concentration of sulfur and nitrogen oxides can be reduced by 62–87% and 12–57%, respectively, when using small masses of plant additives (no more than 10 wt%) and maintaining high combustion heat of the slurry fuel. However, the use of algae and straw in the slurry composition can increase the HCl emissions, which requires extra measures to fight corrosion. A generalizing criterion of slurry fuel vs. coal efficiency has been formulated to illustrate significant benefits of adding plant solid waste to coal-water slurries containing petrochemicals. Straw and sunflower waste (10 wt%) were found to be the best additives to reduce the air pollutant emissions.

Natural background levels (NBLs) and threshold values (TVs) are crucial parameters for identification and the quantification of groundwater pollution, and the evaluation of pollution control measures. The cumulative probability distribution technique was used for the evaluation of NBLs for 36 samples collected during two climate conditions in the part of the desert area from Rajasthan, India. The NBLs for Na⁺, Cl⁻, SO₄²⁻, HCO₃⁻, NO₃⁻ and F⁻ ions were assessed and compared with the natural and anthropogenic processes. The TVs were also calculated for Na⁺, Cl⁻, SO₄²⁻, HCO₃⁻, NO₃⁻ and F⁻ ions, and compared with the drinking limits of the Bureau of Indian Standards. Additionally, the pollution percentage (%) at the individual well was estimated and identified the polluted zones. Results indicate that most of the polluted areas were situated in the southern part, which was influenced by the natural and anthropogenic factors. The sodium concentrations above the TVs, in indicating the saline nature of water. Chloride threshold value above the drinking water limit was mainly observed in the dry season, related to intensive evaporation and industrial waste, which leads to groundwater quality degradation. The NO₃⁻ concentration (∼56% samples) above the TVs indicates extensive use of nitrate fertilizers and sewage effluent. The values of total dissolved solids (TDS) shows the suspicious scenario as about 84% of the samples in the dry period and about 89% in the wet season exceeding the drinking limit. Assessment of background concentrations and threshold values on regional and local scale assigns the basis for the identification of groundwater pollution, and helpful for better water quality guidelines to protecting of water resources.

The performance of the cathode significantly affects the ability of the electro-Fenton (EF) process to degrade chemicals. In this study, a simple method to modify the graphite felt (GF) cathode was proposed, i.e. oxidizing GF by hydrothermal treatment in nitric acid. The surface physical and electrochemical properties of modified graphite felt were characterized by several techniques: scanning electron microscope (SEM), water contact angle, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy and linear scanning voltammetry (LSV). Compared with an unmodified GF (GF-0), the oxygen reduction reaction (ORR) activity of a modified GF was significantly improved due to the introduction of more oxygen-containing functional groups (OGs). Furthermore, the results showed that GF was optimally modified after 9 h (GF-9) of treatment. As an example, the H₂O₂ generation by GF-9 was 2.26 times higher than that of GF-0. After optimizing the process parameters, which include the initial Fe²⁺ concentration and current density, the apparent degradation rate constant of levofloxacin (LEV) could reach as high as 0.40 min⁻¹. Moreover, the total organic carbon (TOC) removal rate and mineralization current efficiency (MCE) of the modified cathode were much higher than that of the GF-0. Conclusively, GF-9 is a promising cathode for the future development in organic pollutant removal via EF.

Most of the previous researches estimate influencing factors impact on air quality average without considering the heterogeneity of influential factors on different levels of air quality. In order to detect the different effects of influencing factors on air quality index (AQI) between lower-AQI and higher-AQI cities, this study applies a spatial quantile regression model (SQRM) to investigate heterogeneity of influential factors on AQI, while accounting for spatial autocorrelation of AQI. The results show that heterogeneity effects of windspeed, terrain slope, urbanization sprawl and spatial autocorrelation on AQI are large across the entire AQI spectrum, while heterogeneity effects of precipitation, temperature, relative humidity, terrain fluctuation and urbanization intensity on AQI are not obvious. The spatial positive autocorrelation of AQI in higher-AQI cities is greater than that in lower-AQI cities. Compared with higher-AQI cities, the negative impact of terrain slope on AQI is lager in lower-AQI cities. One unit increase in wind speed contributes AQI to decrease 9.31 to 5.64 then to 5.39 for lower, medium and higher-AQI cities. One unit increase in urbanization sprawl would lead AQI increase 25.6 to 15.6 then to 10.5 for lower, medium and higher-AQI cities. The heterogeneity analysis of meteorological, topographic and socioeconomic factors effects on air quality are of guiding significance for realizing the differentiation of policy measures for air pollution prevention and control.

To investigate chemical characteristics, abatement mechanisms and regional transport of atmospheric pollutants during the COVID-19 outbreak control period in the Yangtze River Delta (YRD) region, China, the measurements of air pollutants including fine particulate matter (PM₂.₅) and volatile organic compounds (VOCs) on non-control period (NCP, 24 December 2019–23 January 2020) and control period (CP, 24 January–23 February 2020) were analyzed at the urban Pudong Supersite (PD) and the regional Dianshan Lake Supersite (DSL). Due to the stricter outbreak control, the levels of PM₂.₅ and VOCs, and the occurrence frequencies of haze-fog episodes decreased substantially from NCP to CP, with average reduction rates of 31.6%, 38.9% and 35.1% at PD, and 34.5%, 50.7% and 37.9% at DSL, respectively. The major source for PM₂.₅ was secondary sulfate & nitrate in both periods, and the emission control of primary sources such as coal burning and vehicle exhaust decreased the levels of precursors gas sulfur dioxide and nitrogen oxide, which highly contributed to the abatement of PM₂.₅ from NCP to CP. The higher levels of ozone at both PD and DSL on CP might be due to the weak nitrogen monoxide titration, low relative humidity and high visibility compared with NCP. Vehicle exhaust and fugitive emission from petrochemical industry were the major contributors of ambient VOCs and their decreasing activities mainly accounted for VOCs abatement. Moreover, the high frequency of haze-fog events was closely impacted by medium-scale regional transport within Anhui and Jiangsu provinces. Therefore, the decreasing regional transported air pollutants coincided with the emission control of local sources to cause the abatement of haze-fog events in YRD region on CP. This study could improve the understanding of the change of atmospheric pollutants during the outbreak control period, and provide scientific base for haze-fog pollution control in YRD region, China.

Recently, sulfate radical-based advanced oxidation processes (SR-AOPs) have been studied extensively for the removal of pollutants, however, few researches focused on the activation of bisulfite by nanoscale zerovalent iron (nZVI), especially, surface reaction mechanism and sulfate radical-mediated degradation pathway have not been elucidated in detail. In this study, influencing factors, the kinetics, transformation pathway and mechanism of triphenyl phosphate (TPHP) degradation in the nZVI/bisulfite system were systematically discussed. Compared with Fe²⁺, nZVI was found to be a more efficient and long-lasting activator of bisulfite via gradual generation of iron ions. The optimal degradation efficiency of TPHP (98.2%) and pseudo-first-order kinetics rate constant (kₒbₛ = 0.2784 min⁻¹) were obtained by using 0.5 mM nZVI and 2.0 mM bisulfite at the initial pH 3.0. Both Cl⁻ and NO₃⁻ inhibited the degradation of TPHP and the inhibitory effect of Cl⁻ was stronger than that of NO₃⁻ due to the higher reaction rate of Cl⁻ with •SO₄⁻. Furthermore, SEM, XRD and XPS characterization revealed that a thin passivation layer (Fe₂O₃, Fe₃O₄, FeOOH) deposited on the surface of fresh nZVI and a few iron corrosion products generated and assembled on the surface of reacted nZVI. Radical quenching tests identified that •SO₄⁻ was the dominant reactive oxidative species (ROS) for TPHP removal. Based on HRMS analysis, six degradation products were determined and a sulfate radical-mediated degradation pathway was proposed. In a word, this study revealed that the nZVI/bisulfite system had a great potential for the TPHP elimination in waterbody.

In order to tackle China’s severe air pollution issue, the government has released the “Air Pollution Prevention and Control Action Plan” (known simply as the “Action Plan”) since 2013. A recent study reported a decreased trend in PM₂.₅ concentrations over 2013–2017, but O₃ pollution has become more serious. However, the effects of surface O₃ on crops are unclear after the implementation of the “Action Plan”. Here, we evaluated the potential negative effects of surface O₃ on three main food crops (winter wheat, maize and rice) across China during 2015–2018 using nationwide O₃ monitoring data and AOT40-yield response functions. Results suggested that mean O₃ concentration, AOT40 and relative yield loss in China showed an overall upward trend from 2015 to 2018. During winter wheat, maize, single rice, double-early rice, and double-late rice growing seasons, mean O₃ concentration in recent years ranged from 38.6 to 46.9 ppb, 40.2–43.9 ppb, 39.3–42.2 ppb, 33.8–40.0 ppb, and 35.9–39.1 ppb, respectively, and AOT40 mean values ranged from 8.5 to 14.3 ppm h, 10.5–13.4 ppm h, 9.8–11.9 ppm h, 5.2–9.2 ppm h, and 8.0–9.5 ppm h, respectively. O₃-induced yield reductions were estimated to range from 20.1 to 33.3% for winter wheat, 5.0–6.3% for maize, 7.3–8.8% for single rice, 3.9–6.8% for double-early rice and 5.9–7.1% for double-late rice. O₃-induced production losses for winter wheat, maize, single rice, double-early rice, and double-late rice totaled 39.5–88.2 million metric tons, 12.6–21.0 million metric tons, 9.5–11.3 million metric tons, 1.2–1.8 million metric tons, and 2.2–2.7 million metric tons, respectively, and the corresponding economic losses totaled 14.3–32.0 billion US$, 3.9–6.5 billion US$, 3.9–4.6 billion US$, 0.5–0.7 billion US$, and 0.9–1.1 billion US$, respectively. Our results suggested that the government should take effective measures to reduce O₃ pollution and its effects on agricultural production.

Coal-Gas replacement project has been implemented to decrease haze pollution in China in recent years. Airborne arsenic (As) mostly originates from coal burning processes. It is noteworthy to compare the distribution of arsenic fraction in PM₂.₅ before and after coal-gas replacement. Eighty PM₂.₅ samples were collected in Baoding in December 2016 (coal dominated year) and December 2017 (gas dominated year) at different functional areas including residential area (RA), industrial area (IA), suburb (SB), roadside (ST) and Botanical Garden Park (BG). The fraction, bioavailability and health risk of As in the PM₂.₅ samples were investigated and compared between these two years. Arsenic was mainly distributed in the non-specifically sorbed fraction (F1) and the residual fraction (F5). However, the proportion of F1 to the total As in 2017 was higher than that in 2016, while the proportion of As in the amorphous and poorly-crystalline hydrous oxides of Fe and Al fraction (F3) in 2017 was lower. The distributions of fraction and bioavailability showed temporal and spatial characteristics. The total concentration and bioavailability of As in SB and IA were significantly higher than those in RA, ST and BG. The BF (Bioavailability Factor) values of As ranged from 0.30 to 0.61. Health risk assessment indicated that the hazard quotient (HQ) and carcinogenic risk (CR) of As in PM₂.₅ significantly decreased after coal-gas replacement.

Microplastics pollution in the environment is closely determined by the surrounding industrial and human activities. In present study, we investigated microplastics in water and sediment samples collected from a textile industrial area in Shaoxing city, China. The abundance of microplastics varied from 2.1 to 71.0 items/L in surface water samples, and from 16.7 to 1323.3 items/kg (dw) in sediment samples. The polymer type was dominated by polyester both in water (95%) and sediment (79%) samples. The majority of the detected microplastics was predominantly colored fibers smaller than 1 mm in diameter. The high level of microplastic pollution detected in local freshwater and sediment environments was attributed to the production and trading activities of textile industries, for which severe regulations should be envisaged in the future to effectively reduce the local microplastic pollution.