While infants are developing, they are easily affected by toxic chemicals existing in their environments, such as semi-volatile organic compounds (SVOCs): phthalates, polycyclic aromatic hydrocarbons (PAHs), polybrominated diphenyl ethers (PBDEs), and organophosphate esters (OPEs). However, the specific living environment of infants, including increased plastic products and foam floor mats, may increase the presence of these chemicals. In this study, 68 air, dust, and window film samples were collected from homes, with 3- to 6-month-old infant occupants, to analyze phthalates, PAHs, PBDEs, and OPEs. High detection rates and concentrations suggest that these SVOCs are widespread in infant environments and are associated with cooking methods, smoking habits, the period of time after decoration, and room floors. The partitioning behavior of SVOCs indicates that the logarithms of the dust/gas-phase air partition coefficient (logKD) and the window film/gas-phase air partition coefficient (logKF) in homes are not at an equilibrium state when the logarithm of the octanol/air partition coefficient (logKOA) is less than 8 or greater than 11. Considering the 3 exposure routes, ingestion and dermal absorption have become the main routes of infant exposure to phthalates and OPEs, and ingestion and inhalation have become the dominant routes of exposure to PAHs and PBDEs. The total carcinogenic risk of SVOCs, which have carcinogenic toxicities, via ingestion and dermal absorption for infants in homes exceeds the acceptable value, suggesting that the current levels of these SVOCs in homes might pose a risk to infant health.

Ionic liquids (ILs) are extensively used in several chemistry fields. And research about the effects of ILs on soil microbes is needed. In this study, brown soil was exposed to 1-butyl-3-methylimidazolium bromide ([C₄mim]Br), 1-hexyl-3-methylimidazolium bromide ([C₆mim]Br) and 1-decyl-3-methylimidazolium bromide ([C₁₀mim]Br). The toxicities of the three ILs are evaluated by measuring the soil culturable microbial number, enzyme activity, microbial diversity and, abundance of the ammonia monooxygenase (amoA) genes of ammonia-oxidizing bacteria (AOB) and ammonia-oxidizing archaea (AOA). Results showed that all tested ILs caused a decrease in culturable microbial abundance. Tested ILs exposure inhibit urease activity and promote acid phosphatase and β-glucosidase activities. Tested ILs reduced soil microbial diversity and the abundances of AOB-amoA and AOA-amoA genes significantly. After a comparison of the integrated biomarker response (IBR) index, the toxicities of tested ILs to soil microorganisms were as follows: [C₁₀mim]Br > [C₆mim]Br > [C₄mim]Br. Among all collected biomarkers, the abundance of the AOA-amoA gene was the most sensitive one and was easily affected after ILs exposure.

Fly ash (FA), a solid waste generated in thermal power plants, is considered an environmental pollutant. Therefore, measures must be taken to dispose of FA in an environmentally friendly manner. In this paper, an electrospinning technique was employed to incorporate FA particles onto zinc oxide nanofibers (ZnO NFs), and the product (FA/ZnO composite) was used for the removal of methylene blue (MB) from the water. Herein, ZnO NFs may serve as effective semiconductor photocatalysts and provide sufficient surface area for FA, while the FA particles serve as an effective adsorbent. The adsorption capacity and photocatalytic efficiency of the as-synthesized nanocomposite fibers were enhanced compared to those of the pristine ZnO NFs, and this result is attributed to the uniform distribution of FA on the surface of the ZnO NFs. The as-synthesized nanocomposite could have great significance in wastewater treatment.

This study assessed the impact on air quality and health risk by long-range transported (LRT) PM2.5-10- and PM2.5-bound metals and PAHs in Taipei City, Taiwan. Several methods with receptor aerosol measurements were used to quantify the effect of LRT. The hybrid single particle lagrangian integrated trajectory model (HYSPLIT) was used in conjunction with the potential source contribution function (PSCF) to distinguish the LRT aerosols. By using a general linear model (GLM) with a marginal mean and positive matrix fraction (PMF), this study also evaluated the annual increased level of LRT (AIRLRT) for each source contribution to the concentration and the resultant health risk of particle-bound metals and polycyclic aromatic hydrocarbons (PAHs). The LRT influenced fine-sized metals and PAHs rather than coarse-sized ones. We found that the level of PM2.5-bound toxic metals (Pb, Cd, and As) and PAHs (Benzo[a]pyrene and dibenzo[a,e]pyrene) could increase by 90% under the influence of LRT in 2014, while an AIRLRT value of 25% for the PM2.5 mass concentration was observed. Overall, the excess cancer risk (ECR) resulting from PM2.5-bound metal and PAH exposures was 6.40 × 10−5 in relation to coal combustions (20.7%), traffic-related emissions (59.7%) and re-suspended aerosols (19.6%). Among these contributors, LRT-related metals and PAHs in PM2.5 accounted for 51% of the total ECR.

The high acidity of mercury ions (Hg²⁺) contained wastewater can complicate its safe disposal. MgAl-LDHs supported [SnS₄]⁴⁻ clusters were synthesized for Hg²⁺ removal from acid wastewater. The active sites of [SnS₄]⁴⁻ clusters were inserted into the interlayers of MgAl-LDHs using an ion-exchange method. The experimental results indicated that [SnS₄]⁴⁻/MgAl-LDHs composite can obtain higher than 99% Hg²⁺ removal efficiency under low pH values. The maximum mercury adsorption capacity is 360.6 mg g⁻¹. It indicated that [SnS₄]⁴⁻ clusters were the primary active sites for mercury uptake, existing as stable Hg₂(SnS₄) on the surface of the composite. Under low pH values, such a composite seems like a “net” for HgSO₄ molecules, exhibiting great potential for mercury removal from acid solutions. Moreover, the co-exist metal ions such as Zn²⁺, Na⁺, Cd²⁺, Cr³⁺, Pb²⁺, Co²⁺, and Ni²⁺ have no significant influences on Hg²⁺ removal. The adsorption isotherms and kinetics were also studied, indicating that the adsorption mechanism follows a monolayer chemical adsorption model. The [SnS₄]⁴⁻/MgAl-LDHs composite exhibits a great potential for Hg²⁺ removal from acid wastewater.

Polycyclic aromatic hydrocarbons (PAHs) remain a focal concern of the air pollution in China. To discriminate the sources of airborne PAHs in Chinese rural regions, a national-scale tree bark sampling campaign and emission inventory estimation were conducted. The concentrations of the sum of 16 U.S. EPA priority PAHs in rural bark ranged from 6.30 to 3803 ng/g, with the dominance of 3- and 4-ring PAHs. Bark residual PAH concentration correlated significantly with emission flux rate, bark lipid content, ambient PM₂.₅, precipitation and sampling location. Based on the information of emission data, bark PAH congener profiles, principal component analysis, diagnostic ratios and compound-specific isotope analysis, solid fuel combustion was identified as the major source and could explain 40.3%–46.4% of bark PAH residues in rural China. The δ¹³C values of most individual PAHs were more negative at sites with lower longitude and latitude, suggesting a greater contribution of biomass combustion to PAH residues. Our results suggest the importance of regulating solid fuel combustion to significantly improve the air quality in China, and bark samples can provide a wealth of information on effectively monitoring and controlling the sources of PAH emission in rural China.

A comprehensive analysis of 15 target chemical compounds (pharmaceuticals and personal care product, perfluoroalkyl compounds and industrial chemicals) were carried out to determine their concentrations in selected commercially exploited, wild caught small and medium sized pelagic fish species and their organs (Thyrsites atun (snoek), Sarda orientalis (bonito), Pachymetopon blochii (panga) and Pterogymnus laniarius (hottentot)) obtained from Kalk Bay harbour, Cape Town. Solid phase extraction (SPE) method based on Oasis HLB cartridges were used to concentrate and clean-up the samples. Liquid chromatography–mass spectrometry analysis of these chemical compounds revealed the simultaneous presence of at least 12 compounds in different parts of the selected fish species in nanogram-per-gram dry weight (ng/g dw) concentrations. The results revealed that perfluorodecanoic acid, perfluorononanoic acid and perfluoroheptanoic acid were the most predominant among the perfluorinated compounds and ranged between: (20.13–179.2 ng/g), (21.22–114.0 ng/g) and (40.06–138.3 ng/g). Also, diclofenac had the highest concentration in these edible fish species out of all the pharmaceuticals detected (range: 551.8–1812 ng/g). The risk assessment values were above 0.5 and 1.0 for acute and chronic risk respectively which shows that these chemicals have a high health risk to the pelagic fish, aquatic organisms and to humans who consume them. Therefore, there is an urgent need for a precautionary approach and the adequate regulation of the use and disposal of synthetic chemicals that persist in aquatic/marine environment in this province and other parts of South Africa, to prevent impacts on the sustainability of our marine environment, livelihood and lives.

Elevated inorganic arsenic concentrations in groundwater has become a major public and environmental health concern in different parts of the world. Currently, As-contaminated groundwater issue in many countries and regions is a major topic for publications at global level. However, there are many regions worldwide where the problem has still not been resolved or fully understood due to inadequate hydrogeochemical investigations. Hence, this study evaluates for the first time the hydrogeochemical behavior of the arid and previously unexplored inland basin of Sirjan Plain, south east (SE) Iran, in order to assess the controlling factors which influence arsenic (As) mobility and its distribution through groundwater resources. Total inorganic arsenic concentration was measured using inductive-coupled plasma optical emission spectrometry (ICP-OES). Arsenic content in groundwater of this region ranged between 2.4 and 545.8 μg/L (mean value: 86.6 μg/L) and 50% of the samples exceeded the World Health Organization (WHO) guideline value of 10 μg/L in drinking water. Groundwater was mainly of Na-Cl type and alkaline due to silicate weathering, ion exchange and evaporation in arid conditions. Elevated As concentrations were generally observed under weakly alkaline to alkaline conditions (pH > 7.4). Multivariate statistical analysis including cluster analysis and bi-plot grouped As with pH and HCO3 and demonstrated that the secondary minerals including oxyhydroxides of Fe are the main source of As in groundwater in this region. The desorption of As from these mineral phases occurs under alkaline conditions in oxidizing arid environments thereby leading to high levels of As in groundwater. Moreover, evaporation, ion exchange and saltwater intrusion were the secondary processes accelerating As release and its mobility in groundwater. Based on the results of this study, desorption of As from metal oxy-hydroxides surfaces under alkaline conditions, evaporation and intrusion of As-rich saline water are considered to be the major factors causing As enrichment in arid inland basins such as those in southeast Iran. This study proposes the regular monitoring and proper groundwater management practices to mitigate high levels of arsenic in groundwater and related drinking water wells of Sirjan Plain.