Chlorinated aromatic organic compounds are extremely toxic to the environment and cause cancer to the human body. Pentachlorophenol (PCP) is a hydrophobic and ionic organic compound that is employed as a production material in various industries. Although the Taiwanese government has banned the use of PCP for years, large PCP-contaminated areas remain in Southern Taiwan. Chemical oxidation, which has been proposed as a viable method for restoring PCP-contaminated areas, involves the use of micronanosize birnessite (δ-MnO₂), which is a type of manganese oxide and a natural mineral in soil environments. The goal of this study was to simulate the decontamination of the underlying soil of the PCP-contaminated areas, which is situated in anaerobic and lightless environment. Through the use of a self-developed gas release and absorption reaction flask, the oxidative mineral decarboxylation and dechlorination effects of δ-MnO₂ on PCP in aerobic and anaerobic (with oxygen removed through the use of nitrogen) environments without light were investigated. Results indicated that adding δ-MnO₂ facilitated the oxidative decarboxylation and dechlorination of PCP and the release of Cl⁻ in an aerobic, lightless environment without microbial activity. In the anaerobic environment, the oxidative decarboxylation effect of δ-MnO₂ on PCP decreased significantly, and the dechlorination effect was the primary reaction. Accordingly, adding δ-MnO₂ inorganically destroys aromatic benzene and releases CO₂ and Cl⁻. The molar ratio between CO₂ and Cl⁻ was calculated to assess the mechanisms of the distinct reaction systems. The parameters and data acquired from the experiment, which involved simulating the conditions of the contaminated areas, can be used in planning the on-site management of the PCP contamination; in particular, these parameters and data provide a reference for eliminating PCP from underlying soil—including groundwater-saturated layers.

In northern countries, the climate, and consequently the use of studded tyres and winter traction sanding, causes accumulation of road dust over winter and spring, resulting in high PM₁₀ concentrations during springtime dusting events. To quantify the dust at the road surface, a method—the wet dust sampler (WDS)—was developed allowing repeatable sampling also under wet and snowy conditions. The principle of operation is flushing high-pressurised water over a defined surface area and transferring the dust laden water into a container for further analyses. The WDS has been used for some time and is presented in detail to the international scientific community as reported by Jonsson et al. (2008) and Gustafsson et al. (2019), and in this paper, the latest version is presented together with an evaluation of its performance. To evaluate the WDS, the ejected water amount was measured, as well as water losses in different parts of the sampling system, together with indicative dust measurement using turbidity as a proxy for dust concentration. The results show that the WDS, when accounting for all losses, have a predictable and repeatable water performance, with no impact on performance based on the variety of asphalt surface types included in this study, given undamaged surfaces. The largest loss was found to be water retained on the surface, and the dust measurements imply that this might not have as large impact on the sampled dust as could be expected. A theoretical particle mass balance shows small particle losses, while field measurements show higher losses. Several tests are suggested to validate and improve on the mass balances. Finally, the WDS is found to perform well and is able to contribute to further knowledge regarding road dust implications for air pollution.

Annually, a great volume of sediment and suspended particulate matters (SPMs) enters into the seas through estuaries. In the estuarine zone, metals present in SPMs may undergo conservative or non-conservative changes. In the present study, oxidation-reduction potential (ORP) as the most complex chemical parameter of open sea water and its relationship with the behavior of t metals in the estuarine area were investigated. Dissolved oxygen was used as a strong oxidant to increase the ORP. According to the absorption and desorption experiment, Mn and Cu are desorbed from SPMs during estuarine mixing. However, Zn and Pb are absorbed into the SPMs. In addition, the analysis results were indicative of the conservative behavior of Ni. The results of the three-step chemical partitioning of the SPMs revealed that Mn and Cu are desorbed from the SPMs physically, whereas Zn is absorbed into the SPMs chemically. Also, results showed that Pb is physically desorbed from the SPMs, while it is absorbed into SPMs chemically. All metals, except for Ni and Zn, whose reactions with the SPMs are not affected by an increase in the ORP, are affected by the escalation of this parameter.

There is insufficient evidence on the relationship between air pollution and mortality from cardiovascular disease (CVD) in northeast China. Here, we explored the short-term effects of air pollution on CVD mortality and preliminarily investigated differences in population susceptibility to air pollution in Shenyang, China. CVD mortality, air pollution, and meteorological data during 2013–2016 were obtained. Time-series analysis was applied to evaluate the association between air pollution and daily CVD mortality with different lag structures. In the single-pollutant model, each 10 μg/m³ increase in PM₂.₅, PM₁₀, SO₂, NO₂, and O₃ concentrations and 1 mg/m³ increase in CO concentrations at lag0 (same day) was significantly associated with an increase of 0.40% (95% confidence interval, 0.22–0.59%), 0.26% (0.12–0.40%), 0.43% (0.16–0.70%), 0.90% (0.14–1.67%), 0.76% (0.21–1.32%), and 3.33% (0.97–5.75%), respectively, in overall CVD mortality. Susceptibility to air pollutants was higher among females, elderly people, and ischemic heart disease patients. Furthermore, air pollution effects on CVD mortality were 2–8 times greater during the non-heating period. In conclusion, the air pollutants PM₂.₅, PM₁₀, SO₂, NO₂, O₃, and CO showed significant positive effects on CVD mortality in Shenyang, China. These findings highlight the adverse effects of air pollution and suggest the need for personal protective equipment and reduction of air pollution sources.

The synthetic hormone sodium levothyroxine (LTX) is one of the most prescribed drugs in the world and the most effective in hypothyroidism treatment. The presence of LTX in the environment has become a matter of major concern due to the widespread use of this hormone and by the fact that it is only partially removed in conventional water and sewage treatment plants. However, information regarding the photochemical fate of this hormone in environmental or engineered systems is scarce in the literature. In this work, the sunlight-driven direct and indirect LTX degradation was investigated by determining the photolysis quantum yield, ΦLTX = 3.80 (± 0.02) × 10⁻⁵, as well as the second-order kinetic constants of the reactions with hydroxyl radicals, kLTX,•OH = 1.50 (± 0.01) × 10¹⁰ L mol⁻¹ s⁻¹ and singlet oxygen, kLTX,₁O₂ = 1.47 (± 0.66) × 10⁸ L mol⁻¹ s⁻¹. Mathematical simulations indicate that LTX photodegradation is favored in shallow, nitrite-rich, and dissolved organic matter (DOM)-poor environments, with LTX half-life times varying from less than 10 days to about 80 days. LTX removals of 85 and 95% were achieved by UVC photolysis and UVC/H₂O₂ after 120 min, respectively. Three transformation products, triiodothyronine, diiodothyronine, and diiodotyrosine, were identified during LTX degradation by the UVC-based processes studied. The results herein regarding photo-induced kinetics coupled with environmental fate simulations may help evaluate LTX persistence and also the design of water and wastewater treatment processes.

This study aims to evaluate the practical potential of using constructed wetlands (CWs) for treating saline wastewater containing various heavy metals. The results demonstrated that CWs growing Canna indica with porous slag as substrate could efficiently remove heavy metals (Cu, Zn, Cd, and Pb) from saline wastewater at an electrical conductivity (EC) of 7 mS/cm, especially under low influent load. Salts with salinity level (characterized as EC) of 30 mS/cm suppressed the removal of some heavy metals, dependent on heavy metal species and their influent concentrations. The presence of salts in CWs can improve the accumulation of Cu, Zn, and Pb in plant tissues as compared to control treatment, irrespective of metal concentrations in solution. The influence of salts on Cd accumulation depended on both salinity levels and Cd concentrations in solution. Although more heavy metals were accumulated in roots than in shoots, the harvesting of aboveground plant materials is still efficient addition for heavy metal removal due to the greater biomass and growth rate of aboveground plant material. Furthermore, replacing all plants instead of preserving roots from harvested plants in CWs over a period of time is essential for heavy metal removal, because the continued accumulation by roots can be inhibited by the increasing accumulated heavy metals from saline wastewater.

Manganese dioxide nanoparticles/activated carbon (MnO₂/AC) composites and manganese dioxide nanoparticles (MnO₂ NPs) are prepared through chemical reduction method. Morphological study shows that MnO₂ NPs had cylindrical and spherical shape. The morphological study also revealed that MnO₂ NPs were well dispersed on AC while neat Mn NPs present both in dispersed and in agglomerated form. The FT-IR study confirms the synthesis of MnO₂ NPs. Zetasizer study presented that the Mn NPs had uniform size and below 100 nm in size and had zeta potential of − 20 mV, which represent its stability in the suspension form. The synthesized Mn/AC composite and Mn NPs were utilized as photocatalysts for the photodegradation of Congo red (CR) dye. The degradation study shows that MnO₂/AC composite degraded CR dye more efficiently than MnO₂ NPs under UV and normal light irradiation. The efficient degradation of dye by Mn/AC composite is due to the synergistic effect between dye adsorption on AC and rapid photodegradation by supported MnO₂ NPs. The results revealed that Mn/AC composite degraded about 98.53% of CR dye within 5 min while MnO₂ NPs degraded 66.57% of dye within the same irradiation time. The recycled catalyst also significantly degraded dye which verifies its sustainability. The effect of catalyst dosage and initial dye concentration was conducted. The degradation rate of dye was found drastically faster in tap water (in presence of catalyst), which might be due to the presence of various mineral ions in the tap water.

In this paper, a conceptual model was developed to predict the seepage of oil sands process-affected water with capabilities of evaluating the transport and attenuation of naphthenic acids through the dykes and the foundations of oil sands tailings pond. The model incorporates naphthenic acid diffusion, adsorption, dispersion, advection, and biodegradation, and was modeled through the commercial software tools to predict naphthenic acid fate in both spatial and time scales. The tailing pond of the Muskeg River Mine in the Athabasca oil sands deposit was investigated in the case study. The comparison between the onsite monitoring data and the simulation results was in good agreement. In addition, limiting factors for migration of naphthenic acid were also discussed based on a parametric sensitivity study.

The latest research focused on the analysis of algal growth and the dynamics of their growth use the laser diffraction technique, enabling determination of the volume fraction of suspended particles with specific diameters in aqueous solution as well as their fractal dimensions. This study focuses on the possibility of using a laser granulometer to assess the growth dynamics of algae growing in treated wastewater in a hydroponic system, supported by artificial lighting with the use of light-emitting diodes (LEDs). On the basis of the measurements, the fractal dimension (Df) of algae was determined. An attempt was made to apply the modified Avrami equation describing the crystallization process for the analysis of algae growth dynamics in wastewater. Presented results show that the fractal dimension of suspended matter, largely created by algae, in the case of additional lighting of the hydroponic system at night, takes lower values (Df ~ 1.0) than in sewage without additional light source (Df ~ 2.0). In each measurement series, the fractal dimension of particles in the tank with lighting in the end of the experiment was about 33–43% lower than in the tank without LEDs. The analysis of changes in particle diameters calculated on the basis of Avrami equation largely corresponds with the stages of algae growth. During the measurement series with lower air temperatures, the growth of algae in the tank with additional light was faster than in the tank without LEDs. The obtained information can be the basis for determining the effective method of removing algae from wastewater treated in the hydroponic system, before they are discharged to the receiver in order to prevent the outflow of increased concentrations of total suspended solids.

In this study, a chabazite-rich tuff (CHA) from the Bala deposit of Ankara region (Turkey) and its modified forms (CuCHA, AgCHA, FeCHA, and HCHA samples) were investigated at 273 and 298 K using volumetric apparatus up to 100 kPa. The chabazite samples were characterized by using thermal analysis (TG-DTG-DTA), X-ray diffraction (XRD), X-ray fluorescence (XRF), scanning electron microscopy with detector X-ray energy dispersive (SEM-EDX), Fourier transform infrared (FT-IR), and N₂ adsorption methods. It was found that natural chabazite is composed of predominantly chabazite with small amounts of clinoptilolite and erionite. XRD showed that there are major structural changes to Fe- and H-exchanged chabazite samples. Capacity of chabazites for CH₄ ranged from 0.168 and 1.341 mmol/g. Among all the modified forms, it was observed that Ag form of chabazite zeolite had the greatest methane adsorption capacity at both temperatures.