The environmental fate of iodine is of general geochemical interest as well as of substantial concern in the context of nuclear waste repositories and reprocessing plants. Soils, and in particular soil organic matter (SOM), are known to play a major role in retaining and storing iodine. Therefore, we investigated iodide and iodate sorption by four different reference soils for contact times up to 30 days. Selective sequential extractions and X-ray absorption spectroscopy (XAS) were used to characterize binding behavior to different soil components, and the oxidation state and local structure of iodine. For iodide, sorption was fast with 73 to 96% being sorbed within the first 24 h, whereas iodate sorption increased from 11–41% to 62–85% after 30 days. The organic fraction contained most of the adsorbed iodide and iodate. XAS revealed a rapid change of iodide into organically bound iodine when exposed to soil, while iodate did not change its speciation. Migration behavior of both iodine species has to be considered as iodide appears to be the less mobile species due to fast binding to SOM, but with the potential risk of mobilization when oxidized to iodate.

Ethidium bromide (EtBr) is widely used as DNA-staining dyes for the detection of nucleic acids in laboratories and known to be powerful mutagens and carcinogens. In the present paper, the removal of EtBr from aqueous solutions in a batch system using DNA-loaded Fe₃O₄ nanoparticles as a simple and efficient method was investigated. DNA was covalently loaded on the surface of Fe₃O₄ magnetic nanoparticles, which was confirmed by FT-IR analysis and zeta potential measurements. The morphology and crystal structure were characterized by SEM, TEM, and XRD. The influence factors on the removal efficiency such as initial EtBr concentration, contact time, adsorbent dose, pH, and temperature were also studied. The removal process of EtBr can be completed quickly within 1 min. The removal efficiency was more than 99% while the EtBr concentration was routinely used (0.5 mg L⁻¹) in biology laboratories and the dosages of nanoparticles were 1 g L⁻¹. For the different EtBr concentrations from 0.5 to 10 mg L⁻¹ in aqueous solution, the goal of optimized removal was achieved by adjusting the dosage of DNA-loaded Fe₃O₄ nanoparticles. The optimum pH was around 7 and the operational temperature from 4 to 35 °C was appropriate. Kinetic studies confirmed that the adsorption followed second-order reaction kinetics. Thermodynamic data revealed that the process was spontaneous and exothermic. The adsorption of EtBr on DNA-loaded Fe₃O₄ nanoparticles fitted well with the Freundlich isotherm model. These results indicated that DNA-loaded Fe₃O₄ nanoparticles are a promising adsorbent for highly efficient removal of EtBr from aqueous solution in practice.

Since bisphenol A (BPA) exhibits endocrine disrupting action and high toxicity in aqueous system, there are high demands to remove it completely. In this study, the BPA removal by sonophotocatalysis coupled with nano-structured graphitic carbon nitride (g-C₃N₄, GCN) was conducted with various batch tests using energy-based advanced oxidation process (AOP) based on ultrasound (US) and visible light (Vis-L). Results of batch tests indicated that GCN-based sonophotocatalysis (Vis-L/US) had higher rate constants than other AOPs and especially two times higher degradation rate than TiO₂-based Vis-L/US. This result infers that GCN is effective in the catalytic activity in Vis-L/US since its surface can be activated by Vis-L to transport electrons from valence band (VB) for utilizing holes (h⁺VB) in the removal of BPA. In addition, US irradiation exfoliated the GCN effectively. The formation of BPA intermediates was investigated in detail by using high-performance liquid chromatography-mass spectrometry (HPLC/MS). The possible degradation pathway of BPA was proposed.

Variation of volatile organic compound (VOC) concentration and composition in an active landfill were monitored by a developed static chamber for 2 years. The landfill gas from 82 sampling points including 70 points on working face, 8 points on geomembrane (GMB), and 4 points on final cover were analyzed for VOCs by GC-MS. Twenty-eight types of VOCs were detected, including terpenes, sulfur compounds, aromatics, hydrocarbon, oxygenated compounds, aldehyde compounds, and halogenated compounds. Terpenes were the dominant VOCs recorded in the spring, autumn, and winter seasons, whereas sulfur compounds dominated in the summer season. Limonene, ethyl alcohol, and acetone were identified as the main VOCs emitted from the waste working face of the landfill. Limonene dominated the terpenes with a maximum concentration of 43.29 μg m⁻³ in the autumn season. Limonene was also the dominant VOC escaping from the defects of geomembrane temporary cover reaching an average concentration 38 μg m⁻³. The defects of geomembranes can be a great emission source of VOCs. Emission rate of limonene was 2.24 times higher than that on the working face. VOC concentrations on the final cover can be 166 times less than those obtained on the working face. VOC emitted from the landfill did not represent a health threat for human health. However, concentrations of methyl mercaptan and ethanethiol on the working face were 3.4–22.8 times greater than their odor threshold, which were the main compounds responsible for odor nuisance. Results obtained from CALPUFF model indicated that methyl mercaptan and ethanethiol would not be a nuisance for the residents around the landfill. However, these compounds are harmful to the workers on the landfill.

TiO₂ is employed as both photocatalytic and structural materials, leading to its applications in external coatings or in interior furnishing devices, including cement mortar, tiles, floorings, and glass supports. The authors have already demonstrated the efficiency of photoactive micro-sized TiO₂ and here its industrial use is reported using the digital printing to coat porcelain grés slabs. Many advantages are immediately evident, namely rapid and precise deposition, no waste of raw materials, thus positively affecting the economy of the process. Data for the thin films deposited by digital printing were compared with those obtained for the conventional spray method. The use of metal-doped TiO₂ is also reported so that the photoactivity of these materials can be exploited even under LED light. The digital inkjet printed coatings exhibited superior photocatalytic performance owing to both higher exposed surface area and greater volume of deposited anatase, as well as the greater areal distribution density of thinly and thickly coated regions. Moreover, the presence of TiO₂ doped silver increased the efficiency of the materials in NOx degradation both under UVA and LED lights.

Stereocaulon sorediiferum is expected to be a Cu-hyperaccumulator lichen and has fluorescent substances. To clarify the relationship between the fluorescence (FL) of the lichen and its Cu concentration, we collected S. sorediiferum samples at Cu-contaminated and uncontaminated sites in Japan, determined the concentration of Cu, K, Mg, Al, Ca, Mn, Fe, Zn, chlorophyll a,b, and total carotenoids in them, analyzed lichen secondary metabolites and fluorescent substances extracted from them, and measured the FL of them and their extracts. We found that the FL intensity of S. sorediiferum samples is significantly negatively correlated with their Cu concentration. The application of its FL for Cu monitoring may allow a new nondestructive quantitative method for assessing Cu contamination. The spectroscopic and chromatographic analysis shows that the fluorescent substances negatively correlated with Cu concentration are not major lichen secondary metabolites (lobaric acid and atranorin) and remain after immersion in acetone. The correlation analysis and the comparison with the causal relationship between Cu concentration and the chlorophyll a/b ratio suggest that the reason for the decrease in FL intensity with increasing Cu concentration is a structural change of the fluorescent substances by accumulated Cu. These findings lead to a better understanding of the relationship between the FL of S. sorediiferum and its Cu concentration and provide new insights into fluorescent lichen substances.

Groundwater is a major resource for water supply in Canada, and 43 of 68 Saskatchewan municipalities rely on groundwater or combined groundwater and surface water sources. The Regina landfill is built on top of the Condie aquifer, without an engineered liner. Missing data and inconsistent sampling make a traditional groundwater assessment difficult. An integrated statistical approach using principle component analysis, correlation analysis, ion plots, and multiple linear regression is used to study groundwater contamination at the Regina landfill. Geological locations of the water samples were explicitly considered. The abundance of cations in the groundwater was Ca²⁺ > Mg²⁺ > Na⁺ > K⁺ > Mn²⁺; and for anions SO₄²⁻ > HCO₃⁻ > Cl⁻. Correlation analysis and ion plots pointed to gypsum and halite dissolution being the main factors affecting groundwater chemistry. Principal component analysis yielded three principal components, responsible for 80.7% of the total variance. For all monitoring well groups, the sodium absorption ratio was generally less than one. The variation in the ratio from monitoring well groups suggests possible groundwater contamination from landfill operation. Wilcox diagrams indicate groundwater near the landfill is unsuitable for irrigation. A two-step multiple linear regression was used to develop a model for total hardness prediction.

Oyster shells are a type of biogenic materials with excellent characteristics in surface area, porosity, sorption capacity, and high concentration of CaCO₃ (up to 90 wt%), and can be easily converted into a calcium-based alkali adsorbent. In this research, oyster shells calcined at 900 °C were applied as an adsorbent for acid green 25 (AG25) removal from aqueous solutions. The adsorption performances were evaluated, and the FTIR, SEM, and BET techniques were employed to characterize this material. Results showed that AG25 removal performance depended on adsorbent dosage, pH, adsorption temperature, contact time, and initial concentration. Adsorption capacity was maximized at 34.1 mg g⁻¹ at pH of 11.0, an adsorbent dosage of 2.0 g L⁻¹, an AG25 concentration of 70 mg L⁻¹, and adsorption temperature of 40 °C. Both the Ho-McKay model and the pseudo-second-order model correlated with the adsorption kinetics well with the values of R² > 0.99 (closer to unity). The Langmuir isotherm showed an excellent correlation coefficient of R² > 0.99 with the equilibrium data. The thermodynamics study indicates that the adsorption was spontaneous and endothermic. These results demonstrate that the calcined oyster shells has the potential to be used as an eco-friendly and low-cost effective adsorbent for anionic dye removal from water.

Freshwater lakes are important reservoirs for antibiotic resistance genes (ARGs). In this study, we determined the ARG profiles in water samples from Ying Lake, China, using high-throughput quantitative PCR. The high prevalence of ARGs suggested significant pollution with ARGs in the study area, where the ARG diversity and abundance were greater in an area with box-type fish farming than an area with fenced fish farming. Network analysis indicated the widespread co-occurrence of ARGs and mobile genetic elements. cphA-01, blalMP02, and blaCMY202 were identified as adequate indicator genes for estimating the total ARG abundances. Redundancy analysis indicated that changes in the microbial communities caused by variations in the physicochemical parameters with different fish culture methods mainly determined the ARGs in the lake system. Thus, analyzing the factors that affect ARGs provided novel insights into the mechanisms responsible for the maintenance and propagation of ARGs in a lake.

The maximisation of the efficiency of the photovoltaic system is crucial in order to increase the competitiveness of this technology. Unfortunately, several environmental factors in addition to many alterable and unalterable factors can significantly influence the performance of the PV system. Some of the environmental factors that depend on the site have to do with dust, soiling and pollutants. In this study conducted in the city centre of Kraków, Poland, characterised by high pollution and low wind speed, the focus is on the evaluation of the degradation of efficiency of polycrystalline photovoltaic modules due to natural dust deposition. The experimental results that were obtained demonstrated that deposited dust-related efficiency loss gradually increased with the mass and that it follows the exponential. The maximum dust deposition density observed for rainless exposure periods of 1 week exceeds 300 mg/m² and the results in efficiency loss were about 2.1%. It was observed that efficiency loss is not only mass-dependent but that it also depends on the dust properties. The small positive effect of the tiny dust layer which slightly increases in surface roughness on the module performance was also observed. The results that were obtained enable the development of a reliable model for the degradation of the efficiency of the PV module caused by dust deposition. The novelty consists in the model, which is easy to apply and which is dependent on the dust mass, for low and moderate naturally deposited dust concentration (up to 1 and 5 g/m² and representative for many geographical regions) and which is applicable to the majority of cases met in an urban and non-urban polluted area can be used to evaluate the dust deposition-related derating factor (efficiency loss), which is very much sought after by the system designers, and tools used for computer modelling and system malfunction detection.