In this work, photocatalytic degradation of two reactive dyes, Reactive Yellow 84 (RY 84) and Reactive Black 5 (RB 5), on FeTiO₃/TiO₂ heterojunction in the presence of UV–visible radiation and H₂O₂ has been reported. FeTiO₃/TiO₂ heterojunction has been prepared from ilmenite FeTiO₃ and anatase TiO₂ by employing oxalic acid as an organic linker. FeTiO₃/TiO₂ ratios have been varied from 1 to 5 wt.%, and the materials were characterized by X-ray diffraction, scanning electron microscope and diffused reflectance UV–visible spectroscopic analysis. The photocatalytic activity of FeTiO₃/TiO₂ heterojunction for the degradation of the organic dyes RY 84 and RB 5 in the presence of UV–visible light was found to be higher than that of pure TiO₂. The addition of H₂O₂ increases the rate of degradation of both dyes on FeTiO₃/TiO₂ heterojunction. It facilitates the fast degradation of dye solutions even when their concentration was above 100 mg/l, which is otherwise very slow due to the low transmittance of light by the dye solution. The extent of mineralisation of the reactive dye during photocatalytic degradation was estimated from chemical oxygen demand analysis. FeTiO₃/TiO₂ heterojunction photocatalyst was also found to have good photostability; the material retains almost 97 % of its initial activity even in the fifth cycle.

The presence of macrolide antibiotics in aquatic environments causes serious antibiotic resistance propagation in microorganisms. In this study, the use of porous resins as adsorbents for the removal of tylosin from aqueous solutions was evaluated. The effectiveness of the resins (macroporous resin XAD-4, hypercross-linked resin MN-202, and aminated polystyrene resin MN-150) was compared with commercial hydroxylated multiwall carbon nanotubes (H-MWCNTs). Similar patterns of pH-dependent adsorption were observed despite the different surface properties and pore structures of the three resins, implying the importance of the tylosin molecular form in the adsorption process. Tylosin adsorption onto the four adsorbents showed different ionic strengths and temperature dependence consistent with the tylosin speciation and corresponding adsorption mechanism. The adsorption of tylosin onto the XAD-4 and MN-202 is mainly controlled by the intermolecular interactions between the matrix of the adsorbents and the tylosin molecule, whereas specific bonds among multiple surface functional groups are the predominant contributors to MN-150 and H-MWCNTs. The pore size is the key parameter in tylosin adsorption onto the surface of the adsorbents. The adsorption kinetics of the four adsorbents followed the pseudo-second-order model. The adsorption isotherm data well fit the Langmuir models, indicating surface coverage by a monomolecular layer.

Colistin is a peptide antibiotic widely used as a food additive in animal farming, specially swine and poultry, and also has recently been applied in human medicine to treat infections caused by multiresistant gram-negative bacteria strains. When orally administered, colistin is eliminated in feces virtually unaltered; thus, it may reach water bodies and wastewater treatment facilities in its active form. Apart from the risks associated with development of antimicrobial resistance and environmental toxicity issues, the presence of antimicrobials in wastewater can, additionally, interfere in biological processes commonly used to treat them. Nitrifying bacteria are among the most sensitive microorganisms to inhibitory compounds, including pharmaceuticals, and are useful as biosensors to access contaminant toxicity information in wastewater treatment plants. Therefore, in order to assess the colistin acute toxicity to the microorganisms involved in the nitrification processes, the nitritation and nitratation kinetics were monitored under different colistin concentrations. The results showed that only ammonia-oxidizing bacteria are sensitive to the antibiotic, presenting an IC50 of 10.8 mg L⁻¹ of colistin when used as a commercial formulation and 67.0 mg L⁻¹ when used as raw colistin sulfate. For nitrite-oxidizing bacteria, even the highest colistin concentration used in the assays (316 mg L⁻¹) was not sufficient to inhibit the process. According to these results, the colistin concentrations expected in animal farming wastewater, when its dosage is used as a growth promoter, would not be enough to keep nitrification from taking place. Nevertheless, when used in higher concentrations, such as for therapeutic purposes, it could endanger the maintenance of the process.

Coal mine methane is a significant greenhouse gas source as well as a potential lost energy resource if not effectively used. In recent years, mine ventilation air (MVA) capture and use has become a key element of research and development due to comparatively larger methane emissions by MVA than other coal mine sources. Technologies have been evaluated to treat the low methane concentrations in MVA such as thermal-based technologies or processing by biofiltration. This review initially considers the techniques available for treating the low methane concentrations encountered in MVA, after which it focuses on developments in biofiltration systems. Biofiltration represents a simple, energy-efficient, and cheap alternative to oxidize methane from MVA. Major factors influencing biofilter performance along with knowledge gaps in relation to its application to MVA are identified and discussed.

The present study deals with the effect of trace metals on the endangered limpet Cymbula nigra. The Bay of Algeciras (Strait of Gibraltar) was used as the study site. Important industrial activity takes place in the area, including frequent oil spills. However, it is home to important populations of C. nigra. The objective of this work was to determine if these animals were being affected at a subcellular level by the pollutants present in their environment and to analyze the trace metal concentrations in the animal’s soft tissues. To determine the effects of water quality on the antioxidant activity and concentrations through field experimentation, a total of six sites were selected in Algeciras Bay, three located in the inner areas (environmentally degraded sites with higher levels of pollutants) and three in the outermost areas of the Bay. Stress associated to reactive oxygen species formation was assessed on digestive glands and gills as the enzymatic antioxidant activity of catalase (CAT), superoxide dismutase (SOD), and glutathione S-transferase (GST) and as the concentrations of lipid-soluble (α-tocopherol and β-carotene) and the water-soluble antioxidants (reduced and oxidized glutathione (GSH and GSSG)). Gills and digestive glands of those animals located in the inner areas of Algeciras Bay showed higher CAT activity values than those located in the outer areas. As a general pattern, we observed higher antioxidant activities and concentrations in digestive glands that in gills, suggesting the possibility that pollutants are mainly being incorporated by limpets through the food. As a general rule, larger animals showed greater concentrations of these compounds. Iron, zinc, and manganese, in this order, were present in the tissues at the highest concentrations. Chromium and manganese were found in significantly higher concentrations in those animals collected from the inner areas of the Bay. Through the present study, we provide the first data regarding the antioxidant defense levels and metal accumulation capacity of this species, and we reinforce the idea that this endangered species may be, in fact, relatively tolerant to degraded environments.

Stormwater is a potential and readily available alternative source for potable water in urban areas. However, its direct use is severely constrained by the presence of toxic pollutants, such as heavy metals (HMs). The presence of HMs in stormwater is of concern because of their chronic toxicity and persistent nature. In addition to human health impacts, metals can contribute to adverse ecosystem health impact on receiving waters. Therefore, the ability to predict the levels of HMs in stormwater is crucial for monitoring stormwater quality and for the design of effective treatment systems. Unfortunately, the current laboratory methods for determining HM concentrations are resource intensive and time consuming. In this paper, applications of multivariate data analysis techniques are presented to identify potential surrogate parameters which can be used to determine HM concentrations in stormwater. Accordingly, partial least squares was applied to identify a suite of physicochemical parameters which can serve as indicators of HMs. Datasets having varied characteristics, such as land use and particle size distribution of solids, were analyzed to validate the efficacy of the influencing parameters. Iron, manganese, total organic carbon, and inorganic carbon were identified as the predominant parameters that correlate with the HM concentrations. The practical extension of the study outcomes to urban stormwater management is also discussed.

Removal of petroleum hydrocarbon (PHC) contamination that is hazardous and often prevalent in soils would benefit from a rapid detection technique. Visible and near-infrared spectroscopy (VIS-NIRS) has a large potential as a rapid detection technique for PHC in soils. Nevertheless, the combined influence of oil concentration, moisture content and clay content on soil reflectance spectra and the accuracy of the technique have yet received little attention. The objective of this study was to investigate the combined influence of oil concentration and moisture and clay contents on the spectral characteristics of diesel-contaminated soils and the quality of calibration models developed for polycyclic aromatic hydrocarbons (PAH) in soils using VIS-NIRS. With partial least-squares regression data from a systematic experimental design using 150 artificially contaminated soil samples, results showed that soil diffuse reflectance decreased with increasing oil concentration, clay and moisture contents. The trend was less defined in relation to moisture and clay due mainly to the interaction effects of the soil matrices as mediated by the oil. The PAH partial least squares cross-validation showed best performance with the lowest oil concentration and clay content at 20 % moisture with r ² of 0.89, root mean square error of prediction of 0.201 mg/kg and ratio of the standard error of prediction to the standard deviation of the reference data in the validation set of 2.75. Analysis of variance showed that the interaction effects of oil concentration, moisture and/or clay content significantly (p < 0.05) affected the quality of the PAH models.

Buenos Aires Province (República Argentina) has undergone, in the last years, a great increase in agricultural activities based on the incorporation of new technologies and reduction of diversity to meet the increasing food demand. The increase of intensive agricultural systems in Argentina involves the use of fertilizers and pesticides such as herbicides, insecticides, and fungicides. Chlorpyrifos is one of the insecticides most widely used in these crops and constitutes a risk for human health, birds, and aquatic biota such as macroinvertebrates and fishes. In order to assess the possible contamination that the use of this product may represent for the environment, it is necessary to study its interaction with the different types of soils because fate and transport of environmental pollutants may be influenced by their interactions with soil particles. The behavior of chlorpyrifos was analyzed through the study of the recoveries from spiked solid environmental matrices. A strong dependence with organic matter content was observed along with an important dependence with the initial concentrations employed. Here, we show that chlorpyrifos behavior on solid matrices not only depends on soil chemical composition. A significant dependence of recovery percentages with initial concentrations of the pesticide was evident in all cases. Recovery percentages decreased with an increase of the initial concentration employed, no matter the variations in matrices of chemical compositions.

In this work, a coal combustion ash (CCA) has been tested as an alternative low-cost sorbent to commercial activated carbons (GAC) for cadmium and zinc removal from polluted water. To this aim, the effect of pH and metal concentration on CCA adsorption capacity has been investigated, and a comparative analysis with GAC has been carried out in the same experimental conditions. Furthermore, in order to improve CCA adsorption capacity, two different activation treatments of raw CCA have been tested. In particular, the CCA was subjected to a gasification process conducted with steam and to different acidic treatments, conducted either with hydrochloric acid or nitric acid at different acid concentrations. Experimental results showed that all the acid treatments determined a substantial reduction of both cadmium and zinc adsorption capacity. Differently, the steam gasification determined a substantial increase in adsorption capacity with respect to raw CCA, in particular for zinc as its adsorption capacity resulted even higher than the correspondent of GAC. Finally, a thorough analysis of sorbent physical and chemical properties and of adsorption data allowed the individuation of the main cadmium/zinc adsorption mechanism both on CCA and activated carbon, adequately described by the Freundlich model.

N-Nitrosodimethylamine (NDMA) is recently defined as one of nitrogenous disinfection by-products with high carcinogenicity and can be frequently detected in finished water. The decomposition of NDMA in water using nanoscale zero-valent iron (NZVI) in the presence of aluminum and iron salts was investigated in this paper. The results showed that some salts can enhance the removal of NDMA by commercial NZVI in the order of Al(SO) >> AlCl > FeSO > NaSO ≈ NZVI alone, and the highest NDMA removal was 87.3 % in the presence of Al(SO). NDMA removal varied with the addition of Al(SO), NZVI dosage, initial NDMA concentration, solution pH, and temperature. The reduction of NDMA increased with the dosage of Al(SO) and NZVI, which follows a pseudo-first-order kinetics model. The removal of NDMA by NZVI was higher in acidic pHs than in alkaline ones, and the highest removal was found at pH 5. Higher reaction temperature can improve the removal of NDMA and reduce the reaction time. Based on the total nitrogen balance, most nitrogen of NDMA was converted to ammonium and dimethylamine.