The present work investigates the potential of two experimental field columns (FC-2 and FC-4) to reduce volatile organic compound (VOC) emissions from a municipal solid waste (MSW) landfill located in Quebec, Canada. The FC-2 and FC-4 were fed by raw biogas coming from the landfill site. The VOC were identified and quantified in emitted biogas and raw biogas. The emitted biogas was collected at the surface of FC-2 and FC-4, and the raw biogas was obtained directly from the well. The main groups of the VOC in the landfill biogas are BTEX (66 %), alkanes (19 %), cyclic compounds (10 %), and halogenated compounds (5 %). The concentration of VOC in the landfill raw biogas varies from below the limit of detection (BLD) to 22 ppmv, and that of the emitted biogas varies from BLD to 3.1 ppmv. The result of this study showed that the experimental field columns had a very high potential to reduce the VOC emissions from the investigated landfill. The effectiveness of the VOC emission removal for the FC-2 and FC-4 was shown to be practically 100 % for many compounds. The experimental field column elimination capacity of VOC emissions is in the range of 0.1 to 4.6 mg m⁻³ h⁻¹.

Indoor air pollution significantly influences personal exposure to air pollution and increases health risks. Nitrogen dioxide (NO₂) is one of the major air pollutants, and therefore it is important to properly determine indoor concentration of this pollutant considering the fact that people spend most of their time inside. The aim of this study was to assess indoor and outdoor concentration of NO₂ during each season; for this purpose, passive sampling was applied. We analyzed homes with gas and electric stoves to determine and compare the concentrations of NO₂ in kitchen, living room, and bedroom microenvironments (MEs). The accuracy of passive sampling was evaluated by comparing the sampling results with the data from air quality monitoring stations. The highest indoor concentration of NO₂ was observed in kitchen ME during the winter period, the median concentration being 28.4 μg m⁻³. Indoor NO₂ levels in homes with gas stoves were higher than outdoor levels during all seasons. The concentration of NO₂ was by 2.5 times higher in kitchen MEs with gas stoves than with electric stoves. This study showed that the concentration of NO₂ in indoor MEs mainly depended on the stove type used in the kitchen. Homes with gas stoves had significantly higher levels of NO₂ in all indoor MEs compared with homes where electric stoves were used.

Lignin-derived methoxyphenols (MPs) with Fe³⁺-reducing activity were used as potential mediators to increase the decolorization of dyes by classical Fenton (Fe²⁺/H₂O₂) and Fenton-like reactions (Fe³⁺/H₂O₂). In this study, several MPs such as vanillin, vanillic alcohol, syringaldehyde, ferulic, vanillic, and syringic acids were evaluated. The results showed that all MPs displayed similar prooxidant activities in the decolorization of methylene blue, chromotrope 2R, methyl orange, and phenol red. For example, the reaction performed with Fe³⁺/H₂O₂ decolorized 27 % of chromotrope 2R, whereas the treatments with Fe³⁺/H₂O₂/MP decolorized around 70 % of the same dye after 60 min. For Fe²⁺/H₂O₂ systems, two stages of decolorization were visibly observed. In the first stage, the MPs inhibited the treatments, and then they increased the decolorization rate in the second stage. Prooxidant and antioxidant properties were observed for decolorization of methylene blue performed in the presence of low and high concentrations of vanillin, respectively. Overall, the MPs increased dye decolorization without increasing the consumption of H₂O₂.

Textile wastewater was treated by adsorption in batch and column systems using electrochemically modified montmorillonite clay and activated carbon. Textile wastewater was obtained from a denim manufacturing process; according to the characterization of wastewater, non-biodegradable organic matter was found and it limits the application of biological treatments, and then an alternative method was evaluated. The adsorption process was performed with natural and modified materials; iron-modified montmorillonite was prepared at pH 7 using iron electrodes and activated carbon was treated with copper electrodes at pH 2, and 10–12 % of iron and copper respectively were found in the modified materials. Adsorption kinetics and isotherms of chemical oxygen demand (COD), color, and total organic carbon (TOC) were evaluated; the adsorption capacities for color were 50, 37, and 44 U PtCo/g for natural clay, activated carbon, and iron-modified clay, respectively. Adsorption kinetics of COD, color, and TOC data were best adjusted to Elovich model and isotherms data to Freundlich model, indicating chemisorption on heterogeneous materials. The regeneration of materials was performed in the presence and absence of hydrogen peroxide. Continuous systems were evaluated for color and TOC. Fe-modified clay was the best adsorbent, and data were best adjusted to Thomas and Yoon-Nelson models.

Volatile organic compounds (VOCs) decomposition by non-thermal plasma (NTP) has been receiving increasing attention from the scientific communities due to its advantages of easy operation, high efficiency, energy saving, and non-secondary pollution. But most of the researches are doing experiments and existing experiment methods cannot observe the micro physical and chemical processes. In order to make up for the deficiency of the experiment, herein, a numerical method was developed to analyze the decomposition behavior of HCN, C₃H₃N, C₃H₈, C₃H₆, CO, and NO in the VOCs treatment by NTP. Results indicated that increasing electron density or energy was beneficial to VOCs decomposition, but when the electron density and energy was too high, the promotion would be weakened. The influences of initial concentration of O₂ and H₂O on different VOCs decomposition were totally different. The increase of initial concentration of oxygen was beneficial to the decomposition of HCN, C₃H₈, CO, and NO, but the high concentration of oxygen could promote to generate C₃H₆ at the initial reaction stage. The decomposition of HCN and C₃H₃N are not restricted by dry or wet conditions, but the increase of the concentration of water vapor is advantageous to the decomposition of C₃H₈, CO, and NO. Graphical Abstract ᅟ

We conducted a field experiment to determine whether application of biosolids (municipal sewage sludge) to degraded areas of the Brazilian Atlantic rainforest had the potential to contaminate native forest species with trace metals in the sandy soils of the region. Treatments consisted of 0, 2.5, 5, 10, 15, and 20 dry Mg biosolids ha⁻¹, with nine native pioneer, secondary, and climax tree species assessed for metal uptake: capixingui, aroeira-pimenteria, canafístula, cedro-rosa, mutamba, angico-vermelho, copaíba, jatobá, and jequitibá. Biosolid application did not have a statistically significant effect on metal concentrations in soil, and Cd was the only metal with increased availability. No increased metal uptake was seen in tree foliage sampled at 6 and 12 months after application. Additional longer-term study is recommended; however, the results of this study indicate biosolids could be used in Atlantic rainforest reclamation in degraded sandy soils with little impact on soil accumulation and tree uptake of trace metals.

This study evaluated the seed germination and dry mass accumulation of five plant species (Brassica napus L., Brassica rapa L., Celosia cristata L., Tagetes erecta L., and Calendula officinalis L.) grown in five mine tailings collected from Zacatecas, Mexico. Sampled mines were El Bote, Noria de San Pantaleon, Noria de Angeles, Vetagrande, and El Bordo-El Lampotal, in which Pb (3.9–69.7 mg kg⁻¹), As (0.7–26.2 mg kg⁻¹), Hg (0.05–0.10 mg kg⁻¹), and Au (0.01–0.02 mg kg⁻¹) were detected. The most abundant elements at each mine site were as follows: Pb and Au (3.9 and 0.023 mg kg⁻¹, respectively) for El Bote; As, Pb, and Hg (7.4, 6.1, and 0.10 mg kg⁻¹, respectively) for the Noria de San Pantaleon; Pb, As, and Hg (69.7, 26.2, and 0.08 mg kg⁻¹, respectively) for Noria de Angeles; Pb (20.8 mg kg⁻¹) for Vetagrande; and Pb (5.3 mg kg⁻¹) for El Bordo-El Lampotal. Both Noria de Angeles and Vetagrande mine tailings had high values of sodium, sulfates, and electrical conductivity, chemical properties that impaired seed germination and dry mass accumulation. Regardless the mining tailings, B. napus showed high seed germination (66 %), tolerance, growth, and total dry mass accumulation (0.041 g). Either B. napus or C. cristata has good potential for stabilizing or recovering metals from mine tailings.

Accumulation of divalent manganese (Mn) and its toxicity in the green alga Scenedesmus quadricauda was studied at circumneutral pH (6.5). A comparison of two applied concentrations (10 or 100 μM) of MnCl₂, MnSO₄, and Mn(NO₃)₂ indicated that mainly sulfate evoked higher Mn accumulation. On the other hand, nitrate rather depleted antioxidative enzyme activities (APX, CAT, SOD), leading to an increase in ROS formation as proven by fluorescence microscopy. Subsequent experiments revealed that increase in pH (from 4.5 to 9.5) increased also Mn content but typically depleted amounts of reduced glutathione and phytochelatin 2. We also measured the size of particles formed from the manganese salts at pH 9.5. Competitive experiment between Ca/K salts (CaCl₂, CaSO₄, Ca(NO₃)₂, KCl, K₂SO₄, KNO₃) and Mn (as Mn sulfate) showed a negative relation between Ca and Mn amount but KNO₃ stimulated Mn accumulation. Microscopy revealed that mainly K salts elevated plasma membrane damage (Acridine orange staining). Data indicate that not only pH but also accompanying anion affects Mn accumulation and that Ca salts may affect Mn toxicity.

Titania/silica nanomaterials have many possible applications; however, they can be toxic to living organisms, particularly if the material accumulates in niche environments, e.g. areas colonised by actinomycetes. This study therefore investigated the effect of non-activated and UV light-activated titania/silica nanospheres on an environmental Streptomyces strain. The bacteria were incubated with the nanospheres and subsequently cultured on solid medium. The morphology and elemental composition were analysed using optical and electron microscopy (TEM, STEM) and energy-dispersive X-ray spectroscopy (EDX). The appearance of Streptomyces sp. in the experimental and control samples demonstrated that the nanospheres did not have bactericidal properties in the used dose. Furthermore, the observed strain not only survived in the presence of the nanomaterial but also appeared to play a role in its dissolution with an accumulation of the titanium in the intracellular globules of polyphosphate (volutin). Additionally, it was discovered that the UV light-activated titanium dioxide altered the ability of the bacteria to secrete humic acid. The reported phenomenon might be made possible through an accumulation of titanium in the volutin compounds. These findings suggest that streptomycetes could be employed to participate in the dissolution of nanomaterials which enter the natural environment.