Solid-phase extraction (SPE) on activated carbon derived from coconut shell (CSAC) for the preconcentration of four varying polarity pesticides (imidacloprid, acetamiprid, simazine, and linuron) prior to their determination using high performance liquid chromatography with diode array detector (HPLC-DAD) was investigated. The characteristics of the CSAC were analyzed through X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), and Brunauer-Emmett-Teller (BET) method. The effects of the solution pH, eluent type, eluent volume, and flow rate were investigated for optimization of the presented procedure. The adsorption was achieved quantitatively on the CSAC column in the pH range of 2.0–7.0, and then the retained pesticides were eluted with dichloromethane. The detection limit was found to be 0.025–0.039 μg L⁻¹, depending on the pesticide. The proposed SPE-CSAC method was used to determine selected pesticides in tap water samples. The recoveries ranged from 58.2 to 105.3%, with low relative standard deviations. The obtained results indicated that the CSAC could be efficiently used as a low cost alternative to commercially available SPE adsorbents for the determination of the varying polarity pesticides in environmental water samples at trace levels.

This study aimed to determine the mycoremediative capacity of filamentous fungi consortia in landfill heavy metal contaminated soil. Streak plate method was utilized for the isolation of fungi from the landfill soil. Isolates were identified using morphological and molecular techniques. Heavy metal tolerance of the fungi was determined using radial growth diameter technique. Twelve species of landfill indigenous fungi were used for the bioremediation process. Two categories of fungi consortia namely highly tolerant fungi (Perenniporia subtephropora, Daldinia starbaeckii, Phanerochaete concrescens, Cerrena aurantiopora, Fusarium equiseti, Polyporales sp., Aspergillus niger, Aspergillus fumigatus, and Trametes versicolor) and moderately tolerant fungi (Paecilomyces lilacinus, Antrodia serialis, and Penicillium cataractum) were used to amend the contaminated soil; meanwhile, the unamended soil served as control. Maximum tolerance index of 1.0 was reported in Cr-, Cu-, and Fe-amended PDA medium. Meanwhile, the maximum heavy metal bioremoval efficiencies were for highly tolerant fungal consortium treated soil and were recorded as As (62%) > Mn (59%) > Cu (49%) > Cr (42%) > Fe (38%). Likewise, the maximum metal removal rate constant (K) and the half-lives (t₁/₂) were 0.0097/day 71 days, 0.0088/day 79 days, 0.0067/day 103 days, 0.0054/day 128 days, and 0.0048/day 144 days for As, Mn, Cu, Cr, and Fe, respectively, which were all for soil treated with consortium of highly tolerant fungi (P. subtephropora, D. starbaeckii, P. concrescens, C. aurantiopora, F. equiseti, Polyporales sp., A. niger, A. fumigatus, and T. versicolor). Spectra analysis revealed a clear distinction in the functional groups between the fungal treated and the untreated soils. Peaks at 874 ± 2 cm⁻¹ and 1425 ± 2 cm⁻¹ were only found in fungi amended soil. Physicochemical parameters mainly pH and redox potential played a key role in the bioremediation process, and bioaccumulation was believed to be the favored mechanism for the metal bioremoval. The data are suitable for assessing the contribution of bioaugmentation with consortia of fungi. It is equally important for assessing the synergistic effect of fungi on the reduction of extractable heavy metals in contaminated soil.

Two smelters in the North of France emitted potentially toxic metals for more than a century and today, the resulting contamination represents a risk to human health and affects also the biodiversity. To limit health risks and to improve the soil quality, a study using calcium phosphates (monocalcium phosphate, dicalcium phosphate and a mixture of both salts) and Lolium perenne L was conducted. Through this preliminary investigation, we will try to shed some light about (i) the effects of a sustainable amount of calcium phosphates on the agronomic, biological (microbial and fungi communities) and physiological parameters (chlorophyll a and b, antocyanins, carotenoids) as well as the phytoavailability of potentially toxic metals and nutrients in time, and (ii) the potential use of contaminated biomass from ryegrass as a source of new valorisation ways instead of using it as contaminated compost by gardeners. Although slight variations in pH and significant increases of assimilable phosphorus after adding calcium phosphates were registered, the physiology of plants and the biological parameters were statistically unchanged. The germination of the ryegrass seeds was favoured with calcium phosphates regardless the contamination level of the studied soils. No clear effects of calcium phosphates on the microbial and fungi communities were detected. In contrast, results indicated relationships between the physicochemical parameters of soils, their contamination level and the composition of fungal communities. Indeed, for one of the soils studied, calcium could limit the transport of nutrients, causing an increase in fungi to promote again the transfer of nutrients. Surprisingly, the phytoavailability of Pb increased in the most contaminated soil after adding dicalcium phosphate and the mixture of phosphates whereas a slight decrease was highlighted for Cd and Mn. Although minor changes in the phytoavailability of potentially toxic metals were obtained using calcium phosphates, the ability of ryegrass to accumulate Zn and Ca (up to 600 and 20,000 mg kg⁻¹, respectively) make possible to qualify this plant as a bio ‘ore’ resource.

The California Department of Pesticide Regulation conducted indoor air monitoring to estimate sulfury fluoride (SO₂F₂) emissions that bystanders around fumigated houses were potentially exposed to during structural fumigation of residential houses. Monitoring was conducted for 23 fumigations between September 2014 and March 2015. The SO₂F₂ indoor concentrations were measured from four locations inside the fumigated houses once an hour. The decreases of indoor concentrations are due to gas leakage (treatment period) and aeration (aeration period) from the structure to the outdoor environment. Analysis on the monitoring data showed considerable variability of half loss time (11–60 h) and mass loss (22–81%) during treatment periods. The decline of indoor concentrations followed the first-order kinetics; therefore, the hourly flux (g/m²s) of a treatment period can be calculated using initial SO₂F₂ concentration, treatment period mass loss, and house height. Although the California Aeration Plan requires a minimum 12–24 h of aeration after a treatment, the monitoring data showed that 93 ± 5% of the mass at the end of the treatment periods was emitted through the ducting system within the first 2 h. The average ratio of the loss amount in the first hour to the loss in the second was 6:1. These monitoring results provided the critical input for the computer modeling to estimate bystander exposure during structural fumigations of residential houses.

A range of different studies has been performed in order to design and develop photocatalysts that work efficiently under visible (and near-infrared) irradiation as well as to improve photons absorption with improved reactor design. While there is consensus on the importance of photocatalysis for environmental applications and the necessity to utilized solar irradiation (or visible-light) as driving force for these processes, it is not yet clear how to get there. Discussion on the future steps towards visible-light photocatalysis for environmental application is of great interest to scientific and industrial communities and the present paper reviews and discusses the two main approaches, band-gap engineering for efficient solar-activated catalysts and reactor designs for improved photons absorption. Common misconceptions and drawbacks of each technology are also examined together with insights for future progress.

Deca-bromodiphenyl ether (BDE-209) regulates various aspects of spermatogenesis and male fertility through its effect on estrogen receptor α (ERα), but the underlying mechanism remains unclear. Because molecular mechanisms such as remodeling of the blood-testis barrier (BTB) play crucial roles in spermatogenesis, we investigated the disruptive effects of ERα agonists on the BTB in spermatogenesis. In this study, 0, 300, and 500 mg/kg/day of BDE-209 were administered to pregnant adult mice by oral gavage from gestation day 7 to postnatal day 21. SerW3 cells were treated with methylpiperidino pyrazole (MPP) for 30 min before being treated with 50 μg/mL of BDE-209. BDE-209 increases ERα in time- and dose-dependent manners and decreases formin 1 and BTB-associated protein in F1 male mice. Furthermore, BDE-209 impairs the structure and function of the BTB. Activation of ERα signaling could disrupt the BTB, leading to spermatogenesis dysfunction. The results identified the role of ERα in BTB disruption during spermatogenesis and suggested that BTB disruption occurs because of exposure to BDE-209, which could potentially affect spermatogenesis. In conclusion, Sertoli cells seem to be the primary target of BDE-209 in the perinatal period, and this period constitutes a critical window of susceptibility to BDE-209. Also, the SerW3 cell model may not be a particularly useful cell model for studying the function of the cytoskeleton.

The novel waste alkaline battery-sawdust-based adsorbents (WABAs) are prepared by a two-stage activation method with the negative electrode materials as activator and different doping ratio of the positive electrode materials and pine sawdust as raw materials. The characteristics of the WABAs are analyzed by SEM, XRD, FT-IR, and specific surface determination (SBET). The Pb²⁺ adsorption properties of the WABAs are studied by changing the pH of solution, contact time, initial concentration, and temperature. It turns out that when the doping mass ratio is 1:4, the optimum performance of the WABAs is obtained, and comparing with the samples prepared by pure biomass, the iodine adsorption value, total acid groups, and cation exchange capacity (CEC) separately increased by 13, 106, and 22%, respectively. Kinetic studies show that the pseudo-second-order model is more suitable for describing the Pb²⁺ adsorption process and the Langmuir isotherm provides better fitting to the equilibrium data. The thermodynamic parameters indicate the adsorption process would be spontaneous and endothermic. Besides, the prepared WABAs could be reused for 5 cycles with high removal efficiency. This study provides an alternative route for waste alkaline battery treatment. Graphical abstract The schematic diagram of synthesis of waste batteries-sawdust-based adsorbent via a two-stage activation method for Pb²⁺ removal

Hexavalent chromium contamination of groundwater is a worldwide problem caused by anthropogenic and natural processes. We report the rate of Cr(VI) removal by two humic acids (extracted from Miocene age lignite and younger peat soil) in aqueous suspensions across a pH range likely to be encountered in terrestrial environments. Cr(VI) was reduced to Cr(III) in a first-order reaction with respect Cr(VI) concentration, but exhibited a partial order (~ 0.5) with respect to [H+]. This reaction was more rapid with the peat humic acid, where Cr(VI) reduction was observed at all pH values investigated (3.7 ≤ pH ≤ 10.5). ¹³C NMR and pyrolysis GC-MS spectroscopy indicate that the reaction results in loss of substituted phenolic moieties and hydroxyl groups from the humic acids. X-ray absorption spectroscopy indicated that at all pH values the resulting Cr(III) was associated with the partially degraded humic acid in an inner-sphere adsorption complex. The reaction mechanism is likely to be controlled by ester formation between Cr(VI) and phenolic/hydroxyl moieties, as this initial step is rapid in acidic systems but far less favourable in alkaline conditions. Our findings highlight the potential of humic acid to reduce and remove Cr(VI) from solution in a range of environmental conditions.

1,3,5-Tris-(2,3-dibromopropyl)-1,3,5-triazine-2,4,6-trione (TDBP-TAZTO) is an emerging brominated flame retardant which is widely used in several plastic materials (electric and electronic equipment, musical instruments, automotive components). However, until today, no photochemical studies as well as the identification of possible phototransformation products (PTPs) were described in literature. Therefore, in this study, UV-(C) and simulated sunlight irradiation experiments were performed to investigate the photolytic degradation of TDBP-TAZTO and to identify relevant PTPs for the first time. The UV-(C) irradiation experiments show that the photolysis reaction follows a first-order kinetic model. Based on this, the photolysis rate constant k as well as the half-life time t₁/₂ were calculated to be k = (41 ± 5 × 10⁻³) min⁻¹ and t₁/₂ = (17 ± 2) min. In comparison, a minor degradation of TDBP-TAZTO and no formed phototransformation products were obtained under simulated sunlight. In order to clarify the photochemical behavior, different chemicals were added to investigate the influence on indirect photolysis: (i) H₂O₂ for generation of hydroxyl radicals and (ii) two quenchers (2-propanol, sodium azide) for scavenging oxygen species which were formed during the irradiation experiments. Herein, nine previously unknown PTPs of TDBP-TAZTO were detected under UV-(C) irradiation and identified by HPLC-(HR)MS. As a result, debromination, hydroxylation, and dehydrobromination reactions could be presumed as the main degradation pathways by high-resolution mass spectrometry. The direct as well as the OH radical-induced indirect photolysis were observed. Graphical abstract .

Many recent studies have focused on the influencing factors of the ecological footprint, but less attention has been given to human capital. Human capital, which is based on education and rate of return on education, may reduce the ecological footprint since environmental issues are human-induced. The current study investigates the impact of human capital on the ecological footprint in India for the period 1971 to 2014. The outcomes of the newly developed combined cointegration test of Bayer and Hanck disclose the long-run equilibrium relationship between variables. The findings reveal a significant negative contribution of human capital to the ecological footprint. The results of the causality test show that human capital Granger causes the ecological footprint without any feedback. In addition, energy consumption adds to the ecological footprint, while the relationship between economic growth and ecological footprint follows an inverted U-shaped pattern. The findings unveil the potential to reduce the ecological footprint by developing human capital.