Salt-based preservation is practiced for decades in the leather industry because of its versatility, cost-effectiveness, and availability. The salt removed from the soaking process causes significant pollution including organic and elevated total dissolved solids (TDS). Hence, a low-salt skin preservation method using commercial sodium polyacrylate with a reduced quantity of sodium chloride aiming to retain leather properties and pollution reduction was the principal focus of the study. Commercial sodium polyacrylate initially characterized for water absorption capacity along with structural and functional properties is confirmed by NMR and IR spectroscopic techniques. In preliminary experiments, the process parameters attained optimized conditions of sodium polyacrylate (SPA) quantity (5%), a minimal amount of salt (15%), and contact time (4 h) required for skin preservation. Besides, reusability studies after SPA recovery (95%) were applied to skins with an optimized quantity of SPA and salt subsequently stored for 15 days along with control (40% salt). The results revealed that SPA with low salt aided an adequate curing efficiency with a substantial reduction (> 65%) of TDS and comparable physical and organoleptic properties on par with the conventional method. Overall, SPA supported low-salt skin preservation reduces pollutant load (TDS) caused due to using of 40% sodium chloride in the conventional curing process.

The freezing process consists of dissipating heat from the product until the final temperature is lower than the temperature of crystallisation of that product. Freezing can be used for numerous applications, including for disruption of waste-activated sludge (WAS). The aim of this study was to calculate the estimated amount of heat conveyed between the solidified carbon dioxide and the WAS, in the following ratios: 0.25:1; 0.5:1; 0.75:1 and 1:1. In heat of phase transformations, dry ice sublimation, water solidification, the amount of heat transferred by other substances and heat transferred from the sludge (dry sludge) were taken into account during the process of WAS freezing. Heat changes on the surface of WAS were registered using a thermovision camera. The effectiveness of WAS disintegration was confirmed by several biochemical parameters such as soluble chemical oxygen demand (increase over 14 times), degree of disintegration (48%), proteins (increase over 5 times), carbohydrates (increase almost 7 times), RNA (increase by 2.23 mg L⁻¹), ammonia nitrogen (increase over 23 times), phosphates (increase almost 27 times) and turbidity (increased over 7 times). It was found that dry ice pretreatment of WAS can be an intriguing alternative for the conventional methods used.

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.

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 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.

Accurate determination of emerging contaminants in drinking water constitutes a major environmental challenge for which highly sensitive analytical methods are needed. This work details the development of a novel highly sensitive solid-phase extraction-high performance liquid chromatography-tandem mass spectrometry (SPE-HPLC-MS/MS) method for simultaneous determination of a diverse panel of widely used trace contaminants, including two pharmaceuticals (fluoxetine and gemfibrozil), three pesticides (3-hydroxycarbofuran, azinphos-methyl, and chlorpyrifos), and two hormones (testosterone and progesterone) in water. The method is highly reproducible and sensitive with detection limits at subnanogram per liter level (0.05–0.5 ng/L). It was used to monitor the occurrence of these contaminants in source and drinking water across 18 drinking water treatment facilities in Missouri, USA in 1 year including cold winter and hot summer seasons. The experiment results indicated that all of the monitored contaminant concentrations are very low, lower than or close to the method detection limits, in the selected water treatment facilities. Pesticide concentrations were slightly elevated in some source waters during hot season, whereas slightly higher pharmaceuticals were observed during cold season. The concentrations of two hormones were lower than the limits of detection in all the water samples. These contaminants were present, if any, at below detection limits in all treated drinking water samples analyzed, suggesting that treatment processes effectively removed the contaminants studied herein. Graphical Abstract

Indirect potable reuse systems, which consist of wastewater treatment (WWT) and soil aquifer treatment (SAT), offer advantages such as their low cost and the underground storage of reuse water. In this study, the dissolved organic matter (DOM) profile of a sequential treatment system (i.e. WWT followed by SAT) was investigated using a pilot-scale SAT reactor. In addition, the biological DOM removal characteristics in the vadose zone of the SAT, which were found to play an important role in DOM removal for the entire SAT, were investigated using lab-scale reactors (LSRs). Composition of the removed DOM by WWT and SAT showed that the majority fraction of the removed DOM was different for the WWT (hydrophobic neutral 27.9%) and SAT (hydrophobic acids (HoA) 29.1%), suggesting that SAT exhibits unique DOM removal characteristics that contribute to water reclamation. Biological DOM removal was confirmed using the LSRs, and changes in the DOM removal characteristics 10–20 cm from the top of the vadose zone in the LSRs were revealed on the basis of the DOM fractionation and a BIOLOG assay, suggesting that microbial activity in the lower layer of the vadose zone contributed to the unique removal of the HoA fraction in the SAT.

The composition of SrCuₓO mixed metal oxides (MMOs) was engineered via varying the amount of copper relative to strontium. As-synthesized SrCuₓO were highly active for degrading methyl orange (MO) pollutant at dark ambient conditions without the aid of other reagents. The catalytic activity of SrCuₓO demonstrated a reverse-volcano relationship with copper content. Copper-rich MMOs (SrCu₂O) exhibited the highest degradation activity for MO by far and degraded ca. 96% MO within 25 min. MO degradation over SrCu₂O was a surface-catalytic reaction and fitted pseudo-first-order reaction kinetics. The contact between MO molecules and catalyst surface initiated the reaction via the catalytic-active phase (Cu⁺/Cu²⁺ redox pair), which serves as an electron-transfer shuttle ([Formula: see text]) from MO to dissolved O₂, inducing the consecutive generation of reactive oxygen species, which resulted in MO degradation as evidenced by radical trapping experiment. XPS and XRD analysis revealed that active phases in SrCu₂O materials underwent irreversible transformation after reaction, contributing to the observed deactivation in the cycling experiment. The observations in this study demonstrate the significance of chemical composition tailoring in catalyst synthesis for environmental remediation under dark ambient conditions. Graphical abstract

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 .

The fact that hairdressers are exposed to toxic substances through the handling of creams and smoothing products prompted this study whose aim was to quantify the occupational exposure of hairdressers to formaldehyde by comparing the results of exposure for different types of beauty salon. The study population consisted of 23 beauty salons located in the city of Bauru, São Paulo state, Brazil. The samples were collected by inhaled air tests during the most critical 15-min period of the hair straightening procedure and during the 8-h work shift. The concentrations of formaldehyde contained in the formulations of these products were also evaluated and compared with exposure levels. The results were evaluated according to the exposure limits prescribed in Brazilian (NR15) and North American (US OSHA and US NIOSH) standards. The analysis of the smoothing products showed concentrations of formaldehyde of between 3 and 11% in their compositions, i.e., up to 54 times above the 0.2% limit allowed by the National Agency of Sanitary Surveillance (ANVISA). The present study showed that hairdressers are chronically exposed to high concentrations of formaldehyde in the workplace and these exposures are mainly associated with the work process, where many variables of this process influence the intensity of exposure.