Cost-effective recycling of e-waste (from computer printed circuit boards, PCB’s) for the synthesis of metal oxide nanocomposites is demonstrated. Metals in electronic components of waste memory slots were leached out using nitric acid (HNO₃). Compositional analyses of the filtrate obtained after leaching were 66 wt.% Cu, 27.7 wt.% Zn, and 6.2 wt.% Ni. The leached out metal salt solutions were subjected to alkaline hydrothermal treatment to synthesize nanocomposites. Two nanoparticle samples were prepared, one without any stabilizing agent and another sample with PVP as a stabilizing agent. XRD, HR-XRD, HR-TEM, UV-DRS, UV-visible spectroscopy was used to characterize the as-prepared metal oxide nanoparticles. The analysis showed the formation of ZnO/CuO nanocomposites only. No nickel oxide component was precipitated under the studied hydrothermal experimental conditions. Most of the ZnO/CuO nanocomposite particles obtained by this route consisted of fine ZnO nanostructures precipitated on CuO cores. The ZnO and CuO components exhibit both direct and indirect band gaps in the visible range. The nanocomposites demonstrate good visible light photo-Fenton methyl orange (MO) degradation by pseudo-zero order kinetics.

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.

Anaerobic fermentation of waste activated sludge (WAS) for recycling valuable volatile fatty acids (VFAs) is economically valuable. However, the fermentation of protein is the rate-limiting step of VFA production with WAS as a substrate. In this study, the effect of redox mediators (RMs, i.e., riboflavin and lawsone) on the enhanced production of VFAs from WAS was investigated. The results indicate that both RMs can promote protein-dependent fermentation, increasing maximum VFA accumulation by 43.9% and 42.5% respectively. In cultures supplemented with riboflavin and lawsone, VFA production was highly correlated with protease activities, but not with α-glucosidase activities. This implies that RMs affected the redox reaction of amino acids degradation, resulting in an increased release of ammonia. Sequencing results showed that RMs significantly increased the abundance of bacteria related to VFA fermentation and protein/amino acid degradation at the levels of phylum, class, order, family, and even genus.

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 toxic impacts of CuO nanoparticles (NPs) on the marine phytoplankton Nannochloropsis oculata were evaluated by measuring a number of biological parameters. Exposure to different concentrations of CuO-NPs (5–200 mg/L) significantly decreased the growth and content of chlorophyll a of N. oculata. The results showed that CuO-NPs were toxic to this microalga with a half maximal effective concentration (EC50) of 116.981 mg/L. Exposure to CuO-NPs increased the hydrogen peroxide (H₂O₂) content and induced the membrane damages. Moreover, the concentration of phenolic compounds was increased, while the levels of carotenoids were markedly decreased in comparison to the control sample. The activity of catalase (CAT), ascorbate peroxidase (APX), polyphenol oxidase (PPO) and lactate dehydrogenase (LDH) enzymes significantly was increased in response to CuO-NPs treatments. These results indicated that CuO-NPs stimulated the antioxidant defense system in N. oculata to protect the cells against the oxidative damages. The Fourier-transform infrared spectroscopy (FTIR) analyses showed that the main functional groups (C=O and C–O–C) interacted with CuO-NPs. The images of scanning electron microscopy (SEM) and transmission electron microscopy (TEM) revealed the cell membrane damage and the change of cell wall structure which may be contributed to the nanotoxicity. These findings may provide additional insights into the mechanisms of cytotoxicity induced by CuO-NPs.

This article studies the price competition and cooperation in a duopoly that is subjected to carbon emissions cap. The study assumes that in a departure from the classical Bertrand game, there is still a market for both firms’ goods regardless of the product price, even though production capacity is limited by carbon emissions regulation. Through the decentralized decision making of both firms under perfect information, the results are unstable. The firm with the lower maximum production capacity under carbon emissions regulation and the firm with the higher maximum production capacity both seek market price cooperation. By designing an internal carbon credits trading mechanism, we can ensure that the production capacity of the firm with the higher maximum production capacity under carbon emissions regulation reaches price equilibrium. Also, the negotiation power of the duopoly would affect the price equilibrium.

In this study, we investigated the Sb(V) adsorption on ferrihydrite (Fh) at different pH values, in the presence and absence of common competing anions in soil such as phosphate (P(V)) and arsenate (As(V)). Batch adsorption experiments, carried out at pH 4.5, 6.0, and 7.0, showed a greater affinity of Fh towards P(V) and As(V) with respect to Sb(V), especially at higher pH values, while the opposite was true at acidic pH. The capacity of Fh to accumulate greater amounts of phosphate and arsenate in the 6.0–7.0 pH range was mainly linked to the different acid properties of P(V), As(V), and Sb(V) oxyanions. The Sb(V) adsorption on Fh was highly pH-dependent and followed the following order: pH 4.5 (0.957 mmol·g⁻¹ Fh) > pH 6.0 (0.701 mmol·g⁻¹ Fh) > pH 7.0 (0.583 mmol·g⁻¹ Fh). Desorption of antimonate from Sb(V)-saturated Fh, treated with citric and malic acid solutions, was ~equal to 55, 68, and 76% of that sorbed at pH 4.5, 6.0, and 7.0, respectively, while phosphate, arsenate, and sulfate were able to release significantly lower Sb(V) amounts. The FT-IR spectra revealed substantial absorbance shifts related to the surface hydroxyl groups of Fh, which were attributed to the formation of Fe-O-Sb(V) bonds and supported the formation of inner-sphere bonding between Sb(V) and Fh.

Air pollution represents a major health problem in megacities, bringing about 8 million deaths every year. The aim of the study was to evaluate in vivo the ocular and respiratory mucosa biological response after chronic exposure to urban air particles from Buenos Aires (UAP-BA). BALB/c mice were exposed to UAP-BA or filtered air for 1, 6, 9, and 12 months. After exposure, histology, histomorphometry, and IL-6 proinflammatory cytokine level were evaluated in the respiratory and ocular mucosa. Total cell number and differential cell count were determined in the brochoalveolar lavage fluid. In the lung, chronic exposure to UAP-BA induced reduction of the alveolar space, polymorhonuclear cell recruitment, and goblet cell hyperplasia. In the ocular surface, UAP-BA induced an initial mucin positive cells rise followed by a decline through time, while IL-6 level increased at the latest point-time assayed. Our results showed that the respiratory and the ocular mucosas respond differently to UAP-BA. Being that lung and ocular mucosa diseases may be triggered and/or exacerbated by chronic exposure to urban air PM, the inhabitants of Buenos Aires whom are chronically exposed to environmental urban air pollution may be considered a subpopulation at risk. Based on our results, we propose the ocular mucosa as a reliable and more accessible surrogate for pulmonary mucosa environmental toxicity that might also serve as an earlier biomarker for air pollution adverse impact on health.

Macroporous resin-supported reagents have been identified as potential adsorbents for removal of toxic pollutants. This article presents an experimental designed to evaluate the sorption and desorption of nickel(II) with the help of column and batch procedure using simple extractant-impregnated resin (EIR). Isonitroso-4-methyl-2-pentanone (IMP) as an extractant was impregnated on a solid support like Amberlite XAD-4 to prepare the EIR sorbent. Column experimental conditions such as pH, sample flow rate and volume, eluting solution, and interfering ions were studied to optimize the nickel(II) sorption and recovery from aqueous media. The column results suggest that the quantitative nickel(II) sorption was observed at pH 5–6, and the quantitative recovery (≥ 95%) was achieved by using 1.0 M HNO₃. The high concentrations of cations and anions (except EDTA) present in the spiked binary and multi-element mixture solution show no interferences in both quantitative sorption and recovery of nickel(II), whereas the batch experiments were performed to evaluate nickel(II) sorption behavior using the linearized and non-linearized kinetic and isotherm models. By error function analysis, the Freundlich isotherm and the pseudo-first-order kinetic model were found to describe best the experimental data obtained over the studied concentration range and sorption time, respectively. The maximum sorption capacity of nickel(II) onto the EIR sorbent was found to be ~ 81 mg/g. The mean free energy (E = 10.1 kJ/mol) determined using Dubinin-Radushkevich isotherm suggests chemical nature of nickel(II) sorption on EIR. The novelty of the EIR adsorbent lies in its potential for separation and recovery of nickel(II) at trace level in water samples of different origin.

The trace metal pollution in the environment is a highly concerned issue in these days. One of the important causes of trace metal pollution is the exhaust gases released from the vehicles on the roads. These dangerous gases pose life-threatening effects on the forage plants grown along the roadside as these plants are at direct risk to these trace metals. The aims of the present study were to determine the cobalt (Co) concentrations in soil, forages, and blood plasma of the buffaloes and to evaluate the Co deficiencies and toxicities in these samples. All samples were collected from six sites (Faisalabad roadside, Bhalwal roadside, Shaheenabad roadside, Mateela roadside, 50 Chak roadside, and Dera Saudi-control) of Sargodha city. The Co concentrations in these samples were determined by atomic absorption spectrophotometer (AA-6300 Shimadzu Japan). In soil samples, Co level ranged from 1.958 to 3.457 mg/kg in the six sampling sites. The highest Co level was observed at site 6 and the lowest at site 2. In forage samples, Co level ranged from 0.770 to 2.309 mg/kg in the six sampling sites. The highest Co level was observed at site 3 and the lowest at site 2. In blood plasma samples, Co level ranged from 2.644 to 4.927 mg/kg in the six sampling sites. The highest Co level was observed at site 1 and the lowest at site 3. The results showed higher Co values in the samples collected from the site IV while the bioconcentration factor for forage-soil was found highest in the samples collected from Site III. On the other hand, a correlation was found positively significant when soil and forage were correlated, and it was found negatively significant when blood and forage were correlated.