In the present study, magnetic seeding flocculation was applied to remove copper (200 mg/L) and turbidity (180 mg/L) from simulated microetch copper waste. Fe₃O₄ particles (40 to 1600 mesh) were used as magnetic seeds. Poly-aluminum chloride (PAC) and anionic polyacrylamide (PAM) were added as coagulant and flocculant, respectively. The effect of operating factors, such as the dosages of the coagulant and flocculant, initial pH of the wastewater, and dosage and size of the magnetic seeds, on copper and turbidity removal was systematically investigated. In addition, settling speed, floc-size distribution, and volume of sludge were measured with and without the addition of magnetic seeds to compare the efficiency of magnetic seeding to that of traditional flocculation. The results indicated that the highest settling speed, the largest floc size, and the smallest volume of sludge were obtained simultaneously when the dosage and size of magnetic seeds were 2.0 g/L and 300–400 mesh, respectively. High removal efficiencies of 98.53 and 94.72 % for copper and turbidity, respectively, were also achieved under this condition; values that are 4.11 and 0.61 % higher, respectively, than those found in traditional flocculation. The high performance might be attributed to efficient collision of particles and slightly moderate vortex centrifugal force of inertia among the magnetic seeds, which could produce larger magnetic flocs with lower moisture.

Patulin (PAT) is a mycotoxin mainly produced by Aspergillus, Penicillium, and Bissochlamys. Given the high risk associated with this mycotoxin, its potential effects have been investigated by many studies. It is known to be teratogenic, mutagenic, and genotoxic, and it has been shown to induce damages in several organs in experimental animals. Our aim was to investigate the preventive effect against PAT-induced apoptosis in vivo using natural carotenoid, Crocin (CRO). Mice were divided into six groups: a control group, a “PAT alone” group, a “CRO alone” group, and a “PAT plus CRO” groups (pre-treatment conditions). Our results showed that CRO restored the normal levels of biochemical parameters in the liver and kidney. The analysis of the protein expression in these organs revealed that PAT-induced toxicity promotes the induction of apoptosis via the increase in P53, Bax, and cytochrome C and the decrease in Bcl2 expressions. We also found that PAT triggered caspase 3 activation and DNA fragmentation. However, pre-treatment with CRO demonstrated a reduction in the induction of apoptosis via the regulation of all tested biomarkers demonstrating that CRO is effective in the protection against PAT hazards. This could be relevant, particularly with the emergent demand for natural products which may counteract the detrimental toxic effects and therefore prevents multiple human diseases.

Injection of concentrated leachate to landfills is a simple and cost-effective technology for concentrated leachate treatment. In this study, the effects of injection mode of concentrated leachate and its hydraulic loading rate on the stabilization of landfilled waste were investigated. Compared with the injection of concentrated leachate, the joint injection of leachate and concentrated leachate (1:1, v/v) was more beneficial to the degradation of landfilled waste and mitigated the discharge amount of pollutants at the hydraulic loading rate of 5.9 L m⁻² day⁻¹. As the hydraulic loading rate of the joint injection of leachate and concentrated leachate was increased from 5.9 to 17.6 L m⁻² day⁻¹, the organic matter, biologically degradable matter, and total nitrogen of landfilled waste were degraded more rapidly, with the degradation constant of the first-order kinetics of 0.005, 0.004, and 0.003, respectively. Additionally, NO₂ ⁻-N and NO₃ ⁻-N in the concentrated leachate could be well removed in the landfill bioreactors. These results showed that a joint injection of concentrated leachate and raw leachate might be a good way to relieve the inhibitory effect of high concentrations of toxic pollutants in the concentrated leachate and accelerate the stabilization of landfilled waste.

This work investigates influence of different aluminosillicate nanoparticles (NPs) which are found in air in selected workplaces on the properties of the phospholipid (DPPC) monolayer at air–saline interface considered as ex vivo model of the lung surfactant (LS). The measurements were done under physiological-like conditions (deformable liquid interface at 37 °C) for NP concentrations matching the calculated lung doses after exposure in the working environment. Measured surface pressure–area (π–A) isotherms and compressibility curves demonstrated NP-induced changes in the structure and mechanical properties of the lipid monolayer. It was shown that hydrophilic nanomaterials (halloysite and bentonite) induced concentration-dependent impairment of DPPC’s ability of attaining high surface pressures on interfacial compression, suggesting a possibility of reduction of physiological function of natural LS. Hydrophobic montmorillonites affected DPPC monolayer in the opposite way; however, they significantly changed the mechanical properties of the air–liquid interface during compression. The results support the hypothesis of possible reduction or even degradation of the natural function of the lung surfactant induced by particle–phospholipid interactions after inhalation of nanoclays. Presented data do not only supplement the earlier results obtained with another LS model (animal-derived surfactant in oscillating bubble experiments) but also offer an explanation of physicochemical mechanisms responsible for detrimental effects which arise after deposition of inhaled nanomaterials on the surface of the respiratory system.

The dynamics of arsenic (As) and antimony (Sb) in wetland soil periodically submitted to agricultural pressure as well as the impact of soil enrichment with NO₃ ⁻ (50 mg L⁻¹) and PO₄ ³⁻ (20 mg L⁻¹) on As and Sb release were evaluated at both field and laboratory scales. The results showed that As and Sb exhibited different temporal behaviors, depending on the study scale. At field scale, As release (up to 93 μg L⁻¹) occurred under Fe-reducing conditions, whereas Sb release was favored under oxidizing conditions (up to 5 μg L⁻¹) and particularity when dissolved organic carbon (DOC) increased in soil pore water (up to 92.8 mg L⁻¹). At laboratory scale, As and Sb release was much higher under reducing conditions (up to 138 and 1 μg L⁻¹, respectively) compared to oxic conditions (up to 6 and 0.5 μg L⁻¹, respectively) and was enhanced by NO₃ ⁻ and PO₄ ³⁻ addition (increased by a factor of 2.3 for As and 1.6 for Sb). The higher release of As and Sb in the enriched reduced soil compared to the non-enriched soil was probably induced by the combined effect of PO₄ ³⁻ and HCO₃ ⁻ which compete for the same binding sites of soil surfaces. Modeling results using Visual Minteq were in accordance with experimental results regarding As but failed in simulating the effects of PO₄ ³⁻ and HCO₃ ⁻ on Sb release.

Hexavalent chromium Cr(VI) is a toxic water pollutant which can cause serious influence to the health of the human and animals. Therefore, developing new methods to remove hexavalent chromium in water attracts great attention of scholars. In our research, we successfully synthesized a new type of magnetic mesoporous carbon hybrid nitrogen (Fe-NMC) loaded with catalyst Pd nanoparticles (NPs), which performed excellent catalytic reduction efficiency toward Cr(VI). The characterization of Pd/Fe-NMC composite was investigated in detail using scanning electron microscope (SEM), high-resolution transmission electron microscopy (HRTEM), Fourier transform infrared spectroscopy (FTIR), and nitrogen adsorption-desorption measurements. According to the experimental results, we dealt with in-depth discussion and studied on the mechanism of hexavalent chromium removed by Pd/Fe-NMC composite. Furthermore, the batch experiments were conducted to investigate the catalytic reduction ability of composite. It was found that the chromium reduction process conforms to pseudo-first-order reaction kinetics model when the concentrations of chromium and sodium formate were low. It took only 20 min for the Pd/Fe-NMC composite to reach 99.8 % reduction of Cr(VI) (50 mg/L). The results suggested that the Pd/Fe-NMC composite may exhibit significantly improved catalytic activity for the hexavalent chromium reduction at industrial wastewater.

The photocatalytic degradation of furfural in aqueous solution was investigated using N-doped titanium dioxide nanoparticles under sunlight and ultraviolet radiation (N-TiO₂/Sun and N-TiO₂/UV) in a lab-scale batch photoreactor. The N-TiO₂ nanoparticles prepared using a sol-gel method were characterized using XRD, X-ray photoelectron spectroscopy (XPS), and SEM analyses. Using HPLC to monitor the furfural concentration, the effect of catalyst dosage, contact time, initial solution pH, initial furfural concentration, and sunlight or ultraviolet radiation on the degradation efficiency was studied. The efficiency of furfural removal was found to increase with increased reaction time, nanoparticle loading, and pH for both processes, whereas the efficiency decreased with increased furfural concentration. The maximum removal efficiencies for the N-TiO₂/UV and N-TiO₂/Sun processes were 97 and 78 %, respectively, whereas the mean removal efficiencies were 80.71 ± 2.08 % and 62.85 ± 2.41 %, respectively. In general, the degradation and elimination rate of furfural using the N-TiO₂/UV process was higher than that using the N-TiO₂/Sun process.

Exhaust particulate from compression ignition (CI) engines running on engine and chassis dynamometers was studied. Particulate dichloromethane extracts were qualitatively and quantitatively analyzed for polycyclic aromatic hydrocarbons (PAHs) and biomarkers by gas chromatography with flame ionization detector (GC-FID) and gas chromatography-mass spectrometry (GC-MS). PAH group profiles were made and the PAH group shares according to the number of rings (2 or 3; 4; 5 or more) as well as diagnostic indices were calculated. Values of geochemical ratios of selected biomarkers and alkyl aromatic hydrocarbons were compared with literature values. A geochemical interpretation was carried out using these values and biomarker and alkyl aromatic hydrocarbon distributions. It has been shown that geochemical features are unequivocally connected to the emission of fossil fuels and biofuels burned in CI engines. The effect of the exothermic combustion process is limited to low-molecular-weight compounds, which shows that the applied methodology permits source identification of PAHs coexisting in the particulate emitted.

There is compelling evidence in support of interaction between calcium (Ca) and lead (Pb) in thyroid disorders. The aim of present study was to compare the level of Ca and Pb with thyroid hormones such as thyroid-stimulating hormone (TSH), free triiodothyronine (FT3), and free thyroxin (FT4) in serum samples of hyperthyroid (HPRT) and hypothyroid (HPOT) patients of both genders. For comparative purpose, age-matched (25–50 years) subjects having no thyroid disorders were selected as referents/controls. The serum samples were acid-digested prior to analysis by atomic absorption spectrometry. The validity and accuracy of the methodology were checked by certified reference materials. The resulted data indicates that the mean values of Ca in serum samples of HPRT patients were significantly higher than those of referent subjects (p < 0.01), while reverse pattern was observed in the case of HPOT patients. The level of Pb was higher in the serum samples of both types of thyroid patients, but difference was significant in case of HPOT patients as compare to referent subjects (p < 0.01). A negative correlation was observed between serum Ca levels and TSH of HPRT patients (−r = 0.37–0.39, p < 0.01), while FT3 and FT4 have positive correlation (r = 0.49–0.52 and r = 0.46–0.47), p values <0.01. The Pb in serum had positive correlation with TSH (r = 0.48–0.51, p < 0.005), while negative correlation was observed for FT3 and FT4 (−r = 0.55–0.56, 0.5–0.54, p < 0.05) in HPRT patients. On the other hand, a reverse pattern was observed, for correlation of Ca and Pb with thyroid functions in HPOT patients.

The aim of the present work was to complete an exposure assessment in three Mexican indigenous communities using the community-based health risk assessment, which is the first step in the CHILD framework. We used 1-hydroxypyrene (1-OHP) as an exposure biomarker to polycyclic aromatic hydrocarbons (PAHs) and trans, trans-muconic acid (t,t-MA) as an exposure biomarker to benzene, persistent organic pollutants (POPs), lead, manganese, arsenic, and fluoride. Anthropometric measurements were also taken. In these communities, high percentages of children with chronic malnutrition were found (28 to 49 %) based on their weight and age. All communities showed a high percentage of children with detectable levels of four or more compounds (70 to 82 %). Additionally, our results showed that in indigenous communities, children are exposed to elevated levels of certain environmental pollutants, including manganese with 17.6, 16.8, and 7.3 μg/L from SMP, TOC, and CUA, respectively. Lead and HCB levels were similar in the indigenous communities (2.5, 3.1, and 4.2 μg/dL and 2.5, 3.1, and 3.7 ng/mL, respectively). 1-OHP and t,t-MA levels were higher in TOC (0.8 μmol/mol of creatinine, 476 μg/g of creatinine, respectively) when compared with SMP (0.1 μmol/mol of creatinine, 215.5 μg/g of creatinine, respectively) and CUA (0.1 μmol/mol of creatinine, 185.2 μg/g of creatinine, respectively). DDE levels were 30.7, 26.9, and 9.6 ng/mL in CUA, SMP, and TOC, respectively. The strength of this study is that it assesses exposure to pollutants with indications for the resultant risk before an intervention is made by the CHILD program to manage this risk in the indigenous communities. Considering the large number of people, especially children, exposed to multiple pollutants, it is important to design effective intervention programs that reduce exposure and the resultant risk in the numerous indigenous communities in Mexico.