Herein, kitchen waste hydrolysis residue (KWHR) was utilized as the precursor to fabricate nitrogen/oxygen co-doped microporous biocarbons (NOMBs) with ultrahigh specific surface area via KOH activation. Activation temperature was found to be crucial for heteroatom doping and pore structure construction. Attractively, the obtained NOMB with high surface area (2417 m²/g) and microporosity (~ 90%) displayed an outstanding capacity of Cr(VI) removal (526.1 mg/g at pH 2). The kinetics and isotherm studies showed that the adsorption of Cr(VI) onto NOMB was well described by the pseudo-second-order kinetics and Langmuir isotherm. Moreover, it was found that Cr(VI) was partly reduced to Cr(III) during the removal process as the nitrogen/oxygen functionalities and unsaturated carbon bond played crucial roles of electron-donors, which revealed the fact that the removal of Cr(VI) by NOMB was attributed to the coupling of adsorption and reduction reaction. Overall, this study has demonstrated the possibility of preparing microporous biocarbons using KWHR as a renewable material and the resultant NOMB is of great potential to detoxify Cr(VI).

The objective of this study was to analyze and compare the presence of argyrophilic nucleolar organizer regions (AgNORs) in exfoliated cells obtained from the buccal mucosa among crack and cocaine users and non-users by the AgNOR staining technique. Seventy-three males ≥ 18 years were categorized into two groups: 38 crack and/or cocaine users and 35 non-user volunteers. They were interviewed and responded a questionnaire regarding general health and drug addiction. Exfoliative cytology specimens were collected from the clinically intact buccal mucosa, and cytological preparations were fixed and stained by AgNOR technique. The mean number of AgNORs (p = 0.02) and the percentage of epithelial cells with more than 3 (p = 0.01) and 4 (p = 0.04) AgNORs/nucleus were significantly higher in the non-user group. In conclusion, the frequency and diversity of substances present in the drugs—cocaine, crack, and alcohol—consumed by the volunteers of this study may have influenced the number of AgNORs and the response to damage and consequent effect on protein synthesis.

Conventional wastewater treatments are not efficient in removing parabens, which may thus end up in surface waters, posing a threat to aquatic biota and human health. As an alternative treatment, persulfate (PS)-driven advanced oxidation technologies have gained growing attention for removing these pollutants. In this study, the degradation of propylparaben (PrP) by UVA- and zero-valent iron (ZVI)-activated persulfate was investigated. The effects of initial PS concentration ([PS]₀) and irradiance or ZVI concentration were explored using the Doehlert experimental design. For the UVA-activated system, the specific PrP degradation rate (k) and percent removal were consistently higher for increasing [PS]₀ and irradiance, varying in the ranges 0.0053–0.0192 min⁻¹ and 37.9–77.3%, respectively. In contrast, extremely fast PrP degradation was achieved through the ZVI/PS process (0.3304 < k < 0.9212 min⁻¹), with removal percentages above 97.5%; in this case, paraben degradation was hindered for a ZVI dosage beyond 40 mg L⁻¹. Regarding toxicity, ECOSAR predictions suggest that the degradation products elucidated by LC-MS/MS are less toxic than PrP toward fish, daphnid, and green algae. In addition, both processes showed to be strongly dependent on the water matrix, being ZVI/PS more impacted for a MBR effluent, although its performance was much better than that exhibited by the UVA-driven process (t₁/₂ of 65.4 and 276.1 min, respectively).

In this study, it was found that the CeVO₄-CeO₂ nanocomposite possessed remarkably selective catalytic reduction (SCR) performance and wider active temperature scope. And, the promotion principle was explored based on BET, XRD, XPS, H₂-temperature-programmed reduction, NH₃-temperature-programmed desorption, and in situ diffuse reflectance infrared Fourier transform (DRIFT) techniques. The characterization outcomes manifested that the CeVO₄-CeO₂ nanocomposite could inhibit its crystallinity and enhance the concentrations of chemisorbed oxygen species and Ce³⁺, which was advantageous to the SCR process. Moreover, the in situ DRIFT technique manifested that the NH₃-SCR reaction over Ce₀.₇₅V₀.₂₅Oy was enhanced effectively through the mechanism of L-H.

Effects of Polygonum equisetiforme extracts against dichlorvos were investigated in the commercial clam Ruditapes decussatus. The toxicity of this pesticide was firstly tested in R. decussatus gill and digestive gland tissues using five doses varying from 0.05 to 1 mg/l during 2, 4, and 7 days. Results showed that 0.05 mg/l of DDVP induced oxidative stress and neurotoxicity in R. decussatus after 2 days of exposure. Investigations of the effects of P. equisetiforme extracts in R. decussatus exposed to 0.25 mg/l of DDVP were made in clams receiving three concentrations (0.009, 0.045, and 0.09 g/l) during 4 and 7 days. Antioxidant enzymes SOD and CAT as well as H₂O₂ content and AChE were quantified by colorimetric method. Four days of exposure to DDVP increased SOD and CAT activities and enhances H₂O₂ content. AChE levels decreased considerably following DDVP exposure, although a restoration in the enzyme activity was observed with P. equisetiforme extract (E3 = 0.09 g/l). Overall, P. equisetiforme extract at concentration (E1 = 0.009 g/l) prevents oxidative stress caused by DDVP, while 0.09 g/l of P. equisetiforme extract induced an effect similar to that obtained with DDVP alone. Nevertheless, this concentration was found effective for the restoration of the AChE activity.

The widespread use of synthetic polymers has made microplastic (MP) a new type of contaminant that has attracted worldwide attention. Studies have shown that wastewater treatment plants (WWTPs) are an important source of MP collection in the natural environment. This study investigated the removal efficiency and migration characteristics of MPs by sampling the sewage from each treatment section of a WWTP in Zhengzhou, China. The results showed that the abundance of MPs in the influent water and primary, secondary, and tertiary treatment discharges was 16.0, 10.3, 4.5, and 2.9 MP/L, respectively, and the total removal rate of MPs from the influent to the final effluent reached 81.9%. The MPs in the WWTP were mainly small-sized (0.08–0.55 mm), followed by medium-sized (0.55–1.7 mm). Fibers were the dominant MP shape in both the water and sediment samples. Black (36%) and red (23%) were the dominant MP colors. Six different polymer types of MPs were detected, which were mainly polypropylene followed by polyethylene. In general, for the MPs in the WWTP, the removal rate of fragments can reach 97.08%, which is better than that of fibers (70.50%); the removal rate of small-sized can reach 95.86%, which is better than that of medium-sized (83.53%) and large-sized (70.00%). In this study, primary treatment has better effects in eliminating fragments and large-sized MPs; secondary treatment has better effects in eliminating fibers and small-sized MPs. Although WWTPs have a very good removal effect on MPs, 870 million MP/d are still discharged into nearby rivers from WWTPs with a treatment scale of 300,000 m³/day. Graphical Abstract

A novel route is developed for regeneration of deactivated commercial NH₃-SCR catalysts, which includes an initial in situ construction of anatase TiO₂ porous film, followed by loading of MnOₓ, CeOₓ, and Mn-Ce mixed oxides as active components. The regenerated catalysts present largely improved low-temperature denitrification performance due to the synergetic effect of MnOₓ and CeOₓ. The denitrification efficiency could reach a high value of 97% at 200 °C and 100% at 250 °C when the Ce-Mn mixed oxides are loaded at the optimized molar quantity ratio of 10:9 (Ce:Mn). Properties and reaction mechanisms of the regenerated catalysts are investigated with characterizations of X-ray photoelectron spectroscopy (XPS), NH₃ temperature-programmed desorption (NH₃-TPD), H₂ temperature-programmed reduction (H₂-TPR), and in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). Our results demonstrate that the adsorption and oxidation of NO plays a crucial role for these three catalysts even though a difference exists on the reaction pathways. Graphical abstract

The present investigation was conducted to evaluate the effect of penconazole (PEN) fungicide on early embryogenesis of white mice. In the first experiment, 48 pregnant females were divided into different groups; the first group is control (G1). The second group (G2) was treated daily with PEN (30-, 20-, 10-, 5-mg/kg BW). The third group (G3) was treated with PEN (5-mg/kg BW; day after the other day). The fourth group (G4) was treated with PEN (2.5-mg/kg BW daily) during pre-implantation stage (from the 1st to the 4th day of gestation). The fifth group (G5) was treated with PEN (2.5-mg/kg BW daily) during post-implantation (from the 5th to the 8th day of gestation). The pregnant females were sacrificed at the 14th day of gestation. In the second experiment, 63 pregnant females were classified into control, PEN-treated during pre-implantation period (2.5-mg/kg BW), and PEN-administered during post-implantation period (2.5-mg/kg BW). Each group was sacrificed at stages E6.5, E7.5, E8.5, E9.5, E11.5, E14.5, and E18.5. The high doses of PEN in the first experiment showed failed pregnancy, foetoresorption, and embryo disorganization. High doses of PEN induce alterations in the uterus tissue at the level of histology and immunohistochemistry for the expression of TGFβ2, TNFR2, Caspase 10, and HSP70. The low doses of PEN in the second experiment showed upregulated expression of TGFβ2, TNFR2, Caspase 10, and HSP70 at stages E6.5 and E7.5. In conclusion, PEN was found to alter the suitable uterine environment for proper implantation and development at the levels of histological and immunohistochemical that could create a risk during the full course of embryogenesis.

In order to analyze the interaction relationship between heavy metals and other mineral elements during the processes of absorption and translocation by plant grown on heavy metal–contaminated area, the concentrations of Cu, Zn, Mn, Cd, Pb, Ca, Mg, Fe, and K in the medicinal plant Paeonia ostii T. Hong et J. X. Zhang and its rhizospheric soil were determined, which grow around an abandoned copper tailings reservoir in Tongling City, China. Geo-accumulation index (Igₑₒ) calculation indicated that Cu and Pb are the main pollution elements in the rhizospheric soil. Moreover, the Cu and Pb concentrations in the cortex moutan of P. ostii exceeded the maximum permissible limits for food product safety. The bioaccumulation factor values of the tested metals in plant roots were found < 0.50, with the exception of Ca (maximum 5.99). The translocation factor values of detected heavy metals Cd and Pb were more than 1.00, which indicated that P. ostii could be considered a potential accumulator plant for Cd and Pb. Significant positive correlations including Cu-Cd, Cu-Zn, Cu-Pb, Cd-Zn, Cd-Fe, Cd-Fe, Zn-Pb, Pb-Fe, Mn-Fe, and Ca-Mg in the cortex moutan and Cu-Zn, Cu-Fe, Zn-Mg, Zn-Fe, and Mn-K in the leaves were observed (P < 0.05). Significant positive correlation between Cu, Zn, Mg, and Fe was also confirmed in the processes of absorption and translocation from the soil to plant (P < 0.05), which evidenced that synergistic element interactions of the essential elements Cu, Zn, Mg, and Fe are a result of the similarity in their ionic radii and octahedral coordination geometry.

There are many worries about the food safety of seafood contaminated with antibiotic residues. These residues can be potentially dangerous for public health owing to the causation of allergic reactions, toxic effects, and serious health problems. This study was planned to search the occurrence of chloramphenicol (CAP) and sulfonamide residue in sea bream and sea bass. A total of 82 fish samples were collected from 14 different sales points in Afyonkarahisar. The samples were analyzed for CAP and sulfonamide residues using the ELISA method. Results showed that up to 18.3% of the samples were contaminated with CAP. In the positive fish meat samples, the CAP residue concentrations ranged within 0.54–10.6 ng kg⁻¹. The mean CAP residue concentration in positive samples was 4.25 ± 2.78 ng kg⁻¹. No sulfonamide residue was detected from the samples. Despite the prohibition of CAP application in aquaculture, detectable CAP residues in fish meat samples indicate an illegal use of this antibiotic. Therefore, the results obtained in the study are negative signs for food safety. Official controls must be performed rigorously in accordance with the national residue monitoring plan especially for the illegal antibiotics.