3-Phenoxybenzoic acid (3-PBA) is a shared metabolite of several synthetic pyrethroid pesticides (SPs) resulting from environmental degradation of parent compounds and thus occurs frequently as a residue in samples. Hence, the importance of 3-PBA evaluation after pyrethroid application. There is a gap of analytical methods to determine 3-PBA in soil samples. Therefore, an analytical method that combines the solid-phase extraction (SPE) and gas chromatography–mass spectrometry (GC/MS) detection has been developed for the determination of 3-PBA in soil samples. The analytical method was validated in terms of linearity, sensitivity, intra- and inter-day batch precisions, recoveries, and quantification limits. An SPE method using a Strata X cartridge allows obtaining limits of detection and quantification equal to 4.0 and 13.3 ng g⁻¹, respectively. Under optimized conditions, the method average recovery levels ranged from 70.3 to 93.5% with a relative standard deviation below 3.4%. Method intra- and inter-day precision was under 5.0 and 4.8%, respectively. The developed method was applied to 11 agricultural soil samples in the north of Portugal. The developed methodology allowed for the determination of the pyrethroid metabolite, 3-PBA, in agricultural soil samples at levels of few ng g⁻¹. Graphical abstract ᅟ

Several strains of Escherichia coli harbor virulence traits, resulting in E. coli–related intestinal and extra-intestinal infections. Various studies have reported that extra-intestinal pathogenic E. coli (ExPEC) strains were prevalent in nonhuman reservoirs, including environmental waterways. It is therefore important to identify the pathogenic potential and/or ExPEC status of E. coli strains inhabiting the aquatic environments associated with anthropogenic activities. Besides virulence-associated genes, biofilm production also helps in the survival of E. coli in environmental waterbodies. Thus, the aim of the current study was to assess the virulence potential, ExPEC status, and biofilm-producing capability of E. coli isolated from the River Yamuna, a major river traversing the National Capital Region of Delhi, India. We also tried to discern a co-relation, if any, between virulence, biofilm formation, and antimicrobial resistance in these strains. Our results indicated that virulence-associated genes were scarce and none of the strain qualified the molecular criteria essential for ExPEC. This suggested that E. coli strains which can presumably cause human extra-intestinal infections were not prominent in the River Yamuna. However, the fact that more than 80% of the aquatic E. coli isolates were moderate and strong biofilm producers suggests that E. coli in these environments might serve as opportunistic pathogens. Also, no unequivocal association was observed between biofilm production, virulence, and β-lactamase genes in E. coli strains. As per the best of our knowledge, this is the first study where the relationship between virulence, biofilms, and antimicrobials has been examined in E. coli, isolated from an Indian urban aquatic waterbody.

Cadmium is an important widely distributed heavy metal in the environment due to its several industrial uses, while milk thistle is an important herb and is a source of several antioxidant particularly silymarin which is a pharmacological active substance present in seeds of milk thistle plant (Silybum marianum). The current study investigated pathological effects of cadmium (Cd) and their amelioration with silymarin (SL) and milk thistle (MT) quails. A total of 144 quails were equally divided into 9 groups and given different combinations of cadmium chloride (150 and 300 mg/kg feed), SL (250 mg/kg), and MT (10 g/kg) feed. Parameters studied were clinical signs, mortality, organ weights, testes weight and volume, and gross and microscopic pathology. Results of this study indicated an increased mortality and reduced body weight in cadmium-treated quails. Quails were dull, depressed compared with control. Swollen hemorrhagic liver along with atrophied testes were also observed in these groups. No active spermatozoa were observed in lumen of seminiferous tubules of Cd-treated birds presenting arrest of spermatogenesis. Supplementing MT and SL ameliorated mortality, organ weights, spermatogenesis, and histopathological lesions. It may be concluded that MT and SL proved beneficial in cadmium-induced toxicities in Japanese quails.

Sewage sludge has been regarded as an economic and efficient soil amendment for mudflat soil amendment despite of the concern of heavy metal contamination. Converting sewage sludge into vermicompost by earthworms may be effective to minimize the risk of heavy metal contamination caused by direct application of sewage sludge in mudflat soil. The objective of this study was to assess the feasibility of vermicompost amendment (VA), and its influence on heavy metal contamination compared with sewage sludge amendment (SSA) in mudflat soil. The results showed that VA improved the physicochemical properties of mudflat soil by decreasing soil bulk density, salinity, and pH, increasing soil organic carbon, nitrogen, and phosphorus contents in the soil. Consequently, the maize biomass and yield were significantly elevated by VA. For heavy metals, VA increased total Cd, Cu, Ni, Pb, and Zn concentrations in mudflat soil, and the maximum increments occurred at 250 t ha⁻¹. Available Cd, Cu, Mn, Ni, and Zn concentrations significantly increased with increasing VA rates. VA increased the accumulation of Cd, Cu, Mn, Ni, Pb, and Zn in maize tissues, especially in root of maize. Compared with SSA under the condition of maintaining equal carbon input, VA allowed heavy metals to accumulate in a more stable binding form in the top 20-cm layer of mudflat soil. Thus, the risk of runoff and leaching of heavy metals and their bioavailability to plants reduced in mudflat soil. As a result, VA decreased the accumulation of heavy metals in maize plant compared with SSA in mudflat soil. In summary, vermicompost can be an effective and safe substitute for sewage sludge for mudflat amendment.

An in vitro study was conducted to evaluate the effects of thidiazuron (TDZ) growth regulator and magnesium oxide (MgO) nanoparticles on radish (Raphanus sativus L.) under lead (Pb) stress. Effects of TDZ and MgO on seed germination, growth, biomass, total phenolics and flavonoids, antioxidant potential, and Pb phytoaccumulation in different plant parts were assessed. Nanoparticles of MgO were synthesized with leaf extract of Sageretia thea (Osbeck) plant. Thidiazuron and MgO nanoparticles were added to growth media in individual and in combinations. Lead (50 mg L⁻¹) was added to growth media. Thidiazuron and MgO nanoparticles increased plant growth, phenolic and flavonoid contents, free radical scavenging activity, and lead phytoaccumulation. The increase was highly significant in TDZ and MgO nanoparticle combination treatments (T5, T6). Treatment (T6) showed a sixfold increase in Pb accumulation (1721.73 ± 17.4 μg g⁻¹ dry biomass) as compared to control (274.29 ± 4.23 μg⁻¹g⁻¹). Total phenolic and dry biomass showed significantly positive correlation in leaves (R² = 0.73), stem (R² = 0.58), and roots (R² = 0.72). The correlation of Pb accumulation and phenolic contents was significantly positive in root (R² = 0.80), stem (R² = 0.92), and leaves (R² = 0.69). Flavonoid showed a positive correlation with dry biomass and Pb accumulation. Antioxidant activity was highly increased in leaves followed by stem and root. Findings show that TDZ in combination with MgO nanoparticles can play a significant role in secondary metabolite production and Pb phytoaccumulation.

A regional raw clay was used as the starting material to prepare iron-pillared clays with different iron contents. The catalytic activity of these materials was tested in the heterogeneous photo-Fenton process, applied to the degradation of 2-chlorophenol chosen as the model pollutant. Different catalyst loads between 0.2 and 1.0 g L⁻¹ and pH values between 3.0 and 7.0 were studied. The local volumetric rate of photon absorption (LVRPA) in the reactor was evaluated solving the radiative transfer equation applying the discrete ordinate method and using the optical properties of the catalyst suspensions. The photonic and quantum efficiencies of the 2-chlorophenol degradation depend on both the catalyst load and the iron content of the catalyst. The higher values for these parameters, 0.080 mol Einstein⁻¹ and 0.152 mol Einstein⁻¹, respectively, were obtained with 1.0 g L⁻¹ of the catalyst with the higher iron content (17.6%). For the mineralization process, photonic and quantum efficiencies depend mainly on the catalyst load. Therefore, it was possible to employ a natural and cheap resource from the region to obtain pillared clay-based catalysts to degrade organic pollutants in water.

In this study, thermochemical degradation of furfural by sulfate radical has been investigated to find the best-operating conditions. For this purpose, the response surface methodology (RSM) based on central composite design (CCD) was applied to optimize the five independent variables of thermally activated persulfate (TAP)/nZVI oxidation process including pH, PS concentration, furfural concentration, nZVI dosage, and heat. The ANOVA results (“P > F value” < 0.0001 and [Formula: see text] = 0.9701) showed the obtained quadratic model is acceptable to predict furfural removal. Based on the reduced quadratic model PS concentration, nZVI dosage, and heat revealed the positive effects on removal efficiency, while pH and furfural concentration had a negative effect. Accordingly, 98.4% of furfural could be removed within 60 min of reaction under the optimum conditions: pH 5.26, PS concentration of 20.52 mM, furfural concentration of 84.32 mg/L, nZVI dosage of 1.15 mg/L, and a temperature of 79 °C. In such circumstances, the furfural removal efficiency for TAP, PS/nZVI, PS, and nZVI was 94.5, 9, 3, and 2%, respectively. Therefore, based on the synergy index (SI) values, the combination of PS, nZVI, and heat can lead to a synergistic effect in the performance of the thermochemical process.

A novel magnetic bio-adsorbent was prepared from the leaves of Aegle marmelos tree (Indian bael) and Fe₂O₃ nanoparticles. The AMP@Fe₂O₃ nanocomposite (Aegle marmelos leaf powder) was synthesized by pyrolysis process and applied for As(V) removal through batch adsorption process. The synthesized AMP@Fe₂O₃ nanocomposite was analyzed by several instrumental techniques like XRD, FESEM, TEM, HRTEM, FTIR, BET, and VSM studies. Maximum amount of As(V) was removed at pH 3, contact time of 250 min, adsorbent dose of 0.1 g/L, and initial concentration of 0.5 mg/L at room temperature. The model study revealed that the pseudo-second-order kinetics and Langmuir isotherm models were best fitted with the experimental data. The nanocomposite showed a maximum adsorption capacity of 69.65 mg/g. The endothermic nature of the adsorption process was ascertained from the thermodynamics studies. The zeta potential and FTIR analysis before and after adsorption demonstrated two types of adsorption mechanism. The first one was the electrostatic attraction between negatively charged As(V) ions (H₂AsO₄⁻) and protonated −OH group present on the Fe₂O₃ surface and the second one was ligand exchange between the surface hydroxyl groups and As(V) ions. The AMP@Fe₂O₃ nanocomposite was desorbed with 0.5 M NaOH solutions and also used up to four cycles without any major decrease in removal efficiency. Thus, AMP@Fe₂O₃ nanocomposite can be applied as a potential adsorbent for As(V) removal from wastewater.

In this research, we conducted a statistical analysis of ten (metalloid) heavy metals, including Cu, Hg, Cd, Zn, Pb, As, Ni, Cr, Co, and Mn in urban dust of 58 cities in China from 2000 to 2018, and then we analyzed the statistic characters, pollution statue, and health risks of ten heavy metals. Results showed that (1) the maximum (average) values of ten (metalloid) heavy metals in the street dust of 58 Chinese cities all exceeded Chinese background values, and there were obvious differences in contents of heavy metals of Hg, Zn, Co, Cr, and As between industry cities and common cities. A provincial spatial distribution analysis revealed large variations of distributions of heavy metals Cu, Zn, Pb, and Cr, which distributed in cities mainly located in southern, central, and eastern China, ranging from relatively low to high levels, while Ni, Co, and Mn mainly distributed in southern and central China. This is mainly associated with the mining of the cities. (2) Igₑₒ analysis showed that there was no obvious Ni, Mn, or Co pollution in street dust, while the other tested heavy metals had a range of low to high levels of pollution, in particular, seven metals among them had low to extremely strong levels of pollution (Igₑₒ values between 0 and 7.154), and the average Igₑₒ values were in the following order: Cd > Hg > Zn > Pb > Cu > As>Cr > Mn > Co > Ni. (3) Health risks evaluation showed that of the three exposure ways, the HQᵢₙg from hand-mouth intake was the most common exposure route for both children and adults, especially for children, followed by skin absorption and respiration ways. This research showed that the HI value for children was higher than 1, indicative of no carcinogenic risks, while the HI values for both male and female were lower than 1, indicative of carcinogenic risks; calculation of carcinogenic risk through respiratory route showed that the risks of five elements were within the range 10⁻⁶–10⁻⁴, indicative of carcinogenic risk, among which Cr accounting exceeded 90% of total, which needs to be paid more attention to.

Internal micro-electrolysis (IE) coupled with Fenton oxidation (IEF) was a very effective technology for copper (Cu)–ethylenediaminetetraacetic acid (EDTA) wastewater treatment. However, the mechanisms of Cu²⁺ removal and EDTA degradation were scarce and lack persuasion in the IEF process. In this paper, the decomplexation and removal efficiency of Cu–EDTA and the corresponding mechanisms during the IEF process were investigated by batch test. An empirical equation and the oxidation reduction potential (ORP) index were proposed to flexibly control IE and the Fenton process, respectively. The results showed that Cu²⁺, total organic carbon (TOC), and EDTA removal efficiencies were 99.6, 80.3, and 83.4%, respectively, under the proper operation conditions of iron dosage of 30 g/L, Fe/C of 3/1, initial pH of 3.0, Fe²⁺/H₂O₂ molar ratio of 1/4, and reaction time of 20 min, respectively for IE and the Fenton process. The contributions of IE and Fenton to Cu²⁺ removal were 91.2 and 8.4%, respectively, and those to TOC and EDTA removal were 23.3, 25.1, and 57, 58.3%, respectively. It was found that Fe²⁺-based replacement–precipitation and hydroxyl radical (•OH) were the most important effects during the IEF process. •OH played an important role in the degradation of EDTA, whose yield and productive rate were 3.13 mg/L and 0.157 mg/(L min⁻¹), respectively. Based on the intermediates detected by GC-MS, including acetic acid, propionic acid, pentanoic acid, amino acetic acid, 3-(diethylamino)-1,2-propanediol, and nitrilotriacetic acid (NTA), a possible degradation pathway of Cu–EDTA in the IEF process was proposed. Graphical abstract The mechanism diagram of IEF process