Urban market gardening in Africa is suffering from increasing environmental contamination due to sources of contamination as varied as traffic, industry, and agriculture practices. A field study was therefore conducted to determine the global influence of the polluted environment (atmosphere, soil, and irrigation waters) on vegetable quality in a large urban-farming area. For leafy vegetables collected in 15 ha of squatted land belonging to the international airport of Cotonou, total concentrations of metal(loid)s measured in consumed parts of Lactuca sativa L. and Brassica oleracea were 52.6–78.9, 0.02–0.3, 0.08–0.22, 12.7–20.3, 1.8–7.9, and 44.1–107.8 mg kg⁻¹for Pb, Cd, As, Sb, Cu, and Zn, respectively. Human gastric bioaccessibility of the metal(loid)s was measured, and the obtained values varied according to the considered metal(loid) and the plant species. The results identified values that are commonly found in non-polluted soils and roots associated with contaminated edible parts, raising the possibility of atmospheric contamination. Such a hypothesis is in agreement with values of magnetic susceptibility, since iron oxides and probably their associated metal(loid)s do not translocate from the roots toward the upper parts of the plants. (Bioaccessible) estimated dose intake ((B)EDI) and total (bioaccessible) target hazard quotient (Σ(B)THQ) were calculated to assess the health risk of consuming vegetables from this area. Pb and Sb were the major risk contributors. Taking the bioaccessible fractions into account, ΣBTHQ values were lower than ΣTHQ but were all still >1 for both males and females, leading to the conclusion that consuming these vegetables from this area is not risk-free.

Nanoscale zero-valent iron (nZVI) was synthesized and used for the removal of Sb(III) and Sb(V) from aqueous solutions. Results showed that more than 90 % of antimony would be removed in 15 min and that all of antimony could be removed with appropriate nZVI dosage in 90 min. The influence of pH value and possible impurities was investigated. The pH of 4 was found as the optimum pH. Discussion and speculation about the mechanism were presented according to X-ray photoelectron spectroscopy and transmission electron microscopy data. A sheet-like structure was observed after a 90-min reaction, and antimony was detected on the surface by energy-dispersive X-ray spectroscopy. Both Sb(III) and Sb(V) partially reduced in the process. The presence of humic acid transformed the morphology of nZVI but barely influenced the removal efficiency. Competing ions showed diverse influence between Sb(III) and Sb(V). The overall results indicated that nZVI was an efficient and suitable material for the removal of antimony.

The aim of this work was to study the short-term effect of clear-cut harvest on concentrations of dissolved organic carbon (DOC), B, Al, Zn, Cu, Ni, Cr, Cd and Pb in drainage water from northern peatland catchments in Finland underlain by granitic or black shale bedrock, the latter having higher concentrations of several trace elements, such as Ni and Zn. Stem-only harvest (SOH) or whole-tree harvest (WTH) with stump removal were carried out at coniferous sites. Controls were left unharvested. DOC and trace element concentrations were monitored during one pre-treatment and two post-treatment years. There was no constant increase in the element concentrations. However, there were signs that both SOH and WTH clear-cut harvest on northern peatland catchments increases the concentrations of DOC, B, Al, Zn and Ni in ditchwater in some sites irrespective of the bedrock type. The greatest increases were observed in WTH sites but the study does not allow us to assess the statistical significance of the magnitude of the difference between SOH and WTH. We conclude that the element concentrations in ditchwater depend largely on site characteristics masking the possible effect of harvest.

Zn²⁺was added to one of the two identical bench-scale upflow anaerobic sludge blanket (UASB) reactors in steady-state period treating swine wastewater to evaluate the effects of Zn²⁺on performance and methanogenic population. Real-time quantitative PCR (QPCR) was used to quantify the 16S rRNA gene concentrations of the four methanogenic orders. In both reactors, the hydraulic retention time (HRT) was sustained at 48 h and the inner temperature was kept at 35 °C. Both promotion and inhibition of Zn²⁺on chemical oxygen demand (COD) removal, methane production and methanogens community were observed in accordance with different Zn²⁺dosages. COD removal rate and methane production reacted in the same way as methanogens, suggesting that the impact of Zn²⁺on the methanogenic community was the critical reason that caused the changes of UASB performance in treating swine wastewater with unstable Zn²⁺concentration. Among the methanogenic community, Methanomicrobiales (MMB) was the dominant group which got visibly impacted by the dosed Zn²⁺. Overall, lower concentration of Zn²⁺, e.g., less than 17.8 mg/L, was supposed to be advisable for a stable and high efficient treatment of swine wastewater by UASB reactor in practice.

This study demonstrates the potential of a new BiOCl₀.₈₇₅Br₀.₁₂₅ photocatalyst to degrade pharmaceuticals in water (i.e., carbamazepine (CBZ), ibuprofen (IBF), bezafibrate (BZF), and propranolol (PPL)), under simulated solar irradiation. Different parameters were examined through their influence on CBZ degradation. Increasing the catalyst concentration up to 500 mg/L increased CBZ degradation rate; however, above 500 mg/L, CBZ degradation rate was slightly reduced, most likely due to the catalyst’s light-screening effect at high concentrations. Increasing the pH of the tested solution from 4 to 9 decreased the degree of CBZ adsorption to the catalyst and consequently its degradation rate. Quantum yield for CBZ degradation was found to be 0.75 ± 0.05 % using an integrating sphere for absorbance measurements to correctly account for scattering of light by the suspended catalyst. Degradation rates of all examined compounds (at pH 7) followed the order PPL > BZF > IBF > CBZ (highest rate for PPL). Interestingly, PPL was least adsorbed to the catalyst, implying that adsorption is not always mandatory for efficient degradation with BiOCl₀.₈₇₅Br₀.₁₂₅. Different adsorption mechanisms were hypothesized for the different pharmaceuticals, including hydrophobic attraction for the neutrally charged CBZ and ion exchange for the negatively charged IBF and BZF.

A column experiment was conducted to evaluate the effectiveness of nanoscale zerovalent iron (nZVI) for the in situ immobilization of Pb and Zn in an acidic soil. The impact of nZVI on soil was evaluated by monitoring the physicochemical characteristics of the leachates and their ecotoxicological effects on three species, Vibrio fischeri, Artemia franciscana, and Caenorhabditis elegans. Treatment with nZVI resulted in more effective Pb immobilization in comparison to Zn and reduced the leachability by 98 and 72 %, respectively; the immobilization was stable throughout the experiment. Leachates from nZVI-treated soils showed lower toxicity than leachates from untreated ones. The highest toxicity in treated soils was observed in the first leachate, which presented high values of electrical conductivity due to the leachability of soil ions and those provided by the commercial nanoparticle suspension (Na and Fe). V. fischeri and C. elegans were more sensitive to leachates from nZVI-treated soils polluted with Zn than those from soils polluted with Pb; A. franciscana showed the opposite trend.

The article, Pilot-Scale Test for a Phosphate Treatment Using Sulfate-Coated Zeolite at a Sewage Disposal Facility by Jae-Woo Choi, Kyu-Sang Kwon, Soonjae Lee, Byungryul An, Seok-Won Hong, Sang-Hyup Lee, is replete with some fundamental scientific flaws which have the potential to misinform readers. This comment seek to correct these flaws.

Cyanobacterial toxins have caused worldwide concern because of their lethal effects, which has led to intensive search of cost-effective removal techniques. With the application of a Box–Behnken experimental design combined with response surface methodology, the adsorption process of the potent and commonly occurring microcystin-LR (MC-LR) onto nano-sized montmorillonite (NMMT) K10 was investigated through the HPLC-UV system. The quadratic statistical model was established to predict the interactive effects of pH (1–12), NMMT K10 dose (1–10 mg mL⁻¹), and MC-LR initial concentration (100–1,000 μg L⁻¹) on MC-LR adsorption and to optimize the controlling parameters. The MC-LR adsorption by NMMT K10 was pH dependent and was found to reach a maximum at pH 2.96 with a removal peak of 186.37 μg g⁻¹. The range of optimal pH for MC-LR adsorption was 2.96–3.48, and higher adsorption capacities were achieved with increasing adsorbent dose and MC-LR initial concentration. Sorption kinetics revealed that the sorption process of MC-LR on NMMT K10 was rapid (short equilibrium time) and involved several kinetic stages. The Langmuir isotherm model predicted that the theoretical maximum adsorption capacity at pH 3 was 285.20 μg g⁻¹. Alkali eluting media (0.1 M NaOH) showed the highest desorption percentage (75.3 %) during regeneration studies. The high Brunauer–Emmett–Teller (BET) specific surface area (204.65 m² g⁻¹) of NMMT K10 was also characterized. NMMT K10 was determined to be an effective and economic adsorbent for MC-LR removal on a large scale.

Evaluation of variation in the concentration of heavy metal provides vital information about the spatial behavior of the metals affecting the air quality. In the present study, lichen samples of the species Pyxine subcinerea Stirton were collected in the Rudraprayag valley to investigate the metal profile that bioaccumulated in lichens. Multivariate statistical analysis was carried out to elucidate possible contribution of various sources of pollution including anthropogenic sources on heavy metal profile of lichens. Cluster analysis successfully grouped geogenic and anthropogenic inputs represented by Al and Mn and Cu, Cd, Pb, and Zn, respectively. Principal component analysis also segregated sites based on the origin (major contributors).

The present study deals with the synthesis and subsequent application of Fe₃O₄@n-SiO₂nanoparticles for the removal of Cr(VI) from aqueous solutions. Rice husk, an agrowaste material, was used as a precursor for the synthesis of nanoparticles of silica. Synthesized nanoparticles were characterized by XRD and SEM to investigate their specific characteristics. Fe₃O₄@n-SiO₂nanoparticles were used as adsorbent for the removal of Cr(VI) from their aqueous solutions. The effects of various important parameters, such as initial Cr(VI) concentration, adsorbent dose, temperature, and pH, on the removal of Cr(VI) were analyzed and studied. A pH of 2.0 was found to be optimum for the higher removal of Cr(VI) ions. It was observed that removal (%) decreased by increasing initial Cr(VI) concentration from 1.36 × 10⁻²to 2.4 × 10⁻² M. The process of removal was found to be endothermic, and the removal increased with the rise in temperature from 25 to 45 °C. The kinetic data was better fitted in pseudo-second-order model in comparison to pseudo-first-order model. Langmuir and Freundlich adsorption capacities were determined and found to be 3.78 and 1.89 mg/g, respectively, at optimum conditions. The values of ΔG⁰were found to be negative at all temperatures, which confirm the feasibility of the process, while a positive value of ΔH⁰indicates the endothermic nature of the adsorption process. The present study revealed that Fe₃O₄@n-SiO₂nanoparticles can be used as an alternate for the costly adsorbents, and the outcome of this study may be helpful in designing treatment plants for treatment of Cr(VI)-rich effluents.