The comparative effectiveness for hexavalent chromium reduction and removal from irrigation water, using three selected plant species (Phragmites australis, Salix viminalis, and Ailanthus altissima) planted in soil contaminated with hexavalent chromium, has been studied in the present work. The above plant species were irrigated, in a continuous mode, with water, contaminated with 10 mg/L of hexavalent chromium. Hexavalent chromium and total chromium have been measured in all plant tissues species and in the drainage water. Total chromium removal from water was ranging from 56 % (Phragmites) to 70 % (Salix). After 360 days of growth, the chromium content of the contaminated soil dropped from 70 (initial) to 32, 36, and 41 mg Cr/kg₍dᵣy ₛₒᵢₗ₎, for Salix, Phragmites, and Ailanthus, respectively. Salix and Phragmites accumulated the highest amount of chromium in the roots (2,029 and 1,800 mg Cr/kg₍dᵣy ₜᵢₛₛᵤₑ₎, respectively), compared with 358 mg Cr/kg₍dᵣy ₜᵢₛₛᵤₑ₎for Ailanthus roots. Most of chromium was found in trivalent form in all plant tissues. Ailanthus had the lowest affinity for Crⱽᴵreduction in the root tissues. Phragmites indicated the highest chromium translocation potential, from roots to stems, while Salix indicated the highest chromium translocation from roots to leaves. Toxicity effects, expressed as root growth rate inhibition, indicated that Salix is the most chromium-tolerant species, with Ailanthus in the antipode.

Tungsten (W) concentrations were measured along with arsenic (As) in groundwaters from the Murshidabad district of West Bengal, India. Tungsten concentrations range from 0.8 to ~8 nmol kg⁻¹(0.15–1.5 μg kg⁻¹) in the circumneutral pH (average pH ~ 7.3) Murshidabad groundwaters, and attain concentrations as high as 14 nmol kg⁻¹(2.5 μg kg⁻¹) in local ponds (n = 2). Total dissolved As concentrations (AsT) range from 0.013 to 53.9 μmol kg⁻¹(<1 to 4,032 μg kg⁻¹), and As(III) predominates in Murshidabad groundwaters accounting for 70 %, on average, of As in solution. Tungsten concentrations in Murshidabad groundwaters are low compared to alkaline groundwaters (pH > 8) from the Carson Desert in Western Nevada, USA, where W concentrations are reported to reach as high as 4,036 nmol kg⁻¹(742 μg kg⁻¹). Although W is positively correlated with As in groundwaters from the Carson Desert, it is not correlated with AsTor As(III) in Murshidabad groundwaters, but does exhibit a weak relationship with As(V) in these groundwaters. Surface complexation modeling indicates that pH related adsorption/desorption can explain the geochemical behavior of W in Murshidabad groundwaters. However, the model does not predict the high As concentrations observed in Murshidabad groundwaters. The high As and low W concentrations measured in Murshidabad groundwaters indicate that either As and W originate from different sources or are mobilized by different biogeochemical processes within the Murshidabad aquifers. Mobilization of As in Murshidabad groundwaters is presumed to reflect reductive dissolution of Fe(III) oxides/oxyhydroxides and release of sorbed and/or coprecipitated As to the groundwaters. Multivariate statistical analysis of groundwater composition data indicate that W is associated with Mn and Cl⁻, which may point to a Mn oxide/oxyhydroxide, clay mineral, and/or apatite source for W in the Murshidabad sediments.

Recent scientific findings and legislations have clearly highlighted the need for comprehensive approaches and methods to evaluate natural dust contributions to an urban atmosphere. The evaluation of chemical compositions of airborne aerosols is of these methods that may employ several advanced analytical techniques and processes. In this paper, an episodic appearance of Saharan dust incursion over a megacity (Istanbul, Turkey) was investigated using size segregated particulate matter (PM) samples in fine and coarse fractions collected between February 27 and March 8, 2009. The Saharan impact was investigated using satellite observations, backward air trajectory statistics, and chemical analyses of the collected samples. In the chemical analyses, Fourier transform infrared coupled with attenuated total reflectance (ATR-FTIR) spectroscopic method was used to determine the functional groups, namely, alcohols, ammonium, aliphatic carbons, carbonyls, organonitrates, nitrate, silicate, silica, kaolinite, and calcium carbonate. Among all the measured functional groups, it was clearly seen that the intensities of IR peaks related to silicate, silica, kaolinite, and calcium carbonate were associated with the increased mass concentrations during the impact period. The observed IR peaks at 1,030 and 800 cm⁻¹for silicate ions in the samples can be used as an indicator of the large dust incursion into the atmosphere (e.g., Saharan dust episodes observed in Istanbul). This study showed that the ATR-FTIR spectroscopic method is a fast and convenient method to identify these peaks and the IR method in general is useful for identifying a large dust incursion into the atmosphere.

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.

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.