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.

The transformation of less toxic Cr(III) species to harmful Cr(VI) is worth concerning. Compared with free Cr(III), however, the photo-oxidation of Cr(III)–organic acid complexes is seldom reported. In this study, Cr(III)–malate complex was synthesized and purified, and its photo-oxidation was investigated to reveal the potential conversion pathway of Cr(III) to Cr(VI). The results indicated that Cr(III)–malate complex could be gradually photo-oxidized to Cr(VI) through a ligand–metal charge transfer path. Higher pH and stronger light intensity promoted the conversion process. A 50-μM Cr(III)–malate complex was almost completely oxidized to Cr(VI) within 420-min irradiation of 500 W medium-pressure mercury lamp at pH 12. The introduction of H₂O₂, considered as a direct source of hydroxyl radicals (·OH) in the presence of Cr(II), markedly enhanced the yield of Cr(VI), and a complete oxidation of Cr(III)–malate complex (50 μM ) was realized within 20 min. Under a weak acidic condition, the production of Cr(VI) was coupled with the reduction of Cr(VI) by malic acid and its free radical generated from Cr(III)–malate complex, leading a gradual decrease in Cr(VI) concentration with the reaction.

Sorption–desorption behavior of the antibiotic tetracycline (TET) and the synthetic estrogen hormone 17α-ethinylestradiol (EE2) with wastewater sludge and sludge-derived humic substances [humic acid (HA) and humin] was investigated. From acidic functional group capacity and elemental analyses, HA had higher polarity, aromaticity, and acidity than humin; humin contained aliphatic chains with high mineral content. The different physicochemical properties of the pharmaceuticals and sludge components yielded different kinds of sorption–desorption interactions. Partitioning coefficients (Kd) of TET to sludge were higher (1,552 ± 41–4,667 ± 41 L/kg) than EE2 (534 ± 52–609 ± 47 L/kg). TET sorption was highly pH-dependent and maximal at pH 9. Ca²⁺ions enhanced sorption, emphasizing the role of polyvalent metal ions in forming TET–sludge complexes. Humin was the dominant component for TET sorption due to its high inorganic matter content. In contrast, EE2 sorption was independent of solution pH, forming mostly hydrophobic interactions with sludge organic matter. EE2 had a high affinity for HA due to its chemical structure. Desorption of the two pharmaceuticals differed as well. The amount of desorbed TET (18.7 ± 1.3–29.8 ± 2 %) was lower than that of EE2 (60.6 ± 3–62.3 ± 2 %), and the hysteresis index was higher for TET than EE2. While TET desorption tended to be delayed in the solid matrix, EE2 desorbed easily and in accordance with the aqueous equilibrium concentration. The conclusions emphasize the need for further research into frequently used pharmaceuticals with different physicochemical properties and the recognition of sludge application as an important source of distribution for these contaminants in the environment.

Bauxsol is a chemico-physically modified product of red mud and is a promising material for the removal and recovery of phosphorus from wastewater. In this study, response surface methodology (RSM) and artificial neural network (ANN) were employed to develop prediction models and also to investigate the interactions of independent experimental factors for phosphorus adsorption onto acid-activated Bauxsol. The experimental results indicated that HCl activation was effective to improve the adsorption capacity of Bauxsol. The maximum adsorption capacity of acid-activated Bauxsol was 55.72 mg/g (as P) with HCl concentration of 10.20 mol/L, temperature of 41.00 °C, and time of 5.60 h, which increased by 10.53 and 6.62 times compared with the raw red mud and Bauxsol before acid activation, respectively. The relative importance of HCl concentration in RSM and ANN models was 51.78 and 54.25 %, respectively, which illustrated that HCl concentration played the predominant role on improving the adsorption capacity of Bauxsol. The predictive capability of RSM and ANN models was compared, and the results showed that both models provided excellent predictions with R² > 0.93. However, the ANN model showed the superiority over RSM for estimation capability.

Pirina, a waste of olive oil factory, was used as an adsorbent for the removal of remazol brilliant blue R (RBBR) from aqueous solution by adsorption process. The pirina was pretreated with HNO₃before batch adsorption experiments. The effects of contact time, initial concentration, pH, temperature, and ionic strength on dye removal were investigated. While the amount of the dye removed by the pirina was increasing with increasing initial concentration and temperature, it decreased with an increase in pH. Moreover, commercial activated carbon (CAC) was also used to compare with the pirina in removing the RBBR. The maximum amounts of the RBBR removed by the pirina and the CAC were 23.63 and 199.45 mg g⁻¹per unit mass of the adsorbents, and the removal efficiencies of them were found as 94.52 and 99.72 %, respectively. Ionic strength in the presence of NaCl and KCl had also a reducing effect on the removal efficiency. The adsorption isotherm was in the best harmony with Langmuir, Freundlich, and Temkin models. The adsorption kinetic obeyed the pseudo-second-order and the intra-particle diffusion models. The values of the r²from the pseudo-second-order kinetic and intra-particle diffusion were between 0.984–0.999 and 0.85–0.996, respectively. From thermodynamic studies, it was seen that the adsorption was of spontaneous and endothermic nature. The values of ΔG° of the adsorption were between −3,218 and −8,867 J mol⁻¹. The values of ΔH° and ΔS° were 50,134 J mol⁻¹and 179 J mol⁻¹ K⁻¹, respectively. Moreover, SEM and FT-IR studies were also performed.

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.

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.

During this study, the effect of applying several types of treated domestic wastewater on the translocation and accumulation of organic and inorganic micropollutants in soil and radish plants (Raphanus sativus L.) was examined. Primary (PTW), secondary (STW) and tertiary (TTW) treated wastewater as well as tap water (TW) were used for the irrigation of radish plants for a period (transplantating and harvesting) of 67 days. Higher concentrations of polycyclic aromatic hydrocarbons (PAHs) were observed in soils irrigated with PTW. The concentration of PAHs in radish roots ranged between 107.6 ± 12.1 μg/kg for plants irrigated with TTW and 124.1 ± 17.7 μg/kg for plants irrigated with PTW. The root concentration factors (RCFs) expressed as the ratio of PAH concentration in the root mass (dry weight) to the residual concentration in the soil varied from 1.6 to 1.9 indicating a higher accumulation of PAHs in the edible part of radishes than soil. Heavy metals were not detected in the wastewaters utilised and, as a result, no accumulation was found in either the soil or plants in comparison with tap water. RCFs for heavy metals were calculated between 0.91 and 0.99, 0.49 and 0.66, 0.004 and 0.005 for Cu, Zn and Ni, respectively. The results showed that radishes have the ability to concentrate PAHs when they are present in the wastewater and this could have associated health risks.

Surface mining for coal is responsible for widespread degradation of water resources and aquatic ecosystems in the Appalachian Region, USA. Because native topsoils are typically not retained on Appalachian mined sites, mine soils are usually composed of crushed overburden. This overburden tends to contribute high salinity loads to downstream aquatic systems. Also, loss of transpiration from forests and reduced infiltration associated with conventional reclamation procedures lead to altered water budgeting and stream morphology. To investigate the influence of the geologic composition of this overburden on water quality and tree growth, a series of experimental plots were constructed on a reclaimed surface mine site in eastern Kentucky, USA, in 2005. Treatments included unweathered GRAY sandstone, weathered BROWN sandstone, and MIXED sandstones and shale spoils. Plots were composed of end-dumped, uncompacted spoils and were designed to drain interflow through data acquisition stations for sampling purposes. Most water chemical parameters had stabilized across all treatments by 9 years after spoil placement. Discharge volume was not different among treatment types through the first 3 years after placement. However, 9 years after placement, seasonal variation in discharge on BROWN is more extreme than that on MIXED or GRAY. In addition, planted tree growth on BROWN has drastically outpaced growth on GRAY or MIXED, suggesting that evapotranspiration may be influencing seasonal variation in water discharged from BROWN. These results suggest that placement of brown weathered spoils when soil substitutes are required may lessen hydrologic impacts via improved tree growth and water utilization on surface-mined sites in Appalachia.

Drinking water network is vulnerable to toxic chemicals. Anomaly detection-based event detection can provide reliable indication of contamination by analyzing the real-time water quality data, collected by online-distributed sensors in water network. This article reviews the water quality event detection methodologies based on the correlation of water quality parameters and contaminants. Further, we review how to reduce the impact of contamination in water distribution network, including sensor placement optimization and contamination source determination.