The scarcity of water resources in Egypt has necessitated the use of various types of lower quality water. Agricultural drainage water is considered a strategic reserve for meeting increasing freshwater demands. In this study, a novel model series was applied to a drainage basin in the Nile Delta to optimize integrated water quality management for agriculture and the aquatic environment. The proposed model series includes a waste load allocation model, an export coefficient model, a stream water quality model, and a genetic algorithm. This model series offers an optimized solution for determining the required removal levels of total suspended solids (TSS), the chemical oxygen demand (COD) at point and non-point pollution sources, and the source flows that require treatment to meet a given water quality target. The model series was applied during the summer and winter to the El-Qalaa basin in the western delta of the Nile River. Increased pollutant removal and treated fractions at point and non-point sources reduced violations of the TSS standards from 732.6 to 238.9 mg/L in summer and from 543.1 to 380.9 mg/L in winter. Likewise, violations of the COD standards decreased from 112.4 mg/L to 0 (no violations) in summer and from 91.7 mg/L to no violations in winter. Thus, this model is recommended as a decision support tool for determining a desirable waste load allocation solution from a trade-off curve considering costs and the degree of compliance with water quality standards.

The main objective of this study was to investigate the degradation mechanism, the reaction kinetics, and the evolution of toxicity of naproxen in waters under simulated solar radiation. These criteria were investigated by conducting quenching experiments with reactive oxygen species (ROS), oxygen concentration experiments, and toxicity evaluations with Vibrio fischeri bacteria. The results indicated that the degradation of naproxen proceeds via pseudo first-order kinetics in all cases and that photodegradation included degradation by direct photolysis and by self-sensitization via ROS; the contribution rates of self-sensitized photodegradation were 1.4 %, 65.8 %, and 31.7 % via ·OH,¹O₂and O₂•⁻, respectively. Furthermore, the oxygen concentration experiments indicated that dissolved oxygen inhibited the direct photodegradation of naproxen, and the higher the oxygen content, the more pronounced the inhibitory effect. The toxicity evaluation illustrated that some of the intermediate products formed were more toxic than naproxen.

Among the different organic pollutants, persistent organic pollutants and emerging organic contaminants (EOCs) are of particular concern due to their potentially dangerous effects on the ecosystems and on human health. In the framework of the analysis of some of these organic pollutants in water samples, sorptive extraction devices have proven to be adequate for their monitoring. The efficiency of four commercially available and low-cost polymeric materials [polypropylene, poly(ethylene terephthalate), Raffia, and polyethersulfone (PES)] for the simultaneous extraction of 16 organic compounds from five different families from environmental water samples was evaluated in this work. Firstly, the homogeneity of the sorbent materials was confirmed by means of Raman spectroscopy. After the optimization of the parameters affecting the extraction and the liquid desorption steps, it was found that PES showed the largest efficiencies for slightly polar analytes and, to a lesser extent, for nonpolar analytes. Additionally, Raffia rendered good extraction efficiencies for nonpolar compounds. Thus sorptive extraction methods followed by large volume injection-programmable temperature vaporizer-gas chromatography-mass spectrometry were validated using PES and Raffia as sorbent materials. The validation of the method provided good linearity (0.978 < r ² < 0.999 for PES and 0.977 < r ² < 0.999 for Raffia), adequate repeatability (below 19 % and 14 % for PES and Raffia, respectively), and low method detection limits (low ng · l⁻¹ level). Finally, these materials were applied to the analysis of contaminants in environmental water samples.

Many polluted sites are typically characterized by contamination with multiple heavy metals, drought, salinity, and nutrient deficiencies. Here, an Australian native succulent halophytic plant species, Carpobrotus rossii (Haw.) Schwantes (Aizoaceae) was investigated to assess its tolerance and phytoextraction potential of Cd, Zn, and the combination of Cd and Zn, when plants were grown in soils spiked with various concentrations of Cd (20–320 mg kg⁻¹Cd), Zn (150–2,400 mg kg⁻¹Zn) or Cd + Zn (20 + 150, 40 + 300, 80 + 600 mg kg⁻¹). The concentration of Cd in plant parts followed the order of roots > stems > leaves, resulting in Cd translocation factor (TF, concentration ratio of shoots to roots) less than one. In contrast, the concentration of Zn was in order of leaves > stems > roots, with a Zn TF greater than one. However, the amount of Cd and Zn were distributed more in leaves than in stems or roots, which was attributed to higher biomass of leaves than stems or roots. The critical value that causes 10 % shoot biomass reduction was 115 μg g⁻¹for Cd and 1,300 μg g⁻¹for Zn. The shoot Cd uptake per plant increased with increasing Cd addition while shoot Zn uptake peaked at 600 mg kg⁻¹Zn addition. The combined addition of Cd and Zn reduced biomass production more than Cd or Zn alone and significantly increased Cd concentration, but did not affect Zn concentration in plant parts. The results suggest that C. rossii is able to hyperaccumulate Cd and can be a promising candidate for phytoextraction of Cd from polluted soils.

In spite of its wide-world economic relevance, wine production generates a huge amount of waste that threatens the environment. A batch experiment was designed to assess the effect of the amendment of an agricultural soil with two winery wastes (perlite and bentonite wastes) in the immobilization of cyprodinil. Waste addition (0, 10, 20, 40, and 80 Mg ha⁻¹) and different times of incubation of soil-waste mixtures (1, 30, and 120 days) were tested. The addition of wastes improved the soil’s ability to immobilize cyprodinil, which was significantly correlated to total C content in soil-waste mixtures. Longer incubation times decreased the cyprodinil sorption possibly due to the mineralization of organic matter but also as a consequence of the high pH values reached after bentonite waste addition (up to 10.0). Cyprodinil desorption increased as the amount of waste added to soil, and the incubation time increased. The use of these winery wastes contributes to a more sustainable agriculture preventing fungicide mobilization to groundwater.

The ability of certain white-rot fungi (WRF) inocula to transform heptachlor and heptachlor epoxide and its application in artificially contaminated soil were investigated. Fungal inoculum of Pleurotus ostreatus eliminated approximately 89 % of heptachlor after 28 days of incubation, and chlordene was detected as the primary metabolite. The fungal inoculum of Pleurotus ostreatus had the highest ability to degrade heptachlor epoxide; approximately 32 % were degraded after 28 days of incubation, and heptachlor diol was detected as the metabolite product. Because Pleurotus ostreatus transformed heptachlor into a less toxic metabolite and could also effectively degrade heptachlor epoxide, it was then selected to be applied to artificially contaminated soil. The spent mushroom waste (SMW) of Pleurotus ostreatus degraded heptachlor and heptachlor epoxide by approximately 91 and 26 %, respectively, over 28 days. This finding indicated that Pleurotus ostreatus SMW could be used to bioremediate heptachlor- and heptachlor epoxide-contaminated environments.

Current techniques for the ecological risk assessment of chemical substances are often criticised for their lack of environmental realism, ecological relevance and methodological accuracy. ChimERA is a 3-year project (2013–2016), funded by Cefic’s Long Range Initiative (LRI) that aims to address some of these concerns by developing and testing mechanistic fate and effect models, and coupling of these models into one integrated platform for risk assessment. This paper discusses the backdrop against which this project was initiated and lists its objectives and planned methodology.

Oceans play a significant role in the cycling of trace metals and persistent organic pollutants. In this study, aerosol samples covering the whole northern South China Sea (SCS) were collected in 2005 and 2007, respectively, for analysis of trace metals and major elements. The levels of trace metals detected ranged from 0.514 to 119 ng/m³in 2005 and from 0.130 to 24.2 ng/m³in 2007, respectively. Cu, Zn, and Pb were the three predominant metals with high enrichment factors (>10), indicating the strong anthropogenic inputs. The trace metals over SCS were comparable to the values in suburban and background sites of South China, but generally higher than those over other seas and oceans. Considering the fact that they were influenced by their proximity to source regions and air mass origins, the elevated metals in 2005 were probably attributed to the strong wind and long-range atmospheric transport driven by Asian monsoon.

Occurrence, distribution, spatial and seasonal variations, and partitioning between aqueous phase and suspended particulate matters (SPM) of triclocarban (TCC) and triclosan (TCS) in Xiaoqing River, which receives wastewater treatment plant (WWTP) effluents, were studied. The distribution of the total TCC and TCS levels in surface water and sediments along the river were discussed. The highest TCC and TCS concentrations were both found near the discharge port of WWTPs, and the TCC and TCS levels decreased downstream of the WWTPs as a result of their distances from the source of WWTP discharges. The mean values of TCC and TCS in low-flow season were 1.62 and 1.80 times, respectively, as much as in high-flow season in surface water. The study on partitioning of TCC and TCS between aqueous phase and SPM shown the mean level of dissolved TCC accounted for about 10 % of the total level in surface water, whereas the TCS level was about 30 %. The TCC concentrations detected in the surface sediment samples (0 to 5 cm) ranged from 226 to 1,956 ng/g, with a mean value of 733 ng/g. The TCS levels were between 85 and 705 ng/g, with a mean value of 255 ng/g. The distribution and variations of TCC and TCS in sediments along the river were highly consistent with those in the water phase. The TCC and TCS levels in deep sediments (5 to 10 cm) were significantly lower than those in surface sediments. The mean TCC level in surface sediments was about 2.4 times as much as in deep sediments, and the TCS level in surface sediments was 3.1 times as much as in deep sediments.

This study was aimed at investigating the physicochemical and microbiological changes that took place during the ageing process of spent bleaching earth in the presence of autochthonous microorganisms. Research material included fresh spent bleaching earth (SBE₀) and the same material after 3 years of storage at the constant temperature of 20 °C, without aeration and moistening (SBE₃). Changes in the chemical composition of analysed waste material were observed during its ageing process point to a spontaneous bioconversion of fat substance towards formation and/or release of free saturated fatty acids C16:0 and C18:0 (14.3 g 100 g⁻¹D.M.), triterpenes (8.48 g 100 g⁻¹D.M.), cholesterol (3.29 g 100 g⁻¹D.M.), small quantities of carbohydrates and esters (0.80 g 100 g⁻¹D.M.). This process was accompanied by other changes in physicochemical parameters of the waste material, such as colour, odour and viscosity, decrease in fat content from 28.27 to 24.6 % and that of soluble forms of metals (Mo, Cu, Fe, Zn, Ni, Cr and Mn), ranging from 25 to 75 %, and an increase in pH, from 3.85 to 4.2. At the same time, changes in the microbial consortium were observed.