Photodegradation of methylene blue (MB) was studied on TiO₂in the presence of activated carbon (AC) prepared from the sawdust of a soft wood by physical activation under CO₂flow, by pyrolysis under N₂flow, and by chemical activation with ZnCl₂and H₃PO₄under N₂flow. MB photodegradation was performed under UV and UV-visible irradiation to verify the scaling-up of the present TiO₂-AC binary materials. It was verified that oxygenated surface groups on carbon were intrinsically photoactive, and a synergy effect between both solids has been estimated from the first-order apparent rate constants in the photodegradation of MB. This effect enhances the photoactivity of TiO₂up to a factor of about 9 under visible irradiation, and it was associated to the surface properties of AC.

The antioxidant diphenylamine (DPA) is used in fruit-packaging plants for the control of the physiological disorder apple scald. Its use results in the production of DPA-contaminated wastewater which should be treated before finally discharged. Biological treatment systems using tailored-made microbial inocula with specific catabolic activities comprise an appealing and sustainable solution. This study aimed to isolate DPA-degrading bacteria, identify the metabolic pathway of DPA and evaluate their potential for future implementation in bioremediation and biodepuration applications. A Pseudomonas putida strain named DPA1 able to rapidly degrade and utilize DPA as the sole C and N source was enriched from a DPA-contaminated soil. The isolated strain degraded spillage-level concentrations of DPA in liquid culture (2000 mg L⁻¹) and in contaminated soil (1000 mg kg⁻¹) and metabolized DPA via the transient formation of aniline and catechol. Further evidence for the bioremediation and biodepuration potential of the P. putida strain DPA1 was provided by its capacity to degrade the post-harvest fungicide ortho-phenylphenol (OPP), concurrently used by the fruit-packaging plants, although at slower rates and DPA in a wide range of pH (4.5–9) and temperatures (15–37 °C). These findings revealed the high potential of the P. putida strain DPA1 for use in future soil bioremediation strategies and/or as start-up inocula in wastewater biodepuration systems.

The in situ stabilization of metals in soils using plants with great biomass value is a promising, cost-effective, and ecologically friendly alternative to manage metal-polluted sites. The goal of phytostabilization is to reduce the bioavailable concentrations of metals in polluted soil and thus reduce the risk to the environment and human health. In this context, this study aimed at evaluating Miscanthus × giganteus efficiency in phytostabilizing metals on three contaminated agricultural sites after short-term exposure under greenhouse conditions and after long-term exposure under field conditions. Particular attention was paid to the influence of Miscanthus cultivation on (i) Cd, Pb, and Zn fractionation using sequential extractions and (ii) metal bioaccessibility using an in vitro gastrointestinal digestion test. Data gave evidence of (i) different behaviors between the greenhouse and the field; (ii) metal redistribution in soils induced by Miscanthus culture, more specifically under field conditions; (iii) higher environmental availability for Cd than for Pb and Zn was found in both conditions; and (iv) overall, a higher bioaccessible fraction for Pb (about 80 %) and Cd (65–77 %) than for Zn (36–52 %) was recorded in the gastric phase, with a sharp decrease in the intestinal phase (18–35 % for Cd, 5–30 % for Pb, and 36–52 % for Zn). Compared to soils without culture, the results showed that phytostabilization using Miscanthus culture provided evidence for substantial effects on oral bioaccessibility of Cd, Pb, and Zn.

In this study, we investigated the nature of phosphate phase present in sediment of Lake Dang. The phosphate speciation was determined by sequential extraction method. The concentration of phosphate in solution was measured by the ammonium molybdate method with ascorbic acid as the reducing agent. Water and sediment (surface and bottom) were sampled at eight points around the lake by taking into account activities around the lake during dry and rainy seasons. The results showed five forms of phosphorus presents in the sediments. The rank order obtained was Res-P < P-L < P-OM < P-Ca < P-Fe with the prevalence of inorganic phosphorus (P-L + P-Ca + P-Fe) than organic phase. The average phosphorus (P) content was 133, 86, and 52 μg g⁻¹for the surface layer (A, 0–5 cm), medium layer (B, 5–10 cm), and bottom layer (C, 10–15 cm), respectively. This P-content depletion with depth can be explained mainly by oxygen depletion with depth which enhance P desorption. Except P-L form, the P contents were higher in rainy season compared to the dry season. The results of principal component analysis indicate that inorganic phosphorus (P-L + P-Ca + P-Fe) were linked and were provided mainly by car-washing. It appears clearly that phosphorus content vary significantly during the seasons. These results showed also that the amount of (P-Fe) is higher than the others whatever the season. This P form is easily labile and bioavailable which suggest that it can unfortunately enhance greatly the eutrophication of Lake Dang.

Colloidal elemental selenium (Se(0)) adversely affects membrane separation processes and aquatic ecosystems. As a solution to this problem, we investigated for the first time the removal potential of Se(0) by electrocoagulation process. Colloidal Se(0) was produced by a strain of Pseudomonas fluorescens and showed limited gravitational settling. Therefore, iron (Fe) and aluminum (Al) sacrificial electrodes were used in a batch reactor under galvanostatic conditions. The best Se(0) turbidity removal (97 %) was achieved using iron electrodes at 200 mA. Aluminum electrodes removed 96 % of colloidal Se(0) only at a higher current intensity (300 mA). At the best Se(0) removal efficiency, electrocoagulation using Fe electrode removed 93 % of the Se concentration, whereas with Al electrodes the Se removal efficiency reached only 54 %. Due to the less compact nature of the Al flocs, the Se-Al sediment was three times more voluminous than the Se-Fe sediment. The toxicity characteristic leaching procedure (TCLP) test showed that the Fe-Se sediment released Se below the regulatory level (1 mg L⁻¹), whereas the Se concentration leached from the Al-Se sediment exceeded the limit by about 20 times. This might be related to the mineralogical nature of the sediments. Electron scanning micrographs showed Fe-Se sediments with a reticular structure, whereas the Al-Se sediments lacked an organized structure. Overall, the results obtained showed that the use of Fe electrodes as soluble anode in electrocoagulation constitutes a better option than Al electrodes for the electrochemical sedimentation of colloidal Se(0).

Carbonized rice husk (CRH) is a promising material to separate oil from water owing to its abundance, low-cost, and environmentally benign characteristics. However, CRH’s performance is somewhat limited by its similar surface charge to that of oil, leading to repulsive interactions. To improve the separation efficiency of CRH, CRH was modified via impregnation with a cationic biocompatible polymer, polyethlyenimine (PEI) to form PEI-CRH. The modified sample exhibits a remarkably higher (10–50 times) oil/water (O/W) separation efficiency than that of the unmodified one. Small PEI-CRH particles (about 64 μm) are found to adsorb oil droplets faster and larger quantities than bigger particles (about 113 and 288 μm). PEI-CRH exhibits higher separation efficiency at high temperatures owing to the destabilization of the emulsion. It is also found that the oil adsorption mechanism involves a chemical interaction between PEI-CRH and oil droplets. The addition of NaCl considerably improves the separation efficiency, while the addition of a cationic surfactant has the opposite effect. In acidic emulsions, PEI-CRH adsorbs more oil than in neutral or basic conditions owing to favorable attractive forces between oil droplets and the surface of PEI-CRH. PEI-CRH can be easily regenerated by washing with ethanol. These promising features of PEI-CRH indicate that PEI-CRH could be an efficient and low-cost adsorbent for the O/W separation applications.

This study investigated the material/substance flow of polybrominated diphenyl ethers listed in the Stockholm Convention (SC) as persistent organic pollutant (POP-PBDEs) in the most relevant plastic fractions in Nigeria. Considering the prohibition of production and the use of POP-PBDEs and knowing that these pollutants are still contained in electrical and electronic equipment (EEE) and associated wastes (WEEE), it is necessary to determine their flows, especially in developing countries with limited end-of-life management. Following the inventory approach of the SC Guidance and utilizing the existing national e-waste inventory together with monitoring data, a material/substance flow analysis was conducted using the STAN tool. Within the period of 2000 to 2010, the total import for EEE/WEEE in Category 3 and 4 was approximately 8 million tonnes (Mt) containing approximately 2.4 Mt of polymers. For the inventory year 2010, it was estimated that from these polymers, about 0.8 Mt was still in stock and 1.6 Mt has reached the end-of-life. It was also estimated that approximately 1.1 Mt has ended in dumpsites, 0.3 Mt was burned in the open, and 0.2 Mt was recycled. In the plastic fractions, 1,270 t of POP-PBDEs was contained with about 370 t still in use/stock and approximately 900 t has entered the end-of-life phase. All three major end-of-life treatments result in environmental pollution with associated exposure risk. The implementation of the Stockholm Convention represents an important opportunity to improve this management situation in Nigeria and other developing countries.

There is of great interest to develop an economic and high-efficient catalytic ozonation system (COS) for the treatment of biologically refractory wastewaters. Applications of COS require options of commercially feasible catalysts. Experiments in the present study were designed to prepare and investigate a novel manganese–iron–copper oxide-supported alumina-assisted COS (Mn–Fe–Cu/Al₂O₃–COS) for the pretreatment of petroleum refinery wastewater. The highly dispersed composite metal oxides on the catalyst surface greatly promoted the performance of catalytic ozonation. Hydroxyl radical mediated oxidation is a dominant reaction in Mn–Fe–Cu/Al₂O₃–COS. Mn–Fe–Cu/Al₂O₃–COS enhanced COD removal by 32.7 % compared with a single ozonation system and by 8–16 % compared with Mn–Fe/Al₂O₃–COS, Mn–Cu/Al₂O₃–COS, and Fe–Cu/Al₂O₃–COS. The O/C and H/C ratios of oxygen-containing polar compounds significantly increased after catalytic ozonation, and the biodegradability of petroleum refinery wastewater was significantly improved. This study illustrates potential applications of Mn–Fe–Cu/Al₂O₃–COS for pretreatment of biologically refractory wastewaters.