Discharge of synthetic dyes from industries without treatment leads to major environmental problems. Present research highlighted the Mn-doped ZnO along with UV-induced photo degradation of Congo red (CR) dye through batch study. The synthesized Mn-doped ZnO (MDZO) was characterized by Transmission electron microscope (TEM) and Fourier transform infrared spectroscopy (FTIR). The results revealed that MDZO along with UV exposure degraded the CR dye up to 99.3% at concentration 4 mg/L, pH (7), adsorbent dose (0.6 g/L) and contact time (30 min). The degradation data nicely fitted with pseudo-secondary kinetics and the thermodynamic study suggest the said reaction is exothermic in nature. A statistical method, central composite design (CCD) was used to screen out the optimized condition of dye degradation. The interactions of main factors and optimal conditions were also evaluated by 3D surface plots. The statistical output clearly demonstrates that the dye degradation data is nicely fitted with very high goodness of fit and F value (86.19). Present research clearly suggested that Mn-doped ZnO along with UV could be an effective treatment towards degradation of Congo red dye.

In this work, single layered Ti3C2(OH)2 MXene nanosheets have been successfully prepared through a facile approach by etching Ti3AlC2 with alkaline solution treatment (KOH with minimum amounts of water). The structure and morphology of the produced nanosheets were evaluated through X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM) analysis and the chemical composition was determined using an energy dispersion X-ray (EDX) spectrometer. Methylene Blue (MB) as a target pollutant adsorption and photocatalytic degradation tests were subsequently performed to assess the functionalities of hydroxyl-terminated MXene. MB removal using Ti3C2(OH)2 MXene in the dark in 20 minutes achieved an absorption-desorption balance of 51.2%, and then MB was degraded within 80 minutes under UV light irradiation with great efficiency. Our results presented that the powder of as produced exhibited good photocatalytic activity for three cycles photodegradation. The first-order rate constant (k) was calculated to be 0.0372 1/min. About 97% degradation of Methylene Blue dye in the solution was confirmed within 80 min of exposure to ultraviolet light.

Diazinon is an organophosphorus insecticide that was widely used in agriculture to control pests on crops. It acts as an acetylcholinesterase inhibitor, which means that it interferes with the normal functioning of the nervous system of insects, leading to their death. Diazinon can also have an impact on human health and the environment, as it can contaminate water and soil and pose a risk to non-target species, including humans and animals. This review paper shows the progress made in the last years in analytical methods applied for the purpose of extraction, detection and degradation of Diazinon as an important environmental pollutant. A variety of sampling and analytical methods have been developed to measure diazinon and its metabolites in different media. The most popular methods for the identification and analysis of Diazinon are liquid and gas chromatography, liquid-liquid extraction, and solid-phase extraction (SPE). The focus of this review is on the identification, measurement, and elimination of diazinon as a major soil pollutant. It begins with a discussion of analytical techniques, followed by an examination of methods for removing diazinon from soil.

In order to find an effective decolorization method for dye wastewaters, the present work aims at studying the treatment efficiency of an azo dye Acid Red 14 (AR14) by Electro-Fenton process using an undivided electrochemical cell containing different electrode materials. The optimal removal efficiency was obtained using carbon felt or glassy carbon (cathode) and platinum (anode) electrodes. The method is based on the reaction of electrochemically produced hydroxyl radicals leading to oxidative degradation of the AR14. To find the best conditions for treatment of AR14 dye, the effects of Fe2+ concentration, current density, the effect of pH initial, and the nature of support electrolyte were studied. The results showed 94 % removal efficiency in 30 minutes with 120 mA/cm2 of electrolysis current, 0.2 mM of Fe2+, and pH = 3. However, the decolorization efficiency measurements confirmed that the Electro-Fenton process with the platinum anode and the carbon felt cathode was more efficient.

International audience | This review investigates the impact of salinity on the fate of the active compounds of pesticides in a cultivated environment. Due to the over-exploitation of water resources and intensification of agriculture, salinity outbreaks are being observed more often in cultivated fields under pesticide treatments. Nevertheless, there is a poor understanding of the incidence of varying water salt loads on the behavior of pesticides’ active ingredients in soil and water bodies. The present review established that water salinity can affect the diffusion of pesticides’ active ingredients through numerous processes. Firstly, by increasing the vapor pressure and decreasing the solubility of the compounds, which is known as the salting-out effect, salinity can change the colligative properties of water towards molecules and the modification of exchange capacity and sorption onto the chemicals. It has also been established that the osmotic stress induced by salinity could inhibit the biodegradation process by reducing the activity of sensitive microorganisms. Moreover, soil properties like dissolved organic matter, organic carbon,clay content, and soil texture control the fate and availability of chemicals in different processes of persistence in water and soil matrix. In the same line, salinity promotes the formation of different complexes, such as between humic acid and the studied active compounds. Furthermore, salinity can modify the water flux due to soil clogging because of the coagulation and dispersion of clay particle cycles, especially when the change in salinity ranges is severe.

International audience | This review investigates the impact of salinity on the fate of the active compounds of pesticides in a cultivated environment. Due to the over-exploitation of water resources and intensification of agriculture, salinity outbreaks are being observed more often in cultivated fields under pesticide treatments. Nevertheless, there is a poor understanding of the incidence of varying water salt loads on the behavior of pesticides’ active ingredients in soil and water bodies. The present review established that water salinity can affect the diffusion of pesticides’ active ingredients through numerous processes. Firstly, by increasing the vapor pressure and decreasing the solubility of the compounds, which is known as the salting-out effect, salinity can change the colligative properties of water towards molecules and the modification of exchange capacity and sorption onto the chemicals. It has also been established that the osmotic stress induced by salinity could inhibit the biodegradation process by reducing the activity of sensitive microorganisms. Moreover, soil properties like dissolved organic matter, organic carbon,clay content, and soil texture control the fate and availability of chemicals in different processes of persistence in water and soil matrix. In the same line, salinity promotes the formation of different complexes, such as between humic acid and the studied active compounds. Furthermore, salinity can modify the water flux due to soil clogging because of the coagulation and dispersion of clay particle cycles, especially when the change in salinity ranges is severe.

International audience | Temperature is a key factor that influences pesticide degradation. Extrapolating degradation half-lives (DT50) measured at a given temperature to different temperatures remains challenging, especially for tropical conditions with high temperatures. In this study, the use of the standard Arrhenius equation for correcting temperature effects on pesticide degradation in soils was evaluated and its performance was compared with that of alternative Arrhenius-based equations. To do so, a database of 509 DT50 values measured between 5 and 35 °C for 32 pesticides on tropical and temperate soils was compiled for the first time through an extensive literature search. The temperature correction models were fitted to the database using linear mixed regression approaches that included soil type and compound effects. No difference in the temperature dependence of DT50 between tropical and temperate soils was detected, regardless of the model. A comparison of the prediction performances of the models showed that constant activation energy (Ea) cannot be considered valid for the whole range of temperatures. The classical Arrhenius equation with an Ea of 65.4 kJ.mol−1, as recommended by the European Food Safety Authority (EFSA), was shown to be valid for correcting the DT50 only for temperatures ranging from 5 to 20 °C. However, for temperatures greater than 20 °C, which are common in tropical environments, the median Ea was significantly lower at 10.3 kJ.mol−1. These findings suggest the need to adapt the standard temperature correction of the European pesticide risk assessment temperature procedure when it is applied in tropical settings