This study aimed to investigate the degradation of triclosan (TCS) in the presence of p-aminobenzoic acid (PABA) under simulated sunlight irradiation (λ ≥ 290 nm). The effect of PABA concentration, pH, dissolved organic matter (DOM), and DOM-hydrolytic Fe(III) species complexes on the photodegradation of TCS in the presence of PABA (TCS₋PABA) was also studied. The photolysis of TCS₋PABA obeyed pseudo-first-order kinetics well, and the degradation of TCS₋PABA enhanced with increasing solution pH (from 3.0 to 11.0). The presence of PABA inhibited the degradation of TCS₋PABA, and the weakest inhibitory effect was observed while the concentration of PABA was 5 mg L⁻¹. The addition of DOM (Suwannee River fulvic acid standard I [SRFA], Suwannee River HA standard II [SRHA], and Suwannee River natural organic matter [SRNOM]) showed different inhibition effects on TCS₋PABA degradation. However, higher Fe(III) concentration at the DOM concentration of 5 mg L⁻¹ could favor the formation of DOM-hydrolytic Fe(III) species complexes, further accelerating the degradation of TCS₋PABA. In comparison with deionized water (DI water), TCS₋PABA could be better photodegraded in river water nearby the effluent of a wastewater treatment plant. This study provides useful information for understanding the natural behavior of TCS in the presence of other organic contaminants.

Honeybees have become important tools for the ecotoxicological assessment of soil, water and air metal contamination due to their extraordinary capacity to bioaccumulate toxic metals from the environment. The level of heavy metal pollution in the Trieste city was monitored using foraging bees of Apis mellifera ligustica from hives owned by beekeepers in two sites strategically located in the suburban industrial area and urban ones chosen as control. The metal concentration in foraging bees was determined by inductively coupled plasma-mass spectrometry. The chemical analysis has identified and quantified 11 trace elements accumulated in two different rank orders: Zn> Cu > Sr > Bi > Ni > Cr > Pb = Co > V > Cd > As in foraging bees from the suburban site and Zn > Cu > Sr > Cr > Ni > Bi > Co = V > Pb > As > Cd in bees from urban site. Data revealed concentrations of Cr and Cu significantly higher and concentration of Cd significantly lower in bees from urban sites. The spatial difference and magnitude order in heavy metal accumulation along the urban-suburban gradient are mainly related to the different anthropogenic activity within sampled sites and represent a risk for the human health of people living in the city. We discussed and compared results with the range of values reported in literature.

Oleaginous microorganisms such as microalgae, yeasts, bacteria and filamentous fungi are alternative sources of vegetal or animal fats for biodiesel production. This research evaluated the lipid production by the biomass Trichoderma koningiopsis MX1 with a non-stirring culture at room temperature, and fungal lipids were extracted through three techniques for biodiesel generation purposes. The three modified lipid extraction techniques yielded 18.4, 10.3 and 17.1 % of fungal lipids. The trans-esterification of lipids indicated that the controlling components for biodiesel were palmitic (40.8 %) and linoleic acids (ranging from 37.6 % to 41.2 %). Results show that fungal cultural conditions and the lipid extraction technique are determinants for producing biodiesel from fungal lipids. Therefore, the modification of some of these conditions could increase their efficiency and viability.

Activated carbon (AC)/CoFe₂O₄ nanocomposites, MAC-1 and MAC-2, were prepared by a simple pyrolytic method using a mixture of iron(III)/cobalt(II) benzoates and iron(III)/cobalt(II) oxalates, respectively, and were used as efficient adsorbents for the removal of amoxicillin (AMX) and paracetamol (PCT) of aqueous effluents. The synthesized nanocomposites were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), vibrating sample magnetometry (VSM), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX) and transmission electron microscopy (TEM). The sizes of cobalt ferrite nanoparticles formed from benzoates of iron(III)/cobalt(II) and oxalates of iron(III)/cobalt(II) precursors were in the ranges of 5–80 and 6–27 nm, respectively. The saturation magnetization (M ₛ), remanence (M ᵣ) and coercivity (H c) of the MAC-2 nanocomposites were found to be 3.07 emu g⁻¹, 1.36 emu g⁻¹ and 762.49 Oe; for MAC-1, they were 0.2989 emu g⁻¹, 0.0466 emu g⁻¹ and 456.82 Oe. The adsorption kinetics and isotherm studies were investigated, and the results showed that the as-prepared nanocomposites MAC-1 and MAC-2 could be utilized as an efficient, magnetically separable adsorbent for environmental cleanup. The maximum sorption capacities obtained were 280.9 and 444.2 mg g⁻¹ of AMX for MAC-1 and MAC-2, respectively, and 215.1 and 399.9 mg g⁻¹ of PCT using MAC-1 and MAC-2, respectively. Both adsorbents were successfully used for simulated hospital effluents, removing at least 93.00 and 96.77% for MAC-1 and MAC-2, respectively, of a mixture of nine pharmaceuticals with high concentrations of sugars, organic components and saline concentrations.

Eco-ditches are being explored to maximize their capability of capturing pollutants and mitigate any harmful side effects in rivers. In this study, mesocosm plastic drum sediment and field experiments were set up to screen 18 plant species found in ditches and identify those with potential for high biomass production and nutrients removal. Terrestrial plants grown in the mesocosm system were shown to be able to acclimate to aquatic conditions and to survive in primary domestic sewage. About 73–95% increase in plant biomass was recorded. Removal efficiencies for total nitrogen, total phosphorus, and ammonium-nitrogen from the sewage of 72–99%, 64–99%, and 75–100%, respectively, were recorded. Furthermore, complete removal of the applied nitrate-nitrogen load was achieved in mesocosm systems. Findings also show that all species, but especially Acorus calamus, Canna indica, Canna lily, Cyperus alternifolius, Colocasia gigantea, Eichhornia crassipes, Iris sibirica, and Typha latifolia had the highest efficiencies for nitrogen and phosphorous removal. The N and P mass balance analysis demonstrated that plant uptake and sediment N and P accumulation accounted for 41–86% and 18–49% of the total influent TN and TP loads, respectively. In addition, the amounts of nitrogen and phosphorous uptake by these plant species were influenced significantly by biomass. The field-culture experiment further identified Canna indica followed by Cyperus alternifolius as the most promising for high biomass production and nutrients uptake. Therefore, these plants may be recommended for extensive use in treating highly eutrophicated rivers. Outcomes of this work can be useful for model design specifications in eco-ditch mitigation of sewage pollution.

This is the first report on the photodegradation of ofloxacin under simulated solar light and in actual environmental matrices in the presence of a g-C₃N₄ suspension. The catalyst, prepared from the polymerization of dicyandiamide (650 °C, reaction yield 60%), was characterized by means of powder X-ray diffraction (PXRD), UV-vis diffuse reflectance spectroscopy (DRS), scanning electron microscopy (SEM), and BET surface area measurements. The experiments were carried out in a lab-scale batch reactor at concentrations in the range of micrograms/milligrams per liter. The course of the reaction was monitored by high-pressure liquid chromatography with UV-vis and fluorescence detectors. The g-C₃N₄-promoted photodegradation occurred at a rate 10 times faster than the direct photolysis and obeyed a first-order kinetics; in addition, the photodegradation kinetics of sonicated g-C₃N₄ resulted to be of the same order of that caused by P25 TiO₂. Finally, the photochemical paths and the photoproducts have been identified and compared to those obtained by using P25 TiO₂. From the results of this study, it can be concluded that g-C₃N₄ is a very attractive photocatalyst compared to P25 TiO₂ in view of its ease of preparation, low cost, excellent oxidizing properties, large fraction of solar radiation absorbed, and intrinsically layered structure.

To enhance the photocatalytic activity of TiO₂, reduced graphene oxide–TiO₂ (RGO–TiO₂) composites with sandwich-like structure were synthesized using a simple solvothermal method. The morphology, crystalline information, and structural property of the photocatalyst were characterized by field emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and Fourier transmission infrared spectroscopy. The photocatalytic performances of the RGO–TiO₂ composites were evaluated by the degradation of orange II (AO7) in water under UV light irradiation. The results showed that the RGO–TiO₂ composites exhibited much higher photocatalytic activity than TiO₂ and that the removal efficiency of AO7 could reach above 95% only after 20 min of UV light irradiation under the optimum condition. The improved photocatalytic activity might be attributed to the improved charge transfer and significant separation of the photoinduced electrons and holes in the presence of a two-dimensional graphene network. The results of recycling experiments show that RGO–TiO₂ composites have a high photostability, which is expected in the practical application. Radical trapping experiments indicated that ·OH plays a crucial role in the process of AO7 degradation.

Tetravalent (Vᴵⱽ) and pentavalent (Vⱽ) forms of vanadium were selected for testing by the National Toxicology Program via drinking water exposure due to potential human exposure. To aid in the test article selection, drinking water formulations (125–2000 mg/L) of vanadyl sulfate (Vᴵⱽ), sodium orthovanadate, and sodium metavanadate (Vⱽ) were characterized by ultraviolet/visible (UV/VIS) spectroscopy, mass spectrometry (MS), or ⁵¹V nuclear magnetic resonance (NMR) spectroscopy. Aqueous formulations of orthovanadate, metavanadate, and vanadyl sulfate in general were basic, neutral, and acidic, respectively. Changes in vanadium speciation were investigated by adjusting formulation pH to acidic, neutral, or basic. There was no visible difference in UV/VIS spectra of pentavalent forms. NMR and MS analyses showed that the predominant oxidovanadate species in both ortho- and metavanadate formulations at basic and acidic pH, respectively, were the monomer and decamer, while, a mixture of oxidovanadates were present at neutral pH. Oxidovanadate species were not observed in vanadyl sulfate formulations at acidic pH but were observed at basic pH suggesting conversion of Vᴵⱽ to Vⱽ. These data suggest that formulations of both ortho- and metavanadate form similar oxidovanadate species in acidic, neutral and basic pH and exist mainly in the Vⱽ form while vanadyl sulfate exists mainly as Vᴵⱽ in acidic pH. Therefore, the formulation stability overtime was investigated only for sodium metavanadate and vanadyl sulfate. Drinking water formulations (50 and 2000 mg/L) of metavanadate (~pH 7) and vanadyl sulfate (~pH 3.5) were ≥92 % of target concentration up to 42 days at ~5 °C and ambient temperature demonstrating the utility in toxicology studies.

Fine aerosol fraction (particulate matter with aerodynamic diameter <= 1.0 μm (PM)₁.₀) over the Indian Institute of Technology Delhi campus was monitored day and night (10 h each) at 30 m height from November 2009 to March 2010. The samples were analyzed for 5 ions (NH₄⁺, NO₃⁻, SO₄²⁻, F⁻, and Cl⁻) and 12 trace elements (Na, K, Mg, Ca, Pb, Zn, Fe, Mn, Cu, Cd, Cr, and Ni). Importantly, secondary aerosol (sulfate and nitrate) formation was observed during dense foggy events, supporting the fog-smog-fog cycle. A total of 76 samples were used for source apportionment of PM mass. Six factors were resolved by PMF analyses and were identified as secondary aerosol, secondary chloride, biomass burning, soil dust, iron-rich source, and vehicular emission. The geographical location of the sources and/or preferred transport pathways was identified by conditional probability function (for local sources) and potential source contribution function (for regional sources) analyses. Medium- and small-scale metal processing (e.g. steel sheet rolling) industries in Haryana and National Capital Region (NCR) Delhi, coke and petroleum refining in Punjab, and thermal power plants in Pakistan, Punjab, and NCR Delhi were likely contributors to secondary sulfate, nitrate, and secondary chloride at the receptor site. The agricultural residue burning after harvesting season (Sept–Dec and Feb–Apr) in Punjab, and Haryana contributed to potassium at receptor site during November–December and March 2010. The soil dust from North and East Pakistan, and Rajasthan, North-East Punjab, and Haryana along with the local dust contributed to soil dust at the receptor site, during February and March 2010. A combination of temporal behavior and air parcel trajectory ensemble analyses indicated that the iron-rich source was most likely a local source attributed to emissions from metal processing facilities. Further, as expected, the vehicular emissions source did not show any seasonality and was local in origin.

This study presents an effective technology for the olive processing industry to remediate olive washing water. A 14.5-L enclosed tubular photobioreactor was inoculated with a stable microalgal-bacterial consortium obtained by screening strains well adapted to olive washing water. The capacity of an enclosed tubular photobioreactor to remove toxic compounds was evaluated under photosynthesis conditions and without any external supply of oxygen. The results showed that the dominant green microalgae Scenedesmus obliquus, Chlorella vulgaris and the cyanobacteria Anabaena sp. and bacteria present in olive washing water (i.e. Pantoea agglomerans and Raoultella terrigena) formed a synergistic association that was resistant to toxic pollutants present in the effluent and during the initial biodegradation process, which resulted in the breakdown of the pollutant. Total phenolic compounds, COD, BOD₅, turbidity and colour removals of 90.3 ± 11.4, 80.7 ± 9.7, 97.8 ± 12.7, 82.9 ± 8.4 and 83.3 ± 10.4 %, respectively, were recorded in the photobioreactor at 3 days of hydraulic retention time. Graphical abstract Biotreatment of industrial olive washing water by synergetic association of microalgal-bacterial consortia in a photobioreactor