In this study, selective green synthesis of gold nanoparticles (nAu) with the use of Tarragon extract (Artemisia dracunculus) was investigated. Characterization of the synthetized nAu was carried out using several techniques including: UV-Vis, SEM, zeta potential analysis, DLS, and ATR-FTIR. Based on measurements of Tarragon extract by HPLC-MS, significant chemical substances participating as reducing and stabilizing agents were identified. FTIR confirmed typical functional groups that could be found in these acids on the nAu surface, such as O-H, C=O and C-O. The effects of various parameters (concentration of Tarragon extract, Au precursor, and initial pH of the synthesis) on the shape and size of the nanoparticles have been investigated. UV-Vis and SEM confirmed the formation of nAu at various concentrations of the extract and Au precursor and showed correlation between the added extract concentration and shift in maximal absorbance towards higher frequencies, indicating the formation of smaller nanoplates. Zeta potential determined at various pH levels revealed that its value decreased with pH, but for all experiments in the pH range of 2.8 to 5.0, the value is below − 30 mV, an absolute value high enough for long-term nAu stability. In order to evaluate nAu catalytic activity, the reduction of 4-nitrophenol to 4-aminophenol by sodium borohydride was used as a model system. The reaction takes place 1.5 times faster on Au-triangles than on Au-spherical NPs.

Chloroalkenes are among the important anthropogenic organic compounds emitted in the atmosphere as a result of their wide use in synthetic processes in industry. Despite their well-known adverse effects on human health and air quality, the chemistry of these chloroalkenes remains poorly explored. In this work, reactions of 4-chloro-1-butene (CBE), a representative example of chloroalkenes, with O₃, OH, NO₃, and Cl are investigated in a 100-L Teflon reaction chamber equipped with gas chromatography-flame ionization detector (GC-FID). The absolute rate method was used for the reaction with O₃ while the relative rate method was used for reactions with OH, NO₃, and Cl. The following rate constants were obtained at room temperature (298 ± 2) K and atmospheric pressure: (3.96 ± 0.43) × 10⁻¹⁸, (2.63 ± 0.96) × 10⁻¹¹, (4.48 ± 1.23) × 10⁻¹⁵, and (2.35 ± 0.90) × 10⁻¹⁰ cm³ molecule⁻¹ s⁻¹, for reactions with O₃, OH, NO₃, and Cl, respectively. Atmospheric lifetimes of CBE calculated from rate constants of the different reactions obtained in this work showed that reaction with OH is the main loss process for CBE, while in coastal areas and in the marine boundary layer, the CBE loss by Cl reaction becomes important. Estimation of the value of the photochemical ozone creation potential (POCP) indicated that CBE has a large ozone formation potential. The present work underlines the need for further studies on the atmospheric chemistry of chlorinated VOCs.

Graphene oxide (GO)-based membranes provide an encouraging opportunity for oil-in-water emulsion separation with high separation efficiency. In this work, novel hierarchically structured membrane consisting of GO and halloysite nanotubes (HNTs) was successfully fabricated by vacuum-assisted filtration method. XRD and TEM measurements showed the successful intercalation of HNTs into the interlayers of GO nanosheets. With the incorporation of the one-dimensional hollow tubular structure halloysite nanotubes, GO-HNTs(GOH) membrane possessed combined advantages of high oil rejection rate and excellent fouling resistance properties. The permeate fluxes increased from 286.6 L/(m²·h) for GO membrane to 716 L/(m²·h) for GOH membrane. The results indicate that the GOH membranes have great potential applications in water purification and wastewater treatment.

Pollutant removal was compared among subsurface flow constructed wetland (CW) mesocosms used for dairy farm wastewater treatment. Supplemental aeration, flow direction, and the use of phosphorus-reducing filters (PRFs) were varied among the CWs. The following were compared: (1) vertical flow CWs with and without supplemental aeration, (2) aerated CWs with horizontal and vertical flow directions, (3) single-cell and two-cell treatment systems, and (4) wetland-wetland systems (two CWs in series) and wetland-PRF systems (a CW followed by a PRF). The results from this investigation showed that, first, nearly all treatment strategies, either singly or in pairs, substantially reduced almost all the contaminants we tested. Second, supplemental aeration resulted in higher ammonium-nitrogen (NH₄-N) removal efficiencies in aerated vertical flow CWs, compared to unaerated CWs. However, it caused no further improvement in dissolved reactive phosphorus (DRP), total suspended solids (TSS), E. coli, or BOD₅ removal. Third, there was no difference between aerated horizontal and aerated vertical flow CWs in removal of any of the tested contaminants. Fourth, adding a second stage of treatment significantly improved DRP, TSS, E. coli, and NH₄-N removal, but not BOD₅. Finally, treatment systems with PRFs showed superior performance in DRP and E. coli removal.

Environmental concern due to plant accumulation of natural radionuclides is a major concern in uranium mining areas. To evaluate the risk associated with the transfer of radionuclides to edible plants, the uptake of ²³⁸U, ²²⁶Ra, and ²¹⁰Pb by Chinese cabbage (Brassica rapa L. subsp. pekinensis (Lour.) Hanelt) grown in soils contaminated with uranium-mill tailings (UMT) was investigated. Test plants were grown under controlled conditions in substrate composed of soil and UMT in different ratios. Activity concentrations of ²³⁸U, ²²⁶Ra, and ²¹⁰Pb in substrate, leaves, and roots were measured and the concentration ratios determined. Soil characteristics were determined, since they directly affect bioavailability of radionuclides. Concentration ratios of ²³⁸U, ²²⁶Ra, and ²¹⁰Pb in leaves varied from 0.001 to 0.006, 0.024 to 0.172, and 0.004 to 0.011, respectively, and in roots from 0.020 to 0.126, 0.015 to 0.241, and 0.033 to 1.460, respectively. Concentrations of ²³⁸U, ²²⁶Ra, and ²¹⁰Pb in leaves and roots were found to correlate with the amount of ²³⁸U, ²²⁶Ra, and ²¹⁰Pb in the substrate. A higher amount of ²²⁶Ra accumulated in aboveground parts (57–877 Bq kg⁻¹ d. m. for leaves) compared to ²³⁸U (0.6–4.7 Bq kg⁻¹ d. m. for leaves) and ²¹⁰Pb (8–53 Bq kg⁻¹ d. m. for leaves), which were mainly stored in the roots. The relationships between the amount of radionuclides in plants and soil characteristics and their role in radionuclide uptake are discussed and critically evaluated.

Nano zerovalent iron (nZVI) impregnated reduced graphene oxide (nZVI-rGO) hybrid was prepared via gaseous hydrogen reduction of anhydrous iron(III) chloride (FeCl₃) on the surface of thermally exfoliated reduced graphene oxide (rGO) nanosheets without using any toxic reducing agent, surfactant, or stabilizing agent. Characterization of prepared samples was carried out using various techniques. Morphological study showed that prepared rGO possesses a few-layered wrinkled paper-like structures and nZVI particles of ~ 30 nm size were homogeneously dispersed on the surface of rGO nanosheets. Fourier transform infrared (FTIR), X-ray diffraction (XRD), and energy dispersive X-ray spectrometry (EDS) analyses indicated that oxygen-containing functional groups decreased in the order of graphite oxide (GO) > rGO > nZVI-rGO. Removal studies of trinitrotoluene (TNT) were carried out using graphite (G), GO, rGO, and nZVI-rGO with the aid of high-performance liquid chromatography (HPLC). Kinetic models were applied to establish the rate and mechanism of adsorption of TNT on different adsorbents, and intraparticle diffusion model based on initial adsorption characteristics was employed to ascertain mechanism of film and intraparticle diffusion in the adsorption process. The removal rate and adsorption capacity was found to be highest for nZVI-rGO, which renders this adsorbent to be a potential futuristic adsorbent for removal of explosives. Graphical Abstract ᅟ

Bioremediation is a method of removing manganese from wastewaters, and many bacterial species with a role in manganese bioremediation have been identified over several decades. Using K medium with Mn(II), a bacterial consortium was obtained from water sample collected from a mine drainage in southeastern Brazil (Minas Gerais, Brazil), and the isolates were identified as Klebsiella oxytoca using both biochemical and 16S rRNA phylogenetic analysis. Among such isolates, sample SA8 was tested for its manganese removal capability during a week-long experiment in K medium amended with manganese sulfate. Growth of isolate SA8 produced an increase in pH concomitantly to Mn(II) removal, which was not observed in the abiotic control. Manganese removal occurred through oxidation as confirmed by reaction with leucoberbelin blue, and therefore, a new potential application for K. oxytoca in mine water bioremediation is proposed.

This study aims to determine the composition of surfactants in the sea surface microlayer (SML), underlying water (ULW) and atmospheric particles (AP). Surfactants were determined colorimetrically as methylene blue active substances (MBAS) and disulphine blue active substances (DBAS) for anionic and cationic surfactants, respectively. The concentration of dissolved inorganic nutrients (DIN) in ULW was determined so as to indicate the influence of ULW to the surfactants in SML. The results showed that the concentration of MBAS and DBAS in SML at both stations ranged between 0.05 and 0.31 μmol L⁻¹, and between 0.19 and 0.59 μmol L⁻¹, respectively. Surfactants in ULW influence the concentration of surfactants in SML (r = 0.65, p < 0.01, n = 36). The station influenced by anthropogenic sources showed a higher concentration of surfactants in ULW, SML and AP. This finding suggests fine mode atmospheric particles (FMAP) are the main carrier for anionic surfactants as MBAS in the coastal ecosystem. Anionic surfactants as MBAS were found as better indicator of anthropogenic sources than cationic ones.

The impact of nanoparticles (NPs) in zooplankton is poorly studied, particularly when organisms are exposed through diet. Food, constituted mainly by unicellular algae, can act as an important route of contamination for zooplankton. Since unicellular algae have a high surface area in relation to their volume, NPs can interact with their cell membranes and walls, as well as with exopolysaccharides secreted by them. In the present research, we investigated both the acute effects of waterborne titanium dioxide nanoparticles (TiO₂ NPs), and its chronic effects via dietary exposure on the Neotropical freshwater zooplankton Ceriodaphnia silvestrii Daday, 1902 (Crustacea: Cladocera). The observed acute effects served as support for chronic tests, in which we investigated the effects of TiO₂ NPs on survival and life history parameters (body length, numbers of eggs, and neonates produced) of cladoceran adult females, using the freshwater cosmopolitan chlorophycean Raphidocelis subcapitata as source of contamination of TiO₂ NPs for zooplankton. R. subcapitata cells were exposed to concentrations of 0, 0.01, 1, and 10 mg L⁻¹ of TiO₂ NPs for 96 h, and then provided as food for females of C. silvestrii until the third brood was released. Significant toxic effects were observed in body length and total number of neonates and eggs produced by females of C. silvestrii at concentrations of 1 and 10 mg L⁻¹ of TiO₂ NPs. Survival was the most sensitive parameter when exposure was given via food. From the concentration of 0.01 mg L⁻¹ of TiO₂ NPs, there was a decrease in the survival of C. silvestrii females. The quantification of TiO₂ NPs in algae evidenced that they have retained NPs in their cells, being, therefore, an important route of exposure and toxicity of TiO₂ NPs to the studied microcrustacean.

The use of soil additives for toxic metals chemical stabilization aims to decrease in situ the pollutants’ mobility and availability. In this study, the effectiveness of rinsed red mud (RBRM) and annealed animal bones (B400) was compared in terms of Cu, Pb and Ni stabilization in two contaminated soils with contrasting properties Dystric Cambisol (CM dy) and Rendzic Leptosol (LP rz). The mobility of metals in unamended soil samples (control) and samples amended with 1% and 5% of selected additives were compared using sequential extraction protocol. The relative content of metals in readily and potentially available fractions was higher in CM dy (62% Pb, 13% Cu, and 31% Ni in exchangeable fraction) than in LP rz (< 5% of Pb, Cu, Ni in exchangeable fraction). In CM dy, both additives have caused a decrease in metal mobility with an increase of their doses. The effect of 5% sorbent addition was most pronounced related to Pb immobilization, provoking decrease of exchangeable Pb content to < 10%. Furthermore, B400 addition has redistributed investigated metals from the exchangeable to the residual phase more effectively than RBRM, and its effect on metal mobility decreased in the order Pb > Cu > Ni. Amending of LP rz soil had limited effects with no apparent decrease in exchangeable metal content. The effects of soil type variation, the type of additive and the additive dose onto metal mobility were compared according to ANOVA results. The content of readily and potentially available forms of metals was found to be (i) significantly correlated with all investigated variables for Pb, (ii) significantly correlated with soil type for Cu, and (iii) not in significant correlation with selected variables for Ni. Complex impacts of soil properties and treatment conditions on the mobility of co-contaminants emphasize the need for an individual approach to each case of contamination.