Ferrihydrite is often an initial precipitate resulting from the neutralization of Fe(III) solution, and it seems to be one of the products of acid mine drainage forming reactions. Since having the adsorption properties, ferrihydrite can be effective for the remediation of acid mine drainage. This study prepared fresh ferrihydrite by the rapid hydrolysis of Fe(III) ions and investigates its adsorptive behaviours toward Pb(II), Cu(II), and Zn(II). When the sorption data were presented in plot of percent sorbed versus pH, it was found that sorption is strongly dependent on the solution pH and increasing as expected at higher pH for all metal ions investigated. All the observed metal cation sorption began at pH values below zero point charge (ZPC) of ferrihydrite (pH = 7.8–8.0), and almost all removal are achieved at pH values lower than that related metal hydroxide obtained. Enhanced removal of metal ions, as the pH of the solution and initial metal ion concentration are increased, was attributed to surface precipitation of metal hydroxide. The existence of ferrihydrite and adsorption of metal ions onto surfaces are favouring surface precipitation of metal ions at lower pH values than that for metal ion only. Depending on the pH of the solution and initial metal ion concentration, more than one mechanism such as adsorption by complexation and surface precipitation was responsible for the removal.

The efficiency of low-cost, abundantly available local forestry waste, oak (Quercus robur) acorn peel (OP), to remove toxic Cr(VI) from aqueous solutions was studied in a batch system as a function of contact time, adsorbate concentration, adsorbent dosage, and pH. In an equilibrium time of 420 min, the maximum Cr removal by OP at pH 2 and 10 was 100 and 97 %, respectively. The sorption data fitted well with Langmuir adsorption model. Evaluation using Langmuir expression presented a monolayer sorption capacity of 47.39 mg g⁻¹ with an equilibrium sorbent dose of 5 g L⁻¹ and pH 7. Uptake of Cr by OP was described by pseudo-second-order chemisorption model. ICP-OES, LC-ICPMS analysis of the aqueous and solid phases revealed that the mechanism of Cr(VI) removal is by ‘integrated adsorption and reduction’ mechanism. ESEM-EDX and XRD analysis of OP before and after adsorption also confirmed that both adsorption and reduction of Cr(VI) to less toxic Cr³⁺ forms followed by complexation onto the adsorbent surface contributed to the removal of Cr(VI). Consistent with batch studies, OP effectively removed (>95 %) Cr from the real water samples collected from lake and sea. The results of this study illustrate that OP could be an economical, green, and effective biomaterial for Cr(VI) removal from natural aquatic ecosystems and industrial effluents.

Geothermal waters exploited in the southeastern region of Hungary are alkali-hydrogen-carbonate type, and beside the high amount of dissolved salt, they contain a variety of aromatic, heteroaromatic, and polyaromatic hydrocarbons. The majority of these geothermal waters used for heating are directed into surface waters following a temporary storage in reservoir lakes. The aim of this study was to gain information about the temporal and spatial changes of the water quality as well as the bacterial community composition of an alkaline and saline oxbow lake operated as reservoir of used geothermal water. On the basis of the water physical and chemical measurements as well as the denaturing gradient gel electrophoresis (DGGE) patterns of the bacterial communities, temporal changes were more pronounced than spatial differences. During the storage periods, the inflow, reservoir water, and sediment samples were characterized with different bacterial community structures in both studied years. The 16S ribosomal RNA (rRNA) gene sequences of the bacterial strains and molecular clones confirmed the differences among the studied habitats. Thermophilic bacteria were most abundant in the geothermal inflow, whereas the water of the reservoir was dominated by cyanobacteria and various anoxygenic phototrophic prokaryotes. In addition, members of several facultative anaerobic denitrifying, obligate anaerobic sulfate-reducing and syntrophic bacterial species capable of decomposition of different organic compounds including phenols were revealed from the water and sediment of the reservoir. Most of these alkaliphilic and/or halophilic species may participate in the local nitrogen and sulfur cycles and contribute to the bloom of phototrophs manifesting in a characteristic pink-reddish discoloration of the water of the reservoir.

In the last years, several scientific studies have shown that carbamazepine (CBZ) is one of the most frequently detected pharmaceutical in aquatic environment. However, little data is available on its detection and its transformation products (TPs) in marine water. The use of polar organic chemical integrative sampling (POCIS) passive samplers as a semi-quantitative and qualitative tool for screening of pharmaceuticals and TPs in seawater has been studied. Furthermore, the uptake rates of the target compounds were also determined under laboratory experiments to characterize the levels accumulated in devices. The results confirmed the presence of residues of anticonvulsant CBZ as well as some of its main metabolites, over a 1-year monitoring campaign carried out in French coast on the Mediterranean Sea. The work reports for the first time the presence of two TPs (10,11-dihydro-10,11-trans-dihydroxycarbamazepine (TRANS) and 10-hydroxy-10,11-dihydrocarbamazepine (10OH)) in marine water. The results contribute in assessing the environmental and human health risk of pharmaceuticals on coastal areas.

Surfactants always play a special role in wastewater processes due to their amphiphilic properties. The performance of ultrafiltration was investigated for the treatment of wastewater containing low-level anionic surfactant and trace-level nuclides. Results showed that sodium dodecyl benzene sulfonate (SDBS) below the critical micelle concentration (CMC) caused significant effects on membrane fouling and rejection of nuclides. The membrane flux decreased at SDBS concentrations below the CMC but increased at the concentrations near the CMC. The phenomenon was caused by two distinct effects of SDBS, pore blocking by the monomers and enhancement of nuclide scaling caused a decrease in flux, while hydrophilic modification of the membrane surface by micelles caused an increase in flux. The nuclides alone had no significant effect on membrane fouling, but the flux decreased upon an increase in nuclide concentration when coexisting with SDBS. After the addition of low-level SDBS, the rejections of nuclides increased sharply from 20–30 to 60–98 %. The rejections of Sr(II) and Co(II) were higher than those of Ag(I) and Cs(I) due to stronger complexation of SDBS with divalent cations compared with monovalent cations. Deposition of nuclides increased with the addition of SDBS and with increasing of nuclide concentration, resulting in more radioactive solid waste production and more frequent replacement of membrane module.

To achieve the goals of harmful cyanobacterial bloom control and nutrient removal, an eco-engineering project with water hyacinth planted in large-scale enclosures was conducted based on meteorological and hydrographical conditions in Lake Dianchi. Water quality, cyanobacteria distribution, and nutrient (TN, TP) bioaccumulation were investigated. Elevated concentrations of N and P and low Secchi depth (SD) were relevant to large amount of cyanobacteria trapped in regions with water hyacinth, where biomass of the dominant cyanobacteria Microcystis (4.95 × 10¹⁰ cells L⁻¹) was more than 30-fold compared with values of the control. A dramatic increase of TN and TP contents in the plants was found throughout the sampling period. Results from the present study confirmed the great potential to use water hyacinth for cyanobacterial bloom control and nutrient removal in algal lakes such as Lake Dianchi.

Microcystis aeruginosa is a common cause of algal bloom outbreaks in Chinese lakes. This study investigated the effects of phosphate loading on the algal growth and extracellular organic matter (EOM) production of M. aeruginosa. The cell density was monitored by cell counting, and EOMs were characterized by dissolved organic carbon (DOC), carbohydrate, protein, and excitation/emission matrix fluorescence spectroscopy (EEM). DOC concentration peaked during the stationary phase and was contributed primarily by amino acid- and fulvic-like substances. Carbohydrate was a substantially larger fraction than protein. Phosphate showed positive influence on the cell growth and EOMs. As its concentration increased, the EOMs concentration increased. So did EOM and β-ionone as typical taste and odor compounds. Whatever the phosphate concentration was, the peak of β-ionone concentration exceeded its odor threshold (7.0 ng/L), resulting in a severe fruit-like odor. Additionally, the disinfection by-products involved with EOM were evaluated in both chlorination and chloramination, indicating that trihalomethanes were the dominated toxic by-products and the chloramination showed more significant effect on its formation as an interesting result.

In earlier studies in the existing literature, concentration balance in the feeding solution has never been considered as an influencing factor when the studies were carried out under several feeding conditions to examine effects of different carbon sources on the enhanced biological phosphorus removal (EBPR) process. For a better understanding of a stable operation of an EBPR reactor, it is thought that effects of the concentration balance need to be combined and evaluated with effects of the type of carbon sources in EBPR studies. Therefore, this study was aimed at determining the effect of concentration balance on the performance stability and the phosphorus and glycogen dynamics of a sequencing batch reactor (SBR). In this study, the SBR operation was divided into two main stages. In the first stage, two different ratios of the total concentration of monovalent (M) to divalent (D) cations (in milliequivalent per liter, meq/L) (7.6 and 1.5, 30 days of operation for each) was applied in the feeding solution to investigate the effect of the concentration balance on the performance stability of the SBR. During this stage, sodium acetate was used as the sole carbon source. To investigate the effect of the type of carbon source on the EBPR process under the condition of constant M/D ratio, sodium acetate was used as the sole carbon source during the first half of the reactor operation of 120 days, and, then, the carbon source was abruptly switched to glucose in the second stage.

Chitosan-montmorillonite composite was extensively used for the removal of heavy metals from wastewater. In wastewater, copper (Cu²⁺) usually coexist with the organic ligands, which had unknown effect on Cu²⁺ adsorption by the composite materials. In order to understand further on that, the adsorption of copper by the composite materials must be studied. In the present study, montmorillonite was coated with chitosan, and X-ray diffraction (XRD) patterns of the composite proved the intercalation of chitosan in the montmorillonite. Fourier transform infrared (FTIR) spectra of the composite identified the presence of amino group on the composite, and that of the composite saturated with metals identified the interaction between the amino groups and metals. Langmuir adsorption isotherm indicated that the composite had more capacity to adsorb Cu²⁺ from wastewater than montmorillonite. The adsorption capacity of Cu²⁺ by montmorillonite and chitosan-montmorillonite composite was studied, respectively, as a function of pH and in the presence of acetate. Compared to the montmorillonite at low ligand concentration (0.08 mmol/L) or low pH (<4.0), the coexisting acetate increased more Cu²⁺ adsorption by the composite. The acetate ligand presented less depression on the adsorption by the composite than that by montmorillonite at high ligand concentration (4 mmol/L) or high pH (>4.5). Therefore, the composite is more suitable for removing Cu²⁺ than montmorillonite in acid aqueous medium.

The ability of water hyacinth (WH) and pondweed (PW) to accumulate mercury from water in gold mine tailing area was studied. Experiments were carried out in the field conditions without using a model system. An approach for mercury fractionation according to its association with various types of biomolecules (water soluble compounds, oxygen-containing ligands such as polycarboxylic acids and cell wall components) was suggested. It is based on sequential extraction of mercury to recover different compounds according to the binding strength. In all cases for WH and PW, the most portion of mercury is bound to the cell wall (63–67 and 54–64 %, for WH and PW, respectively) that works as a physiological barriers and protects the plants from negative impact of mercury ions. An approach based on the ability of plants to extract elements from tailings drainage waters that are characterized by milder conditions in comparison with strongly acidic waste material was suggested. The highest BCF values (66,500 and 32,700 for WH and PW, respectively) were obtained for plants grown in natural stream. At low levels of mercury in water (C Hgwₐₜₑᵣ = 0.01–0.05 ppb) typical for tailing solutions, translocation of the element from roots to shoots decreases as concentration of mercury in WH increases. PW is preferable to use in practice for tailings remediation from mercury contamination since it does not require cultivation in a greenhouse and shows BCF values comparable with WH.