In this study, we investigated the effect of olive mill wastewater on selected soil physical and hydraulic properties. Olive mill wastewater was added to each column every week at different loading rates (0, 50, 100, and 200 m³ ha⁻¹). Physicochemical and hydraulic properties were determined for surface (0–8 cm) and subsurface layers (8–16 and 16–24 cm). The highest loading rate (200 m³ ha⁻¹) showed an increase in aggregate stability from 18% (control) to 31 and to 38%, penetration resistance from 1.8 kg cm⁻² (control) to 3.5 and to 4.5 kg cm⁻², hydraulic conductivity from 43 cm day⁻¹ (control) to 15.3 and 3.3 cm day⁻¹, and water repellency from < 5 s (control) to 120 and 261 s in the first and second months for the surface layer, respectively. The opposite was observed for the infiltration rate, where it decreased from 39.01 mm h⁻¹ (control) to 1.26 and 0.42 mm h⁻¹ for the first and second months, respectively. This study showed that application of olive mill wastewater deteriorated the physical and hydraulic properties of soil proportional to loading rates and more specifically at the surface layer.

In this work, a novel functionalized graphene oxide (GO) was used as an effective and selective adsorbent for removal of mercury (Hg²⁺). The magnetic nanocomposite adsorbent (MNA) based on GO was prepared through surface reversible addition–fragmentation chain transfer copolymerization of acrylic monomers and then the formation of Fe₃O₄ nanoparticles. The structure of MNAs was characterized by using FTIR, SEM, TEM, VSM, XRD, and nitrogen adsorption/desorption isotherms. The results of ion adsorption of MNAs demonstrated high selectivity and adsorption efficiency for Hg²⁺ in the presence of competing ions. Furthermore, the removal of Hg²⁺ obeyed a pseudo-second-order model and fitted well to the Langmuir isotherm model with the maximum Hg²⁺ uptake of 389 mg g⁻¹. The MNA was also confirmed as good materials for re-use and maintained 86% of its initial adsorption capacity for mercury after the fifth regeneration cycles. Finally, the experimental results demonstrated that the solution pH, ion concentration, and temperature had a major impact on Hg(II) adsorption capacity. The results indicate that the MNAs with high adsorption abilities could be very promising adsorbents for the selective recovery of ions in wastewater treatment process. Graphical abstract

The use of pyrolysis to produce oil from sludge by the evaporation–condensation process is a promising technique. However, the resulting lipids are prone to be acidized under exposure to oxygen, which can affect their quality and use. To eliminate the need for this oil separation process, the present work uses blended pyrolysis to preserve the oil in the char and to prevent it from deteriorating. At the same time, metals are eliminated to a secure level of combustion emissions. The sludge was pyrolyzed into a sintering fuel through blended pyrolysis with SiO₂, Al₂O₃, and sand. These materials are the main components of the sintered ceramsite obtained. Therefore, the influence of these substances and residence time on lipid formation and metal residue in the char were investigated. Non-blended pyrolysis required a 40-min duration, whereas sand-pyrolysis required 10 min to achieve the same yield. The concentration of C₁₆:₀ produced by blended pyrolysis with sand reached 2177 mg kg⁻¹, which is 57% higher than that of non-blended pyrolysis. Blended pyrolysis with SiO₂ required at least 20 min to immobilize As metal. In summary, blended pyrolysis simplifies the process, reduces time, and produces char with lipid-rich and low metal leaching, which can be used as a sintering fuel.

Nitrogen loss in karst sloping farmland will lead to declining land productivity and environmental pollution, in which the nitrogen loss through underground pore fissures will directly lead to groundwater pollution. The characteristics of total nitrogen (TN) production were studied by simulating the “dual structure” microenvironment of sloping farmland in a karst region using an artificial rainfall simulation method. The results show that rainfall was the main driving factor of TN loss in karst sloping farmland. TN was mainly lost through underground pore fissures when the rainfall intensity was ≤ 30 mm · h⁻¹. TN was lost at the surface and underground when the rainfall intensity was ≥ 50 mm · h⁻¹, TN loss on the surface accounted for a large proportion, and the surface flow was the main carrier of TN loss. The TN loss underground is easily ignored because it is hidden underground. Therefore, TN loss belowground in karst sloping farmland should receive increased attention. It would be interesting to explore the influences of connectivity and type of underground pore fissure system on TN loss in karst sloping farmland. The prevention and control of TN loss in karst sloping farmland should be considered both at the surface and underground. Reducing the formation of slope flows and slowing rainwater filtration by increasing slope vegetation coverage can be considered to reduce TN loss. The results of this study provide a theoretical reference for agricultural non-point source pollution control in a karst region. Graphical abstract

Ammonia is one of the most common aquatic pollutants. To analyze the effect of ammonia exposure on the glutathione redox system, we investigated the levels of hydrogen peroxide (H₂O₂) and glutathione, and transcription and activities of glutathione-related enzymes in liver and gills of FFRC strain common carp (Cyprinus carpio L.) exposed to 0, 10, 20, and 30 mg/L of ammonia. The results showed that H₂O₂ content reached a maximum level at 48 h of exposure in the liver of fish. In gills, H₂O₂ increased rapidly at 6 h and reached to maximum levels at 24 h of exposure, indicating that gills experienced oxidative stress earlier than the liver of fish exposed to ammonia. Reduced glutathione (GSH) content and reduced glutathione/oxidized glutathione (GSH/GSSG) ratio increased significantly within 24 h of exposure. Meanwhile, the transcription and activities of glutathione S-transferase (GST) and glutathione reductase (GR) increased significantly in the liver, and glutathione peroxidase (GSH-Px) and GST increased in the gills of fish exposed to ammonia. Malondialdehyde (MDA) content kept at a low level after exposure to low concentration of ammonia, but increased significantly after exposure to 30 mg/L ammonia for 48 h along with a decrease in GSH content and GSH/GSSG ratio. These data showed that the glutathione redox system played an important role in protection against ammonia-induced oxidative stress in the liver and gills of FFRC strain common carp, though the defense capacity was not able to completely prevent oxidative damage occurring after exposure to higher concentration of ammonia. This research systematically studied the response of the glutathione redox system to ammonia stress and would provide novel information for a better understanding of the adaptive mechanisms of fish to environmental stress.

Since decades, surface water bodies have been exposed to pesticides from agriculture. In many places, retention systems are regarded as an important mitigation strategy to lower pesticide pollution. Hence, the processes governing the transport of pesticides in and through a retention system have to be understood to achieve sufficient pesticide attenuation. In this study, the temporal dynamics of metazachlor and its transformation products metazachlor-oxalic acid (OA) and –sulphonic acid (ESA) were observed in an agricultural retention pond and hydrologic tracers helped to understand system-inherent processes. Pesticide measurements were carried out for 80 days after their application during transient flow conditions. During a short-term (3 days) experiment, the tracers bromide, uranine and sulphorhodamine B were used to determine hydraulic conditions, residence times and sorption potential. A long-term experiment with sodium naphthionate (2 months) and isotopes (12 months) provided information about inputs via interflow and surface-groundwater interactions. During transient conditions, high concentration pulses of up to 35 μg L⁻¹ metazachlor, 14.7 μg L⁻¹ OA and 22.5 μg L⁻¹ ESA were quantified that enduringly raised solute concentrations in the pond. Mean residence time in the system accounted for approximately 4 h showing first tracer breakthrough after 5 min and last tracer concentrations 72 h after injection. While input via interflow was confirmed, no evidence for surface-groundwater interaction was found. Different tracers illustrated potentials for sorption and photolytic degradation inside the system. This study shows that high-resolution sampling is essential to obtain robust results about retention efficiency and that hydrological tracers may be used to determine the governing processes.

A challenge in side-stream treatment of anaerobic digester supernatant is that the effluent does not meet discharge standards. To address this challenge, this study tested tubular multichannel ceramic microfiltration (MF) and ultrafiltration (UF) membranes for the post-treatment of anaerobic digester supernatant. Pollutant rejection (total suspended solids (TSS), COD, total nitrogen (TN), and total phosphorus (TP)), color removal, and membrane susceptibility to fouling were determined at various transmembrane pressures (TMPs) (0.2, 0.3, 0.4, 0.5 MPa). Both methods completely removed TSS. In MF, COD was removed with 48–76% efficiency at 0.2–0.4 MPa. In UF, COD removal efficiency was slightly higher, reaching 83.7% at 0.4 MPa. With both methods, pollutant removal did not increase at TMP of 0.5 MPa. With both MF and UF, color was reduced by 54–100%, irrespective of the TMP. At 0.2–0.4 MPa, membrane resistance was lower and permeate flux was much higher with MF than UF. At 0.5 MPa, the methods differed only slightly from each other. Due to the larger cut-off, flux decline was slower in MF (0.7 h⁻¹) than in UF (1.1 h⁻¹), as the larger pore-size favors less foulant deposition. Thus, taking into account rejection efficiency, capacity, washing frequency, and cost (pressure), these results indicate that MF at 0.4 MPa is the most effective variant for post-treatment of anaerobic digester supernatant. With this variant, the almost colorless permeate contained 25 mg COD/L, no TSS, 55 mg TN/L (75% in the form of nitrites and nitrates), and 8.5 mg TP/L, thus meeting criteria for water to be used in irrigation or algae cultivation.

Polycyclic aromatic hydrocarbons (PAH) are persistent organic compounds of major concern that accumulate in the environment, especially soils, and require remediation. Researches to develop bioremediation and phytoremediation (alternative eco-friendly technologies) are being conducted. First, a bioaccessibility measurement protocol was adapted to a brownfield soil using Tenax® beads in order to compare PAHs bioaccessibility in soil samples. PAHs desorption kinetics were established, described by a site distribution model, and a common extraction time was calculated (48 h). Second, the role of two Fabaceae (Medicago sativa L. or Trifolium pratense L.) root exudates in enhancing PAHs bioaccessibility and biodegradation in the studied soil was evaluated during microcosms experiments (28 °C). The CO₂ emissions were significantly higher in presence of T. pratense exudates; the dehydrogenase activities showed improvements of the soil microbial activity in presence of two types of root exudates compared to untreated soil samples; the PAHs residual contents decreased more in untreated samples than in the presence of T. pratense exudates; and M. sativa exudates lowered PAHs bioaccessibility but not residual contents.

Polycyclic aromatic hydrocarbons (PAHs) upset the basic biological parameters of the soil, such as enzymatic activity, which can be used to identify the direction and intensity of organic and mineral substance transformation in the soil environment. The aim of this study was to determine the impact of soil contamination with naphthalene, phenanthrene, anthracene and pyrene at rates of 0–4000 mg kg⁻¹ DM (dry matter) of soil on the activity of acid phosphatase and alkaline phosphatase. An analysis was also conducted on how some organic substances, such as cellulose, sucrose and compost at rates of 0 and 9 g kg⁻¹ DM alleviate the PAH impact on the enzymes under study. The experiment was carried out in a laboratory with loamy sand as the soil material. Phosphatase resistance (RS) and soil resilience (RL) were calculated. The enzyme activity was found to depend significantly on the PAH rate, time of PAH deposition in soil and the type of organic substance added to the soil. The activity of acid and alkaline phosphatase increased with the degree of soil contamination with PAHs. Naphthalene had the greatest stimulating effect on enzyme activity. Biostimulation of soil with cellulose, sucrose and compost had a positive effect on acid and alkaline phosphatase activity, with cellulose and compost being the most effective in boosting acid and alkaline phosphatase activity, respectively. Naphthalene had the greatest effect on acid and alkaline phosphatase resistance and pyrene had the least effect. Low RL indices indicate that the presence of PAHs permanently disturbed the activity of acid and alkaline phosphatase.

The utilization of construction and demolition waste materials for the radionuclide immobilization by sorption processes was investigated. Given that the liquid radioactive waste usually has a complex composition and that effects of competition may significantly influence the efficiency of the treatment, the Simplex Centroid experimental design was used to explore ions sorption from multi-component solutions. For the purpose of this study, the common components of construction and demolition waste, such as pathway concrete and different bricks samples, were used along with the multi-component Sr²⁺, Co²⁺, and Ni²⁺ ions solutions. The equations for the prediction of metal ions sorption capacities were derived. The coefficients that correspond to the linear and interaction terms were obtained using a special cubic model. Likewise, by analysis of variance, statistically significant terms of the obtained polynomial were defined. The investigation has shown that the most effective sorption was onto the pathway concrete for all three cations, while the highest sorption capacity was found for Co²⁺ ions. Also, it has been determined that concerning Sr²⁺ ion removal there was a competition with coexisting Co²⁺ and Ni²⁺ ions, reducing its sorption capacity, while sorption of Co²⁺ and Ni²⁺ occurred more independently on other cations in multi-component solutions. Based on the obtained results, the applied experimental design can be efficiently used for the description of competitive sorption process and could be a powerful tool for the prediction of cation immobilization in liquid radioactive waste treatment.