Excess fluoride concentration in drinking water is a global issue, as this has an adverse effect on human health. Several adsorbents have been synthesized from natural raw material to remove fluoride from water. Reported adsorbents have some problems with the leaching of metal ions, fewer adsorption sites, and low adsorption capacity. Therefore, to address this, an effective biomaterial derived from the Luffa cylindrica (LC), containing many active sites, was integrated with a nano form of cerium oxide to form a robust, biocompatible, highly porous, and reusable LC–Ce adsorbent. This synthesized biosorbent offers better interaction between the active sites of LC–Ce and fluoride, resulting in higher adsorption capacity. Several factors, influence the adsorption process, were studied by a central composite design (CCD) model of statistical analysis. Langmuir’s and Freundlich’s models well describe the adsorption and kinetics governed by the pseudo–second–order model. The maximum monolayer adsorption capacity was found to be 212 and 52.63 mg/g for LC–Ce and LC, respectively determined by the Langmuir model. Detailed XPS and FTIR analyses revealed the underlying mechanism of fluoride adsorption via ion-exchange, electrostatic interaction, H–bonding, and ion-pair formation. All the results indicate that LC–Ce could serve as a suitable adsorbent for efficient fluoride removal (80–85%).

Riverbed sediments are the interface layer in riverine ecosystems connecting the overlying medium of water and the vadose zone. The transport behavior of phosphorus (P), which has been recognized as the primary cause of freshwater eutrophication, in riverbed sediments remains unclear. Understanding the impact of riverbed sediments on P transport is a necessary prerequisite for the development of appropriate strategies to reduce potential groundwater pollution. In this study, riverbed sediments were collected from the upstream, midstream, and downstream sections of the Beiyun River, China, and packed into vertical soil columns to perform leaching experiments to quantify P transport characteristics. In addition, the impact mechanisms were further explored by conducting laboratory batch tests of P adsorption and desorption. The results demonstrated that approximately 80% of P can be adsorbed by riverbed sediments in soil column leaching experiment, and a tailing phenomenon was observed in its desorption. The hydraulic conductivity properties of riverbed sediments were evaluated by the advection-dispersion equation, showing a gradually decreasing adsorption capacity for P from upstream to downstream sections, which was supported by the results obtained from adsorption–desorption thermodynamic and kinetic batch tests. The estimated annual leaching masses of P increased from 60.72 g/(m² a) in the upstream section to 132.31 g/(m² a) in the downstream section. The role of riverbed sediments as a source or sink of P is possibly determined by their coarse sand particles content, and the mean equilibrium P concentration (EPC0). The competitive relationship between P and other forms of nutrients also has an important influence on its source-sink role. These findings suggest that the prevention of the potential P leaching is most needed in the downstream sections of Beiyun River, and corresponding control strategies should be developed to avoid groundwater pollution.

Microplastics with extremely high abundances are universally detected in marine and terrestrial systems. Microplastic pollution in the aquatic environment, especially in ocean, has become a hot topic and raised global attention. However, microplastics in soils has been largely overlooked. In this paper, the analytical methods, occurrence, transport, and potential ecological risks of microplastics in soil environments have been reviewed. Although several analytical methods have been established, a universal, efficient, faster, and low-cost analytical method is still not available. The absence of a suitable analytical method is one of the biggest obstacles to study microplastics in soils. Current data on abundance and distribution of microplastics in soils are still limited, and results obtained from different studies differ significantly. Once entering into surface soil, microplastics can migrate to deep soil through different processes, e.g. leaching, bioturbation, and farming activities. Presence of microplastics with high abundance in soils can alter fundamental properties of soils. But current conclusions on microplastics on soil organisms are still conflicting. Overall, research on microplastics pollution in soils is still in its infancy and there are gaps in the knowledge of microplastics pollution in soil environments. Many questions such as pollution level, ecological risks, transport behaviors and the control mechanisms are still unclear, which needs further systematical study.

Land application of biosolids is a major route for the introduction of silver (Ag) into the terrestrial environment. Previous studies have focused on the risks from Ag to the human food chain but there is still a lack of quantitative information on the flow of biosolid-borne Ag in the soil-crop system. Two long-term field experiments were selected to provide contrasting soil properties and tillage crops to investigate the fate of Ag from sequentially applied biosolids. Biosolid-borne Ag accumulated in the soil and < 1‰ of applied Ag was taken up by the crops. The biosolid-borne Ag also migrated down and accumulated significantly (p < 0.05) in the soil profile to a depth of 60–80 cm at an application rate of 72 t biosolids ha⁻¹. Soil texture significantly affected the downward transport of biosolid-borne Ag and the migration of Ag appeared to be more pronounced in a soil profile with a low clay content. Moreover, loss of Ag by leaching may not be related to the biosolid application rate. Leaching losses of Ag may have continued for some time after biosolid amendment was suspended. The results indicate that soil texture may be a key factor affecting the distribution of biosolid-borne Ag in the soil-crop system.

In compliance to European Union directives to reuse urban wastes as secondary fuels, the aim of present work was to investigate and control the environmental impact from disposal of ashes generated by combustion of a bio-solid, an olive by-product and their blend. Two waste materials were admixed with the ash and their performance as potential stabilizers was assessed. Metals and ions leached through a soil were measured.The results showed that dissolution of some alkaline substances raised the pH of water effluents, decreasing the extractability of heavy metals from the ashes. In some cases Cr and As leached reached hazardous levels. Upon addition of waste materials to ash, the concentration of Cr in liquid extracts was reduced by 35–97%, while that of Cu and As by 100%. All heavy metal values measured in the leachates were decreased to values below legislation limits. The mineralogy, the chemistry and the pH of solids involved were key factors for the retention of elements.

Cadmium (Cd) concentration was investigated in parent rocks, surrounding soil of black shales outcrop, stream water, stream sediments, paddy soil as well as rice plants. Leaching test and sequential extraction procedure were applied to evaluate Cd mobility and bioavailability in soil samples. This study aims to emphasize ecological risk of Cd induced by black shales by combining various natural medias in black shales area and control area. The black shales parent rocks have elevated Cd concentration and act as a source of Cd. The liberated Cd from black shales outcrop temporarily accumulated in the acidized surrounding soil and could arise potential adverse impacts on environment due to rainfall. Although high concentration of Cd was not detected in stream water, Cd concentrated stream sediment was a hidden toxin for surface water system. Cd in paddy soil was primarily from geogenic source and effected little by anthropogenic source. The concentration as well as mobility and bioavailability of Cd were high in paddy soil in black shales area, which lead to elevated Cd concentration in roots, shoots and grains of rice. As a result, residents in black shales area suffer increased non-carcinogenic risk of Cd via food chain.

Soil nitrogen (N) leaching is recognized to have negative effects on the environment. There is a lack of studies on different simultaneously occurring drivers of environmental change, including changing rainfall and N deposition, on soil N leaching. In this study, a two factorial field experiment was conducted in a Korean pine forest with the following four treatments: 30% of throughfall reduction (TR), 50 kg N ha⁻¹ yr⁻¹ of N addition (N+), throughfall reduction plus N addition (TRN+) and natural forest (CK). The zero-tension pan lysimeter method was used to assess the response of soil N leaching loss to manipulated N addition and throughfall reduction. The results showed that the soil N leaching loss in natural forest was 5.0 ± 0.4 kg N ha⁻¹yr⁻¹, of which dissolved organic nitrogen (DON) accounted for 48%. Compared to natural forest, six years of N addition (NH₄NO₃, 50 kg N ha⁻¹ year⁻¹) significantly (P < 0.05) increased soil N leaching losses by 122%, especially in the form of NO₃⁻; a 30% reduction in throughfall slightly decreased N leaching losses by 23%; in combination, N addition and throughfall reduction increased N leaching losses by 48%. There was a strong interaction between N addition and throughfall reduction, which decreased N leaching loss by approximately 2.5 kg N ha⁻¹ yr⁻¹. Our results indicated that drought would diminish the enhancing effect of N deposition on soil N leaching. These findings highlight the importance of incorporating both N deposition and precipitation and their impacts on soil N leaching into future N budget assessments of forest ecosystems under global environmental change.

Oil-contaminated soils resulted from drilling activities can cause significant damages to the environment, especially for living organisms. Treatment and management of these soils are the necessity for environmental protection. The present study investigates the field study of seven oil-contaminated soils treated by different stabilization/solidification (S/S) methods, and the selection of the best treated site and treatment method. In this study, first, the ratios of consumed binders to the contaminated soils (w/w) and the treatment times for each unit of treated soils were evaluated. The ratios of consumed binders to the contaminated soils were between 6 and 10% and the treatment times for each unit of treated soils were between 4.1 and 18.5 min/m³. Physicochemical characteristics of treated soils were also determined. Although S/S methods didn’t change the water content of treated soils, they increased the porosity of soils. Unexpectedly, the cement-based S/S methods didn’t increase the pH of the treated soils. The highest and the lowest leaching of petroleum hydrocarbons was belonging to S/S using diatomaceous earth (DE) and the combination of Portland cement, sodium silicate and DE (CS-DE), respectively. The best acid neutralization capacity was obtained for soils treated using the combination of Portland cement and sodium silicate (CS). Based on the best-worst multi-criteria decision-making method (BWM-MCDM), the soils treated using CS-DE was select as the best. The BWM-MCDM can be used as an effective tool for the selection of the best alternative in all areas of environmental decontamination.

It is of environmental significance to study the leaching performance of additives from microplastics (MPs) and further evaluate the toxicity of leachate to microalgae. Here, we investigated the effects of accelerated aging on characteristics, leaching, and toxicity of commercial lead chromate pigmented MPs. Results show that aging of MPs caused surface cracks and fragmentation, increased their surface area and carbonyl contents, and promoted the release of lead chromate pigment. Chromium (Cr) and lead (Pb) tend to leach under acidic condition, rather than neutral and alkali environment. Aging treatment facilitates the leaching performance and a high concentration of NaCl solution also favors the leaching process. Toxicology experiments demonstrate that only high concentration of leachate (>10 μg L⁻¹) exerted significant inhibitory influence (p < 0.005) on cell photosynthesis of Microcystis aeruginosa. The growth inhibition of algal cells remarkably increased with increasing leachate concentrations. We observed more inhibiting effects on cell growth and photosynthesis using the leachates of aged MPs. Longer aging time leads to more release of Cr and Pb, rendering higher toxicity to microalgae. These novel findings will benefit us from assessing the leaching behavior of additives in MPs and their toxicological risks to aquatic organisms.

In this study, samples of soil and particulate matter obtained from the highly industrialized region of Ostrava, Czech Republic, are used for the toxicity evaluation of the selected metal(loid)s (Cd, Cr, Cu, Ni, Pb, Zn, As). We investigated the samples from sites supposedly affected the most by the local pollution sources using mineralogical techniques (XRD, SEM/EDS) to understand the solid speciation of the contaminants as the crucial factor affecting their release. Although the bulk composition was defined by common silicates and oxides that are rather resistant to leaching, the presence of tiny Ni, Pb, and/or Zn sulfate-like droplets indicated a potential increase of the solubility of these metals. In vitro tests simulating gastric and lung fluids were used to assess the exposure risk for humans, as well as metal(loid) bioaccessibility. Based on the results, the potential risk for the observed age group (3-year-old children) could be recognized, particularly in the cases of As, Pb and Cd for both oral and inhalation exposure. Arsenic exhibits high bioaccessibility (7.13–79.7%, with the median values of 10.6 and 15.6 for SGL and SLF, respectively), high daily intake (1.4- to 8.5-fold higher than the tolerable daily intake) and high concentrations in atmospheric PM₁₀ (2.5 times the tolerable concentration in air). In contrast, Ni exceeded tolerable concentrations in the atmosphere up to 20-fold, but its bioaccessibility remained relatively low (0.1–22%), and Ni did not pose a major threat to human health. Cadmium, Pb and As originating from industrial activities and domestic heating have been suggested to be the most important pollutants (tolerable daily intake was exceeded by up to 74-, 34- and 8-fold for Cd, Pb and As, respectively).