A mathematical model is developed to investigate the effect of pH and salinity fluctuation on biogeochemical reactions and metals' behavior in sediments. The model includes one-dimensional vertical advective and diffusive transport of species, serial reductions of electron acceptors, and precipitation/dissolution of species, acid–base chemistry, and metal sorption to sediments. The model was tested using data obtained from laboratory microcosm experiments which exposed metal (Cd, Zn) contaminated sediment to alternating fresh and salty overlying water. The model successfully reproduces the contrasting metal's release behavior and the vertical profiles of pH, Cl⁻, SO₄²⁻, Mn and Fe in porewater and the acid volatile sulfides (AVS) and simultaneously extracted metals (SEM) in sediments. The model showed that FeOOH₍ₛ₎was the dominant sorption phase controlling the solubility of the metals at the surficial sediments while AVS controlled the solubility of the metals in anoxic sediments. The model also showed that the release of the metals to overlying water was controlled by the oxidation of metal sulfides in a very thin layer of oxic sediments (2–3 mm). The proposed model can be useful in managing metal contaminated sediments where pH and salinity are fluctuating by assessing the underlying biogeochemical processes and metals' behavior.

The main objective of this study was to evaluate the degradation of a ternary mixture of n-hexane, benzene, and methanol fed to two Trickle Bed Air Biofilters (TBABs) designated as “A” and “B”. Both TBABs were loaded with pelletized diatomaceous earth support media and run at an empty bed residence time (EBRT) of 120 s. TBABs “A” and “B” were operated at pH 4 and fed with n-hexane:benzene:methanol (CH:CB:CM) concentrations ratios of 1:3:10 and 1:3:6.6, respectively under different loading rates. The influent total loading rates varied from 39.2 to 117.7 g/m³h and from 32 to 96.4 g/m³h for TBABs “A” and “B”, respectively. In both TBABs, methanol and benzene were the most eliminated volatile organic compounds (VOCs), while the removal of n-hexane was controlled by the VOCs ratios. Higher removal efficiencies were obtained for the VOCs ratio of 1:3:6.6 corresponding to a total VOCs load of 96.4 g/m³h. The addition of VOCs mixture to the TBABs resulted in change of the fungi community within the TBABs as compared to the fungi community when the TBABs were previously receiving only n-hexane as a sole substrate.

In order to determine human exposure to the indoor toxicant, selection of dust fraction and understanding dust particle size distribution in settled indoor dust are very important. This study examined the influence of dust particle size on the concentration of polybrominated diphenyl ethers (PBDEs) congeners, assessed the distribution of dust particle size and characterized the main indoor emission sources of PBDEs. Accordingly, the concentrations of PBDE congeners determined in different indoor dust fractions were found to be relatively higher in the order of dust particle size: 45–106 μm > (<45 μm) > 106–150 μm. The finding shows arbitrary selection of dust fractions for exposure determination may result in wrong conclusions. Statistically significant moderate correlation between the concentration of Σ₉PBDEs and organic matter content calculated with respect to the total dust mass was also observed (r = 0.55, p = 0.001). On average, of total dust particle size <250 μm, 93.4 % (m/m%) of dust fractions was associated with less than 150 μm. Furthermore, of skin adherent dust fractions considered (<150 μm), 86 % (v/v%) is in the range of particle size 9.25–104.7 μm. Electronic materials treated with PBDEs were found the main emission sources of PBDE congeners in indoor environment. Based on concentrations of PBDEs determined and mass of indoor dust observed, 150 μm metallic sieve is adequate for human exposure risk assessment. However, research in this area is very limited and more research is required to generalize the fact.

In view of the fatal illnesses caused by methylene blue (MB) which is contained in the dye wastewater, the present study focused on the use of natural sunlight in heterogeneous photocatalysis to decolorize and degrade MB. The present study also investigated the effects of enhancers (hydrogen peroxide and persulfate ion) and inhibitors (chloride and carbonate ions) on photodecolorization of MB. Pseudo-first-order rate constants for each studied effect were determined through Langmuir-Hinshelwood model. The recommended conditions to photodecolorize 60 ppm of MB under natural sunlight were 1.0 g/L of titanium dioxide nanopowder at initial pH 10.5 in order to achieve 85.3 % decolorization (rate constant of 10.8 × 10⁻³ min⁻¹). The addition of 4,080 ppm of hydrogen peroxide and persulfate ion significantly enhanced the decolorization efficiency up to 96.6 and 99.3 %, respectively (rate constants of 66.2 and 91.0 × 10⁻³ min⁻¹, respectively). However, the addition of 2,000 ppm of chloride and carbonate ions reduced the decolorization efficiency of MB to 74.7 and 70.2 %, respectively (rate constants of 7.8 and 7.3 × 10⁻³ min⁻¹, respectively). The present study implied that it was possible to use natural sunlight as a light source for photocatalytic treatment of dye in tropical countries like Malaysia.

Effect of biochar, derived from unfertilized dates, on the immobilization of Cd and Ni, in a sandy loam alkaline soil, was investigated. The biochar was applied to the soil columns at the rate of 0.5, 1, and 2 % (w/w) artificially polluted with 10 mg kg⁻¹Cd and 100 mg kg⁻¹Ni. After 1 month incubation of soil-biochar mixture under ambient conditions, the soil bulk density was reduced by 0.19 g cm⁻³as compared with no biochar addition with increase in soil pH. A reduction of 53 % in the NH₄NO₃-extractable soil Ni was recorded as compared with the corresponding control without biochar addition. After incubation, the water-soluble Ni and NH₄NO₃-extractable soil Cd and Ni contents were significantly lower in all the biochar treatments than the control. A reduction of 53 % in the NH₄NO₃-extractable soil Ni was recorded as compared with the corresponding control. The biochar content separated from the incubated soil showed low concentrations of NH₄NO₃-extractable Cd and Ni. The total Ni and Cd contents recovered from biochar samples after incubation were 35.2 and 3.7 mg kg⁻¹, respectively. Their contents in soil were substantially reduced by the incorporation of biochar amendment (114 to 57.2 mg kg⁻¹Ni, 9 to 5.6 kg⁻¹Cd) as compared with the no-biochar control. Therefore, addition of the biochar improved the soil physical properties and succeeded in immobilizing the studied metals.

In the present study, we investigate the effects of a possible protective role of vitamin E (vit E) or selenium (Se) on glucose metabolism disruption induced by static magnetic field (SMF) in rats. Rats have been exposed to SMF (128 mT, 1 h/day during 5 days). Our results showed that SMF failed to alter body weight and relative liver weight. Our data demonstrated that exposure to SMF increased (+21 %) blood glucose level and caused a decrease (−15 %) in liver glycogen content. Moreover, the same treatment induced a reduction of pancreatic islet area. Interestingly, supplementation with vit E (DL α-tocopherol acetate, 150 mg/kg per os during 5 days) prevented alterations induced by SMF on glucose metabolism and liver glycogen content, whereas supplementation with Se (Na₂SeO₃, 0.20 mg/l, in drinking water for 4 weeks) restored only hepatic glycogen contents. By contrast, both vit E and Se failed to correct the area of pancreatic islets.

Preliminary analysis on dredged marine sediments from Benoi basin in Singapore was carried out showing elevated concentrations of Zn, Cu, Pb, Cd, Cr and Ni. Ethylenediamine tetraacetic acid (EDTA) thermal washing experiments were conducted for heavy metal extraction at temperature 100 °C. Results indicated the significant efficiency of thermal washing to extract Pb, Zn and Ni. However, there was little or no influence in the removal of Cu and Cr and a slight effect to Cd indicating multiple mechanisms. In addition, agitation was found to have great influence on the removal efficiency of heavy metals as experiments without agitation performed lesser or no extraction due to limited contact of the washing solution and the dredged sediment. Sequencing processes of thermal treatment followed by EDTA washing showed limited performance, likely due to thermal stabilization of the contaminants particularly at low liquid-to-soil (L/S) ratio. Furthermore, sequential extraction analysis on the metal speciation was performed before and after thermal washing. It was revealed that metals mainly extracted from fractions bound to carbonates and Fe-Mn oxides, the relative mobile fraction. On the contrary, metals in the residual fraction displayed a considerable stability.

When released into natural aquatic systems, cerium oxide (CeO₂) nanoparticles (NPs) may have toxic effects to the ecosystems and public health; it is thus important to understand their environmental fate and transport. This work studied the effects of humic acid (HA) concentrations (0–10 mg L⁻¹) and solution chemistry (ionic strength (IS) and pH) on the retention and transport of CeO₂NPs in water-saturated porous media under environmental relevant conditions. HA and IS showed remarkable effect on the retention and transport of CeO₂NPs in the porous media. Even at low concentrations (i.e., 5 and 10 mg L⁻¹), HA stabilized CeO₂NPs in the suspensions by introducing both negative surface charge and steric repulsion and thus enhanced their mobility in the porous media. When solution HA concentration increased or ionic strength decreased, mobility of CeO₂NPs in the porous media enhanced dramatically. Solution pH, however, had little influence on the mobility of the CeO₂NPs under the tested experimental conditions, and increasing solution pH only slightly increased the transport of the NPs. Mathematical models were applied to describe the experimental data. Predictions from the extended Derjaguin–Landau–Verwey–Overbeek (XDLVO) theory and advection–dispersion–reaction (ADR) model matched the experimental data well.

Stabilization of sewage sludge (SS) prior to its land disposal may help control the mobility of SS-borne contaminants, particularly potentially toxic metals. We examined the effects of stabilized SS application on soil properties, biomass production, and phytoavailability of Cu and Zn to plants grown in two contrasting soils, Entisol and Aridisol. Stabilized SS mixtures were created by mixing SS in a 3-to-1 ratio with bentonite (B), sugar beet factory lime (SL), brick factory fly ash (BFA), rice straw (RS), water hyacinth (WH), and 50:50 mixture of RS and SL. Mixtures were applied at 50 Mg ha⁻¹, and Sorghum vulgare L. and Eurica sativa were grown in a pot experiment. All the amendments increased plant availability and uptake of both Cu and Zn compared to the unamended control. The application of stabilized SS increased dry plant biomass significantly and decreased DTPA-extractable elements compared to the non-stabilized SS treatment. We conclude that of the six amendments studied, especially sugar beet factory lime (SL) and bentonite (B), are promising for the stabilization of metal-contaminated biosolids and should be tested under field conditions.