Leachable chromium in the incineration fly ash and wastewater sludge has been thermally stabilized by plasma melting at the temperature of 1,773 K. To better understand how chromium is stabilized with the high-temperature treatment, chemical structure of the slags sampled at temperature zones of 1,100–1,700 K has been studied by synchrotron X-ray absorption spectroscopy. The component-fitted X-ray absorption near edge structure spectra of chromium indicate that the main chromium compounds in the sludge and fly ash are Cr(OH)₃, Cr₂O₃, and CrCl₃. A small amount of toxic CrO₃ is also observed in the fly ash. In the plasma melting chamber under the reducing environment, the high-oxidation state chromium is not found. The slags in the plasma melting chamber have much less leachable chromium, which is due to chemical interactions between chromium and SiO₂ in the slags. The existence of the interconnected Cr-O-Si species is observed by refined extended X-ray absorption fine structure spectroscopy. In the Cr₂O₃ phase of the slags, their bond distances, and coordination numbers for the first (Cr-O) and second (Cr-(O)-Cr) shells have insignificant perturbation when experienced with different melting temperatures between 1,300 and 1,700 K. It seems that Cr₂O₃ and chromium encapsulated in the silicate matrix of the slags have relatively much lower leachability. With this concept, to obtain a low chromium leachability slag from the plasma melting process, the residence time of the melting chamber may be decreased, and the slag discharge temperatures may be increased to 1,300 K. This work also exemplifies utilization of molecule-scale data obtained from synchrotron X-ray absorption spectroscopy to reveal how chromium is thermally stabilized in a commercial scale plasma melting process.

Plant growth-promoting rhizobacteria (PGPR) play an important role in the biodegradation of natural and xenobiotic organic compounds in soil. They can also alter heavy metal bioavailability and contribute to phytoremediation in the presence or absence of synthetic metal chelating agents. In this study, the inhibitory effect of Cd2+ and Ni2+ at different concentrations of Ca2+ and Mg2+, and the influence of the widely used chelator EDTA on growth of the PGPR Pseudomonas brassicacearum in a mineral salt medium with a mixture of four main plant exudates (glucose, fructose, citrate, succinate) was investigated. Therefore, the bacteriostatic effect of Cd2+, Ni2+ and EDTA on the maximum specific growth rate and the determination of EC50 values was used to quantify inhibitory impact. At high concentrations of Ca2+ (800 μmol L-1) and Mg2+ (1,250 μmol L-1), only a small inhibitory effect of Cd2+ and Ni2+ on growth of P. brassicacearum was observed (EC50 Cd2+, 18,849 ±â€‰80 μmol L−1; EC50 Ni2+, 3,578 ±â€‰1,002 μmol L−1). The inhibition was much greater at low concentrations of Ca2+ (25 μmol L−1) and Mg2+ (100 μmol L−1) (EC50 Cd2+, 85 ±â€‰0.5 μmol L−1 and EC Ni2+, 62 ±â€‰1.8 μmol L−1). For the chosen model system, a competitive effect of the ions Cd2+ and Ca2+ on the one hand and Ni2+ and Mg2+ on the other hand can be deduced. However, the toxicity of both, Cd2+ and Ni2+, could be significantly reduced by addition of EDTA, but if this chelating agent was added in stoichiometric excess to the cations, it also exhibited an inhibitory effect on growth of P. brassicacearum.

Solution pH is among the most important parameters that influence heavy metal biosorption. This work presents a kinetic study of the effects of pH on chromium biosorption onto Cupressus lusitanica Mill bark from aqueous Cr(VI) or Cr(III) solutions and proposes a mechanism of adsorption. At all assayed contact times, the optimum pH for chromium biosorption from the Cr(III) solution was 5.0; in contrast, optimum pH for chromium biosorption from the Cr(VI) solution varied depending on contact time. The kinetic models that satisfactorily described the chromium biosorption processes from the Cr(III) and Cr(VI) solutions were the Elovich and pseudo second-order models, respectively. Diffuse reflectance infrared Fourier transform spectroscopy studies suggest that phenolic compounds present on C. lusitanica Mill bark play an important role in chromium biosorption from the Cr(III) solution. On the other hand, chromium biosorption from the Cr(VI) solution involved carboxyl groups produced on the bark by redox reactions between oxygen-containing groups and Cr(VI), and these were in turn responsible for the biosorption of Cr(III) produced by Cr(VI) reduction.

The Loxahatchee National Wildlife Refuge (Refuge) developed as a system with waters low in nutrients. Today, the Refuge wetlands are impacted by inflows containing elevated nutrient concentrations originating from agricultural sources flowing into canals surrounding the west side and from urban and horticultural areas flowing into canals surrounding the eastern side of the Refuge. We analyzed water quality sampled at 40 sites divided into eastern and western areas and four zones in the Refuge. We defined four zones as the canals surrounding the Refuge marsh, the perimeter zone, the transition zone, and the interior zone. The canal receiving agricultural inflows had greater alkalinity and conductivity (SpC), Si and SO4 but lower turbidity and total suspended solids than the canal receiving urban and horticultural inflows. Alkalinity, total dissolved solids (TDS), SpC, Ca, Cl, and SO4 concentrations were greater in the perimeter than in transition and interior zones. Alkalinity and SpC values and SO4 concentrations were greater in the transition than in interior zone. Alkalinity, SpC, and TDS values and Ca, SO4, and Cl concentrations correlated in negative curvilinear relationships with distance from the canal (r 2 = 0.78, 0.70, 0.61, 0.78, 0.64, 0.57, respectively). Analysis of multiple water quality parameters may reveal the complexity of interactions that might be overlooked in a simple single parameter analysis. These data show an impact of canal water containing high nutrient concentrations on water quality flowing from the canal towards the Refuge interior.

This article describes the synthesis of p-sulfonated calix[4,6]arene derivatives and firstly their immobilization onto magnetic nanoparticles for removal of some carcinogenic aromatic amines. The prepared new water-soluble calix[4,6]arene appended magnetic nanoparticles (p-C[4]-MN and p-C[6]-MN) were characterized by a combination of Fourier transform infrared spectroscopy, scanning electron microscopy, and thermogravimetric analyses. The separation and quantification of aromatic amines were performed by high performance liquid chromatography. In batch sorption experiments, the compounds 7 and 8 were found to be effective sorbent for aromatic amines. It was observed that the percentage of aromatic amine removal was 44–97 % for compound 7 and 63–97 % for 8 when the pH of the aromatic amine solution was in the range of 3.0–8.5. The sorption of aromatic amines by p-sulfonated calix[n]arenes-based magnetic nanoparticles shows that sulfonic acid groups play a major role for the formation of hydrogen bonds and electrostatic interactions.

An effective adsorbent for the removal of heavy metals was manufactured by immobilization of jujube powder. The adsorptions of Cd, Zn and Cu from aqueous solutions by jujube complex beads (Type 1 and Type 2) were studied in a batch adsorption system. The adsorption data were fitted well with the Langmuir isotherm models. The adsorption capacities (β) for Cd, Zn and Cu were 4.23, 2.93 and 3.64 mg/g in Type 1 and 1.24, 0.70 and 1.35 mg/g in Type 2 beads. The removal efficiencies of the Type 2 beads, with a larger unit surface area, were lower than those of the Type 1 due to part of the casein or cyclic AMP being destroyed during the drying process of the Type 1. These values for Type 1 beads were higher than those of all other adsorbents for each heavy metal. A comparison of the kinetic models on the overall adsorption rate showed that the adsorption system was best described by pseudo-first-order kinetics. The removal efficiencies of Cd, Zn and Cu exhibited similar tendencies to those observed in the equilibrium tests. This indicates that the jujube complex beads developed in this study can be used as promising adsorbents for the removal of heavy metals from wastewater.

We investigated the influence of cadmium stress on zinc hyperaccumulation, mineral nutrient uptake, and the content of metal-binding proteins in Arabidopsis halleri. The experiments were carried out using plants subjected to long-term cadmium exposure (40 days) in the concentrations of 45 and 225 μM Cd²⁺. Inductively coupled plasma-mass spectrometry, size exclusion chromatography coupled with plasma-mass spectrometry, and laser ablation inductively coupled plasma-mass spectrometry used for ablation of polyacylamide gels were employed to assess the content of investigated elements in plants as well as to identify metal-binding proteins. We found that A. halleri is able to translocate cadmium to the aerial parts in high amounts (translocation index >1). We showed that Zn content in plants decreased significantly with the increase of cadmium content in the growth medium. Different positive and negative correlations between Cd content and mineral nutrients were evidenced by our study. We identified more than ten low-molecular-weight (<100 kDa) Cd-binding proteins in Cd-treated plants. These proteins are unlikely to be phytochelatins or metallothioneins. We hypothesize that low-molecular-weight Cd-binding proteins can be involved in cadmium resistance in A. halleri.

Conventional clay capping for post-closure management of landfill commonly cracks and deteriorates over time. As a consequence, water ingress into waste increases as a function of time, potentially causing a range of environmental issues. An alternative approach is known as phytocapping, which utilizes select plant species to control cap stability and moisture percolation. In this study, growth of Arundo donax L. (giant reed), Brassica juncea (L.) Czern. (Indian mustard), and Helianthus annuus L. (sunflower) on a landfill site was studied with different biosolid amendment rates (0, 25, and 50 Mg ha−1). Cultivation of the landfill cap and amendment with biosolids significantly improved the characteristics of the soil. Growth of each plant species increased due to biosolid addition. Giant reed produced the largest biomass in the 50 Mg ha−1 biosolid amendment rate (38 Mg ha−1 dry weight). The high pH and clay content of landfill cap soil, and the low metal concentrations of the biosolid resulted in low heavy metal (copper, zinc, cadmium, and lead) accumulation in leaves of most treatments. The improvement in growth and limited uptake of metal contaminants to plant shoots indicated that biosolid application to landfill clay caps improves the application of phytocapping of old landfill sites.

Nitrogen (N) deposition to the ocean is thought to be increasing worldwide, but the amount of coastal and open ocean measurements is very limited. In this paper, we assess N deposition in the coastal zone of Cayo Coco, in central Cuba, during a multi-annual period (2005–2007). Wet and dry N depositions were estimated based on the NH 4 + and NO x – concentrations in the rain. Cold fronts and troughs, coming from the west, contributed most to rain (41%) and to N deposition, followed by tropical waves and storms coming from the east, which caused 31% of the rain. Average concentrations of NH 4 + and NO x – in the rain were 8.8 and 8.3 μM. NO x – presented a clearly decreasing trend (0.26 μM per month), decreasing by half during 2005–2007. Total N deposition averaged 3.23 kg N ha−1 year−1, similar to that found in Virgin Islands and Puerto Rico, but lower than previously measured in Cuba and in nearby areas of the USA and than model predictions for the oceanic region around Cuba. These low values and the decreasing trend found are attributed to drastic reduction of fossil fuel and fertilizer use in Cuba since 1990. Because land input has decreased even more drastically, deposition seems to be nowadays the most important N source to the coastal zone of Cayo Coco. The δ15N range of seagrass (Thalassia testudinum) and macroalgae (Penicillus dumetosus) in the area (−1.83‰ to 3.02‰ and +1.02‰ to +4.17‰, respectively) sustain that atmospheric sources (deposition and N2 fixation) comprise 70–90% of the N budget.

The effect of activated sludge acclimation on the biodegradation of toluene and dimethyldisulphide (DMDS) in the presence of a non-aqueous phase liquid, polydimethylsiloxane (PDMS), in a two-phase partitioning bioreactor was characterized. The influence of the presence of PDMS, at a ratio of 25% (v/v), and acclimation of activated sludge on two hydrophobic VOC biodegradation was studied. Activated sludge were acclimated to each VOC and in the presence of the non-aqueous phase liquid, namely in the emulsion of PDMS in water. Using acclimated cells, 97.9% and 108.7% improvement of the mean biodegradation rates were recorded for toluene and DMDS, respectively, if compared to the values recorded in the absence of acclimation. While and in agreement with the lower solubility in water of DMDS if compared to toluene, a most significant effect of PDMS addition on the rate of DMDS removal was recorded, 87.0% and 153.6% for toluene and DMDS, respectively. In addition and if both biomass acclimation and PDMS addition were considered, overall improvements of the removal rates were 204% and 338% for toluene and DMDS.