Ca-Al layered double hydroxides (LDHs) with different Ca/Al molar ratios were composited at pH ranges, using a co-precipitation method, and were experimented to remove fluoride from wastewater and studied in terms of isotherm models such as Langmuir and Freundlich reactions. The composite LDHs were characterized with X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and Thermogravimetric analysis (TGA). The results showed that different synthesis conditions of Ca-Al LDHs had an influence on their morphology, layered structure, and particle size distribution, which substantially affected the uptake capacity for aqueous fluoride. LDHs with the Ca/Al molar ratio of 2 and synthesized at the pH of 12 had the highest capacity for the fluoride removal (e.g., 146.6 mg/g) and such reaction reached an equilibrium within 1 h. The Freundlich model was a better fit for this study. The high adsorption method of Ca-Al LDHs can be favorable to removing fluoride from wastewater streams.

Because of their adverse effects, such as their toxicity and carcinogenicity, volatile organic compounds (VOCs) are the most important and common pollutants produced by urbanization and industrial processes that contaminate air and water streams. VOCs, commonly originating from many industrial syntheses, and their derivatives, especially halogen, produce an unpleasant odor in the air when present in excess. All the issues related to VOCs make them a severe threat to whole ecosystems and environments as well as humans. Globally growing environmental awareness and knowledge have resulted in strict regulations to control VOC emissions into the air. It is necessary for each component of emitted VOCs to be controlled or removed from the air. NaZSM-5 and HZSM-5, having high ratios of SiO₂/Al₂O₃ (50), which are necessary for good adsorbents of organics, were prepared. Characterization of the prepared materials was done by XRD, SEM, FTIR, N₂ adsorption, NH₃-TPD, ²⁷Al-NMR, and TGA analysis. The adsorptive removal of VOCs from the air by Na-ZSM-5 and H-ZSM-5 was explored. These adsorption materials were tested with respect to the adsorption capacity, renewability, and selectivity for benzene, toluene, ethylbenzene, and xylene. The effects of the contact time, adsorbent dose, and initial concentration of pollutant on the adsorption process were also studied. Finally, the adsorption data were applied to Langmuir, Freundlich, and Temkin isotherms and two different kinetic models.

Despite its isolation and scarce occupation, Antarctica is not exempt from the input of contaminants related to present and past human activities. Several deleterious compounds, such as the persistent organic pollutants (POPs) may reach Antarctic ecosystems, mostly via atmospheric long-range transport and further deposition. In this context, snow and its seasonal melting water represent a sink to these pollutants and also the last compartment before they reach marine primary producers. In order to assess the concentration of a selection of organic contaminants, a PDMS headspace extraction method was chosen due to its improvement in fieldwork sampling. Samples were collected in King George Island, during the austral summers from 2007 to 2010. PBDEs and PAHs remained under the method detection limits in all of the cases, restricting data interpretation to organochlorine compounds: average Σ HCHₛ ranged from 1.46 to 4.17, HCBs from 1.36 to 3.77, Σ Dᵣᵢₙₛ from <0.35 to 4.29, Σ Cₕₗₒᵣdₐₙₑₛ from 5.72 to 13.3, Σ DDTₛ from 4.32 to 24.4, and PCBs from 132 to 156 (always in pg kg⁻¹). Results were, in general, in agreement with previous literature. Nevertheless, due to the fact that samples were collected progressively later into the austral summer, one trend can be noticed: the sum of the concentrations in both matrixes seems to decrease, with a proportional increase in snow. Some exceptions can be remarked, hypothetically linked to the passage of South American frontal systems. Finally, results for these two compartments are compatible with the exposure expected for lower trophic-level organisms from such ecosystem.

In two soils from Central Greece, a pot experiment was conducted with the addition of mixture at various ratios of zeolite and compost (based on Posidonia oceanica (L.) leaves) applied at a rate of 5% w/w (calculated on a soil dry weight basis). Three varieties of tobacco (Burley, Virginia, and Oriental) were cultivated, and Cu, Zn, and Cd concentrations in tobacco leaves were measured at first, second, and third primings. We found that the addition of zeolite in the soil1 led to a significant reduction of metal concentration in all three tobacco varieties compared to the control. Also, zeolite addition reduced significantly the water-soluble, as well as, DTPA-extractable metal concentrations, compared to the other treatments. Our results suggest that the most effective amendment in soil 1 was the mixture consisting of 20% compost and 80% zeolite; this mixture led to higher reduction of metal concentration in all tobacco varieties. As for soil 2, which had almost twice as high Cd concentrations as than in soil 1, Posidonia compost was more effective in reducing Cd concentrations from all three tobacco varieties. In all cases studied, both in soils 1 and 2, Cd concentration was higher in Burley tobacco leaves. The results indicate that a mixture of zeolite and compost consisting of Posidonia oceanica (L.) is a low-cost soil conditioner that is effective in reducing tobacco Cu, Zn, and Cd uptake.

A set of chitosan-g-poly(acrylic acid)/rice husk ash hydrogel composites was successfully employed as methylene blue (MB) adsorbent. Maximum MB adsorption capacity of 1952 mg/g of dried hydrogel was obtained with the composite at 5 wt% of rice husk ash (RHA) at pH ≥ 5. The adsorption capacity varied from 1450 to 1950 mg/g with increasing the initial MB concentration from 1500 to 2500 mg/L. The MB removal efficiency was higher than 90% for all samples. At pH ≥ 5, negatively charged groups (–COO⁻) in the adsorbent were generated, which could strongly interact with the positive charges from MB, favoring adsorption. Adsorption kinetics followed the pseudo-second-order model, which is based on the chemisorption phenomenon, reaching saturation as fast as 1 h of experiments due to the formation of an adsorbed MB monolayer, as suggested by the Langmuir isotherm model (type I). Desorption experiments showed that 75% of loaded MB can be removed from the adsorbent by immersing it in a pH 1 solution. CHT-g-PAAc/RHA5% composite was submitted to five cycles of adsorption/desorption, maintaining its MB removal efficiency at 91%. Therefore, chitosan-g-poly(acrylic acid)/RHA hydrogel composites present outstanding capacity to be employed in the remediation of MB-contaminated wastewaters.

Energy development in the Bakken and Three Forks formations of the USA has led to an increase in fugitive dust from unpaved roads. A dust abatement alternative that has been considered in this region is oil-well produced waters. The objectives of this study were to compare dust loading at sites abated with produced water to non-abated control sites and to determine if the elemental constituents in released dust are different compared to control roads. Three previously untreated unpaved roads were selected, and passive dust collectors were placed at 10, 20, 40, and 60 m from the road on the downwind side of the dominant prevailing wind in each mile section. Eighty-four days post-application, two sections treated with produced waters failed to reduce dust when compared to the controls. Dust elemental changes were found on two of the three roads. Elements that were found to have differences included Mo, Mn, Fe, As, Au, and Hg. Overall results indicated that oil-well produced water is not effective at controlling road dust. Results of this study are important to road managers who are contemplating the usage of produced waters to reduce dusts from unpaved roads.

Genetically modified agricultural products have been introduced to increase food supply by enhancing their resistance to pests and diseases, along with easily adapting to environmental conditions. Due to the modification of DNA, public objections are prevalent, including concerns on the impact on the ecosystem. In this research, adsorption and transport of Cry1Ab, a toxin exuded by the transgenic Bt maize in alumino-silica clays, were evaluated in laboratory columns under steady-state flow conditions. Since Cry1Ab fate and transport were very responsive to animal waste field applications, during which humic acids were released, Cry1Ab adsorption and transport in humic acid-coated alumino-silica clays were also investigated. Cry1Ab breakthrough curves were simulated using the convection-dispersion transport models. It was discovered that the humic acid coating increased Cry1Ab deposition during the transport. Based on analysis of the breakthrough curves, adsorption isotherms of Cry1Ab in alumino-silica clays were obtained and compared with those of batch experiments. The humic acid coating changed the bonding energy between Cry1Ab and the adsorption receptor sites on alumino-silica clay surfaces, thereby changing Cry1Ab partition between the aqueous phase and the solid phase.

Alpine lakes of the Tatra Mountains were severely affected by acidification, with minimum recorded values of pH ∼4.5 in the mid-1980s. Since the 1990s, a dramatic decrease in the deposition of acidifying compounds has led to a considerable reversal in lake water chemistry (to pH∼5 in the most severely affected lakes). We studied changes of planktonic crustaceans and chironomid occurrence during the acidification period and the following period of recovery from acidification in three categories of 50 Tatra Mountain lakes (non-acidified, acidified and strongly acidified, according to their status at the beginning of the 1980s). In acidified and strongly acidified lakes, the planktonic crustaceans completely disappeared already by about 1976 except for a few individuals of ubiquitous species in littoral zone due to acidification-induced oligotrophication. In strongly acidified lakes, the original planktonic crustaceans disappeared and littoral species became more abundant already before 1976 due to acidification-induced eutrophication and aluminium toxicity. These processes were quickly reversed following the increase in lake water pH. Extinct species started to return to several acidified and strongly acidified lakes already in the beginning of 1990s. The process of recovery was delayed in many other lakes of the same categories, however, or it did not even start before 2008 despite the improved water chemistry and feeding resources (concentration of chlorophyll-a). Compared to planktonic crustaceans, the reaction of chironomids to acidification and recent recovery has been less pronounced. An analysis of sediment records showed that fluctuations in relative abundance of the dominant chironomid taxa and a decrease of their density occurred. In spite of the fact that chironomid fauna exhibited clear signs of recovery in the last two decades, the recovered assemblage does not exactly reflect the pre-acidification status in the lake. The occurrence and higher proportion of more thermophilous chironomid species in some alpine lakes of all categories could be correlated with increasing air temperature. The considerable effect of climatic factors may thus prevent the full re-establishment of the original status even when the acidification stress completely ceases. The delayed return of planktonic crustaceans to some recovered lakes could be a consequence of the short water residence time of these lakes. In addition, a shortening of the water residence time in recent decades, probably related to recent climate change, in interaction with the ecology of planktonic crustaceans, may possibly be causing further delays in their return.

The contamination of drinking water with arsenic has been a problem in a lot of countries around the world because of its toxicological and carcinogenic effects on human health. Porous materials modified with Fe₃O₄ nanoparticles (Fe₃O₄ NPs) represent convenient removers for that contaminant. A co-precipitation method of Fe(III) and Fe(II) in alkaline media was applied to obtain Fe₃O₄ NPs. In a first stage, single nanoparticles were synthesized and stabilized with carboxylic acids. A characterization with attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR), Raman spectroscopy, and X-ray diffraction (XRD) confirms a magnetite-type structure. Moreover, transmission electron microscopy (TEM) and calculations from XRD data using Scherrer’s equation indicate an average particle size of 13 nm and an average crystallite size of 10 nm, both independent of the stabilizer used. Then, the co-precipitation method studied was applied to modify kaolin, bentonite, diatomite, and silica and thus prepare magnetic composites having support-magnetite weight ratios of 2:1. Among them, silica-modified material presented the best hydraulic characteristics, an important aspect for large-scale applications such as removal under gravity. This composite has the capacity to remove up to 80 and 70% for initial concentrations of 25 and 50 μg/L, respectively, representing a convenient remover for processes developed in subsequent stages or in continuous flow.

In Portugal, the industrial production of phosphate fertilizers, has been dealing with a specific raw material—north African phosphate rock—with a high content of trace metals and natural radioactive elements mainly from the ²³⁸U decay series. A disabled phosphate plant located in the vicinity of the river Tejo estuary has produced phosphoric acid for several decades (1950–1989) and dumped tons of phosphogypsum (PG) on retention lagoons, formerly decanted and deposited into a stockpile. This paper deals with the assessment of radionuclides, rare earth elements (REEs) and heavy metals transfer to plants (fam. Plantaginaceae, Plantago sp.) and mosses (fam. Bryaceae, Bryum sp.) growing naturally on the PG pile. In Plantago sp., the concentration ratio (CR, plant tissue/PG) was 0.187 for ²²⁶Ra and 0.293 for ²¹⁰Pb. The translocation factor (TF, aerial parts/roots) was 0.781 for ²²⁶Ra and 0.361 for ²¹⁰Pb. In contradiction to the high CR, the leachability of ²²⁶Ra from PG was low, lower than 2%. The results confirmed the role of mosses as biomonitors. A high quantity of contaminants collected in its biomass confirmed the hypothesis of their significant transport by air and rain water. High concentrations of heavy metals (As, Cd, Zn, W) in samples collected on the stockpile are an evidence of their transport from former industrial zones in the surroundings and present even more important risk for public health and environment than natural radionuclides and REEs from the PG stockpile.