Sequestration of heavy metals from soil with Fe–Mn concretions and nodules

In recent years, heavy metal contamination has become a major environmental issue in many parts of the world. Fe and Mn oxides, oxyhydroxides and hydroxides have long been recognized as scavengers playing an important role in controlling the location, mobility and bioavailability of metal contaminants in soils. Fe–Mn concretions and nodules are discrete bodies made of soil or sediment materials cemented together under the influence of Fe and Mn oxides. Here metals sorption by Fe–Mn concretions and nodules are surveyed and critical reviewed. Valuable available literature data demonstrate that the formation of Fe–Mn concretions and nodules is the most efficient and durable process for metal contaminants sequestration in the soils. The papers discussed in this review show that the application of Fe–Mn concretions and nodules, as geochemical scavengers for remediating metal contaminated soils, is strongly recommended.     

Arsenic and chromate removal from water by iron chips—Effects of anions

The purpose of this study is to estimate the removal efficiency of As and Cr (VI) by one kind of industrial waste — iron chips, as well as to estimate the effects of typical inorganic anions (sulfate, phosphate, and nitrate), and typical organic anions (citrate, oxalate, and humate) on As or Cr (VI) removal. The results showed that 98% of As (V) and 92% of As (III) could be removed from aqueous phase by the iron chips within 60 min. Compared with As species, Cr (VI) was removed much more rapidly and efficiently with 97% of Cr (VI) being removed within 25 min. The removal efficiency for arsenic was in the order: As (III) (sulfate), As (III) (nitrate) or As (III), As (III) (humate), As (III) (oxalate), As (III) (citrate), As (III) (phosphate), and for chromate was in the order: Cr (VI) (sulfate), Cr (VI) (phosphate) or Cr (VI) (nitrate) or Cr (VI) (oxalate), Cr (VI), Cr (VI) (citrate), Cr (VI) (humate). In all the treatments, pH level increased with time except for As (III), the removal of which was either without anions or in the presence of humate or nitrate.     

Recent developments on gas–solid heterogeneous oxidation removal of elemental mercury from flue gas

Environmental Chemistry Letters - Mercury is a toxic and persistent environmental pollutant which has been recognized as a global threat to human health and our ecosystem because mercury...     

Simultaneous removal of arsenate and fluoride from water by AI-Fe （hydr）oxides

A1-Fe （hydr）oxides with different A1/Fe molar ratios （4：1, 1：1, 1：4, 0：1） were prepared using a co- precipitation method and were then employed for simultaneous removal of arsenate and fluoride. The 4A1 ： Fe was superior to other adsorbents for removal of arsenate and fluoride in the pH range of 5.0-9.0. The adsorption capacity of the A1-Fe （hydr）oxides for arsenate and fluoride at pH 6.50.3 increased with increasing A1 content in the adsorbents. The linear relationship between the amount of OH released from the adsorbent and the amount of arsenate or fluoride adsorbent by 4A1 ： Fe indicated that the adsorption of arsenate and fluoride by A1- Fe （hydr）oxides was realized primarily through quantita- tive ligand exchange. Moreover, there was a very good correlation between the surface hydroxyl group densities of A1-Fe （hydr）oxides and their adsorption capacities for arsenate or fluoride. The highest adsorption capacity for arsenate and fluoride by 4A1 ： Fe is mainly ascribed to its highest surface hydroxyl group density besides its largest pHpzc. The dosage of adsorbent necessary to remove arsenate and fluoride to meet the drinking water standard was mainly determined by the presence of fluoride since fluoride was generally present in groundwater at much higher concentration than arsenate.     

Application of magnesite–bentonite clay composite as an alternative technology for removal of arsenic from industrial effluents

This study evaluated the feasibility of integrating amorphous magnesite and bentonite clay (composite) as an alternative technology for removing arsenic from industrial effluents. The removal of arsenic from industrial effluents by using magnesite–bentonite clay composite was carried out in batch mode. The effects of equilibration time, adsorbent dosage, adsorbate concentration, and pH on removal of arsenic were investigated. The experiments demonstrated that ≈100% arsenic removal is optimum at 30 minutes of agitation, 2 g of adsorbent dosage (2 g: 100 mL, S/L ratio), and 20 mg L^?1 of arsenic concentration. The adsorption data fitted well to both Langmuir and Freundlich adsorption models, hence proving monolayer and multilayer adsorption. The kinetic studies revealed that the data fitted better to a pseudo-second-order reaction than to a pseudo-first-order reaction, hence proving chemisorption. At optimized conditions, the composite was able to remove arsenic to below World Health Organization water quality guidelines, hence depicting that the composite is effective and efficient in removing arsenic from contaminated water. Based on that, this comparative study proves that the composite is a promising adsorbent with high adsorption capacity for arsenic and can be a suitable substitute for the conventional treatment methods.     

High performance of multi-layered alternating Ni–Fe–P and Co–P films for hydrogen evolution

Judiciously engineering the electrocatalysts is attractive and challenging to exploit materials with high electrocatalytic performance for hydrogen evolution reaction. Herein, we successfully perform the interface engineering by alternately depositing Co–P and Ni–Fe–P films on nickel foam, via facile electroless plating and de-alloying process. This work shows that there is a significant effect of de-alloying process on alloy growth. The electronic structure of layered alloys is improved by interface engineering. The multilayer strategy significantly promotes the charge transfer. Importantly, the Co–P/Ni–Fe–P/NF electrode fabricated by interface engineering exhibits excellent electrocatalytic hydrogen evolution activity with an overpotential of 43.4 mV at 10 mA cm-2 and long-term durability for 72 h in alkaline medium (1 mol L-1 KOH). The innovative strategy of this work may aid further development of commercial electrocatalysts.     

Effect of Ca(II), Fe(II), and Fe(III) on Cu(II) adsorption by a polyvinylidene fluoride-based chelating membrane from Cu(II)–EDTA complex solution

A polyvinylidene fluoride-based membrane bearing the diethylenetriaminepentaacetic acid chelating group was employed to recover Cu(II) from the Cu(II)-ethylenediaminetetraacetic acid complex aqueous solution. Effects of Ca(II), Fe(II), and Fe(III) on Cu(II) uptake were investigated by static batch adsorption tests and dynamic adsorption filtration. Isotherms, kinetics, and breakthrough curves of Cu(II) uptakes in the presence of the three cations at concentrations of 1 mmol L^?1 were elucidated. The three cations showed a positive effect on the Cu(II) uptake; the stimulative roles were in the order of Fe(III) > Fe(II) > Ca(II). They did not alter the adsorption behavior of the membrane; adsorption isotherms and kinetics could be described by Langmuir and Lagergren second-order models, and Cu(II) adsorption was a spontaneous and exothermic process. The presence of Ca(II), Fe(II), and Fe(III) increased the sorption capacity of the membrane stack by 1.3, 1.9, and 3 times. Breakthrough time and the exhaustion time of membrane stacks were also extended.     

Using adsorption and sulphide precipitation as the principal removal mechanisms of arsenic from a constructed wetland – a critical review

This review has been undertaken to understand the role of various parameters such as redox potential, microbes, and organic matters on the fate and transport of arsenic in the constructed wetland. A conceptual diagram of arsenic fate and transport in the constructed wetland was developed. Role of various minerals which are produced due to microbial activities are described. The role of these minerals on arsenic adsorption is discussed. It was envisaged that iron sulphide would be the main adsorbent for arsenic in microbe-mediated adsorption process. Beside microbe-mediated arsenic adsorption, roles of various microbes, such as sulphate reducers and methane producers, on arsenic transformation are discussed. Role of various organic carbon sources and electron acceptors on the proliferation of the above mentioned microbes with respect to arsenic transformation was envisaged. Role of dissolved organic matters on arsenic transformation and transport was also discussed in details. To strengthen the review, laboratory studies and modelling of arsenic adsorption and transformation using the Visual Minteq were appended.     

Characteristics of soil micro-and macro-arthropods and soil properties in Songnen Grassland of China during different periods of freeze–thaw season

ABSTRACT

Soil properties have an important influence on soil fauna in the grassland ecosystem. However, the relationship between the structural characteristics of soil fauna and properties in the grassland ecosystem in freeze–thaw season remains unclear. Hence, the feature of soil arthropods and properties in Songnen Grassland of China were investigated in fall–winter alternating (T1), completely frozen (T2) and winter–spring alternating periods (T3) during freeze–thaw season in three years. Results showed slight differences in the community composition of soil animals with Oribatida, Prostigmata and Mesostigmata as co-dominant groups in all sampling periods. The total number of individuals of soil arthropod at low temperature was low. The pH value, electrical conductivity (EC), and moisture content had the same order of T3?>?T2?>?T1. The activities of invertase and urease increased with increasing soil temperature, whereas protease activity had no relationship with soil temperature, soil moisture, EC and soil organic matter (SOM), activities of protease and urease were principal factors affecting individual abundance of soil animals. The sequence of their effect degrees was moisture content > EC > SOM > protease activity > urease activity. The changes in the quantitative characteristics of soil animals were related to soil properties. Therefore, soil properties can affect the structural characteristics of soil arthropod in the Songnen Grassland of China in the freeze–thaw season.     

Synthesis and antibacterial activity of a Fe3O4–AgCl nanocomposite against Escherichia coli

In this investigation, Fe₃O₄ magnetic nanoparticles (MNPs) were prepared by the alkalinization of an aqueous medium containing ferrous sulfate and ferric chloride. In the next step, a Fe₃O₄–AgCl magnetic nanocomposite was fabricated by the drop-by-drop addition of silver nitrate solution into a NaCl solution containing Fe₃O₄ MNPs. All prepared nanoparticles were characterized by transition electron microscopy (TEM), X-ray diffraction (XRD), and energy-dispersive X-ray spectroscopy (EDS). Both particle types varied in size from 2.5 to 20?nm, with an average size of 7.5?nm for Fe₃O₄ MNPs and 12.5?nm for Fe₃O₄–AgCl nanocomposites. The antibacterial effect of the Fe₃O₄ MNPs and fabricated Fe₃O₄–AgCl nanocomposites against Escherichia coli (ATCC 35218) were investigated by conventional serial agar dilution method using the Müller–Hinton Agar medium. The minimum inhibitory concentration was 4?mg?mL^?1 for Fe₃O₄ MNPs and 2?mg?mL^?1 for the Fe₃O₄–AgCl magnetic nanocomposites. Time-kill course assays showed that the Fe₃O₄–AgCl magnetic nanocomposites successfully killed all inoculated bacterial cells during an exposure time of 60?min. The antibacterial activity of recycled Fe₃O₄–AgCl magnetic nanocomposites over four 60?min cycles of antibacterial treatment was further tested against E. coli by the colony-forming unit (CFU) method. The antibacterial efficiency of the nanocomposites was constant over two cycles of antibacterial testing.     

An assessment of coastal land-use and land-cover change from 1974–2008 in the vicinity of Mobile Bay,Alabama

The purpose of this research is to quantify and assess geospatial land-use and land-cover (LULC) changes in the coastal counties of Mobile and Baldwin, Alabama using nine Landsat images from 1974–2008. A study-specific classification scheme was devised comprising upland herbaceous, upland forest, non-woody and woody wetlands, open water, and urban categories. Upland forest was the most dominant terrestrial cover type. Wetlands averaged 17% and urban averaged 7%. A majority of the urban expansion occurred between 1974 and 1979 (26%). Thirty-four percent of the 2008 urban areas were upland forest in 1974. Watershed-scale analysis of Three Mile Creek and D’Olive Bay highlights the temporal and spatial differences of urbanization for watersheds found within the same region. This study is a Gulf of Mexico Alliance (GOMA) Application Pilot project that uses NASA data products to benefit coastal environmental managers and community members. Results have led to increased effectiveness of coastal conservation decision-making, increased understanding of post-hurricane LULC change, continued research on habitat change impacts, and contributed to timely conservation planning efforts. This study has benefited the development of watershed management plans by the Mobile Bay National Estuary Program, which is especially important given projected climate change.     

Correction to: Facile synthesis of the magnetic metal–organic framework Fe3O4/Cu3(BTC)2 for efficient dye removal

Environmental Chemistry Letters - Dyeing wastewaters present high hazards for the environment and human health. Advanced dye removal may be achieved by magnetic metal–organic frameworks...     

Degradation of Ni–EDTA complex by Fenton reaction and ultrasonic treatment for the removal of Ni<Superscript>2+</Superscript> ions

It is difficult to meet the increasingly stringent environmental regulations by the application of conventional precipitation processes treating complex heavy metal wastewaters. We studied the potential of a new method for removing heavy metals from metal–EDTA wastewater by Fenton reaction followed by hydroxide precipitation. This process is referred to as Fenton reaction-hydroxide precipitation (FR-HP) process. This study investigated the use of FR-HP and ultrasonic/FR-HP processes for the removal of Ni(II) from Ni–EDTA wastewater. The results indicate that ultrasonic/FR-HP process is more effective for the removal of nickel ions than FR-HP process.     

Performance and mechanism of carbamazepine removal by FeS-S2O82– process: experimental investigation and DFT calculations

● Synergistic removal of carbamazepine (CBZ) was obtained in the FeS-S₂O₈^2– process. ● SO₄^•− and •OH were identified as the main radicals in the FeS-S₂O₈^2– process. ● Heterogeneous oxidation would be dominant first, followed by homogeneous reaction. ● Degradation pathway of CBZ was well elucidated by experiments and DFT calculations. As persulfate (S₂O₈^2–) is being increasingly used as an alternative oxidizing agent, developing low-cost and eco-friendly catalysts for efficient S₂O₈^2– activation is potentially useful for the treatment of wastewater containing refractory organic pollutant. In this study, the degradative features and mechanisms of carbamazepine (CBZ) were systematically investigated in a novel FeS- S₂O₈^2– process under near-neutral conditions. The results exhibited that CBZ can be effectively eliminated by the FeS-S₂O₈^2– process and the optimal conditions were: 250 mg/L FeS, 0.5 mmol/L S₂O₈^2–, and pH = 6.0. The existence of Cl⁻ (1 and 50 mmol/L) has little influence on the CBZ elimination, while both HCO₃⁻ and HPO₄²⁻ (1 and 50 mmol/L) significantly suppressed the CBZ removal in the FeS-S₂O₈^2– process. CBZ could be degraded via a radical mechanism in the FeS-S₂O₈^2– process, the working radical species (i.e., SO₄^•− and •OH) were efficiently formed via the promoted decomposition of S₂O₈^2– by the surface Fe²⁺ on the FeS and the dissolved ferrous ions in solution. Based on the identified oxidized products and Fukui index calculations, a possible degradation pathway of CBZ was speculated. More importantly, a two-stage oxidation mechanism of CBZ elimination was speculated in the FeS-S₂O₈^2– process, the activation of S₂O₈^2– by the surface-active Fe^(II) of FeS dominated in the initial 5 min, while homogeneous oxidation reactions played more essential parts than others in the following reaction stage (5–60 min). Overall, this study demonstrated that the FeS-S₂O₈^2– process is capable of removing CBZ from water efficiently.     

Role of the natural and anthropogenic radiative forcings on global warming: evidence from cointegration–VECM analysis

Over the last few years there has been much debate about the hypothesis that anthropogenic emissions of CO₂ and other greenhouse gases increase global temperature permanently. By using recent advances in time series econometrics, this paper tries to answer the question on how human activity affects Earth’s surface temperatures. Bearing in mind this goal, we estimated the long-run cointegration relations between global temperatures and changes in radiative forcings by a set of perturbing factors. We found that the temperature response to a doubling in radiative forcing of anthropogenic greenhouse gases is + 2.94 °C [95 % CI: + 1.91, + 3.97], in perfect accordance with prior research, and that the orthogonalized cumulated effect over a 100 year time period, in response to a unit increase of size of one standard deviation in greenhouse gas radiative forcing, is + 3.86 °C [95 % CI: + 0.03, + 6.54]. Conversely, the amplitude of solar irradiance variability is hardly sufficient to explain observed variations in the Earth’s climate. Our results show that the combined effect of stochastic trends attributable to anthropogenic radiative forcing variations are driving the Earth’s climate system toward an ongoing phase of global warming, and that such long-run movement is unlikely to be transient.     

Chemical and isotopic composition of CO2-rich magnesium–sodium–bicarbonate–sulphate-type mineral waters from volcanoclastic aquifer in Rogaška Slatina,Slovenia

Environmental Geochemistry and Health - Bottled natural mineral waters from an andesitic aquifer in Slovenia are enriched in magnesium (1.1&nbsp;g/l), sulphate (2.2&nbsp;g/l) and dissolved...