The reaction of Hg²⁺with sulfite is a major identified reduction pathway in the atmosphere. UV absorption spectroscopy was used to study the kinetics of Hg²⁺reduction by sulfite (Na₂SO₃) in the presence of fly ash. Upon the addition of Cumberland and Shawnee fly ash samples, the reduction rates were 0.0071 ± 0.0008 and 0.0009 ± 0.0006 s⁻¹, respectively. This represents c.a. 40 and 90 % decreases in the homogeneous rate, 0.013 ± 0.007 s⁻¹. The reduction reaction was also observed when Cumberland was added without Na₂SO₃. Sulfur elemental analyzer and high-resolution field emission scanning microscopy with energy dispersive X-ray spectroscopy (HR-FE-SEM-EDS) characterization confirmed that Cumberland fly ash particles were rich in sulfur. Nanoparticle Tracking Analysis (NTA) determined the mean particle size in solution to be 246 ± 25 nm for Cumberland fly ash and 198 ± 14 nm for Shawnee. To obtain further insight on observed Hg²⁺homogeneous reduction rates by sulfite, the effects of several environmental variables were investigated. Hg(NO₃)₂and HgO were used as the sources of Hg²⁺. Extended pH (1–7) and temperature (1.0–45.0 °C) ranges were studied for the first time. The enthalpies of activation for the HgO reduction were 94 ± 3 kJ mol⁻¹at pH 1 and 92 ± 4 kJ mol⁻¹at pH 3, while the entropies were 33 ± 9 J mol⁻¹ K⁻¹at pH 1 and 30 ± 10 J mol⁻¹ K⁻¹at pH 3. It was determined that increasing ionic strength, especially with nitrate species, slows down the reaction at pH = 7. Significance of the results on the variability of mercury reduction by sulfite at various environmental conditions, and its implication in modelling are discussed.

Surfactant can reduce the interfacial tension in liquid–gas system and may probably improve the rate and/or extent of dissolution. This study was conducted to evaluate the effect of three different surfactants (viz., sodium dodecyl sulfate (SDS), Triton X-100, and cetyltrimethylammonium chloride (CTAC)) on CO₂biomineralization by two ureolytic microorganism—Sporosarcina pasteurii and Bacillus megaterium. In S. pasteurii-mediated biomineralization, headspace CO₂content (2.5 mM) was decreased by 40, 52, and 68 % in the presence of SDS, Triton X-100 or CTAC, respectively within the first 8 h of incubation. CO₂removal with B. megaterium in the presence of Triton X-100 (64 %) and CTAC (56 %) was better in comparison to control without surfactant (48 %). However, appreciable CO₂depletion was not observed with SDS, which was just 4 %. On other hand, headspace CO₂loss in the presence of CTAC with B. megaterium did not get biomineralized, as no calcium carbonate was detected. Crystalline phase and morphology of CaCO₃precipitate also varied between ionic and nonionic surfactants. The result suggests that the effect of surfactant on CO₂capture and biomineralization can be largely different, depending on the surfactant and concerned microbial species involved.

The disposal of potentially toxic element (PTE)-loaded sludge that is produced during industrial or commercial wastewater treatments evoke concerns because of the probability of hazardous environmental consequences. In the current work, we proposed a chelant-assisted decontamination technique of the laboratory-produced PTE-loaded (As, Cd, Pb) polymeric-Fe-coated sludge and subsequent recovery of the chelants and PTEs. The chelant options include both biodegradable (EDDS, GLDA, and HIDS) and non-biodegradable (EDTA) alternatives. The washing performance was compared and discussed in terms of the solution pH and relative stabilities of the complexes of PTEs and chelants in solution. The changes in solution pH or chelants have no significant effect on the chelant-induced removal efficiency of Cd, and the same result was observed for Pb at extreme and moderate acidic pH. The As-extraction rate is also improved with chelant in the solution despite a limited interaction between the chelant and the arsenic species in the solution. The column-packed solid-phase extraction (SPE) system, which was equipped with macrocycle, chelating resin, or ion-exchange resin, was used to explore the corresponding separation performance of the PTEs and chelant. The macrocycle-equipped SPE system shows better selectivity than other SPEs in terms of extraction and recovery performance of the PTEs regardless of the chelants. Some unique points of the proposed process are minimum environmental burden due to the use of biodegradable materials in the washing solution and cost minimization by recycling the ingredients.

Here, we report on the ability of two different water treatment residues, a Fe-based (Fe-WTR) and an Al-based (Al-WTR) ones, to accumulate Cd(II) and Zn(II) from aqueous solutions at different pH values (pH 4.5, 5.5, and 7.0). Fe-WTR showed a greater Zn(II) and Cd(II) sorption capacity than Al-WTR at all the pH values investigated, in particular at pH 7.0 (e.g., ∼0.200 and ∼0.100 mmol g⁻¹ of Me(II) sorbed by Fe- and Al-WTR at pH 7.0, respectively). The greater capacity of the Fe-WTR to accumulate Me(II) seems to be linked to its higher content of iron and manganese ions and to its higher CEC value compared to Al-WTR. The role of the inorganic and organic fractions of WTRs in metal sorption was also assessed. A higher affinity of Cd(II) with respect to Zn(II) toward functional groups of the organic matter of both WTRs was observed, while Zn(II) showed a stronger association with the inorganic phases. The sorption of both metal ions appeared mainly governed by the formation of inner-sphere surface complexes with the inorganic and organic phases of WTRs, as suggested by the sequential extraction data.

In situ burning is a method by which oil is burned at a spill site under controlled conditions, and this method is subject to increased interest due to its applicability in the Arctic. This paper reviews the literature regarding the characterization and environmental effects of burn residues in Arctic waters. The results of a systematic literature search indicate that only a very limited number of studies have arctic pertinence. From the review, it is also indicated that the properties and composition of the residues depend on the efficiency of the burning and the oil type. Furthermore, the studies within the frame of the literature search reach consensus that in situ burning may increase the concentrations of large poly-aromatic hydrocarbons (PAHs; high ring number) while reducing small PAHs (low ring number). There are very few toxicity studies of burn residues on aquatic and arctic organisms, and to enhance the knowledge base, more organisms as well as oil types must be studied. Furthermore, there is a lack of studies investigating the potential effect of sinking burn residues on benthic organism and the smothering effects of the more viscous burn residues on birds and other organisms related to the sea surface. More knowledge regarding environmental fate and effect of residues is crucial to complete a robust net environmental benefit analysis prior to an oil spill response operation in arctic waters.

The electrokinetic transport of sulfate was investigated as a means of treating and restoring a sulfate-accumulating saline soil. The electrokinetic treatment decreased the electrical conductivity of the soil, an indicator of soil salinity, to 58.6, 73.1, and 83.5 % for 7, 14, and 21 days, respectively. More than 96 % of the chloride and nitrate were removed within 7 days. However, the removal of sulfate was highly influenced by the anode material. An iron anode removed sulfate effectively, whereas sulfate was hyper-accumulated in the anodic region when an inert anode was used. The iron anode was oxidized in a sacrificial anodic reaction, which competed with the electrolysis reaction of water at the anode, and finally, the reaction prevented the severe acidification of the soil in the anodic region. However, the competing reactions produced hydrogen ions at the anode and the ions were transported toward the cathode, which, in turn, acidified the soil, especially in the anodic region. The acidification switched the surface charge of the soil from negative to positive, increasing the interaction between the soil surface and sulfate and thus inhibiting the transport of sulfate under the electric field. The zeta potential analysis of the soil provided an explanation. The results indicate that preventing severe acidification is an important factor which influences the transport of anions and iron anode for the enhanced removal of anionic pollutants by electrokinetic remediation.

The processing, storage, and flux of inorganic carbon in rivers and streams play an influential role in the lateral transfer of atmospheric and terrestrial carbon to the marine environment. Quantifying and understanding this transfer requires a rapid and accurate means of measuring representative concentrations of dissolved inorganic carbon (DIC) and CO₂in field settings. This paper describes a field method for the determination of DIC based on the direct measurement of dissolved CO₂using a commercial carbonation meter. A 100-mL water sample is combined with 10 mL of a high ionic strength, low-pH, citrate buffer, mixed well, and the dissolved CO₂concentration is measured directly. The DIC is then calculated based on the dissolved CO₂concentration, buffer-controlled ionic strength, pH, and temperature of the mixture. The method was accurate, precise, and comparable to standard laboratory analytical methods when tested using prepared sodium bicarbonate solutions up to 40 mM DIC, North Atlantic seawater, commercial bottled waters, and carbonate spring waters. Coal mine drainage waters were also tested and often contained higher DIC concentrations in the field than in subsequent laboratory measurements; the greatest discrepancy was for the high-CO₂samples, suggesting that degassing occurred after sample collection. For chemically unstable waters and low-pH waters, such as those from high-CO₂mine waters, the proposed field DIC method may enable the collection of DIC data that are more representative of natural settings.

The influence of long-term exposure to background pollution on the response and recovery of the invasive species Corbicula fluminea to ammonia stress was investigated using a multi-marker approach. Wild clams of the tidal freshwater areas of two estuaries of the NW Iberian coast with different levels of pollution, the estuaries of Minho river (reference) and of Lima river (contaminated), were collected and exposed individually to different treatments: 8 and 14 days in dechlorinated tap water (DTW), 8 and 14 days in 1 mg L⁻¹of ammonia (AM), and 8 days in AM followed by 6 days in DTW. After each defined time (0, 8, and 14 days), the clams were sacrificed and the activity of the enzymes glutathione S-transferase (GST), catalase (CAT), glutathione reductase (GR), glutathione peroxidase (GPx), cholinesterase (ChE), octopine dehydrogenase (ODH), and the lipid peroxidation (LPO) levels were used as effect criteria. At the beginning of the bioassay, the clams from the polluted estuary presented significantly higher background levels of GST, CAT, GR, GPx, and LPO than those from the reference one indicating long-term exposure to oxidative stressors. In general, C. fluminea from both estuaries presented little sensibility to ammonia with no significant differences found between exposed and control clams for most of the biomarkers. That low sensibility of C. fluminea could be seen as advantageous for its invasion ability.

This paper presents the efficacy of zero-valent iron nanoparticles (ZVINs), magnetic iron oxide nanoparticles (MINs), zero-valent iron nanoparticles/sugarcane bagasse (ZVIN-SB) composite and magnetic iron oxide nanoparticles/sugarcane bagasse (MIN-SB) composite in immobilizing chromium present in tannery sludge. The optimized values for the immobilization of chromium by the adsorbents were found to be 48 h, 100 g/kg and 7, respectively, for time, adsorbent dosage and pH. The maximum uptake capacity was found to be 429.75, 539.25, 587.25 and 625.8 mg/kg, respectively, for ZVIN, MIN, ZVIN-SB and MIN-SB. The desorption study of the unamended sludge and sludge amended by ZVIN, MIN, ZVIN-SB and MIN-SB was carried out with three different desorbing media (0.1 N HCL, DIW and 0.1 N NaOH). It was found that the cumulative concentration of leachate chromium was more in basic condition than in neutral and acidic conditions. In column studies, the concentration of leachate chromium attained 0 mg/L at 24, 15, 18 and 14 pore volumes, respectively, for the sludge amended by ZVIN, MIN, ZVIN-SB and MIN-SB. The experimental adsorption data fitted well with pseudo-first-order kinetics. The zero-order kinetics accurately predicted the experimental desorption capacity (q ₑ) of the sludge amended by ZVIN, MIN, ZVIN-SB and MIN-SB. The Fourier transform infrared spectroscopy (FTIR) analysis showed that the amine, carboxyl, iron compounds, etc. present in the adsorbents were the chief causes for the immobilization of chromium. The X-ray diffraction (XRD) analysis of the sludge showed the presence of trivalent chromium compounds at a higher concentration.

In this study, stable carbon and nitrogen isotope ratios in the samples of pine needles collected in 2013 and 2014 from heavily urbanized area in close proximity to point-source pollution emitters, such as a heat and power plant, nitrogen plant, and steelworks in Silesia (Poland), were analyzed as bio-indicators of contemporary environmental changes. The carbon isotope discrimination has been proposed as a method for evaluating water-use efficiency. The measurement of carbon and nitrogen isotopes was carried out using the continuous flow isotope ratio mass spectrometer. The isotope ratio mass spectrometer allows the precise measurement of mixtures of naturally occurring isotopes. The δ¹⁵N values were calibrated relative to the NO-3 and USGS34 international standards, whereas the δ¹³C values were calibrated relative to the C-3 and C-5 international standards. The strong year-to-year correlations between the δ¹³C in different sampling sites, and also the inter-annual correlation of δ¹⁵N values in the pine needles at each of the investigated sampling sites confirm that the measured δ¹³C and δ¹⁵N and also intrinsic water-use efficiency (iWUE) trends are representative of the sampling site. Diffuse air pollution caused the variation in δ ¹³C, δ¹⁵N, and iWUE dependent on type of emitter, the localization in the space (distance and direction) from factories and some local effect of other human activities. The complex short-term variation analysis can be helpful to distinguish isotopic fractionation, which is not an effect explainable by climatic conditions but by the anthropogenic effect. Between 2012 and 2014, an increase in iWUE is observed at leaf level.