Bismuth(III) Forms Exceptionally Strong Complexes with Natural Organic Matter.

The use of bismuth in the society has steadily increased during the last decades, both as a substitute for lead in hunting ammunition and various metallurgical applications, as well as in a range of consumer products. At the same time, the environmental behavior of bismuth is largely unknown. Here, the binding of bismuth(III) to organic soil material was investigated using extended X-ray absorption spectroscopy (EXAFS) and batch experiments. Moreover, the capacity of suwannee river fulvic acid (SRFA) to enhance the solubility of metallic bismuth was studied in a long-term (2 years) equilibration experiment. Bismuth(III) formed exceptionally strong complexes with the organic soil material, where >99% of the added bismuth(III) was bound by the solid phase, even at pH 1.2. EXAFS data suggest that bismuth(III) was bound to soil organic matter as a dimeric Bi3+ complex where one carboxylate bridges two Bi3+ ions, resulting in a unique structural stability. The strong binding to natural organic matter was verified for SRFA, dissolving 16.5 mmol Bi per gram carbon, which largely exceeds the carboxylic acid group density of this compound. Our study shows that bismuth(III) will most likely be associated with natural organic matter in soils, sediments, and waters.

The Adsorption of Per- and Polyfluoroalkyl Substances (PFASs) onto Ferrihydrite Is Governed by Surface Charge.

An improved quantitative and qualitative understanding of the interaction of per- and polyfluoroalkyl substances (PFASs) and short-range ordered Fe (hydr)oxides is crucial for environmental risk assessment in environments low in natural organic matter. Here, we present data on the pH-dependent sorption behavior of 12 PFASs onto ferrihydrite. The nature of the binding mechanisms was investigated by sulfur K-edge X-ray absorption near-edge structure (XANES) spectroscopy and by phosphate competition experiments. Sulfur K-edge XANES spectroscopy showed that the sulfur atom of the head group of the sulfonated PFASs retained an oxidation state of +V after adsorption. Furthermore, the XANES spectra did not indicate any involvement of inner-sphere surface complexes in the sorption process. Adsorption was inversely related to pH (p < 0.05) for all PFASs (i.e., C3-C5 and C7-C9 perfluorocarboxylates, C4, C6, and C8 perfluorosulfonates, perfluorooctane sulfonamide, and 6:2 and 8:2 fluorotelomer sulfonates). This was attributed to the pH-dependent charge of the ferrihydrite surface, as reflected in the decrease of surface ζ-potential with increasing pH. The importance of surface charge for PFAS adsorption was further corroborated by the observation that the adsorption of PFASs decreased upon phosphate adsorption in a way that was consistent with the decrease in ferrihydrite ζ-potential. The results show that ferrihydrite can be an important sorbent for PFASs with six or more perfluorinated carbons in acid environments (pH ≤ 5), particularly when phosphate and other competitors are present in relatively low concentrations.

Biochar and peat amendments affect nitrogen retention, microbial capacity and nitrogen cycling microbial communities in a metal and polycyclic aromatic hydrocarbon contaminated urban soil.

Soil contaminants may restrict soil functions. A promising soil remediation method is amendment with biochar, which has the potential to both adsorb contaminants and improve soil health. However, effects of biochar amendment on soil-plant nitrogen (N) dynamics and N cycling microbial guilds in contaminated soils are still poorly understood. Here, a metal- and polycyclic aromatic hydrocarbon (PAH) contaminated soil was amended with either biochar (0, 3, 6 % w/w) and/or peat (0, 1.5, 3 % w/w) in a full-factorial design and sown with perennial ryegrass in an outdoor field trial. After three months, N and the stable isotopic ratio δ15N was measured in soil, roots and leaves, along with microbial responses. Aboveground grass biomass decreased by 30 % and leaf N content by 20 % with biochar, while peat alone had no effect. Peat in particular, but also biochar, stimulated the abundance of microorganisms (measured as 16S rRNA gene copy number) and basal respiration. Microbial substrate utilization (MicroResp™) was altered differentially, as peat increased respiration of all carbon sources, while for biochar, respiration of carboxylic acids increased, sugars decreased, and was unaffected for amino acids. Biochar increased the abundance of ammonia oxidizing archaea, while peat stimulated ammonia oxidizing bacteria, Nitrobacter-type nitrite oxidizers and comB-type complete ammonia oxidizers. Biochar and peat also increased nitrous oxide reducing communities (nosZI and nosZII), while peat alone or combined with biochar also increased abundance of nirK-type denitrifiers. However, biochar and peat lowered leaf δ15N by 2-4 ‰, indicating that processes causing gaseous N losses, like denitrification and ammonia volatilization, were reduced compared to the untreated contaminated soil, probably an effect of biotic N immobilization. Overall, this study shows that in addition to contaminant stabilization, amendment with biochar and peat can increase N retention while improving microbial capacity to perform important soil functions.

Large-scale arsenic mobilization from legacy sources in anoxic aquifers: Multiple methods and multi-decadal perspectives.

While geogenic arsenic (As) contamination of aquifers have been intensively investigated across the world, the mobilization and transport of As from anthropogenic sources have received less scientific attention, despite emerging evidence of poor performance of widely used risk assessment models. In this study we hypothesize that such poor model performance is largely due to insufficient attention to heterogeneous subsurface properties, including the hydraulic conductivity K and the solid-liquid partition (Kd), as well as neglect of laboratory-to-field scaling effects. Our multi-method investigation includes i) inverse transport modelling, ii) in-situ measurements of As concentrations in paired samples of soil and groundwater, and iii) batch equilibrium experiments combined with (iv) geochemical modelling. As case study we use a unique 20-year series of spatially distributed monitoring data, capturing an expanding As plume in a Chromated Copper Arsenate (CCA)-contaminated anoxic aquifer in southern Sweden. The in-situ results showed a high variability in local Kd values of As (1 to 107 L kg-1), implying that over-reliance of data from only one or few locations can lead to interpretations that are inconsistent with field-scale As transport. However, the geometric mean of the local Kd values (14.4 L kg-1) showed high consistency with the independently estimated field-scale "effective Kd" derived from inverse transport modelling (13.6 L kg-1). This provides empirical evidence for the relevance of using geometric averaging when estimating large-scale "effective Kd" values from local measurements within highly heterogenous, isotropic aquifers. Overall, the considered As plume is prolonged by about 0.7 m year-1, now starting to extend beyond the borders of the industrial source area, a problem likely shared with many of the world's As-polluted sites. In this context, geochemical modelling assessments, as presented here, provided a unique understanding of the processes governing As retention, including local variability in, e.g., Fe/Al-(hydr)oxides contents, redox potential and pH.

Effect of pH, surface charge and soil properties on the solid-solution partitioning of perfluoroalkyl substances (PFASs) in a wide range of temperate soils.

The pH-dependent soil-water partitioning of six perfluoroalkyl substances (PFASs) of environmental concern (PFOA, PFDA, PFUnDA, PFHxS, PFOS and FOSA), was investigated for 11 temperate mineral soils and related to soil properties such as organic carbon content (0.2-3%), concentrations of Fe and Al (hydr)oxides, and texture. PFAS sorption was positively related to the perfluorocarbon chain length of the molecule, and inversely related to solution pH for all substances. The negative slope between log Kd and pH became steeper with increasing perfluorocarbon chain length of the PFAS (r2 = 0.75, p ≤ 0.05). Organic carbon (OC) alone was a poor predictor of the partitioning for all PFASs, except for FOSA (r2 = 0.71), and the OC-normalized PFAS partitioning, as derived from organic soil materials, underestimated PFAS sorption to the soils. Multiple linear regression suggested sorption contributions (p ≤ 0.05) from OC for perfluorooctane sulfonate (PFOS) and FOSA, and Fe/Al (hydr)oxides for PFOS, FOSA, and perfluorodecanoate (PFDA). FOSA was the only substance under study for which there was a statistically significant correlation between its binding and soil texture (silt + clay). To predict PFAS sorption, the surface net charge of the soil organic matter fraction of all soils was calculated using the Stockholm Humic Model. When calibrated against charge-dependent PFAS sorption to a peat (Oe) material, the derived model significantly underestimated the measured Kd values for 10 out of 11 soils. To conclude, additional sorbents, possibly including silicate minerals, contribute to the binding of PFASs in soil. More research is needed to develop geochemical models that can accurately predict PFAS sorption in soils.

Binding of per- and polyfluoroalkyl substances (PFASs) by organic soil materials with different structural composition - Charge- and concentration-dependent sorption behavior.

The charge- and concentration-dependent sorption behavior of a range of per- and polyfluoroalkyl substances (PFASs) was studied for three organic soil samples with different organic matter quality, one Spodosol Oe horizon (Mor Oe) and two Sphagnum peats with different degrees of decomposition (Peat Oi and Peat Oe). Sorption to the two peat materials was, on average, four times stronger compared to that onto the Mor Oe material. In particular, longer-chained PFASs were more strongly bound by the two peats as compared to the Mor Oe sample. The combined results of batch sorption experiments and 13C NMR spectroscopy suggested sorption to be positively related to the content of carbohydrates (i.e., O-alkyl carbon). Sorption of all PFAS subclasses was inversely related to the pH value in all soils, with the largest pH effects being observed for perfluoroalkyl carboxylates (PFCAs) with C10 and C11 perfluorocarbon chain lengths. Experimentally determined sorption isotherms onto the poorly humified Peat Oi did not deviate significantly from linearity for most substances, while for the Mor Oe horizon, sorption nonlinearity was generally more pronounced. This work should prove useful in assessing PFAS sorption and leaching in organic soil horizons within environmental risk assessment.

Effect of acid deposition on quantity and quality of dissolved organic matter in soil-water.

The aim of this study was to explore how acid deposition may affect the concentration and quality of dissolved organic matter (DOM) in soil-water. This was done by a small-scale acidification experiment during two years where 0.5 × 0.5 m(2) plots were artificially irrigated with water with different sulfuric acid content, and soil-water was sampled using zero-tension lysimeters under the O-horizon. The DOM was characterized using absorbance, fluorescence, and size exclusion chromatography analyses. Our results showed lower mobility of DOM in the high acid treatment. At the same time, there was a significant change in the DOM quality. Soil-water in the high acid treatment exhibited DOM that was less colored, less hydrophobic, less aromatic, and of lower molecular weight, compared to the low acid treatment. This supports the hypothesis that reduction in sulfur deposition is an important driver behind the ongoing brownification of surface waters in many regions.

Projecting impacts of climate change on metal mobilization at contaminated sites: Controls by the groundwater level.

Heavy metal and metalloid contamination of topsoils from atmospheric deposition and release from landfills, agriculture, and industries is a widespread problem that is estimated to affect >50% of the EU's land surface. Influx of contaminants from soil to groundwater and their further downstream spread and impact on drinking water quality constitute a main exposure risk to humans. There is increasing concern that the present contaminant loading of groundwater and surface water systems may be altered, and potentially aggravated, by ongoing climate change, through large-scale impacts on recharge and groundwater levels. We investigated this issue by performing hydrogeological-geochemical model projections of changes in metal(loid) (As and Pb) mobilization in response to possible (climate-driven) future shifts in groundwater level and fluctuation amplitudes. We used observed initial conditions and boundary conditions for contaminated soils in the temperate climate zone. The results showed that relatively modest increases (0.2 m) in average levels of shallow groundwater systems, which may occur in Northern Europe within the coming two decades, can increase mass flows of metals through groundwater by a factor of 2-10. There is a similar risk of increased metal mobilization in regions subject to increased (seasonal or event-scale) amplitude of groundwater levels fluctuations. Neglecting groundwater level dynamics in predictive models can thus lead to considerable and systematic underestimation of metal mobilization and future changes. More generally, our results suggest that the key to quantifying impacts of climate change on metal mobilization is to understand how the contact between groundwater and the highly water-conducting and geochemically heterogeneous topsoil layers will change in the future.

Stabilization and solidification remediation of soil contaminated with poly- and perfluoroalkyl substances (PFASs).

Remediation methods for soils contaminated with poly- and perfluoroalkyl substances (PFASs) are urgently needed to protect the surrounding environment and drinking water source areas from pollution. In this study, the stabilization and solidification (S/S) technique was tested on aged PFAS-contaminated soil that were artificially spiked with 14 PFAS. To further reduce leaching of PFASs in S/S-treated soil, seven different additives were tested at 2% concentration: powdered activated carbon (PAC), Rembind®, pulverized zeolite, chitosan, hydrotalcite, bentonite, and calcium chloride. Standardized leaching tests on S/S-treated soil revealed that leaching of 13 out of 14 target PFASs (excluding perfluorobutane sulfonate (PFBA)) was reduced by, on average, 70% and 94% by adding PAC and Rembind®. Longer-chained PFASs such as perfluorooctane sulfonate (PFOS), which is considered persistent, bioaccumulative and toxic, were stabilized by 99.9% in all S/S treatments when PAC or Rembind® was used as an additive. The S/S stabilization efficiency depended on PFAS perfluorocarbon chain length and functional group, e.g., it increased on average by 11-15 % per CF3-moeity and was on average 49% higher for the perfluorosulfonates (PFSAs) than the perfluorocarboxylates (PFCAs). Overall, the S/S treatment with active carbon-based additives showed excellent performance in reducing leaching of PFASs, without marked loss of physical matrix stability.

Evaluating the ability of standardised leaching tests to predict metal(loid) leaching from intact soil columns using size-based elemental fractionation.

Laboratory-based leaching tests are frequently used for in situ risk assessments of contaminant leaching to groundwater and surface waters. This study evaluated the ability of three standardised leaching tests to assess leaching of lead (Pb), zinc (Zn), arsenic (As) and antimony (Sb) from four intact soil profiles, by considering particulate (0.45-8 µm; percolation test), colloidal (10 kDa-0.45 µm) and truly dissolved (<10 kDa) fractions of these elements. Deionised water was used as the percolation test leachant, while either deionised water or 1 mM CaCl2 was used in batch tests. Data from an irrigation experiment were used as reference. The results indicated that in percolation tests, leachate should be collected at a liquid:solid ratio (L/S) range of 2-10, instead of 0-0.5 or 0.5-2. Even at L/S = 2-10, the percolation test overestimated total Pb concentration, mainly because of greater mobilisation of particle-bound Pb, but appeared suitable for categorising soils into high/low risk with respect to mobilisation of particulate and colloidal contaminants. The batch test performed better with CaCl2 than with deionised water when standard membrane filtration (0.45 µm) was used, as the high Ca2+ concentration reduced colloidal mobilisation, avoiding overestimation of concentrations of elements such as Pb. However, the higher Ca2+ concentration and lower pH could result in overestimated concentrations of weakly sorbed elements, e.g. Zn.

Solubility and transport of Cr(III) in a historically contaminated soil - Evidence of a rapidly reacting dimeric Cr(III) organic matter complex.

Chromium is a common soil contaminant and, although it has been studied widely, questions about its speciation and dissolutions kinetics remain unanswered. We combined information from an irrigation experiment performed with intact soil columns with data from batch experiments to evaluate solubility and mobilization mechanisms of Cr(III) in a historically contaminated soil (>65 years). Particulate and colloidal Cr(III) forms dominated transport in this soil, but their concentrations were independent of irrigation intensity (2-20 mm h-1). Extended X-ray absorption fine structure (EXAFS) measurements indicated that Cr(III) associated with colloids and particles, and with the solid phase, mainly existed as dimeric hydrolyzed Cr(III) bound to natural organic matter. Dissolution kinetics of this species were fast (≤1 day) at low pH (<3) and slightly slower (≤5 days) at neutral pH. Furthermore, it proved possible to describe the solubility of the dimeric Cr(III) organic matter complex with a geochemical equilibrium model using only generic binding parameters, opening the way for use of geochemical models in risk assessments of Cr(III)-contaminated sites.

Influence of particle size distribution, organic carbon, pH and chlorides on washing of mercury contaminated soil.

Feasibility of soil washing to remediate Hg contaminated soil was studied. Dry sieving was performed to evaluate Hg distribution in soil particle size fractions. The influence of dissolved organic matter and chlorides on Hg dissolution was assessed by batch leaching tests. Mercury mobilization in the pH range of 3-11 was studied by pH-static titration. Results showed infeasibility of physical separation via dry sieving, as the least contaminated fraction exceeded the Swedish generic guideline value for Hg in soils. Soluble Hg did not correlate with dissolved organic carbon in the water leachate. The highest Hg dissolution was achieved at pH 5 and 11, reaching up to 0.3% of the total Hg. The pH adjustment was therefore not sufficient for the Hg removal to acceptable levels. Chlorides did not facilitate Hg mobilization under acidic pH either. Mercury was firmly bound in the studied soil thus soil washing might be insufficient method to treat the studied soil.