Schwertmannite is a poorly-crystalline Fe(III) oxyhydroxysulfate mineral that may control Sb(V) mobility in acid sulfate environments, including acid mine drainage and acid sulfate soils. However, the mechanisms that govern uptake of aqueous Sb(V) by schwertmannite in such environments are poorly understood. To address this issue, we examined Sb(V) sorption to schwertmannite across a range of environmentally-relevant Sb(V) loadings at pH 3 in sulfate-rich solutions. Antimony K-edge extended X-ray absorption fine structure (EXAFS) spectroscopy revealed that Sb(V) sorption (at all loadings) involved edge and double-corner sharing linkages between SbVO6 and FeIIIO6 octahedra. The coordination numbers for these linkages indicate that sorption occurred by Sb(V) incorporation into the schwertmannite structure via heterovalent Sb(V)-for-Fe(III) substitution. As such, Sb(V) sorption to schwertmannite was not limited by the abundance of surface complexation sites and was strongly resistant to desorption when exposed to 0.1 M PO43-. Sorption of Sb(V) also conferred increased stability to schwertmannite, based on changes in the schwertmannite dissolution rate during extraction with an acidic ammonium oxalate solution. This study provides new insights into Sb(V) sorption to schwertmannite in acid sulfate environments, and highlights the role that schwertmannite can play in immobilizing Sb(V) within its crystal structure.

Alloy-type materials are attractive for anodes in sodium-ion batteries (SIBs) owing to their high theoretical capacities and overall performance. However, the accumulation of stress/strain during repeated cycling results in electrode pulverization, leading to rapid capacity decay and eventual disintegration, thus hindering their practical applications. Herein, we report a 3D coral-like Sb-Cu alloy nanoarray with gradient distribution of both elements. The array features a Sb-rich bottom and a Cu-rich top with increasing Sb and decreasing Cu concentrations from top to bottom. The former is the active component that provides the high capacity, whereas the latter serves as an inert additive that acts against volume variation. The gradual transition in composition within the electrode introduces a ladder-type volume expansion effect, facilitating a smooth distribution and effective release of stress, thereby ensuring the wanted mechanical stability and structural integrity. The as-developed nanoarray affords a high reversible capacity (460 mAh g-1 at 0.5 C), stable cycling (89% retention over 120 cycles at 1.0 C), and superior rate capability (354 mAh g-1 at 10 C). The concentration dual-gradient strategy paves a new pathway of designing alloy-type materials for SIBs.

Introduction: Comorbid insomnia and obstructive sleep apnea (COMISA) is not a well-identified sleep disorder, despite having a significant impact on health. This study investigates the relationship between sleep bruxism (SB) and sleep architecture in patients with COMISA, obstructive sleep apnea (OSA), and in those without any sleep disorders. Methods: 119 patients were included in the study and divided into three groups: OSA, COMISA, and a control group. Polysomnographic (PSG) examination provided parameters related to sleep architecture, OSA, and characteristics of SB. Results: The bruxism episode index (BEI) and other SB parameters were not found to be statistically different between the three groups (p > 0.05). There was no statistical difference in measured sleep architecture between the COMISA and OSA groups (p > 0.05). In comparison to the control group, participants in the COMISA group were found to have an increased apnea-hypopnea index (AHI), oxygen desaturation index (ODI), respiratory disturbance index (RDI), all arousals (AA), and respiratory arousals (RA) (p < 0.05). Among COMISA patients, AA and RA were shown to have a positive linear correlation with the number of bradycardia events per hour (r = 0.49, r = 0.48, p < 0.05). Conclusions: SB does not occur in patients with COMISA more frequently than in patients with OSA or those without any sleep disorders. PSG parameters are not specific for COMISA; therefore, in order to differentiate this disorder from OSA alone, a comprehensive patient assessment has to be performed.

The soil-plant transfer of trace elements is a complex system in which many factors are involved such as the availability and bioavailability of elements in the soil, climate, pedological parameters, and the essential or toxic character of the elements. The present study proposes the evaluation of the use of multielement contents in vascular plants for prospecting ore deposits of trace elements of strategic interest for Europe. To accomplish this general goal, a study of the soil-plant transfer of major and trace elements using Quercus ilex as a study plant has been developed in the context of two geological domains with very different characteristics in geological terms and in the presence of ore deposits: the Almadén syncline for Hg and the Guadalmez syncline for Sb. The results have made it possible to differentiate geological domains not only in terms of individual elements, but also as a combination of major and trace elements using Factor Analysis. The bioconcentration factors have demonstrated the uptake of macronutrients and micronutrients in very high concentrations but these were barely dependent, or even independent of the concentrations in the soil, in addition to high values of this factor for Sb. The Factor Analysis allowed for the differentiation of geogenic elements from other linked to stibnite ore deposits (Sb, S, and Cu). This element (Sb) can be uptake by Quercus ilex via the root and from there translocating it to the leaves, showing a direct relation between concentrations in soil and plants. This finding opens the possibility of using Quercus ilex leaves for biogeochemical prospecting of geological domains or lithological types of interest to prospect for Sb deposits.

While antimony (Sb) and arsenic (As) co-contamination in subsurface soil systems due to the legacy of Sb smelting wastes has been documented, the role of inherent heterogeneity on pollutant migration is largely overlooked. Herein this study investigated Sb and As migration in a slag impacted, vertically stratified subsurface at an abandoned Sb smelter. A 2-dimensional flume was assembled as a lab-scale analogue of the site and subject to rainfall and stop-rain events. Reactive transport modeling was then performed by matching the experimental observations to verify the key factors and processes controlling pollutant migration. Results showed that rainfall caused Sb and As release from the shallow slag layer and promoted their downward movement. Nevertheless, the less permeable deeper layers limited physical flow and transport, which led to Sb and As accumulation at the interface. The re-adsorption of Sb and As onto iron oxides in the deeper, more acidic layers further retarded their migration. Because of the large difference between Sb and As concentrations, Sb re-adsorption was much less effective, which led to higher mobility. Our findings overall highlight the necessity of understanding the degree and impacts of physicochemical heterogeneity for risk exposure assessment and remediation of abandoned Sb smelting sites.

Antimony (Sb) is a potential candidate anode for potassium-ion batteries (PIBs) owing to its high theoretical capacity. However; in the process of potassium alloying reaction; the huge volume expansion (about 407%) leads to pulverization of active substance as well as loss of electrical contact resulting in rapidly declining capacity. Herein; uniformly dispersed Sb-Nanodot in carbon frameworks (Sb-ND@C) were constructed by in situ confined polymerization of ionic liquids. Attributed to the uniformly dispersed Sb-ND and confinement effect of carbon frameworks; as anode for PIBs; Sb-ND@C delivered a superior rate capability (320.1 mA h g-1 at 5 A g-1) and an outstanding cycling stability (486 mA h g-1 after 1000 cycles; achieving 89.8% capacity retention). This work offers a facile route to prepare highly dispersed metal-Nanodot via the in situ polymerization of ionic liquid for high-performance metal-ion batteries.

Incorporation of oxophilic metals into Pd-based nanostructures has shown great potential in small molecule electrooxidation owing to their superior anti-poisoning capability. However, engineering the electronic structure of oxophilic dopants in Pd-based catalysts remains challenging and their impact on electrooxidation reactions is rarely demonstrated. Herein, we have developed a method for synthesizing PdSb-based nanosheets, enabling the incorporation of the Sb element in a predominantly metallic state despite its high oxophilic nature. Moreover, the Pd90Sb7W3 nanosheet serves as an efficient electrocatalyst for the formic acid oxidation reaction (FAOR), and the underlying promotion mechanism is investigated. Among the as-prepared PdSb-based nanosheets, the Pd90Sb7W3 nanosheet exhibits a remarkable 69.03% metallic state of Sb, surpassing the values observed for the Pd86Sb12W2 (33.01%) and Pd83Sb14W3 (25.41%) nanosheets. X-ray photoelectron spectroscopy (XPS) and CO stripping experiments confirm that the Sb metallic state contributes the synergistic effect of their electronic and oxophilic effect, thus leading to an effective electrooxidation removal of CO and significantly enhanced FAOR electrocatalytic activity (1.47 A mg-1; 2.32 mA cm-1) compared with the oxidated state of Sb. This work highlights the importance of modulating the chemical valence state of oxophilic metals to enhance electrocatalytic performance, offering valuable insights for the design of high-performance electrocatalysts for electrooxidation of small molecules.

Antimony (Sb) has been considered a promising anode for sodium-ion batteries (SIBs) owing to its high theoretical capacity (660 mA h g-1) and low redox voltage (0.2-0.9 V vs Na+/Na). However, the capacity degradation caused by the volumetric variation during battery discharge/charge hinders the practical application. Herein, guided by the DFT calculation, Sb/Fe2S3 was fabricated by annealing Fe and Sb2S3 mixed powder. Next, Sb/Fe2S3 was blended with 15 wt % graphite by ball milling, yielding nano-Sb/Fe2S3 anchored on an exfoliated graphite composite (denoted as Sb/Fe2S3-15%). When applied as an anode of SIBs, Sb/Fe2S3-15% delivered reversible capacities of 565, 542, 467, 366, 285, and 236 mA h g-1 at current rates of 1, 2, 4, 6, 8, and 10 A g-1, respectively, surpassing most of the Sb-based anodes. The co-existence of highly conductive Fe2S3 and Sb minimizes the polarization of the anode. Our experiments proved that the Sb and Fe2S3 phases were reversible during discharge/charge cycling, and the exfoliated graphite can accelerate the Na+ diffusion and e- conduction. The proposed synthesis method of this work can also be applicable to synthesize various antimony/transition metal sulfide heterostructures (Sb/M1-xS), which may be applied in a series of fields.

Jarosite, a common mineral in acidic sulfur-rich environments, can strongly sorb both As(V) and Sb(V). However, little is known regarding the mechanisms that control simultaneous co-sorption of As(V) and Sb(V) to jarosite. We investigated the mechanisms controlling As(V) and Sb(V) sorption to jarosite at pH 3 (in dual and single metalloid treatments). Jarosite was found to sorb Sb(V) to a greater extent than As(V) in both single and dual metalloid treatments. Relative to single metalloid treatments, the dual presence of both As(V) and Sb(V) decreased the sorption of both metalloids by almost 50%. Antimony K-edge EXAFS spectroscopy revealed that surface precipitation of an Sb(V) oxide species was the predominant sorption mechanism for Sb(V). In contrast, As K-edge EXAFS spectroscopy showed that As(V) sorption occurred via bidentate corner-sharing complexes on the jarosite surface when Sb(V) was absent or present at low loadings or by formation of similar complexes on the Sb(V) oxide surface precipitate when Sb(V) was present at high loadings. These results point to a novel mechanism by which Sb(V) impacts the co-sorption of As(V). Overall, these findings highlight a strong contrast in the sorption mechanisms of Sb(V) versus As(V) to jarosite under acidic environmental conditions.

Antimony (Sb) is a toxic metalloid, which has been increasingly used in the brake lining of vehicles, and increased concentrations have been found in soils near abundant traffic. However, since very few investigations of Sb accumulation in urban vegetation have been undertaken there exists a knowledge gap. We studied the concentrations of Sb in leaves and needles of trees in the Gothenburg City area, Sweden. In addition, lead (Pb), also associated with traffic, was investigated. Sb and Pb concentrations of Quercus palustris leaves at seven sites with contrasting traffic intensity varied substantially, correlated with the traffic-related PAH (polycyclic aromatic hydrocarbon) air pollution at the sites and increased during the growing season. Sb but not Pb concentrations were significantly higher in needles of Picea abies and Pinus sylvestris near major roads compared to sites at larger distances. In Pinus nigra needles at two urban streets both Sb and Pb were higher compared to an urban nature park environment, emphasising the role of traffic emissions for these elements. A continued accumulation of Sb and Pb in three years old needles of Pinus nigra, two years old needles of Pinus sylvestris and eleven years old needles of Picea abies was observed. Our data suggest a pronounced link between traffic pollution and Sb accumulation in leaves and needles, where the particles carrying Sb seem not to be transported very far from the source. We also conclude that there exists a strong potential for Sb and Pb bioaccumulation over time in leaves and needles. Implications of these findings are that increased concentrations of toxic Sb and Pb are likely to prevail in environments with high traffic intensity and that Sb can enter the ecological food chain by accumulation in leaves and needles, which is important for the biogeochemical cycling.