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Major sources of pollution during the antimony (Sb) mining and processing are mining waste rock, smelting waste, tailings dam, and underground tunnel wastewater. The aim of the present study was to assess magnitude of pollution from Sb mine by taking four types of samples: soil in the mining waste rock zone, soil in the smelting zone, soil in tailings zone, and soil in underground tunnel wastewater zone. Sixty soil samples from the four zones were taken for experimental work, and the contents and morphological characteristics of the six potentially toxic elements (PTEs) such as Sb, As, Hg, Pb, Cd, and Zn in the soil samples were measured by using a hydride generation atomic fluorescence spectrometer (AFS-9700). The results show that the soil of the mine area is seriously polluted. The average contents of Sb, As, Hg, Pb, Cd, and Zn in the soil reach 1267.20 mg·kg−1, 94.44 mg·kg−1, 1.46 mg·kg−1, 184.19 mg·kg−1, 8.54 mg·kg−1, and 1054.11 mg·kg−1, respectively. There exists good correlation between the PTEs in the soil, with Sb strongly positively correlated with As, Hg, Pb, and Zn. The intensity of pollution is highest in the antimony-smelting zone, where the potential ecological risk index is over 15,000, followed by the tailings zone and mining waste rock zone, with the underground tunnel wastewater zone being the lowest. Using sequential chemical extraction, the elements are associated with the residual fraction, followed by organic-sulfide fraction, and smaller portions in the Fe-Mn oxide, carbonate, and exchangeable fractions. There are great differences in the speciation content of different elements in different sampling zones. The study implicates that Sb-smelting zone is the potential source of PTEs and maximum metals are associated with residual phase, out of which significant portion is associated with mobile fraction or phase. [ABSTRACT FROM AUTHOR]

Abstract: Most research on direct solvolytic liquefaction (DSL) focuses on hydrothermal liquefaction or organic model solvents and is dominated by catalytic processes. This review highlights the much less understood aspects of non‐catalytic DSL including the solvent recycling required for continuous processing. Results from earlier studies indicate both the feasibility of recycling and the non‐catalytic suppression of char formation. However, a proof of continuous operation under steady state with a stationary solvent composition and an extensive investigation of process parameters are missing to date. [ABSTRACT FROM AUTHOR]

High quality and accurate environmental investigations and analysis are essential to any assessment of contamination and to the decision-making process thereafter. Remediation decisions may be focused by health outcomes, whether already present or a predicted risk. The variability inherent in environmental media and analysis can be quantified statistically; uncertainty in models can be reduced by additional research; deep uncertainty exists when environmental or biomedical processes are not understood, or agreed upon, or remain uncharacterized. Deep uncertainty is common where health and environment interact. Determinants of health operate from the individual's genes to the international level; often several levels act synergistically. We show this in detail for lead (Pb). Pathways, exposure, dose and response also vary, modifying certainty. Multi-disciplinary approaches, built on high-quality environmental investigations, enable the management of complex and uncertain situations. High quality, accurate environmental investigations into pollution issues remain the cornerstone of understanding attributable health outcomes and developing appropriate responses and remediation. However, they are not sufficient on their own, needing careful integration with the wider contexts and stakeholder agendas, without which any response to the environmental assessment may very well founder. Such approaches may benefit more people than any other strategy. [ABSTRACT FROM AUTHOR]

Detecting sources of insects attacking grain stores can help to develop more effective pest management tools. This study considers combinations of chemical elements as intrinsic markers for tracing resource use by Prostephanus truncatus ( Horn) ( Coleoptera: Bostrichidae), a pest of stored maize ( Zea mays L., Poaceae) which occurs in natural environments where alternative hosts may support reservoirs of infestation. Prostephanus truncatus were laboratory-reared on maize or field-caught in pheromone-baited flight-traps. Beetles and hosts were screened for multiple elements using inductively coupled plasma atomic emission spectrometry (ICP-AES). For elements above detection limits, we tested relationships between determinations for various host plants, and for beetles according to environment where captured. An alternative host, Spondias purpurea L. ( Anacardiaceae), contained more Al, B, Ca, Cu, Fe, Mg, Si, and Sr than maize, and less P and Zn. Elemental profiles of beetles were associated with environment, with significantly lower Al, Ca, Cu, Cr, Fe, P, S, Si, Sr, Ti, and Zn determinations in maize-reared beetles than in beetles captured in agricultural or natural environments. Additionally, Al, Ba, K, P, Sr, and Ti determinations of field beetles captured in agricultural vs. natural environments were significantly different. This suggests Al, Sr, and Ti as candidate markers for environment, and possibly others as elemental concentrations (except B, Ba, Ni, and P) were significantly different in comparisons of all field-collected vs. maize-reared beetles. We present a robust practical solution which successfully identified combinations of elemental markers for remotely tracing resource use and dispersal by P. truncatus. We discuss the application of chemical characterisation for identifying intrinsic markers of pests, particularly species with alternative hosts. We discuss how to manage the low replication and unbalanced sample sizes inherent in insect elemental screening, particularly when rarer elements are potential markers. [ABSTRACT FROM AUTHOR]

Abstract: Cork oak forests in the MED region are of critical social and ecological value and under stress from both environmental change and variation in management practice. This study, as part of a NATO Science for Peace project (SfP 981674), evaluated geochemical methods to assess potentially toxic element (PTE) input to field sites from Quercus suber forests in Tabarka (Tunisia) and an experimental control forest managed by ARGIS-Sardega (Italy). Surface and subsurface soil samples were collected from environmentally comparable sites in the two regions. Sites were identified with varied stand and shrub density and characterised for basic soil properties and multi element content. The data were evaluated using principle component analysis (PCA) and soil enrichment factors (SEF). Soils showed chemical variability associated with differences in parent material and the effects of biomass density. Contributions from events such as fire damage, as well as biomass, sea salt and geogenic sources can be identified, and evaluation is enhanced using a combination of assessment methods. Ultimately despite concerns for the regulation of forest activities in the study area, little direct anthropogenic impact was on soil quality. [Copyright &y& Elsevier]

Abstract: Cobalt is a naturally occurring element found in rocks, soil, water, plants, and animals and has diverse industrial importance. It is cycled in surface environments through many natural processes (e.g. volcanic eruptions, weathering) and can be introduced through numerous anthropogenic activities (e.g. burning of coal or oil, or the production of cobalt alloys). The environmental behaviour of cobalt in terrestrial environment is relatively poorly studied and in particular where Co is used in industrial processes, the baseline information to support wider and long-term environmental impacts is widely dispersed. To support the adoption of new EU regulations on the risk assessment of chemicals, we review here the various aspects of the environmental chemistry, fate and transport of Co across environmental interfaces and discuss the toxicology and potential for bio magnification and food chain accumulation. The soil-to-plant transfer of Co appears to be viable route to expose lower trophic levels to biologically significant concentrations and Co is potentially accumulated in biomass and top soil. Evidence for further accumulation through soil-invertebrate transfer and to higher trophic levels is suggested by some studies but this is obscured by the relatively high variability of published transfer data. This variation is not due to one particular aspect of the transfer of Co in terrestrial environments. Influences are from the variability of geological sources within soil systems; the sensitivity of Co mobility to environmental factors (e.g. pH) and the variety of life strategies for metal elimination/use within biological species. Toxic effects of Co have been suggested for some soil–plant animal studies however, uncertainty in the extrapolation from laboratory to field is a major limitation. [Copyright &y& Elsevier]

The mobility and bioavailability of As and Sb in relation to soil-biota transfer were evaluated at a former Sb mining and smelting site (Glendinning, SW Scotland, UK). The study specifically assessed the accumulation of As and Sb in different environmental components (soil, plants and earthworms) across mining area to estimate risk factors for the biota. Total concentrations and fractions of As and Sb in soils were determined. The latter using both a single solute and a non-specific stepwise sequential extraction (CISED) method. Mineralogical information was gathered from XRD and SEM analysis used to identify element distribution patterns. Pseudo-total (aqua-regia) levels of As and Sb in the soils varied between 50-17,400 mg kg- 1 and 10-1,200 mg kg- 1, respectively. Both elements are predominantly associated with Fe (or Al) oxides/hydroxides, by adsorption around silicate grains, representing a potentially bioavailable fraction. Antimony was also associated with sulphide phases. The highest values of As and Sb in biota were recorded in the earthworms (960 mg kg-1 and 27 mg kg- 1, respectively). Bioconcentration factors for both elements were below 1 and the highest for earthworms. Total and leached As levels in soils and biota were positively and significantly correlated, but only for Sb in earthworms and grass. Bioavailability of As in the biota, was shown to be limited by pH. In spite of the considerably high As and Sb contents of the soil the plant contamination remained comparably low, but still exceeded background values. [ABSTRACT FROM AUTHOR]

Total concentrations and extractable fractionations of As and Sb were determined in soil samples from former mining sites in Scotland and Italy. Pseudo-total levels of As and Sb in the sample were between 50–17,428 mg/kg and 10–1,187 mg/kg (Scotland), and 16–691 mg/kg and 1.63–11.44 mg/kg (Italy). Between 0.001–0.63% and <0.001−8.82% of the total soil As and Sb, were extractable using, a single extraction bioavailability estimate. Data from an As-specific extraction procedure revealed that up to 60% of As was associated to amorphous Fe-Al oxyhydroxide phase in all soils. A non-specific-sequential extraction test also showed As to be strongly associated with Fe (and Al) oxyhydroxides at both locations. In the case of Sb, in addition to the crystalline Fe-oxide bound Sb the Al-silicate phase also appeared to be significant. At both sites Sb appears to be chemically more accessible than As with consistent availability despite the varied origin and host soil properties. [ABSTRACT FROM AUTHOR]

Abstract: This study investigated the sorption characteristics and release of selected heavy metals (Cd, Cu, Cr, Pb and Zn) from a typical urban soil material from a derelict brownfield site in Western Scotland, UK. The study aimed to evaluate contaminant interactions with an urban substrate, comprising a mix of mineral soil and residue materials (e.g. brick, concrete, wood). This type of material has received little consideration in the literature to date. Soil samples were subject to a sequence of test involving batch equilibration and dynamic leaching, in single (non-competitive) and multi-element (competitive) solutions. The batch experiments were carried out in unadjusted and close to soil field pH conditions (pH 2 and 7, respectively). The equilibrium adsorption capacity for heavy metals was measured and extrapolated using the Langmuir isotherm. The parameters of the isotherms x m (the maximum amount adsorbed per unit mass of adsorbent (mg/g)) and b (adsorption constant (m3/g)) were calculated for Cd, Cu, Cr, Pb as single-element and multi-element solutions. The adsorption from the single-element solution was more effective than adsorption under multi-element conditions, due to competitive effects. For example, the adsorption of copper from a single-element solution was over four times greater than for a multi-element solution. In the case of Cr and Zn, migration of metal from soil to solution was observed. Adsorption capacity at pH 2 followed the order Cr>Cu>Pb>Cd and at pH 7 Cd>Zn, with precipitation affecting Cu and Pb behaviour. During the column leaching experiment, most of the heavy metals were irreversibly bound to the soil, but in the case of Cr some movement from soil into solution was observed. The results also showed that Cd, Cu, Pb and Zn were removed from the solution and adsorbed on the soil. No significant difference in the metal removal from single- and multi-element solutions was observed. Overall, the urban residue behaved in a similar manner to mineral soils despite a significant component of anthropogenic solid materials. [Copyright &y& Elsevier]

A pilot study of production of respirable and inhalable dusts from sawing and sanding medium density fibreboard (MDF) and softwood in a typical cabinet-making workshop produced high but variable exposure levels at the bench and operator position. Exposure levels for the total inhalable fraction (∼ < 100 μm) were 6.9 - 91 mg m  - 3 for MDF and 2.5 - 45 mg m  - 3 for softwood. For the respirable fraction ( < 10 μm) levels were 0.4 - 13 mg m  - 3 for MDF and 0.4 - 2.9 mg m  - 3 for softwood. These results show significant dust loading is produced in the coarser fraction and that the material used has a significant impact on levels produced. It suggests that fuller evaluation of operator influence of fine dust production is needed and may question the common application of a single inhalable exposure standard for wood dust to all wood working scenarios. [ABSTRACT FROM AUTHOR]

The revised, four-step BCR sequential extraction for soil or sediment has been compared with an alternative procedure in which 0.2 mol l−1 ammonium oxalate (pH 3) replaced 0.5 mol l−1 hydroxylammonium chloride (pH 1.5) in step 2, the reducible step. A variety of substrates were studied: BCR CRM601, a sewage sludge amended soil, two industrial soils, and a steel manufacturing by-product (basic oxygen furnace filter cake). Greater amounts of iron were recovered in step 2 when acid ammonium oxalate was used, for all substrates. Similar trends were observed for copper. Manganese and zinc were not strongly affected by the procedural modification, except for zinc in the two industrial soils, where oxalate extraction proved more efficient than use of hydroxylammonium chloride. A large proportion of the calcium and lead isolated in step 2 of the BCR procedure was not released until step 3 when the alternative procedure with oxalate in step 2 was used. This is probably due to rapid precipitation of analyte oxalates from solution. Thus, whilst oxalate offers superior dissolution of iron-containing matrix components, it should not be used if calcium or lead concentrations are to be measured. Selection of the most appropriated sequential extraction protocol for use in a particular study must always be carried out on the basis of “fitness for purpose” criteria. However, the revised BCR protocol, involving use of 0.5 mol l−1 NH2OH·HCl in the reducible step, appears to be more generally applicable than procedures involving acid ammonium oxalate. [Copyright &y& Elsevier]

The concept that total organic C (TOC) is the main factor dominating the sorption of PCBs to sediment is over simplified. Numerous discrepancies are found when trying to compare concentrations predicted from laboratory observations to field concentrations. Some studies show a lack of correlation between PCB and TOC or particle size, but state that it is the origin of the organic matter or the clay swelling that is most important in determining the partitioning to sediment. It may also be argued that the discrepancies are merely a reflection of localised inputs of PCBs. An evaluation of the influence of these factors was undertaken at an intertidal site in the Clyde Estuary, previously highlighted as being highly contaminated by PCBs. Analysis of a series of sediment samples failed to show a strong correlation of PCB content with TOC or particle size. Separation into grain-size fractions and subsequent analysis suggested that both variation in organic matter source and mineralogical composition exerts an influence on congener distribution with implications for the mobility of PCBs within intertidal sediments. [Copyright &y& Elsevier]

A black colouration and strong odours of highly polluted water are often associated with high levels of ammonical nitrogen (NH 4 +-N), which is a priority for pollution control. Treatment technology needs to be cost-effective and the natural mineral, bentonite (Be) is widely used in water treatment, but without activation performs poorly in NH 4 +-N removal. We report on a new adsorbent (denoted as Be-TA-Fe) prepared by the coupling of bentonite and a metallic phenolic network, ferric tannate (Fe-TA). Advanced characterisation techniques and batch adsorption tests were used to determine its structural features and adsorption behavior for NH 4 +-N. After modification by Fe-TA, the bentonite showed a larger BET surface area up to 75.842 m2/g. The optimal conditions for the preparation of Be-Fe-TA which resulted in the highest removal of NH 4 +-N were a mass ratio of bentonite to Fe-TA (m Be/ m Fe-TA) of 8:1, with 8% w/w starch and 8% w/w polyvinyl alcohol (PVA). As expected, lower adsorbent doses produced higher adsorption capacity. The main mechanisms for the removal of NH 4 +-N by Be-Fe-TA were through electrostatic adsorption, ion exchange and ionic bonding. The novel sorbent performed well in a weak acid and neutral environment, and some parameters, such as dissolved oxygen and microorganisms, did not affect the removal significantly. For example, the removal efficiency could reach 92.85% removal of NH 4 +-N at 13.5 mg/L and pH 6.8 with 25 g/L of Be-TA-Fe. Overall, Be-TA-Fe shows significant promise as a method of treatment for contaminated by ammonical nitrogen. [ABSTRACT FROM AUTHOR]

The use of the term "heavy metal" is regularly questioned by the scientific community. Here, we followed the evolution (1970–2020) in the number of published papers including this term in their title. Thus, we can evidence a continuous, albeit sometimes stabilizing, increase especially in environmental journals. After several other warning opinions, we propose that it should be replaced in the scientific literature by terms like "metal", "metalloid", "trace metal elements" or "potentially toxic element". [ABSTRACT FROM AUTHOR]

The Community Bureau of Reference (BCR) four-step sequential extraction has been adapted for fractionation of potentially toxic elements (PTE) in simulant airborne particulate matter (APM) samples presented on 47 mm filter dynamics measurement system (FDMS) filters as used in routine air quality monitoring. Simulants were prepared from an urban soil reference material and from BCR CRM 701, which is certified for analytes extractable by the BCR procedure. Analysis was performed by inductively coupled plasma mass spectrometry using an Agilent 7700x instrument. Fractionation patterns similar to the full-scale protocol were obtained when test portions as small as 0.0625 g were extracted in 2–3 mL of reagents. However, changing the extraction vessel used was found to affect the outcome. This highlights the operational nature of sequential extraction procedures and the need carefully to evaluate the effects of procedural modifications. When the method developed was applied to blank FDMS filters, large amounts of Zn were detected, especially in step 3, the oxidisable fraction, and step 4, the residual fraction. Despite this, following blank-correction, fractionation patterns similar to certified values were obtained for BCR CRM 701, with overall recoveries (∑(steps 1–4)) of 84.2-113%. Given the increased awareness of public health risks associated with poor air quality, a sequential extraction procedure specifically designed for use with APM samples collected during routine air quality represents a valuable tool for use in source apportionment and to improve understanding of human exposure to PTE through inhalation. [ABSTRACT FROM AUTHOR]

The release of metals from a mine tailings pond to groundwater is an important pathway to assess the environmental impact of mining residues and implications for wider environmental risk. We research the impact of manganese ore area in Heling Town, Xiangtan City, Hunan Province, central China. The focus is to assess the migration of manganese (Mn) using the Visual MODFLOW model of groundwater flow and the MT3DMS software platform to model solute transport. The modelling objective focuses on evaluating the migration of the pollution plume of manganese over a 20 year time period. The results show the sustained release and transport of Mn from the tailing pond. The concentration of Mn in the central pollution halo is 1.97 mg/L, and the maximum detectable range is at 2291 m, with the concentration range exceeding the third level of national groundwater standard is 1280 m. The result provides a basis for the development and utilization of the mining area and the pollution prediction and protection of the tailings pond. [ABSTRACT FROM AUTHOR]

Conventional methods for water and wastewater treatment are energy-intensive, notably at the stage of coagulation–flocculation, calling for new strategies to predict pollutant reduction because the amount of energy consumed is related to how much of the pollutant is treated. Here we developed a model, named Bio-logic, inspired by ecosystems, where pollutants represent organisms, coagulants are food, and the wider environmental conditions are the living environment. Artificial intelligence was used to learn the biological behavior, which enabled an accurate prediction of the amount of pollutant reduction. Results show that pseudo-biological objects that have a strong affinity for biological food, such as turbidity, total phosphorus, ammonia nitrogen and the potassium permanganate index, induced a strong correlation, between measured pollutant consumption capacity and predicted values. For instance, R2 correlation coefficients are 0.97 for turbidity and 0.92 for the potassium permanganate index in the laboratory; and 0.99 for turbidity, 0.90 for total phosphorus, 0.75 for ammonia nitrogen and 0.63 for the potassium permanganate index in water treatment plants. Overall, our findings demonstrate that artificial intelligence can use the water Bio-logic model to predict the pollutant consumption capacity. [ABSTRACT FROM AUTHOR]

Significant criteria for choosing materials (consolidants and protective coatings) for the conservation of the built cultural heritage were gathered from the literature and by consultation with experts working on the preservation of cultural heritage. Ten criteria were chosen from these, and a questionnaire was prepared and sent to stakeholders in the cultural heritage conservation domain in order to evaluate, score and rank the importance of the proposed criteria. Based on the results obtained a decision support tool was developed, aimed at conservators and other stakeholders, to help them to make sustainable decisions with regard to the selection of conservation materials for treatment of the built cultural heritage. Performance characteristics and health and safety were identified to be the most important criteria. A preliminary decision can be made based on these two criteria, however, reversibility, minimum intervention and re-treatability are also of very high importance and additional information about these characteristics of the material are required to support decisions. Information about environmental performance, peer recommendation, the application techniques, the price and availability of the materials, which are also integrated in decision support tools, can help conservators and stakeholders to reach a final decision on interventions. The study also provides feedback for the manufacturers of conservation materials. For the users of material, it is very important that the manufacturers clearly identify key characteristics (i.e. criteria) on the product, including those related with environmental performance of the materials. [ABSTRACT FROM AUTHOR]

Since waste residues of antimony ores are piled in a disorderly way long-term, heavy metal elements of the residues are dissolved and precipitated under the eluviation effect of snow and rain, causing serious pollution to the surrounding soil. This paper takes the antimony ore of Hunan stannary as the research area, and the surrounding soil of the storage yard of antimony ores as the research object, and carries out research on the migration rules of Sb in the leachate of waste residues of antimony ores in soil by means of spot sampling, lab analysis, and test and simulation, and simulates the migration of Sb in the surrounding soil of mining areas. The results show that through the dynamic penetration experiment of indoor soil columns, the hydrodynamic dispersion coefficient (D = 2.485 cm2 /h), adsorption distribution coefficient (Kd = 48.826 cm3/g), retardation factor (Rd = 78.50), and other parameters of Sb migrating in soil are obtained; the study makes use of the HYDRUS-1D model to conduct dynamic simulation of Sb in the soil nearby the antimony mine areas on the stannaries of Hunan Province, and the results indicate that the measured value is quite close to the fitted value, and in the correlation analysis of double variables, R is equal to 0.986, indicating that the simulation effect is fairly good. This study aims to provide a theoretical foundation and scientific basis for evaluating, controlling, curbing, and repairing the surrounding ecological environment of antimony mine areas. [ABSTRACT FROM AUTHOR]

Antimony ore tailings slag was used analyze heavy metals, chemical speciation, and leaching characteristics. The results show that the residual silicate phases account for 65.44% of Sb, 77.22% of As, 87.94% of Hg, 58.53% of Pb, 71.27% of Cd, and 96.34% of Zn. Although the exchangeable and carbonate phases account for 7.71% of Sb, 0.71% of As, 3.77% of Hg, 4.82% of Pb, 1.83% of Cd, and 1.73% of Zn, the water-or-acid-soluble phases contribute more to the chemical speciation of heavy metals. Concentrations of Sb, As, and Hg in the leachates increased with increasing solid-liquid ratio, decreasing particle size and increasing temperature. In simulated rainfall conditions, the total quantity increased in the order Sb > As > Hg and were 42.508 mg, 52.940 μg, and 0.876 μg, respectively, at 500 g antimony ore tailings. Under different rainfall intensity simulations, the maximum quantity in the leachates of Sb, As, and Hg were 93.894 mg, 255.451 μg, and 1.690 μg, respectively, and increased in the order of moderate > heavy > rainstorm. Finally, the cumulative leaching of Sb at pH 6.0 is 42.025 mg/L (higher than at 4.0 and 5.0), and the As and Hg at pH 4.0 are 107.097 μg/L and 0.989 μg/L, respectively. [ABSTRACT FROM AUTHOR]

A cubic crystal form Co3O4 was synthesized using the sol-gel method and applied as catalyst in the visible light-driven photocatalytic degradation of 1,2,4-trichlorobenzene (1,2,4-TCB). 1,2,4-TCB removal efficiency initially increased and was followed by a gentle decrease as the Co3O4 dosage increased, with the optimal dosage of 2.0 g/L. The degradation rate changed positively with light intensity and reaction temperature. However, pH exerted only a slight effect on 1,2,4-TCB degradation. Strong acidic and basic conditions were conducive to the photocatalytic degradation of 1,2,4-TCB. The optimal parameters for the photocatalytic degradation of 1,2,4-TCB were found at a Co3O4 dosage of 2.0 g/L, 350 W of illumination intensity, initial 1,2,4-TCB concentration of 7.5 mg/L at 30ºC, with 1,2,4-TCB removal efficiency of 90.13% after 6.0 hours photocatalytic degradation. The Co3O4 synthesized in the study with high-purity and stable properties guaranteed its high catalytic activity and stability. The possible mechanisms of visible light-driven photocatalytic degradation of 1,2,4-TCB with synthesized Co3O4 photocatalyst were also proposed. [ABSTRACT FROM AUTHOR]

The prediction of heavy metal pollution load at the soil-water interface of a mining area was studied through an improved soil and water assessment tool (SWAT) model. The Red Flag Mining Area of Xiangtan Manganese Mine in Hunan Province, China, was selected as the research district. GPS, ARCGIS, RS technology, and field experiments were employed in this study. A modified one-dimensional migration model was embedded in the sediment migration source module of SWAT in order to establish an Improved SWAT model for the prediction of manganese pollution load at the soil-water interface. The key pollution areas identified by the improved model were consistent with actual mine pollution, with the Nash-Sutcliffe efficiency Ens and regression R² coefficients of 0.88 and 0.91, respectively. The tudy would provide the theoretical foundation and scientific basis for management and repair at the site. [ABSTRACT FROM AUTHOR]

Sediment cores and bottom water samples from across the Baltic Sea region were analyzed for freely dissolved concentrations (C free ), total sediment concentrations (C T ) and the dissolved aqueous fraction in water of seven indicator PCBs. Ex-situ equilibrium sampling of sediment samples was conducted with polydimethylsiloxane (PDMS) coated glass fibers that were analyzed by automated thermal desorption GC-MS, which yielded PCB concentrations in the fiber coating (C PDMS ). Measurements of C PDMS and C T were then applied to determine (i) spatially resolved freely dissolved PCB concentrations; (ii) baseline toxicity potential based on chemical activities (a); (iii) site specific mixture compositions; (iv) diffusion gradients at the sediment water interface and within the sediment cores; and (vi) site specific distribution ratios (K D ). The contamination levels were low in the Gulf of Finland and moderate to elevated in the Baltic Proper, with the highest levels observed in the western Baltic Sea. The SPME method has been demonstrated to be an appropriate and sensitive tool for area surveys presenting new opportunities to study the in-situ distribution and thermodynamics of hydrophobic organic chemicals at trace levels in marine environments. [ABSTRACT FROM AUTHOR]

Natural organic matter (NOM) found in water sources is broadly defined as a mixture of polyfunctional organic molecules, characterized by its complex structure and paramount influence on water quality. Because the inevitable release of pollutants into aquatic environments due to an ineffective control of industrial and agricultural pollution, the evaluation of the interaction of NOM with heavy metals, nanoparticles, organic pollutants and other pollutants in the aquatic environment, has greatly increased. Three-dimensional (3-D) fluorescence has the potential to reveal the interaction mechanisms between NOM and pollutants as well as the source of NOM pollution. In water purification engineering system, the 3-D fluorescence can indicate the variations of NOM composition and gives an effective prediction of water quality as well as the underline water purification mechanisms. Inadequately treated NOM is a cause of precursors of disinfection byproducts (DBPs), posing a potential threat to human health. Effective control and measurement/evaluation of NOM have long been an important factors in the prevention of water pollution. Overall, 3-D fluorescence allows for a rapid identification of organic components thus indicating possible sources of water pollution, mechanisms of pollutant interactions, and possible DBPs formed during conventional treatment of this water. This article reviews the 3-D fluorescence characteristics of NOM in natural water and typical water purification systems. The 3-D fluorescence was effective for indicating the variabilities in NOM composition and chemistry thus providing a better understanding of NOM in natural water system and water engineering system. [ABSTRACT FROM AUTHOR]

The increasing quantities of polluted waters are calling for advanced purification methods. Flocculation is an essential component of the water purification process, yet flocculation is commonly not optimal due to our poor understanding of the flocculation process. In particular, there is little knowledge on the mechanisms ruling the migration of pollutants during treatment. Here we have created the first tensor diagram, a mathematical framework for the flocculation process, analyzed its properties with a deep learning model, and developed a classification scheme for its relationship with pollutants. The tensor was constructed by combining pixel matrices from a variety of floc images, each with a particular flocculation period. Changing the factors used to make flocs images, such as coagulant dose and pH, resulted in tensors, which were used to generate matrices, that is the tensor diagram. Our deep learning algorithm employed a tensor diagram to identify pollution levels. Results show tensor map attributes with over 98% of sample images correctly classified. This approach offers potential to reduce the time delay of feedback from the flocculation process with deep learning categorization based on its clustering capabilities. The advantage of the tensor data from the flocculation process improves the efficiency and speed of response for commercial water treatment. [ABSTRACT FROM AUTHOR]

Simple Summary: Fish kept as pets are almost always held in tanks with substrate such as gravel or sand on the bottom of the tank. This may be added as a form of enrichment to encourage natural fish behaviours, or for aesthetic reasons. However, substrate can also harbour elevated levels of waste products and unwanted bacteria; therefore, whether the use of substrate in home aquaria is advantageous or disadvantageous has not been fully considered. Here, we investigated whether there was a difference in water quality in home aquaria that contained either no substrate (bare tanks), plastic plants as enrichment but no substrate, sand or gravel substrate. Water quality (e.g., temperature, oxygen, pH and ammonia) and the presence of bacteria were measured over a 7-week period. As water quality can also vary with the season, the study was repeated at different times of the year. Addition of both gravel and sand substrate resulted in increased pH and the waste products ammonia and nitrate. Substrate was also associated with a greater presence of bacteria. In conclusion, the use of substrate affected water quality, with further research needed on the use of substrate in home aquaria. Almost all home aquaria contain substrate, either as intentional enrichment or for aesthetic purposes. For fishes, benefits of structural enrichment have been well considered, particularly in research and aquaculture settings. However, our understanding of the impacts of tank substrate as enrichment is limited. While substrate can induce foraging in some species, a major drawback is the potential of substrate to harbour elevated levels of waste and pathogenic bacteria. Here, we considered whether substrate as a form of environmental enrichment significantly altered water quality and bacterial presence in home aquaria. Water quality (temperature, oxygen, pH, TAN, unionised ammonia, nitrate, Ca2+, Na+, Mg2+ and K+) and bacterial presence (Pseudomonas spp.) were measured over two seven-week periods in stand-alone, tropical, freshwater tanks that simulated home aquaria. The following four enrichment conditions were considered: bare tanks, plastic plants, gravel substrate or sand substrate. The addition of both gravel and sand resulted in increased pH, concentrations of total ammonia nitrogen and nitrate. Substrate was also associated with a greater Pseudomonas presence. Decreased pH alongside an increased concentration of ions were also observed depending on the time of year. In conclusion, enrichment type affected the water quality of home aquaria, with further research needed on the role of the tank biome in fish welfare. [ABSTRACT FROM AUTHOR]

Black-odorous waters are an increasingly common phenomenon characterized by excessive levels of nutrients, the formation of metal sufide precipitates, volatile sulfurous compounds, low dissolved oxygen and high chemical oxygen demand. Black-odorous waters frequently occur in lake and river systems where inputs have restricted circulation. The key remediation issue is the removal of nitrogen and phosphorus. Here, we present a novel aeration-adsorption system using fiber balls and we study treatment parameters and removal mechanism. Kinetics and changes of the solid phase were followed using Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and X-ray diffraction. Results show complete removal of ammonia N, initially at 31 mg/L, and 92.8% removal of total nitrogen, initially at 29 mg/L, after a 24 h reaction time at pH 9.67. At pH 5.67 and 9.67, total phosphorus and phosphate could be significantly reduced by 90–92% at 3.2–5.2 mg/L after 24 h. Treatment met China's integrated wastewater discharge standards, demonstrating an effective and robust treatment capability. First-order and second-order kinetic models provided a good fit to the treatment data, indicating physical and chemical adsorption were involved in the treatment reactions. The reaction mechanism involved hydrogen substitution and binding to oxygen. These results present a cost effective and robust approach for the removal of N and P from black, odorous water, providing opportunity to abate environmental contamination. [ABSTRACT FROM AUTHOR]

Forest parks in many urbanized areas are affected by the anthropogenic pollution as demonstrated by the poor health status of many trees. The concentrations of harmful agents like Potentially Toxic Elements (PTEs) can be very high in urban soils and their availability is an important issue for biological components in these environments. This study focuses on the mobile forms of PTEs extracted by 1 М NH 4 OAc at pH = 7 in relation to determining their bioavailability for forest trees in oak ecosystems in urban areas. The area studied is along an urban–rural gradient from the Sofia region, Bulgaria. The NH 4 OAc extracts mainly “biologically active” fraction of elements in soils comprising primarily the soluble and exchangeable forms and in some cases showed good positive correlation with PTE accumulation in trees. Four experimental forest park sites (U1, U2, U3 and U4) created on Hortic/Technic Anthrosols were selected along the urban gradient in the Sofia region. The control sites located in rural zones with natural soils Cambisols and Luvisols (R1, R2, R3 and R4) were used as reference. Strong correlations were found between mobile forms of Cu, Zn, Pb, Cd in urban soils and a number of soil parameters (pH, CEC and texture). The mobility is related to soil pH and with more acidic soils a higher mobility is shown, which is statistically significant for Pb. The element Cu is less mobile in the soil and is localized in the top layer, where it is mainly associated with soil organic matter. The mobile (NH 4 OAc extractable) portions of Cu, Zn, Pb, and Cd (mg/kg soils) in Urban Soils ranged between: 0.74 and 2.61; 2.94 and 3.29; 1.34 and 3.28; and 0.02 and 0.16, respectively and those in Natural Soils ranged between: 0.73 and 1.65; 1.20 and 5.29; 1.10 and 6.80; and 0.02 and 0.07. The significance of the mobile proportion was greatest for Cd in urban soils where it reached 33.3% of the total content. Despite the determined correlation between mobile forms of Pb and Cd with their total content in leaves of oak trees there is no clear visible effect on the tree health characteristics using parameters as defoliation and decoloration of crowns. [ABSTRACT FROM AUTHOR]

Aims: Rare earth elements (REEs) and normalized REE patterns determined in plant and soil samples represent powerful tools to trace biogeochemical processes during weathering, soil genesis and processes in the rhizosphere, and thus publications reporting REE concentrations and normalized REE patterns in soil systems and plants are rapidly increasing.A normalized REE pattern allows for the recognition of anomalous concentrations of an individual REE. In the literature, anomalies are predominantly reported/focused for/on the redox-sensitive elements cerium (Ce) and europium (Eu) that can shift their oxidation state during interactions with organic and inorganic soil phases and the biological processes affecting their mobility in soil and uptake by plants. Thus positive Eu anomalies in plants are often interpreted as a consequence of reduction of Eu3+ to Eu2+ in the rhizosphere followed by a preferential uptake of Eu2+.Due to an analytical artefact in ICP-MS analysis, a false Eu anomaly may be reported. This can be avoided by using a barium (Ba) interference correction. We draw attention to the possibility of this problem and to being aware of its potential occurrence when Eu anomalies are reported.We recommend (i) including information on how this potential problem was dealt with in the Materials and Methods section of articles and (ii) how to implement Findable Accessible Interoperable and Reusability (FAIR) guiding principles in that section (including data availability in an open repository).Methods: Rare earth elements (REEs) and normalized REE patterns determined in plant and soil samples represent powerful tools to trace biogeochemical processes during weathering, soil genesis and processes in the rhizosphere, and thus publications reporting REE concentrations and normalized REE patterns in soil systems and plants are rapidly increasing.A normalized REE pattern allows for the recognition of anomalous concentrations of an individual REE. In the literature, anomalies are predominantly reported/focused for/on the redox-sensitive elements cerium (Ce) and europium (Eu) that can shift their oxidation state during interactions with organic and inorganic soil phases and the biological processes affecting their mobility in soil and uptake by plants. Thus positive Eu anomalies in plants are often interpreted as a consequence of reduction of Eu3+ to Eu2+ in the rhizosphere followed by a preferential uptake of Eu2+.Due to an analytical artefact in ICP-MS analysis, a false Eu anomaly may be reported. This can be avoided by using a barium (Ba) interference correction. We draw attention to the possibility of this problem and to being aware of its potential occurrence when Eu anomalies are reported.We recommend (i) including information on how this potential problem was dealt with in the Materials and Methods section of articles and (ii) how to implement Findable Accessible Interoperable and Reusability (FAIR) guiding principles in that section (including data availability in an open repository).Results: Rare earth elements (REEs) and normalized REE patterns determined in plant and soil samples represent powerful tools to trace biogeochemical processes during weathering, soil genesis and processes in the rhizosphere, and thus publications reporting REE concentrations and normalized REE patterns in soil systems and plants are rapidly increasing.A normalized REE pattern allows for the recognition of anomalous concentrations of an individual REE. In the literature, anomalies are predominantly reported/focused for/on the redox-sensitive elements cerium (Ce) and europium (Eu) that can shift their oxidation state during interactions with organic and inorganic soil phases and the biological processes affecting their mobility in soil and uptake by plants. Thus positive Eu anomalies in plants are often interpreted as a consequence of reduction of Eu3+ to Eu2+ in the rhizosphere followed by a preferential uptake of Eu2+.Due to an analytical artefact in ICP-MS analysis, a false Eu anomaly may be reported. This can be avoided by using a barium (Ba) interference correction. We draw attention to the possibility of this problem and to being aware of its potential occurrence when Eu anomalies are reported.We recommend (i) including information on how this potential problem was dealt with in the Materials and Methods section of articles and (ii) how to implement Findable Accessible Interoperable and Reusability (FAIR) guiding principles in that section (including data availability in an open repository).Conclusions: Rare earth elements (REEs) and normalized REE patterns determined in plant and soil samples represent powerful tools to trace biogeochemical processes during weathering, soil genesis and processes in the rhizosphere, and thus publications reporting REE concentrations and normalized REE patterns in soil systems and plants are rapidly increasing.A normalized REE pattern allows for the recognition of anomalous concentrations of an individual REE. In the literature, anomalies are predominantly reported/focused for/on the redox-sensitive elements cerium (Ce) and europium (Eu) that can shift their oxidation state during interactions with organic and inorganic soil phases and the biological processes affecting their mobility in soil and uptake by plants. Thus positive Eu anomalies in plants are often interpreted as a consequence of reduction of Eu3+ to Eu2+ in the rhizosphere followed by a preferential uptake of Eu2+.Due to an analytical artefact in ICP-MS analysis, a false Eu anomaly may be reported. This can be avoided by using a barium (Ba) interference correction. We draw attention to the possibility of this problem and to being aware of its potential occurrence when Eu anomalies are reported.We recommend (i) including information on how this potential problem was dealt with in the Materials and Methods section of articles and (ii) how to implement Findable Accessible Interoperable and Reusability (FAIR) guiding principles in that section (including data availability in an open repository). [ABSTRACT FROM AUTHOR]

The release of lanthanides (Ln) into the environment has increased in recent decades due to their expanding applications in society. Studying their toxicity in aquatic ecosystems is urgent and challenging, with contradictory evidence presented in the literature. This study compared the biodistribution of La and Gd in Daphnia magna exposed to sub-chronic conditions and developed the first Toxicokinetic-Toxicodynamic (TKTD) model for these lanthanides with this model crustacean. D. magna were initially exposed for 7 days to concentrations close to the LC 50 of La (2.10 mg L-1) and Gd (1.70 mg L−1). After exposure, half of the live daphnids were introduced in a clean media to allow depuration over 24 h, while the other organisms were directly prepared for synchrotron imaging measurements. Synchrotron X-ray fluorescence analysis revealed that metal distribution in the organisms was similar for both La and Gd, predominantly localized in the intestinal tract, even after the depuration process. These results indicate that ingested metal can adversely affect organisms under sub-chronic exposure conditions, highlighting the importance of using nominal concentrations as a more suitable indicator of metal bioavailability for risk assessment. The General Unified Threshold Model of Survival (GUTS) TKTD framework, in its reduced form (GUTS-RED), was developed for La and Gd using dissolved and nominal concentrations. D. magna were exposed for 7 days to concentrations from 0.5 to 5 mg L−1 of La or Gd and mortality monitored daily. The mechanistic model revealed a faster toxicokinetics for La than Gd and a higher toxicity for Gd than La in the organism. This study confirmed, despite similar chemical properties, the variation in both toxicity and toxicokinetics between these two metals. [Display omitted] • La and Gd were similarly biodistributed in the gut of D. magna. • Metals in the gut were not depurated by the organism. • La and Gd show different toxicokinetic and toxicodynamic. • Nominal or "whole" metal concentrations should be considered under long-term exposures. [ABSTRACT FROM AUTHOR]

Several physiologically based extraction procedures have been proposed to estimate the fraction of the potentially toxic element content that would be bioaccessible in the human gastro-intestinal tract following accidental ingestion of soil. Many of these procedures are complex, they have been applied to a very limited range of soils, and most work has focussed on arsenic and lead. In the present study, a simplified, two-stage extraction, simulating the human stomach and intestine, was developed and applied to urban soil samples from ten public-access areas in the City of Torino, Italy. The human oral bioaccessibility of chromium, copper, nickel, lead and zinc was estimated. Lead and zinc bioaccessibilities were found to be higher in the stomach, but chromium was more bioaccessible in the intestine. Analyte concentrations were higher in roadside soils than in soils from parks. A higher proportion of the soil metal content was found in bioaccessible forms at roadsides than in parks. Comparison of the current findings with results of earlier work involving sequential extraction of the same soils indicated that the sequential procedure gave a relative, but not an absolute, indication of bioaccessibility. Calculations based on the bioaccessible analyte concentrations suggest that ingestion of only 2-3 g of some of the roadside soil samples from Torino could deliver the tolerable daily oral intake of chromium, nickel and lead to a 20-kg child. The developed procedure is useful for preliminary screening of soils and prediction of whether their bioaccessible metal contents are likely to pose a risk to human health. [ABSTRACT FROM AUTHOR]

The chemistry of semiconductor wafer processing liquid waste, contaminated by heavy metals, was investigated to determine arsenic content. Arsenic and gallium concentrations were determined for waste slurries collected from gallium arsenide (GaAs) wafer processing at three industrial sources and compared to slurries prepared under laboratory conditions. The arsenic and gallium content of waste slurries was analyzed using inductively coupled plasma mass-spectrometry (ICP-MS) and it is reported that the arsenic content of the waste streams was related to the wafer thinning process, with slurries from wafer polishing having the highest dissolved arsenic content at over 1,900 mgL-1. Lapping slurries had much lower dissolved arsenic (< 90 mgL-1) content, but higher particulate contents. It is demonstrated that significant percentage of GaAs becomes soluble during wafer lapping. Grinding slurries had the lowest dissolved arsenic content at 15 mgL-1. All three waste streams are classified as hazardous waste, based on their solids content and dissolved arsenic levels and treatment is required before discharge or disposal. It is calculated that as much as 93% of material is discarded through the entire GaAs device manufacturing process, with limited recycling. Although gallium can be economically recovered from waste slurries, there is little incentive to recover arsenic, which is mostly landfilled. Options for treating GaAs processing waste streams are reviewed and some recommendations made for handling the waste. Therefore, although the quantities of hazardous waste generated are miniscule in comparison to other industries, sustainable manufacturing practices are needed to minimize the environmental impact of GaAs semiconductor device fabrication. [ABSTRACT FROM AUTHOR]

Six forest locations were chosen from urban (U) and semi-urban (SU) zones of Sofia, Bulgaria. Soil profiles characterised for their generic physico-chemical properties: particle size distribution, pH, C-content (%) and N-content (%). From the ratio silt/clay and C/N, significant differences were observed for the Ah horizon in the urban and semi-urban locations. Clay formation appeared to be reduced in this horizon in the urban soils and the C-content is higher in semi-urban soils in comparison with the urban soils. On the base of the results obtained, a reduction of the buffering capability is noted for the topsoil of the urban sites compared to the semi-urban sites. [ABSTRACT FROM AUTHOR]

Fluorescence excitation-emission matrix spectroscopy (EEMs) has become a very popular technique in characterization of aquatic dissolved organic matter (DOM) coupled with a parallel factor (PARAFAC) model, denoted as (EEMs-PARAFAC). This research addresses the poorly researched relationship correlation between dissolved ions and fluorescence in a natural water environment. The relationship between the EEMs-PARAFAC components and ionic composition was studied in freshwater lakes, rivers, and seawater from locations in China. The natural water environment is different from a simulated environment having a fixed ionic composition. We used electrical conductivity (EC) to reflect the ionic strength as an indicator to evaluate the relationship in a series of water bodies. Results show that the EC generally had a positive correlation with DOM in natural water environment, but no correlation was found with water from the highly saline Yellow Sea. The Chaohu Lake samples contained one component having a significant negative correlation with EC, i.e., r > 0.6, p < 0.05, while other surface waters contained components having both positive and negative correlations (r > 0.5, p < 0.05). The negative correlation with EC also highlighted that humic acid-like components and protein-like materials (c1-c3) were positively correlated with DOM, while the protein-like component (c4) was negatively correlated with DOM. The EC equation proposed provided a good fit with the EC values of surface waters. The use of EC would be a useful and rapid method for analyzing the variation in the fluorescence component and its effect on water quality. This study highlights the need to account for variation in EC when assessing EEMs-PARAFAC of natural waters. [ABSTRACT FROM AUTHOR]

Chemical oxidation is a key technique used in dye wastewater treatment via the formation of hydroxyl radicals. To obtain optimal treatment effects, it is critical to understand the interaction of the molecular structure of the dye with the hydroxyl radical. We evaluated fluorescence excitation-emission matrix spectroscopy to study the decay of an azo-dye (Procion Red MX-5B) by a hydroxyl radical generated from catalytic Fe (III) on H2O2. Results showed that fluorescence signal reliably indicated the variations of the chemical groups and components during degradation, and the degradation could be divided into three stages: initial degradation (decolorisation), rapid intermediate degradation, and final degradation. Under control of uncorrected matrix correlation, the fluorescence fractions could be fitted successfully by parallel factor model (PARAFAC) model: two fluorescence components in initial degradation including mono substituted benzene and mono substituted naphthalene, three components as multi substituted benzene in rapid degradation, and no components could be resolved in the final degradation. The results from the study demonstrate the utility fluorescence characterization of dye degradation mechanisms and enhance the understanding of the degradation mechanisms. [ABSTRACT FROM AUTHOR]

How to effectively remove excess Sb(III) in the water environment by biosorption is receiving close attention in the international scientific community. To obtain the maximum biosorption efficiency, response surface methodology (RSM) was employed to optimize a total of 13 factors for biosorption of Sb(III) onto living Rhodotorula mucilaginosa DJHN070401. The mechanism of biosorption and bioaccumulation was also studied. The results showed that biosorption reached 56.83% under the optimum conditions. Besides, pH, Fe2+, and temperature are significant influencing factors, and control of Ca2+ and Fe2+ has a beneficial impact on Sb(III) biosorption. The characterization explained that physical adsorption occurred readily on the loose and porous surface of DJHN070401 where carboxyl, amidogen, phosphate group, and polysaccharide C-O functional groups facilitated absorption by complexation with Sb(III), accompanied by ion exchange of Na+, Ca2+ ions with Sb(III). It was also noted that the living cell not only improved the removal efficiency in the presence of metabolic inhibitors but also prevented intracellular Sb(III) being re-released into the environment. The results of this study underpin improved and efficient methodology for biosorption of Sb(III) from wastewater. [ABSTRACT FROM AUTHOR]

Mining activities have introduced various heavy metals and metalloids to surrounding soil environments, causing adverse impacts to the ecological environment system. The extremely high concentration of various heavy metals and metalloids make the Xikuangshan (Hunan, China) an excellent model to assess their ecological risk. In this study, the soil samples from 26 locations of different land use methods in four areas (smelting area, road nearby ore, mining area, and ore tailing area) in Xikuangshan with different levels of various heavy metals and metalloids (Sb, As, Pb, and Cd) were analyzed; in addition, the index of geo-accumulation and the potential ecological risk index were used to evaluate ecological risk. The results showed that the average contents of Sb, As, Pb, and Cd in all soil samples were 4368.222 mg·kg−1, 40.722 mg·kg−1, 248.013 mg·kg−1, and 40.941 mg·kg−1, respectively, implying serious contamination of compound pollution of heavy metals in soil. The concentration of heavy metals in soil among smelting area, road nearby ore, mining area, and ore tailing area showed significant distribution characteristics of region because different mining activities such as smelting, mining, transportation, and stacking caused different pollution intensity. Moreover, the contents of Sb in soil samples decreased successively in residue field, wasteland, forestland, sediment, grassland, and vegetable field, and the contents of Sb in vegetable-field and ecological restoration grassland were relatively low, which indicate that the method of grassland ecological restoration is an effective method to control antimony pollution in soil. The results of ecological risk assessment showed that the antimony mining area was seriously polluted by Sb, As, Pb, and Cd, and had strong ecological risk, and Sb and Cd were the most important pollution factors, which indicated that the pollution of Sb and Cd should be a major concern of relevant departments of environment and health. [ABSTRACT FROM AUTHOR]

Dissolved organic matter (DOM) is not only a vector for the migration of aquatic environmental pollutants, but is also key to the control of water pollution. Economic and effective DOM removal through coagulation is essential in water treatment processes. This work investigated the role of carboxylated magnetic metal organic frameworks (MMOFs) nanoparticles in polymeric iron-based coagulation for the removal of aquatic DOM using a MMOFs-doped polyferric iron-based coagulant (MMOF-PIC). Analytical methodologies and tools used in this research included scanning electron microscopy (SEM), zeta potential, molecular weight cut off (MWCO), vibrating sample magnetometer (VSM) measurement, excitation emission matrix spectroscopy (EEMs), and X-ray photoelectron spectroscopy (XPS). The results showed that MMOF-PIC had the potential to change the structure of the polyferric iron-based coagulant (PIC) and charge, as determined by a porous surface morphology, a higher medium polymeric species distribution, and a more positive zeta potential. The MMOFs consequently enhanced PIC action on the removal of UV254 exposed DOM species with molecular weight <30 kDa, including aromatic C C based compounds, org-N as primary amines and amide/peptide bound species, water containing microbial metabolites and protein-like materials. The coagulation of DOM was enhanced by improving charge neutralization, adsorption-bridging and sweep-flocculation in the presence of MMOFs nanoparticles. This was due to hydrogen bonds, π-π bonds and covalent bonds resulting from actions of nanoparticles and pollutants. These results indicate that magnetic MOF nanoparticles can improve PIC coagulation for DOM, enhancing future removal of target pollutants. Image 1 • Carboxyl magnetic MOFs (MMOFs) doped polymeric-iron was prepared. • MMOFs and PIC coexisting in the same system can enhance coagulation for DOM. • MMOFs changed PIC's structure, charge and adsorption properties. • Chemical bond binding force contributed to enhanced adsorption. [ABSTRACT FROM AUTHOR]

Removal of dissolved organic matter (DOM) is a major problem in drinking water treatment, because DOM modifies color, taste and odor, and carcinogenic by-products of DOM can be created during disinfection. Efficient water remediation is limited by our poor knowledge of DOM structure and properties, thus calling for advanced methods of characterisation. Here, we tested the influence of two coagulants, polymeric ferric sulfate and cationic polyacrylamide, on the three-dimensional fluorescence excitation–emission wavelength spectra of DOM during coagulation. Results of the parallel factor model reveal 3 fluorophore components C1–3. Cationic polyacrylamide decreases the linear correlation between DOM and fluorescence, e.g., from 0.92 to 0.82 for C1 and from 0.84 to 0.79 for C2. The C3 component, a protein-like material, was the most affected. Findings demonstrate the need to consider residual polymer as a potential interference when using fluorescence to assess DOM removal by coagulation. [ABSTRACT FROM AUTHOR]

The injection of oxidants is one of the useful remediation technologies for eliminating hydrogen sulfide (H2S) and ammonia (NH3/NH4+) in aquatic sediments. In the current work, the impact of calcium nitrate injection on the release of heavy metals associated with phosphate was evaluated in a column test of sediment with overlying water at a volume ratio of 1:1 for 131 days. Sulfide was significantly oxidized by calcium nitrate, as its amount was reduced substantially by 85% from the 20th to the 30th day, with a decrease in the oxidation–reduction potential to −68 mV and a simultaneous increase in pH to 9.83. Over 50% of the mobile Zn, Pb, and Cu were reprecipitated in the sediment when the phosphate was partially released. It is proposed that the heavy metal immobilization was related to the phosphate content in the pore water due to the precipitation of heavy metals and phosphorus on the surface of Fe hydroxide particles after oxidation. This is supported by chemical fraction analysis of the heavy metals in the sediment, which indicated increased residual fractions of heavy metals. Our results provide an insight into the remediation of sediment by oxidation with a self‐stabilization of heavy metals and phosphate. Practitioner points: Effective removal of sulfide after calcium nitrate injection was achieved.Metal immobilization was related to the phosphate content in pore water.Over 50% of mobile Zn, Pb, and Cu might be reprecipitated in sediment.Oxidizable fraction of heavy metal predominantly transformed to its residual fraction. [ABSTRACT FROM AUTHOR]

Elevated soil concentrations of antimony (Sb) and co-contaminants are frequently encountered where antimony has been mined on a large scale. For instance, the Xikuangshan antimony mine in central South China has sustained, over many centuries, dispersed and spatially variable input of toxic elements into the soil ecosystem. We utilized this unique environment to assess the impact of geochemical conditions on soil microbiology. Geochemical conditions were assessed by monitoring absolute and available fractions of toxic elements and disrupted soil properties. Soil microbiology was studied by high-throughput sequencing and statistical analysis, including principle component analysis and canonical correspondence analysis. Results show that Sb concentrations were ranged from 970 to more than 24,000 mg/kg. As concentrations were three times higher than the regional background values and ten times higher for Pb, 590 times higher for Cd and 30 times higher for Hg. About 5–10% of the total soil Sb was environmentally mobile. Microbial diversity was high, and soil properties such as pH, organic matter, iron and sulfate controlled the absolute microbial activity. We identified strong positive and negative correlations with specific bacterial taxonomic groups which show: (1) an intolerance of available fractions for all elements, e.g., Gemmatimonas, Pirellula, Spartobacteria; (2) a good tolerance of available fractions for all elements, e.g., Povalibacter, Spartobacteria; and (3) a mixed response, tolerating available Sb, Hg and Cd and inhibition by As, Pb, e.g., Escherichia/Shigella and Arthrobacter, and in reverse, e.g., Gemmatimonas and Sphingomonas. The site hosts great diversity dominated by Gram-negative organisms, many with rod (bacillus) morphologies but also some filamentous forms, and a wide range of metabolic capabilities: anaerobes, e.g., Saccharibacteria, metal oxidizing, e.g., Geobacter, chemoautotrophs, e.g., Gemmata, and sulfur reducing, e.g., Desulfuromonas. The bioremediation potential of Arthrobacter and Escherichia/Shigella for Sb control is highlighted. [ABSTRACT FROM AUTHOR]

Nanoscale pore characteristics of the Upper Permian Longtan transitional mudrocks and their equivalent strata Wujiaping Formation marine mudrocks in and around the eastern Sichuan Basin was investigated using field emission scanning electron microscopy (FE‐SEM) and low‐pressure N2 adsorption experiments. The results indicate that the Upper Permian mudrock is at a mature stage with total organic carbon (TOC) values ranging between 0.47% and 12.3%. The Longtan mudrocks mainly contain vitrinite, and their mineral composition is primarily clay. In contrast, the Wujiaping mudrocks are dominated by sapropelinite and solid bitumen, and their mineral compositions are mainly quartz and a notably high amount of pyrite. The FE‐SEM reveals that clay mineral pores and microcracks are the common pore types in the Longtan mudrocks. The specific surface area and pore volume depend on the clay content but are negatively correlated with the TOC. The generation of nanometer pores in the Longtan mudrocks is caused by high clay mineral contents. Meanwhile, the Wujiaping mudrock mainly contains OM pores, and the pore parameters are positively correlated with the TOC. The OM pore development exhibits remarkable differences in the Longtan and Wujiaping mudrocks, which might be related to their sedimentary facies and maceral fractions. Vitrinite and inertinite appear as discrete particles in these mudrocks and cannot generate pores during thermal maturation. Sapropelinite often contains many secondary pores, and solid bitumen with large particles, usually with several pores, is not the major contributor to the pore system of the investigated mudrock. [ABSTRACT FROM AUTHOR]

Antimicrobial resistance (AMR) represents a major global health threat, as well as a major hazard to sustainable economic development and national security. It remains, therefore, vital that current research aligns to policy development and implementation to alleviate a potential crisis. One must consider, for example, whether drivers of antibiotic resistance can be controlled in the future, or have they already accumulated in the past, whether from antibiotics and/or other pollutants? Unfortunately, industrial heritage and its pollution impact on the prevalence of environmental AMR have largely been ignored. Focussing on industrialised estuaries, we demonstrate that anthropogenic pollution inputs in addition to the natural diurnal environmental conditions can sufficiently create stressful conditions to the microbiome and thus promote selective pressures to shift the resistome (i.e., collection of resistance traits in the microbiological community). Unfortunately, the bacteria's survival mechanisms, via co-selective pressures, can affect their susceptibility to antibiotics. This review highlights the complexity of estuarine environments, using two key contaminant groups (metals/toxic elements and polyaromatic hydrocarbons), through which a variety of possible chemical and biological pollutant stressors can promote the emergence and dissemination of antimicrobial resistance. We find compelling divers to call on more focused research on historically disrupted ecosystems, in propagating AMR in the real world. [ABSTRACT FROM AUTHOR]

In this study, adsorption behaviors and mechanisms of Sb(III) ions onto Fe(III)-treated humus sludge adsorbent (FTHSA) from aqueous solutions was investigated using batch adsorption techniques, Fourier transform infrared (FT-IR) spectra and scanning electron microscopy were coupled to an energy-dispersive spectrometer (EDS). FTHSA was prepared via immersion with 1 mol/L FeCl3. The effects of dosage, contact time, Sb(III) initial concentration, and pH on the adsorption of Sb(III) onto FTHSA were investigated. Sb(III) adsorption was favored at pH with 2.0 and decreased dramatically with increasing pH. The description of equilibrium data of Sb(III) adsorption by Langmuir, Freundlich, and Dubbin-Radushkevich isotherm models showed that Langmuir model provided the best fit for Sb(III) adsorption with maximum adsorption amount of 9.433 mg/g. Pseudo first-order, pseudo second-order, Elovich, and intraparticle diffusion model were applied to describe the adsorption process of Sb(III) ions onto FTHSA. The results showed that the pseudo second-order model described well how Sb(III) adsorption and chemical adsorption played a dominant role in the adsorption process. The FT-IR spectra also indicated that the chemical interactions as ion exchange among the metal ions and N-H, O-H, C=O, COO, and C-O were mainly involved in the adsorption process. Therefore, FTHSA has a suitable potential removal for Sb(III) ions in the practical process. [ABSTRACT FROM AUTHOR]

Graphical abstract Highlights • MEBR coupling intermittent DC and MBR was established to treat coal chemical industry wastewater. • MEBR exhibited significant efficiency improvement and membrane fouling reduction. • Changes in properties of mixed liquor caused by electrokinetics accounted for fouling migration. • MEBR with intermittent DC and iron anode promoted microbial community evolution. Abstract A membrane electro-bioreactor (MEBR) embracing biological treatment, electrokinetic phenomena and membrane filtration was established by applying intermittent direct current (DC) to MBR. MEBR exhibited significant improvement of treatment performance and reduction of membrane fouling. COD and total phenols removal efficiencies increased to 83.53% and 93.28% at an exposure mode of 24′-OFF/6′-ON, compared to 71.24% and 82.43% in MBR. Trans-membrane pressure increment rate declined dramatically in MEBR, which was mainly attributed to the increase of sludge floc size and decrease of zeta potential, soluble microbial products and specific resistance to filtration, resulted from electrokinetic effects such as electrocoagulation, electrophoresis, electroosmosis and electromigration of ions. It was notable that DC exposure exerted distinct evolution on microbial community, with the improvement of microbial community richness and diversity. The relative abundances of functional genera were promoted noticeably in MEBR. An interactive relevance existed among microbial community structure, mixed liquor properties and operational parameters. [ABSTRACT FROM AUTHOR]

For linear noise such as seismic ground roll, 3-D frequency-wavenumber-wavenumber (3-D FKK) domain filtering suppression is better than 2-D frequency-wavenumber (F-K) domain filtering. In recent years, with the continuous development of computer processing speed and memory capacity, high-density data acquisition in seismic exploration has been widely applied in the hydrocarbon industry, opening up the application of 3-D FKK filtering methods. We applied the 3-D FKK filtering software to a 3-D high-density onshore seismic field dataset from a coal mine in western China. The case study demonstrates that the linearity of the noise in the field data is better represented by constructing the single shot records as a minimum dataset. Both theoretical synthetic models and the 3-D high-density onshore seismic field data numerical filtering experiments demonstrate that the feasibility of 3-D FKK filtering. [ABSTRACT FROM AUTHOR]

Shock metamorphism of minerals in meteorites could help to understand the shock history of its parent body and also provide a window into the interior of the Earth. Although shock features in olivine have been well known within and adjacent to shock melt veins and shock melt pockets in meteorites, there are processes that are not yet completely understood. Ringwoodite is formed by crystallization from olivine melts or solid-state phase transformation of olivine. Typically, olivine clasts with a ringwoodite rim around an olivine core have been documented from only a handful of meteorites. Here we report results from GRV053684, a highly shocked L6 chondrite that was collected by Chinese Antarctic Research Expedition in 2006 to Antarctica. The investigations of the shock pressure history and the transformation mechanism of olivine to ringwoodite use optical microscope, electron probe microanalyzer (backscattered electron images, major element quantitative analyses, and quantitative wavelength-dispersive spectrometry elemental X-ray maps), and Raman spectrograph. Ringwoodite in the shock melt vein generally displays as Fe-rich (Fa37-43) polycrystalline rims around Fe-poor (Fa11-20) olivine core and as small individual clasts embedded in shock melt vein matrix. The difference in FeO between ringwoodite rim and olivine core implies that Fe was preferentially partitioned to ringwoodite. The occurrence of maskelynite (An17) indicates a shock pressure ~30 GPa. The FeO and MgO diffusion indicates the transformation process of olivine to ringwoodite is a diffusion-controlled incoherent nucleation and growth. The spatial association between ringwoodite and the shock melt vein matrix suggests that high temperature plays a key role in prompting phase transformation. [ABSTRACT FROM AUTHOR]

Three-dimensional seismic survey is widely applied, but 3-D filtering technology has yet to be fully utilized for the analysis of seismic field data. The common approach is to first filter inline and then crossline. However, an effective 3-D filtering method is expected to eliminate coherent noise, such as the ground roll. We propose a 3-D Butterworth filtering method in the time-space domain. Firstly, a Butterworth-type filter in the frequency-wavenumber-domain is designed to suppress the linear noise with a specific apparent velocity. Secondly, transforming this filter to the time and space domain yields 3-D partial differential equations (PDEs), which are applied to suppress the linear noise. Factorizing the finite-difference equations in a different direction other than decreasing the 3-D PDEs to 2-D PDEs produces a highly accurate and efficient algorithm. Designing the 3-D Butterworth filter, selecting the filtering parameters, and showing its application to synthetic data and a 3-D high-density onshore seismic field data from a region in western China are discussed in detail. Numerical experiments with 3-D high-density onshore seismic field data demonstrate that it is more effective than the 3-D frequencywavenumber- wavenumber (FKK) filtering method. [ABSTRACT FROM AUTHOR]