High Concentrations Of Arsenic Research Articles

Granulometric and Geochemical Distribution of Arsenic in a Mining Environmental Liability in a Semi-arid Area.

This study focuses on the "El Lavadero" tailings deposit, a mining environmental liability (MEL) located near the town of San Felipe de Jesús, Sonora, in northwest Mexico. The objective was to determine the total arsenic (As) content, its granulometric and geochemical distribution, as well as its mobilization capacity and bioavailability. The results from oxidized and unoxidized tailings showed low potential of hydrogen (pH) values (2.4-5.7) and high concentrations of total arsenic (8235-36,004mgkg-1), predominantly in the finer granulometric fractions (< 0.05mm). Arsenic also prevails in the finest fraction of agricultural soil (> 2mm). These fine particles could present adverse environmental effects due to their potential to be transported by leaching and water suspension. In contrast, arsenic in the effluent sediments is primarily found in the coarser fraction (> 2mm). A significant proportion of arsenic in the tailings (5-40%) was found in the non-residual geochemical fractions (I + II + III) (1106-7675mgkg-1), indicating potential for mobilization and bioavailability. Depending on environmental conditions (redox potential and pH), arsenic can redissolve and exhibit high mobility in abiotic media, which may ultimately impact the environment and human health. Therefore, it is crucial to rehabilitate the "El Lavadero" MEL to prevent further environmental damage. This study provides useful information to understand some phenomena in other global mining environmental liabilities, such as mobilization and bioavailability of arsenic and its possible impact on the surrounding environment and biota, contributing to the worldwide research of ecosystems polluted by mining activity, especially in arid and semi-arid climates.

Taxonomic revision of the genus Sarcosphaera (Ascomycota: Pezizales) in Europe and North America revealed unexpected diversity

Sarcosphaera (Ascomycota: Pezizales) is a genus of rare spring fungi, currently encompassing a single species, S. coronaria, which is red-listed in many European countries. The genus is characterized by large bright-colored fruit-bodies and high arsenic content. This study investigates the genetic diversity across Europe and North America. Using integrated molecular techniques, including ITS and 28S rDNA sequencing, we aimed to resolve the taxonomic ambiguities and assess their arsenic hyperaccumulation capabilities, a rare trait among fungi. We identified the presence of two species in the Western Palearctic (S. coronaria, S. crassa) and at least 12 additional lineages in North America, indicating a more complex taxonomic structure than previously recognized. To consolidate the taxonomy and nomenclature of these fungi, we selected reference specimens for S. coronaria and S. crassa and discussed their morphological and ecological differences. Two genera, Caulocarpa (C. montana) and Hydnotryopsis (H. setchellii), a genus comprising hypogeous fungi, are newly placed in the genus Sarcosphaera. Sarcosphaera is thus another genus where the rapid evolution of hypogeous forms from their above-ground ancestors took place. Furthermore, two new Sarcosphaera species, S. columbiana and S. pacifica, are described from the Pacific Northwest. Investigation of arsenic content of Sarcosphaera species revealed that arsenic mass fractions in ascocarps vary significantly between species and even within species across different geographical locations. Our findings have important implications for the taxonomy and conservation of the S. coronaria species complex and also point to future directions for further research in the taxonomy, geomycology, and toxicology of this group of fungi.

Hydrogeochemical processes of as enrichment and migration in the Surface’s critical zone of the Shiquan River basin in the western Qinghai–Tibet Plateau

The enrichment of As in the western Qinghai–Tibet Plateau and its surrounding basins has been widely reported. However, the spatial distribution of arsenic content in the Surface’s Critical Zone (SCZ) of the Shiquan River Basin in the western Qinghai–Tibet Plateau is poorly understood, as is the mechanisms through which water–rock interactions and surface water-groundwater interactions influence arsenic enrichment and migration. In this study, the contents of arsenic and other chemical components in surface water, groundwater, sediment, soil, and rock in the Shiquan River Basin were analyzed to investigate the hydrogeochemical process of arsenic migration. The results indicate that the concentration ratios of HCO3–/(Na++K+), Ca2+/(Na++K+), Na+/(Na++Ca2+) and δ18O in the surface water of the Shiquan River Basin vary along the runoff path. Carbonate and silicate weathering dominate the middle and upper reaches, while evaporite dissolution gradually increases in the lower reaches. Arsenic is enriched in rocks, soil, surface water, and groundwater in the SCZ, with slightly higher concentrations found in the surface water, sediment, and soil in the middle reaches than in the upper and lower reaches. This spatial distribution suggested that the hydrogeochemical processes along the runoff path controlled the distribution of As in the basin. Water–rock interactions and hot spring discharge of arsenic-bearing minerals contributed to its enrichment in the basin, while adsorption by riverbed sediment led to the gradual decay of dissolved arsenic. The underlying aquifer (alluvial-diluvial layer) recharged by surface water is the main source of high arsenic concentration in groundwater. The findings of this study can serve as a reference for studying arsenic in similar high-arsenic basins worldwide.

Effect of Curing Time and Ferric Chloride on a Copper Concentrate with a High Arsenic Content

As a result of changes in copper mineralogy, various treatment options for copper sulfides have been explored, including pretreatment processes aimed at enhancing material permeability and improving the dissolution of valuable minerals. Despite its significance, this topic has only recently gained attention. In this research, a copper concentrate with a high arsenic content was studied, with enargite (Cu3AsS4) as the main mineral phase. The objective was to evaluate the effect of pretreatment on copper extraction efficiency prior to leaching. Three key variables were investigated: curing time (0, 5, 10, and 15 days), H2SO4 dosage (0, 70, 140, and 210 kg/t), and FeCl3 concentration (0, 0.5, 1, and 1.5 M). The sample was characterized both before and after pretreatment, revealing the formation of new species such as CuSO4·5H2O and Cu2Cl(OH)3 under optimal conditions of 15 days curing time, 70 kg/t of H2SO4, and 1 M FeCl3. Copper extraction solely through curing reached 20.79%. The analysis suggests that curing time is the most influential factor in the process, accounting for 46% of the overall contribution. In comparison, sulfuric acid and ferric chloride contribute less, with 20% and 10% contributions, respectively.

Hydrothermal precipitation of copper from leaching solutions of metallurgical dusts

In this work, we aim to establish the main regularities of hydrothermal precipitation of copper from the previously unstudied sulfuric-nitric acid and sulfate solutions of atmospheric and autoclave processing of metallurgical dusts. Pyrite was used as a sulfidizer. The elemental composition of the products was determined by X-ray fluorescence, inductively coupled plasma atomic emission spectrometry, and atomic absorption analysis. It was found that copper precipitation by the proposed technology enables its recovery at a level of more than 95%. For sulfate solutions with a high arsenic concentration, a two-stage scheme of oxidation-hydrothermal treatment with the following parameters was proposed: temperature 180°С, duration 2 h, oxygen consumption 0.026 dm3/g pyrite (for the 1st stage), and 200°С and 2 h (for the 2nd stage). Extraction in the cake amounted to 95.4% of copper (in the form of Cu2S) and 91.4% of arsenic (in the form of FeAsO4), which allowed further separation of these metals by flotation. An autoclave treatment of a Cu–Zn–Fe–As–NO3 solution in the presence of pyrite at 180–220°С produced the activation energy values (kJ/mol) corresponding to the kinetic regime calculated by the two methods: 64.6 by the conventional method and 60.5 by the shrinking core model. The kinetic parameters of CuSO4–H2SO4–FeS2–H2O and CuNO3–H2SO4–FeS2–H2O systems were also determined. Flotation enrichment of copper autoclave precipitation cake was shown to result in a high degree of Cu and As separation, with the recovery amounting to Cu ˃ 95% and As ˂ 5%. Precious metals contained in pyrite are transferred to a flotation concentrate by 92.7% (Au) and 96.5% (Ag). The composition of the resulting flotation concentrate comprised (%): 12 Cu; 37 Fe; 38 S; 13 other elements. It is shown that, in order to obtain a product with the required content of copper, flotation concentrate should be separated into pyrite and copper concentrates followed by an additional flotation of primary copper concentrate in an alkaline medium in the presence of lime. Hence, our study has established the main regularities of hydrothermal precipitation of copper from the sulfuric-nitric acid and sulfate solutions of atmospheric and autoclave processing of metallurgical dusts.

Removal of Arsenic from Contaminated Water by Polypyrrole-Based Adsorbents

Worldwide, there is growing concern over the toxicity of arsenic in drinking water. The US Environmental Protection Agency and Central Pollution Control Board (India) have set a safe limit of 50 parts per billion for arsenic in drinking water. Millions of people are at immediate risk due to high concentrations of arsenic in drinking water, particularly in developing nations where arsenic poisoning symptoms have been observed. One of the essential techniques described in this article is the absorption of arsenic from contaminated water by sustainable cellulosic materials like jute and wood sawdust after suitable modification. Jute and sawdust are cheap and abundantly available in South Asia. They are functionalized with polypyrrole coating by in situ chemical polymerization of pyrrole in aqueous medium in the presence of ferric chloride. Polypyrrole-coated jute fabric (with 11.28% polypyrrole add-on) and polypyrrole-coated sawdust (with 5.28% polypyrrole add-on) are found to be excellent adsorbers of arsenic ion (As3+) from water. The effect of dosage of polypyrrole-coated adsorbents, treatment time and pyrrole concentration on the As removal efficiency have been investigated in this work. The arsenic concentration in water is determined using a microwave plasma atomic emission spectrometer with the highest level of accuracy. Maximum As removal efficiency by the polypyrrole-coated sawdust and polypyrrole-coated jute fabric is found to be 80.90% and 97.3%, respectively, from a 50 mL, 7.5 parts per million As solution with a dosage of 1 g at neutral pH. The polypyrrole-coated jute and sawdust are characterized by Fourier-transform infrared spectroscopy to understand the chemical interaction between cellulose and polypyrrole molecules. The scanning electron microscope studies reveal a uniform coating of polypyrrole around the surface of jute fibre and sawdust particles. Thermo-gravimetric analysis shows good thermal stability of jute and sawdust after polypyrrole coating.

Feasibility of riverbank filtration in Vietnam

Riverbank filtration (RBF) could contribute to meeting the growing demand for drinking water in Vietnam. This study investigates the feasibility of implementing RBF in different regions of Vietnam, with a focus on the Red River Delta (RRD) and Binh Dinh (a province in central Vietnam). Although Vietnam’s extensive river network and shallow aquifers generally provide favorable hydrogeological conditions for RBF, regional variations in hydrogeology introduce specific challenges. In the RRD, complex hydrogeological settings, such as thick clay layers near the surface and low hydraulic conductivity in the Holocence aquifer, can limit the effectiveness of RBF in maximizing the portion of bank filtrate and improving water quality. In contrast, Binh Dinh generally presents more favorable conditions, with absence of clay layers on top and higher hydraulic conductivity leading to successful RBF implementation. Water quality issues such as high concentrations of ammonium, arsenic, and other pollutants persist in both RBF and groundwater in the RRD, requiring careful site-specific evaluations. The study also highlights that while surface water remains underutilized compared to groundwater, its use may be economically preferable in regions where groundwater quality is compromised. Lessons learned from the RRD and Binh Dinh can serve as good practice for RBF implementation in other parts of Vietnam. The findings indicate that while RBF holds significant promise for enhancing water supply in Vietnam, its application needs to be carefully tailored to local hydrogeological and water quality conditions.

Evaluation of the Bioavailability of Iodine and Arsenic in Raw and Cooked Saccharina japonica Based on Simulated Digestion/Caco-2 Cell Model.

Kelp is a traditional healthy food due to its high nutritional content; however, its relatively high contents of iodine and arsenic have raised concerns about its edible safety. This study explored the effects of different cooking treatments on the contents of iodine and arsenic in kelp, evaluated the bioaccessibility and bioavailability of iodine and arsenic in kelp using in vitro digestion, and compared the differences in the transport characteristics of iodine in kelp and KIO3 using a Caco-2 monolayer cell transport model. The results show that the content of target elements that reached systemic circulation could be reduced by cooking and gastrointestinal digestion. The highest reductions in iodine and arsenic were 94.4% and 74.7%, respectively, which were achieved by boiling for 10 min. The bioaccessibility and bioavailability of iodine and arsenic were significantly improved by a cooking treatment. However, the contents of iodine and arsenic decreased significantly, with the bioaccessibility of iodine reducing from 3188.2 μg/L to 317.0 μg/L and that of arsenic reducing from 32.5 μg/L to 18.1 μg/L in the gastric phase after boiling. The findings also show that the efficiency of iodine transport in kelp and KIO3 was positively correlated with the transport time and negatively correlated with the concentration of iodine. With the increase in the iodine concentration, the rate of iodine transport in kelp decreased from 63.93% to 3.14%, but that of KIO3 was stable at around 35%, which indicates that the absorption efficiency of iodine from kelp was limited, even when too much kelp was ingested. In conclusion, the edible safety of kelp is significantly improved after cooking. The risk of excessive iodine and arsenic intake caused by consuming kelp is extremely low, and as an effective iodine supplement source, kelp has higher edible safety compared with KIO3. This study clarifies the safety of algae based on iodine and arsenic contents and also provides a basis for the formulation of food safety standards.

Potential of Heavy Metals and Microplastics Contamination in River Mpanga, Fort Portal, Kabarole District, Uganda

Anthropogenic environmental pollution is a major development challenge in Ugandan rivers and lakes, the key drivers being industrialization, agriculture, and urbanization. The aim of the study was to assess the potential of heavy metal and microplastic contamination in River Mpanga, Fort Portal, Uganda. Triplicate water and sediment samples were collected from three sampling sites, preserved, and analyzed at the Chemistry Department, Makerere University for heavy metals, while microplastics analysis was conducted at NaFIRRI, Jinja. Sediment heavy metal contamination was assessed from the geoaccumulation index, while microplastic characterization and quantification were determined from stereomicroscopy and morphological features. Arsenic was the most prevalent metal with a mean concentration of 13.2 ppm thus higher than permissible maximum limits of WHO. The mean concentrations (ppm) of copper, lead, and cadmium were 0.01, 0.01, and 0.001 respectively, and below the permissible maximum. Sediment samples revealed very strong arsenic contamination, strong contamination for copper, moderate to strong contamination for lead, and a potential lack of contamination for cadmium. The higher concentrations of the heavy metals in the sediments compared to water could be attributed to bioaccumulation, as evidenced by the high geoaccumulation values. Microplastics occurred throughout the river and included fragments, filaments, film, pellets, form, and fibers. The presence of heavy metals and microplastics was attributed to anthropogenic activities within the river vicinity, which discharged heavy metal-laden waste into River Mpanga. High arsenic concentrations and sediment accumulation of contaminants pose serious potential public health threats to the local communities.

Turning waste into wonder: Arsenic removal using rice husk based activated carbon

In this study, rice husk activated carbon (RHAC) was synthesized by physicochemical activation, which consists of heat treatment with CO2 gasification and KOH chemical treatment to eliminate arsenic (As) from the polluted water. Initial arsenic concentrations, solution pH, solution temperature and contact time are the parameters that have been tested in this study. The characterization study showed that RHAC has a high BET surface area (815.52 m2/g) and its pore structure was found to be mesoporous with an average pore diameter of 2.96 nm. Characterization studies, including X-ray diffraction analysis (XRD), Raman spectroscopy and scanning electron microscopy (SEM) were employed to determine the RHAC’s performance. The adsorption of As towards RHAC followed the Freundlich isotherm model and pseudo-first order with adsorption process was favorable at higher arsenic concentrations. The mechanism study also signified that the adsorption of As-RHAC was limited by film-diffusion. Thermodynamic studies indicated that the As-RHAC adsorption system was endothermic, random, spontaneous, feasible in nature and governed by the chemisorption process. Desorption and regeneration studies of RHAC showed that it can be utilized up to 5 cycles and is stable for the water treatment facilities.

Concurrent elimination of arsenic and nitrate from aqueous environments through a novel nanocomposite: Fe3O4-ZIF8@eggshell membrane matrix

The high concentration of nitrate and arsenic as potentially toxic elements (PTEs) with carcinogenic properties in many groundwater sources worldwide is a concern for health and the environment. This work checked the capacity of a novel nanocomposite, Fe3O4-ZIF8@eggshell membrane matrix (F-ZIF8@EMM) for concurrently eliminating arsenic and nitrate, two of the most encountered hazardous pollutants in drinking water. Contact time (30–120 min), pH (3–10), initial arsenic concentration (25–100 μg/L), initial nitrate concentration (60–120 mg/L) and adsorbent dose (0.25–5 mg/L) as various operating influences were investigated on the co-adsorption of arsenic and nitrate from water by a new nanocomposite thru diverse experimental tests. Characteristics of F-ZIF8@EMM were determined through X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), Fourier transform infrared spectroscopy (FTIR) and Brunauer–Emmett–Teller (BET) analyses. Taguchi model was used to determine the optimal co-adsorption conditions. The results revealed that the optimal conditions for the simultaneous adsorption of 94.32 % of these two elements were at pH = 7, adsorbent dose 1 mg/L, primary nitrate concentration 120 mg/L, initial arsenic concentration 100 μg/L, and contact time 90 min. Correspondingly, the simultaneous adsorption of arsenic and nitrate best fit the Langmuir isotherm, and the pseudo-second-order (PSO) model was the best model that fitted with experimental kinetic data (R2 = 1). The maximum experimental adsorption capacity of F-ZIF8@EMM was 128.5 mg/g. This study indicated that the efficiency of nanocomposite F-ZIF8@EMM in the co-adsorption of arsenic and nitrate was promising.

Extraction of arsenic from fine dust of copper smelters by reduction roasting with natural gas

One of the current trends in the complex processing of fine dust from copper smelters is their direct leaching with sulfuric acid. As practical results show, high reliable technological parameters are not achieved due to the high content of arsenic in dust. During sulfuric acid leaching of dust, arsenic is distributed between the lead cake and the solution at a ratio of 40 and 60%, respectively. The redistribution of arsenic between leaching products significantly reduces the technological performance and leads to the accumulation of arsenic in the technological scheme. The paper presents the results of comprehensive studies of the elemental and phase composition of fine dust from one of the copper smelters in Kazakhstan. In the initial dust, along with the main phases presented in the form of lead and zinc sulfate, the following typical components were found: oxides of copper, lead, zinc and copper and zinc ferrites. Arsenic is found in two forms—As(III) and As(V). The laboratory installation and technique for conducting reduction roasting of dust with natural gas are presented. The influence of roasting duration, temperature and natural gas consumption on the extraction of arsenic from dust was studied. It has been established that almost complete, up to 99%, extraction of arsenic from dust is achieved with optimal technological roasting parameters: duration τ = 40 min.; natural gas consumption is 1.5 times higher than the stoichiometrically required amount for the reduction of As2O5, and temperature 500 °C.

Trace Elements Anomalous Concentrations in Building Materials-The Impact of Secondary Mineralisation Processes.

The Pb, Cr, Cd, Ni, Zn, Cu, Co, As, Sr, Ba, and Zr content has been determined in the tested rock raw materials. The concentration of cadmium (Cd) was found to be elevated in all types of rock materials and was found on average to be: 1.39 mg/kg in limestones, 0.86 mg/kg-sandstones, 0.44 mg/kg-diatomites, 0.55 mg/kg-opoka rocks, 0.89 mg/kg-marls, 0.21 mg/kg-gaizes 0.42 mg/kg-kaolin clays, and 2.13 mg/kg-decalcified opoka rocks. Higher concentrations of arsenic (As) have also been recorded in sandstones and diatomites, as well as lead (Pb) in limestones and sandstones. The results obtained indicate that the anomalous level of elements is of natural origin and the results of identified secondary mineralisation processes that have affected the tested materials. Pyritization and sulfatization processes have been detected. Mineralogical research has shown that these processes can be associated with the activity of biochemical processes caused by the decomposition of the soft tissues of animal organisms and the organic substances of plant origin that fill the stylolites. It has been shown that the content of strontium (Sr) increases in geologically older Jurassic formations compared to younger Cretaceous formations, which can be used in the monitoring of building materials.

From Inundations to Golden Opportunity: Turning Holopelagic Sargassum spp. into a Valuable Feed Ingredient through Arsenic Removal

For over a decade, numerous Greater Caribbean and Western African coasts have received enormous masses of holopelagic Sargassum spp. (sargasso). A promising use of this beached biomass as a feed ingredient in the animal industry is restricted by its high arsenic (As) content. This proof of concept aimed to demonstrate that simple, low-cost processes involving hot water (either fresh or seawater) and/or citric acid can remove arsenic from the sargasso. Sargasso collected from a Mexican Caribbean beach in December 2023 had a total arsenic level of 62.2 mg/kg, which decreased to 7.2 mg/kg after treatment with hot freshwater (90 °C for 15 min), and then further decreased to 0.8 mg/kg when followed up with a citric acid treatment. Sargasso collected in March 2024 had total arsenic of 89 mg/kg, which was lowered to 2.6 mg/kg by applying hot freshwater and citric acid sequentially. Employing only citric acid reduced the arsenic concentration to 8.0 mg/kg, while treating the sargasso only with hot seawater reduced the As level to 10.1 mg/kg. Thus, simply using hot water, either fresh or seawater, lowered the arsenic levels to acceptable levels for the animal feeding sector. These straightforward and potentially cost-effective methods may transform the restraint of high arsenic contents into a valuable opportunity to use these seaweeds as animal feed.

Functional genomics and taxonomic insights into heavymetaltolerant novel bacterium Brevibacterium metallidurans sp. nov. NCCP-602T isolated from tannery effluent in Pakistan.

The strain designated NCCP-602T was isolated from tannery effluent, and displayed aerobic, gram-positive, rod-shaped cells that were characterized by oxidase negative, catalase positive, and non-motile features. The most favourable growth conditions were observed at a temperature of 30°C, pH 7.0, and NaCl concentration of 1% (w/v). It tolerated heavy metals at high concentrations of chromium (3600 ppm), copper (3300 ppm), cadmium (3000 ppm), arsenic (1200 ppm) and lead (1500 ppm). The results of phylogenetic analysis, derived from sequences of the 16S rRNA gene, indicated the position of strain NCCP-602T within genus Brevibacterium and showed that it was closely related to Brevibacterium ammoniilyticum JCM 17537T. Strain NCCP-602T formed a robust branch that was clearly separate from closely related taxa. A comparison of 16S rRNA gene sequence similarity and dDDH values between the closely related type strains and strain NCCP-602T provided additional evidence supporting the classification of strain NCCP-602T as a distinct novel genospecies. The polar lipid profile included diphosphatidylglycerol, glycolipid, phospholipids and amino lipids. MK-7 and MK-8 were found as the respiratory quinones, while anteiso-C15:0, iso-C15:0, iso-C16:0, iso-C17:0, and anteiso-C17:0 were identified as the predominant cellular fatty acids (> 10%). Considering the convergence of phylogenetic, phenotypic, chemotaxonomic, and genotypic traits, it is suggested that strain NCCP-602T be classified as a distinct species Brevibacterium metallidurans sp. nov. within genus Brevibacterium with type strain NCCP-602T (JCM 18882T = CGMCC1.62055T).

Safety assurance and nutritional quality enhancement of Phyllospora comosa biomass using hydrothermal treatment derived ensemble machine learning models

One of the major barriers to the mass industrial utilisation of brown seaweeds as food sources stem from the food safety risks associated with their iodine and arsenic concentrations, which typically exceed regulatory limits. Hydrothermal treatments might effectively reduce the high iodine and arsenic concentration of Phyllospora comosa below the Australian maximum residual limits (iodine = 1 mg/g and arsenic = 0.00667 mg/g; dry weight) set for brown seaweeds. The experimental hydrothermal treatments dictated that the 82 °C–250 s treatment reduced the iodine concentration from 2.76 mg/g to 0.88 mg/g (68% reduction) and arsenic concentration from 0.01693 mg/g to 0.00965 mg/g (43% reduction). Machine learning models predicted that blanching at 100 °C for ∼4 minutes will reduce the arsenic concentration below its maximum residual limit. Additive log-ratio transformations showed that around 50% (dw) of the hydrothermally treated Phyllospora comosa samples were leached out during the highest treatment intensity, 82 °C–250 s. Even though, a half of the biomass is lost, hydrothermally treated Phyllospora comosa products are safer for human consumption and thus may permit the expansion of seaweed production and consumption in Australia.

Ultra-efficient peroxymonosulfate utilization and trichloroethylene degradation in heterogeneous catalytic system guided by sheet-like Cu2MnO4 nanoparticles: The role of Cu(III)–O species and free radicals

Synthesizing cubic spinel Cu2MnO4 with nanosheet structure (SCMO) aimed to construct a “non-radical-mediated radical-oxidative reaction”, for increasing PMS utilization efficiency, and solving the defects of SO4•− and •OH through indirect PMS activation by electron transfer process. Compared with box-like Cu2MnO4 (11.1%, 0.0035 min−1) and ordinary Cu2MnO4 nanoparticles (21.3%, 0.0070 min−1), SCMO/PMS showed excellent trichloroethylene removal (98.8%, 0.1577 min−1). The pivotal role of Cu(III) was determined based on EPR analysis, quenching experiments, chemical probe experiments, hydrogen temperature-programmed reduction and Raman spectroscopy analysis, in-situ FTIR and Raman analyses. In brief, the interaction between PMS and SCMO could produce surface-bonded reactive complexes and the subsequent breaking of O–O bond in the sub-stable structure allowed the conversion of Cu(II) to Cu(III), which in turn facilitates the generation of •OH and SO4•−. The density functional theory (DFT) calculations provided supporting evidence for the electron donor role of SCMO and the increase of the electron acceptance capacity of PMS. SCMO/PMS system showed good resistance and degradation efficiency to complex composition and combined pollutants in actually contaminated groundwater, respectively. However, the coexistence of high concentrations of arsenic could significantly affect SCMO performance due to their adsorption on –OH groups, which still need in-depth study.

Toxicological risk assessment using spring water quality indices in plateaus of Giresun Province/Türkiye: a holistic hydrogeochemical data analysis

Water scarcity is a growing concern due to rapid urbanization and population growth. This study assesses spring water quality at 20 stations in Giresun province, Türkiye, focusing on potentially toxic elements and physicochemical parameters. The Water Quality Index rated most samples as "excellent" during the rainy season and "good" during the dry season, except at stations 4 (40° 35′ 12″ North/38° 26′ 34″ East) and 19 (40° 44′ 28″ North/38° 06′ 53″ West), indicating "poor" quality. Mean macro-element concentrations (mg/L) were: Ca (34.27), Na (10.36), Mg (8.26), and K (1.48). Mean trace element values (μg/L) were: Al (1093), Zn (110.54), Fe (67.45), Mn (23.03), Cu (9.79), As (3.75), Ni (3.00), Cr (2.84), Pb (2.70), Co (1.93), and Cd (0.76). Health risk assessments showed minimal non-carcinogenic risks, while carcinogenic risk from arsenic slightly exceeded safe limits (CR = 1.75E−04). Higher arsenic concentrations during the rainy season were due to increased recharge, arsenic-laden surface runoff, and human activities. Statistical analyses (PCA, PCC, HCA) suggested that metals and physico-chemical parameters originated from lithogenic, anthropogenic, or mixed sources. Regular monitoring of spring water is recommended to mitigate potential public health risks from waterborne contaminants.

Assessment of heavy metals and its treatment through phytoremediation in groundwater along River Kabul in district Charsadda

Life cannot exist without water. Water scarcity is caused by massive groundwater decline. Water contamination is the most common problem spreading worldwide quicker than ever, along with anthropogenic water scarcity. Since tainted water can harm health, water contamination is also contributing to water scarcity. Heavy metals in drinking water have plagued most Asian, African, and European nations for decades. Studies reveal that heavy metals have caused damage in Pakistan, India, and China. This study detects heavy metals in groundwater and treats them with phytoremediation along the river Kabul in district Charsadda. It also measures pH, EC, TDS, turbidity, fluoride, phosphates, nitrites, and nitrates. All indicators meet the WHO and national environmental quality criteria for drinking water, except for turbidity, which exceeds the limit of ≤5 NTU in four examined regions, reaching a maximum of 9.99 NTU. Chemical parameters were within the standard limits, except for high concentrations of arsenic (As) and cadmium (Cd) in samples from S2 (15.20 μg/L) and S1 (20.50 μg/L) compared to WHO’s 10 and 5 μg/L standards. However, the limit is within EPA Pakistan’s 50 and 100 μg/L standards for drinking water, which Pakistan still follows. Heavy metals can harm health, even at low levels. Since the majority of the study area’s population relies on groundwater for drinking and other needs, heavy metal pollution of the groundwater can cause many ailments. Thus, phytoremediation is increasingly vital to reduce these heavy metals to WHO limits to protect human health and the environment.

Arsenic accumulation in spolic technosols in the area of a large copper smelting plant in the Middle Urals

Relevance. The necessity to study arsenic behaviour in soils as one of the main pollutants of depositing environments in areas of mining and metallurgical industry. In recent decades, arsenic emissions into the environment have reached a huge scale, so this element attracts the attention of researchers around the world. But in spite of all the studies of this problem, there are still some aspects that need to be clarified to understand the geochemistry of arsenic. This paper deals with spolic technosols with critically high arsenic content in the soil profile with alternating water-logged and dry conditions. As one of the main soil-forming elements, orthosteins contain significant amounts of iron and manganese compounds and are capable of adsorption and involvement of the elements in nodule formation. Aim. To determine the influence of orthosteins on arsenic accumulation in soil subjected to intensive anthropogenic load. Object. Ortsteins spolic technosols in the zone of operation of copper smelting plant and background soils not exposed to pollution. Methods. Arsenic was determined by inversion voltammetry method. Morphological characterisation and patterning of the orthosteins were performed by scanning electron microscopy using a Thermo Fisher Phenom XL G2 Desktop SEM unit. Results. The study of morphological features of orthosteins revealed differences in soils subjected to greater anthropogenic load. Arsenic was not detected inside the orthosteins in all studied soils. Also arsenic concentrations in the total mass of ortstein is up to 40–50% of the soil mass. This fact indicates the accumulation of arsenic by surface adsorption and the appearance of orthosteins as a geochemical barrier. The data obtained in the course of this work can contribute to the search for ways to clean up soils contaminated with arsenic, as well as provide an understanding of the basic processes of the behaviour of this element in soil formation.