Search Results (131)

This study addresses the microbial corrosion of cement-based materials in coastal urban sewer networks, systematically investigating the kinetic mechanisms of sulfur biogeochemical cycling under seawater infiltration conditions. Through dynamic monitoring of sulfide concentrations and environmental parameter variations in anaerobic pipelines, a multiphase coupled kinetic model integrating liquid-phase, gas-phase, and biofilm metabolic processes was developed. The results demonstrate that moderate salinity enhances the activity of sulfate-reducing bacteria (SRB) and accelerates sulfate reduction rates, whereas excessive sulfide accumulation inhibits SRB activity. At 35 °C, the mathematical model coefficient “a” for sulfate reduction in the reactor with 3 g/L salinity was significantly higher than those in reactors with 19 g/L and 35 g/L salinities, with no significant difference observed between the latter two. Overall, high sulfate concentrations do not act as limiting factors for sulfide oxidation under anaerobic conditions; instead, they enhance the reaction within specific concentration ranges. The refined kinetic model enables prediction of sulfur speciation in tropical coastal urban sewer pipelines, providing a scientific basis for corrosion risk assessment. Full article

Active and abandoned mining sites are significant sources of heavy metals and metalloid pollution, leading to serious environmental issues. This study assessed the environmental risks posed by potentially toxic elements (PTEs), specifically arsenic (As) and antimony (Sb), in the Technosols (mining residues) of the former Pejão coal mine complex in Northern Portugal, a site impacted by forest wildfires in October 2017 that triggered underground combustion within the waste heaps. Our methodology involved determining the “pseudo-total” concentrations of As and Sb in the collected heap samples using microwave digestion with aqua regia (ISO 12914), followed by analysis using hydride generation-atomic absorption spectroscopy (HG-AAS). The concentrations of As an Sb ranging from 31.0 to 68.6 mg kg⁻¹ and 4.8 to 8.3 mg kg⁻¹, respectively, were found to be above the European background values reported in project FOREGS (11.6 mg kg⁻¹ for As and 1.04 mg kg⁻¹ for Sb) and Portuguese Environment Agency (APA) reference values for agricultural soils (11 mg kg⁻¹ for As and 7.5 mg kg⁻¹ for Sb), indicating significant enrichment of these PTEs. Based on average I_geo values, As contamination overall was classified as “unpolluted to moderately polluted” while Sb contamination was classified as “moderately polluted” in the waste pile samples and “unpolluted to moderately polluted” in the downhill soil samples. However, total PTE content alone is insufficient for a comprehensive environmental risk assessment. Therefore, further studies on As and Sb fractionation and speciation were conducted using the Shiowatana sequential extraction procedure (SEP). The results showed that As and Sb levels in the more mobile fractions were not significant. This suggests that the enrichment in the burned (BCW) and unburned (UCW) coal waste areas of the mine is likely due to the stockpiling of lithic fragments, primarily coals hosting arsenian pyrites and stibnite which largely traps these elements within its crystalline structure. The observed enrichment in downhill soils (DS) is attributed to mechanical weathering, rock fragment erosion, and transport processes. Given the strong association of these elements with solid phases, the risk of leaching into surface waters and aquifers is considered low. This work underscores the importance of a holistic approach to environmental risk assessment at former mining sites, contributing to the development of sustainable remediation strategies for long-term environmental protection. Full article

The widespread implementation of anaerobic digestion (AD) systems for organic waste treatment is increasingly challenged by emerging contaminants, including microplastics (MPs), antibiotics, and heavy metals (HMs), which exhibit environmental persistence and pose risks to ecological and human health. This review critically examines the sources, transformation pathways, and advanced mitigation strategies for these contaminants within AD systems. MPs, primarily derived from fragmented plastics and personal care products, accumulate in digestates and act as vectors for adsorbing toxic additives and pathogens. Antibiotics, introduced via livestock manure and wastewater, exert selective pressures that propagate antibiotic resistance genes (ARGs) while disrupting methanogenic consortia. HMs, originating from industrial and agricultural activities, impair microbial activity through bioaccumulation and enzymatic interference, with their bioavailability modulated by speciation shifts during digestion. To combat these challenges, promising mitigation approaches include the following: (1) bioaugmentation with specialized microbial consortia to enhance contaminant degradation and stabilize HMs; (2) thermal hydrolysis pretreatment to break down MPs and antibiotic residues; (3) chemical passivation using biochar or sulfides to immobilize HMs. Co-digestion practices inadvertently concentrate these contaminants, with MPs and HMs predominantly partitioning into solid phases, while antibiotics persist in both liquid and solid fractions. These findings highlight the urgency of optimizing mitigation strategies to minimize contaminant mobility and toxicity. However, critical knowledge gaps persist regarding the long-term impacts of biodegradable MPs, antibiotic transformation byproducts, and standardized regulatory thresholds for contaminant residues in digestate. This synthesis underscores the necessity for integrated engineering solutions and policy frameworks to ensure the safe resource recovery from AD systems, balancing energy production with environmental sustainability. Full article

Cadmium (Cd) mobilization in paddy soils during redox fluctuations poses significant risks to rice safety. This study investigated the efficacy of nano-calcium carbonate (NCC), nano-hydroxyapatite (NHAP), and their composite (C+P) in immobilizing Cd under simulated flooding–drainage cycles. Soil treatments (0.5% and 1.0% w/w) were subjected to 40 day anaerobic and 20 day aerobic incubation. The results demonstrated that NCC and C+P elevated the soil pH by 1.35–1.39 and 0.72–1.01 units during the anaerobic and aerobic phases, respectively. These amendments suppressed Fe(II) and Mn(II) release by 41–75%, correlating with reduced Cd bioavailability. While nanomaterials minimally influenced Cd speciation during flooding, aerobic conditions triggered a marked shift: residual Cd fractions increased by 80.8–116.4% under NCC, driven by CdCO₃ precipitation and phosphate complexation. Cd release rates decreased by 53.6–66.8% in NCC and C+P treatments during oxidation. Microbial analysis revealed diminished bacterial diversity but enriched Firmicutes (up to 58.9%), which positively correlated with pH and residual Cd. Redundancy analysis identified pH and Fe/Mn dynamics as key regulators of the microbial community structure. NCC emerged as the most effective amendment. This study highlights the potential of NCC-based strategies for mitigating Cd risks in acidic paddy soils, particularly during post-flooding drainage. Full article

The microbial conversion of inorganic Se into bioactive organoselenium compounds represents a cutting-edge strategy for developing functional foods with enhanced nutritional value. This study introduces Lactiplantibacillus plantarum S1, a novel Se-enriched probiotic strain isolated from traditional Chinese sauerkraut, and systematically optimizes its capacity for selenite biotransformation. Critical fermentation parameters—including sodium selenite supplementation timing (2 μg/mL added at mid-log phase, 7 h post-inoculation), pH (5.0), and anaerobic cultivation duration (12 h)—were identified as key determinants of conversion efficiency. The optimized protocol achieved a 72.3% organoselenium conversion yield, producing 626.6 μg/g cellular organoselenium while maintaining probiotic viability (2.28 × 10⁹ CFU/mL). Se speciation analysis demonstrated that 78.51% of intracellular Se existed in organic forms, with protein-bound Se constituting the predominant fraction (85.33%), followed by polysaccharide-associated (6.42%) and nucleic acid-linked (3.38%) species. The strain’s dual functionality as both an efficient Se bioconverter and a resilient probiotic carrier highlights its potential for nutraceutical applications. These findings not only establish a robust bioprocess for Se-enriched probiotic production but also reveal mechanistic insights into preferential Se incorporation into protein matrices. This work bridges microbial Se metabolism research with scalable functional food innovation, offering a sustainable platform for developing Se-fortified products with dual health benefits. Full article

The antihypertensive drugs indapamide, atenolol, metoprolol, propranolol and bisoprolol were considered in this research. Because they have structures that are affected by pH, developing a chromatographic method was challenging. Based on the speciation diagram of these compounds versus pH scale, a mixed-mode stationary phase (hydrophobic stationary phase, C18 and strong cation exchanger (SCX)) was our first choice. Design of Experiments (DoE) was used to estimate how various factors such as pH, mobile phase composition and flow rate influenced chromatographic performance. As a result, the separation was achieved in 24 min using an aqueous phosphate buffer phase (pH 7.20) and 20 mM triethylamine, with methanol being used as organic modifier (30%). Their retention mechanism was investigated. The new method was validated in term of linearity, limits of detection and quantification, precision, accuracy, and robustness. The method was applied to river water samples, and good results were obtained. Full article

Sexual selection is a major driver of speciation and evolution, with mate choice being a key component. Individuals assess mate quality by integrating various mating cues. The Western mosquitofish (Gambusia affinis), a species exhibiting pronounced sexual dimorphism in body size and secondary sexual traits, serves as an ideal model for studying mate choice. This study examines the impact of mating cues on mate choice in different sexes of G. affinis through a combination of morphological parameter database construction, computer-simulated animations, and dichotomous association preference tests. The results showed that male gonopodium status significantly affects female mate choice. Females exhibited a preference for males with resting-phase gonopodia, suggesting their aversion to forced copulation and sexual harassment in coercive mating systems. Furthermore, males preferred younger females, with this preference being positively correlated with male body size. This suggests that males are sensitive to sperm competition intensity and may base their choice on social rank. Geometric morphometric analysis and simulation experiments showed that males preferred females with larger gravid spots, regardless of age, suggesting that gravid spot size reflects female fecundity. Male preference for younger females with streamlined bodies and smaller abdomens was significant, but body size did not affect mate choice in general. Our findings highlight that female and male G. affinis employ different mate choice strategies, with females prioritizing male harassment avoidance and males considering multiple mating cues, not solely one dominant characteristic, in their mate choice decisions. These findings demonstrate that mate choice in G. affinis involves balancing conflicting preferences for traits associated with reduced harassment risk (e.g., resting-phase gonopodium in males) and those linked to reproductive potential (e.g., large gravid spot in females), highlighting the nuanced decision-making processes in both sexes. Full article

A sol-gel approach was used to prepare a thin hydrogel membrane based on an organic-inorganic polymer matrix embedded with pre-synthesized gold nanoparticles (AuNPs). The organic polymers utilized were poly(vinyl alcohol) (PVA) and poly(ethylene oxide) 400 (PEO) while tetraethoxysilane (TEOS) served as a precursor for the inorganic silica polymer. AuNPs were synthesized using D-glucose as a reducing agent and starch as a capping agent. A mixture of PVA, PEO, pre-hydrolyzed TEOS, and AuNP dispersions was cast and dried at 50 °C to obtain the hybrid hydrogel membrane. The structure, morphology, and optical properties of the nanocomposite membrane were analyzed using TEM, SEM, XRD, and UV-Vis spectroscopy. The newly designed hybrid hydrogel membrane was utilized as an efficient sorbent for the simultaneous speciation analysis of valence species of chromium and manganese in water samples via solid-phase extraction. This study revealed that Cr(III) and Mn(II) could be simultaneously adsorbed onto the PVA/PEO/SiO₂/AuNP membrane at pH 9 while Cr(VI) and Mn(VII) remained in solution due to their inability to bind under these conditions. Under optimized parameters, detection limits and relative standard deviations were determined for chromium and manganese species. The developed analytical method was successfully applied for the simultaneous speciation analysis of chromium and manganese in drinking water and wastewater samples. Full article

Although total selenium content is still useful in many areas, knowledge of its speciation is gaining importance as its various chemical forms have different environmental effects, toxicities and biological utilization. Among several methods used for the isolation and enrichment of selenium species, solid-phase extraction and its alternative approaches are often applied due to their simplicity and high efficiency. This brief overview summarizes the progress made in using different nanostructure sorbents to separate and preconcentrate inorganic selenium species in environmental waters. Nanomaterials are finding increasing applications as they have a large specific surface area and high chemical stability. Functionalizing their surface by covalent or noncovalent interactions with other components, grafting or doping with heteroatoms can improve the separation and removal efficiency. Strategies based on combining selective chemical reactions and separation procedures are discussed. Full article

Tellurium, recognized as one of the technology-critical elements, should be considered as a xenobiotic. Its application, i.a. in the growing photovoltaic industry, raises concerns about Te(IV) and Te(VI) release to the environment. As both forms differ in mobility and toxicity, Te speciation should be included in water monitoring, but problems with speciation changes occurring during sampling, transport, and sample storage require the use of on-site separation of Te forms. A simple procedure based on solid phase extraction (SPE) with the anionic exchange mechanism (SAX, involving commercially available columns), followed by their quantification with elemental techniques, has a high potential for implementation in routine analysis. The proposed SPE-ICP-MS (inductively coupled plasma mass spectrometry) method allows direct analysis of Te(VI) and Te(IV), with Te(IV) determined after elution from the column. The detection limits obtained for the 5.0 mL sample are 0.02 ng mL⁻¹ and 0.05 ng mL⁻¹ for Te(VI) and Te(IV), respectively. Hydride generation inductively coupled plasma optical emission spectrometry (HG-ICP-OES) was used to control possible changes in tellurium speciation occurring during species isolation using SPE. The simple and fast water pretreatment proposed here offers the possibility of separating Te(IV) and Te(VI) at the sampling site, and the elution of Te(IV) does not have to be conducted on-site. Application to the river water and seawater matrix proved the feasibility of incorporating Te speciation analysis into routine water analysis. Full article

Existing studies have demonstrated the positive effects of nano-sized iron oxide on compost maturity, yet the impact of nano-sized iron oxide on phosphorus speciation and bacterial communities during the composting process remains unclear. In this study, pig manure and straw were used as raw materials, with biochar-supported nano-sized iron oxide (BC-Fe₃O₄NPs) as an additive and calcium peroxide (CaO₂) as a co-agent, to conduct an aerobic composting experiment with pig manure. Four treatments were tested: CK (control), F1 (1% BC-Fe₃O₄NPs), F2 (5% BC-Fe₃O₄NPs), and F3 (5% BC-Fe₃O₄NPs + 5% CaO₂). Key findings include the following. (1) BC-Fe₃O₄NPs increased compost temperatures, with F3 reaching 61℃; F1 showed optimal maturity (C/N ratio: 12.90). (2) BC-Fe₃O₄NPs promoted stable phosphorus forms; Residual-P proportions were higher in F1, F2, and F3 (25.81%, 51.16%, 51.68%) than CK (19.32%). (3) Bacterial phyla Firmicutes, Actinobacteria, and Proteobacteria dominated. BC-Fe₃O₄NPs altered community composition, especially on day 7. Firmicutes dominated CK, F1, and F3; Proteobacteria dominated F2. At the genus level, day 7 showed Corynebacterium (CK), Clostridum (F1, F3), and Caldibacillus (F2) as predominant. (4) Pearson correlation analysis revealed shifted correlations between phosphorus forms and bacterial phyla after BC-Fe₃O₄NPs addition. Firmicutes positively correlated with NaOH-OP in F1 during the thermophilic phase, facilitating phosphate release and adsorption by BC-Fe₃O₄NPs. The significance of correlations diminished with increasing additive concentration; in F3, all phyla positively correlated with various phosphorus forms. Full article

Geogenic chromium (Cr) and vanadium (V) contamination of groundwater in the Piedmont region of North Carolina poses threats to public health. These contaminants are naturally derived from saprolite and aquifer materials, but geochemical variability in these materials makes it difficult to predict specific risks of Cr and V in well water. The objectives of this study were to (1) determine host phases of Cr and V in representative subsurface materials; (2) characterize contaminant binding parameters of chemically variable saprolites; and (3) examine the influence of saprolite chemistry on contaminant sorption, speciation, and phase associations. Isotherm experiments revealed that saprolite samples sorbed roughly an order of magnitude more V than Cr. Chemical extractions and synchrotron-based X-ray fluorescence showed that substantial Cr and V were bound with metal oxide/oxyhydroxides in native and Cr-and V-sorbed saprolites; however, electrostatically bound fractions were also present, representing potentially important sources of groundwater contamination. X-ray absorption-near-edge-structure spectroscopy indicated that sorbed Cr was found as reduced Cr(III), whereas sorbed V was dominated by the oxidized V(V) and intermediate V(IV) species. Results from this study could be used to help parameterize mechanistic models and improve prediction of the Cr and V contamination potential of shallow aquifers. Full article

The oxidative desulfurization (ODS) of heavy fuel oil (HFO) offers a promising solution for desulfurizing marine fuels under mild conditions, in line with current environmental regulations. While most studies focus on model or light fuels, explaining deactivation through leaching or sulfone adsorption, the deactivation mechanisms of catalysts in HFO remain poorly understood. In this work, Mo-based catalysts supported on alumina were extensively characterized before and after catalytic reactions, and regeneration through air calcination was considered. Techniques such as XRD, Raman spectroscopy, XRF, and TGA, alongside catalytic testing with H₂O₂ as an oxidant, revealed that Mo surface speciation significantly impacted both activity and deactivation. Contrary to well-dispersed polymolybdates, crystalline MoO₃ induced low activity and hindered regeneration. No leaching of the active phase was demonstrated during the reaction. Sulfone adsorption had minimal impact on deactivation, while non-sulphur compounds appeared to be the key contributors. Regeneration outcomes were found to be molybdenum content-dependent: 10Mo/Al recovered its activity, while 20Mo/Al formed inactive phases, like Al₂(MoO₄)₃. Using an organic oxidant (tBHP) during ODS influenced the regeneration, as it prevented Al₂(MoO₄)₃ formation and redispersed crystalline MoO₃, enhancing performance. These findings advance understanding of catalyst deactivation and suggest strategies to extend catalyst life in the ODS of HFO. Full article

The historical use of lead (Pb) poses ongoing health risks via exposure to contaminated urban soils. However, there is limited information about heterogeneity in Pb speciation and distribution at the house lot scale. This study determined highly spatially resolved Pb and other metal speciation along horizontal transects and vertical soil cores from three homes in the Akron, Ohio (USA) municipal. Solid phase characterization was coupled with a sequential extraction protocol to determine operationally defined speciation (exchangeable (M_EX), reducible (M_RED), oxidizable (M_OX), and residual (M_RES)). Lead and Zn were strongly correlated across all fractions (R² = 0.92). Total extractable Pb and Zn were found in low weight percent concentrations nearest to the homes, and speciation was dominated by M_EX and M_RED. High Pb in the M_EX fraction was correlated with the presence of Pb-bearing paint chips in the soil. Lead in the M_EX fraction in soils near the homes decreased with increasing time due to exterior renovations coupled with increases in Pb and Zn in the M_RED fraction. These results suggest that homes are the dominant source of Pb and Zn due to the weathering of exterior surfaces and highlight the acute risk of exposure to more labile Pb immediately following exterior renovations and damage to home exteriors in areas of older housing stock. Full article

The Kingdom of Saudi Arabia (KSA) has millions of date palm trees for commercial scale date-fruit production. The respective industry also generates agricultural waste including date palm tree branches. This rich bio-resource can be used for several beneficial applications. The present study therefore investigated the application of granular activated carbon (GAC) produced using date palm tree branches to successfully remove phenol, p-cresol, and copper from synthetic wastewater. The respective adsorption equilibrium results fitted well to the Langmuir-type adsorption isotherm. Furthermore, the pH-dependent adsorption results both for phenol and p-cresol appeared to follow an anionic-type adsorption behavior (i.e., decreasing adsorption with an increase in aqueous phase equilibrium pH). However, the pH-dependent adsorption finding for copper showed a cationic-type adsorption behavior. These adsorption trends were explained employing the pH-dependent speciation of the respective pollutants. In general, findings from the present work indicate that a high-specific-surface-area (SSA_BET) GAC material from the date palm tree branches can be successfully employed for aqueous phase pollution control. Full article