Search Results (438)

The windowpane oyster (Placuna placenta) is common in coastal areas of the Philippines, thriving in brackish waters. Its shells underpin the local craft industries. While its meat is edible, only small amounts are consumed locally, most going to waste. Utilization of this potential nutrient source is hindered by the lack of information concerning its organic and mineral content, the possible presence of heavy metal ions, and the risk of microbial pathogens. We report extensive analysis of the meat from Placuna placenta, harvested during three different seasons to account for potential variations. This comprises proximate analysis, mineral, antioxidant, and microbial analyses. While considerable seasonal variation was observed, the windowpane oyster was found to be a rich source of protein, fats, minerals, and carbohydrates, comparing well with the meats of other shellfish and land animals. Following pre-cooking (~90 °C, 25–30 min), the standard local method for food preparation, no viable E. coli or Salmonella sp. were detected. Mineral content was broadly similar to that reported in fish, although iron, zinc, and copper were more highly represented, nevertheless, heavy metals were below internationally acceptable levels, with the exception of one of three samples, which was slightly above the only current standard, FSANZ. Whether the arsenic was in the safer organic form, which is commonly the case for shellfish, or the more toxic inorganic form remains to be established. This and the variation of arsenic over time will need to be considered when developing food products. Overall, the meat of the windowpane oyster is a valuable food resource and its current (albeit low-level) use should lower any barriers to its acceptance, making it suitable for commercialization. The present data support its development for high-value food products in urban markets. Full article

The increasing demand for rapid, sensitive, and eco-friendly methods for the detection of trace heavy metals in environmental samples, attributed to their serious threats to health and the environment, has spurred considerable interest in the development of sustainable sensor materials. Toxic metal ions, namely, lead (Pb²⁺), cadmium (Cd²⁺), mercury (Hg²⁺), arsenic (As³⁺), and chromium, are potential hazards due to their non-biodegradable nature with high toxicity, even at trace levels. Acute health complications, including neurological, renal, and developmental disorders, arise upon exposure to such metal ions. To monitor and mitigate these toxic exposures, sensitive detection techniques are essential. Pre-existing conventional detection methods, such as atomic absorption spectroscopy (AAS) and inductively coupled plasma-mass spectrometry (ICP-MS), involve expensive instrumentation, skilled operators, and complex sample preparation. Electrochemical sensing, which is simple, portable, and eco-friendly, is foreseen as a potential alternative to the above conventional methods. Carbon-based nanomaterials play a crucial role in electrochemical sensors due to their high conductivity, stability, and the presence of surface functional groups. Biochar (BC), a carbon-rich product, has emerged as a promising electrode material for electrochemical sensing due to its high surface area, sustainability, tunable porosity, surface rich in functional groups, eco-friendliness, and negligible environmental footprint. Nevertheless, broad-spectrum studies on the use of biochar in electrochemical sensors remain narrow. This review focuses on the recent advancements in the development of biochar-based electrochemical sensors for the detection of toxic heavy metals such as Pb²⁺, Cd²⁺, and Hg²⁺ and the simultaneous detection of multiple ions, with special emphasis on BC synthesis routes, surface modification methodologies, electrode fabrication techniques, and electroanalytical performance. Finally, current challenges and future perspectives for integrating BC into next-generation sensor platforms are outlined. Full article

This article presents the potential use of a humic agent called ‘Superhumate’, obtained from weathered coal from the Shubarkol deposit in Kazakhstan. The experiment was conducted using model solutions and surface mine water samples from the “Degelen” site at the Semipalatinsk Test Site. The adsorption of heavy metals and toxic elements using the “Superhumate” agent was carried out under dynamic conditions using a chromatographic column. Tests were conducted at a natural pH range of 5–8 (mine waters) and with a model solution at pH 1.7. Assessing the sorption efficiency of this preparation revealed that at pH 1.7, the agent does not adsorb elements such as Cd, Cu, Pb, and Zn. Under dynamic experimental conditions, using the preparation for mine waters at natural pH levels (pH 5–8), elements such as Be, Sr, Mo, Cd, Cs, Zn, and U were efficiently adsorbed at levels of 60–95%. The sorption efficiency of Pb ions was found to be almost independent of pH. The experimental results obtained with mine water samples indicate that alkaline solutions have the highest sorption efficiency, with pH ≥ 7, which is attributed to the solubility of the agent. Full article

The primary worldwide variables limiting plant development and agricultural output are the ever-present threat that environmental stressors such as salt (may trigger osmotic stress plus ions toxicity, which impact on growth and yield of the plants), drought (provokes water stress, resulting in lowering photosynthesis process and growth rate), heavy metals (induced toxicity, hindering physiological processes also lowering crop quantity and quality), and pathogens (induce diseases that may significantly affect plant health beside productivity). This review explores the integrated effects of these stressors on plant productivity and growth rate, emphasizing how each stressor exceptionally plays a role in physiological responses. Owing to developments in technology that outclass traditional breeding methods and genetic engineering techniques, powerful alleviation strategies are vital. New findings have demonstrated the remarkable role of nanoparticles in regulating responses to these environmental stressors. In this review, we summarize the roles and various applications of nanomaterials in regulating abiotic and biotic stress responses. This review discusses and explores the relationship between various types of nanoparticles (metal, carbon-based, and biogenic) and their impact on plant physiology. Furthermore, we assess how nanoparticle technology may play a role in practices of sustainable agriculture by reducing the amount of compounds used, providing them with a larger surface area, highly efficient mass transfer abilities, and controlled, targeted delivery of lower nutrient or pesticide amounts. A review of data from several published studies leads to the conclusion that nanoparticles may act as a synergistic effect, which can effectively increase plant stress tolerance and their nutritional role. Full article

Heavy metal ions pose a significant threat to the environment and human health due to their high toxicity and bioaccumulation. Traditional instrumentations, although sensitive, are often complex, costly, and unsuitable for on-site rapid detection of heavy metal ions. Lateral flow assay technology has emerged as a research hotspot due to its rapid, simple, and cost-effective advantages. This review summarizes the applications of lateral flow assay technology based on nucleic acid molecules and antigen–antibody interactions in heavy metal ion detection, focusing on recognition mechanisms such as DNA probes, nucleic acid enzymes, aptamers, and antigen–antibody binding, as well as signal amplification strategies on lateral flow testing strips. By incorporating these advanced technologies, the sensitivity and specificity of lateral flow assays have been significantly improved, enabling highly sensitive detection of various heavy metal ions, including Hg²⁺, Cd²⁺, Pb²⁺, and Cr³⁺. In the future, the development of lateral flow assay technology for detection of heavy metal ions will focus on multiplex detection, optimization of signal amplification strategies, integration with portable devices, and standardization and commercialization. With continuous technological advancements, lateral flow assay technology will play an increasingly important role in environmental monitoring, food safety, and public health. Full article

The persistent contamination of aquatic environments by heavy metals, particularly Pb²⁺, Cd²⁺, and Cu^2+, poses a serious global threat due to their toxicity, persistence, and bioaccumulative behavior. In response, low-cost and eco-friendly adsorbents are being explored, among which CaCO₃-based biocomposites derived from mollusk shells have shown exceptional performance. In this study, a hybrid biocomposite composed of poly(vinyl alcohol) (PVA) and oyster shell-derived CaCO₃ was computationally investigated using Density Functional Theory (DFT) to elucidate the electronic and structural basis for its high metal-removal efficiency. Calculations were performed at the B3LYP/6-311++G(d,p), M05-2X/6-311+G(d,p), and M06-2X/6-311++G(d,p) levels using GAUSSIAN 16. Among them, B3LYP was identified as the most balanced in terms of accuracy and computational cost. The hybridization with CaCO₃ reduced the HOMO-LUMO gap by 20% and doubled the dipole moment (7.65 Debye), increasing the composite’s polarity and reactivity. Upon chelation with metal ions, the gap further dropped to as low as 0.029 eV (Cd²⁺), while the dipole moment rose to 17.06 Debye (Pb²⁺), signaling enhanced charge separation and stronger electrostatic interactions. Electrostatic potential maps revealed high nucleophilicity at carbonate oxygens and reinforced electrophilic fields around the hydrated metal centers, correlating with the affinity trend Cu²⁺ > Cd²⁺ > Pb²⁺. Fukui function analysis indicated a redistribution of reactive sites, with carbonate oxygens acting as ambiphilic centers suitable for multidentate coordination. Natural Bond Orbital (NBO) analysis confirmed the presence of highly nucleophilic lone pairs and weakened bonding orbitals, enabling flexible adsorption dynamics. Furthermore, NCI/RDG analysis highlighted attractive noncovalent interactions with Cu²⁺ and Pb²⁺, while FT-IR simulations demonstrated the formation of hydrogen bonding (O–H···O=C) and Ca²⁺···O coordination bridges between phases. Full article

In this study, kaolinite-based clay (Ka-Clay) was used as an adsorbent for the efficient removal of Pb(II), Cd(II) and Hg(II) ions from aqueous media. The selection of Pb(II), Cd(II) and Hg(II) ions for experimental studies took into account their high toxicity, while the choice of Ka-Clay, the ease of preparation and high availability of this material were the most important arguments. Ka-Clay exhibits high adsorption performance, with removal percents over 98% for Pb(II) and 93% for Cd(II), even at high concentrations of metal ions (over 150 mg/L, pH = 6.5, 4 g adsorbent/L, 21 ± 1 °C). For Hg(II) ions, the adsorption percent does not exceed 55%, and this moderate value is mainly due to the significant change in pH. The adsorption behavior was in accordance with the Langmuir model (R² > 0.95) and the pseudo-second order kinetic model (R² > 0.99), indicating an adsorption process that occurs mainly through chemical interactions at the adsorbent surface between the metal ions and the functional groups. Adsorption processes are spontaneous (ΔG = −8.66 ÷ −15.76 kJ/mol) and endothermic (ΔH = 7.09 ÷ 21.81 kJ/mol), and the adsorption mechanism is the results of elementary processes of electrostatic attraction, ion exchange and superficial complexation. The insignificant effect of other ions (Ca(II), Mg(II), Na(I), K(I)) present in real wastewater samples as well as the desorption behavior of exhausted adsorbent highlight the practical utility of this adsorbent on a large scale. The experimental results included in this study suggest that Ka-Clay can be used as a promising adsorbent for the removal of high concentrations of toxic heavy metals with low cost and high efficiency, and this can contribute to the design of a sustainable wastewater treatment method. Full article

In this study, Ni²⁺ and Cd²⁺ resistant Pseudomonas aeruginosa 18, Enterobacter ludwigii 11Uz, and Enterobacter cloacae Uz_5 strains were isolated from soils contaminated with heavy metals in the Samarkand and Kashkadarya regions (Uzbekistan), and tested to remove Ni²⁺ and Cd²⁺ ions from the environment via biosorption. The biosorption capacity of these strains was observed under in vitro conditions. The biosorption process was highly dependent on the growing conditions, with the highest biosorption rate observed after 300 min of incubation at pH 7.0, and 40 °C. The presence of functional groups such as S=O, NH₂, and COOH in the biosorbing microorganisms was confirmed by IR spectroscopy. The adsorption capacity decreased when the initial metal concentration was increased and was enhanced with higher microbial biomass. Enterobacter ludwigii 11Uz strain was found to alter the toxic oxidation state of Ni²⁺ and Cd²⁺ cations, while Pseudomonas aeruginosa 18 and Enterobacter cloacae Uz_5 strains reduced the toxicity of Ni²⁺ cations only by changing their oxidation state. It was confirmed in our studies that the three selected bacterial strains actively participated in the detoxification of Cd²⁺ through the synthesis of cysteine amino acid. Full article

In the wake of global energy transition and the “dual-carbon” goal, the rapid growth of electric vehicles has posed challenges for large-scale lithium-ion battery decommissioning. Retired batteries exhibit dual attributes of strategic resources (cobalt/lithium concentrations several times higher than natural ores) and environmental risks (heavy metal pollution, electrolyte toxicity). This paper systematically reviews pyrometallurgical and hydrometallurgical recovery technologies, identifying bottlenecks: high energy/lithium loss in pyrometallurgy, and corrosion/cost/solvent regeneration issues in hydrometallurgy. To address these, an integrated recycling process is proposed: low-temperature physical separation (liquid nitrogen embrittlement grinding + froth flotation) for cathode–anode separation, mild roasting to convert lithium into water-soluble compounds for efficient metal oxide separation, stepwise alkaline precipitation for high-purity lithium salts, and co-precipitation synthesis of spherical hydroxide precursors followed by segmented sintering to regenerate LiNi_1/3Co_1/3Mn_1/3O₂ cathodes with morphology/electrochemical performance comparable to virgin materials. This low-temperature, precision-controlled methodology effectively addresses the energy-intensive, pollutive, and inefficient limitations inherent in conventional recycling processes. By offering an engineered solution for sustainable large-scale recycling and high-value regeneration of spent ternary lithium ion batteries (LIBs), this approach proves pivotal in advancing circular economy development within the renewable energy sector. Full article

Non-invasive Micro-test Technology (NMT) represents a pioneering approach in the study of physiological functions within living organisms. This technology possesses the remarkable capability to monitor the flow rates and three-dimensional movement directions of ions or molecules as they traverse the boundaries of living organisms without sample destruction. The advantages of NMT are multifaceted, encompassing real-time, non-invasive assessment, a wide array of detection indicators, and compatibility with diverse sample types. Consequently, it stands as one of the foremost tools in contemporary plant physiological research. This comprehensive review delves into the applications and research advancements of NMT within the field of plant abiotic stress physiology, including drought, salinity, extreme temperature, nutrient deficiency, ammonium toxicity, acid stress, and heavy metal toxicity. Furthermore, it offers a forward-looking perspective on the potential applications of NMT in plant physiology research, underscoring its unique capacity to monitor the flux dynamics of ions/molecules (e.g., Ca²⁺, H⁺, K⁺, and IAA) in real time, reveal early stress response signatures through micrometer-scale spatial resolution measurements, and elucidate stress adaptation mechanisms by quantifying bidirectional nutrient transport across root–soil interfaces. NMT enhances our understanding of the spatiotemporal patterns governing plant–environment interactions, providing deeper insights into the molecular mechanism of abiotic stress resilience. Full article

This study investigates the development and sensing profile of synthetic melanin nanoparticle-coated electrodes for the electrochemical detection of heavy metals, including lead (Pb), cadmium (Cd), cobalt (Co), zinc (Zn), nickel (Ni), and iron (Fe). Synthetic melanin films were prepared in situ by the deacetylation of diacetoxy indole (DAI) to dihydroxy indole (DHI), followed by the deposition of DHI monomers onto indium tin oxide (ITO) and glassy carbon electrodes (GCE) using cyclic voltammetry (CV), forming a thin layer of synthetic melanin film. The deposition process was characterized by electrochemical quartz crystal microbalance (EQCM) in combination with linear sweep voltammetry (LSV) and amperometry to determine the mass and thickness of the deposited film. Surface morphology and elemental composition were examined using scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX). In contrast, Fourier-transform infrared (FTIR) and UV–Vis spectroscopy confirmed the melanin’s chemical structure and its polyphenolic functional groups. Differential pulse voltammetry (DPV) and amperometry were employed to evaluate the melanin films’ electrochemical activity and sensitivity for detecting heavy metal ions. Reproducibility and repeatability were rigorously assessed, showing consistent electrochemical performance across multiple electrodes and trials. A comparative analysis of ITO, GCE, and graphite electrodes was conducted to identify the most suitable substrate for melanin film preparation, focusing on stability, electrochemical response, and metal ion sensing efficiency. Finally, the applicability of melanin-coated electrodes was tested on in-house heavy metal water samples, exploring their potential for practical environmental monitoring of toxic heavy metals. The findings highlight synthetic melanin-coated electrodes as a promising platform for sensitive and reliable detection of iron with a sensitivity of 106 nA/ppm and a limit of quantification as low as 1 ppm. Full article

Heavy metals in lead refining waste slag pose persistent environmental risks, challenging conventional treatment methods that struggle to balance long-term stabilization with resource recovery potential. To address this issue, we developed a sustainable stabilization strategy. The simultaneous and long-lasting stabilization of Zn, Pb, and As heavy metals in lead refining waste slag was achieved by using an Fe-S(II) stabilizer, and the leaching toxicity of Zn, As and Pb was less than 1 mg/L, which is lower than the concentration limit of the Identification standards for hazardous wastes–Identification for extraction toxicity (GB5085.3-2007). The samples were analyzed by characterization before and after stabilization, and it was found that Fe-S(II) formed a protective layer of sulfide capsule on the surface of the samples. This stabilization mechanism, which has been termed the “nucleation-capture-sulfide encapsulation” process, involves after the oxidation of Fe⁰ to form a core–shell structure for trapping metal ions, where the external oxide layer undergoes mineralization via S(II) sulfide reduction. This microencapsulation-based passivation not only ensures long-term heavy metal immobilization but also preserves the slag’s potential for secondary resource recovery, aligning with circular economy principles. By minimizing environmental leakage risks while retaining metal reclamation feasibility, this approach offers a green and sustainable solution for heavy-metal-laden industrial waste management. Full article

Mercury (Hg) pollution has led to a serious decline in crop yields. Methyl jasmonate (MJ), as a plant hormone, regulates plant responses to heavy metal stress. Nonetheless, the pathways by which MJ modulates Hg tolerance in plants are still not well elucidated. Our study aimed to elucidate the positive impacts of MJ in alleviating Hg-induced toxicity in maize (Zea mays L.) seedlings using an integrated approach combining physiological assessments and transcriptomic analysis. The findings indicated that exogenous MJ mitigated Hg-induced inhibition of photosynthetic performance by up-regulating photosynthesis-related and light-harvesting-related genes and increasing chlorophyll content. Under Hg stress, MJ enhances proline accumulation in maize seedlings by up-regulating essential genes in the proline biosynthesis pathway and down-regulating critical genes in the proline degradation pathway. MJ also elevates the expression of key enzymes involved in phenylpropanoid biosynthesis in maize seedlings, decreases malondialdehyde (MDA) content, and enhances root vitality. In addition, MJ may exert a detoxification effect on maize seedlings under Hg stress by regulating the expression of various genes linked to basic nutrient transport proteins, as well as those involved in the transport, influx, and distribution of metal ions. These findings indicate that MJ is essential for enhancing plant tolerance to Hg stress, thereby establishing a theoretical framework for the advancement and utilization of environmentally friendly agricultural methods involving plant hormones. Full article

This study focuses on the synthesis and characterization of a cationic ion-exchange sorbent derived from vermiculite and epoxy acrylate copolymers, designed to address freshwater scarcity by removing toxic metal ions from aqueous environments. The sorbent was engineered to preserve the chemical integrity of freshwater while adhering to environmental safety standards. Vermiculite served as the base material, modified with glycidyl methacrylate (GMA), acrylonitrile (ACN), and orthophosphoric acid (H₃PO₄) in a mass ratio of 1:0.35:0.15:3. Optimization experiments explored varying H₃PO₄ proportions (two- and threefold increases) to refine the synthesis conditions. The materials underwent microwave irradiation at 300 W for 10 min. Infrared (IR) spectroscopy confirmed the presence of functional groups (P=O, P−O−C), enhancing sorption capacity, while scanning electron microscopy (SEM) revealed a porous structure crucial for adsorption. Sorption properties, assessed via atomic emission spectroscopy, demonstrated capacities of 39.80 mg/g for MoO₄²⁻ and 39.06 mg/g for ReO₄⁻, with extraction efficiencies of 79% and 78%, respectively. Chemical stability tests indicated the sorbent retained up to 90% of its functionality in aggressive environments, highlighting its robustness. The developed sorbent offers a high-performance, cost-effective solution for heavy metal removal from wastewater, advancing sustainable water purification technologies. Full article

Heavy metal and pesticide contaminations represent significant environmental and health hazards to humans and animals. Toxic heavy metals such as lead (Pb), cadmium (Cd), mercury (Hg), and copper (Cu) persist in the environment, bioaccumulating in beverages and food products from both natural and anthropogenic sources. Traditional remediation techniques, such as chemical precipitation and ion exchange, are effective but often costly and challenging to apply at a large scale. In recent years, grape pomace—a winemaking by-product rich in bioactive compounds—has emerged as a promising, low-cost biosorbent for the removal of such pollutants. Its high adsorption capacity, environmental friendliness, and availability make it a strong candidate for water and food decontamination processes. This study evaluates grape pomace and its biochar as sustainable biosorbents for heavy metal removal from water and soil, examining their adsorption efficiency, adsorption mechanisms, environmental benefits, advantages, limitations, and perspectives for future industrial-scale applications. Full article