Search Results (21)

Building on the successful demonstration of hypernuclear spectroscopy using heavy-ion beams, the HypHI Collaboration is shifting its focus to investigating proton- and neutron-rich hypernuclei. A crucial component of this research is the implementation of a fragment separator, which facilitates the production and separation of rare isotope beams and is vital for accessing hypernuclei far from the stability line. High-precision spectroscopy of these exotic hypernuclei is planned to be conducted at GSI first, which will be followed by experiments at the FAIR facility utilizing the FRS and Super-FRS fragment separators. A thorough systematic investigation paired with an optimization analysis was employed to establish the most favorable experimental setup for producing high-isospin hypernuclei. Theoretical models describing heavy-ion-induced reactions and hypernuclear synthesis guided this process, which was complemented by Monte Carlo simulations to obtain experimental efficiencies for the production and transmission of the exotic secondary beams. The outlined methodology offers insights into the anticipated yields of ${}_{\Lambda }{}^6\mathrm{He}$, ${}_{\Lambda }{}^9\mathrm{C}$, and a range of both proton- and neutron-rich hypernuclei. Full article

In this study, we report a green, one-step synthesis of fluorescent carbon quantum dots (PET-FCQDs) derived from polyethylene terephthalate (PET) waste using an environmentally friendly pyrolytic method. The PET-FCQDs were systematically characterized using techniques such as UV-Vis spectroscopy, fluorescence spectroscopy, ATR-FTIR, TGA, and fluorescence microscope, confirming their nanoscale size (2–50 nm), rich functional groups and thermal stability. Thermal stability and dynamics evaluated by the Coats–Redfern method showed endothermic reactions with an activation energy of 88.84–125.05 kJ/mol. Density functional theory studies showed a binding energy, highest occupied molecular orbital, lowest unoccupied molecular orbital, and energy gap of −675.39, −5.23, −5.07, and 0.17 eV, respectively. The as-synthesized PET-FCQDs demonstrated excellent optical properties with quantum yield ($\Phi$) of 49.6% and were applied as a dual-mode fluorescent sensing probe for the detection of Pd²⁺, ciprofloxacin (CIP), and fluoxetine (FLX) in aqueous systems via fluorescence quenching and enhancement mechanisms. For Pd²⁺, the fluorescence emission intensity at 470 nm was quenched proportionally to the increasing concentration, while CIP and FLX induced fluorescence enhancement. The Stern–Volmer analysis confirmed strong interaction between the analytes and PET-FCQDs, distinguishing dynamic quenching for Pd²⁺ and static interactions for CIP and FLX. The method exhibited linear detection ranges of 1–10 mg/L for Pd²⁺, 50–150 µg/L for CIP, and 100–400 ng/L for FLX, with corresponding limits of detection (LOD) of 1.26 mg/L, 3.3 µg/L, and 134 ng/L, respectively. Recovery studies in spiked tap water and river water samples demonstrated the practical applicability of PET-FCQDs, although matrix effects were observed, particularly for FLX. This work not only highlights a sustainable route for PET waste upcycling but also demonstrates the potential of PET-FCQDs as cost-effective, sensitive, and versatile fluorescent probes for environmental monitoring of heavy metal ions and pharmaceutical pollutants. Further optimization of the sensing platform could enhance its selectivity and performance in real-world applications. Full article

True ternary fission, the fission of a nucleus into three fragments of nearly equal mass, is an elusive and poorly known process influenced by shell effects. An increase in the probability of this process with respect to binary fission, which is very low in spontaneous and neutron-induced fission, has been envisaged. Heavy-ion-induced reactions are adopted due to the possibility of an increase in the fissility parameter and the excitation energy of the compound nuclei. Nuclei with mass number around A = 250, accessible in heavy-ion-induced reactions, are favorable and should be investigated. It is still debated if the process takes place in a single step, direct ternary fission, or in a two step, sequential ternary fission. The purpose of this work is to define experimental conditions and observables that allow the disentangling of the products from the direct and sequential ternary fission, as well as from the usual most probable binary fission. This step is essential for gaining insights into the ternary fission dynamics and the binary to ternary fission competition. The method proposed here is for simulating the kinematics of the ternary and binary fission processes to compute the energy distributions and angular correlations of direct and sequential ternary fission products, as well as those of binary fission. The reaction taken as a benchmark is ⁴⁰Ar + ²⁰⁸Pb at 230 MeV and is supposed to form the ²⁴⁸Fm* compound nucleus. The simulation results have been filtered by considering the response function of a multi-coincidence detection system virtually constructed using the Geant4 simulation toolkit. The simulations support the possibility of separating the products of different multimodal fission decays with the proposed setup that consequently represents an effective tool to obtain insights into ternary fission from the observables selected. Full article

Lead (Pb) contamination in loess poses a significant environmental challenge that impedes sustainable development. Microbially induced carbonate precipitation (MICP) is an innovative biomimetic mineralization technology that shows considerable promise in remediating soil contaminated with heavy metals. However, the toxicity of lead ions to Bacillus pasteurii reduces the efficiency of mineralization, subsequently diminishing the effectiveness of remediation. Although biochar can immobilize heavy metal ions, its adsorption instability presents a potential risk. In this study, we first compared the pH, electrical conductivity (EC), unconfined compressive strength (UCS), permeability coefficient, and toxicity leaching performance of lead-contaminated loess specimens remediated using biochar (BC), red mud (RM), red-mud-modified biochar (MBC), and MICP technology. Additionally, we evaluated the mechanism of MICP combined with varying amounts of MBC in remediating lead-contaminated loess combing Zeta potential, X-ray diffraction (XRD) analyses, and scanning electron microscopy (SEM) tests. The results showed that MICP technology outperforms traditional methods such as RM, BC, and MBC in the remediation of lead-contaminated loess. When MICP is combined with MBC, an increase in MBC content results in a higher pH (8.71) and a lower EC (232 us/cm). Toxic leaching tests reveal that increasing MBC content reduces the lead leaching concentration in loess, with optimal remediation being achieved at 5% MBC. Microscopic analysis indicates that the remediation mechanisms of MICP combined with MBC involve complexation, electrostatic adsorption, ion exchange, and precipitation reactions. The synergistic application of MICP and MBC effectively adsorbs and immobilizes lead ions in loess, enhancing its properties and demonstrating potential for pollution remediation and engineering applications. Full article

The theory of heavy ion double charge exchange (DCE) reactions proceeding by effective rank-2 isotensor interactions is presented. Virtual pion–nucleon charge exchange interactions are investigated as the source for induced isotensor interactions, giving rise to the Majorana DCE (MDCE) reaction mechanism. MDCE is of a generic character, proceeding through pairs of complementary (${\pi }^{\pm },{\pi }^{\mp }$) reactions in the projectile and target nucleus. The dynamics of the elementary processes is discussed, where the excitation of pion–nucleon resonances are of central importance. Investigations of initial and final state ion–ion interactions show that these effects are acting as vertex renormalizations. In closure approximation, well justified by the finite pion mass, the second-order transition matrix elements reduce to pion potentials and effective two-body isotensor DCE interactions, giving rise also to two-body correlations in either of the participating nuclei. Connections to neutrinoless Majorana double beta decay (MDBD) are elucidated at various levels of the dynamics, from the underlying fundamental electro-weak and QCD scales to the physical scales of nuclear MDBD and MDCE physics. It is pointed out that heavy ion MDCE reactions may also proceed by competing electro-weak charge exchange processes, leading to lepton MDCE by electrons, positrons, and neutrinos. Full article

This study specifically validates the migration patterns of lead ions under sodium ion stress in soil and concludes that a high concentration of sodium ions, when coexisting with lead ions, diminishes the migration rate of lead ions, consequently reducing the removal efficiency of lead ions. 1. Introduction: Treatment of lead-contaminated soil has become a prominent research concern, with electrochemical treatment (ECT) technology demonstrating significant potential in this regard. ECT not only overcomes the drawbacks of traditional technology of soil remediation, such as long remediation periods, low efficiency, and high costs, but also enables in situ remediation. However, the influence of varying concentrations of non-contaminant ions on the removal efficiency of heavy metal ions during electrochemical treatment remediation of different naturally polluted soils remains unclear. Therefore, investigating the impact of sodium ion stress on the migration of lead ions is essential. 2. Methods: This study applies a DC power supply connected to an experimental device. The device is made of plexiglass and consists of three compartments: one soil compartment and two electrolytic compartments. A multimeter is installed with a wire between the DC power and the soil reaction device for monitoring the current. 3. Results: This study indicates a significant influence of the presence of sodium ions on the migration of lead ions during ECT. A high concentration of sodium ions induces ion competition in the soil, hindering the migration of lead ions and causing a decrease in their migration rate. Additionally, the competitive interaction between sodium ions and lead ions has a pronounced effect on the efficiency of ECT, leading to a reduction in the removal efficiency of lead ions. 4. Conclusion: These results emphasize the importance of considering sodium ion stress in the electrochemical remediation of lead-contaminated soil and provide valuable insights for optimizing electrochemical remediation strategies. Full article

The role of initial state (ISI) and final state (FSI) ion–ion interactions in heavy-ion double-charge-exchange (DCE) reactions $A(Z,N)\to A(Z\pm 2,N\mp 2)$ are studied for double single-charge-exchange (DSCE) reactions given by sequential actions of the isovector nucleon–nucleon (NN) T-matrix. In momentum representation, the second-order DSCE reaction amplitude is shown to be given in factorized form by projectile and target nuclear matrix elements and a reaction kernel containing ISI and FSI. Expanding the intermediate propagator in a Taylor series with respect to auxiliary energy allows us to perform the summation in the leading-order term over intermediate nuclear states in closure approximation. The nuclear matrix element attains a form given by the products of two-body interactions directly exciting the $n^2{p}^{-2}$ and $p^2{n}^{-2}$ DCE transitions in the projectile and the target nucleus, respectively. A surprising result is that the intermediate propagation induces correlations between the transition vertices, showing that DSCE reactions are a two-nucleon process that resembles a system of interacting spin–isospin dipoles. Transformation of the DSCE NN T-matrix interactions from the reaction theoretical t-channel form to the s-channel operator structure required for spectroscopic purposes is elaborated in detail, showing that, in general, a rich spectrum of spin scalar, spin vector and higher-rank spin tensor multipole transitions will contribute to a DSCE reaction. Similarities (and differences) to two-neutrino double-beta decay (DBD) are discussed. ISI/FSI distortion and absorption effects are illustrated in black sphere approximation and in an illustrative application to data. Full article

Lithium-sulfur (Li-S) batteries have emerged as one of the most hopeful alternatives for energy storage systems. However, the commercialization of Li-S batteries is still confronted with enormous hurdles. The poor conductivity of sulfur cathodes induces sluggish redox kinetics. The shuttling of polysulfides incurs the heavy failure of electroactive substances. Tremendous efforts in experiments to seek efficient catalysts have achieved significant success. Unfortunately, the understanding of the underlying catalytic mechanisms is not very detailed due to the complicated multistep conversion reactions in Li-S batteries. In this review, we aim to give valuable insights into the connection between the catalyst activities and the structures based on theoretical calculations, which will lead the catalyst design towards high-performance Li-S batteries. This review first introduces the current advances and issues of Li-S batteries. Then we discuss the electronic structure calculations of catalysts. Besides, the relevant calculations of binding energies and Gibbs free energies are presented. Moreover, we discuss lithium-ion diffusion energy barriers and Li₂S decomposition energy barriers. Finally, a Conclusions and Outlook section is provided in this review. It is found that calculations facilitate the understanding of the catalytic conversion mechanisms of sulfur species, accelerating the development of advanced catalysts for Li-S batteries. Full article

Nitric oxide (NO) is an endogenous signaling molecule that plays an important role in plant ontogenesis and responses to different stresses. The most widespread abiotic stress factors limiting significantly plant growth and crop yield are drought, salinity, hypo-, hyperthermia, and an excess of heavy metal (HM) ions. Data on the accumulation of endogenous NO under stress factors and on the alleviation of their negative effects under exogenous NO treatments indicate the perspectives of its practical application to improve stress resistance and plant productivity. This requires fundamental knowledge of the NO metabolism and the mechanisms of its biological action in plants. NO generation occurs in plants by two main alternative mechanisms: oxidative or reductive, in spontaneous or enzymatic reactions. NO participates in plant development by controlling the processes of seed germination, vegetative growth, morphogenesis, flower transition, fruit ripening, and senescence. Under stressful conditions, NO contributes to antioxidant protection, osmotic adjustment, normalization of water balance, regulation of cellular ion homeostasis, maintenance of photosynthetic reactions, and growth processes of plants. NO can exert regulative action by inducing posttranslational modifications (PTMs) of proteins changing the activity of different enzymes or transcriptional factors, modulating the expression of huge amounts of genes, including those related to stress tolerance. This review summarizes the current data concerning molecular mechanisms of NO production and its activity in plants during regulation of their life cycle and adaptation to drought, salinity, temperature stress, and HM ions. Full article

The current state of heavy metal (HM) environmental pollution problems was considered in the review: the effects of HMs on the vital activity of plants and the functioning of their antioxidant system, including phenolic antioxidants. The latter performs an important function in the distribution and binding of metals, as well as HM detoxification in the plant organism. Much attention was focused on cadmium (Cd) ions as one of the most toxic elements for plants. The data on the accumulation of HMs, including Cd in the soil, the entry into plants, and the effect on their various physiological and biochemical processes (photosynthesis, respiration, transpiration, and water regime) were analyzed. Some aspects of HMs, including Cd, inactivation in plant tissues, and cell compartments, are considered, as well as the functioning of various metabolic pathways at the stage of the stress reaction of plant cells under the action of pollutants. The data on the effect of HMs on the antioxidant system of plants, the accumulation of low molecular weight phenolic bioantioxidants, and their role as ligand inactivators were summarized. The issues of polyphenol biosynthesis regulation under cadmium stress were considered. Understanding the physiological and biochemical role of low molecular antioxidants of phenolic nature under metal-induced stress is important in assessing the effect/aftereffect of Cd on various plant objects—the producers of these secondary metabolites are widely used for the health saving of the world’s population. This review reflects the latest achievements in the field of studying the influence of HMs, including Cd, on various physiological and biochemical processes of the plant organism and enriches our knowledge about the multifunctional role of polyphenols, as one of the most common secondary metabolites, in the formation of plant resistance and adaptation. Full article

Some road systems are unpaved due to limited governmental finance and fewer maintenance techniques. Such unpaved roads become vulnerable during heavy rainy seasons following restrained accessibility among cities and traffic accidents. Considering the circumstances, innovative and cost–effective approaches are required for unpaved roads. Microbially induced carbonate precipitation (MICP) is an emerging soil improvement technology using microbes to hydrolyze urea generating carbonate ions, and precipitates calcium carbonate in the presence of calcium ion. Induced calcium carbonate bonds soil particles enhancing stiffness and strength when the MICP reaction takes place within the soil system. This study introduces the use of microbes on unpaved road systems consisting of in situ lateritic soils. The MICP technology was implemented to improve soil strength through two approaches: surface spraying and mixing methods. A series of soil testing was performed with varying chemical concentrations to measure precipitation efficiency, strength, and quality for construction material and see the feasibility of the proposed methods. The laboratory test results indicated that the surface spraying method provided improved; however, it was highly affected by the infiltration characteristics of used soils. The mixing method showed promising results even under submerged conditions, but still required improvement. Overall, the proposed idea seems possible to apply to improving unpaved road systems in the lateritic region but requires further research and optimization. Full article

Experimental liver injury with hepatocelluar necrosis and abnormal liver tests is caused by exposure to heavy metals (HMs) like aluminum, arsenic, beryllium, cadmium, chromium, cobalt, copper, iron, lead, mercury, molybdenum, nickel, platinum, thallium, titanium, vanadium, and zinc. As pollutants, HMs disturb the ecosystem, and as these substances are toxic, they may affect the health of humans and animals. HMs are not biodegradable and may be deposited preferentially in the liver. The use of animal models can help identify molecular and mechanistic steps leading to the injury. HMs commonly initiate hepatocellular overproduction of ROS (reactive oxygen species) due to oxidative stress, resulting in covalent binding of radicals to macromolecular proteins or lipids existing in membranes of subcellular organelles. Liver injury is facilitated by iron via the Fenton reaction, providing ROS, and is triggered if protective antioxidant systems are exhausted. Ferroptosis syn pyroptosis was recently introduced as mechanistic concept in explanations of nickel (Ni) liver injury. NiCl₂ causes increased iron deposition in the liver, upregulation of cyclooxygenase 2 (COX-2) protein and mRNA expression levels, downregulation of glutathione eroxidase 4 (GPX4), ferritin heavy chain 1 (FTH1), nuclear receptor coactivator 4 (NCOA4) protein, and mRNA expression levels. Nickel may cause hepatic injury through mitochondrial damage and ferroptosis, defined as mechanism of iron-dependent cell death, similar to glutamate-induced excitotoxicity but likely distinct from apoptosis, necrosis, and autophagy. Under discussion were additional mechanistic concepts of hepatocellular uptake and biliary excretion of mercury in exposed animals. For instance, the organic anion transporter 3 (Oat3) and the multidrug resistance-associated protein 2 (Mrp2) were involved in the hepatic handling of mercury. Mercury treatment modified the expression of Mrp2 and Oat3 as assessed by immunoblotting, partially explaining its impaired biliary excretion. Concomitantly, a decrease in Oat3 abundance in the hepatocyte plasma membranes was observed that limits the hepatic uptake of mercury ions. Most importantly and shown for the first time in liver injury caused by HMs, titanium changed the diversity of gut microbiota and modified their metabolic functions, leading to increased generation of lipopolysaccharides (LPS). As endotoxins, LPS may trigger and perpetuate the liver injury at the level of gut-liver. In sum, mechanistic and molecular steps of experimental liver injury due to HM administration are complex, with ROS as the key promotional compound. However, additional concepts such as iron used in the Fenton reaction, ferroptosis, modification of transporter systems, and endotoxins derived from diversity of intestinal bacteria at the gut-liver level merit further consideration. Full article

Exogenous heavy metals or non-metallic waste products, for example lanthanide or iodinated contrast media for radiological procedures, may interfere with the biochemical pools in patients and in common food sources, creating an excess buildup of exogenous compounds which may reach toxic levels. Although the mechanisms are unknown, our experiments were designed to test if this toxicity can be attributed to “transmetallation” or “chelation” reactions freeing up lanthanides or chelated transition metals in acidic fruits used as phantoms representing the biologically active and mineral-rich carbohydrate matrix. The rapid breakdown of stable contrast agents have been reported at a lower pH. The interaction of such agents with native metals was examined by direct imaging of contrast infused fresh apples and sweet potatoes using low energy X-rays (40–44 kVp) and by magnetic resonance imaging at 1.5 and 3T. The stability of the exogenous agents seemed to depend on endogenous counterions and biometals in these fruits. Proton spin echo MR intensity is sensitive to paramagnetic minerals and low energy X-ray photons are sensitively absorbed by photoelectric effects in all abundant minerals and were compared before and after the infusion of radiologic contrasts. Endogenous iron and manganese are believed to accumulate due to interactions with exogenous iodine and gadolinium in and around the infusion spots. X-ray imaging had lower sensitivity (detection limit approximately 1 part in 10⁴), while MRI sensitivity was two orders of magnitude higher (approximately 1 part in 10⁶), but only for paramagnetic minerals like Mn and Fe in our samples. MRI evidence of such a release of metal ions from the native pool implicates transmetallation and chelation reactions that were triggered by infused contrast agents. Since Fe and Mn play significant roles in the function of metalloenzymes, our results suggest that transmetallation and chelation could be a plausible mechanism for contrast induced toxicity in vivo. Full article

This paper presents a new analysis of the experimental transmission spectra of polyethylene terephthalate (PET) films before and after irradiation with swift heavy ions (SHI) films, as reported previously by the authors. It is shown that the absorption edge red shift for irradiated films contains two regions of exponential form, one of which is located in the UV region and the other at lower energy, mainly in the visible part of the spectrum. The behaviour of the transmission curves under different irradiating fluences demonstrates that these two regions reflect respectively the electron-enriched core of the latent track and its electron-depleted peripheral halo. The focal point method yields a bandgap energy of 4.1 eV for the electron-enriched core of the latent track, which is similar to n-doped semiconductors, and a bandgap of about 1.3–1.5 eV for the electron-depleted halo, similar to p-doped semiconductors. The boundary between the latent track cores and halos corresponds to a conventional semiconductor p-n junction. The values of the characteristic Urbach energy determined from experimental data correspond to the nonradiative transition energy between the excited singlet and triplet levels of benzene-carboxyl complexes in repeat units of the PET chain molecule. A parallel is drawn between the SHI-induced redistribution of electrons held in structural traps in the PET film and chemical redox reactions, which involve the redistribution of electrons in chemical bonds. It is suggested that alkali etching triggers the release of excess electrons in the latent track cores, which act as a catalyst for the fragmentation of PET chain molecules along the latent tracks of the SHI irradiation. Full article

Heavy metals are essential for a wide range of biological processes, including the growth and reproduction of cells, synthesis of biomolecules, many enzymatic reactions, and the body’s immunity, but their excessive intake is harmful. Specifically, they cause oxidative stress (OS) and generate free radicals and reactive oxygen species (ROS) in metabolism. In addition, the accumulation of heavy metals in humans can cause serious damage to different organs, especially respiratory, nervous and reproductive and digestive systems. Biologically, metal chelation therapy is often used to treat metal toxicity. This process occurs through the interaction between the ligand and a central metal atom, forming a complex ring-like structure. After metals are chelated with appropriate chelating agents, their damage in metabolism can be prevented and efficiently removed from the body. On the other hand, heavy metals, including Zn, Fe and Cu, are necessary for the suitable functioning of different proteins including enzymes in metabolism. However, when the same metals accumulate at levels higher than the optimum level, they can easily become toxic and have harmful effects toward biomolecules. In this case, it induces the formation of ROS and nitrogen species (RNS) resulting in peroxidation of biological molecules such as lipids in the plasma membrane. Antioxidants have an increasing interest in many fields due to their protective effects, especially in food and pharmaceutical products. Screening of antioxidant properties of compounds needs appropriate methods including metal chelating assay. In this study, a general approach to the bonding and chelating properties of metals is described. For this purpose, the basic principles and chemical principles of metal chelation methods, both in vivo and in vitro, are outlined and discussed. Hence, in the main sections of this review, the descriptions related to metal ions, metal chelating, antioxidants, importance of metal chelating in biological system and definitions of metal chelating assays as widely used methods to determine antioxidant ability of compounds are provided. In addition, some chemical properties, technical and critical details of the used chelation methods are given. Full article