Heavy Ion Research Articles

Sequestration of divalent heavy metal ions from aqueous environment by adsorption using biomass-bentonite composites as potential adsorbent: Equilibrium and kinetic studies

Hybrid clay adsorbents have been investigated in recent studies as cheap and effective adsorbents for eliminating micropollutants, such as heavy metal ions from aqueous solution. Here, we modified bentonite (BEN) with palm kernel shell and groundnut shell by calcination to obtain palm kernel shell-modified bentonite (BPKS) and groundnut shell-modified bentonite (BGS). We studied the batch equilibrium adsorption of Pb2+, Cd2+ and Ni2+ ions under the influence of dosage, solution pH, contact time and concentration. Under these conditions, we found that the modified adsorbents (BGS and BPKS) had a higher equilibrium adsorption (qe) for the metal ions than unmodified BEN. BEN exhibited Langmuir adsorption capacities (Qo) of 32.47, 14.04 and 14.16 mg/g for Pb2+, Cd2+ and Ni2+, respectively. BGS and BPKS had Qo values of 29.15, 14.27, 16.61 and 31.75, 17.67, 15.625 mg/g for Pb2+, Cd2+, Ni2+, respectively. Investigations revealed that the rate of adsorption on the three adsorbents is best described by a pseudo-second-order kinetic model, with R2 values ≥ 0.9; the intra-particle diffusion model establishes a surface interaction mechanism involving the exchange of electrons between the surfaces of the adsorbents and the adsorbate. Scanning electron microscopy results suggest porous and heterogeneous adsorbent surfaces, indicating a physio-sorption phenomenon. The modifications increased the surface area of BEN from 78.435 to 194.850 and 140.650 m2/g in BGS and BPKS, respectively, using BET surface area analysis. However, the average pore width of BEN reduces from 3.8 to 3.3 nm in both BGS and BPKS. Also, the modification enhanced the cation exchange capacity in BPKS only. The findings from this study offered invaluable insights into how biomass can enhance the physicochemical properties of BEN, as needed for practical environmental application and/or optimization, during the removal of Pb2+, Cd2+ and Ni2+ ions from aqueous media.

N-Doping CQDs as an Efficient Fluorescence Probe Based on Dynamic Quenching for Determination of Copper Ions and Alcohol Sensing in Baijiu.

To address an accurate detection of heavy metal ions in Baijiu production, a nitrogen-doping carbon quantum dots (N-CQDs) was prepared by hydrothermal method from citric acid and urea. The as-prepared N-CQDs had an average particle size of 2.74 nm, and a large number of functional groups (amino, carbonyl group, etc.) attached on its surface, which obtained a 9.6% of quantum yield (QY) with relatively high and stable fluorescence performance. As a fluorescent sensor, the fluorescence of N-CQDs at 380 nm excitation wavelength could be quenched quantitatively by adding Cu2+, due to the dynamic quenching of electron transfer caused by the binding of amine groups and Cu2+, which showed excellent sensitivity and selectivity to Cu2+ in the range of 0.5-5 μM with a detection limit (LOD) of 0.032 μM. In addition, the N-CQDs as well as could be applied to quantitative determine alcohol content in the range of 10-80 V/V% depending on the fluorescence enhancement. Upon the experiment, the fluorescent mechanism was studied by Molecular dynamics (MD) simulations, which demonstrated that solvent effect played an influential role on sensing alcohol content in Baijiu. Overall, the work provided a theoretically guide for the design of fluorescence sensors to monitor heavy metal ion in liquid drinks and sense alcohol content.

Unlocking the potential of biochar: an iron-phosphorus-based composite modified adsorbent for adsorption of Pb(II) and Cd(II) in aqueous environments and response surface optimization of adsorption conditions.

In this work, iron-phosphorus based composite biochar (FPBC) was prepared by modification with potassium phosphate and iron oxides for the removal of heavy metal ions from single and mixed heavy metal (Pb and Cd) solutions. FTIR and XPS characterization experiments showed that the novel modified biochar had a greater number of surface functional groups compared to the pristine biochar. The maximum adsorption capacities of FPBC for Pb(II) and Cd(II) were 211.66mg·g-1 and 94.08mg·g-1 at 293K. The adsorption of Pb(II) and Cd(II) by FPBC followed the proposed two-step adsorption kinetic model and the Freundlich isothermal adsorption model, suggesting that the mechanism of adsorption of Pb(II) and Cd(II) by FPBC involved chemical adsorption of multiple layers. Mechanistic studies showed that the introduction of -PO4 and -PO3 chemisorbed with Pb(II) and Cd(II), and the introduction of -Fe-O increased the ion exchange with Pb(II) and Cd(II) during the adsorption process and produced precipitates such as Pb3Fe(PO4)3 and Cd5Fe2(P2O7)4. Additionally, the abundant -OH and -COOH groups also participated in the removal of Pb(II) and Cd(II). In addition, FPBC demonstrated strong selective adsorption of Pb(II) in mixed heavy metal solutions. The Response Surface Methodology(RSM) analysis determined the optimal adsorption conditions for FPBC as pH 5.31, temperature 26.01°C, and Pb(II) concentration 306.30mg·L-1 for Pb(II). Similarly, the optimal adsorption conditions for Cd(II) were found to be pH 5.66, temperature 39.34°C, and Cd(II) concentration 267.68mg·L-1. Therefore, FPBC has the potential for application as a composite-modified adsorbent for the adsorption of multiple heavy metal ions.

Fermion self-energy and damping rate in a hot magnetized plasma

We derive a general expression for the fermion self-energy in a hot magnetized plasma by using the Landau-level representation. In the one-loop approximation, the Dirac structure of the self-energy is characterized by five different functions that depend on the Landau-level index n and the longitudinal momentum pz. We derive general expressions for all five functions and obtain closed-form expressions for their imaginary parts. The latter receive contributions from three types of on shell processes, which are interpreted in terms of Landau-level transitions, accompanied by a single photon (gluon) emission or absorption. By making use of the imaginary parts of the self-energy functions, we also derive the Landau-level dependent fermion damping rates Γn(pz) and study them numerically in a wide range of model parameters. We also demonstrate that the two-spin degeneracy of the Landau levels is lifted by the one-loop self-energy corrections. While the spin splitting of the damping rates is small, it may be important for some spin and chiral effects. We argue that the general method and the numerical results for the rates can have interesting applications in heavy-ion physics, astrophysics, and cosmology, where strongly magnetized QED or QCD plasmas are ubiquitous. Published by the American Physical Society 2024

Rapid Detection of Heavy Metal Ions Co3+, Cu2+, Ni2+, and Zn2+ in Wastewater By Pyrimidine–Thiourea Ligand

Rapid Detection of Heavy Metal Ions Co3+, Cu2+, Ni2+, and Zn2+ in Wastewater By Pyrimidine–Thiourea Ligand

Determination of Binding Constants for the Complexes Between Heavy Metal Ions and Cucurbit[n]uril

AbstractOne of the major concerns worldwide is the rapid increase in water pollution with hazardous heavy metals. The Cucurbit[n]uril (CB[n]) structure provides an inner hydrophobic cavity accessible through two electrostatically negative portals with polar carbonyl groups, allowing for charged ion–dipole interaction between cationic species with excellent binding affinities. In this work we selected CB[5], and CB[7] for the titrimetric and electrochemical evaluation of the heavy metal complexes formed with Copper(II), Cadmium(II) and Lead(II). The host–guest interaction was found by either attenuation of the redox peaks, the formation of a new peak, or the slight shift in the redox peaks of the heavy metal ions. Titration data were obtained for CB[n] with the heavy metal solutions to determine the molar coefficient of binding. The stoichiometry of the complexes was 1 : 1 by Job′s plot. We calculated the binding constants using the Benesi–Hildebrand method achieving relatively good binding constants (K) ranging from (1.80±0.14)×105–(4.98±0.13)×105 M−1. The results showed that the complexes of Cadmium(II) and Lead(II) with both CB[5] and CB[7] are highly stable in aqueous media. Copper(II) was able to bind to the smaller sized portal of CB[5], whereas with CB[7] the heavy metal ion could not form a favourable complex. This phenomenon suggests that the CB[5] is an ideal host at forming stable host–guest interactions than their larger homologue.

Heavy metals removal in a graphene engineered concrete-based filter column

In this study, crushed aggregate surfaces were coated with reduced graphene oxide (RGO) using a chitosan-derived solution and included in porous concrete-based filter column samples to improve heavy metal removal. The RGO coating strengthened the aggregate and cement interfaces, thus improving the compressive strength of these samples by up to 18 %. The removal of lead and copper in samples containing RGO coated aggregate (GCA) operated with a minimum hydraulic load was found to be 97 % and 92 %. Increasing the hydraulic load reduced this heavy metal removal, but the presence of GCA increased the active sites for heavy metal ions to immobilize, leading to improved copper removal under such operating conditions. Calcium ions from the cement hydrates were found to leach from the concrete matrices during such a wastewater passage. This leaching of calcium ions was determined to be relatively lesser in RGO decorated concrete samples, pointing out the positive effects of GCA on the resistance of the concrete matrices to aggressive chemicals. Clay particles containing highly turbid water were also passed through these concrete samples to examine the effects on the infiltration rate. Clay particles were found to clog pores, marginally reducing the infiltration rate. Concrete-based water filters are easy to operate and have low maintenance requirements, and industries responsible for heavy metal pollution in aquatic environments can widely adopt them instead of complex treatment methods.

Enhanced detection of heavy metal ions using Ag nanoparticles and single-walled carbon nanotubes within Cu-based metal-organic frameworks

Heavy metal ions (HMIs) are major water pollutants, and their toxicity for humans is a great concern for scientists and environmentalists. They are harmful to health even at trace levels; therefore, identifying and removing heavy metals from water is critical. Herein, we report highly selective and sensitive multi-analyte detection of HMIs in water using an electrochemical sensor probe based on Ag nanoparticles and single-walled carbon nanotubes incorporating copper benzene tri-carboxylate metal–organic frameworks (Ag/SWNTs@CuBTC-MOFs). The materials were characterized using FTIR, XPS, XRD, and FE-SEM with EDX mapping, TEM, TG-DTA, BET surface area, CV, and EIS. The Ag/SWNTs@CuBTC-MOF electrochemical sensor was tested by differential pulse voltammetry over a pH range of 3–10 for various HMIs. It shows high pH-dependent sensitivity towards Hg2+ (pH-5.0), Ni2+ (pH-7.0), and Fe3+ (pH-10.0) ions and a limit of detection of 1.39 nM, 2.6 nM, and 3.03 nM, respectively. The fabricated sensor probe exhibits high selectivity, good linearity, and a limit of detection below the maximum contamination limit, as the US Environmental Protection Agency suggested.

A Ratiometric Green Fluorescent Carbazole-bis(hydrazinobenzothiazole) Probe for the Selective Detection of Toxic Hg2+ Ions in Real Water Samples.

A dyad Carbazolyl-bis(hydrazinobenzothiazole) was designed to form a symmetrical structure that containing two-arm active binding sites facilitates coordination with Hg2+ ion. This sensor has imparted a colorimetric and fluorometric changes in presence of Hg2+ ions. The ligand showed a selective blue shift in presence of Hg2+even in co-existence with heavy metal ions with luminescence change from colorless to blue and colorless to green under day light. Enhanced Intramolecular charge transfer process is responsible for fluorescence transformation when ligand interacts with Hg2+ ion. The emission spectra showed a ratiometric response to increasing addition of Hg2+ ions. The sensor is capable of detecting above the lower concentration of 6.8025 × 10-8 M. The fluorescence efficiency of CBT-2 with Hg2+ ion is quite stable under different co-metal ions and wide range of pH 6 to 9. The sensor CBT-2 forms a 1:1 stoichiometric complex with Hg2+ ions and the binding nature is confirmed from the 1H-NMR, FTIR, and mass spectroscopic studies. The sensor CBT-2 and its Hg2+ complex possess good binding nature to protein in Bovine Serum Albumin which could be good in biological applications. Additionally, wedevelop a practical application in real water sample analysis and electrochemical detection viaoxidation potential discrimination.

Effect of Heavy Ion Irradiation on Friction of GNSs: Implications for Aerospace Lubrication

Effect of Heavy Ion Irradiation on Friction of GNSs: Implications for Aerospace Lubrication

Impact of Nitrate on the Removal of Pollutants from Water in Reducing Gas-Based Membrane Biofilm Reactors: A Review

The membrane biofilm reactor (MBfR) is a novel wastewater treatment technology, garnering attention due to its high gas utilization rate and effective pollutant removal capability. This paper outlines the working mechanism, advantages, and disadvantages of MBfR, and the denitrification pathways, assessing the efficacy of MBfR in removing oxidized pollutants (sulfate (SO4−), perchlorate (ClO4−)), heavy metal ions (chromates (Cr(VI)), selenates (Se(VI))), and organic pollutants (tetracycline (TC), p-chloronitrobenzene (p-CNB)), and delves into the role of related microorganisms. Specifically, through the addition of nitrates (NO3−), this paper analyzes its impact on the removal efficiency of other pollutants and explores the changes in microbial communities. The results of the study show that NO3− inhibits the removal of other pollutants (oxidizing pollutants, heavy metal ions and organic pollutants), etc., in the simultaneous removal of multiple pollutants by MBfR.

Asymmetric jet shapes with two-dimensional jet tomography

Two-dimensional (2D) jet tomography is a promising tool to study jet medium modification in high-energy heavy-ion collisions. It combines gradient (transverse) and longitudinal jet tomography for selection of events with localized initial jet production positions. It exploits the transverse asymmetry and energy loss that depend, respectively, on the transverse gradient and jet path length inside the quark-gluon plasma (QGP). In this study, we employ 2D jet tomography to study medium modification of the jet shape of γ-triggered jets within the linear Boltzmann transport (LBT) model for jet propagation in heavy-ion collisions. Our results show that jets with small transverse asymmetry (ANn⃗) or small γ-jet asymmetry (xJγ=pTjet/pTγ) exhibit a broader jet shape than those with larger ANn⃗ or xJγ, since the former are produced at the center and go through longer path lengths while the later are off center and close to the surface of the QGP fireball. In events with finite values of ANn⃗, jet shapes are asymmetric with respect to the event plane. Hard partons at the core of the jet are deflected away from the denser region while soft partons from the medium response at large angles flow toward the denser part of QGP. Future experimental measurements of these asymmetric features of the jet shape can be used to study the transport properties of jets and medium responses. Published by the American Physical Society 2024

Ultra-high performance concrete with metal mine tailings and its properties: a review

Abstract Metal mine tailings (MMT) are a kind of industrial solid waste, with an increasing accumulation year by year, which has seriously damaged the ecological environment. Incorporating MMT in ultra-high performance concrete (UHPC) is an effective means to achieve green sustainable development, which can not only make wastes be resources and prevent pollution but also save raw material costs and reduce energy consumption. However, metal mine tailings contain complex and diverse metal oxides and other chemical substance and even contain certain radioactive elements and heavy metal ions. These factors can affect the corrosion resistance of UHPC, accelerate its aging and damage, and in addition may have serious impacts on the environment and human health. This paper summarizes the material properties of MMT and its application in UHPC; analyzes the effects of MMT as powder or fine aggregate on the workability, mechanical properties, durability, and leaching toxicity of UHPC; and elaborates the hydration products, interfacial transition zone, and pore structure of UHPC incorporating MMT (MMT-UHPC). Based on previous research results, the relationship between flowability, flexural strength, porosity, and compressive strength of MMT-UHPC is established.

Microfluidics Evolution and Surface Functionalization: A Pathway to Enhanced Heavy Metal Ion Detection

AbstractThis review delves into the significant advancements in microfluidic technology since 2017, highlighting its critical role in shrinking device sizes and integrating advanced surface functionalization techniques. It showcases how microfluidics, an interdisciplinary field, has revolutionized fluid manipulation on a microscale, enabling the creation of cost‐effective, portable devices for on‐the‐spot analyses, like heavy metal ion detection. From its early days rooted in ancient observations to cutting‐edge uses of materials like silicon, glass, polydimethylsiloxane (PDMS), and paper, this review charts microfluidics’ dynamic evolution. It emphasizes the transformative impact of surface functionalization methods, including silanization and plasma treatments, in enhancing device materials' performance. Moreover, this review anticipates the exciting convergence of microfluidics with emerging technologies like droplet microfluidics and three‐dimensional (3D) printing, alongside nanotechnology, forecasting a future of sophisticated analytical tools, point‐of‐care diagnostics, and improved detection systems. It acknowledges the hurdles in scaling production and achieving universal reliability and standardization. This review highlights the transformative impact of microfluidic technology on diagnostics and environmental surveillance, emphasizing its utility in deploying compact sensors for comprehensive and concurrent evaluations of water quality.

High-energy particle observations from the Moon.

The Moon is a unique natural laboratory for the study of the deep space plasma and energetic particles environment. During more than 3/4 of its orbit around the Earth it is exposed to the solar wind. Being an unmagnetized body and lacking a substantial atmosphere, solar wind and solar energetic particles bombardthe Moon's surface, interacting with the lunar regolith and the tenuous lunar exosphere. Energetic particles arriving at the Moon's surface can be absorbed, or scattered, or can remove another particle from the lunar regolith by sputtering or desorption. A similar phenomenon occurs also with the galactic cosmic rays, which have fluxes and energy spectra representative of interplanetary space. During the remaining part of its orbit the Moon crosses the tail of the terrestrial magnetosphere. It then provides the opportunity to study in-situ the terrestrial magnetotail plasma environment as well as atmospheric escape from the Earth's ionosphere, in the form of heavy ions accelerated and streaming downtail. The lunar environment is thus a unique natural laboratory for analysing the interaction of the solar wind, the cosmic rays and the Earth's magnetosphere with the surface, the immediate subsurface, and the surface-bounded exosphere of an unmagnetized planetary body. This article is part of a discussion meeting issue 'Astronomy from the Moon: the next decades (part 2)'.

Investigation of Single-Event Effects for Space Applications: Instrumentation for In-Depth System Monitoring

Ionizing radiation induces the degradation of electronic systems. For memory devices, this phenomenon is often observed as the corruption of the stored data and, in some cases, the occurrence of sudden increases in current consumption during the operation. In this work, we propose enhanced experimental instrumentation to perform in-depth Single-Event Effects (SEE) monitoring and analysis of electronic systems. In particular, we focus on the Single-Event Latch-up (SEL) phenomena in memory devices, in which current monitoring and control are required for testing. To expose the features and function of the proposed instrumentation, we present results for a case study of an SRAM memory that has been used on-board PROBA-V ESA satellite. For this study, we performed experimental campaigns in two different irradiation facilities with protons and heavy ions, demonstrating the instrumentation capabilities, such as synchronization, high sampling rate, fast response time, and flexibility. Using this instrumentation, we could report the cross section for the observed SEEs and further investigate their correlation with the observed current behavior. Notably, it allowed us to identify that 95% of Single-Event Functional Interrupts (SEFIs) were triggered during SEL events.

Adsorption Potential, Speciation Transformation, and Risk Assessment of Hg-, Cd-, and Pb-Contaminated Soils Using Biochar in Combination with Potassium Dihydrogen Phosphate

The objective of this study is to develop a remediation technology for composited heavy metal-contaminated soil. Biochars (BC300, BC400, and BC500) derived from corn were combined with potassium dihydrogen phosphate (KH2PO4) to immobilize and remove heavy metal ions, including mercury (Hg2+), cadmium (Cd2+), and lead (Pb2+). The adsorption kinetics of metal ions in aqueous solutions with different concentrations was tested, and the fitting effects of the two models were compared. The findings demonstrate that the joint application of biochar and KH2PO4 could markedly enhance the immobilization efficacy of Pb2+, whereas the utilization of KH2PO4 on its own exhibited a more pronounced immobilization impact on Cd2+. Furthermore, the present study underscores the shortcomings of various remediation techniques that must be taken into account when addressing heavy metal-contaminated soils. It also emphasizes the value of comprehensive remediation techniques that integrate multiple remediation agents. This study offers a novel approach and methodology for addressing the intricate and evolving challenges posed by heavy metal contamination in soil. Its practical value and potential for application are significant.

Real-time and specific monitoring of nitric oxide and evaluating of the oxidative stress in living cells and zebrafish under the pollutant exposure using a carbon dot-based composite fluorescent probe

Nitric oxide (NO) functions as an essential signalling molecule in various physiological and pathological pathways. In vitro and vivo redox processes mediated by reactive oxygen species (ROS) and nitric oxide (NO) directly influence the intracellular state. In this study, a red-emitting fluorescent nanoprobe, N,S-CDs@Zn-ICA, was synthesized to monitor NO fluctuations in living cells and zebrafish under the exposure to various pollutants. Red-emissive carbon dots (N,S-CDs) were synthesized by a hydrothermal method using o-phenylenediamine and urea as carbon / nitrogen sources, and H2SO4 as sulfur source. Glutathione (GSH) was introduced to link N,S-CDs with metal organic complexes (Zn-ICA) through an amidation reaction to fabricate a carbon dot-based composite fluorescent probe, which greatly improved the selectivity, stability, and response time of the N,S-CDs. The composite probe has high selectivity and sensitivity with limit of detection (LOD) of 96.0 nM. Furthermore, the proposed probe was successfully used to monitor the dynamic changes in NO levels and evaluate oxidative stress in MCF-7 cells and zebrafish under the exposure to various pollutants, including seven heavy metal ions (such as Pb2+, Cd2+, and Hg2+) and nine organic pollutants at different concentrations and exposure times. This work provides a novel strategy for constructing highly selective and red-emitting fluorescent probe for real-time and dynamic monitoring of NO and further evaluating oxidative stress induced by pollutants in vitro and in vivo via fluorescence imaging.

Unleashing the potential of Cajanus cajun biochar polymer composite for Cu (II) removal: mechanism, modification, and application.

This study introduces a cost-effective approach to fabricating a porous and ionically surface-modified biochar-based alginate polymer networks composite (SBPC) through air drying. The study critically analyzes the role and concentrations of various components in the success of SBPC. Characterization techniques were employed to evaluate the microstructure and adsorption mechanism, confirming the ability of the adsorbent's carboxyl and hydroxyl groups to eliminate various heavy metal ions in water simultaneously. The SBPC demonstrated high copper binding capacities (937.4mg/g and 823.2mg/g) through response surface methodology (RSM) and column studies. It was also influential in single and natural systems, exhibiting competitive behavior and efficient removal of Cu2+. The Langmuir isotherm and pseudo-second-order kinetics strongly correlate with experimental data, with R2 values of 0.98 and 0.99, respectively. SBPC showed remarkable stability, up to 10 desorption cycles, and achieved 98% Cu2+ adsorption efficiency and 91.0% desorption. Finally, the cost analysis showed a cost of 125.68 INR/kg or 1.51 USD/kg, which is very low compared to the literature. These results highlight the potential of SPBC and show that it provides an efficient and cost-effective solution for removing Cu2+ from a real system.

CHARACTERISTICS OF THE ADSORPTION OF HEAVY METAL IONS Pb2+, Cd2+, AND Ni2+ FROM INDUSTRIAL WASTEWATER

The aim of the study is to research of the adsorption properties of heavy metal ions Pb2+, Cd2+ and Ni2+ from industrial wastewater. For the adsorption of heavy metal ions, natural clinoptilolite was used, which belongs to the Ai-Dag deposit of the Tovuz-Kazakh region of Azerbaijan. Isotherms and kinetic curves of adsorption of heavy metal ions Pb2+, Cd2+ and Ni2+ were determined. The dependence of the adsorption of heavy metal ions on the pH value is also shown. It was revealed that the separation process proceeds more intensively at pH values ​​of 5-6. It has been established that the maximum adsorption capacity of the clinoptilolite adsorbent for the adsorption of Pb2+, Cd2+, and Ni2+ ions is 7.5, 6.7, and 5.9 mmol/g, respectively.