Element Solution Research Articles

Study on Enhancing the Quantitative Performance of LIBS for Cu Element in Liquids Based on the Chitosan-Parafilm Enrichment Method

Abstract To enhance the accuracy of laser-induced breakdown spectroscopy (LIBS) in detecting heavy metal elements in solutions, a Chitosan (CS)-Parafilm (PM) enrichment method is proposed. This method involves drying chitosan-heavy metal complexes on a Parafilm substrate. During the drying of droplets, electrostatic attraction and chelation by CS effectively concentrate analytes. Additionally, the hydrophobic effect of the PM substrate induces Marangoni flow, which drags analytes from the bottom edge to the central top of the droplet surface, effectively suppressing the coffee ring effect (CRE).LIBS spectra were collected in a uniform array on the surface of sediments, and spectral stability was assessed through cumulative excitation spectra measurements. The results showed that the spectral stability of emission lines Cu I 324.754 nm and Cu I 327.396 nm decreased to 3.85% and 3.78%, respectively, indicating that the CS-PM enrichment method allows for uniform deposition of analytes within samples, effectively enhancing detection repeatability.Quantitative analysis of Cu elements using the CS-PM enrichment method was conducted using PSO-SVM, PSO-BPNN, and RF algorithms. The RF algorithm demonstrated the best predictive performance with Rp² of 0.979, RMSEP of 4.60 mg/L, MAE of 3.19 mg/L, and RPD of 6.75. These results indicate that CS-PM effectively improves spectral stability and quantitative analysis accuracy, providing a technical reference for enhancing the stability and quantitative performance of element analysis in liquids using LIBS.

A Catalyst Tube-Equipped Dual-Stage Tube Furnace System for Accurate Hg Isotopic Determination of Ore Samples Using Neptune Plus Multicollector Inductively Coupled Plasma Mass Spectrometry.

Mercury (Hg) isotopes, which display mass-dependent fractionation and mass-independent fractionation, provide a multidimensional tracer to decipher the source of metals in mineral deposits. However, mineral ore samples usually contain abundant interfering elements (e.g., Te) that can cause inaccurate Hg isotopic analysis. Available acid digestion and combustion methods failed to remove these interfering elements, hindering the application of Hg isotopes for metallogenetic tracing. Here, we developed a new dual-stage tube furnace system employing a Mn-containing catalyst tube to pretreat mineral ore samples. This method yielded good Hg recoveries (100.5 ± 3.8%, 1SD, n = 15) and low levels of interfering elements in sample solutions, allowing for accurate analysis of a series of ore standard reference materials (GBW-11108v: coal; GSO-3: Cu-Ag sulfide ore; GBW 07859: Au-Te sulfide ore). The new method was also successfully applied to measure the Hg isotopic composition of magmatic and hydrothermal ore deposits, which yielded a large range in Δ199Hg value (-0.19 to 0.22‰) for ore deposits formed in different geological settings, highlighting the future applications of this method for metallogenic tracing, especially tracing the source of metals in mineral ore deposits.

Theoretical investigation on crash performance of bamboo-inspired energy absorption systems based on systematic experimental and numerical analysis

The need for energy-absorbing devices with adaptable crashworthiness is increasingly urgent in various engineering fields with diverse load environments. For this aim, bamboo-inspired modular energy absorption systems have recently been proposed to integrate mechanical efficiency, tunability, and robustness. However, their mechanical responses under varying load velocities have not been systematically studied, which limits the effective prediction and optimization of their crashworthiness. In this study, quasi-static and dynamic experiments were performed on bamboo-inspired systems, discretely assembled using 3D printed steel tube specimens. Matched finite element simulations were conducted using ABAQUS/Explicit. Specific energy absorption and efficiency of these systems respectively exceeded 12.9 J/g and 47 %, surpassing existing discretely assembled systems and rivaling typical cellular materials. Efficient deformation mode with self-locking capability was observed, and sharp impact peak was avoided when the crash velocity was less than 50 m/s. Building upon these findings, a modified spherical shell theory under crashing was developed to predict energy absorption performance of bamboo-inspired system based on the traveling plastic hinge model. The average relative error between the analytical solution and finite element results was found less than 6.5 %. The mean effective stress of the system could exceed 35 MPa under thickness-to-diameter ratio of 5 %. This work presents an efficient and effective approach for optimizing and estimating the crash performance of modular protective devices.

Rapid quantitative analysis of three elements (Al, Mg and Fe) in molten zinc based on laser-induced breakdown spectroscopy combined with machine learning algorithm

Hot-dip galvanizing represents one of the most cost-effective methods for the prevention of metal corrosion, and is therefore employed extensively across a range of fields. Carrying out the research and development of technology and devices for quantitative analysis of chemical elements in hot-dip galvanising process can provide theoretical basis and technical support for the efficiency of hot-dip galvanising process and reduction of energy consumption. A machine learning-assisted LIBS combined with a programmable logic controller (PLC) for simultaneous on-line/in-site monitoring of multiple elements in hot-dip galvanising solution (molten zinc) was developed in the current study. The LIBS spectral data of the on-site hot-dip galvanising solution was collected under optimised experimental conditions. In order to further reduce the influence of experimental noise on the analysis performance, the on-site LIBS spectral data were preprocessed and anomalous spectral data were screened based on normalisation and principal component analysis-mahalanobis distance (PCA-MD). On the basis of the optimised data, component prediction models for three key elements of on-site hot-dip galvanising solution were constructed. The storage and re-call of the model was achieved based on python combined with LabVIEW, thus real-time prediction of the on-site component content of hot-dip galvanising solution was achieved. The results show that the random forest model presents the best prediction results, in which the R2 is 0.9978 and the RMSE is 0.0013% for Al, the R2 is 0.9984 and the RMSE is 0.0011% for Mg, and the R2 is 0.9932 and the RMSE is 0.0001% for Fe. From the on-site analysis results of the constructed model, its MRE of Al, Mg and Fe is 0.0098, 0.0236, and 0.2102, respectively. In summary, the in-situ/on-line analysis system of hot-dip galvanising solution combined with machine learning constructed in this study shows excellent performance, which can satisfy the needs of hot-dip galvanising solution production site. This study is expected to provide theoretical basis and technical reference for quality control and process optimisation in other production sites in the metallurgical field.

Element release from lead crystal ware and metallic hip flasks

The release of 21 elemental ions from lead crystal ware and metallic hip flasks into different food simulants as well as alcoholic beverages was investigated in this study. For this purpose, an ICP-MS method including a sample pre-treatment based on microwave-assisted digestion was developed and validated. Elemental ion release from lead crystal glasses into artificial tap water, 0.5% citric acid solution and white wine, respectively, was only analysed for Pb. Within 24 h, Pb release from crystal glass was shown to increase with time. To account for repeated use, at least three consecutive release experiments were performed, which showed – with one remarkable exception – constant or decreasing levels of element ion release. However, after four months resting period, Pb release from crystal glass was higher than before. In contrast, all 21 elemental ions were detected to be released from the hip flasks into 0.5% citric acid solution, apple liqueur and herb liqueur, respectively. Release of Cd, Cr, Ni, As, TI, Sn and most prominently Pb from hip flasks was in the range of and above the respective release limit (SRL) as set by the Council of Europe (CoE). When focussing on the third repetition, only one out of six hip flasks met the suggested SRL for all determined elements in all test solutions. This demonstrates both, that the SRLs of the CoE can be met and that producers of hip flasks may have to review their manufacturing processes.

The effect of impurity in vanadium-rich solution on vanadium precipitation of VO2(B) by hydrothermal method

The effect of iron, aluminum, silicon and phosphorus in the vanadium-rich solution on the vanadium precipitation of VO2(B) by hydrothermal method were studied. Through the analysis of vanadium conversation efficiency, the content of V and impurity elements in precipitates and their existing form, product crystal structure and micromorphology, it is concluded that the effect following the order of P > Fe > Si > Al. As the impurity concentration increased, V content of the precipitates decreased to varying degrees, while impurity content increased. The exist of Al, Si, Fe and P could alter the diffraction peaks intensity of some crystal faces and the micromorphology of VO2(B). The high concentrations of Fe and P transformed the VO2(B) to Fe2.5V7.1O16 and Na0.45VOPO4·1.58 H2O, respectively. V and P are easily combined by covalent bonds, affecting the precipitation of VO2(B). Silicon is adsorbed on the surface of the precipitate as silica gel, thereby reducing the purity of the precipitate. The influence of impurity elements in vanadium-rich solution on the precipitation of VO2(B) by hydrothermal method is studied, which will provide a theoretical basis for the application of the new process of vanadium precipitation by hydrothermal method.

Research on the Two-Pillar Solution and Its Implication

With the rapid development of economic globalization and digitalization, new business models are activating the world economy while exacerbating the remaining problems of base erosion and profit shifting (BEPS). In the face of intensifying international tax avoidance, The Organisation for Economic Co-operation and Development (OECD) has announced its Two-pillar solution to the international community, proposing a global minimum tax regime, which is effectively a coordination of global anti-tax avoidance measures. At present, Pillar 2 has come into effect, and Pillar 1 has also been opened for signature, marking the implementation stage of the two-pillar solution. In this paper, the two-pillar solution is the main research object. Firstly, from the perspective of large-scale tax avoidance by multinational corporations, this paper systematically analyzes the historical background of the introduction of the two-pillar solution of the OECD. After a detailed analysis of the provisions of the two-pillar solution, the existing institutional deficiencies and obstacles to its implementation are proposed. Finally, in response to the issues raised, practical recommendations are made that the elements of the two-pillar solution should aim to achieve general equity, balance the interests of developing countries and be in harmony with existing international tax policies. The governments should also optimize the structure of tax incentives.

Effects of solute alloying elements on solid solubility of TiC in austenite

Solute elements in microalloying steel affect the solid solubility of microalloying elements, and thus affect the second phase precipitation in steels. In this work, the influences of solid solution elements, especially Si and Al, on the solubility product of TiC in austenite were studied using the two-sublattice model. The results show that both Al and Si additions reduced the solubility product of TiC in the austenite region, and the reduction degree of TiC solubility product with Al addition was increased with increasing temperature, while it was decreased with Si addition. In addition, Mn, Mo and Cr additions all increased the solubility product of TiC in the austenite region, and the increment degree of TiC solubility product with Mo addition was decreased with increasing temperature, while it changed slightly with Mn or Cr addition with temperature. The model of solubility product of TiC without alloying additions in austenite was modified, and the calculating result was highly consistent with findings of literatures. Finally, a calculation model of TiC solubility product considering the influence of alloying elements was established.

The nitrogen deficiency influence on the growth and development of spring two-nuclear barley varieties grown under photoculture conditions

The purpose of the research is to study, the effect of N deficiency in irrigation solutions on the structural and functional characteristics of spring barley (Hordeum vulgare L.), the Oplot variety under controlled environmental conditions, in comparison with the structural and functional characteristics of Takmak barley, which has been the standard in all variety testing sites of the Krasnoyarsk Territory since 2022. The plants were grown under light culture conditions using hydroponics on expanded clay with constant environmental conditions at a photoperiod day/night of 17h / 7h, respectively. The basis for the preparation of irrigation solutions was Knop solution (control) and a solution in which, in order to reduce the concentration of N-NO3, the salt content was changed 2 times so as not to change the concentration of other macronutrients. A comparison of the rate of absorption of macronutrients by barley plants of the Oplot and Takmak varieties, depending on the composition of the irrigation solution, shows a higher demand of the barley of the Oplot variety for the presence of mineral nutrition elements in the irrigation solution in comparison with the barley of the Takmak variety. The deficiency of N in the irrigation solution led to a decrease in total tillering by about 2.5 times, but productive tillering in the barley of the Oplot variety decreased to a greater extent than in the barley of the Takmak variety. When growing on Knop solution the barley of the Oplot variety showed higher productivity than the barley of the Takmak variety. When grown on solutions with a deficiency of N, the grain yield of the barley of the Oplot variety decreased by 2.8 times, and in the barley of the Takmak variety, the differences between the control and experimental variants were unreliable. The barley of the Takmak variety showed higher resistance to N deficiency in the irrigation solution, thereby showing higher plasticity compared to the barley of the Oplot variety.

Adsorption of natural dye phycocyanin by means of Laponite®: Synthesis and characterization of the hybrid obtained

This work addresses the use of Laponite® clay in various applications, focusing on its adsorption capacity and improvement of properties in water-based products. It describes the synthesis of Laponite® hybrids with the pigmented cyanobacterium phycocyanin (PC) to evaluate the adsorption capacity of the dye. This research addresses the importance of Laponite® clay in improving rheological properties of water-based products due to its ability to interact with components in aqueous solutions. Laponite® can be effectively dispersed in water, enhancing the dispersion of other elements in solution and preventing aggregation of solids. The structure and properties of synthetic Laponite® are described, highlighting its use in the textile industry as an additive for pigments and the formation of gels. Experimentally, Laponite® is used to adsorb phycocyanin, a cyanobacterial pigment, with the aim of achieving maximum adsorption. A design of experiments with different experimental conditions, including pH, addition of silane and surfactant, is used. A detailed analysis of the characterization of the resulting hybrids is presented, including colour, total solar reflectance (TSR), thermal analysis (TGA), EDS, FTIR and X-ray diffraction (XRD) measurements. The results show successful adsorption of the pigment in all experiments, with adsorption percentages above 97%. The colour of the hybrids is evaluated and the total solar reflectance is analyzed, highlighting their importance in applications such as coatings and printed textiles. Infrared spectroscopy and X-ray diffraction are used to study the structural properties of the hybrids. For future work, it is intended to be able to apply the hybrids obtained on an industrial scale in the colouring of textiles and plastic polymers.

A non-uniform compound strip method for effective buckling analysis of stiffened structures

In this paper, a versatile compound strip method (CSM) with non-uniform spline functions is developed for buckling analysis of stiffened structures. The proposed method further extends the existing CSM by permitting the flexible modification of local knots to place the stiffeners along the strip arbitrarily. In addition, a reasonable knot arrangement can achieve an accurate solving procedure with improved convergence. The displacements of stiffeners are expressed compatibly by the fundamental parameters of skin according to the beam-plate model. Consequently, the reinforcement of stiffeners is naturally incorporated by adding the beam stiffness matrix to the corresponding strips. Based on the first-order shear deformation plate theory and non-uniform spline functions, the semi-analytical formulations of stiffened structures are established. The present method provides the possibility to achieve the local mesh refinement in the finite strip methods. The convergence and validation study is demonstrated through the comparisons with the results of the existing literature solution and finite element method. In conclusion, a more efficient and applicable CSM is proposed to analyze the buckling behaviors of stiffened structures.

Mn-controlled martensitic variant selection significantly affects the strength and toughness of 2.3 GPa ultra-high strength spring steel

In this study, the microstructure and mechanical properties of 55SiCrVNb ultra-high strength spring steel with 0.7 and 1.5 wt.% Mn were systematically investigated. The results show that 0.7Mn steel exhibited higher strength and toughness. The morphology and content of retained austenite, content of element in solid solution and the type and quantity of precipitates were basically the same in 0.7Mn and 1.5Mn steels. Hence, the variant reconstruction, as a unique perspective, was used to unravel the strengthening and toughening mechanisms governing the evolution of variants across varying Mn contents. Compared with the 1.5Mn steel, the decrease in Mn content deteriorated the variant selectivity (decreased variant frequency over 50 %), which led to a more uniform distribution of close-packed plane (CP) and Bain groups in 0.7Mn steel, thus refining the block size and improving the grain refinement strengthening (σp). The 0.7Mn steel with a higher density of high angle grain boundaries (HAGBs) effectively constrained dislocation slip, thereby enhancing dislocation strengthening (σd). As the Mn content decreased, the block size decreased from 0.24 to 0.14 μm, and the contribution of σp and σd increased by about 107 and 96 MPa, thus improving the yield strength. In addition, the increased HAGBs, which were dominated by the highly selective V1/V2, V1/V3(V5) and V1/V6 variant pairs, and the uniform CP and Bain group also contributed to inhibiting crack deflection and enhancing the impact toughness. Moreover, the higher Schmid factor with high geometrically necessary dislocation of 0.7Mn steel improved the deformation resistance of variants and strength. This work provided a new mechanism of strengthening and toughening dominated by variants.

(Invited) Degradation and Poisoning of Proton-Exchange Membrane Water Electrolyzer Anode Catalysts

Hydrogen production through water electrolysis is a crucial technology to enable the transition to a carbon neutral, hydrogen-based economy. One of the primary types of electrolyzers is the low-temperature proton-exchange membrane water electrolyzer (PEMWE). As with the analogous proton-exchange membrane fuel cells, platinum group metal electrocatalysts are utilized due to their activity and stability in acidic environment. Electrocatalysis R&D efforts for PEMWEs primarily focus on the oxygen evolution reaction (OER) since it is several orders of magnitude kinetically slower than the hydrogen evolution reaction (HER).1 Iridium-based metal oxides (IrOx) are regarded as the best PEM electrolyzer electrocatalysts as they balance activity and stability.2 However, improvements are needed in both areas to enable minimization of Ir loading to meet system cost targets while also meeting challenging performance and lifetime targets.3 An understanding of the factors affecting both the activity and stability of Ir-based OER catalysts is needed to develop strategies to enable both high OER activity and long-term stability of the PEMWE anode catalyst.This presentation will describe our studies of the effects of perfluorosulfonic acid (PFSA) binder on the OER kinetics and the factors influencing the stability of two commercial Ir-based OER catalysts, one comprised of IrOx only and the other also containing TiOx. Measurements of OER kinetics as a function of ionomer to catalyst ratio utilizing rotating disc electrode and cavity microelectrode methods in an acidic aqueous electrochemical environment will be described. Dissolution and loss of Ir under the operating conditions of the PEMWE anode is considered to be one of the main PEMWE anode degradation mechanisms.4 To understand the factors affecting this phenomenon, the potential and time-dependence of Ir (and Ti) were determined using an electrochemical flow cell system connected to an inductively-coupled plasma-mass spectrometer (ICP-MS) capable of detecting trace concentrations (<ppb) of dissolved elements in solution. The electrochemical data combined with the ICP-MS data have been used to evaluate the influence of various factors such as potential, potentiodynamic profile parameters (e.g., scan rate, upper and lower potential limits) on the dissolution processes in acidic aqueous electrolyte at room temperature.AcknowledgementsThis research is supported by the U.S. Department of Energy, Energy Efficiency and Renewable Energy, Hydrogen and Fuel Cell Technologies Office under the auspices of the H2NEW Consortium. Argonne National Laboratory is managed for the U.S Department of Energy by the University of Chicago Argonne, LLC, also under contract DE-AC-02-06CH11357.References A. Raveendran, M. Chandran, and R. Dhanusuraman, RSC Adv., 13 (2023) 3843.J. Ouimet, J.R. Glenn, D.D. Porcellinis, A.R. Motz, M. Carmo, K.E. Ayers, ACS Catalysis, 12 (2022) 6159."Technical Targets for Proton Exchange Membrane Electrolysis", U.S. Department of Energy, Energy Efficiency and Renewable Energy, Hydrogen and Fuel Cell Technologies Office, March, 2023.Zeng, R. Ouimet, L. Bonville, A. Niedzwiecki, C. Capuano, K. Ayers, A.P. Soleymani, J. Jankovic, H. Yu, R. Maric, et al., J. Electrochem. Soc., 169(5) (2022) 054536.

Investigating Corrosion Degradation of Porous Transport Layers for PEM Water Electrolyzers Using on-Line ICP-MS

The degradation of polymer electrolyte membrane water electrolyzer (PEMWE) is the net result of degradation phenomena across each component, which includes structural changes to the catalyst layer, deactivation of the electrolyte, loss of performance due to impurities in the feed water, and the corrosion and passivation of titanium-based bipolar plates (BPPs) and porous transport layers (PTLs).1, 2 This presentation will focus on PTL degradation, which has received relatively little attention compared to loss of performance related to catalyst and electrode degradation mechanisms. Generally, PTL degradation can be categorized into chemical/corrosion degradation and mechanical degradation. 3 In this work, we focus on corrosion degradation of the anode PTL. Titanium (Ti) is the state-of-the-art material for PTLs due to its stability and intrinsic electrical conductivity. Ti can however, develop an oxide layer in the harsh oxidizing conditions of the anode, thus reducing the effective electrical conductivity and cell performance. Coating the Ti parts with platinum group metals (Pt or Ir) is often used to protect against oxidation.4 An electrochemical flow cell system connected to an inductively-coupled plasma-mass spectrometer (ICP-MS) capable of detecting trace concentrations (<ppb) of dissolved elements in solution has been used to investigate the corrosion rates of the Ti-PTLs with and without coatings toward understanding factors influencing degradation mechanisms. The influence of various parameters such as potential, potentiodynamic profile parameters (e.g., scan rate, upper and lower potential limits), electrolyte type, and pH on the corrosion processes has been investigated. References Feng, X. Yuan, G. Liu, B. Wei, Z. Zhang, H. Li, H. Wang, J. Power Sources 2017, 366, 33.Babic, M. Suermann, F. N. Büchi, L. Gubler, T. J. Schmidt, J. Electrochem. Soc. 2017, 164, F387.Park, H. Oh, T. Ha, Y.I. Lee, K. Min, Appl. Energy 155 (2015) 866-880.Rakousky, U. Reimer, K. Wippermann, M. Carmo, W. Lueke, D. Stolten, J. Power Sources 326 (2016) 120–128. Acknowledgements This research is supported by the U.S. Department of Energy, Energy Efficiency and Renewable Energy, Hydrogen and Fuel Cell Technologies Office under the auspices of the H2NEW consortium. Argonne National Laboratory is managed for the U.S Department of Energy by the University of Chicago Argonne, LLC under contract DE-AC-02-06CH11357.

Electrical conductivity of binary magnesium alloys: Integrating first-principles and machine learning studies

The electrical conductivity is the fundamental physical property of Mg alloys and the basic information for the design of comprehensive high-performance Mg alloys. In this work, the electrical conductivity of 29 Mg-based binary alloys has been calculated using the first-principles methods and the main factors have been analyzed by machine learning. It is found that the electrical conductivity values of the binary alloys containing elements located in the s region and p region of the periodic table are bigger than others of alloys contain alloying elements in the f region and d region. The results of machine learning show that the difference ratio of volume (∆V/VMg), extra-nuclear electron configuration and difference of valence () play the main controlling role, followed by solid solubility and electronegativity of the alloying element. For solid solution elements in Mg-based binary alloys, the impact weight on the electrical conductivity is: difference ratio of volume > number of extra-nuclear electron vacancy > difference of valence.

Utilizing the Perfluoronaphthalene Radical Cation as a Selective Deelectronator to Access a Variety of Strongly Oxidizing Reactive Cations.

A selective deelectronation reagent with very high potential of +2.00 (solution)/+2.41 V (solid-state) vs. Fc+/0 and based on a room temperature stable perfluoronaphthalene (naphthaleneF) radical cation salt was developed and applied. The solid-state deelectronation of commercial naphthaleneF with [NO]+[F{Al(ORF)3}2]- generates [naphthaleneF]+⋅[F{Al(ORF)3}2]- (ORF=OC(CF3)3) in gram scale. Thermochemical analysis unravels the solid-state deelectronation potential of the starting [NO]+-reagent to be +2.34 V vs. Fc+/0 with [F{Al(ORF)3}2]- counterion, but only +1.14 V vs. Fc+/0 with the small [SbF6]- ion. Selective reactions demonstrate the selectivity of [naphthaleneF]+⋅ for deelectronation of a multitude of organ(ometall)ic molecules and elements in solution: providing the molecular structures of the acene dications [tetracene]2+, [pentacene]2+ or spectroscopic evidence for the carbonyl complex of the ferrocene dication [Fc(CO)]2+, the [P9]+ cation from white phosphorus, the solvent-free copper(I) salt starting from copper metal and the dicationic Fe(IV)-scorpionate complex [Fe(sc)2]2+.

The effects of refractory elements on mechanical properties in CoCrNiFe concentrated solid solution alloys across different temperatures

Mo, W and Re are all important strengthening elements in either single phase solid solution (SS) alloys or the SS phases in precipitation-strengthened Ni/Co-based superalloys, of which the compositions are usually complicated. To directly compare the effects of Mo, W and Re on the mechanical properties of concentrated SS alloys, a model CoCrNiFe concentrated SS alloy as the base and three alloys with 3 at.% Mo, W and Re additions are fabricated and their mechanical properties are examined in both quasi-static tensile and creep tests at room and two high temperatures. Experimental and modeling results demonstrate that at room and low temperatures, the order of strengthening effect is W > Mo > Re, in accordance with solid solution strengthening model and thermal activation analysis. On the other hand, Re can significantly decrease the minimum creep rate at 1273 K, primarily due to the reduced diffusivity as confirmed from the diffusion couple analysis.

Chelator-impregnated polydimethylsiloxane beads for the separation of medical radionuclides

Chelator-impregnated resins have been studied earlier for the chemical separation of elements in aqueous solutions, but issues with their chemical stability have limited their use in the separation of (medical) radionuclides from their respective irradiated targets. We developed a polydimethylsiloxane (PDMS)-based chelator-impregnated resin that showed a high chemical stability against leaching. Several different chelators were tested in this study. After impregnation of the PDMS beads with the di-2-ethylhexylphosphoric acid (D2EHPA) chelator, an in-flow separation study with various radionuclides (Y-90, La-140, and Ac-225) was conducted. These three radionuclides have potential use in nuclear medicine and a production route through irradiation of Sr-, Ba-, and Ra-targets respectively, necessitating their chemical separation. The D2EHPA-impregnated beads achieved high adsorption efficiencies of 99.89% ± 0.14%, 99.50% ± 0.10%, and 98.51% ± 0.25%, for Y-90, La-140, and Ac-225, respectively, while co-adsorption of minor amounts (<3%) of the targets were reported. These results, together with the high chemical stability of the PDMS-based resin, highlight the potential of chelator-impregnated resins in the rapidly growing field of (medical) radionuclide production.

Exploring the Application of Terahertz Metamaterials Based on Metallic Strip Structures in Detection of Reverse Micelles.

Terahertz spectroscopy has unique advantages in the study of biological molecules in aqueous solutions. However, water has a strong absorption capability in the terahertz region. Reducing the amount of liquid could decrease interference with the terahertz wave, which may, however, affect the measurement accuracy. Therefore, it is particularly important to balance the amount and water content of liquid samples. In this work, a terahertz metamaterial sensor based on metallic strips is designed, fabricated, and used to detect reverse micelles. An aqueous confinement environment in reverse micelles can improve the signal-to-noise ratio of the terahertz response. Due to "water pool" trapped in reverse micelles, the DOPC (1,2-dioleoyl-sn-glycero-3-phosphocholine) solution and DOPC emulsion can successfully be identified in intensity by terahertz spectroscopy. Combined with the metamaterial sensor, an obvious frequency shift of 30 GHz can be achieved to distinguish the DOPC emulsion (5%) from the DOPC solution. This approach may provide a potential way for improving the sensitivity of detecting trace elements in a buffer solution, thus offering a valuable toolkit toward bioanalytical applications.

Quantitative analysis of microstructural evolution in cold-sprayed CuCrZr: Understanding heat transfer mechanisms from room temperature to 600°C

Cold-sprayed CuCrZr coating offers interesting multifunctional properties with a combination of high mechanical property, good thermal stability and substantial deposition thickness. Despite these advantages, the incorporation of solid solution elements and the deposit’s unique microstructure often result in suboptimal heat transfer capabilities. This study delved into the thermal conductivity of cold-sprayed CuCrZr coatings over a temperature range from room temperature to 600 °C. Furthermore, it quantitatively analyzed their microstructural evolution post-thermal testing and its correlation with thermal properties, employing techniques such as FESEM, EBSD, TEM, and XRD. Findings indicate the CuCrZr coating exhibits significant thermal sensitivity, with conductivity increasing from 65.83±1.79 W/(m∙K) at 25 °C to 198.42±0.63 W/(m∙K) at 600 °C. The annealing effect during thermal testing significantly enhances the coatings’ room temperature thermal properties, chiefly through the enhancement of interparticle metallurgical bonding, grain enlargement, solid solution precipitation, and a reduction in dislocation density. The thermal conduction across the coating/substrate interface is intricately influenced by the interplay between electrons and phonons, with impediments at the interface becoming markedly pronounced beyond 300 °C. The investigation pinpointed interparticle interfaces as the predominant barriers to heat transfer, contributing to 73.77 % of the total resistance. Meanwhile, the effects of solid solution elements, grain boundaries, and dislocations on thermal conductivity were comparatively minor, contributing 9.36 %, 1.04 %, and 0.44 %, respectively. However, it is also noted that the annealing effect can induce the coalescence of microcracks into pores and promote the precipitation or oxidation of Cr at the interfaces, which, in turn, limits the potential for further enhancements in thermal conductivity.