Ion Precipitation Research Articles

Utilization of Schiff base ligands to chelate Ag+ for highly specific and sensitive Hg2+/Ag+ immunoassay

In this study, a planar benzothiazole Schiff base derivative ZX1 was designed and synthesized to selectively precipitate silver ions, in conjunction with the immunoassay detection of Hg2+ ions. The silver chelation process was highly effective in the pH range of 7–10, with a silver ion precipitation ratio of 99.9 %. The coordination behavior of ZX1 with Ag+ was studied using a series of spectroscopic measurements, topography analysis and DFT calculation. The shortest bond distances were 2.251 and 2.254 Å between nitrogen atom of thiazole and Ag+. Weak interactions were analyzed using the interaction region indicator (IRI) method and VMD. The immunoassay was developed through an anti-Hg2+/Ag+ monoclonal antibody, which showed similar sensitivities for Ag+ and Hg2+. The selectivity and anti-interference ability of the Schiff base ligands were tested for some hard metal ions and several anions. With co-existence of interference ion Ag+, Hg2+ was detected in rice matrix solution with 77 %∼123.5 % recovery by addition of ZX1 as the masking reagent and 90.3 %∼115 % for wheat matrix. This research provides a promising immunoassay strategy for simultaneous detection of silver ions and mercury ions in food matrix by utilization of Schiff base ligands. This novel Schiff base ligand was then used as the pre-treatment reagent to remove silver ions within 5 min for detection of Hg2+ or detection of both Ag+ and Hg2+ based on a novel bi-specific heavy metal antibody.

Metal-modified biochars prepared from blue algae and their ability of adsorbing phosphates from water and utilization as soil amendment

The problem of blue algae accumulation can be alleviated by utilizing blue algae as biomass for resource utilization, which can remove excess phosphates from water to alleviate eutrophication. Herein, Magnesium (Mg) and/or lanthanum (La) were used to modify biochar via high-temperature slow pyrolysis with blue algae as the raw biomass. These modified biochars exhibited abundant carbon (18.0%-50.3%), oxygen content (17.4%-49.1%), along with a high specific surface area (82.26-233.80 m2/g). The surface of metal-modified biochar was enriched with hydroxyl and carboxyl groups and metal elements were efficiently incorporated into biochars. Adsorption kinetic and isotherm experiments were conducted under the optimal pyrolysis temperature of 600 °C, pH of 6.0, and adsorbent dosage of 2.0g/L. The adsorption kinetics studies by metal-modified biochars for phosphate fitted well pseudo-second-order model Redlich-Peterson isotherm model. Biochar modified by Mg and La exhibited the highest removal efficiency (97.8%) for phosphate at adsorption equilibrium. The adsorption mechanism involved the electrostatic interaction between hydroxylated metal oxides and negatively charged phosphate ions and the precipitation of phosphate ions through chemical reactions with metal oxides in the solution. After phosphate adsorption, the pristine and metal-modified biochars derived from blue algae were applied as the soil amendment. Biochar adsorbed phosphate apparently improved the germination rate of seeds facilitated the height, width, weight, and chlorophyll content of vegetable seedlings, and induced oxidative stress, which proved that the biochar recovered after adsorption was a high-quality soil amendment. This study provides a new approach for the treatment of phosphate wastewater and the algae application.

Preparation of large specific surface rare earth oxides from calcium-containing rare earth solution by carbon dioxide carbonization method☆

The calcium-containing rare earth solution is generated during the recovery processes of NdFeB waste, which is treated as wastewater by enterprises. In this paper, the carbon dioxide carbonization method was applied to the separation of rare earths and calcium in the solution, as well as the preparation of rare earth oxides with a large specific surface. It is shown that the process of CO2 carbonization of solution includes reactions such as the dissolution, diffusion and ionization of CO2, the carbonate precipitation of rare earth ions, and the neutralization of hydrogen ions. At a pH of 4.5, the carbonization precipitation rate is effectively controlled, enabling homogeneous precipitation and ensuring both high precipitation yield and rare earth oxides purity. In this way, the crystallization of carbonization products is a process dominated by the oriented attachment theory and coexisting with the Ostwald ripening theory, resulting in abundant pores formed by multiple layers of stacking in the products. With the optimal carbonization conditions, the rare earth precipitation yield solution reaches 99.32%. The obtained carbonization products are crystalline (LaCe)(CO3)3·8H2O, and the purity of the rare earth oxides is as high as 99.22 wt%. The specific surface area of the rare earth oxides reaches 94.7 m2/g, and its adsorption efficiency for tetracycline hydrochloride in solution can reach 92.6% in a short time. The rare earth oxides are expected to be used as an adsorption material for wastewater treatment and other adsorption environments.

Carbon dioxide sequestration through mineralization from seawater: The interplay of alkalinity, pH, and dissolved inorganic carbon

Marine carbon dioxide removal technologies rely on the equilibration of the seawater with atmospheric CO2, where a pH increase can facilitate carbon dioxide removal either through increased absorption capacity of CO2, or precipitation of minerals. Here, we focus on explicitly defining the governing factors that influence seawater alkalinity with respect to CaCO3 mineralization and atmospheric CO2 uptake. We utilize an electrochemical setup and different water types, from near-shore Mediterranean seawater as well as Red Sea Salt water. The setup allows us to separate mineralization from alkalinity enhancement via an electrochemical membrane cell, and a second compartment with controlled environment, where the interplay of ion concentration, precipitation, pH, DIC concentration, and total alkalinity are evaluated. The effect of sparging additional carbon dioxide before, and after the precipitation of CaCO3 was evaluated while utilizing both a mild pH swing (from, ∼8.3 to ∼9.5), and a larger pH swing (from, ∼8.3 to ∼10.2). A thermodynamic model is presented defining the energy consumption to increase the pH, and the influence of Mg thereon is explicated. Furthermore, we detail theoretical aquatic chemistry simulations via PHREEQC to rationalize the observed intricate dynamics of the carbonate system in seawater. We end with a discussion of the implications of total alkalinity, pH, salt complexation, and carbon uptake capacity relevant to of all ocean alkalinity enhancement and marine based carbon dioxide removal systems, concluding that the carbon uptake capacity of water returned to the ocean must be verified in such technologies

A Comprehensive Flow–Mass–Thermal–Electrochemical Coupling Model for a VRFB Stack and Its Application in a Stack Temperature Control Strategy

In this work, a comprehensive multi-physics electrochemical hybrid stack model is developed for a vanadium redox flow battery (VRFB) stack considering electrolyte flow, mass transport, electrochemical reactions, shunt currents, and as heat generation and transfer simultaneously. Compared with other VRFB stack models, this model is more comprehensive in considering the influence of multiple factors. Based on the established model, the electrolyte flow rate distribution across cells in the stack is investigated. The distribution and variation in shunt currents, single-cell current and single-cell voltage are analyzed. The distribution and variation in temperature and heat generation and heat transfer are also researched. It can be found that the VRFB stack temperature will exceed 40 °C when operating at 60 A and 100 mA cm−2 at an ambient temperature of 30 °C, which will lead to electrolyte ion precipitation, affecting the performance and safety of the battery. To control the stack temperature below 40 °C, a new tank cooling control strategy is proposed, and the suitable starting cooling point and the controlled temperature are specified. Compared with the common room cooling strategy, the new tank cooling strategy reduces energy consumption by 27.18% during 20 charge–discharge cycles.

Effect of Curing Light with Different Intensities on the Penetration of Silver and Fluoride Ions and Dentin Hardness in Primary Carious Molars Following Silver Diamine Fluoride Application: A Comparative Microscopic Ex Vivo Study.

A paradigm shift from surgical to medical approach for caries management has popularized silver diamine fluoride (SDF) as a preventive and interim caries arrest medicament. Few studies conducted have explored the effect of curing light on SDF's microbial property, its penetration, and effect on dentin. However, there is a research gap regarding the effect of different intensities of curing light on SDF performance. To determine the effect of different curing light intensities on SDF penetration depth and dentin hardness in carious lesions of primary molars. Silver diamine fluoride was applied on 30 extracted carious primary molars. Teeth were randomly allocated into three groups-(1) control group, no light curing after application of SDF; (2) light curing of SDF with low intensity (1000 mW/cm2); and (3) light curing of SDF with high intensity (2500 mW/cm2). A scanning electron microscopy (SEM) with energy dispersive X-ray (EDX) analysis was performed to check ion penetration after 1 week, and a Vickers hardness test was used to assess dentin hardness of both infected and affected dentin layers at 1-week and 1-month intervals. Based on the distribution of data, parametric and nonparametric tests were applied. Statistical Package for the Social Sciences (SPSS) version 26 was used for statistical analysis. The level of significance was set at 5%. Silver diamine fluoride penetrated beyond the carious lesion in all three groups. The mean silver ion precipitation in infected dentin in group III (16.90 ± 0.68) was maximum, whereas it was found to be minimum in group II (7.31 ± 0.63). The mean fluoride ion precipitation in affected dentin in group III (4.06 ± 0.41) was highest and least in group II (3.09 ± 0.58). A considerable increase in mean dentin hardness of infected dentin was observed in all three groups (214.00 ± 89.06, 218.00 ± 75.17, 231.00 ± 98.86, respectively; p < 0.001) after 1 month. Applying SDF to carious lesions using a high-intensity dental curing light induced more silver ion precipitation in infected dentin and increased its hardness. Bhatt R, Patel M, Thakkar A, et al. Effect of Curing Light with Different Intensities on the Penetration of Silver and Fluoride Ions and Dentin Hardness in Primary Carious Molars Following Silver Diamine Fluoride Application: A Comparative Microscopic Ex Vivo Study. Int J Clin Pediatr Dent 2024;17(7):766-772.

Novel utilization exploration for the dephosphorization waste of Ca–modified biochar: enhanced removal of heavy metal ions from water

Phosphorus-modified biochar has been proven to enhance the precipitation and complexation of heavy metal ions from wastewater. However, the current modification methods require large amounts of exogenous P and have high energy consumption. Hence, this study proposes and analyzes a strategy integrating biochar production, phosphorus wastewater treatment, dephosphorization waste recovery, and heavy metal removal. “BC-Ca-P” was derived from Ca-modified biochar after phosphorus wastewater treatment. The adsorption of Pb(II) by BC-Ca-P followed the Langmuir isotherm and pseudo–second–order kinetic models. The maximum adsorption capability of 361.20 mg·g−1 at pH 5.0 for 2 h was markedly greater than that of external phosphorous-modified biochar. The adsorption mechanisms were dominated by chemical precipitation and complexation. Furthermore, density functional theory calculations indicated that oxygen-containing functional groups (P-O and C-O) contributed the most to the efficient adsorption of Pb(II) onto BC-Ca-P. To explore its practical feasibility, the adsorption performance of BC-Ca-P recovered from an actual environment was evaluated. The continuous-flow adsorption behavior was investigated and well-fitted utilizing the Thomas and Yoon–Nelson models. There was a negligible P leakage risk of BC-Ca-P during heavy metal treatment. This study describes a novel and sustainable method to utilize dephosphorization waste for heavy metal removal.Graphical

ELECTRO RECOVERY OF TELLURUM IONS FROM NON-AQUEOUS N-N DIMETHYLFORMAMIDE ELECTROLYTE

The work presents studies of the mechanism of recovery of tellurium ions from non-aqueous N-N dimethylformamide. For this, linear and cyclic current-voltage polarization curves have been recorded. The influence on the process of the concentration of tellurium ions, change of potential sweep rate and temperature has been investigated. By recording linear polarization curves, it has been established that the reducing process of tellurium ions is controlled by their diffusion to the cathode surface. The influence of the concentration of its ions in the electrolyte, the rate of change of the potential and the temperature on the tellurium deposition process was studied. By recording the cyclic polarization curve, the potential area where tellurium ions precipitate and its anodic dissolution occurs is determined. It was determined that the increase in the concentration of tellurium ions and the temperature increases the speed of the reduction process of tellurium, and the reduction process itself is controlled by the diffusion of tellurium ions on the cathode surface. To confirm the obtained data, polarization curves have been recorded on a rotating platinum disk electrode. Data received, exactly the linear dependence of ip on the electrode rotation speed (ω) to the power of 0.5, confirms that, that the process of reduction of tellurium electrodes in non-aqueous N-N dimethylformamide is controlled by diffusion polarization

The rare-earth elements recovered from the leachate of discarded phosphor by electrodeposition

ABSTRACT Recovering rare-earth elements (REEs) from discarded phosphors is an important solution to alleviate the current shortage of rare-earth resources, the aluminum element in discarded phosphors will badly affect the purity and recovery of rare-earth elements. An electrodeposition method for recovering the rare earth from the discarded phosphoric leachate was proposed to avoid the effecting of aluminum elements. The results show that the purity of the rare-earth oxides recovered reached 99.13% and the recovery rate of rare-earth elements reached 98.89% by adopting the optimal electrodeposition process with the help of the complexing agent glycine. Research has found that adding the complexing agent glycine can help rare-earth hydroxides precipitate at the cathode and inhibit aluminum ion precipitation by changing the aluminum deposition potential. Moreover, it was also found that the generation of OH- ions by reduction of NO3- in acid aqueous solution was a one-step irreversible reaction in the deposition process by cyclic voltammetry, which ensured the reliability of rare-earth hydroxide precipitation reaction.

β-Lactoglobulin Separation from Whey Protein: A Comprehensive Review of Isolation and Purification Techniques and Future Perspectives

Cow milk, although rich in essential nutrients, is a well-known allergic food that can cause allergic reactions in infants and young children. β-Lactoglobulin accounts for 10% of the total protein in milk and 50% of the whey protein, which has high nutritional value and excellent functional properties but is also the main allergen leading to milk protein allergy. Exploring the mechanism of milk allergy and selecting suitable separation and purification methods to obtain high-purity β-Lactoglobulin is the premise of research on reducing allergenicity. In this review, the research progress in membrane technology, gel filtration chromatography, ion exchange chromatography, affinity chromatography, precipitation and aqueous 2-phase system separation for the separation and purification of milk β-Lactoglobulin is reviewed in detail to promote the further development of milk β-Lactoglobulin separation and purification methods and provide a new method for the development of hypoallergenic dairy products in the future. Among these methods, ion exchange chromatography and gel chromatography are widely used, precipitation is generally used as a crude purification step, and high-performance liquid chromatography and membrane technology are used for further purification to improve the purity of allergens.

Study on separation and purification of titanium alloys (TC4-6Al-4V) by molten salt electrolysis

With the widespread expansion of titanium applications and its significant increase in usage, the issue of recycling titanium resources after consumption has emerged. Focusing on titanium alloys with high usage, such as TC4 (Ti-6Al-4V), this article proposes a titanium separation and recovery method based on molten salt electrolysis. This method thoroughly analyzes the characteristics of elements in TC4 and electrochemical principles, ensuring that vanadium in the TC4 alloy does not undergo electrochemical dissolution when the electrolysis potential is below 0.3 V vs Pt. Subsequently, through electrochemical analysis, it was discovered that the precipitation of aluminum ions is influenced by concentration. Therefore, by controlling the concentration of aluminum in the eutectic molten salt, such as increasing the electrolyte concentration and shortening the electrolysis time, the precipitation of aluminum can be effectively avoided. Under the experimental conditions mentioned above, vanadium elements deposit at the bottom of the crucible in the form of anode slime, while aluminum dissolves and remains in the electrolyte. Meanwhile, titanium ions in the cathode region undergo electron reduction and deposit in the cathode area in the form of titanium, thus achieving precise separation of alloy elements. Experimental verification shows that the purity of the obtained titanium reaches 99.17 atomic percent. Therefore, this molten salt electrolysis method, which combines the physical properties of alloy elements with electrochemical principles, not only provides a new perspective for the separation and recovery of titanium and other critical metals, but also offers new research directions for the recovery technology of other alloy elements.

Effects of light curing on silver diamine fluoride-treated carious lesions: A systematic review.

This systematic review aims to evaluate the potential benefits and underlying mechanisms of combining SDF with light curing, based on available studies. A systematic search of publications was conducted with the keywords "silver diamine fluoride" or "silver fluoride" and "dental light curing," "LED curing," "dental laser," and "dental polymerization" in 4 databases: PubMed, EBSCO, Scopus, and Google Scholar to identify English-language articles published up to March 2023. Duplicate publications were deleted. Two reviewers screened the titles and abstracts and excluded irrelevant publications. The full text of the remaining publications was retrieved. Studies investigating the effect of light-curing on SDF-treated carious lesions were included. The 175 publications initially found included 5 laboratory studies investigating the effects of light curing on 38% SDF-treated dentine carious lesions, but no clinical study was found. Four of these studies were conducted on extracted primary teeth, and one was on extracted permanent teeth. SDF with light curing increased microhardness (n = 3, p < .05) showed a higher mineral density (n = 1, p < .041) and had more silver ion precipitation in infected dentine (n = 1, p < .016) compared to SDF without light curing. Moreover, no significant differences in the antibacterial activity were observed between SDF with light curing and SDF alone (n = 1, p > .05). Drawing from the limited number of laboratory studies, incorporating light curing subsequent to the SDF application yields potential favorable outcomes that include augmented microhardness, elevated mineral density, and heightened silver ion precipitation within infected dentine. Future clinical research is required to confirm or refute the benefit of light curing on SDF-treated carious lesions.

Evolution of 2D Nanostructures on Charged Surfaces through the Precipitation of Hydrolyzable Ions

The significance of surface charge at solid-liquid interfaces extends to crucial roles in diverse chemical processes, including crystallization, self-assembly, fuel cell reactions, and heterogeneous catalysis. Building upon the classical mean field description derived from the Gouy–Chapman model, the electrostatic attraction between a charged interface and counterions in solutions prompts oppositely charged ions from the solution to accumulate at the interface, forming an electric double layer (EDL), with distinct properties from those observed in bulk solutions. While the model accounts for the distribution of ions based on their spatial average perpendicular to the surface, the discussion regarding the lateral structure at the interface, particularly the local molecular-level details, is relatively limited.In this study, we explored the interfacial structure of mica, a mineral with an atomically flat surface and intrinsic negative charge, in electrolytes containing different multi-valent cations, utilizing in-situ liquid phase atomic force microscopy (LP-AFM). We find that, as the solution pH is gradually raised, cations precipitate and form a monolayer hydroxide film on mica surface. Divalent ions such as Mg2+, Ni2+, and Co2+, form large continuous monolayers in a manner that aligns with expectations based on classical nucleation theory. For trivalent ions like Al3+, Fe3+, and Cr3+, hydrolyzed species adsorb in increasing amounts as pH is increased. Instead of exhibiting a random distribution, these ions reveal intricate lateral ordering and eventually evolve into an ordered ion network. Upon further pH increase, the ion network undergoes a transition to a discontinuous film with a persistent network of gaps. The links between the surface nanostructure and local surface charge were investigated using three-dimensional fast force mapping (3D FFM) and complementary streaming potential apparatus (SPA) measurements. As films form, an inversion from negative to positive zeta potential on mica is observed through SPA and is accompanied by the appearance of a long-range tip-sample forces through 3D FFM. These findings suggest that electrostatic interactions between positively charged ions/films and a negatively charged substrate stabilize the surface nanostructure. Furthermore, films created by trivalent ions are more strongly charged compared to those formed by divalent ions.The lateral structure at mica-electrolyte interfaces was simulated using a charge-frustrated lattice gas model, where the ions experience competing interactions between short-range chemical bonding and long-range electrostatic forces. For weak charge effects, the film undergoes a first-order transition from sparse adsorbates to large continuous sheets, aligning with the behavior observed with divalent ions. When the charge effect is sufficiently strong, the surface forms various states, including ordered patterns of ions, ion clusters, and microphase-separated partial films, corresponding to the behavior observed with trivalent ions. This study provides molecular-level understanding of how electric fields control the spontaneous formation of interfacial nanostructures, and offers valuable insights into using electric fields to control crystallization processes for the development of functional materials.

Synergistic effect of YAG particulate reinforcement on microstructural and thermo-mechanical properties of pressureless sintered MgAl2O4 spinel ceramic composites

Yttrium aluminum garnet (YAG) powders, synthesized through a partial wet chemical process, exhibit controlled morphology, high phase purity, and uniform homogeneity etc. This process involves the precipitation of aluminum ions onto Y2O3 particles. The transformation process of the Al-compound/Y2O3 precursor structure leads to the direct crystallization of pure YAG at 900 °C, passing through an intermediate stage where hexagonal YAH phase forms. A comprehensive study was conducted on the impact of preformed YAG as a reinforcing phase on the densification, mechanical, and thermo-mechanical properties of MgAl2O4-YAG composite, sintered under pressureless sintering in temperature range of 1500 °C–1600 °C. The inclusion of YAG particulate up to 5.0 wt% significantly enhances the densification, hardness, fracture toughness, flexural strength and high-temperature mechanical behavior of magnesium aluminate spinel (MAS) ceramics, however, increasing the YAG content beyond 5.0 wt% causes a reduction in these properties. The optimized addition of YAG particulate contributes to reducing the average grain size and refining the microstructure of the spinel ceramic matrix.

Ion Precipitation Into Io's Poles Driven by a Strong Sub‐Alfvénic Interaction

AbstractJuno performed two close flybys of Io and found enhanced field‐aligned proton fluxes are absorbed by Io. These protons are absorbed at mass input rates comparable to previous estimates for hydrogen losses from Io, hence Jupiter is likely the source of hydrogen at Io. The conditions necessary for this to occur are: (a) formation of Alfvén waves at Io, (b) wave‐particle coupling to energize protons, (c) anti‐planetward transport of ions due to the magnetic mirror force and/or parallel acceleration, and (d) strong sub‐Alfvénic interaction slowing the flow connected to Io's fluxtube allowing for sufficient travel time for energized ions to transit to Io. The derived slowdown of ≤12% the upstream value is linked to filamentation within the Alfvén wing. This mechanism is likely operating at all strongly interacting satellites and provides an avenue to transfer material from a planetary body to its satellites, including exoplanets and brown dwarfs.

Red mud/steel slag three-dimensional electrochemical system for the removal of organic pollutant with Na2S2O3 as electrolyte: Contribution of •OHads

The dynamic changes in the iron redox cycle (Fe2+/Fe3+) played a crucial role in the electro-Fenton degradation of organic pollutants. The synthesis of composite particle electrodes RMSSx:y from a mixture of steel slag (SS) and red mud (RM) was applied in a three-dimensional electrochemical system for the remediation of hydrochloric tetracycline (TCH) in wastewater, utilizing Na2S2O3 as an electrolyte. Further, some investigations were conducted to determine the effects of RM/SS, electrolyte, particle electrode dosage, cell voltage, and pH on TCH degradation efficiency. Under optimal conditions such as 8 g/L RMSS5:5 particle electrodes, a cell voltage of 4 V, an initial pH of 3, and 6 mM Na2S2O3 electrolyte, the degradation rate of TCH in wastewater was 98.3 %. Meanwhile, its total organic carbon (TOC) was reduced by 88 % within 60 min. Cyclic experiments with consistently high degradation efficiency demonstrated the stability of the particle electrode RMSS5:5. The practical applicability of RMSS5:5 was further confirmed through its successful treatment of various industrial wastewaters, including dyeing (DW), chemical (CW), and pharmaceutical (PW) effluents, achieving chemical oxygen demand (COD) removal rates of 67.8 %, 67.6 %, and 65.0 % respectively. The enhancement of TCH degradation through the utilization of Na2S2O3 as the electrolyte was primarily attributed to the complexation and reduction effects exerted by S2O32- ions. These effects prevented the leaching and precipitation of iron ions, facilitated the reduction of Fe (III), and consequently enabled •OHads to play a dominant role in the degradation process. These findings demonstrated the potential of RMSS5:5 in efficiently degrading emerging contaminants, thereby offering an innovative approach for utilizing SS and RM as functional materials in electro-Fenton processes.

Remote sensing of electron precipitation mechanisms enabled by ELFIN mission operations and ADCS

The Electron Loss and Fields INvestigation (ELFIN) mission comprising two 3U+ CubeSats was developed, built, and operated by several generations of undergraduate students at UCLA. The spin-stabilized CubeSats (spin-rate: 21 RPM) produced high-resolution measurements of precipitating, trapped, and backscattered fluxes of electrons and ions in the radiation belts. Launched in September 2018, ELFIN operated successfully until its deorbit just over four years later. Initially, however, mission operations was very challenging and only tapped the full mission potential after a thorough redesign of the operations paradigm. This mid-mission adjustment yielded the higher data downlink volume necessary to acquire a comprehensive data set, therefore enabling ensemble studies with sufficient statistical significance. The new operational framework also led to additional improvements across the mission. Most notably, the Attitude Determination and Control System (ADCS) benefited from more reliable collections of magnetometer data for attitude determination, enabling knowledge and control to <1°. This allowed high pitch-angle resolution (especially within the loss cone) and high energy resolution spectrograms, both powerful diagnostics of radiation belt electron and ion precipitation. This paper highlights the scientific advancements made possible by ELFIN’s efficient mission operations and ADCS design, unique for CubeSats, and emphasizes the role of electron precipitation measurements for future studies in magnetospheric, ionospheric, and atmospheric physics.

Targeting Bacterial Persisters via Reactive Oxygen Species‐Generating Hydrogel Microspheres

AbstractThe presence of bacterial persisters is a key factor contributing to chronic infection. However, no effective treatment methods are currently available. Thus, a platform is developed, called reactive oxygen species (ROS) bomb, based on microenvironment‐adaptive hydrogel microspheres, to oxidize the cell membranes of persisters in chronic periprosthetic joint infection (PJI). Fenton reagent hydroxy iron oxide (FeOOH) and a glucose oxidase (GOx)/calcium phosphate (CaP) acid‐responsive shell are sequentially induced on the surface of mesoporous polydopamine (PDA) nanoparticles by the PDA‐mediated ion precipitation and interfacial adhesion, followed by the coloaded with glucose into microfluidic hyaluronic acid hydrogel microspheres. Hydroxyl radicals are explosively generated through GOx‐mediated glucose oxidase, H2O2 production, and its Fenton‐like reactions with FeOOH, which also benefit from the weakly acidic microenvironment around persisters, result in the destruction of bacterial cell membrane, and subsequent overflow of cellular contents such as dsDNA, proteins, and K+. The bactericidal rates of methicillin‐resistant Staphylococcus aureus and Staphylococcus epidermidis persisters are up to 99.14% and 98.96%, and the bacterial loads in lesion location are significantly decreased after ROS bombs treated, effectively alleviated the inflammation and bone resorption damage. This work provides a new strategy toward persisters clearance and shows great application potential in other chronic infection‐related diseases.

Effect of temperature on binding process of calcium carbonate concrete through aragonite crystals precipitation

This study investigated the impact of temperature on the strength development of calcium carbonate concrete (CCC) comprising calcium carbonate and concrete waste. CCC exhibited its highest compressive strength when manufactured at temperatures between 60 and 70 °C, thereby demonstrating strengths 1.5 and 2.7 times greater than those achieved at 40 and 90 °C, respectively. At this temperature range (60–70 °C), CCC showed the highest amount of precipitated aragonite with large acicular aragonite crystals, which decreased the porosity of CCC. This temperature range governed the homogeneous distribution of calcium carbonate deposition within the CCC specimen. Moreover, the carbonated cement paste particles within the CCC continuously underwent aqueous carbonation, thereby providing an additional Ca source for calcium carbonate precipitation in CCC. At high temperatures, this process promotes the precipitation of Ca ions as needle-like aragonite crystals during reprecipitation with accelerating the transformation of calcium carbonate polymorphs. The CCC strength arose from the deposition of calcium carbonate from input calcium bicarbonate solution and the reprecipitation of calcium carbonate during aqueous carbonation. The calcium carbonate precipitation from aqueous carbonation accounts for 30 % of the total calcium carbonate precipitation of CCC. Needle-like aragonite crystals functioned as interlocking bridges between the particles and frame connections, effectively strengthening the CCC composite.

Chronoamperometric investigations on electrochemical synthesis of iron nitrides in molten salt system

A systematic investigation of the electrochemical iron nitride synthesis in a LiCl/KCl salt melt at 723 K shows an optimum of ϵ\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\epsilon$$\\end{document}-Fe3\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$_3$$\\end{document}N1+x\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$_{1+x}$$\\end{document} formation in the range of 2.2 to 2.3 V and for γ′\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\gamma '$$\\end{document}-Fe4\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$_4$$\\end{document}N between 2.4 and 2.5 V enabling the control of the desired iron nitride phase by setting the supplied terminal voltage. The product formation of iron nitrides starts when the electrochemical window is reached, which could be verified by linear sweep voltammetry. Hence, a maximum of nitrogen content in the formed iron nitride phases is observed for 2.27 V. During elongated synthesis periods, convection emerges as the predominant transport mechanism hindering an accelerated reaction rate with higher overpotential applied. Real-time analysis of the background current allows conclusions about the remaining nitride concentration. Additionally, there is concurrent iron nitride formation at the electrode surface through nitride adsorption and autonucleation-induced precipitation of iron and nitride ions. The analysis of the amount of sediment in comparison to the layer thickness of the nitrided working electrode suggests that the autonucleation mechanism dominates over the adsorption mechanism with increasing overpotential and can be further enhanced by this feature.Graphical abstract