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Rationale: Sulfur isotopes have been widely used to solve some key scientific questions, especially in the last two decades with advanced instruments and analytical schemes. Different sulfur speciation and multiple isotopes analyzed in laboratories worldwide and in situ microanalysis have also been reported in many articles. However, methods of sampling to measurements are multifarious, and occasionally some inaccuracies are present in published papers. Vague methods may mislead newcomers to the field, puzzle readers, or lead to incorrect data-based correlations., Methods: We have reviewed multiple methods on sulfur isotopic analyses from the perspectives of sampling, laboratory work, and instrumental analysis in order to help reduce operational inhomogeneity and ensure the fidelity of sulfur isotopic data. We do not deem our proposed solutions as the ultimate standard methods but as a lead-in to the overall introduction and summary of the current methods used., Results: It has been shown that external contamination and transformation of different sulfur species should be avoided during the sampling, pretreatment, storage, and chemical treatment processes. Conversion rates and sulfur isotopic fractionations during sulfur extraction, purification, and conversion processes must be verified by researchers using standard or known samples. The unification of absence of isotopic fractionation is needed during all steps, and long-term monitoring of standard samples is recommended., Conclusion: This review compiles more details on different methods in sampling, laboratory operation, and measurement of sulfur isotopes, which is beneficial for researchers' better practice in laboratories. Microanalyses and molecular studies are the frontier techniques that compare the bulk sample with the elemental analysis/continuous flow-gas source stable isotope ratio mass spectrometry method, but the latter is widely used. The development of sulfur isotopic measurements will lead to the innovation in scientific issues with sulfur proxies., (© 2024 John Wiley & Sons Ltd.)

This study demonstrates an all-graphene, additive-free, aqueous-based ink for direct ink writing (DIW) to 3D-print functional aerogels for applications in electronics and electromagnetic interference (EMI) shields. We employ a two-step electrochemical method with a specially designed intercalation step that controls the surface functionality of graphene nanosheets. Comprehensive characterization reveals the significant impact of the physicochemical properties of graphene nanosheets on homogeneity, rheology, electrical conductivity, and EMI shielding effectiveness (SE). A critical observation is that rheology alone is insufficient to predict the printability of two-dimensional particulate systems, while ink homogeneity, dictated by inter-sheet interactions, plays a vital role. By focusing on optimizing intercalation conditions, we find that phosphoric acid treatment is most effective in enhancing both printability and conductivity, achieving an electrical conductivity of 158 S cm−1 and an EMI SE of 50 dB (at 50 μm thickness) without requiring any post-processing reduction. Systematic experiments with varying durations of phosphoric acid intercalation establish that a 10-minutes treatment produces inks with superior 3D printing fidelity. This innovative approach to graphene ink production enables rapid, continuous, and large-scale manufacturing of lightweight, porous materials, avoiding the need for environmentally harmful reductant chemistries or high-temperature processing. Furthermore, eliminating the reduction step in the fabrication process aligns with industrial demands for energy-efficient production processes and high output rates, marking a significant advancement in the field of materials science and offering promising prospects for applying graphene-based inks in advanced manufacturing technologies. [ABSTRACT FROM AUTHOR]

This article investigated the charge and discharge management structure of electric vehicles (EVs) in intelligent parking lots (IPLs). It seems that with the expansion of renewable energy sources (RESs) as clean energy and investigation of the effects of EVs on the operation and planning of future distribution networks around the way EVs exchange energy with each other and the upstream network operator, RESs such as solar and wind sources, along with hydrogen storage are essential. Therefore, a new stochastic multi‐scenario approach for charge/discharge management of EVs parked in IPL was proposed, in which a newly developed model for the IPL with a hydrogen storage system (HSS) consisting of a fuel cell, an electrolyzer, and a hydrogen storage tank was presented. In the proposed model, the constraints of upstream network and power balance constraints, with the operating constraints related to the IPL, including EVs, renewable energy sources, and the hydrogen storage system, were formulated as the most important objectives of the optimization problem. The optimization algorithm, Competitive Swarm Optimizer (CSO), was formulated for implementation, and its results were compared with those of the PSO and GWO algorithms. The CSO must handle a variety of practical, large‐scale optimization problems. Based on the obtained results, the excess energy purchased from the upstream network or renewable sources was used as hydrogen storage for consumption during peak hours. As expected, the technical constraints and financial goals of the system were met, and the proposed system was evaluated on a 33‐bus network. As the expected benefits will be the most beneficial with the presence of renewable sources, the final profit will be reduced by taking into account uncertainty for charge/discharge management in EVs such as the uncertainty of electric load, market price, wind turbine, and photovoltaic cell sources. Nonetheless, the profit obtained from renewable resources is preferable to losses resulting from the uncertainty of the system, and according to expectation, the performance of the system for managing the optimal charging and discharging of EVs in the IPL will be acceptable with the maximum profit for the grid. [ABSTRACT FROM AUTHOR]

A novel method for the speciation and quantification of polysulfide anions and molecular sulfur in lithium polysulfide solutions in organic solvents is reported. The technique is based on hyphenation of highperformance liquid chromatography (HPLC) and inductively coupled plasma mass spectrometry (ICPMS). A sector-field mass-spectrometer was utilized which made it possible to quantify various sulfur compounds without the need for single component standards and conduct the direct detection of the main isotope of sulfur regardless of interferents such as highly abundant 16O2. Key aspects of separation and sample preparation were considered which allowed complete separation of derivatized polysulfide anions. Gradual adjustment of essential parameters and hardware is described. Variation of plasma settings allowed for obtaining chromatograms with desired analyte peak shapes. The optimized method was applied for the quantification of various lithium polysulfide mixtures in organic solvents showing the accessibility of the corresponding polysulfide distributions with this technique. [ABSTRACT FROM AUTHOR]

Metal micro/nanoparticle ink-based printed circuits have shown promise for promoting the scalable application of flexible electronics due to enabling superhigh metallic conductivity with cost-effective mass production. However, it is challenging to activate printed metal-particle patterns to approach the intrinsic conductivity without damaging the flexible substrate, especially for high melting-point metals. Here, we report a pressure-constrained sonication activation (PCSA) method of the printed flexible circuits for more than dozens of metal (covering melting points from room temperature to 3422 °C) and even nonmetallic inks, which is integrated with the large-scale roll-to-roll process. The PCSA-induced synergistic heat-softening and vibration-bonding effect of particles can enable multilayer circuit interconnection and join electronic components onto printed circuits without solder within 1 s at room temperature. We demonstrate PCSA-based applications of 3D flexible origami electronics, erasable and foldable double-sided electroluminescent displays, and custom-designed and large-area electronic textiles, thus indicating its potential for universality in flexible electronics. It is challenging to activate the flexible printed metal circuit to approach the intrinsic conductivity with minimal damage to the substrate. Here, the authors report a large-scale pressure-constrained sonication activation method for various metals and non-metallic inks. [ABSTRACT FROM AUTHOR]

The recent investigation targets to use adapted carbon paste (CP) with copper nanoparticles (CuNs) operating in a phosphate buffer (PBS) medium with a pH range of 5.0–8.0, to synthesize a novel, susceptible, and simple electrochemical sensor for the detection of one of the most important drugs, vitamin B6. Copper (Cu) is one of the most three common essential trace elements found in the bodies of both humans and animals, along with iron and zinc for all crucial physiological and biochemical functions. Its properties, which are assessed using a variety of methods including scanning electron microscopy (SEM), cyclic voltammetry (CV), differential pulse voltammetry (DPV), and electrochemical impedance spectroscopy (EIS), have also drawn a lot of attention recently. We considered the effects of pH, buffer, scan rate, interference, and calibration curve. The susceptible electrode's linear calibration curve encompassed concentration values between 8.88 and 1000.0 µM. The calculated limits of detection and quantification were 32.12 and 107.0 µM, respectively. Furthermore, this method was established in real human urine samples and drug validation which have been shown satisfactory results for vitamin B6 detection. [ABSTRACT FROM AUTHOR]

The kinetics of phase transformations in the nitriding process α-Fe → γ'-Fe4N → ε-Fe3-2N of the pre-reduced iron ammonia synthesis catalyst was investigated under in situ conditions (atmospheric pressure, 350 °C) by measuring changes of mass, gas phase composition, and magnetic permeability in a differential tubular reactor. The iron nanocrystallite size distribution according to their specific active surface areas was measured, and it was found that the catalyst is bimodal as the sum of two Gaussian distributions, also differing in the value of the relative magnetic permeability. Relative magnetic permeability of small α-Fe crystals in relation to large crystals is higher by 0.02. In the area of α → γ' transformation, the magnetic permeability dependencies change, proving the existence of two mechanisms of the α-Fe structure change in the α-Fe → γ'-Fe4N transformation. In the first area, a solution of α-Fe (N) is formed with a continuous and insignificant change of the crystal lattice parameters of the iron lattice. In the second area, there is a step, oscillatory change in the parameters of the iron crystal lattice in FexN (x = 0.15, 0.20, 0.25 mol/mol). In the range of γ'-Fe4N → ε-Fe3-2N transformation, a solution is formed, with nitrogen concentration varying from 0.25–0.45 mol/mol. During the final stage of the nitriding process, at a constant value of the relative magnetic permeability, only the concentration of nitrogen in the solution εr increases. The rate of the phenomenon studied is limited by a diffusion rate through the top layer of atoms on the surface of iron nanocrystallite. The estimated value of the nitrogen diffusion coefficient varied exponentially with the degree of nitriding. In the area of the solution, the diffusion coefficient is approximately constant and amounts to 5 nm2/s. In the area of oscillatory changes, the average diffusion coefficient changes in the range of 3–11 nm2/s, and is inversely proportional to the nitrogen content degree. The advantage of the research method proposed in this paper is the possibility of simultaneously recording, under reaction conditions, changes in the values of several process parameters necessary to describe the process. The research results obtained in this way can be used to develop such fields of knowledge as heterogeneous catalysis, materials engineering, sensorics, etc. [ABSTRACT FROM AUTHOR]

Silver-coated copper microparticles combine the oxidation resistance of silver with the low cost of copper. They are interesting components for printed conductive structures. We studied whether printed films of such particles can be printed and sintered at low temperatures in air to create highly conductive films and whether it is possible to recover the particles from them for recycling. Pastes containing 1.5 μm to 5 μm spheres and 3 μm flakes with L -ascorbic acid were prepared, screen-printed, and treated at temperatures of 110 °C to 300 °C in air. The bulk resistance of films treated below 160 °C were two orders of magnitude higher than that of bulk copper, ρCu, and limited by particle–particle contact resistances. They were reduced by treating the prints at 160 °C to 250 °C, leading to bulk film resistances down to 41ρCu. We demonstrate that the high mobility of silver enables the formation of necks that bridge the copper cores and reduce resistivity in this temperature window. The sintered prints retained their conductivity for at least 6 months. Treatments at higher temperatures in air were detrimental: resistances increased above 250 °C. These temperatures led to dewetting of the silver coating and fast copper oxidation, resulting in a continuously increasing resistance. In a final study, we demonstrated that films treated below 200 °C can be recycled by recovering the metal powder from the printed conductors and that the powder can be printed again. [ABSTRACT FROM AUTHOR]

The field of bioelectronics is developing exponentially. There is now a drive to interface electronics with biology for the development of new technologies to improve our understanding of electrical forces in biology. This builds on our recently published work in which we show wireless electrochemistry could be used to grow bioelectronic functional circuitry in 2D cell layers. To date our ability to merge electronics with in situ with biology is 3D limited. In this study, we aimed to further develop the wireless electrochemical approach for the self-assembly of microwires in situ with custom-designed and fabricated 3D cancer spheroids. Unlike traditional electrochemical methods that rely on direct electrical connections to induce currents, our technique utilises bipolar electrodes that operate independently of physical wired connections. These electrodes enable redox reactions through the application of an external electric field. Specifically, feeder electrodes connected to a power supply generate an electric field, while the bipolar electrodes, not physically connected to the feeder electrodes, facilitate the reduction of silver ions from the solution. This process occurs upon applying a voltage across the feeder electrodes, resulting in the formation of self-assembled microwires between the cancer spheroids.Thereby, creating interlinked bioelectronic circuitry with cancer spheroids. We demonstrate that a direct current was needed to stimulate the growth of conductive microwires in the presence of cell spheroids. Microwire growth was successful when using 50 V (0.5 kV/cm) of DC applied to a single spheroid of approximately 800 µm in diameter but could not be achieved with alternating currents. This represents the first proof of the concept of using wireless electrochemistry to grow conductive structures with 3D mammalian cell spheroids. [ABSTRACT FROM AUTHOR]

Conducting metal interconnections are essential to link electronic components or multiple circuits for electronic device fabrication. Scalable, rapid, and sustainable methods for printing adherent metal interconnections on dielectric materials are lacking, which stifles the development of new electronic consumer devices. Here a breakthrough single‐step and rapid process to deposit highly conducting metal tracks is introduced, using an atmospheric pressure plasma jet. The deposition process used a rudimentary aqueous solution of metal salts as ink, that was introduced as a mist into a helium plasma gas. The metal salt was reduced and deposited with spatiotemporal control using a plasma jet generated at radio frequency with 15 W power at room temperature and pressure. The conductive metal layers were highly adhesive on glass, ceramics, polymeric materials, even biological surfaces such as plant leaves and animal skin, depostedwith little damage to the substrate. The conductivity of deposited tracks on glass shows 50.8 ± 8.6% and 5.2 ± 1.6% of bulk silver and copper metal conductivity respectively. [ABSTRACT FROM AUTHOR]

Herein, we propose an analytical approach based on intermolecular fluorescent resonant energy transfer (FRET) pairs for the visualization of specific enzyme activity in model biomembranes and in living cells. Cell visualizations with fluorescent confocal laser microscopy usually rely on fluorescent probes, such as Fluorescein isothiocyanate (FITC), Alexa488, Tetramethylrhodamine isothiocyanate (TRITC) and many others. However, for more specific tasks, such as the detection of certain enzymatic activity inside the living cell, the toolbox is quite limited. In the case of enzyme-hydrolases for example, the choice is limited to organic molecules comprising a fluorescent dye (typically, 4-methylumbelliferone (MUmb) or 7-amino-4-methylcoumarin (AMC) derivatives) and a fluorescence quencher, bound via an enzyme-sensitive linker—so that when the linker is degraded, the fluorescent signal increases. Unfortunately, both MUmb and AMC are quenched and have a relatively low quantum yield in cells, and their excitation and emission ranges overlap with that of intracellular fluorophores, often producing a strong background noise. R6G, on the other hand, has excellent quantum yield apart from intracellular fluorophores, but there are no efficient quenchers that could be chemically linked to R6G. Herein, we show that R6G is able to form intermolecular FRET pairs with MUmb or AMC, with the latter serving as fluorescence donors. This yields a combination of R6G's excellent fluorescence properties with a possibility to use an enzyme-sensitive linker in MUTMAC or AMC derivatives. This phenomenon was initially discovered in a model system, reversed micelles, where the donor, the acceptor, and the enzyme are forced to be in close proximity to each other, so that proximity could serve as an explanation for the intermolecular FRET effect. Surprisingly enough, the phenomenon has been reproduced in living cells. Moreover, we were able to create working intermolecular donor–acceptor FRET pairs for several different enzymes, including chymotrypsin, phosphatase, and asparaginase. This appears counterintuitive, as besides the overlap of the emission spectra of the donor and the absorption spectra of the acceptor, there are other criteria for the FRET effect, including the convergence of two fluorophores at a distance of about 1–10 nm, and the orientation of their dipoles at a certain angle, which is difficult to imagine in a bulk system like a living cell. We hypothesize that FRET-enabling donor–acceptor interaction may be taking place at the inner surface of the lipid bilayer, to which both donor and acceptor molecules would likely have an affinity. This hypothesis would require a more detailed investigation. Therefore, we have shown that the method suggested has good potential in the visualization of enzyme functioning inside living cells, which is often a challenging task. Shifting of the fluorescence signal to the long-wavelength region would increase the signal selectivity, making it easily distinguishable from autofluorescence. [ABSTRACT FROM AUTHOR]

With the rapid development of integrated circuits, glass substrates are frequently utilized for prototyping various functional electronic circuits due to their superior stability, transparency, and signal integrity. In this experiment, copper wire was printed on a glass substrate using inkjet printing, and the electronic circuit was sintered through laser irradiation with a 532 nm continuous green laser. The relationship between resistivity and microstructure was analyzed after laser sintering at different intensities, scanning speeds, and iterations. The experimental results indicate that the conductivity of the sintered lines initially increases and then decreases with an increase in laser power and scanning speed. At the same power level, multiple sintering runs at a lower scanning speed pose a risk of increased porosity leading to reduced conductivity. Conversely, when the scanning speed exceeds the optimal sintering speed, multiple sintering runs have minimal impact on porosity and conductivity without altering the power. [ABSTRACT FROM AUTHOR]

Acid mine drainage (AMD), containing large quantities of heavy metals and acidic components, poses a severe threat to the environment and human health. Acidithiobacillus ferrooxidans (A. ferrooxidans) plays a crucial role in the treatment of AMD, but its activity is significantly influenced by environmental conditions. This study systematically analyzes the stress effect of high phosphorus concentration on A. ferrooxidans during AMD treatment and its biomineralization effect. The results indicate that with phosphorus concentrations ranging from 0 g/L to 2 g/L, the system's pH and Fe2+ oxidation rate initially decrease and then increase, with higher phosphorus concentrations delaying the time of increase. When the phosphorus concentration exceeds 2 g/L, both pH and Fe2+ oxidation rates generally show a downward trend. The morphology and elemental composition of the precipitates obtained under different phosphorus concentrations exhibit significant differences, indicating that phosphorus concentration notably affects the oxidation activity of A. ferrooxidans and its mediated biomineralization process. Under high phosphorus concentrations, the activity of A. ferrooxidans is inhibited, hindering the Fe2+ oxidation process and resulting in the formation of a large quantity of amorphous ferric phosphate precipitates. The findings provide a scientific basis for optimizing AMD treatment technologies, suggesting that reasonable control of phosphorus concentration in practical applications can improve AMD treatment efficiency and pretreatment effects. [ABSTRACT FROM AUTHOR]

Efficient neutrophil migration to infection sites plays a vital role in the body's defense against bacterial infections and natural immune responses. Neutrophils have a short lifespan and cannot be mass‐cultured in vitro. Therefore, developing more stable artificial neutrophils (AN) in a controllable manner has become a research focus. However, existing AN lack chemotaxis, which is the ability to migrate toward high‐signal‐concentration positions in a dynamic blood‐ flow environment. Supplying AN with chemotaxis is key to designing AN that are more similar to natural neutrophils in terms of morphology and function. In this study, micrometer‐sized, spherical, biocompatible AN are developed. These AN consist of zeolitic imidazolate framework‐8 nanoparticles encapsulating two enzymes, coacervate droplet frameworks, and outer phospholipid bilayers carrying enzymes. The AN exhibit responsiveness to elevated hydrogen peroxide levels at inflammation sites, actively chemotaxing toward these sites along concentration gradients. They also demonstrate effective combat against Staphylococcus aureus infections. The capabilities of the AN are further validated through in vitro experiments and in vivo evaluations using vascular graft infection models. This study replicates natural neutrophils in terms of chemical composition, functionality, and physiological impact. It introduces new ideas for advancing the development of advanced artificial cells. [ABSTRACT FROM AUTHOR]

Flexible transparent electrodes (FTEs) have become a vital component of many devices such as heaters, solar cells, light-emitting diodes (LEDs), and smart windows. Recently, great endeavors have been undertaken to develop new-generation FTE materials as an alternative to conventional rigid indium tin oxide (ITO). Owing to their outstanding conductivity and flexibility, metallic nanowires have been considered as one of the most potential candidates for FTEs. This review summarizes recent advances in understanding the relationship among the dispersion uniformity of metallic nanowires, the optical and electrical properties of metallic nanowire FTEs, and the stability of devices based on metallic nanowire FTEs. Based on the importance of uniformity in FTE properties, this progress report presents strategies to enhance the uniformity of metallic nanowires for a high-performance FTE. Representative devices based on metallic nanowire FTEs with high stability and reliability are presented. [ABSTRACT FROM AUTHOR]

Smart windows effectively respond to the ever‐changing climatic conditions, offering a smart solution for low‐carbon buildings. However, current smart windows derived from chromic materials often have inferior solar modulation ability, or showcase high haze that obstructs outdoor views. Here, instead of developing new chromic materials, a new bistatic window is proposed for ultra‐high solar modulation and luminous transmission. The new developed window can reduce the indoor surface temperature for ≈11 °C, and reduce the building space cooling and heating energy consumption by 30% to 40%, providing significant energy‐related advances over traditional smart windows. In detail, the bistatic window exhibits excellent solar modulation ability (ΔTsol = 61%), high visible transmittance in both bleached (Tlum,bleached = 91%) and colored (Tlum,colored = 56%) states, low haze (< 1%), rapid switching response (switching time < 1 min), high color rendering index (CRI > 80), and long‐cyclic stability after 1000 cycles. With the advantages of facile fabrication and scalability, it is foreseen the developed bistatic window holds promising prospect for the next‐generation low‐carbon buildings, paving a new way for future advancements in the fields of smart windows. [ABSTRACT FROM AUTHOR]

Miniaturization and flexibility are becoming the trend in the development of electronic products. These key features are driving new methods in the manufacturing of such products. Printed electronics technology is a novel additive manufacturing technique that uses active inks to print onto a diverse set of substrates, realizing large-area, low-cost, flexible and green manufacturing of electronic products. These advantageous properties make it extremely compatible with flexible electronics fabrication and extend as far as offering revolutionary methods in the production of flexible electronic devices. In this paper, the details of a printing process system are introduced, including the materials that can be employed as inks, common substrates, and the most recently reported printing strategies. An assessment on future setbacks and developments of printed flexible electronics is also presented. [ABSTRACT FROM AUTHOR]

This study focuses on the successful fabrication of a cost-effective strain sensor using exclusively additive manufacturing Fused Deposition Modeling (FDM) technology, enabling fast on-site production, which is particularly advantageous in maritime settings, reducing downtime, and supporting a circular economy approach by minimizing inventory needs and environmental footprint. The principle of operation of the developed device is based on the piezoresistive characteristics of a carbon nanotube (CNT)-enriched building material, from which the main sensing element consists. The prototype exhibited reliable piezoresistive properties, and a clear correlation was observed between the thermal treatment of the printed piezoresistor and the resulting gauge factor, linearity, and hysteresis. Its robustness, simple design, and single-step manufacturing process, together with its ability to be integrated into the readout circuitry through standard soldering, enhance its reliability and durability. The key advantages of the proposed device include its low cost, simple design, and rapid remote production. [ABSTRACT FROM AUTHOR]

Copper-based conductive ink has received attention to fabricate thin, flexible, and lightweight devices through printing techniques. In particular, the copper formate based conductive inks, called metal organic decomposition (MOD) inks, which are fabricated by using amine ligand coordinated copper formate have been well studied because of higher oxidative resistant against air than that of metallic copper before thermal annealing. The copper formate moiety of amine ligand coordinated copper formate complexes varies by changing the coordinated amine species, however, for the thermal decomposition temperature of such ink is not well understand. Here, we analyzed the influence of the amine ligand on the thermal decomposition temperature drop of copper formate moiety. Amine-copper formate complexes bearing several amine ligands containing primary amine, pyridine, and imidazole groups were fabricated. The relationship between the evaluated decomposition temperature and the differences between the wavenumbers of symmetric and antisymmetric vibration mode peaks in Fourier transform infrared (FTIR) spectra was found to be nearly linear. This finding demonstrates that the thermal decomposition temperature is governed by the structural modification of formate ions by the coordination of amine groups. Based on this finding, the order of thermal decomposition temperature of the copper moiety is predictable by using FTIR measurement. [ABSTRACT FROM AUTHOR]

The properties of natural rubber foam (NRF) containing gamma-synthesized chitosan (CS) powder were investigated to address the growing demand for efficient methods to treat industrial wastewater contaminated with heavy metals. The CS powder was prepared by irradiating chitin (CT) powder with varying doses of gamma rays (0–100 kGy), followed by deacetylation using 40% sodium hydroxide (NaOH) at 100 °C for 1 h. The resulting CS powders were then mixed with natural rubber latex (NRL) at different contents (0, 3, 6, and 9 parts per hundred parts of rubber by weight; phr) and processed using Dunlop techniques to prepare the foam samples. The experimental findings indicated that the degree of deacetylation (%DD) of the CS powder increased initially with gamma doses up to 60 kGy but then decreased at 80 and 100 kGy. In addition, when the CS powder was incorporated into the NRF samples, there were increases in total surface area, density, compression set, and hardness (shore OO), with increasing gamma doses and CS contents. Furthermore, the determination of heavy metal adsorption properties for Cu, Pb, Zn, and Cd showed that the developed NRF sample exhibited high adsorption capacities. For instance, their removal efficiencies reached 94.9%, 82.5%, 91.4%, and 97.0%, respectively, in NRF containing 9 phr of 60 kGy CS. Notably, all adsorption measurements were determined using 3 cm × 3 cm × 2.5 cm specimens submerged in respective metal solutions, with an initial concentration of 25 mg/L. However, the removal capacity per unit mass of the sample (mg/g) showed less dependencies on CS contents, probably due to the higher density of CS/NRF composites in comparison to pristine NRF, resulting in a smaller volume of the former being submerged in the solution, subsequently suppressing the effects from CS in the adsorption. Lastly, tests on the reusability of the developed NRF indicated that the samples could be reused for up to three cycles, with the Cu removal capacity remaining relatively high (83%) in the sample containing 9 phr of 60 kGy CS. The overall outcomes implied that the developed NRF with the addition of gamma-synthesized CS not only offered effective and eco-friendly heavy metal adsorption capacity to improve public health safety and the environment from industrial wastewater but also promoted greener and safer procedures for the synthesis/modification of similar substances through radiation technologies. [ABSTRACT FROM AUTHOR]

LCS-1, a putative selective inhibitor of SOD1, is a substituted pyridazinone with rudimentary similarity to quinones and naphthoquinones. As quinones catalytically oxidize H2S to biologically active reactive sulfur species (RSS), we hypothesized LCS-1 might have similar attributes. Here, we examine LCS-1 reactions with H2S and SOD1 using thiol-specific fluorophores, liquid chromatography–mass spectrometry, electron paramagnetic resonance (EPR), UV–vis spectrometry, and oxygen consumption. We show that LCS-1 catalytically oxidizes H2S in buffer solutions to form RSS, namely per- and polyhydrosulfides (H2Sn, n = 2–6). These reactions consume oxygen and produce hydrogen peroxide, but they do not have an EPR signature, nor do they affect the UV–vis spectrum. Surprisingly, LCS-1 synergizes with SOD1, but not SOD2, to oxidize H2S to H2S3-6. LCS-1 forms monothiol adducts with H2S, glutathione (GSH), and cysteine (Cys), but not with oxidized glutathione or cystine; both thiol adducts inhibit LCS-1-SOD1 synergism. We propose that LCS-1 forms an adduct with SOD1 that disrupts the intramolecular Cys57-Cys146 disulfide bond and transforms SOD1 from a dismutase to an oxidase. This would increase cellular ROS and polysulfides, the latter potentially affecting cellular signaling and/or cytoprotection. [ABSTRACT FROM AUTHOR]

Hydrogen sulfide (H2S) in environments with temperatures below 100 °C is generally assumed to be of microbial origin, while abiotic H2S production is typically restricted to higher temperatures (T). In this study, we report an abiotic process for sulfidogenesis through the reduction of elemental sulfur (S0) by hydrogen (H2), mediated by pyrite (FeS2). The process was investigated in detail at pH 4 and 80 °C, but experimental conditions ranged between 40 and 80 °C and pH 4–6. The experiments were conducted with H2 as reducing molecule, and µm-sized spherical (but not framboidal) pyrite particles that formed in situ from the H2S, S0 and Fe2+ present in the experiments. Fe monosulfides, likely mackinawite, were identified as potential pyrite precursors. The absence of H2 production in controls, combined with geochemical modelling, suggests that pyrite formation occurred through the polysulfide pathway, which is unexpected under acidic conditions. Most spherical aggregates of authigenic pyrite were composed of nanometric, acicular crystals oriented in diverse directions, displaying varying degrees of organization. Although it was initially hypothesized that the catalytic properties were related to the surface structure, commercially sourced, milled pyrite particles (< 50 μm) mediated H2S production at comparable rates. This suggests that the catalytic properties of pyrite depend on particle size rather than surface structure, requiring pyrite surfaces to act as electron shuttles between S0 and H2. [ABSTRACT FROM AUTHOR]

Graphene composite conductive inks are promising for the scalable production of printable electronics, and multifunctional coatings, owing to their cost-effectiveness, high conductivity, and remarkable flexibility. However, the restacking of graphene (Gr) sheets and agglomeration of carbon black (CB) significantly reduce the conductivity of aqueous graphene composite inks, limiting the exploration of high-performance devices. Herein, a highly conductive and dispersed graphene composite ink, based on a composite system of two- and zero-dimensional carbon materials was developed by a scalable sand-milling method. Carboxymethyl cellulose (CMC) can effectively address the aggregation issues of Gr and CB through steric hindrance. Functionalized Gr and CB can synergistically form an interpenetrating conductive network structure. The synthesis of a highly dispersed Gr/CB composite was facilitated by an in situ exfoliation process, which resulted in a high electrical conductivity of 2.12 × 104 S m−1 (i.e., a sheet resistance of 2.16 Ω sq−1). A screen-printed Gr/CB @ thermoplastic polyurethane fabric based on the Gr/CB composite ink exhibited an excellent electrical conductivity (7.08 Ω sq−1). The resulting composite fabric demonstrated promising potential for application in low-voltage driven wearable heaters and ultra-sensitive flexible strain sensors, while being waterproof, stable, and comfortable, suggesting significant potential for use in flexible wearable electronics. [ABSTRACT FROM AUTHOR]

Bio-based plant oil-derived elastomers are an attractive alternative to petroleum polymers due to a growing demand for flexible, high-strain materials in the 3D printable soft robotics field. So far, such solutions have been limited to slow and labor-demanding molding techniques, making them unable to achieve high design flexibility and exceptional resolution. Herein, we present a vat photopolymerization 3D printable and easily tailorable plant oil acrylate-based system with a bio-based carbon content ranging from 62% to 80%. By targeting the tuning of macromolecular design and post-processing conditions, a broad mechanical and functional contrast from soft and stretchable elastomers, with up to 180% elongation, to hard and ductile shape-memory polymers, is realized in 3D-printed parts. To further demonstrate the capability of the developed materials, we created a fully 3D-printed soft robotic actuator capable of fast and delicate movement. The proposed approach enables 3D printing of sustainable, high-resolution structures with targeted mechanical properties for application in various advanced fields. [ABSTRACT FROM AUTHOR]

Carbon black particles possess dimensions on the nanometer or sub-nanometer scale. When utilized, these particles have a tendency to aggregate, which compromises their stability under storage conditions. To address this issue, a dispersant was prepared using cotton short fibers as raw materials through etherification and graft polymerization with acrylamide (AM) and 2-acrylamido-2-methylpropane sulfonic acid (AMPS) as raw materials. The dispersant was then used to disperse carbon black to test its dispersing performance. A response surface optimization test was utilized to ascertain the influence of AMPS monomer mass, AM monomer mass, and potassium persulfate (KPS) initiator mass on the dispersibility of carbon black during dispersant preparation, and a set of optimal preparation conditions were obtained. The dispersion stability of carbon black in water was assessed using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), elemental analysis (EA), thermogravimetric analysis (TG), zeta potential analysis, high magnification scanning electron microscopy (SEM), and contact angle measurements. Results revealed that the optimum mass ratio of carboxymethyl cellulose (CMC) to AMPS to AM was 1:0.69:1.67, with the KPS initiator comprising 1.56% of the total monomer mass. By incorporating the dispersant at a concentration of 37.50%, the particle size of carbon black particles was observed to decrease from 5.350 μm to 0.255 μm, and no agglomeration of carbon black particles occurred even after 3 weeks of storage. [ABSTRACT FROM AUTHOR]

Hydrogels with particulates, including proteins, drugs, nanoparticles, and cells, enable the development of new and innovative biomaterials. Precise control of the spatial distribution of these particulates is crucial to produce advanced biomaterials. Thus, there is a high demand for manufacturing methods for particle-laden hydrogels. In this context, 3D printing of hydrogels is emerging as a promising method to create numerous innovative biomaterials. Among the 3D printing methods, inkjet printing, so-called drop-on-demand (DOD) printing, stands out for its ability to construct biomaterials with superior spatial resolutions. However, its printing processes are still designed by trial and error due to a limited understanding of the ink behavior during the printing processes. This review discusses the current understanding of transport processes and hydrogel behaviors during inkjet printing for particulate-laden hydrogels. Specifically, we review the transport processes of water and particulates within hydrogel during ink formulation, jetting, and curing. Additionally, we examine current inkjet printing applications in fabricating engineered tissues, drug delivery devices, and advanced bioelectronics components. Finally, the challenges and opportunities for next-generation inkjet printing are also discussed. Highlights: • Inkjet printing recently emerged to construct hydrogels with particulates into advanced biomaterials and biomedical devices. • A fundamental understanding of intra and inter-drop transport processes begins to be established. • Challenges and opportunities for next-generation inkjet printing are also discussed. [ABSTRACT FROM AUTHOR]

High iron ore production generates substantial solid waste. Storing this waste in dams poses environmental issues and safety risks for the population. The aim of this study was to valorize sterile waste (IOT) from an inactive iron mine in the Nador region of northeastern Morocco, as an additive in the manufacture of fired bricks made from a red clay (AJH) extracted from the Oujda region. For this purpose, brick specimens were obtained using a mix of a 40% of AJH and 60% of IOT. Physico-chemical, geotechnical and mineralogical characterization techniques were applied to qualify raw material. IOT consisted of hematite, magnetite, pyrite, jarosite and quartz and AJH of kaolinite, chlorite, calcite, hematite, dolomite, quartz and vermiculite. After firing the specimens at 500 °C, 850 °C and 1100 °C, mineralogical composition, bulk density, compressive strength and microstructure behavior of the specimens was assessed. The compressive strength of the bricks containing IOT is 1.25 MPa at T = 500 °C and it varies little at 1100 °C. The compressive strength of the reference sample is 2.94 MPa at 1100 °C. The material has low vitrification and greater porosity compared to the reference bricks. Adding IOT brings significant changes to the color of fired bricks. [ABSTRACT FROM AUTHOR]

Flexible fiber electrodes offer new opportunities for bioelectronics and are reliable in vivo applications, high flexibility, high electrical conductivity, and satisfactory biocompatibility are typically required. Herein, we present an all-metal flexible and biocompatible fiber electrode based on a metal nanowire hybrid strategy, i.e., silver nanowires were assembled on a freestanding framework, and further to render them inert, they were plated with a gold nanoshell. Our fiber electrodes exhibited a low modulus of ∼75 MPa and electrical conductivity up to ∼4.8 × 106 S m−1. They can resist chemical erosion with negligible leakage of biotoxic silver ions in the physiological environment, thus ensuring satisfactory biocompatibility. Finally, we demonstrated the hybrid fiber as a neural electrode that stimulated the sciatic nerve of a mouse, proving its potential for applications in bioelectronics. [ABSTRACT FROM AUTHOR]

Current additive manufacturing technologies wherein as-printed simple two-dimensional (2D) structures morph into complex tissue mimetic three-dimensional (3D) shapes are limited to multi-material hydrogel systems, which necessitates multiple fabrication steps and specific materials. This work utilizes a single shape memory thermoplastic polymer (SMP), PLMC (polylactide-co-trimethylene carbonate), to achieve programmable shape deformation through anisotropic design and infill angles encoded during 3D printing. The shape changes were first computationally predicted through finite element analysis (FEA) simulations and then experimentally validated through quantitative correlation. Rectangular 2D sheets could self-roll into complete hollow tubes of specific diameters (ranging from ≈6 mm to ≈10 mm) and lengths (as long as 40 mm), as quantitatively predicted from FEA simulations within one minute at relatively lower temperatures (≈80 °C). Furthermore, shape memory properties were demonstrated post-shape change to exhibit dual shape morphing at temperatures close to physiological levels. The tubes (retained as the permanent shape) were deformed into flat sheets (temporary shape), seeded with endothelial cells (at T < Tg), and thereafter triggered at ≈37 °C back into tubes (permanent shape), utilizing the shape memory properties to yield bioresorbable tubes with cellularized lumens for potential use as vascular grafts with improved long-term patency. Additionally, out-of-plane bending and twisting deformation were demonstrated in complex structures by careful control of infill angles that can unprecedently expand the scope of cellularized biomimetic 3D shapes. This work demonstrates the potential of the combination of shape morphing and SMP behaviors at physiological temperatures to yield next-generation smart implants with precise control over dimensions for tissue repair and regeneration. [ABSTRACT FROM AUTHOR]

Silver-based metal–organic decomposition inks composed of silver salts, complexing agents and volatile solvents are now the subject of much research due to the simplicity and variability of their preparation, their high stability and their relatively low sintering temperature. The use of this type of ink in inkjet printing allows for improved cost-effective and environmentally friendly technology for the production of electrical devices, including flexible electronics. An approach to producing a silver salt-based reactive ink for jet printing has been developed. The test images were printed with an inkjet printer onto polyimide substrates, and two-stage thermal sintering was carried out at temperatures of 60 °C and 100–180 °C. The structure and electrical properties of the obtained conductive lines were investigated. As a result, under optimal conditions an electrically conductive film with low surface resistance of approximately 3 Ω/square can be formed. [ABSTRACT FROM AUTHOR]

The physical properties as well as thermal and electrical stability of copper particles can be improved by surface protection, which mainly depends on the coating material. Our study was, therefore, focused on the rheological, thermal, mechanical and electrical characterization of polymer composites by comparing uncoated (Cu), silver-coated (Cu@Ag) and silica-coated (Cu@Si) copper flakes in low-density polyethylene at various volume concentrations (up to 40%). Interactions among particles were investigated by rheological properties, as these indicate network formation (geometrical entanglement), which is important for mechanical reinforcement as well as establishing an electric pathway (electrical percolation). The results showed that geometrical and electrical percolation were the same for Cu and Cu@Si, ~15%, while, surprisingly, Cu@Ag exhibited much lower percolation, ~7.5%, indicating the fusion of the Ag coating material, which also decreased crystal growth (degree of crystallinity). Furthermore, the magnitude of the rheological and mechanical response remained the same for all investigated materials, indicating that the coating materials do not provide any load transfer capabilities. However, they profoundly affect electron transfer, in that, Cu@Ag exhibited superior conductivity (74.4 S/m) compared to Cu (1.7 × 10−4 S/m) and Cu@Si (1.5 × 10−10 S/m). The results obtained are important for the design of advanced polymer composites for various applications, particularly in electronics where enhanced electrical conductivity is desired. [ABSTRACT FROM AUTHOR]

Windows are an important part of buildings and transmit light between indoors and outdoors. Frequent heat exchange through windows increases building energy consumption. Smart windows can change optical properties and modulate solar radiation, which are recognized as frontrunners in building energy saving. Among various smart windows, thermochromic windows usually passively regulate light transmittance in response to environmental temperature and have showed great potential for practical applications. Thermochromic materials are key to constructing thermochromic smart windows. Usually, a reversible phase transition takes place for thermoresponsive materials near the critical transition temperature, leading to changes in transmittance over different spectrum bands. Representative thermochromic materials include metal oxides, hydrogels, perovskites, ionic liquids, liquid crystals, etc. The intrinsic phase transition temperature, luminous transmittance, and solar modulation ability are among the critical parameters defining the performance of smart windows. New strategies have been developed to modulate the performance of thermochromic materials and smart windows to meet demands from different environments and climates. Such endeavors have boosted smart windows to modulate fullspectrum solar regulation and to achieve efficient all-climate building energy saving. Next generation smart windows will not only modulate solar transmission, but also convert and store solar energy through new power technologies such as thermoelectricity conversion and solar cells. Challenges and future prospects of smart windows are discussed to inspire future building energy saving. [ABSTRACT FROM AUTHOR]

In the present work, we examined the antibacterial activity of novel silver@cuprous oxide core-shell/hydroxyapatite (Ag@Cu2O/HAp) hetero-nanohybrids against Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli bacteria. The hydrothermal technique was used to easily synthesise Ag@Cu2O/HAp core-shell nanohybrid structures. Immobilisation of Ag@Cu2O core shells on HAp nanoparticles was done by controlling the relative concentrations of Ag, Cu2O, and HAp. The Ag@Cu2O/HAp nanohybrids were characterised using XRD, FTIR, Raman, UV-vis, SEM, EDX, TEM, and SAED methods. By observing the growth of S. aureus and E. coli populations in the presence and absence of Ag, Ag@Cu2O, HAp, and Ag@Cu2O/HAp nanoparticles, their antibacterial impact was compared. MIC Alamar Blue assay was performed to study the cytotoxicity of Ag@Cu2O/HAp nanomaterials. In addition, reactive oxygen species (ROS) studies were conducted to understand the type of active species produced under light and dark conditions. The possible photochemical and antibacterial mechanisms of the Ag@Cu2O/HAp nanohybrids against S. aureus and E. coli bacteria were proposed. In addition, the promising antibacterial nature of Ag@Cu2O/HAp materials suggests that they are good candidates for industrial and biomedical applications. [ABSTRACT FROM AUTHOR]

Iron formations (IFs) are marine chemical sediments that are confined to the Precambrian rock record and provide unique insights into the co-evolution of the atmosphere-hydrosphere and biosphere through almost three billion years of Earth's history. IFs commonly appear throughout the Archaean until the Palaeoproterozoic ca. 1.8 billion years ago and re-appear during the "Snowball Earth" epoch in the Neoproterozoic. The formation and deposition mechanism(s) of IFs are, however, still incompletely understood, hindering unique interpretations of palaeoenvironments. Many IFs are banded iron formations (BIFs) with layer thickness of alternating Fe- and Si-rich layers ranging over several orders of magnitude from the nanometre to the metre scale. A second textural type, so called granular iron formations (GIFs) that form above storm wave base become widespread in the Palaeoproterozoic. Understanding the fundamental mechanisms that are responsible for the textural types and the periodicity of banding in BIFs is crucial to link these features to the environmental and geochemical evolution of the Earth. We here provide a conceptual model that highlights the role of changing light conditions and water transparency for Iron Formation (IF) precipitation. We show that the model is particularly feasible for IFs deposited in shallow waters but may also be applicable for some IFs deposited in deeper water settings. The model builds on other primary Banded Iron Formation (BIF) precipitation models postulating that Fe(III)- (oxyhydr)oxide production can be dominated by anoxygenic photoautotrophic Fe2+-oxidising bacteria. These so called photoferrotrophs are adapted to very low light levels corresponding to about 1% of the light level required by oxygenproducing phototrophs allowing them to thrive deep down in the water column. The depth of Fe(III)-(oxyhydr)oxide production is mainly controlled by water turbidity which controls how deep photosynthetically available radiation (PAR) penetrates the water column. Eutrophic conditions result in relatively shallow Fe(III)-(oxyhydr)oxide production depth due to turbidity either induced by the biomass itself and/or by particles that are actively or passively produced by microorganisms (e.g., Fe(III) and Mn(IV)-(oxyhydr)oxides, sulphides), triggering the formation of Fe-rich bands. During oligotrophic stages, Fe(III)-(oxyhydr)oxides are only produced relatively deep down in the water column, so that only silica-rich bands form in the Fe(III)-(oxyhydr)oxide free upper water column. Reactive transport modelling adopted from Ozaki et al., (2019) shows that besides upwelling and nutrient supply, alternating Fe(III) production depth is mainly associated with changing light conditions as a result of water transparency. Periodicities reflected by alternating Fe- and Si-rich bands in IFs in our model can thus be associated with: (1) nutrient supply patterns; (2) additional sources of turbidity in the water column such as Fe(III) and Mn(IV) oxide particles, sulphides, and wind blown silicate particles; or (3) formation and clearing of organic haze in the atmosphere. One or all of these reasons for low light conditions seem to become more important in the Palaeoproterozoic (<2.4 Ga) and could be partly responsible for the more widespread occurrences of shallow marine granular IFs relative to former epochs, which is often assigned to the gradual oxidation of the ocean. Our model shows that variable water transparency should be considered as additional factor for IF deposition especially for shallow marine settings. This model also reasonably explains the prominent layering in BIFs as syn-depositional feature. [ABSTRACT FROM AUTHOR]

In this article, the particle concentration of finely dispersed copper(II) oxide nanosuspensions as precursors for reductive laser sintering (RLS) is optimized on the basis of rheological investigations. For this metallization process, a smooth, homogeneous and defect-free precursor layer is a prerequisite for adherent and reproducible copper structures. The knowledge of the rheological properties of an ink is crucial for the selection of a suitable coating technology as well as for the adjustment of the ink formulation. Different dilutions of the nanosuspension were examined for their rheological behavior by recording flow curves. A strong shear thinning behavior was found and the viscosity decreases exponentially with increasing dilution. The viscoelastic behavior was investigated by a simulated doctor blade coating process using three-interval thixotropy tests. An overshoot in viscosity is observed, which decreases with increasing thinning of the precursor. As a comparison to these results, doctor blade coating of planar glass and polymer substrates was performed to prepare precursor layers for reductive laser sintering. Surface morphology measurements of the resulting coatings using laser scanning microscopy and rheological tests show that homogeneous precursor layers with constant thickness can be produced at a particle–solvent ratio of 1.33. A too-high particle content results in an irregular coating layer with deep grooves and a peak-to-valley height S z of up to 7.8 μm. Precise dilution control allows the fabrication of smooth surfaces with a S z down to 1.5 μm. [ABSTRACT FROM AUTHOR]