Common Metal Research Articles

Computational Evidence for Bisartan Arginine Blockers as Next-Generation Pan-Antiviral Therapeutics Targeting SARS-CoV-2, Influenza, and Respiratory Syncytial Viruses

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), influenza, and respiratory syncytial virus (RSV) are significant global health threats. The need for low-cost, easily synthesized oral drugs for rapid deployment during outbreaks is crucial. Broad-spectrum therapeutics, or pan-antivirals, are designed to target multiple viral pathogens simultaneously by focusing on shared molecular features, such as common metal cofactors or conserved residues in viral catalytic domains. This study introduces a new generation of potent sartans, known as bisartans, engineered in our laboratories with negative charges from carboxylate or tetrazolate groups. These anionic tetrazoles interact strongly with cationic arginine residues or metal cations (e.g., Zn2+) within viral and host target sites, including the SARS-CoV-2 ACE2 receptor, influenza H1N1 neuraminidases, and the RSV fusion protein. Using virtual ligand docking and molecular dynamics, we investigated how bisartans and their analogs bind to these viral receptors, potentially blocking infection through a pan-antiviral mechanism. Bisartan, ACC519TT, demonstrated stable and high-affinity docking to key catalytic domains of the SARS-CoV-2 NSP3, H1N1 neuraminidase, and RSV fusion protein, outperforming FDA-approved drugs like Paxlovid and oseltamivir. It also showed strong binding to the arginine-rich furin cleavage sites S1/S2 and S2′, suggesting interference with SARS-CoV-2’s spike protein cleavage. The results highlight the potential of tetrazole-based bisartans as promising candidates for developing broad-spectrum antiviral therapies.

Non-Noble Metal Catalysts for Electrooxidation of 5-Hydroxymethylfurfural.

2,5-Furandicarboxylic acid (FDCA) is a class of valuable biomass-based platform compounds. The creation of FDCA involves the catalytic oxidation of 5-hydroxymethylfurfural (HMF). As a novel catalytic method, electrocatalysis has been utilized in the 5-hydroxymethylfurfural oxidation reaction (HMFOR). Common noble metal catalysts show catalytic activity, which is limited by price and reaction conditions. Non-noble metal catalyst is known for its environmental friendliness, affordability and high efficiency. The development of energy efficient non-noble metal catalysts plays a crucial role in enhancing the HMFOR process. It can greatly upgrade the demand of industrial production, and has important research significance for electrocatalytic oxidation of HMF. In this paper, the reaction mechanism of HMF undergoes electrocatalytic oxidation to produce FDCA are elaborately summarized. There are two reaction pathways and two oxidation mechanisms of HMFOR discussed deeply. In addition, the speculation on the response of the electrode potential to HMFOR is presented in this paper. The main non-noble metal electrocatalysts currently used are classified and summarized by targeting metal element species. Finally, the paper focus on the mechanistic effects of non-noble metal catalysts in the reaction, and provide the present prospects and challenges in the electrocatalytic oxidation reaction of HMF.

Detection of Silver and Mercury Ions Using Naphthalimide-Based Fluorescent Probe.

A multifunctional fluorescent probe P based on a naphthalimide derivative for the detection of Ag+ and Hg2+ through a dual-signal was designed and characterized. P exhibited a large Stokes shift (107 nm), high selectivity, good sensitivity, and fast response time. By adjusting the testing medium and the order of reagent addition, multifunctional detection with P was achieved. The addition of Ag+ or Hg2+ to P solution in either ethanol or an ethanol-water mixture resulted in a significant quenching of fluorescence emission at 537 nm and caused a decrease in the absorbance at 440 nm accompanied by the appearance of a new absorption peak at around 340 nm, and there was an obvious color change from yellow to colorless. In contrast, the addition of other common metal ions and anions did not produce substantial spectral or color changes. The detection limit of probe P for Ag+ and Hg2+ was calculated to be 0.33 μM. The sensing mechanism was proposed and validated through MS and 1H NMR spectrometry methods. Additionally, P demonstrated the capability to recognize Ag+ and Hg2+ in living cells with satisfactory results.

Novel amino-functionalized MOF-based sensor for zinc ion detection in water and blood serum samples

Aquatic systems with low zinc levels can experience a significant decrease in carbon dioxide uptake and limited growth of phytoplankton species. In this study, we describe the use of a new fluorescent sensor based on NH2-MIL-53(Al), and modified with glutaraldehyde and sulfadoxine, for selectively detecting zinc ions in water and blood serum samples. Characterization of the synthesized material was performed using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), Brunauer–Emmett–Teller (BET) surface area analysis, X-ray photoelectron spectroscopy (XPS), and scanning electron microscopy (SEM), confirming successful functionalization and preservation of the MOF structure. The sensor’s performance for Zn2+ detection was evaluated by spectrofluorometry, demonstrating a significant fluorescence enhancement upon Zn2+ binding due to the interaction between Zn2+ ions and the sulfonamide groups. With a detection limit as low as 3.14 × 10–2 ppm, the sensor demonstrates high selectivity for Zn2+ over other common metal ions. The sensor’s response is rapid, stable, and reproducible, making it suitable for practical applications. Real sample analysis was conducted in tap water and blood serum samples, with the results compared to those obtained using ICP-OES and a colorimetric test with 5-bromo-PAPS. The comparison confirmed the high accuracy and reliability of the fluorescent sensor in detecting Zn2+ ions in complex matrices. NH2-MIL-53(Al) modified with glutaraldehyde and sulfadoxine shows potential as a selective fluorescent sensor for Zn2+ detection, making it a valuable tool for monitoring the environment and biology.

Microstructural Evaluation and Linkage to the Engineering Properties of Metal-Ion-Contaminated Clay.

The rapid progress of urbanization and industrialization has led to the accumulation of large amounts of metal ions in the environment. These metal ions are adsorbed onto the negatively charged surfaces of clay particles, altering the total surface charge, double-layer thickness, and chemical bonds between the particles, which in turn affects the interactions between them. This causes changes in the microstructure, such as particle rearrangement and pore morphology adjustments, ultimately altering the mechanical behavior of the soil and reducing its stability. This study explores the effects of four common metal ions, including monovalent alkali metal ions (Na+, K+) and divalent heavy metal ions (Pb2+, Zn2+), with a focus on how ion valence and concentration impact the soil's microstructure and mechanical properties. Microstructural tests show that metal ion incorporation reduces particle size, increases clay content, and transforms the structure from layered to honeycomb-like. Small pores decrease while large pores dominate, reducing the specific surface area and pore volume, while the average pore size increases. Although cation exchange capacity decreases, cation adsorption density per unit surface area increases. Monovalent ions primarily disperse the soil structure, while divalent ions induce coagulation. Macro-mechanical tests reveal that metal ion contamination reduces porosity under loading, with compressibility rises as the ion concentration increases. Soils contaminated with alkali metal ions shows higher compression coefficients at all loads, while heavy metal ions cause higher compression under lower loads. Shear strength, the internal friction angle, and cohesion in metal-ion-contaminated clay decrease compared to uncontaminated field-state clay, with greater declines at higher ion concentrations. The Micropore Morphology Index and hydro-pore structural parameter effectively characterize both micro- and macrostructural properties, establishing a quantitative relationship between HPSP and the engineering properties of metal-ion-contaminated clay.

Metabolipidomic changes induced by dermal nickel penetration determined in an ex vivo porcine ear skin model.

Nickel is one of humans' most prevalent triggers of allergic contact dermatitis. However, the underlying mechanisms of this allergy still need to be fully understood. One aspect that has yet to be explored is the direct impact of common metal allergens on the skin's metabolites and lipids composition. Our study employed matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI MSI) to analyze spatially resolved metabolic alterations induced by nickel exposure. Cross-sections of ex vivo porcine ear skin exposed to increasing nickel (II) ion concentrations (17-167 μg/cm2) were measured with an AP-SMALDI5 AF ion source coupled to Q Exactive HF Orbitrap mass spectrometer. Additionally, the penetration of nickel ions into the skin was observed through its pink complexation with dimethylglyoxime under light microscopy. For nickel ion concentrations up to 84 μg/cm2, most nickel ions were stopped within the stratum corneum, while only a very small proportion of nickel ions penetrated the viable epidermis and dermis. Stratum corneum locations with high nickel ion concentrations showed a decrease in arginine and ceramides. Furthermore, several phosphatidylcholine and sphingomyelin species were found to be downregulated in the viable epidermis and dermis due to the nickel exposure. Nickel penetrates at a trace level into the viable skin and induces severe metabolomic and lipidomic changes in the stratum corneum, epidermis, and dermis, indicating a change in the skin (barrier) function. These findings contribute to a deeper understanding of nickel-induced skin allergies and provide a solid foundation for further research.

The Application of Sulfur–Metal Mass Ratios in Metal Sulfides in Assessing Prospects for Deep Metallogeny: A Case Study of the Tongshan Copper Deposit in Heilongjiang Province, Northeast China

Sulfur–metal mass ratios (SMMRs) between sulfur and metal elements (Cu, Pb, Zn, Ag, Fe, etc.) in metal sulfides are fixed in idealized compositions, so they should have a relatively fixed proportion in terms of mass without considering the presence of structural defects such as vacancies or substitution elements. Rock bodies with an SMMR of S far greater than the common metal sulfides may contain additional sulfides of other metals. We studied the Tongshan copper deposit in NE China and calculated the mass transfer of various elements in drill hole ZK611 samples. The data show a S influx of 7160 g/t, a Cu influx of 5469 g/t, and an Fe influx of 8796 g/t in the Cu ore body. Below the Cu ores, the average influx is 18,600 g/t of S, 650 g/t of Cu, and 5360 g/t of Fe, which provides an SMMR far above common mineral sulfide values. Further studies indicated that this rock unit contains fine-grained sphalerite and galenite, and when Zn and Pb are included in the rock SMMR calculations, values closer to the mineral sulfides emerge. These results imply that the coordinating balance relationship of S content with Fe and other ore-forming metals could provide direct information for assessing metallogenic prospects.

Metal Peroxide Nanoparticles for Modulating the Tumor Microenvironment: Current Status and Recent Prospects.

Background: The significant expansion of nanobiotechnology and nanomedicine has led to the development of innovative and effective techniques to combat various pathogens, demonstrating promising results with fewer adverse effects. Metal peroxide nanoparticles stand out among the crucial yet often overlooked types of nanomaterials, including metals. These nanoparticles are key in producing oxygen (O2) and hydrogen peroxide (H2O2) through simple chemical reactions, which are vital in treating various diseases. These compounds play a crucial role in boosting the effectiveness of different treatment methods and also possess unique properties due to the addition of metal ions. Methods: This review discusses and analyzes some of the most common metal peroxide nanoparticles, including copper peroxide (CuO2), calcium peroxide (CaO2), magnesium peroxide (MgO2), zinc peroxide (ZnO2), barium peroxide (BaO2), and titanium peroxide (TiOx) nanosystems. These nanosystems, characterized by their greater potential and treatment efficiency, are primarily needed in nanomedicine to combat various harmful pathogens. Researchers have extensively studied the effects of these peroxides in various treatments, such as catalytic nanotherapeutics, photodynamic therapy, radiation therapy, and some combination therapies. The tumor microenvironment (TME) is particularly unique, making the impact of nanomedicine less effective or even null. The presence of high levels of reactive oxygen species (ROS), hypoxia, low pH, and high glutathione levels makes them competitive against nanomedicine. Controlling the TME is a promising approach to combating cancer. Results: Metal peroxides with low biodegradability, toxicity, and side effects could reduce their effectiveness in treating the TME. It is important to consider the distribution of metal peroxides to effectively target cancer cells while avoiding harm to nearby normal cells. As a result, modifying the surface of metal peroxides is a key strategy to enhance their delivery to the TME, thereby improving their therapeutic benefits. Conclusions: This review discussed the various aspects of the TME and the importance of modifying the surface of metal peroxides to enhance their therapeutic advantages against cancer, as well as address safety concerns. Additionally, this review covered the current challenges in translating basic research findings into clinical applications of therapies based on metal peroxide nanoparticles.

Determination of Hafnium in Zirconium by Spectrophotometry

Zirconium and hafnium have opposite nuclear properties and are used very differently in the nuclear industry. However, hafnium is a common metal impurity in zirconium, and the chemical properties of the two are very similar except for nuclear properties, and it is difficult to separate and detect them. At present, the detection of hafnium content in zirconium is usually achieved by using an inductively coupled plasma (ICP) spectrometer, but ICP equipment is expensive, and the detection cost is high. Therefore, it is necessary to develop a simple and low-cost method for the determination of hafnium content in zirconium. Based on this, this paper takes the spectrophotometric method as a starting point. Through a series of experiments on the influence of pH and concentrations of the color-developing agent xylenol orange sodium salt on the absorbance of zirconium and hafnium ions, the appropriate variables are selected to detect the content of hafnium in zirconium. Finally, according to the measured absorbance and total ion concentration, by comparing the working curve of zirconium and hafnium ions, the content of hafnium in zirconium is calculated based on the lever principle.

Choline supplementation reduces cadmium uptake and alleviates cadmium toxicity in Solanum lycopersicum seedlings

Sustainable plant production in soil polluted with heavy metals requires that novel strategies are developed for the benefit of humans and other living things. Cadmium (Cd) is a common heavy metal pollutant for plants, and there is limited information on the use of exogenous bio-regulators to reduce the accumulation and toxic effects of Cd pollution in plants. Choline is an endogenous quertarnary amine that is known to improve stress tolerance in plants, while its mechanism of action in certain conditions is yet to be determined. This study investigated the effects of foliar choline supplementation (10 mM) on Solanum lycopersicum seedlings exposed to Cd application (50 mg/L in soil). The seedlings were randomized to five groups: Control (E1), Cd stress (E2), Choline supplementation after Cd stress (E3), Choline (E4), and Choline supplementation before Cd stress (E5). Following the applications, the Cd content, growth and development parameters (chlorophyll content, fresh and dry weight), oxidative stress parameters (H2O2 and MDA contents), as well as antioxidative defense system (SOD, GSH, AsA, and TPC contents) were analyzed. Choline supplementation after Cd stress reduced the enhanced Cd content in roots by 38% but did not alter it in leaves (p > 0.05) compared to the Cd group. Choline supplementation before Cd stress decreased Cd content both in roots by 87.5% and in leaves by 50%. Choline supplementation after and before Cd stress increased fresh and dry weights in both roots and leaves. While the Cd group (E2) increased the H2O2 level and SOD activity, no remarkable change was observed in H2O2 levels in all choline supplementations (E3, E4, E5). Therefore, lipid peroxidation (MDA) was not observed in choline supplementation before Cd stress (E5), however, when the choline was applied after Cd stress (E3) MDA content was reduced by 40% compared with the Cd stress group (E2). Choline supplementations after and before Cd stress (E3, E5) increased AsA content by 30%, while the Cd group (E2) decreased it by 60% compared with the control group (E1). Choline supplementations before Cd stress (E5) increased TPC by 33%, while the Cd group (E2) decreased it by 18%, moreover, when choline was applied after Cd stress (E3), no change was observed compared to the control group. These data suggest that choline prevents inhibition of plant growth due to Cd toxicity by reducing Cd uptake. The results provided in the present study are likely to enhance the quality and efficiency of crop production in heavy metal-polluted areas.

Agro-waste based biomass residues valorization for effective adsorption of heavy metal.

In this experiment four agro-waste based biomass residues (soybean stover-SSb, buckwheat stover-BWb, Artemisia vulgaris- AVb and Chromolaena odorata-COb) was valorized into low cost amendment called biochar followed by compositional characterization for their application in heavy metal removal. Investigation was carried out on the removal of the most common heavy metal ions including arsenic, cadmium, lead, nickel, zinc, and copper through adsorption on four types of biomass valorised biochar. According to preliminary testing, all the biochar was effective to eliminate a mixture of six heavy metals from the aqueous phase, with the removal of arsenic being the most removed and nickel being the least. In comparison to no biochar treatment, the average removal rate of heavy metal from aqueous solution using four distinct types of biochar was 45.75-62.42% (Cd), 43.64-56.33% (Pb), 41.85-59.73% (Ni), 42.87-60.28% (Zn), 45.64-59.51% (Cu), and 49.02-60.53% (As). The percent decrease of cadmium heavy metal adsorption with increase in maximum contaminant level (MCL) from 1- to fivefold was 20.0 (SSb), 20.7 (COb), 21.6 (BWb), and 22.9 (AVb). The results of the dosage study indicated that As adsorption was the most beneficial on all four types of biochar, whereas Ni adsorption was the least effective. With increase in application rate of biochar the heavy metals adsorption (%) was also increased. Four different agro-waste valorized biochar were used to treat the wastewater, and the physical and chemical changes that occurred both before and after the biochar treatment were noted. There was a drop in the wastewater CODT, CODD, TSS, ammonia, TKN, TP and pH values of 79.7-103.5%, 57.7-81.5, 52.3-68.4%, 1.23-2.23%, 14.1-20.6%, and 1.23-3.03%, respectively. Furthermore, after being passed through a biochar, the wastewater's Zn, Pb, Cd, As, Cr and Cu levels decreased by 3.26-6.15%, 0.06-0.34%, 0.01-0.08%, 2.37-3.65%, 3.95-5.53%, and 2.24-3.34%, respectively at 2.5 and 5.0g/litre of wastewater. Thus, in order to comply with regulations for the disposal of wastewater effluent, the process of valorizing biomass into biochar offered enormous potential for the removal of heavy metals in addition to wastewater treatment.

Restricted Intramolecular Rotation: A Dual Fluorescence Response to Hg2+ Quenching and Ag+ Enhancement in Live Rhizoctonia Solani Cells.

A novel imidazo[1,2-a]pyridine derivative probe (R) was designed, synthesized, and characterized via various characterization techniques, such as ESI-MS, 1H NMR, 13C NMR, and Dept-135 NMR. The data obtained from single-crystal XRD reveal that probe R has a coplanar configuration and is part of the monoclinic crystal system, designated the P2(1)/n space group. The fluorescence of (R) is further enhanced by silver (I) ions. On the other hand, Hg2+ significantly quenches the fluorescence of probe R. The presence of other common metal ions does not influence the fluorescence of probe R in the CH3CN: H2O (1:1) mixture, as they neither increase nor quench it. From the fluorescence enhancement data, the low detection limit (LOD) for Ag + ions was determined to be 1.24 × 10- 8 M, whereas the quenching caused by Hg2+ resulted in an LOD of 5.69 × 10- 9 M. The complex of probe R with Ag+/Hg2+ exhibited a 1:1 stoichiometry, as confirmed by mass spectrometry and a Job plot. Single-crystal XRD analysis of R and its complex with Hg2+ revealed a loss of coplanarity, which confirmed their nonfluorescent behavior. We present a promising application of probe R in visualizing living Rhizoctonia oryzae cells exposed to silver (I) and mercury (II) ions.

Development and Biomedical Application of Non-Noble Metal Nanomaterials in SERS.

Surface-enhanced Raman scattering (SERS) is vital in many fields because of its high sensitivity, fast response, and fingerprint effect. The surface-enhanced Raman mechanisms are generally electromagnetic enhancement (EM), which is mainly based on noble metals (Au, Ag, etc.), and chemical enhancement (CM). With more and more studies on CM mechanism in recent years, non-noble metal nanomaterial SERS substrates gradually became widely researched and applied due to their superior economy, stability, selectivity, and biocompatibility compared to noble metal. In addition, non-noble metal substrates also provide an ideal new platform for SERS technology to probe the mechanism of biomolecules. In this paper, we review the applications of non-noble metal nanomaterials in SERS detection for biomedical engineering in recent years. Firstly, we introduce the development of some more common non-noble metal SERS substrates and discuss their properties and enhancement mechanisms. Subsequently, we focus on the progress of the application of SERS detection of non-noble metal nanomaterials, such as analysis of biomarkers and the detection of some contaminants. Finally, we look forward to the future research process of non-noble metal substrate nanomaterials for biomedicine, which may draw more attention to the biosensor applications of non-noble metal nanomaterial-based SERS substrates.

Glucose‐based Ionic Liquid Organocatalysts for Asymmetric aza‐Diels‐Alder Reactions

AbstractCarbohydrate‐based ionic liquids and salts (CHILS) have recently emerged as an uprising sub‐class of ionic liquids. Their starting materials are available in abundant natural resources from plants and fauna. Carbohydrates are not only sustainable; they also exhibit natural chirality. To use this, novel glucosyl imidazolium NTf2 ionic liquids were synthesized and applied as organocatalysts in aza‐Diels‐Alder reactions in this work, where we used aldimines and Danishefsky's diene as substrates. We investigated the structure‐activity relationships of these glucosyl imidazolium NTf2 organocatalysts through several functionalizations on the carbohydrate and the imidazole and compared them with common metal catalysts and ionic liquids. Our organocatalysts improved the yield of the model aza‐Diels‐Alder reaction highly and also had a positive effect on the overall diastereomeric excess.

In situ growth of large-scale and ultrathin carbon nitride films shield common metal substrates from corrosion and oxidation

A centimeter-size carbon nitride (CN) film, with nanoscale thickness, is in situ deposited on various metals through the thermal condensation of melamine, achieving broad and uniform coverage, without any pre- and post-treatments. As the temperature rises, the nitrogen content in the film increases, leading to the part of CN to transform into g-C3N4. Benefit from higher Gibbs adsorption free energies of g-C3N4 with Cl- and O2 in aqueous environment, a 30 nm CN film deposited at 475 ℃ with large g-C3N4 network, minimal segregation and low internal stress enables pure metals and alloys to achieve over 90 % protection efficiency.

The influence of adult urine lead exposure on bone mineral densit: NHANES 2015-2018.

Previous studies have indicated that exposure to heavy metals related to bone health is primarily limited to some common harmful metals, and the impact of lead has not been fully understood. This study aims to explore the relationship between urine lead exposure and bone density. 1,310 adults were included from the NHANES database (2015-2018), and through generalized linear regression analysis and constrained cubic spline models, the association between lead levels and total bone density as well as lumbar spine bone density was explored. The study also examined the impact of combined exposure to lead and cadmium on bone density. Urinary lead levels were significantly negatively correlated with total bone mineral density (β: -0.015; 95%CI: -0.024, -0.007) and lumbar spine bone mineral density (β: -0.019; 95%CI: -0.031, -0.006). Compared to the lowest three quartiles of lead levels, the adjusted odds ratios for T3 changes in total bone mineral density and lumbar spine bone mineral density were 0.974 (95%CI: 0.959, 0.990) and 0.967 (95%CI: 0.943, 0.991), indicating a significant negative trend. Further analysis with constrained cubic spline models revealed a non-linear decreasing relationship between urinary lead and total bone mineral density as well as lumbar spine bone mineral density. Stratified analyses suggested that the relationship between urinary lead levels and bone mineral density might be significantly influenced by age, while gender showed no significant impact on the relationship. Moreover, combined exposure to lead and cadmium was found to be associated with decreased bone mineral density, emphasizing the potential synergistic effects between lead and cadmium on bone health. However, the specific mechanisms of lead and its effects on different populations require further comprehensive research. This study provides valuable insights for further exploration and development of relevant public health policies.

Experimental and theoretical examination and development of methods to calculate required pull force in wire drawing

Wire drawing is one of the oldest and most common cold metal forming processes. Wire is drawn through a single die or a set of conical dies to make it longer and stronger. In the drawing die there are three geometrical parameters that affect the drawing force: die diameter, die angle and bearing length. The force required to pull the wire through the drawing die has been investigated numerous times over the years and new drawing force equations have been developed. However, some of today’s most widely used equations do not include the influence of the bearing length. In this paper the most common methods to calculate the drawing force are evaluated by means of wire drawing experiments and finite element studies. From the results, a novel equation for calculating the drawing force is proposed. The proposed equation is dependent on the bearing length and was compared with experiments and validated using finite element simulations with promising results.

Development of smart molecularly imprinted tetrahedral amorphous carbon thin films for in vitro dopamine sensing

This study investigates how varying the thickness of tetrahedral amorphous carbon (ta-C) thin films and incorporating a titanium adhesion layer influences the structural and electrochemical properties of molecularly imprinted ta-C thin film-based sensing platforms, aiming to develop a molecularly imprinted ta-C electrochemical sensor for dopamine (DA) detection with physiologically relevant sensitivity. This electrochemical sensing platform was designed by integrating ta-C with molecularly imprinted polymers (MIPs). The process involved depositing a ta-C thin film onto boron-doped p-type silicon wafers through a filtered cathodic vacuum arc (FCVA) system. Subsequently, the ta-C sensing platforms were electrochemically coated with the MIP layer (DA-imprinted polypyrrole). We evaluated three configurations: (i) a 15 nm ta-C layer, (ii) a 7 nm ta-C layer with a 20 nm titanium adhesion layer, and (iii) a 15 nm ta-C layer with a 20 nm titanium adhesion layer. Comprehensive structural and electrochemical characterization was performed to understand how these modifications affect sensor performance. The optimized MIP/ta-C sensor demonstrated a sensitivity of 0.16 μA μM−1 cm−2 and a limit of detection (LOD) of 48.6 nM, suitable for detecting DA at physiological levels. Leveraging the synergistic effects of ta-C coatings and molecular imprinting, as well as its compatibility with common complementary metal–oxide–semiconductor (CMOS) processes underlines its potential for integration into microanalytical systems, paving the way for miniaturized and high-throughput sensing platforms.

Integrating Data Mining and Natural Language Processing to Construct a Melting Point Database for Organometallic Compounds.

As semiconductor devices are miniaturized, the importance of atomic layer deposition (ALD) technology is growing. When designing ALD precursors, it is important to consider the melting point, because the precursors should have melting points lower than the process temperature. However, obtaining melting point data is challenging due to experimental sensitivity and high computational costs. As a result, a comprehensive and well-organized database for the melting point of the OMCs has not been fully reported yet. Therefore, in this study, we constructed a database of melting points for 1,845 OMCs, including 58 metal and 6 metalloid elements. The database contains CAS numbers, molecular formulas, and structural information and was constructed through automatic extraction and systematic curation. The melting point information was extracted using two methods: 1) 1,434 materials from 11 chemical vendor databases and 2) 411 materials identified through natural language processing (NLP) techniques with an accuracy of 86.3%, based on 2,096 scientific papers published over the past 29 years. In our database, the OMCs contain up to around 250 atoms and have melting points that range from -170 to 1610 °C. The main source is the Chemsrc database, accounting for 607 materials (32.9%), and Fe is the most common central metal or metalloid element (15.0%), followed by Si (11.6%) and B (6.7%). To validate the utilization of the constructed database, a multimodal neural network model was developed integrating graph-based and feature-based information as descriptors to predict the melting points of the OMCs but moderate performance. We believe the current approach reduces the time and cost associated with hand-operated data collection and processing, contributing to effective screening of potentially promising ALD precursors and providing crucial information for the advancement of the semiconductor industry.

Exploring acid mine drainage treatment through adsorption: a bibliometric analysis.

Discharge of acidic wastewater from mining activities (acid mine drainage (AMD)) is a major global environmental and public health issue. Although several approaches, including chemical precipitation and membrane technology, have been developed to treat AMD, adsorption has emerged as the most promising technology due to its cost-effectiveness and efficacy. Despite the wide adoption of adsorption in treating AMD, the evolution of research in this area remains poorly understood. To address this gap, a bibliometric analysis of the most recent literature involving the application of adsorption in AMD remediation was conducted by merging datasets of articles from Scopus (1127) and the Web of Science Core Collection (1422), over the past decade (2013-2022). This analysis revealed a yearly increase of 11% in research publications, primarily contributed by China, the United States, and South Africa. Keyword analysis revealed that natural schwertmannites and their transformations, activated carbon, zeolites, and clay minerals, are the most extensively employed adsorbents for the removal of common metals (arsenic, chromium, iron, manganese, among others). The findings underscore the need for future focuses on recovering rare earth elements, using nanoparticles and modified materials, pursuing low-cost, sustainable solutions, integrating hybrid technologies, pilot-scale studies, exploring circular economic applications of AMD sludges, and inter-continental collaborations. These insights hold significant future implications, serving as a valuable reference to stakeholders in the mining industry.