Search Results (131)

A scalable synthesis of two-dimensional titanium nitride chloride (TiNCl) via flash Joule heating (FJH) using titanium tetrachloride (TiCl₄) precursor has been developed. This single-step method overcomes traditional synthesis challenges, including high energy consumption, multi-step procedures, and hazardous reagent requirements. The structural and chemical properties of the synthesized TiNCl were characterized through multiple analytical techniques. X-ray diffraction (XRD) patterns confirmed the presence of TiNCl phase, while Raman spectroscopy data showed no detectable oxide impurities. Fourier transform infrared spectroscopy (FTIR) analysis revealed characteristic Ti–N stretching vibrations, further confirming successful titanium nitride synthesis. Transmission electron microscopy (TEM) imaging revealed thin, plate-like nanostructures with high electron transparency. These analyses confirmed the formation of highly crystalline TiNCl flakes with nanoscale dimensions and minimal structural defects. The material exhibits excellent structural integrity and phase purity, demonstrating potential for applications in photocatalysis, electronics, and energy storage. This work establishes FJH as a sustainable and scalable approach for producing MXenes with controlled properties, facilitating their integration into emerging technologies. Unlike conventional methods, FJH enables rapid, energy-efficient synthesis while maintaining material quality, providing a viable route for industrial-scale production of two-dimensional materials. Full article

To enhance agricultural soil health and soil organic carbon (SOC) sequestration, it is important to accurately measure SOC. The aim of this study was to compare common methods for measuring SOC in soils in order to determine the most effective approach among different agricultural land types. The measurement methods of loss-on-ignition (LOI), automated dry combustion (Dumas), and real-time near-infrared spectroscopy (NIRS) were compared. A total of 95 soil core samples, ranging in clay and calcareous content, were collected across a range of agricultural land types from forty-eight fields across five farms in the Southwest of England. There were similar and positive correlations between all three methods for measuring SOC (ranging from r = 0.549 to 0.579; all p < 0.001). On average, permanent grass fields had higher SOC content (6.6%) than arable and temporary ley fields (4.6% and 4.5%, respectively), with the difference of 2% indicating a higher carbon storage potential in permanent grassland fields. Newly predicted conversion equations of linear regression were developed among the three measurement methods according to all the fields and land types. The correlation of the conversation equations among the three methods in permanent grass fields was strong and significant compared to those in both arable and temporary ley fields. The analysed results could help understand soil carbon management and maximise sequestration. Moreover, the approach of using real-time NIRS analysis with a rechargeable portable NIRS soil device can offer a convenient and cost-saving alternative for monitoring preliminary SOC changes timely on or offsite without personnel risks from the high-temperature furnace and chemical reagent adopted in the LOI and Dumas processes, respectively, at the laboratory. Therefore, the study suggests that faster, lower-cost, and safer methods like NIRS for analysing initial SOC measurements are now available to provide similar SOC results as traditional soil analysis methods of the LOI and Dumas. Further studies on assessing SOC levels in different farm locations, land, and soil types across seasons using NIRS will improve benchmarked SOC data for farm stakeholders in making evidence-informed agricultural practices. Full article

From an occupational health perspective, if not stored, handled, and disposed of properly, laboratory chemicals exhibit hazardous properties such as flammability, corrosion, and explosibility. Additionally, they can also cause a range of health effects in handlers, including irritation, sensitization, and carcinogenicity. Additionally, the chemical waste generated during the planned assay is a significant byproduct and, if left untreated, can cause detrimental effects on both living organisms and non-living elements when released into the environment. Chemically, laboratory waste contains reagents, organic and inorganic compounds, and diagnostic stains. These agents are more toxic and hazardous than residential waste and affect the personnel handling them and the environments in which they are released. Considering this, it is crucial to adhere to waste management regulations during the various stages including generation, segregation, collection, storage, transportation, and treatment. This is extremely important and necessary if we are to avoid harm to individuals and environmental contamination. This review encompasses the examination of laboratory medical waste, various categories of chemical waste, and strategies to minimize and ensure the safe disposal of these toxic agents. As far as the authors are aware, this is the first review that focuses on the effects of laboratory-generated chemical wastes and environmental ethics. This is a neglected topic in healthcare education, and this review will serve as a valuable resource for students. Full article

The aim of this study is to explore the feasibility of using flotation wastewater from copper–porphyry ore processing to synthesize a gel that serves as a precursor for a polymer nanocomposite used in supercapacitor electrode fabrication. These wastewaters—characterized by high acidity and elevated concentrations of metal cations (Cu, Ni, Zn, Fe), sulfates, and organic reagents such as xanthates, oil (20 g/t ore), flotation frother (methyl isobutyl carbinol), and pyrite depressant (CaO, 500–1000 g/t), along with residues from molybdenum flotation (sulfuric acid, sodium hydrosulfide, and kerosene)—are byproducts of copper–porphyry gold-bearing ore beneficiation. The reduction of Ni powder in the wastewater induces the degradation and formation of a gel that captures both residual metal ions and organic compounds—particularly xanthates—which play a crucial role in the subsequent steps. The resulting gel is incorporated during the oxidative polymerization of aniline, forming a nanocomposite with a polyaniline matrix and embedded xanthate-based compounds. An asymmetric supercapacitor was assembled using the synthesized material as the cathodic electrode. Electrochemical tests revealed remarkable capacitance and cycling stability, demonstrating the potential of this novel approach both for the valorization of industrial waste streams and for enhancing the performance of energy storage devices. Full article

The aim of this study is to investigate a green and efficient hydrothermal synthesis method for obtaining a high-purity MIL-100(Fe) metal–organic framework (MOF) without using hazardous HF acid or other toxic reagents. The influence of various synthesis conditions (reactant ratios and reaction times) and washing protocols on the MOF’s properties and crystallinity was investigated. Additionally, the adsorption capacities of the synthesized MIL-100(Fe) for hydrogen (H₂), carbon dioxide (CO₂), and water vapor were evaluated at different temperatures and pressures. By analyzing the adsorption behavior, this research study aims to assess the potential of this material for thermal or specific gas storage applications. MF-S1 synthesis, using less iron and water, produces the purest MIL-100(Fe), as confirmed by XRD and FTIR. MF-S1-W2, with additional washing, is ideal for gas adsorption due to its crystallinity, purity, and high surface area. It effectively stores hydrogen (0.25 wt.% at 5 °C), CO₂ (32.6 wt.% at 5 °C), and water vapor (47.5 wt.% at 30 °C). Full article

Nipah virus (NiV) is a severe zoonotic pathogen that substantially threatens public health. Pigs are the natural hosts of NiV and can potentially transmit this disease to humans. Establishing a rapid, sensitive, and accurate point-of-care detection method is critical in the timely identification of infected pig herds. In this study, we developed an NiV detection method based on reverse transcription–recombinase polymerase amplification (RT-RAA) and the clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein 13a (Cas13a) system for the precise detection of NiV. The highly conserved region of the NiV gene was selected as the detection target. We first designed eleven pairs of RT-RAA primers, and the optimal primer combination and reaction temperature were identified on the basis of RT-RAA efficiency. Additionally, the most efficient crRNA sequence was selected on the basis of the fluorescence signal intensity. The results revealed that the optimal reaction temperature for the developed method was 37 °C. The detection limit was as low as 1.565 copies/μL. Specificity testing revealed no cross-reactivity with nucleic acids from six common swine viruses, including Seneca virus A (SVA), foot-and-mouth disease virus (FMDV), classical swine fever virus (CSFV), porcine epidemic diarrhea virus (PEDV), African swine fever virus (ASFV), and pseudorabies virus (PRV). A validation test using simulated clinical samples revealed a 100% concordance rate. The detection results can be visualized via a fluorescence reader or lateral flow strips (LFSs). Compared with conventional detection methods, this RT-RAA-CRISPR/Cas13a-based method is rapid and simple and does not require scientific instruments. Moreover, the reagents can be freeze-dried for storage, eliminating the need for cold-chain transportation. This detection technology provides a convenient and efficient new tool for the point-of-care diagnosis of NiV and for preventing and controlling outbreaks. Full article

Surface-enhanced Raman spectroscopy (SERS) is widely employed due to its high sensitivity and distinctive fingerprinting capabilities. Colloidal nanoaggregates are commonly used as SERS substrates because of their mobility and the abundance of “hotspots”. Although the reagent-free “freeze-thaw-ultrasonication” method for preparing Ag nanoaggregates (AgNAs) does not introduce additional background interference and maintains the original interfacial properties of AgNAs, their unstable physical nanostructure limits SERS detection to just 7 days. Herein, we demonstrate mesoporous silica-encapsulated colloidal Ag nanoaggregates (AgNAs@m-SiO₂) by combining a freeze-thaw-ultrasonication method and a cetyltrimethylammonium bromide (CTAB)-assisted silanization reaction, achieving long-term SERS stability of more than two months. The prepared AgNAs@m-SiO₂ serve a dual capability: (1) preserving electromagnetic “hotspots” for ultra-sensitive detection (e.g., malachite green detection limit: 3.60 × 10⁻⁸ M), and (2) maintaining structural stability under harsh conditions. The AgNAs@m-SiO₂ substrate exhibited superior structural stability after 50 min of ultrasonic treatment, with an initial SERS signal retention of 91.8%, which is twice that of the bare AgNAs (retention of 45%). The long-term performance further highlighted its superiority: after 70 days of storage, the composite maintained 84.3% of its original signal strength, outperforming the uncoated controls by over ten times (which retained only 8%). Crucially, the substrate’s robust design enables the direct detection of contaminants in real environmental matrices (river and seawater) for qualitative analyses and water quality assessments, thus validating its suitability for environmental sensing applications in the field. Full article

The implementation of sodium-ion batteries for renewable energy storage requires the development of sustainable electrode materials. Usually, these materials are produced through complex energy-intensive processes that are challenging to scale and involve expensive and/or toxic reagents. In this study, sustainable hard carbon materials, some doped with iron, synthesized from sucrose using a simple, fast, and cost-effective two-step eco-friendly process, are investigated as anodes for sodium-ion batteries. The influence of physicochemical and structural material properties on electrode reversible capacity, cycling stability, and efficiency is analyzed. The SC900 material, which exhibits a certain development of graphite-like structure, though not strictly graphitic, showed the best electrochemical performance, providing discharge capacities exceeding 100 mAh g⁻¹ after 400 cycles with excellent cycling stability and high coulombic efficiency. The capacity of the materials increases as d₀₀₂ decreases, (i.e., as the degree of structural order increases), to the optimum value of ~0.3700 nm. However, a further decrease in d₀₀₂ to values characteristic of quasi-graphitic materials, as a consequence of the catalytic effect of iron, hinders Na⁺-ion storage, which, in addition to the low electrochemical activity of the iron oxides present, leads to much lower capacities. Full article

Cyanide is a crucial reagent for the synthesis of biomolecules in prebiotic chemistry. However, effective organic synthesis requires cyanide to be concentrated. One proposed mechanism for cyanide storage and concentration on Early Earth involves the formation of aqueous ferrocyanide complexes. In basic pH conditions, cyanide will spontaneously form ferrocyanide complexes in the presence of aqueous Fe(II). While ferrocyanide aqueous complex formation is well defined, the potential for Fe(II)-bearing minerals to react with cyanide to form ferrocyanide complexes or store cyanide on the mineral surface has yet to be explored under prebiotically relevant conditions. In this study, we demonstrate that when cyanide interacts with ferroan brucite (Mg_xFe_1−x(OH)₂), cyanide will both form aqueous and mineral-surface-adsorbed ferrocyanide implying that there are two reservoirs that cyanide will partition into. In addition, we found that cyanide decreased the amount of hydrogen gas produced by the oxidation of ferroan brucite, indicating that cyanide alters the mineral’s redox reactivity. The cyanide adsorbed on brucite can be released by a decrease in pH, which leads to the dissolution of ferroan brucite, thus releasing the adsorbed cyanide. Our findings suggest that iron-bearing minerals may represent an overlooked storage reservoir of cyanide on Hadean Earth, potentially playing a significant role in cyanide availability for prebiotic chemistry. Full article

The complex chemical composition of honey presents significant challenges for its analysis with variations influenced by factors such as botanical source, geographical location, bee species, harvest time, and storage conditions. This study aimed to employ high-performance thin-layer chromatography (HPTLC) fingerprinting, coupled with multivariate data analysis, to characterise the chemical profiles of Australian stingless bee honey samples from two distinct bee species, Tetragonula carbonaria and Tetragonula hockingsi. Using a mobile phase composed of toluene:ethyl acetate:formic acid (6:5:1) and two derivatisation reagents, vanillin–sulfuric acid and natural product reagent/PEG, HPTLC fingerprints were developed to reveal characteristic patterns within the samples. Multivariate data analysis was employed to explore the similarities in the fingerprints and identify underlying patterns. The results demonstrated that the chemical profiles were more closely related to harvest time rather than bee species, as samples collected within the same month clustered together. The quality of the clustering results was assessed using silhouette scores. The study highlights the value of combining HPTLC fingerprinting with multivariate data analysis to produce valuable data that can aid in blending strategies and the creation of reference standards for future quality control analyses. Full article

Achieving the New World Sustainability Vision 2030 leads to enacting environmental restrictions, which aim to partially or totally reduce the negative impacts of different forms of waste and develop alternative technologies for eco-friendly and cost-effective utilization. Solid waste is a hazardous waste with many environmental and economic problems resulting from its storage and disposal. However, at the same time, these wastes contain many valuable elements. One of these solid wastes is heavy oil fly ash “HOFA” generated in power stations using heavy oil as fuel. HOFA is produced annually in massive amounts worldwide, the storage of which leads to the contamination of water resources by the contained heavy metals, resulting in many cancerogenic diseases. At the same time, these ashes contain many valuable metals in significant amounts, such as vanadium “V” and nickel “Ni” that can be extracted effectively compared to their low content and difficulty processing in their main ores. Hence, recycling these types of wastes reduces the environmental adverse effects of their storage and the harmful elements in their composition. This paper critically reviews the world resources of vanadium-bearing waste and various approaches described in the literature for recovering V, Ni, as well as other valuable metals from (HOFA) and other wastes, including pyro- and hydro-metallurgical processes or a combination. Hydro-metallurgical processes include alkaline or acidic leaching using different reagents followed by chemical precipitation, solvent extraction, and ion exchange to extract individual elements. The pyro-metallurgical processes involve the non-salt or salt roasting processes followed by acidic or alkaline leaching processes. The operational parameters and their impact on the efficiency of recovery are also discussed. The digestion mixtures of strong mineral acids used to dissolve metal ions in HOFA are also investigated. Bioleaching is a promising eco-friendly technology for recovering V and Ni through appropriate bacteria and fungi. Oxidation leaching is also a promising environmentally friendly approach and more effective. Among all these processes, the salt roasting treatment showed promising results concerning the cost, technological, and environmental effectiveness. The possibility of complex processing of HOFA has also been investigated, proposing innovative technology for completely utilizing this waste without any remaining residue. Effective zeolite for wastewater treatment has been formulated as a good alternative for conserving the available water resources. Full article

The European Union (EU) regulations mandate 10% of all food packaging to be reusable by 2030. United States (U.S.) exporters of specialty crops face new challenges in ensuring microbiological food safety using reusable packaging. A novel antimicrobial formulation consisting of ammonium carboxylate salt of capric acid and L-arginine (GS-2) was recently developed as a spray coating chemical for food packaging materials. In this study, we evaluated the antimicrobial efficacy of GS-2 against microbial strains representing three foodborne bacterial pathogens (Escherichia coli O157:H7, Listeria monocytogenes, Salmonella enterica), one fungal spoilage organism (Aspergillus niger), and one surrogate viral pathogen (murine norovirus) on three reusable plastic materials (acrylonitrile butadiene styrene, high-density polyethylene, and polypropylene) and one cardboard packaging material, respectively. Different chemical concentrations, exposure times, and storage conditions were individually evaluated for the relative antimicrobial efficacies of GS-2 against these microorganisms. Our results showed that GS-2 was highly effective for inactivating bacterial pathogens on both plastic and cardboard surfaces. For instance, 3% GS-2 achieved a >5 log CFU/in² reduction in E. coli O157:H7, L. monocytogenes, and S. enterica on tested plastic surfaces at an exposure time of 60 min. However, its efficacy against A. niger and murine norovirus was less optimal, resulting in a ≤1 log CFU/in² reduction on all tested surfaces. Based on our study, GS-2 demonstrated a strong potential as an antibacterial coating reagent for reusable food packaging materials to minimize pathogen contamination and ensure the safety of the specialty crops. Full article

When processing low-quality gibbsite–kaolinite bauxites, technologies that involve different methods of mechanical and chemical enrichment with the separation of a difficult-to-utilize fine kaolinite fraction for disposal are used. Before production, problems related to waste storage and disposal arise. To solve the problem of utilization, it is necessary to develop an effective technology for the selective processing of the kaolinite fraction. The efficiency of the technology will depend on the quality of pretreatment of raw materials prior to processing for Al₂O₃ extraction. Preliminary preparation of kaolinite fraction is associated with the maximum removal of excess silica during chemical enrichment by treatment with an alkaline solution. The presence of silica reduces the quality of final alumina products and requires a large consumption of reagents during the desiliconization of aluminate solutions. During the chemical enrichment of kaolinite fraction in alkaline solution, a serious problem of the co-dissolution of Al₂O₃ with silica arises. The solution to this problem can be the transformation of phase composition with the transformation of kaolin into a chemically resistant compound corundum, which will create conditions for the selective removal of silica. Kazakhstan’s alumina refinery, Pavlodar Aluminum Smelter, processes low-quality gibbsite–kaolinite bauxite from the Krasnogorsk deposit. To improve the quality of bauxite, preliminary gravity enrichment is carried out to separate the kaolinite fraction to a quantity greater than 50%. The purpose of this work was to study the possibility of the selective processing of the kaolinite fraction via various techniques, including preliminary thermal transformation, through sintering, chemical enrichment, autoclave leaching in a circulating aluminate solution, and low-temperature desiliconization, to obtain a solution for decomposition. As a result of this study, the possibility of obtaining a corundum phase after sintering at a temperature of 900–1000 °C was established, which made it possible to obtain 58.8% chemical enrichment through the extraction of SiO₂ into solution. Further use of the enriched kaolinite fraction in autoclave leaching in a circulating aluminate solution with low-temperature desiliconization made it possible to obtain an aluminate solution with a caustic modulus of 1.65–1.7, which is suitable for decomposition. Full article

To maintain the carbon dioxide concentration below the no-return threshold for climate change, we must consider the reduction in anthropic emissions coupled to carbon capture methods applied in synergy. In our recent papers, we proposed a green and reliable method for carbon mineralization using ascorbic acid aqueous solution as the reducing agent for carbon (IV) to carbon (III), thus obtaining oxalic acid exploiting green reagents. Oxalic acid is made to mineralize as calcium (as the model cation) oxalate. Oxalates are solid-state reservoirs suitable for long-term carbon storage or carbon feedstock for manufacturing applications. The carbon mineralization reaction is a double-step process (carbon reduction and oxalate precipitation), and the carbon capture efficiency is invariably represented by a double-slope curve we formerly explained as a decrease in the reducing effectiveness of ascorbic acid during reaction. In the present paper, we demonstrated that the reaction proceeds via a “pure CO₂-capture” stage in which ascorbic acid oxidizes into dehydroascorbic acid and carbon (IV) reduces to carbon (III) and a “mixed” stage in which the redox reaction competes with the degradation of ascorbic acid in producing oxalic acid. Despite the irreversibility of the reduction reaction, that was demonstrated in abiotic conditions, the analysis of costs according to the market price of the reagents endorses the application of the method. Full article

Flow cytometry facilitates the detection of multiple cell parameters simultaneously with a high level of resolution and throughput, enabling in-depth immunological evaluations. High data resolution in flow cytometry depends on multiple factors, including the concentration of reagents used in the staining protocol, and reagent validation and titration should be the first step in any assay optimization. Titration is the process of finding the concentration of the reagent that best resolves a positive signal from the background, with the saturation of all binding sites, and minimal antibody excess. The titration process involves the evaluation of serial reagent dilutions in cells expressing the antigen target for the tested antibody. The concentration of antibody that provides the highest signal to noise ratio is calculated by plotting the percentage of positive cells and the intensity of the fluorescence of the stained cells with respect to the negative events, in a concentration–response curve. The determination of the optimal antibody concentration is necessary to ensure reliable and reproducible results and is required for each sample type, reagent clone and lot, as well as the methods used for cell collection, staining, and storage conditions. If the antibody dilution is too low, the signal will be too weak to be accurately determined, leading to suboptimal data resolution, high variability across measurements, and the underestimation of the frequency of cells expressing a specific marker. The use of excess antibodies could lead to non-specific binding, reagent misuse, and detector overloading with the signal off scale and higher spillover spreading. In this publication, we summarized the titration fundamentals and best practices, and evaluated the impact of using a different instrument, sample, staining, acquisition, and analysis conditions in the selection of the optimal titer and population resolution. Full article