Mixture Of Nitrate Research Articles

On the formation of ammonia from the thermal decomposition of hydroxylammonium nitrate vapor

The ionic liquid hydroxylammonium nitrate (HAN) is a promising propellant for various types of spacecraft propulsion systems. With respect to combustion and plasma-based electric propulsion, the thermal decomposition of HAN into gas phase species provides a convenient feed gas supply. While the decomposition of HAN in the liquid phase has been extensively studied, little is known about the decomposition chemistry of HAN vapor interacting with heated surfaces. The ability to decompose HAN vapor on a reactive surface could provide a means to control the feed gas composition and enhance the performance of spacecraft propulsion systems.In this initial qualitative study, HAN was vaporized and thermally decomposed using porous 316-stainless-steel and quartz disks under vacuum conditions. Decomposition products with low vapor pressures would condense on an in-line quartz tube which was subsequently collected and analyzed with Raman spectroscopy, NMR spectroscopy, and FT-IR spectroscopy. At temperatures above 440 K the 316-stainless-steel system produced significant quantities of ammonia which reacted with vaporized nitric acid to form ammonium nitrate. Temperatures below 440 K yielded partial HAN decomposition which resulted in a binary mixture of HAN and ammonium nitrate. The degree to which HAN was consumed was determined by analysis of the 1008 cm−1N-OH asymmetric Raman band of HAN and the 1049 cm−1 symmetric stretching Raman band of the nitrate ion, NO3−. The quartz system yielded significantly different results with no ammonium nitrate detected at temperatures above 440 K. Reformed HAN was the primary product detected at lower temperatures. The difference in reported measurements and visual observations highlights the distinct differences in HAN vapor decomposition chemistry from the two materials examined.

An Alternative Method for the Selective Synthesis of Ortho-nitro Anilines Using Bismuth Nitrate Pentahydrate.

Nitroaromatic compounds are important scaffolds used for the syn-thesis of a variety of compounds, such as explosives, herbicides, dyes, perfumes and phar-maceuticals. Bismuth nitrate pentahydrate is a widely used reagent in organic synthesis; how-ever, its utility as a nitrating agent for anilines is underexplored. The aim of this work is to propose and find the proper reaction conditions of an alternative nitrating agent constituted by a mixture of bismuth nitrate / acetic anhydride in DCM with a series of substituted anilines under mild reflux. Several anilines having both activating and deactivating substituents in the ortho, meta and para positions were the substrate for the nitration reaction. Experimental conditions were performed in "one-pot" conditions before product purification. Bi(NO3)3•5H2O demonstrated to be effective and somehow regioselective when it came to the nitration of anilines in the ortho position. Although other products were also identified under these conditions, in most cases, the ortho derivative was the major or even the only product obtained with moderate to high yields in the range of 50% - 96%. Bi(NO3)3•5H2O is an efficient and safe nitrating agent since the use of concen-trated and corrosive acids like sulfuric and nitric is avoided; furthermore, bismuth nitrate is low-priced and no special care nor equipment is required.

Detonability of Ammonium Nitrate Mixtures with the Addition of Organic Materials

As an oxygen carrier and a strong oxidising agent, ammonium nitrate can create an explosive mixture when mixed with organic material. A typical example is the mixture of ammonium nitrate and fuel oil (ANFO), which is the most used explosive for civilian applications. In this work, we studied the detonability and detonation properties of mixtures of ammonium nitrate with recycled rubber and hay. The main goal of this study was to determine the optimal volume ratio of ammonium nitrate and organic materials in terms of achieving the best performance (working capacity). Using small experiments, it was determined that the maximum burst velocity for the ammonium nitrate/hay mixture is achieved at 8% hay by volume, while the maximum burst velocity for the ammonium nitrate/rubber mixture is achieved at 15% rubber by volume. A thermochemical calculation has shown that the maximum detonation heat is achieved at the zero oxygen balance at the volume ratios of 89.2/10.8 for AN/Rubber and 72.85/27.15 for AN/Hay.

Photocatalytic Degradation of Rhodamine-B and Water Densification via Eco-Friendly Synthesized Cr2O3 and Ag@Cr2O3 Using Garlic Peel Aqueous Extract

The purification and densification of wastewater play an important role in water recycling, especially if the materials used in water recycling are other types of recycled waste. Therefore, considering this view in this study, the biosynthesis of silver-decorated chromium oxide nanoparticles utilizing a wasted Allium sativum (garlic) peel extract is investigated. The aqueous extract of garlic peel (GPE) was treated with silver nitrate, chromium nitrate, and a mixture of silver nitrate and chromium nitrate to synthesize silver nanoparticles (Ag-garlic), chromium oxide nanoparticles (Cr2O3-garlic), and silver-decorated chromium oxide nanoparticles (Ag@Cr2O3-garlic), respectively. The synthesized nanoparticles were elucidated via thermal gravimetric analysis (TGA), infrared spectra (FT-IR), absorption spectra (UV-Vis), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). Antimicrobial activity studies were conducted against waterborne germs, bacterial strains (Bacillus subtilis, Enterococcus faecium, Escherichia coli, and Pseudomonas aeruginosa), and fungal strains (Alternaria porri, Aspergillus flavus, Aspergillus niger, Fuserium oxysporum, and Trichoderma longibrachiatum) and showed significant levels of antimicrobial activity. The results revealed that Ag@Cr2O3 significantly improved antimicrobial activity due to their synergistic effect. The photocatalytic activity of nanoparticles was assessed using Rhodamine B dye (5 ppm) under solar irradiation. Cr2O3-garlic exhibited the best activity as a photocatalyst among the studied nanoparticles, with 97.5% degradation efficiency under optimal conditions.

One-pot synthesis of near-infrared absorbing silver nanoprisms via a simple photochemical method using an ultraviolet-C light source

This study describes a simple one-pot photochemical method to synthesize triangular silver nanoprisms (T-AgNPs), for which a mixture of silver nitrate (AgNO3) and citrate was irradiated with an ultraviolet-C (UVC) lamp reactor. We successfully synthesized T-AgNPs with edge lengths ranging from 50 to 150 nm, showing a significant localized surface plasmon resonance (LSPR) band over a wavelength of 1200 nm. This photochemical reaction appears to be unrestricted by plasmon resonance conditions, allowing for the formation of colloidal T-AgNPs with an LSPR band in the near-IR region. In addition, this new method does not require any highly reactive reducing agents or initially prepared silver seed solution. The reduction of Ag+ ions by citrate is induced by UVC light, and the nascent Ag first undergoes nucleation to form spherical or quasi-spherical silver nanoparticles (S-AgNPs). Subsequently, continuous irradiation with UVC light facilitates the transformation of these S-AgNPs into T-AgNPs. The growth kinetics of the nanoparticles with different reaction conditions were examined using ultraviolet–visible–near-infrared spectroscopy and transmission electron microscopy. This new method offers a simple, efficient, and cost-effective means to synthesize T-AgNPs with near-IR LSPR, contributing to wider applications in the fields of optoelectronics, spectroscopics, photovoltaics, etc.

Ferrimagnetic devitrified glass doped with copper by ion exchange: Microstructure, bioactivity and antibacterial properties

In this work, the ion-exchange technique in molten salts was investigated to introduce copper ions in a bioactive and ferrimagnetic devitrified glass. This approach aimed to develop a magnetic and bioactive material for oncologic bone implants, able to join the ability to promote bone bonding to hyperthermic therapy while simultaneously lowering the risk of developing post-surgery infections. The ion-exchange approach was developed in order to overcome experimental critical issues related to the influence of copper introduction as a starting reagent, during the material synthesis, on magnetite nucleation.The magnetic devitrified glass was prepared by melt and quenching route, followed by ion exchange in a mixture of molten sodium and copper nitrates, in three different Na/Cu molar ratios (20, 200, 2000). The obtained samples were analysed in terms of morphology, composition, ability to release heat, bioactivity and antibacterial properties. The results revealed that copper ion-exchange involved both sodium and calcium ions and the precipitation of few amounts of copper oxide aggregates occurred. The crystalline nature of the starting material and its ability to reach the temperature needed for hyperthermia, under exposition to an alternating magnetic field, were not affected. A bacteriostatic effect was obtained by samples with the highest copper amount and the copper doping did not affect the bioactivity of the glass ceramic.

Разработка и исследования перспективного материала для высокомощных фторуглеродных катодов

An original method for the synthesis of silver vanadium oxide (Ag2V4O11) has been developed, including mechanical activation of a mixture of vanadium pentoxide and silver nitrate in a planetary mill followed by heat treatment in a muffle furnace at a temperature of 700 °C for 5 hours in an air atmosphere and providing a product yield of 99.5 % in a highly dispersed state. Based on the data obtained, it was found that the introduction of 8 wt. % Ag2V4O11 made it possible to double the polarization characteristics in comparison with a conventional (CFx)n sample. According to the results of testing the samples, it was shown that at a discharge current density above 1.0 mA/cm2, there is a significant decrease in the discharge specific capacity and medium-discharge potential in the traditional (CFx)n sample and in samples with a low content of silver vanadium oxide. An increase in the content of Ag2V4O11 over 8 wt. % leads to a decrease in the specific capacity of the samples due to the lower energy intensity of this material compared to the energy intensity (CFx)n. The sample with 8 wt. % of silver vanadium oxide has the highest energy consumption at a higher discharge potential (630 mAh/g versus 570 mAh/g for traditional). Electrodes based on the composition of fluorocarbon – silver vanadium oxide and primary elements based on them surpass known analogues in capacity, stability and preservation.

Handheld portable device for delivering capped silver nanoparticles for antimicrobial applications

Abstract We describe a simple, cost-effective, green method for producing capped silver nanoparticles (Ag NPs) using a handheld portable mesh nebulizer. The precursor solution containing a 1:1 mixture of silver nitrate (AgNO3) and ligand (glycerol or sodium alginate) was sprayed using the nebulizer. The Ag NPs were generated in the water microdroplets within a few milliseconds under ambient conditions without any external reducing agent or action of a radiation source. The synthesized nanoparticles were characterized by using high-resolution transmission electron microscopy (HR-TEM), X-ray photoelectron spectroscopy (XPS), and X-ray diffraction analysis (XRD), which validated the formation of Ag NPs. The synthesized glycerate-capped silver nanoparticles (Ag-gly NPs) were used as a catalyst to show the oxidative coupling of aniline to form azobenzene products with a yield of up to 61%. Experiments conducted using Ag NPs produced in the droplets demonstrated more than 99% antibacterial activity when contacting Escherichia Coli. Our in-situ synthesis-cum-fabrication technique using a portable sprayer represents a viable alternative to the existing fiber or hydrogel-based antimicrobial wound healing.

Method of calculation of satellite flow parameters behind the point of Mach reflection

A mathematical model for the calculation and express analysis of triple configurations of air shock waves arising from an “elevated” explosion of a condensed high-energy material is presented. The considered blast waves with a long duration of the positive phase (compression phase) can take place in industrial and agricultural applications: in the explosion of fuel-air mixtures, explosive dust in elevators and granaries, as well as high-energy materials for agricultural and industrial applications based on ammonium nitrate and explosive saltpetre mixtures with petroleum products. The developed mathematical model uses exact and semi-empirical relationships developed earlier in the theory of optimal shock wave systems.

Effect of ammonium and potassium nitrate on winter hardiness and yield of winter rye (<i>Secale cereale</i> L.)

The results of research for 3 years (2019–2021) on winter rye (Secale cereale L.) crops in the North-West region of the Russian Federation (Leningrad region) are presented. The effect of different doses and timing of ammonium and potassium nitrate application on winter hardiness and productivity of winter rye plants on the example of Volkhova and Eureka varieties was studied. The soil in the experimental fields was sod-podzolic loamy with the depth of the arable horizon of 20–25 cm. Humus content – 2.0–2.3%, pH of the salt extract – 5.2–5.5. Fertilizers were applied in dry form in the autumn one week after the emergence of the seedlings, and in the spring – at the resumption of vegetation. The studied fertilizer doses in terms of active substance for nitrogen were 0 (control), 30, 60 and 90 kg/ha. It is shown that winter hardiness of both varieties practically did not depend on the doses and timing of the application, as well as on the type of fertilizers. The maximum grain yield was shown by the Volkhova variety at a dose of nitrogen of 60 kg/ha, the Eureka variety – 90 kg/ha, with the maximum yield of the Eureka variety for all the years exceeding that of the Volkhova variety by 24.5%. Within the specified doses of nitrogen for both varieties, the best option was a single spring application of a mixture of ammonium and potassium nitrate, the worst - a single spring application of ammonium nitrate alone. On average for both varieties, potassium nitrate application in spring increased the grain yield by 16% compared to the variants where potassium nitrate was not used.

Controlled fabrication of Fe3N@NG composites as superior oxygen evolution reaction electrocatalysts

We report the controlled fabrication of nitrogen doped graphene (NG) nanoplates, which are uniformly decorated with iron nitride (Fe3N) nanoparticles, via ball milling of mixtures of graphite and iron nitrates and the following ammonia annealing. The obtained Fe3N@NG composites demonstrate excellent electrocatalytic activity and durability for oxygen evolution reaction, both of which outperform those of the state-of-the-art iridium oxide catalysts. This may be attributed to nitrogen doping as well as the synergistic effect between Fe3N and graphene nanoplates.

Synthesis of highly active oxygen evolution reaction electrocatalysts using balsa woods

Balsa woods derived carbons (BCs), which are decorated with ruthenium (Ru) and cobalt (Co) nanoparticles, are fabricated by simply annealing mixtures of BCs, ruthenium chloride and cobalt nitrates in hydrogen. Electrochemical measurement results demonstrate that the obtained BC/Ru/Co composites exhibit high oxygen evolution reaction (OER) activity and excellent durability, both of which are better than those of the state-of-the-art iridium oxide catalysts. The superior OER performances of the BC/Ru/Co composites may be ascribed to the collaborative contributions of Ru, Co and their large surface areas.

The Efficacy of Silver Nanoparticles in Combating Biofilm Formation by Uropathogenic Escherichia coli

Uropathogenic Escherichia coli (UPEC) is prevalent in urinary tract infections (UTIs). UPEC’s biofilm production enables it to invade and persist in the uroepithelium, leading to recurrent UTIs. The biofilm formation is associated with antibiotic resistance. To overcome this resistance, non-conventional compounds must be developed as an alternative to conventional antibiotics. Silver nanoparticles (AgNPs) are significant due to their antibacterial activity against diverse organisms. This study was done to investigate the antibacterial and anti-biofilm effects of AgNPs on UPEC. AgNPs were biosynthesized using Pseudomonas aeruginosa ATCC 27853. AgNPs were characterized using visual inspection and scanning electron microscopy. The Agar well diffusion method was employed to assess the antibacterial activity of AgNPs against UPEC isolates. The study utilized the tissue culture plate method to investigate both the biofilm and anti-biofilm properties of AgNPs. Following incubation, Ps.aeruginosa and silver nitrate (AgNO3) mixture exhibited a colour change from pale yellow to dark brown. The mean size of spherical AgNPs observed under a scanning electron microscope was 24.187 ± 8.019 nm. 130 UPECs were obtained. AgNPs exhibited antibacterial activity at a concentration of 20 µg/ml against all tested UPEC strains. Among UPEC strains that produced biofilms, a significant inhibition of 99.89 ± 0.45% was observed at a higher concentration of 512 µg/ml of AgNPs. Ps.aeruginosa produces nitrate reductase enzyme that can potentially convert AgNO3 to AgNPs. The biosynthesized AgNPs exhibit antibacterial and anti-biofilm activity against all tested UPEC strains.

Heat transfer and thermal resistance analysis under various heat transfer fluid flow rates based on a medium-temperature pilot-scale latent heat storage system

Assessments often rely on experimentally observed factors when examining heat transfer variations due to different heat transfer fluid (HTF) flow rates. To better comprehend limiting factors and guide operational parameter design for shell-and-tube latent heat system (LHS) systems, a quantitative analysis of thermal resistance hindering heat transfer is crucial. Hence, this article conducted experimental evaluations at various flow rates to critically analyze its thermal performance based on a large-capacity (1000 MJ) medium-temperature LHS system loaded with 4130 kg commercial nitrate mixture (peak melting temperature: 219.90 °C). The heat transfer coefficient and thermal resistance during charging and discharging were quantitatively investigated to identify the main factors influencing heat transfer and dominant mechanisms. The results suggested that augmenting the charging flow rate from 5 to 15 L/min resulted in 2.65 times increase in average power (from 24.01 to 63.64 kW). Besides, during charging, the overall thermal resistance primarily came from the phase change material (PCM) side initially. As PCM melted, the thermal resistance on the PCM side became equivalent to that on the HTF side. Increasing the charging flow rate enhanced heat transfer through two mechanisms: reducing the thermal resistance on the HTF side and increasing the driving force of heat transfer by elevating the average HTF temperature. During discharging, the overall thermal resistance was predominantly derived from the PCM side after solidification. Increasing the discharging flow rate caused a limited influence on decreasing thermal resistance. Enhancing the discharging flow rate only bolstered the driving force for heat transfer by elevating the average HTF temperature. This study provides valuable insights into the factors influencing heat transfer in LHS systems and contributes to optimizing LHS technology.

Technical note: Gas-phase nitrate radical generation via irradiation of aerated ceric ammonium nitrate mixtures

Abstract. We present a novel photolytic source of gas-phase NO3 suitable for use in atmospheric chemistry studies that has several advantages over traditional sources that utilize NO2 + O3 reactions and/or thermal dissociation of dinitrogen pentoxide (N2O5). The method generates NO3 via irradiation of aerated aqueous solutions of ceric ammonium nitrate (CAN, (NH4)2Ce(NO3)6) and nitric acid (HNO3) or sodium nitrate (NaNO3). We present experimental and model characterization of the NO3 formation potential of irradiated CAN / HNO3 and CAN / NaNO3 mixtures containing [CAN] = 10−3 to 1.0 M, [HNO3] = 1.0 to 6.0 M, [NaNO3] = 1.0 to 4.8 M, photon fluxes (I) ranging from 6.9 × 1014 to 1.0 × 1016 photons cm−2 s−1, and irradiation wavelengths ranging from 254 to 421 nm. NO3 mixing ratios ranging from parts per billion to parts per million by volume were achieved using this method. At the CAN solubility limit, maximum [NO3] was achieved using [HNO3] ≈ 3.0 to 6.0 M and UVA radiation (λmax⁡ = 369 nm) in CAN / HNO3 mixtures or [NaNO3] ≥ 1.0 M and UVC radiation (λmax⁡ = 254 nm) in CAN / NaNO3 mixtures. Other reactive nitrogen (NO2, N2O4, N2O5, N2O6, HNO2, HNO3, HNO4) and reactive oxygen (HO2, H2O2) species obtained from the irradiation of ceric nitrate mixtures were measured using a NOx analyzer and an iodide-adduct high-resolution time-of-flight chemical ionization mass spectrometer (HR-ToF-CIMS). To assess the applicability of the method for studies of NO3-initiated oxidative aging processes, we generated and measured the chemical composition of oxygenated volatile organic compounds (OVOCs) and secondary organic aerosol (SOA) from the β-pinene + NO3 reaction using a Filter Inlet for Gases and AEROsols (FIGAERO) coupled to the HR-ToF-CIMS.

Co–Fe–oxide nanoparticles supported on the various highly dispersed matrices: the effect of the carrier on structural and magnetic properties

sA series of mixed oxides was synthesized by deposition of the guest phase on the highly dispersed oxide matrix. Fumed nanooxides SiO2, Al2O3, SiO2/Al2O3, and SiO2/Al2O3/TiO2 with the specific surface area of 65–91 m2/g were selected as highly dispersed matrices. Co–Fe mixed oxides with the general formula Co4xFexOy (Co: Fe = 4: 1) were deposited as the guest oxides using the two-step method: (i) solvate-stimulated modification of the surface of fumed nanocarriers with the mixture of cobalt nitrate (II) and iron (III) formate and (ii) subsequent heat treatment up to 600 °C to form Co4xFexOy. The aim of this paper was to study the influence of the composition and structure of fumed oxide matrices and deposited guest phase on the morphology of the resulting composites in the gaseous and aqueous media using the XRD, XPS, FTIR, nitrogen adsorption and SEM/EDX, as well as quasi-elastic light scattering (QELS) methods. The low-temperature nitrogen adsorption isotherms have a sigmoidal shape with a narrow hysteresis loop characteristic of mesoporous materials. The specific surface area (SBET) of the composites varies from 48 to 82 m2/g, showing a tendency towards a decrease in the SBET values by 10–26% in comparison with the initial nanocarriers. The SEM data show the denser aggregate structure of nanocomposites compared to the initial carriers. The primary particle size was in the 30–60 nm range and the EDX data confirm the formation of a guest phase on the mixed aluminosilicate carriers, mainly in the surface patches corresponding to the alumina structure. According to the QELS data, there is a tendency to form aggregates of 100–10 μm in size in the aqueous media. The XRD method shows that the deposited metal oxides are in the form of crystalline phases of Co3O4 with the crystallites of 25–26 nm in size for the individual SiO2 and Al2O3 nanocarriers and 34–37 for the mixed ones, but the iron oxide reflections were not identified for the composites. XPS observation demonstrates the signal of Fe 2p electrons as the form of Fe2O3 oxide in the surface layer of nanocomposites as well as Co 2p as the Co3O4 and Co(OH)2.

Best billiard ball in the 19th century: Composite materials made of celluloid and bone as substitutes for ivory.

The demystification of how 19th-century novelly designed materials became significant elements of modern technological, economic, and cultural life requires a complete understanding of the material dimensions of historical artifacts. The objects frequently described as the earliest manufactured plastic products-the billiard balls made by John Wesley Hyatt and his associates from the late 1860s-are examined closely for the first time and are found to be more complex and functionally more successful than has been described. Modern analytical techniques such as optical microscopy, scanning electron microscope-energy dispersive X-ray spectroscopy, X-ray fluorescence, micro-Fourier transformed infrared, and handheld/micro-Raman spectroscopies were used to reveal the complex composition of the Smithsonian Institution's "original" 1868 celluloid billiard ball. Comparisons with billiard and pool balls commercialized from the 1880s to the 1960s showed an unexpected consistency in material formulations. All specimens were made of an unprecedented composite material prepared with a mixture of cellulose nitrate, camphor, and ground bone; the source of the bone was identified as cattle by peptide mass fingerprint (ZooMS). Patent specifications and contemporary journal descriptions explained how and when these formulations emerged. Combining the technical analyses of compositions with a careful reading of the historical record and contemporary descriptions reveals the key elements of the first successful efforts to substitute materials to assist the survival of endangered animals.

Evaluation of handheld Raman spectrometers for the detection of intact explosives

The detection of intact explosives in the field provides a unique challenge for investigators, considering the sensitive and dangerous nature of these samples. Handheld Raman instruments have grown in popularity for the analysis of unknown samples in the field, combining speed of data collection and reliability with a size that allows for the instruments to be field portable. Handheld Raman instruments are used commonly in the field, and yet there is very little research on the detection capabilities of these instruments, specifically for explosive compounds. The present study aimed to evaluate the detection capabilities of two handheld Raman spectrometers, the Rigaku ResQ-CQL and the Field Forensics HandyRam™, using explosives analytical standards, including 2,4,6-trinitrotoluene (TNT), nitromethane (NM), ammonium nitrate (AN) and smokeless powder components such as diphenylamine (DPA), ethyl centralite (EC), and methyl centralite (MC). The spectrometers were evaluated on their sensitivity, the repeatability of the data, and the performance of the internal library when available. In addition, an interference study with glass and plastic containers was also performed. Finally, authentic intact explosive samples, including TNT flakes, a mixture of ammonium nitrate and fuel oil (ANFO), smokeless powder and nitromethane were analyzed to evaluate the developed method and test the detection capabilities of the spectrometers with authentic samples. Spectra were reproducible for all the analytes across both instruments, with regards to the peak location and the intensity. Spectra obtained with the Rigaku ResQ-CQL displayed better resolution for all analytes, including the authentic samples. In addition, its wider scan range allowed for the detection of more detailed peaks below 400 cm−1. Identifying the detection capabilities of these handheld instruments can therefore help guide investigators on how to best utilize them in the field.

Morphological features of Co3O4 nanoparticles obtained by solution combustion method

The global environmental crisis has made it imperative to enhance tools and techniques for monitoring and analyzing environmental parameters. Gas sensors, crucial for air quality assessment, continually under go technological advancements to enhance accuracy and efficiency in detecting harmful substances. They play an essential role in ensuring safety in workplaces, urban areas, and industries, aiding pollution control efforts. Enhanced gas sensor performance hinges on careful selection and control of gas-sensitive materials and their structure. This involves optimizing gas-sensitive compounds, employing advanced materials, and developing technologies for sensitive and rapid substance detection. One promising compound for this purpose is Co3O4 oxide, synthesized efficiently using the solution combustion method. This method off ers simplicity and allows for precise control over product structures and properties, enabling customization for specific requirements and ensuring high detection efficiency and accuracy. In this study, Co3O4 particles were synthesized from a mixture of cobalt nitrate and glycine with the addition of nitric acid using the solution combustion method. The influence of nitric acid addition and the fuel-to-oxidizer ratio on the morphological characteristics of the cobalt oxide was investigated. The results from SEM, TEM, XRD, and SAXS analyses confi rmed that the addition of nitric acid and a fuel-rich mixture lead to nanoparticles with smaller diameter spread and more stable characteristics.

A blue emission of zirconium (IV) complex based on 2, 6-pyridinedicarboxylic acid ligand: Syntheses, crystal structure, and luminescence sensing

A novel blue emission of zirconium complex, formulated as [Zr(pydc)3]·[(CH3)2NH2]2 (1), has been synthesized by using a mixture of zirconium nitrate and 2, 6-pyridinedicarboxylic acid (H2pydc). The complex 1 presents a three-dimensional supramolecular network structure due to the intermolecular NH···O, OH···O hydrogen bonds. Additionally, the crystals of 1 exhibit blue luminescence and demonstrate a highly selective and sensitive sensing capability for detection of Co2+ ions with a Ksv value of 1.22 × 104 M−1 and limit of detection (LOD) of 1.20 × 10−5 M. Furthermore, the fluorescence lifetime and quantum yield of the complex 1 is τ = 6.22 μs and Φ = 25.9 %.