Atomic Emission Research Articles

Mechanism of a Novel Carrier Buffer in Arc Atomic Emission Spectroscopy

Mechanism of a Novel Carrier Buffer in Arc Atomic Emission Spectroscopy

Revolutionizing sensing technologies: Crafting a green, ultra-sensitive bismuth optical sensor via fixation of 5-(2′,4′-dimethyl-phenylazo)-6-hydroxypyrimidine-2,4-dione on PVC membrane

An innovative and exceptionally responsive optical sensing device engineered to selectively identify Bi(III) ions in water-based solutions. The sensing component, 5-(2′,4′-dimethylphenylazo)-6-hydroxypyrimidine-2,4-dione (DMPAHPD), is incorporated into a plasticized polyvinyl chloride (PVC) membrane. The sensor demonstrates an exceptional selectivity for Bi(III) within a broad dynamic range spanning from 7.5 × 10−10 to 4.2 × 10−5 M at pH 2.25. Notably, it achieves lower quantification and detection limits of 7.25 × 10−10 and 2.15 × 10−10 M, respectively. The optode membrane’s response to Bi(III) proves to be entirely reversible, demonstrating remarkable selectivity for Bi(III) ions over a diverse range of other cations and anions. The sensor exhibits favorable performance characteristics, including good reversibility, a wide dynamic range, a prolonged lifespan, sustained response stability over the long term, and high reproducibility. This visual chemical sensor exhibits potential for real-world usage, offering consistent outcomes when assessing Bi(III) levels in matrices such as water, soil, plants, biological and synthetic mixtures. Importantly, the sensor’s performance is comparable to corresponding data achieved from inductively coupled plasma atomic emission spectroscopy (ICP-AES).

Determination of rare earth elements in ferrocarbonatite using ICP-AES and ICP-MS

AbstractA method has been developed for the determination of Rare Earth Elements (REEs) in ferrocarbonatite using Inductively Coupled Plasma—Atomic Emission Spectrometer (ICP-AES) and Inductively Coupled Plasma—Mass Spectrometer (ICP-MS). The conventional dissolution procedures are tedious, with large measurement uncertainty and are thus not suitable for certified reference material (CRM) production and exploration of REEs. The described method involves leaching of sample using 3 M HCl followed by dissolution of residue (silica and REEs) by HF then determined REEs using ICP-AES and ICP-MS. The leaching step prevents formation of fluoride precipitates of matrix (Ca, Mg, Ba and Al). The method has been validated using CRMs.

Studying the process of metals and non-metals transfer in a low-temperature gas flow over sulfide tailings materials

ABSTRACT A large number of publications have been devoted to the study of aerosol atmospheric transport, but the low-temperature transfer of metals and metalloids as a part of gas flow remains poorly understood. The present work is devoted to the study of gas stream composition using an approach based on the collection of nascent condensate upon cooling of the air flow formed over the surface of contaminated sites. A special laboratory unit was designed to collect the condensate followed by the study of its composition using atomic emission and mass spectrometry. The main novelty of this work consists of the application of the single-particle ICP‒MS technique to obtain qualitative information concerning the state of the elements in the condensates. Gold and silver are most likely present in the samples as nanoparticles; arsenic, selenium, tin and lead are present both as nanoparticles and as soluble forms; and barium and mercury are present only in soluble forms. The condensed phase contains As, Hg, Au, Ag, Pb and Sn at the ppb level, while the main elements of the tailings material (Fe, Ba, Cu, Zn and others) are present at the ppm level, which exceeds the background concentration.

Comparative Analysis of Biochar Derived from Rice Straw and Soybean Straw

Aim: Recycling agricultural postharvest waste and re-introducing it again into farmland is one of the tangible ways to address zero waste dream, soil infertility and climate change. Pyrolysis of crop leftovers into biochar remains the most acceptable alternative for proper management of crop waste. The possibility of sustainable biochar production practices and multi-functionality features makes it promising to fufill an increasing demand for soil amendment, agricultural sustainability, environmental protection, cutting-edge materials and mitigation of climate change. Methodology: Same amount (14450 g) in feedstock of rice straw (RS) and soybean straw (SS) undergo slow pyrolysis separately to produce biochar. Physical (percentage yield, moisture, ash, volatile matter, bulk density, pH, electrical conductivity), chemical characterization (Microwave Plasma Atomic Emission Spectroscopy (MP-AES), Scanning Electron Microscope Energy Dispersive X-ray (SEM-EDX), Fourier Transformed Infrared (FTIR) and Thermogravimetric Analysis and Derivative Thermogravimetry (TGA and DTA)) and evaluation of bochar was determined. Results: Rice straw biochar (RSB) recorded a higher char yield of 42.1%. Both lignocellulosic biochars were black and porous with a higher silica (10.6%) content in RSB and higher carbon (82.2%) content in SSB as was revealed by SEM-EDX. Higher ash 27.1%, volatile matter (VM) 31.3% and moisture 29.4% content was seen in RSB compared to SSB because of feedstock composition. Rice straw biochar show higher peaks of macro and micro mineral elements K(14561.21mg/kg), Ca (2401.28 mg/kg), and Na(1735.27 mg/kg) than soybean straw biochar. FTIR was used to identify functional groups that might act as cation adsorbents. As the temperature increased, the TGA and DTG graphs showed mass loss and sample breakdown. Conclusion: Rice and soybean crop wastes were converted into biochar, a nutrient-rich material that maybe utilized to balance acidic soils promoting healthy plant growth and also protecting the environment.

Optimal Conditions for Demetallization of the Heavy Fraction of Low-Temperature Coal Tar of Shubarkol Komir JSC in the Presence of “Coal Shale” Catalytic Additive

The optimal conditions for demetallization of the heavy fraction of coal tar from Shubarkol Komir JSC were determined by means of full factorial experiment. Optimal conditions for demetallization of the aforementioned fraction were found to be a proportion of “Coal shale” catalytic additive to the heavy fraction of coal tar with boiling point above 300 °С equal to 0.04, process temperature in the range of 420–430 °С, duration from 20 to 30 minutes and initial pressure between 3 and 5 MPa. Experiments conducted under these conditions demonstrated the demetallization rates of 87–89 %. Conversion of the heavy fraction of coal tar in hydrogen medium at pressure of 4.0 MPa and temperature of 420 °C was examined, with and without the use of the “Coal Shale” catalytic additive. The findings demonstrate that the incorporation of the “Coal Shale” catalytic additive is associated with a notable enhancement in the production of liquid hydrogenate, reaching up to 57 %. Atomic emission spectral analysis was used to investigate the content of rare and dispersed elements including Ge, Ga, Y, Yb, Zr, Nb the ash of the heavy fraction of coal tar and the “Coal shale” catalytic additive, as well as in the solid product of demetallization of the heavy fraction of coal tar using the catalytic additive. The results showed that the use of “Coal shale” as the catalytic additive leads to an increase in the content of Ga, Yb, Y elements by 3-3.8 times, and Zr — by 7.5 times compared to the initial heavy fraction of coal tar in the absence of the catalytic additive.

Determination of selenium in polyheteroatomic organic compounds by microwave plasma atomic emission spectrometry

Currently, the problem of selenium determination in various objects attracts a large number of scientists. Interest in this area is attributed to the biological importance of selenium, since it is both an important nutrient and has a toxic effect on the body, depending on its amount and the properties of the compounds in which it is contained. Checking the purity of selenium-containing organic compounds (both determination of impurities and analysis of the basic composition), which is carried out by methods of elemental analysis, is an important task, however, in modern literature there is lack of information regarding this problem. The purpose of the presented study is to develop a method for the determination of selenium in the basic composition of synthetic polyheteroatomic organic compounds by microwave plasma atomic emission spectrometry. Various selenodiazole derivatives were mainly used for analysis. Optimal conditions for sample preparation and atomic emission determination of the selenium content were specified. To mineralize the substances under study, oxygen flask combustion was used with the addition of potassium nitrate, which improves combustion and prevents the formation of soot. Hydrochloric acid at a concentration of 0.1 M was used as an absorption solution. It is noted that before measurements it is necessary to purge the monochromator and optimize the pressure in the atomic emission spectrometer nebulizer and optimize pressure in the atomizer. In addition, the number of replicates and sampling time were increased to optimize selenium measurement. Under specified conditions, the metrological characteristics of the technique were determined: the detection limit and quantitation limit, intra-laboratory precision and accuracy. Selenium was determined in 11 synthetic organic compounds with selenium content ranged from 12 to 51%. The error of the analysis did not exceed 0.3%, which meets the requirements of organic elemental analysis.

Removal of Arsenic from Contaminated Water by Polypyrrole-Based Adsorbents

Worldwide, there is growing concern over the toxicity of arsenic in drinking water. The US Environmental Protection Agency and Central Pollution Control Board (India) have set a safe limit of 50 parts per billion for arsenic in drinking water. Millions of people are at immediate risk due to high concentrations of arsenic in drinking water, particularly in developing nations where arsenic poisoning symptoms have been observed. One of the essential techniques described in this article is the absorption of arsenic from contaminated water by sustainable cellulosic materials like jute and wood sawdust after suitable modification. Jute and sawdust are cheap and abundantly available in South Asia. They are functionalized with polypyrrole coating by in situ chemical polymerization of pyrrole in aqueous medium in the presence of ferric chloride. Polypyrrole-coated jute fabric (with 11.28% polypyrrole add-on) and polypyrrole-coated sawdust (with 5.28% polypyrrole add-on) are found to be excellent adsorbers of arsenic ion (As3+) from water. The effect of dosage of polypyrrole-coated adsorbents, treatment time and pyrrole concentration on the As removal efficiency have been investigated in this work. The arsenic concentration in water is determined using a microwave plasma atomic emission spectrometer with the highest level of accuracy. Maximum As removal efficiency by the polypyrrole-coated sawdust and polypyrrole-coated jute fabric is found to be 80.90% and 97.3%, respectively, from a 50 mL, 7.5 parts per million As solution with a dosage of 1 g at neutral pH. The polypyrrole-coated jute and sawdust are characterized by Fourier-transform infrared spectroscopy to understand the chemical interaction between cellulose and polypyrrole molecules. The scanning electron microscope studies reveal a uniform coating of polypyrrole around the surface of jute fibre and sawdust particles. Thermo-gravimetric analysis shows good thermal stability of jute and sawdust after polypyrrole coating.

Assessment of Heavy Metals (Cr, Cu, Pb, and Zn) Bioaccumulation and Translocation by Erigeron canadensis L. in Polluted Soil

This work aims to assess the bioavailability and bioaccumulation of Cr, Cu, Pb, and Zn in the soil–plant system (Erigeron canadensis L.) in the zone of anthropogenic impact in Dnipro city, a significant industrial and economic centre of Ukraine. Sampling was carried out at three locations at distances of 1.0 km, 5.5 km, and 12.02 km from the main emission sources associated with battery production and processing plants in Dnipro. The concentrations of heavy metals such as Cr, Cu, Pb, and Zn were analysed using atomic emission spectrometry from soil and parts of Erigeron canadensis L. The highest concentrations of elements in the soil, both for the mobile form and the total form, were determined to be 48.96 mg kg−1 and 7830.0 mg kg−1, respectively, for Pb in experimental plot 1. The general ranking of accumulation of elements in all experimental plots, both for the plant as a whole and for its parts, was as follows: Zn > Cu > Cr > Pb. Zn for plants was the most available heavy metal among all studied sites and had the highest metal content in the plant (339.58 mg kg−1), plant uptake index (PUI-506.84), bioabsorption coefficient (BAC-314.9), and bioconcentration coefficient (BCF-191.94). According to the results of the study, it is possible to evaluate Erigeron canadensis L. as a hyperaccumulator of Zn, Cu, and Cr and recommend it for phytoextraction of soils contaminated with Zn, Cu, and Cr and phytostabilization of soils contaminated with Pb.

Efficient Cu‐Based Mixed Oxides Catalyst for α‐Alkylation of Ketones with Alcohols

AbstractA series of Cu‐based mixed oxides were prepared by calcinations of corresponding CuMgAl‐layered double hydroxides precursors at different temperatures with nominal Cu/Mg/Al ratios of 1 : 1 : 2(Cu‐LDH‐1), 1 : 2 : 1(Cu‐LDH‐2),1 : 1 : 1(Cu‐LDH‐3), and 2 : 1 : 1(Cu‐LDH‐4). The synthesized catalysts were characterized using X‐ray diffraction, high‐resolution transmission electron microscopy, scanning electron microscopy, X‐ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, inductively coupled plasma atomic emission spectroscopy (ICP‐AES), and N2 physisorption analysis techniques. All as‐obtained catalysts showed adequate catalytic performance for the α‐alkylation of ketones with alcohols through a hydrogen autotransfer mechanism. The catalyst CuMgAl‐I‐650 (obtained by calcining Cu‐LDH‐1 at 650 °C) displayed the highest activity and selectivity. Using this catalyst system, a wide range of branched ketones were synthesized in good to excellent isolated yields. Moreover, the catalyst CuMgAl‐I‐650 could be recycled and reutilized for four cycles without any significant loss of activity and selectivity. This study provides a very simple and inexpensive catalysis based on transition metals, which are in abundance on earth.

Cooperative atomic emission from a line of atoms interacting with a resonant plane surface

Cooperative atomic emission from a line of atoms interacting with a resonant plane surface

Element accumulation in the tracheal and bronchial cartilages of monkeys

Compositional changes in the tracheal and bronchial cartilages can affect respiratory ventilation and lung function. We aimed to elucidate element accumulation in the tracheal and bronchial cartilages of monkeys and divided it into four sites: the tracheal, tracheal bifurcation, left bronchial, and right bronchial cartilages. The elemental content was analyzed using inductively coupled plasma atomic emission spectrometry.The average calcium content was two to three times higher in the tracheal cartilage than in the other three cartilages. The trends of phosphorus and zinc were similar to those of calcium. The average calcium, phosphorus, and zinc cartilage contents were the highest in the tracheal cartilage and decreased in the following order: the left bronchial, right bronchial, and tracheal bifurcation cartilages. These findings revealed that differences existed in element accumulation between different sites within the same airway cartilage and that calcium, phosphorus, and zinc accumulation mainly occurred in the tracheal cartilage.A substantial direct correlation was observed between age and calcium content in the tracheal and bronchial cartilages and all such monkeys with high calcium content were > four years of age. These results suggest that calcium accumulation occurs in the tracheal and bronchial cartilages after reaching a certain age.An extremely substantial direct correlation was observed between calcium and phosphorus contents in the tracheal and bronchial cartilages. This finding is similar to the previously published calcium and phosphorus correlations in several other cartilages, suggesting that the calcium and phosphorus contents of cartilage exist in a certain ratio.

Analytical Method Development and Validation Based on Simple Color Reactions and Microwave Plasma–Atomic Emission Spectrometry (MP-AES) for the Detection of Adulteration in Teff Injera (Ethiopian Flatbread)

Analytical Method Development and Validation Based on Simple Color Reactions and Microwave Plasma–Atomic Emission Spectrometry (MP-AES) for the Detection of Adulteration in Teff Injera (Ethiopian Flatbread)

Role of modified calcium montmorillonite and 5 A zeolite in microstructure and efflorescence formation of metakaolin-based geopolymer

To reduce the efflorescence extent of metakaolin (MK)-based geopolymer, this study introduced thermally activated modified calcium montmorillonite (MT) and 5 A zeolite (ZT) into MK-based geopolymer, and the optimal mixing ratio was acquired by response surface methodology. The effect of the two modified clay minerals on the microstructural and mechanical properties of the MT-ZT-MK geopolymer was explored by compressive strength testing, phase analysis (XRD and FTIR), pore structure analysis (MIP), and morphology analysis (SEM-EDS). To investigate the performance and mechanism of efflorescence inhibition of the ternary geopolymer, the cation concentration in the leaching solution was detected by inductively coupled plasma atomic emission spectrometry (ICP-OES), and the efflorescence area of the geopolymer was calculated using Image Pro Plus (IPP) software. The results of the experiment showed that the optimal mixing ratio, as determined by RSM, was 1.5 wt% of modified MT and 2.9 wt% of modified ZT, with the highest compressive strength at 65.1 MPa and the lowest degree of efflorescence after 28 days of curing. It can be concluded that the two clays gradually exhibit the effect of cation exchange and internal curing. The pore structure is optimized and (N, C)-A-S-H gels are formed with the extension of curing time. On the other hand, the lesser extent of efflorescence possibly is attributed to the restricted channels for Na+ in the matrix to undergo carbonation with CO2 in the air.

Dancing bubble sonoluminescence in phosphoric acid solution

Abstract Sonoluminescence is more distinctly observed in phosphoric and sulfuric acid, which exhibit high viscosity and lower vapor pressures relative to water. Within an 85-wt% phosphoric acid solution saturated with argon (Ar), variations in the light-emitting regimes of bubbles were noted to correspond with increments in the driving acoustic intensity. Specifically, the bubbles were observed to perform a dance-like motion 2 cm below the multi-bubble sonoluminescence (MBSL) cluster, traversing a 25-mm2 grid during the camera exposure period. Spectral analysis conducted at the beginning of the experiment showed a gradual attenuation of CN (B2Σ–X2Σ) emission concurrent with a strengthening of Ar (4p–4s) atom emission lines. The application of a theoretical temperature model to the spectral data revealed that the internal temperature of the bubbles escalates swiftly upon their implosion. This study is instrumental in advancing the comprehension of the underlying mechanisms of sonoluminescence and in the formulation of a dynamic model for the behavior of the bubbles.

Efficacy of silver nanoparticle-modified bullfrog skin as an antimicrobial wound dressing

This research explores the synthesis of silver nanoparticles and their incorporation into bullfrog skin for potential use as a wound dressing. The study addresses the need for wound dressings that exhibit biocompatibility, low cytotoxicity, superior biodegradability, and antimicrobial activity. Silver nanoparticles were synthesized using silver nitrate and sodium citrate solutions and integrated into bullfrog skin at varying concentrations (0%, 0.5%, 1%, and 1.5%). The modified and unmodified bullfrog skin samples were characterized using dynamic light scattering(DLS), X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and Energy Dispersive Spectroscopy (EDS). Antimicrobial analyses were conducted to assess the efficacy of the modified skin against common pathogens, including Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, and Candida albicans. The results demonstrated that samples containing 1% and 1.5% silver nanoparticles exhibited significant inhibitory effects on all tested microorganisms. This indicates that these concentrations are optimal for antimicrobial activity, suggesting the potential of silver nanoparticle-modified bullfrog skin as an innovative and effective wound dressing material.

Exact stark analytical function for Hα line based on the FFM model related with plasma parameters

Optical Emission Spectroscopy is a widely used technique for plasma diagnosis, with particular interest in hydrogen atomic emission due to its prevalence in plasmas. However, accurately determining plasma parameters like electron density, electron temperature, and gas temperature starting from the experimental profiles remains a challenge. This paper introduces a comprehensive model for Stark broadening of the Hα line in a wide range of plasma conditions, addressing the limitations of existing analytical expressions for line shapes. The proposed model encompasses the full splitting of the transition into fifteen Lorentzian profiles and electric micro-field fluctuations surrounding the emitting atoms due to collisions with charged particles. Starting from accurate spectral data obtained from realistic computer simulations, fitting parameters of the model, have been obtained by using an optimization method based on a genetic algorithm. The set of parameters of the model are reported for a wide range of plasma conditions. The behavior of these parameters is analyzed to understand their dependence in terms of the electron density and temperature and gas density of the plasma. The model parameters here obtained constitute a useful tool in plasma diagnosis to obtaining the values of the physical parameters of the plasma starting from the experimental profiles.

Size-segregated content of heavy metals and polycyclic aromatic hydrocarbons in airborne particles emitted by indoor sources

Indoor air quality is negatively affected by the emission of different combustion sources releasing airborne particles and related particle-bound toxic compounds (e.g., heavy metals and polycyclic aromatic hydrocarbons). To date, very few studies focused on the chemical characterization of the airborne particles emitted by indoor sources were carried out; moreover, no data on their size-resolved chemical compositions are available. In the present study, an experimental analysis aimed at determining the size-segregated content of heavy metals and polycyclic aromatic hydrocarbons in airborne particles (including sub-micrometric ones) emitted by widely-used indoor combustion sources (i.e., incenses, candles, mosquito-coils, and cooking activities) was carried out. To this purpose, airborne particles were collected through an electric low-pressure impactor and were post-analyzed by means of chromatography–mass spectrometry and atomic emission spectrometry techniques. Results of the analyses showed that the chemical composition of the emitted particles is not invariant to the particle size, indeed, an important contribution of sub-micrometric particle range to the total mass of chemical compounds emitted by the sources was noticed. These findings also demonstrated that significant underestimations of particle-bound compounds depositing in the lungs could occur if size-dependent compositions are not adopted.

Application of sculptured Mn conical (Spiral+helical) thin films for monitoring N2-CO and N2-CO2 gas mixtures: Gas ionization and field emission sensors

This study deals with the design and fabrication of Mn sculptured conical (spiral + helical) thin films as electrodes for the detection of gas mixtures of different percentages (N2-CO and N2-CO2) in a gas ionization and field emission face to face sensor. The electrodes were produced using oblique angle deposition (OAD) technique. X-ray diffraction (XRD), atomic force microscopy (AFM) and field emission electron microscopy (FESEM) as well as energy dispersive x-ray spectroscopy (EDS) confirmed crystallography, morphology and elemental composition of materials of the designed samples. The sharp tip of the nano-helices were aimed to act as an electric field enhancer by applying voltage. The results indicated that Paschen's law is not applicable for inter-electrodes gaps less than 15 μm at pressures higher than 250 mbar where the field emission process becomes the dominant reaction. Enhanced selectivity and sensitivity were obtained for CO, CO2 and their mixtures with N2 gas at lower concentrations and shorter inter-electrodes gaps (<100 μm). The ionization energies of different ionization channel reactions of N2, CO and particularly CO2 in the gas mixtures were used to explain the behavior of Paschen's curves in different pressure ranges. Highest sensitivity of the sensor was obtained for inter-electrodes gaps of less than 100 μm. Comparison of the results with the published literature showed better performance of the present sensors relative to previously reported works.

Elemental tracer determination and modeling for geographical origin designation of sweet oranges

Sweet oranges have long been an integral part of global health and culinary practices, offering a wealth of nutrients and bioactive compounds. Ensuring the authenticity of these citrus fruits is essential for maintaining consumer confidence, promoting transparency in sourcing, and protecting producers' reputations in the marketplace. In this study, we explored the feasibility of using multi-element profiling combined with pattern recognition algorithms to trace the origin of sweet orange samples. To achieve this, we employed an optimized microwave plasma atomic emission spectroscopy (MP-AES) method to analyze the elemental composition (Al, Ba, Ca, Cd, Co, Cr, Cu, Fe, K, Li, Mg, Mn, Mo, Na, Ni, Pb, Sr, and Zn) of 183 orange samples from four production regions in northeastern Argentina. Support vector machine (SVM), random forest (RF), and gradient boosting tree (GBT) models were then built using the collected data to identify elemental tracer's indicative of origin. Based on a comprehensive evaluation of overall accuracy, receiver operating characteristic (ROC) curves, and area under the curve (AUC), the GBT model demonstrated the best classification performance, achieving a 96.5 % correct prediction rate on test samples, as confirmed by the ROC curve (AUC = 0.973). Consequently, this approach provides compelling evidence for the potential utility of MP-AES combined with supervised modeling to determine the geographic origin of sweet oranges produced in Argentina, thereby contributing to consumer protection against fraud.