Optical Emission Spectroscopy Research Articles

Evaluations of Groundwater Quality using Principal Component Analysis and Associated Multivariate Techniques: A Case History in Ewekoro Communities, South-West Nigeria

The quest for quality water consumption is comprised of integration of numerous techniques from different professionals whose contributions go a long way in determining overall health status and wellness of any given society. The water quality status of boreholes in Ewekoro communities of Ewekoro Local Government Area, South-West Nigeria was investigated in this work. Water samples were collected from 25 boreholes at various sampling stations across the study area. Standard analytical water quality methods using Inductively Coupled Mass Spectrometry (ICP-MS)/Optical Emission Spectrometry (ICP-OES) and Pour Plate Techniques were respectively employed in the laboratory for the samples’ geochemical and bacteriological analyses. The raw data were processed and analyzed using Principal Component Analysis and other multivariate techniques with Excel and SPSS 20.0 statistical software packages with the corresponding outcomes systematically compared with water quality standards. For the PCA, the varimax rotation converged in 23 iterations with 6 components extracted which accounted for 92.76% of the total cumulative variance respectively observed for geochemical parameters. Na2+, K+, Ca2+, Cl-, SO42-, NH4+, PO43-, and HCO3-, Mg3+, Cu2+, Cd2+, Zn2+, Ni, S , Si, Fe3+, NO3− and Al3+ played a significant contribution with higher factor loading supported by the dominance of HCO3− among the water quality determinants. The rotation converged in 8 iterations with 3 extracted components that accounted for a total cumulative variance of 90.99% % with pH, TEMP, EC, BOD, TS, TURB, ALK, TH, TDS, THC, and DO in the Physico-chemical Parameters series. Most quality determinants in the sampled water are within allowable limits of the approved water quality standards including WHO except Alkalinity, HCO3−, MgCO3−, Cl−, BOD, Cd2+, Fe3+ and Zn2+. The overall ionic dominance pattern follows the same trend K+ >Na2+ > Fe3+ >Mn2+ and Cl- >NO3- >NO2-. The results of the microbial analyses revealed the highest Total Coliform Count of 17 x 102 MPN/100 ml while that of THBC and FCC were reported as 7.8 ×102 cfu/ml and 1.2×102 cfu/ml respectively. The hygienic status of the water sources was found to be poor. High BOD, Coliform Count and BOD5:NO3- ratios of 248.23 recorded for the groundwater samples were suggestive of possible organic pollution due to faecal invasion with the lowest measured depth of 35m. Multivariate statistical approaches namely Correlation, Principal Component Analysis and Descriptive statistics simplified and identified the interrelationship among the analyzed physicochemical parameters and the pollution sources. This study has therefore revealed that boreholes in Ewekoro were polluted and posed potential risk to biomedical safety and overall human health. Intervention measures are therefore necessary to safeguard the inhabitants from water-related diseases and their consequences.

Occupational exposure assessment of heavy metals among construction workers in Rawalpindi Pakistan

Construction is one of the primary drivers of development and economic activity in Pakistan. Many activities are performed at the construction site including cement mixing, carpentry, and painting. Workers working in these activities are exposed to toxic heavy metals. Due to exposure to these heavy metals, subjects are at high risk of developing diseases mainly respiratory diseases. Human hair and nail samples of construction workers in Rawalpindi, Pakistan were collected to assess the heavy metals. Heavy metals such as Al, As, Cd, Cr, Ni, K, Pb, and Zn were analyzed in the hair and fingernails of the construction workers. To determine the level of selected heavy metals, Inductively Coupled Plasma optical emission spectrometry was used. Results revealed that Al was the highest with a mean concentration of 7.54 μg/g in all three groups. Whereas Cd was below the detection limit. Heavy metal concentration was high in hair (1.77 μg/g) in two groups including cement mixing and carpentry. However, in the carpentry group heavy metal concentration was high in nails (1.19 μg/g). Additionally, the workers of the carpentry group have higher metal concentrations when compared to the other two groups and this group was at high risk of toxic metal exposure. After the correlation analysis, the results revealed that age was significantly correlated to body burden of metals (r = 0.496, p ≤ 0.05). Moreover, some of the heavy metals in hair and nails were significantly correlated with each other. Since all groups, especially carpenters, show high levels of heavy metals, there is a need for regular monitoring of heavy metals at construction sites. Most importantly, the implementation of training programs is needed to raise awareness among construction workers.

Height-resolved emission spectroscopy and high-speed imaging of the TiAl6V4 vapor plume under laser powder bed fusion conditions

Optical emission spectroscopy is increasingly used as an in situ monitoring technique during laser powder bed fusion (LPBF) because plume emission holds elemental information not found in other in situ sensing techniques. This work explores the shape, stability, and temperature of the emission plume above the melt pool of Ti6Al4 V undergoing laser scans under LPBF-like processing conditions, using high-speed video and height-resolved spectroscopy to study the details of plume dynamics. Optical emission spectroscopy is conducted in the 480 nm to 525 nm region, where Ti emission is strong, with 0.3 mm vertical resolution above the baseplate. The Boltzmann plot method is used to determine temperature at each probed elevation, which indicates that the hottest location of the plume is occasionally elevated 0.3 mm to 0.6 mm above the scanning surface. The results show that the plume shape, stability, temperature, and spectra are highly dependent on the processing conditions. We highlight some of the complexities of optical emission spectroscopy and discuss potential challenges for implementing optical emission spectroscopy across an entire build.

Impact of Manufacturing Process and Compounding on Properties and Quality of Follow-On GLP-1 Polypeptide Drugs.

The prevalence of follow-on and compounded products of glucagon-like peptide-1 analogs is increasing. We assessed glucagon-like peptide-1 analogs semaglutide and liraglutide for purity, potential immunogenicity, and expected stability, by comparing a representative selection of commercially available follow-on drug substances (DSs) and drug products (DPs) with their corresponding originators. Tests included several chromatography methods coupled with ultraviolet and mass spectrometry detectors, inductively coupled plasma optical emission spectroscopy, inductively coupled plasma mass spectrometry, nuclear magnetic resonance, dissolution analyses, in silico peptide/major histocompatibility complex II-binding prediction, and fibrillation assays. Overall, 16 injectable semaglutide, 8 oral semaglutide, and 2 injectable liraglutide follow-on products were analyzed alongside originator products. Compared with originator, follow-on injectable semaglutide DSs and DPs had new impurities and impurity patterns, including high molecular weight proteins, trace metals, anions, counterions, and residual solvents. Analyses showed that several commercialized follow-on oral semaglutide DPs had a markedly lower quantity of semaglutide than the label claim, while dissolution tests indicated different semaglutide and sodium N-(8-[2-hydroxybenzoyl] amino)caprylate (SNAC) release profiles, which may reduce bioavailability. Neoepitopes were identified in DS and DP semaglutide follow-ons, indicating potential immunogenicity. Fibrillation assays showed increased fibrillation tendency and reduced physical stability in liraglutide follow-on DP samples compared with originator. This study highlights that differences in the manufacturing processes of follow-on semaglutide and liraglutide (vs those used for originators) can result in several changes to the DSs and DPs. The impact of these changes on efficacy and safety outcomes remains unknown and should be investigated by clinical studies.

Utilizing a medicinal plant and soil assays for heavy metal pollution assessment and its impacts in a Turkish Industrial Zone

Due to the worldwide growth in population, agricultural and industrial activities are expanding quickly, which pollutes the air, water, and soil and leads to the buildup of potentially hazardous substances in medicinal plants. The current study sought to determine the concentrations of various metals in Silybum marianum plants and soils in order to highlight the level of pollution in a Turkish Organized Industrial Zone in Dilovasi District, Kocaeli, and to investigate the effects of these heavy metals on plants. In order to determine the concentrations of elements evaluated within the scope of this study inductively coupled plasma optical emission spectroscopy was employed, due to the benefits of ICP that provides few or no organic molecules, few ionization interferences, as well as the ability to analyze many elements sequentially. Furthermore, in order to evaluate elemental analysis in terms of nutritional values, risk assessments using RDA, EDI, THQ, and HI parameters were conducted. The value of heavy metals in co-located soil samples is relatively high. However, except for Co, Mn, and Ni, it has stayed within the World Health Organization’s permitted limits. The evaluation of the co-located soil samples found that the highest contents (mg kg−1) of Al, Ca, Cd, Cr, Cu, Fe, K, Mn, Na, Ni, Pb, and Zn, were recorded as 7825.10, 4365.86, 4768.59, 2.50, 30.45, 38.49, 8352.00, 17452.26, 1495.82, 1495.82, 163.53, 1452.23, 28.67, 136.55 and 125.45, respectively, belonging to Location 1. These findings are in accordance with the Industrial Status Report since the place specified as Location 1 in the current study is characterized by its pronounced industrial activity and the robust electrical plant station with an industrial facility for generating electric power. Furthermore, the hazard index, the estimated daily intake and target hazard quotient for potentially harmful components and recommended daily allowance values for mineral nutrients were computed. Therefore, even though mineral nutritional values in some areas were found to be higher than Buyukada control location, this should be ignored. Consequently, this study warns against using S. marianum plants as food or medicine collected from current regions. As a result, ongoing inspection is necessary to prevent an excessive buildup of metals in the area and other places with similar human life-related features.

Potentially Toxic Metals Enrichment in Soils of Ishiagu Mining Community, Southeastern Nigeria

This Study was carried out to evaluate potentially toxic metals enrichment, pollution and potential ecological risk in the soils of Ishiagu. The concentrations of Cadmium (Cd), Chromium (Cr), Cobalt (Co), Copper (Cu), Lead (Pb), Manganese (Mn), Nickel (Ni), Zinc (Zn), Aluminum (Al) and Iron (Fe) in soil samples from the area were analyzed by Bureau Veritas Laboratory, Vancouver, Canada, using inductively-coupled plasma optic emission spectrometry (ICP-OES). Descriptive statistics, enrichment factor, pollution load and potential ecological risk indices were employed to analyze the data in order to understand the characteristics of potentially toxic metals in the study area. The potentially toxic metals statistic show the mean values (mg/kg-1 ) of Pb, Zn, Mn, Fe, Al, Cd, Cr, Ni, Co, and Cu to be 205.7, 162, 527, 35892, 11374, 1.3, 21.6, 15, 14.6 and 11.1 respectively. The soil enrichment varied considerably between mining and non-mining areas with mining area being extremely enriched with Pb, Zn and Cd, and significantly enriched with Co, Cu, Ni and Fe. Non- mining areas are minimally enriched with all investigated metals. The soils around the mines are polluted with Pb and Cd, where both metals also pose very high ecological risks.

Exploration of catalytic activities of Caesalpinia bonduc (L.) Roxb. ash on green-oxidation of small organic substrates: an effective way to reduce the use of harsh chemicals

In this modern era, large-scale industrial use of harsh chemicals is an alarming problem as it can cause serious environmental damage. Among industrial pollutants, harsh chemical oxidizing agents are one of the leading chemicals that can cause severe environmental threats. These harmful harsh chemicals are practically omnipresent in industries and are used to oxidize numerous small organic substrates. Replacement of these harsh chemicals with some plant-based products might be helpful to safeguard our environmental damage. In this study, Caesalpinia bonduc (L.) Roxb. ash is used as a catalyst to activate aerial oxygen for promoting the oxidation of 3,5-di-tert-butylcatechol (3,5-DTBC) and o-aminophenol (OAPH) like small organic substrates. Detailed kinetic studies for these catalytic oxidation reactions have been performed spectrophotometrically, which confirms that catalytic reactions follow Michaelis–Menten kinetics. Several enzyme-kinetics plots such as the Michaelis–Menten plot, Lineweaver–Burk plot, Hanes–Woolf plot, and Eadie–Hofstee plot have been used to determine the maximum rate achieved by the reaction (Vmax) and Michaelis constant (KM) like kinetic parameters. The average values of Vmax and KM for catalytic oxidation of 3,5-DTBC are (8.6669 ± 0.6519) × 10–5 M S−1 and (21.4289 ± 0.4741) × 10–4 M, respectively. Similarly, the average values of Vmax and KM for catalytic oxidation of OAPH are (2.1781 ± 0.2071) × 10–5 M S−1 and (20.1062 ± 1.2690) × 10–3 M, respectively. The mineral composition of Caesalpinia bonduc (L.) Roxb. ash has also been evaluated by using inductively coupled plasma optical emission spectroscopy (ICP-OES).Graphical

Processing and Characterization of Spent Nickel–Metal Hydride Type AA Batteries to Recover Valuable Materials (Cobalt, Nickel and Rare Earth Elements)

The experimental research was focused on the investigation of valuable material from spent Ni-MH type AA batteries, namely the metal grid anodes and the black mass material (anode and cathode powder). The materials of interest were analyzed by X-ray fluorescence spectroscopy (XRF), ICP-OES (inductively coupled plasma optical emission spectrometry), optical microscopy, scanning electron microscopy (SEM), energy-dispersive X-ray analysis (EDX), electron backscatter diffraction (EBSD), and X-ray diffraction (XRD). The analyzed grids have a high Fe content, but some of them correspond to the Invar alloy with approx. 40% Ni. In the black mass material, round particles and large aggregations were observed by SEM analysis, showing a high degree of degradation. The XRD analysis reveals the presence of only three compounds or phases that crystallize in the hexagonal system: La0.52Ce0.33Pr0.04Nd0.11Co0.6Ni4.4, Ni(OH)2, and La5Ni19. The obtained results provide useful and interesting information that can be used for further research in the recycling and economic assessment of metals from spent Ni-MH batteries.

Bones or Stones: How Can We Apply Geophysical Techniques in Bone Research?

Some studies have used physical techniques for the assessment of bone structure and composition. However, very few studies applied multiple techniques, such as those described below, at the same time. The aim of our study was to determine the chemical and mineralogical/organic composition of bovine tibial bone samples using geophysical/geochemical reference techniques. X-ray diffraction (XRD), thermogravimetry (TG), Fourier-transform infrared spectrometry with attenuated total reflectance accessory (FTIR-ATR), inductively coupled mass spectrometry (ICP-MS) and inductively coupled optical emission spectrometry (ICP-OES) were applied to measure the organic and inorganic composition of 14 bovine bone samples. In addition, peripheral quantitative CT (QCT) was used to assess BMD in these bones. We were able to define the total composition of the studied bone samples. ICP-OES and ICP-MS techniques were used to determine the major and trace element composition. The X-ray analysis could detect inorganic crystalline compounds of bones, such as bioapatite, and its degree of ordering, indicating whether the bones belong to a younger or older individual. The total volatile content of the samples was calculated using TG and resulted in about 35 weight% (wt%). This, together with the 65 wt% total resulting from the chemical analysis (i.e., inorganic components), yielded a total approaching 100 wt%. As a large portion of the volatile content (H2O, CO2, etc.) was liberated from the organic components and, subordinately, from bioapatite, it could be concluded that the volatile-to-solid ratio of the examined bone samples was ~35:65. The FTIR-ATR analysis revealed that the organic portion consists of collagens containing amide groups, as their typical bands (OH, CH, CO, NC) were clearly identified in the infrared spectra. Numerous parameters of bone composition correlated with BMD as determined by QCT. In conclusion, we performed a complex evaluation of bovine bones to test multiple geophysical/geochemical techniques in bone research in association with QCT bone densitometry. From a medical point of view, the composition of the studied bones could be reliably examined by these methods.

Groundwater geochemistry using modified integrated water quality index (IWQI) and health indices with special emphasis on nitrates and heavy metals in southern parts of Tirupati, South India.

Groundwater is particularly vulnerable to pollution in places with a high population density and extensive human usage of the land, especially in southern parts of Tirupati, India. To assess this, 60 bore-well samples were obtained and assessed for physical specifications, ion chemistry, and heavy metals during the pre- and post-monsoon seasons 2022. The current investigation employed a modified integrated water quality index (IWQI), conventional graphical and human health risk assessment (HHRA) of nitrates and heavy metals to know the groundwater chemistry and its detrimental health effects on humans. The major ions were analyzed using American public health association (APHA)standards, whereas heavy metals were analyzed using inductively coupled plasma optical emission spectrometry(ICP-OES). Additionally, pH Redox Equilibrium and C (PHREEQC),a geochemical model written in C programming language was employed to determine the saturation indices of mineral facies and ArcGIS 10.3.1 was used for spatial distribution patterns of IWQI. Then, the HHRA of nitrates and heavy metals was performed using United States environmental protection agency (USEPA)guidelines. The noteworthy outcomes include elevated levels of Ca2+, Mg2+, Cl-, NO3-, Cu,Fe, Mn, and Pb, demonstrating rock-water interaction, silicate weathering, Ca-Mg-HCO3 followed by mixed water facies, dissolution/precipitation, reverse exchange, and anthropogenic contamination are the major controlling processes in groundwater of southern Tirupati, India. The modified IWQI reveals that most groundwater samples (38%) fall under the bad quality class, with (47%) in the poor quality class and only (15%) classified as medium qualityclass in pre- and post-monsoon seasons. Elevated IWQI were observed in all directions except in the east, which is suitable for drinking. Moreover, the major hazard quotient (HQ) and hazard index (HI)for nitrates (NO3-) and heavy metals like copper(Cu), iron (Fe), manganese (Mn), lead (Pb) and zinc (Zn) are above the critical value of 1, revealing potential risk to humans, especially infants, followed by children and adults, entailing the instantaneous implementation of proper remedial measures and stringent policies to reduce the risk associated with groundwater pollution in the southern parts of Tirupati.

Analytical Techniques for Detecting Rare Earth Elements in Geological Ores: Laser-Induced Breakdown Spectroscopy (LIBS), MFA-LIBS, Thermal LIBS, Laser Ablation Time-of-Flight Mass Spectrometry, Energy-Dispersive X-ray Spectroscopy, Energy-Dispersive X-ray Fluorescence Spectrometer, and Inductively Coupled Plasma Optical Emission Spectroscopy

Rare earth elements (REEs) hold significant industrial, scientific, and modern technological worth. This study focused on detecting and quantifying REEs in various geological ore samples. These samples were collected from different REE-bearing locations recommended by geological experts. The analysis was conducted using laser-induced breakdown spectroscopy (LIBS) and laser ablation time-of-flight mass spectrometry (LA-TOF-MS). In this work, LIBS methodology was employed using three different configurations: standard LIBS, LIBS with an applied magnetic field, and LIBS with both an applied magnetic field and target sample heating within an optimal temperature range. Elements from the REE group, specifically lanthanum (La), cerium (Ce), and neodymium (Nd), were identified and quantified. To detect, quantify, and validate the results from LIBS and LA-TOF-MS, we utilized an array of analytical techniques—Energy-Dispersive X-ray Spectroscopy (EDX), Energy-Dispersive X-ray Fluorescence Spectrometer (ED-XRF), and Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES). Interestingly, the quantitative results for REEs (La, Ce, and Nd) in the ore samples obtained using the LIBS technique with various configurations were found to be in agreement with those from LA-TOF-MS, EDX, XRF, and ICP-OES. In addition, LIBS enables detailed microchemical imaging, allowing the map of the spatial distribution of elements within the mineral–ore matrix. The high-resolution microscale elemental mapping of REEs was accomplished using the emission lines Ce (II) at 446.0 nm, La (II) at 492.1 nm, and Nd (II) at 388.8 nm. By integrating multiple analytical techniques, our study enabled the construction of a complete elemental distribution map, providing new insights into the geochemical processes and mineral composition of rare earth ores, while advancing geochemistry and contributing valuable data for rare earth resource exploration.

Flotation of Li Pegmatite with a Soybean Oil-Based Collector: Fundamental Studies

ABSTRACT In this work, the effect of a soybean oil-based collector on the surface properties of spodumene, feldspar, quartz, and muscovite was characterized and evaluated. By means of gas chromatography, it was determined that the reagent was composed of a mixture of carboxylic acids: linoleic (48%), oleic (28%), palmitic (13.3%), stearic (3.6%), α-linolenic (3.4%), and elaidic (3.2%). The reagent contained ~14 ppm Ca (determined by inductively coupled plasma optical emission spectroscopy – ICP-OES) and a critical micellar concentration (CMC) of 100 mg/L. At pH 6, the spodumene recovery was 50–60% higher than the other mineral recoveries, ascribed to chemical adsorption of the collector ionic-molecular species, which has high hydrophobicity power, on Al3+ sites on the spodumene surface. For pH values >10, the recoveries of feldspar and quartz were higher than spodumene, due to their activation by hydroxyl and hydroxide of Ca and subsequent adsorption of ionic specimen of the collector. The electrokinetic potential curves of spodumene, feldspar, and muscovite with collector were shifted toward more negative values compared to their electrokinetic potential curves without reagent. Fourier transform infrared spectroscopy (FT-IR) showed chemical adsorption of the anionic species of the collector at pH 6 with the Al3+, Fe3+, and Ca sites on the surface of aluminosilicates and Ca for quartz.

Arsenic in Rice and Rice-Based Products with Regard to Consumer Health

Most articles on the exposure to arsenic (As) associated with rice and rice products come from Asia where these products are consumed in the largest quantities; relatively few of the articles have focused on European consumers. Since rice products can represent a significant contribution to overall arsenic exposure, the aim of the study was to determine the total arsenic content (tAs) in rice and the most commonly-consumed rice products available on the Polish market. The tAs determination was performed by hydride generation coupled to inductively-coupled plasma optical emission spectrometry (HG-ICP-OES). Because an inorganic form of As (iAs) is mutagenic and carcinogenic and about 100-fold more toxic than the organic form, an additional aim of the study was to assess the risk of its ingestion, assuming that it constitutes 67.7%, 72.7%, or 90% of tAs. In all products tested, the calculated iAs content was below the maximum permissible levels, and no threat was found for any of the analyzed Polish consumers, based on the mean rice consumption in Poland and the mean calculated iAs content. However, a potential health risk was noted among infants and young children, assuming maximum iAs levels and threefold higher consumption (16.2 g d−1). To avoid a risk of developing cancer, infants up to one year of age should consume no more than 32.2 g of the studied products per week, children under three years of age up to 68.7 g, and adults 243 g. Consumers should strive to include a variety of cereals in their daily diet and choose products shown to have low arsenic contamination levels based on testing and inspection rankings.

Multi-diagnostic of dust growth in a capacitive Ar/C2H2 plasma

Abstract The interest in the production of nanoparticles (NPs) within Ar/C2H2 reactive plasmas is increasing, driven by their potential applications in functional materials or for their analogy to cosmic dust. The growth process of NPs has been thoroughly examined using a broad array of diagnostic tools. Significant among these tools are those that determine two-dimensional distributions of NP sizes and densities. The inherent complexity of these techniques has resulted in a limited number of works that integrate these measurements with a multitude of other diagnostic tools. Here, we show a multi-diagnostic exploration of the growing process of NPs in Ar/C2H2 plasmas. The combination of in-situ techniques, such as scattered light images, optical emission spectroscopy, light extinction, quadrupole mass signals, or self-bias voltage, with ex-situ scanning electron microscopy images and FTIR spectra of the deposited dust, provides a detailed picture of the growth process. The temporal evolution of plasma parameters, coupled with chemical composition measurements, provides a comprehensive description of the dust growth phases, and the FTIR measurements reveal an appreciable difference in chemical composition between the core and shell of the NPs. Furthermore, employing a method based on the terminal falling velocity of NPs in the afterglow, the intrinsic mass density of NPs is estimated. The asymmetries observed in the spatial distributions of NP size and density are qualitatively discussed in terms of neutral drag, ion drag, and electrostatic forces.

Low-damage etching of poly-Si and SiO2 via a low-energy electron beam in inductively coupled CF4 plasma

Abstract Electron-assisted etching of poly-Si and SiO2 is performed via a grid system in inductively coupled CF4 plasma. The feasibility of electron-assisted etching is discussed with a focus on the low-surface damage of the etching. The etch rate increases with electron beam energy, which indicates that the electrons assist the surface etching process. To verify this, etching of poly-Si and SiO2 is performed in several plasma conditions, which leads to differences in etch rate that depend on the presence or absence of radicals and electron beams. Poly-Si and SiO2 are not etched without radicals of CF4 plasma, but they are etched when such radicals are present. When the electron beam and radicals exist simultaneously, the etch rate increases more dramatically than in the case of a CF4 plasma without an electron beam, demonstrating that the electron beam assists the etching process. Optical emission spectroscopy is employed to verify the F radical does not affect the etch rate increase. The surface roughness is measured after electron-assisted etching and compared with the surface roughness after ion-assisted etching.

Design and first tests of the trapped electrons experiment T-REX.

Gyrotrons are essential for electron cyclotron resonance heating in fusion reactors, making efficient operation crucial for advancing fusion energy. Past experiments revealed instability issues due to trapped electrons in the magnetron injection gun (MIG) region, causing undesired currents and operational failures. To address this, tight manufacturing tolerances are required for the MIG geometry [Pagonakis etal., Phys. Plasmas 23, 023105 (2016)]. We present the initial findings of the trapped electrons experiment developed at the Swiss Plasma Center, designed to understand the physics of electron clouds in gyrotron MIGs. T-REX replicates MIG geometries, as well as their typical electric and magnetic fields, and it is supported by 2D particle-in-cell simulations with the FENNECS code [Le Bars etal., Phys. Plasmas 29, 082105 (2022); Le Bars, Ph.D. thesis, EPFL, Lausanne, 2023]. The setup includes two coaxial electrodes in a vacuum chamber atop a superconducting magnet, with a central electrode biased to negative DC voltages and an outer one at the ground, creating a radial electric field (1-2MV/m) and an axial magnetic field (B < 0.4T). This setup mimics Penning-Malmberg traps. We present the experimental device and first findings on current distribution and also a qualitative comparison with FENNECS simulations [Le Bars etal., Comput. Phys. Commun. 303, 109268 (2024)]. Planned diagnostics include optical emission spectroscopy, phosphor screen imaging, streak camera imaging, and potentially electric field distribution via the Stark effect. This research aims to enhance gyrotron performance and reliability in fusion energy systems.

Migration of Platinum Nanoparticles via Volatile Platinum Dioxide during Lean High-Temperature Ageing of Diesel Oxidation Catalysts

When platinum-containing diesel oxidation catalysts (DOC) are exposed to high temperatures under lean conditions, the platinum nanoparticles form volatile platinum dioxide on the catalyst surface. The exhaust flow carries the volatile platinum dioxide to the downstream aftertreatment catalyst, such as the selective catalytic reduction (SCR) catalyst, that is responsible for reducing the nitrogen oxides (NOx) emissions and can negatively impact its performance, by promoting the parasitic oxidation of ammonia. Here we investigate the factors such as exposure time, temperature and DOC design characteristics for their impact on the platinum dioxide migration, by characterising the amount of platinum deposited on the SCR catalyst at very low levels (&lt;5 ppm), using inductively coupled plasma optical emission spectroscopy (ICP-OES) fire assay technique. Our results indicate that well-dispersed platinum, not associated with palladium, is most prone to platinum dioxide migration. We also compare several methods to suppress the platinum dioxide migration from the DOC, such as sintering of the platinum nanoparticles, stabilising the platinum nanoparticles via interaction with palladium or covering the platinum nanoparticles with a high surface area capture layer to trap the volatile platinum dioxide.

Construction of Multi-Channel Radio Frequency Plasma Jet System in Atmospheric Pressure and the Diagnosis of Plasma Parameters and I-V Characteristics

In order to produce cold plasma at atmospheric pressure, a multi-channel RF, of (1, 2, 3, and 4 MHz) frequencies, plasma jet system is developed using argon as the working gas. This system consists of two parts, a multi-channel power supply (of a power of 100 W) and a plasma jet. A strong electric field is created that ionizes and excites argon ions. The I-V characteristics of the system and the electron temperature and density for different powers (20, 50, 70, and 80 W), gas flow rates (10, 20, 30, and 40 sccm) (standard centimeter cubic per minute) at different frequencies (1, 2, 3, and 4 MHz) are studied, using the optical emission spectroscopy method. This system can be used in medical applications and material treatment with high efficiency.

Operating Characteristics of a Wave-Driven Plasma Thruster for Cutting-Edge Low Earth Orbit Constellations

This paper outlines the development phases of a wave-driven Helicon Plasma Thruster for cutting-edge Low Earth Orbit (LEO) constellations. The two-stage ambipolar electric propulsion (EP) system combines the efficient ionization of an ultra-compact helicon reactor with plasma acceleration based on an ambipolar electric field provided by a magnetic nozzle. This paper reveals maturation challenges associated with an emerging EP system in the hundreds-watt class, followed by outlook strategies. A 3 cm diameter helicon reactor was operated using argon gas under a time-modulated RF power envelope ranging from 250 W to 500 W with a fixed magnetic field strength of 400 G. Magnetically enhanced inductively coupled plasma reactor characteristics based on half-wavelength right helical and Nagoya Type III antennas under capacitive (E-mode), inductive (W-mode), and wave coupling (W-mode) were systematically investigated based on Optical Emission Spectroscopy. The operation characteristics of a wave-heated reactor based on helicon configuration were investigated as a function of different operating parameters. This work demonstrates the ability of two-stage HPT using a compact helicon reactor and a cusped magnetic field to outperform today’s LEO spacecraft propulsion.

Iron, Zinc and Total Phenolic Content in Cooked Biofortified NUA 45 and Gloria Sugar Beans: The Case of Zimbabwe

Biofortification involves breeding of staple crops that are micronutrient-dense and high yielding for example iron-biofortified beans. The biofortification of crops has been found to be cost effective and feasible to fight micronutrient deficiencies. The aim of the study was to determine the iron, zinc and total phenolic composition for the biofortified NUA 45 and Gloria sugar beans in raw as well as cooked samples with and without previous soaking. Determination of iron and zinc content in the raw, cooked bean grain samples with and without soaking was carried out by Inductively Coupled Plasma (ICP) Optical Emission Spectrometry whereas the determination of Total Phenolic Content was done using the Folin-Ciocalteau colorimetric method. The highest zinc concentration (0.295ppm) was found in raw Gloria sugar beans whilst the raw NUA 45 sugar beans had the highest iron content (0.755ppm) and total phenolic composition (352.8mg/100g). For the cooked bean samples Gloria sugar beans had the highest zinc concentration (0.247ppm) cooked after soaking. NUA 45 sugar beans had no significant difference on the zinc content after being cooked with and without soaking. Amongst the cooked samples the biofortified NUA 45 sugar beans cooked after soaking had the highest iron content (0.373ppm) as well as the highest total phenolic content in the beans cooked without soaking (200.5mg/100g). Biofortified NUA 45 and Gloria sugar beans proved to be good sources of iron, zinc and phenolic compounds. However, cooking with and without soaking diminished the iron, zinc and the total phenolic composition of the cooked NUA 45 and Gloria sugar beans.