Optical Emission Spectroscopy Research Articles

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.

Investigating the Level of Metal’s Toxicity in Used Cell Phone Batteries by TCLP and WET Methods

Introduction: Batteries are widely used in all kinds of electrical and electronic equipment. These batteries contain several metals that lead to the leakage of metals into the soil and underground water in the burial places, which pose serious risks to human health and the environment. Materials and Methods: In this study, the concentration of 15 metals (Ag, Al, As, Ba, Cd, Co, Cs, Cu, Fe, Li, Mn, Pb, Sr, Zn, Ni) in different components of 7 used battery models was investigated using Waste Extraction Test (WET) and Toxicity Characteristic Leaching Procedure (TCLP) toxicity. The concentration of metals was measured by Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES). Metal concentrations were compared with the United States Environmental Protection Agency (USEPA) and California Department of Toxic Substances Control (CDTSC) standards. Results: The results showed that the average concentration of metals in both WET and TCLP methods was high, but the concentration of most metals in WET method was relatively higher than in TCLP method. Conclusion: The results showed that the recovery of metals from batteries is necessary, moreover safe burial of batteries is essential to reduce environmental risks.

Characterization and potential application of microspheres from sodium alginate cross-linked with pectin from Citrus depressa Hayata’s peels

BackgroundPectin from Taiwan Citrus depressa Hayata’s peels (CDH pectin) and sodium alginate (Na alginate) were mixed in neutral acidity to produce microhydrogel beads or microspheres. The potential use of the microspheres such as encapsulation materials for quercetin and nobiletin, DPPH (2,2-diphenyl-1-picrylhydrazyl) scavenging activity, toxic elements absorption ability, and thermal characteristics were explored.ResultsDifferent ratios of CDH pectin and Na alginate produced microspheres of varying sizes and shapes. The highest yield (47.59%) with the broadest diameter was obtained at a Na alginate—CDH pectin ratio of 2:1, while the smallest yield was obtained from Na alginate—CDH pectin ratio of 1:3 (24.13%). Increasing the amount of Na alginate resulted in more spherical microspheres, higher heavy metals (cobalt and nickel) removal rates, yet a lower swelling ratio. A high pectin concentration also increased the encapsulation efficiency of quercetin and nobiletin, reaching 91.5% and 86.74%, respectively. Quercetin and nobiletin release analysis (in vitro) showed a slow release of drugs from the microspheres. Less than 20% quercetin and nobiletin were released from the microspheres in SGF (simulated gastric fluid) pH 1.2 solution after 2 h and more than 40% of the encapsulated drug was released in SIF (simulated intestinal fluid) pH 6.8 after 4 h. The strong DPPH scavenging activity of quercetin (99%) was not hindered by encapsulation materials. ICP-OES (inductively coupled plasma–optical emission spectrometry) analysis demonstrated that the biopolymer can absorb cobalt and nickel from water. Thermogravimetric analysis (TGA) result showed that the combination of CDH pectin and Na alginate produced a biopolymer that exhibited a weight loss of only 1.86–4.33% at 100 °C.ConclusionsThese findings suggest that microspheres produced from CDH pectin cross-linked with sodium alginate had potential in nobiletin and quercetin encapsulation. Moreover, the polymer could absorb heavy metals and exhibit an important characteristic for hot food and beverage packaging applications.

AI-powered precursor quantification in atmospheric pressure plasma jet thin film deposition via optical emission spectroscopy

AI-powered precursor quantification in atmospheric pressure plasma jet thin film deposition via optical emission spectroscopy

Analysis of discharge parameters of an argon cold atmospheric pressure plasma jet and its impact on surface characteristics of White Grapes

An argon cold atmospheric-pressure plasma (CAP) jet operated using bipolar pulsed power supply has been characterised electro-optically and the discharge parameters are optimized. An analysis has been done on the impact of the argon CAP jet treatment on the surface properties of white grapes for different treatment time period. The developed argon CAP jet is a plasma source based on dielectric barrier discharge (DBD) that has been tuned at various input parameters including applied voltage, frequency, average power consumption, and argon flow rate. Optical Emission Spectroscopy (OES) is used to identify the generated species along with plasma parameters. The collisional–radiative (CR) model is employed to extract the electron density (ne) and electron temperature (Te) from the spectra at the optimised applied voltage of 4 kV, frequency 20 kHz and argon flow rate of 4 slpm. The OES results coupled with the CR model (ne ∼ 1014 cm−3 and Te ∼ 1 eV) and the plasma gas temperature measurement through OH (A-X) transitions (Tg ∼ 310.5 K) show the non-equilibrium nature of the argon CAP jet. A comparative analysis between untreated and treated white grapes reveals that the argon CAP jet treatment influences surface microstructure, increasing hydrophilicity (with a ∼49.3% decrease in water contact angle) along with slight changes in surface temperature (∼5 °C increase), colour (ΔE* < 1.5), and physiochemical properties such as chemical composition (no change) and Total Soluble Solid (TSS) content (∼8.3%). It is inferred that this type of CAP jet treatment of white grapes only affects the physical characteristics of the grape surface and does not alter any chemical compositions.

Multi-energy calibration and induced plasma optical emission spectrometry (MEC-MIP OES) as an alternative method for the multi-elemental determination of essential elements in cocoa.

The challenge of combining MEC-MIP OES arises from the limited number of emission lines available in this analytical technique. For the MEC-MIP OES optimization, the emission line wavelengths, sample dilution, proportion sample:standard for preparing MEC solutions, and nebulizer gas flow rate were studied. Then, the use of multi-energy calibration (MEC) and microwave-induced plasma optical emission spectrometry (MIP OES) was proposed as an alternative method for the determination of essential elements (Ca, K, Mg, Mn, and Na) in cocoa. In the optimized conditions, the method presented adequate analytical performance, with recoveries of 94-104% and relative standard deviations lower than 5%, showing adequate precision. The limits of detection (mg kg-1) were 12 for Ca, 2 for K, 3 for Mg, 3 for Mn, and 6 for Na. The proposed method was applied to analyze cocoa samples cultivated in Brazil and Ecuador after acid decomposition. The results were in the range (mg kg-1) of 409-1530 for Ca, 5520-13300 for K, 1460-3210 for Mg, 16-34 for Mn, and 28-61 for Na. Samples cultivated in Ecuador presented higher metal concentrations than the Brazilian samples. The proposed procedure was an easy and reliable approach for determining metals in cocoa samples, enabling multi-elemental determination with a lower cost and simplified calibration to be applied in routine applications.

Propriedades físico-químicas do óleo da castanha de baru e análise da qualidade nutricional dos ácidos graxos e minerais: uma rica fonte de selênio, um oligoelemento

Baru nut (Dipteryx alata Vogel) oil obtained by cold pressed machine yielded 24% (mg g–1), primarily composed of unsaturated fatty acids (⁓ 79%), with oleic and linoleic acids in the proportion of 2:1. The oxidative stability assessed by Rancimat method, Thermogravimetry analysis and Differential Scanning Calorimetry revealed thermal stability, which attributed to a higher amount of oleic than linoleic fatty acids, synergistic action of the natural antioxidants and low iodine index. The nutritional qualities were calculated to atherogenic (AI = 0.07), thrombogenic (TI = 0.22) and hypocholesterolemic/ hypercholesterolemic (HH = 13.77), and physicochemical indices: acidity (0.62), peroxide (9.99), saponification (179.93) were higher, whereas iodine (93.00) and relative density (0.9121) were found between the recommended Codex Alimentarius parameters. Mineral elements were quantified using ICP OES (inductively coupled plasma optical emission spectroscopy) in decreased order of Mg &gt; Se &gt; Zn &gt; Mn &gt; Al &gt; Cu, whereas As, Co, Cd, Cr, Fe, Ni, and Pb &lt; LOD. In addition, this oil showed optimal indices to non-cancer risk (CR &lt; 10–6), and non-carcinogenic: hazard quotient (HQ), and total hazard indices (HI) &lt; 1. Nevertheless, major attention is necessary for children and Se hypersensitive consumers, which baru oil daily consumption quantity was estimated based on selenium (Se) trace element at 0.7964 g kg–1. Thus, we recommend the consumption of baru nut oil for human health promotion and metabolic disease prevention.

Analysis of pulsed direct current reactive magnetron sputtering on a silicon target

Reactive sputtering is a very useful technique, particularly, for producing inhomogeneous interference filters, where the refractive index changes smoothly during deposition. In such a context, precise control of deposition parameters is crucial for replicating the desired optical properties. This study employed a pulsed DC power source to investigate the influence of a duty cycle on target poisoning, sputtering plasma characteristics, electric signals, and optical and morphological properties of synthesized films. Reactive pulsed DC magnetron sputtering was characterized by analyzing the behavior of plasma emission via optical emission spectroscopy and voltage-current signals, while modulating parameters such as the oxygen content within the vacuum chamber. A set of thin films was coated on glass substrates under different system conditions. These films underwent characterization employing spectroscopic ellipsometry to ascertain their optical constants, atomic force microscopy for surface morphology analysis, and x-ray diffraction for the determination of crystalline structures. The results indicate that longer duty cycles required higher oxygen levels to poison the target. Additionally, a detailed analysis of electrical signals revealed nonsquare waveforms, whose characteristics were influenced by both the duty cycle and the oxygen content within the sputtering chamber, resulting in higher effective voltages during the on-time of the voltage pulse. Grown films via reactive pulsed DC magnetron sputtering were also compared to films grown via conventional DC magnetron sputtering at equivalent conditions of target poisoning.

Development and Validation of an ICP‐OES Method to Determine Extractable and Leachable Metals in HDPE (Plastic) Pharmaceutical Packaging Material

ABSTRACTThe safety and effectiveness of pharmaceutical medicines depend heavily on extractables and leachables. Patients may be adversely affected by contaminants that enter drug products through packing materials. As a result, regulatory organizations like the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA) have set standards and regulations for evaluating and managing extractables and leachables. Characterizing the packing materials, carrying out extraction experiments and checking the extracted solutions for contaminants are all parts of this research. As part of the process for approving new drugs, regulatory agencies make use of these data. In present work, an inductively coupled plasma optical emission spectroscopy (ICP‐OES) method is developed and validated for quantifying trace elements from a high‐density polyethylene (HDPE) packaging material. The approach delineated in accordance with United States Pharmacopoeia (USP) &lt;661.1&gt; and &lt;661.2&gt; for the comprehensive analysis of 16 metallic elements including aluminium, arsenic, cadmium, chromium, cobalt, lead, mercury, nickel, titanium, vanadium, zinc, zirconium, barium, manganese, calcium and tin is applicable for evaluating the efficacy of packaging materials. The method detection limits (MDLs) complied as per USP 39‐NF 34 &lt;661.1&gt; along with relative standard deviations (RSDs) obtained were ranging from 0.3% to 3.1% and recoveries of all elements spiked at two different trace levels in HDPE samples were within 97%–110%, providing sensitive, accurate and reproducible methodology.

CaviPlasma: Parametric study of discharge parameters of high-throughput water plasma treatment technology at glow-like discharge regime

Abstract AC discharge in dense hydrodynamic cavitation cloud in water named CaviPlasma has been studied at different discharge parameters.&amp;#xD;CaviPlasma stands for the cavitation and plasma that are two coupled basic phenomena of the novel technology enabling very high throughput of plasma water processing compared to other current technologies. In this article the diagnostic and the properties of CaviPlasma discharge are discussed based on optical and electric characterization of the discharge phenomena together with the physico-chemical characterisation of the plasma treated water. The so-called unbridged mode of CaviPlasma operation is described, where the discharge propagates from a metal electrode towards a liquid electrode at the collapsing end of the cavitation cloud. Production of H, O and OH species in the discharge was proved by optical emission spectroscopy. Formation of hydrogen peroxide (H2O2) in water was determined by chemical methods. The energy yield for H2O2 generation is as high as 9.6 g/kWh and the generation rate is up to 2.4 g/h. The degradation of phenol admixture in water was also studied. The article covers a parametric study enabling development of tailored applications.

A chemometric approach using I-optimal design for optimising Pb(II) removal using bentonite-chitosan composites and beads

This paper reports adsorption studies of Pb(II) ions onto Bentonite-Chitosan (Bt-Ch) composites or beads when using an I-optimal design experiment approach. Three adsorption factors (pH, adsorbent dosage, and initial concentration) were optimised whilst simultaneously investigating multiple adsorbents. The Bt-Ch composites and beads (type A and B) adsorbents were made using weight ratios 90%/10% and differed characteristically due to their preparation methods of solution blending and precipitation, respectively. A batch procedure was used for adsorption experiments, and the amounts of Pb(II) ions (adsorbed onto Bt-Ch composites/beads) were analysed using inductively coupled plasma optical emission spectrometry (ICP-OES). Adsorption experimental parameters were analysed and optimised by using a response surface method (I-optimal design) generated from Design-Expert® 13.0 software. The main achievements of this study were to intensify the understanding and application of I-optimal experimental designs, which allow simultaneous determination of adsorption capacities and efficiencies across multiple adsorbents in an economical manner. A reduced quadratic model provided the best fit for the experimental data and exhibited minimal deviation between predicted and experimental values. This was evidenced by the very small covariance (CV) values of 1.81% and 1.33% observed for adsorption capacity and adsorption efficiency, respectively, also suggesting high reproducibility. It was observed that the adsorption factors studied (pH, adsorbent dose, and initial concentration) have a more pronounced effect on the adsorption capacity (F-value = 714.37) compared to adsorption efficiency (F-value = 140.62). Adsorbent dosage was found to have the greatest effect on adsorption capacity, while the initial pH of Pb(II) solution had the greatest effect on adsorption efficiency. Under optimal conditions, the adsorption capacities of beads-A (73.2 mg/g) and beads-B (77.6 mg/g) were found to be higher than that of the corresponding composite (51.7 mg/g). Whilst the optimum adsorption efficiency values for all three adsorbents were ∼100% (with ranges of pH 2–5, initial concentrations 50–200 mg/L, and adsorbent dosage 0.05–0.5 mg). The desirability indexes for the optimised conditions for these respective responses (and each adsorbent) were found to be within the ranges of 0.892–0.974 and 0.945–0.967 for adsorption capacity and adsorption efficiency, respectively. These high desirability index values for both responses indicate that the optimised conditions lead to very good performance for both measures. The information obtained in this study provides detailed understanding of the adsorption phenomena of the adsorbents studied. It gives confidence in the use of I-optimal designs to be applied as a chemometric tool for the specific adsorbents studied herein and others.

Optical emission spectroscopy as a method for evaluating the change in Si etching structures profile in ICP SF6/C4F8 plasma: Microstructures

In this work, a method for in situ diagnostics of the etching profile of silicon structures (etching window sizes 15–400 μm) using optical emission spectroscopy was proposed. To determine the relationship between the etching profile and plasma parameters, the influence of technological parameters on the etching characteristics (vertical and lateral etching rate, selectivity in relation to photoresist, and sidewall angle) was studied. As a general parameter, which reflects the changes in plasma characteristics depending on the selected technological parameters, the parameter X (C/F ratio in SF6/C4F8 plasma) was introduced. Based on the results obtained, a general pattern between the lateral etching rate, sidewall angle, and optical emission spectra was identified. Thus, ranges of X values, at which the lateral etching rate does not exceed 5 nm/min for 15–30 μm structures and 15 nm/min for 100 μm structures, were estimated: 0.38 ≤ X ≤ 0.77 and 0.28 ≤ X ≤ 0.46, respectively. For 250–400 μm structures, ranges of X values, at which the sidewall angle is acute, straight, and obtuse, were determined: 0.16 ≤ X &amp;lt; 0.29, 0.29 ≤ X ≤ 0.41, 0.41 &amp;lt; X ≤ 0.75, respectively.

Failure Analysis of a Welded 316L Stainless-Steel Stack with Premature Damage Due to Stress-Corrosion Cracking

AbstractThis study analyzed the premature failure of a stainless-steel stack obtained from a mining company. The stack was manufactured using ASTM A240 Type 316L stainless steel. After one year of its service, massive leakages and cracks were observed near the welds. Following a visual examination of the stack, a representative sample was extracted and analyzed using visual and radiographic inspection, metallographic examination, scanning electron microscopy, energy-dispersive spectrometry, optical emission spectrometry, ferrite number analysis, and leak testing. Furthermore, corrosion mechanisms and the sequence of events leading to failure were determined. Two different mechanisms were identified: acid dew point corrosion caused by the condensation of H2SO4 and HCl at the inner walls of the chimney, followed by stress-corrosion cracking near the welded joints.

Electric field components within a micro-scaled DBD measured by Stark shifting and splitting of helium lines

Abstract Atmospheric pressure dielectric barrier discharges (DBDs), such as the micro cavity plasma array (MCPA), have emerged as promising technologies for the conversion of volatile gases. These conversion processes' effectiveness can be enhanced by integrating catalytically active surfaces. To deepen the understanding of the plasma-catalyst interaction, it is crucial to study the transport dynamics of charged species to the catalytic surface, which, due to collisions with neutrals, also directly affects the transport of reactive species to the catalyst. Thereby the transport of the charged species is in particular influenced by the electric field perpendicular to the catalytic surface. &amp;#xD;However, experimental data on the component-wise electric field strength within DBDs are rare. To address this issue, we performed polarized optical emission spectroscopy (OES) on the shifting and splitting of the allowed 492.19 nm (1D→1P0) and forbidden 492.06 nm (1F0→1P0) helium line pair. This diagnostic approach requires a non-radially symmetric geometry, which leads to an adapted reactor design of the MCPA allowing the side-on observation of the discharge. The discharge operates in pure helium at atmospheric pressure, utilizing a triangular excitation voltage with a frequency of 15 kHz and an amplitude of 600 V. We performed phase-resolved measurements of the electric field components with a temporal resolution of 1 µs. Our results revealed an electric field strength of approximately 22 kV cm-1 for the component perpendicular to the dielectric surface, while the component parallel to the dielectric surface is about 5 kV cm-1 larger during the decreasing potential phase of the applied voltage.

Microstructural evolution and formation of defect complexes in diamond films by nitrogen-containing plasma

Abstract The morphology and crystalline quality of polycrystalline diamond samples were studied by systematically varying the flowrate of nitrogen gas in the microwave plasma. A slight improvement in both crystallite size and crystalline quality is observed for a low concentration of 0.5 sccm nitrogen. With a further increase in nitrogen concentration, diamond switches from micro-crystalline (MCD) to nanocrystalline (NCD) with a nitrogen flow of 2.5 sccm (10% of methane concentration). The surface roughness of the sample is found to depend strongly on the crystallite size of the sample. Extensive spectroscopic studies have been done to understand the presence and formation of different defect complexes in diamond. The presence of nitrogen-containing defect complexes has been studied thoroughly and their concentration has been found to be limited by the solubility limit rather than the availability of reactants in the gas environment. In contrast, the effect these complexes have on the strain of the diamond film is found to be negligible. Optical emission spectroscopy (OES) of the plasma reveals the presence of C2 dimers as well as C-N radicals. However, they have little role in modifying diamond grain morphology or crystalline quality.

Copper abietate/polyvinyl acetate composite film for enhanced humidity sensing in Chinese herbal medicine monitoring systems

Sensing materials derived from natural and biodegradable sources are increasingly being developed and applied to realize environmentally friendly technologies. In this paper, we present the synthesis, characterization, and application of a novel copper abietate/polyvinyl acetate (CuA/PVAc) composite film, specifically engineered to enhance the humidity-sensing capabilities of Chinese herbal medicine monitoring systems. The sensing material was synthesized by strategically melding copper abietate, a natural renewable material, with PVAc to exploit their combined synergistic properties for optimal humidity-sensing performance. Comprehensive characterization techniques, including inductively coupled plasma optical emission spectrometry (ICP-OES), field-emission scanning electron microscopy (FESEM), water contact angle measurements, and Fourier transform infrared (FT-IR) spectroscopy, were employed to confirm the formation of CuA/PVAc composites. These analyses confirmed the homogeneity and intended chemical composition of the composite films.The resultant CuA-1/PVAc-4 (0.4 μg/μL) composite film exhibited a good logarithmic relation (0.9988) with relative humidity (RH) over a wide range (11 %–97 %) and high sensitivity (24.55 Hz/%RH). Moreover, this study introduces a novel, eco-friendly approach by integrating the CuA/PVAc composite with a quartz crystal microbalance (QCM) sensor and a sophisticated wireless circuit that enables real-time, Wi-Fi-based humidity monitoring tailored for the preservation of Chinese herbal medicines. The implementation of this wireless humidity detection system represents a significant advancement in the application of environmentally friendly materials in sensor technology and offers a practical and scalable approach for precise environmental monitoring.

Evaluation of analytical uncertainty in quantitative determination of elements - The case of boron

BackgroundThe uncertainty including accuracy and precision is the most vital factor that determines the overall quality of quantitative analysis. The uncertainty has been, however, evaluated relatively within the same analytical technique. Given this background, the present study evaluates the uncertainty on quantitative elemental analysis with a quasi-absolute approach. The objectives of this study are (1) to investigate the analytical uncertainty of prompt gamma-ray analysis (PGA), a chemical interference-free method in principle, on the quantitative analysis of boron and (2) to evaluate the applicability of inductively coupled plasma optical emission spectrometry (ICP-OES), a common technique for quantitative elemental analysis including boron. ResultsPGA provided analytical quantity that is equivalent to the true quantity. The quantity values determined for a series of boron-containing samples are all well above the detection limit of the PGA system, the quantity resolution of which is also much smaller than the minimum difference in quantity among the samples. These facts confirm that the evaluation of analytical uncertainty with the present PGA system is statistically meaningful. The analytical uncertainty in both methods was adequately evaluated by comparing the results from PGA and ICP-OES for a series of boron-containing materials with different physical/chemical properties (i.e. CrB2, B4C, and solidified products of stainless steel-B4C melt) and the major sources of uncertainty in both methods are specified. The conditions for sample preparation/pretreatment were optimized to lower the uncertainty. Significance and noveltyThis study proposes a new concept to perform the quasi-absolute evaluation of analytical uncertainty by employing a chemical interference-free technique. The proposed concept is not limited to the combination of PGA and ICP-OES as demonstrated in this study, but it is applicable to any combination of any analytical methods for any element. Hence, the concept demonstrated in this study could be beneficial to a wide range of analytical chemistry.

A comparative study of Fibre Bragg Grating for spatially and temporally resolved gas temperature measurements in cold atmospheric pressure plasma jets

Abstract Cold atmospheric pressure plasma jets (CAP-Jet) are successfully used in medical ther-apy for healing of chronic wounds and are widely researched in inactivation of patho-gens and in assisting in cancer therapy. A crucial parameter for these plasma applica-tions is that CAP-Jets operate at temperatures that are tolerable for biological tissues. While tools characterizing the plasma's gas temperature are well developed, there are only a few methods that work with an agreeable limit of uncertainty, complexity and limited perturbation properties to accurately determine that the studied plasma jet operates at tissue tolerable temperatures at all times. In the current work, time resolved measurements of the gas temperature in the effluent of a CAP-Jet are performed using the innovative technique of a Fibre Bragg Grating (FBG), in which the temperature dynamics is measured by a shift of the FBGs resonant wavelength through its thermo-optic coefficient. Comparing with other temporal and spatial diagnostic tools such as thermocouple measurement, Schlieren imaging, and optical emission spectroscopy, we demonstrate reliable calorimetric measurements at different plasma duty cycles. The plasma source maintains tissue tolerable temperatures inside the plasma active zone with values below 35°C at 1 cm distance from the jet nozzle. The calorimetric measure-ments have revealed that the heat power dissipation in comparison to electric energy of our plasma source is at least 50%.