Coupled Plasma Optical Emission Spectrometry Research Articles

Impact of industrial effluent on selected grass species

Industrial wastewater contains a variety of substances such as organic carbon, salts and heavy metals, which along with arsenic (As), cadmium (Cd), lead (Pb) and nickel (Ni) are known to be highly toxic even in very low concentrations. This study was carried out to test the impact of industrial effluent from the Industrial Estate Islamabad, the capital city of Pakistan, on four local grass species of the Pothohar region, i.e., Panicum maximum (Mombasa grass), Cenchrus ciliaris (Dhaman grass), Cynodon dactylon (Khabbal grass) and Chloris gayana (Rhodes grass). These grasses were grown in tap water (T0), industrial effluent (T1), and in industrial effluent-tap water ratio (50:50; T2). The concentrations of As, Cd, Pb, and Ni accumulated by these grasses were appraised with inductively coupled plasma optical emission spectrometry (ICP-OES). All four grasses differed significantly in terms of their accumulation of different types of metal elements in the shoot and root organs. The analysis of industrial effluent, and root and shoot biomass samples of all four grasses did not have high amounts of heavy metals with reference to the levels of the metals documented by WHO. It is generally recommended that the effluents from the Industrial Estate Islamabad can be used with some caution for growing forage grasses including the four species tested in this study.

Analysis of Zinc and Copper Content in Selected Tissues and Organs of Wild Mallard Ducks (Anas platyrhynchos L.) in Poland

The research material included selected muscles and liver of mallard ducks obtained in two research areas. A total of 28 mallards were obtained for the study—six males and six females from the Siedlce hunting district and eight males and eight females from the Leszno hunting district. Zinc and copper concentrations were determined by inductively coupled plasma optical emission spectrometry (ICP OES). It was concluded from the study that the Leszno hunting district is more polluted than the Siedlce hunting district. Among the examined tissues of mallard ducks from both hunting districts, the highest content of zinc and copper was found in the liver. In this organ, birds shot in the Leszno hunting district were characterized by a significantly higher content of these elements compared to birds shot in the Siedlce hunting area. The significantly higher average zinc and copper concentrations in the liver of mallards harvested in this hunting district may have been influenced by fertilization of crop fields in this area with fertilizers containing these elements and by extraction of ore containing zinc and copper minerals in the Legnica-Głogów Copper District. This is an important problem with regard to the safety of consumers of game meat. It was shown that the tissues of male mallards were characterized by higher average levels of zinc and copper than those of females, but the differences were statistically significant only in the case of the average copper content in the leg muscles.

Ensuring the Quality of the Analytical Process in a Research Laboratory

This paper discusses approaches for verification of methods of measurements of chemical and physical characteristics of specific samples. The limitations of well-known approaches are discussed. Some examples of alternatives are given to demonstrate specific issues encountered in the research laboratory analyzing new materials or characterizing new properties of materials. Application of sequential procedure using lower quantities of samples and reagents is presented. A standard addition to solid samples is discussed. The approach of control charts for estimation of method uncertainty for determination of plant available phosphorus is presented. The method comparison is applied as an approach to verification of alkaline reactivity by inductively coupled plasma–optical emission spectroscopy (ICP-OES) measurement, as well as density of newly synthesized chalcogenide glass materials. The presented examples demonstrated that alternative approaches are needed in order to verify the methods applied due to the great variety of activities and corresponding tasks in a research laboratory.

Effect of bioceramic powder abrasion on different implant surfaces.

Bioceramic coatings have been shown to promote bone repair, which aids in the early integration of implants. This study aimed to evaluate the influence of air abrasion with a bioceramic abrasive on the surface characteristics of different implant materials and surfaces. The dissolution of the applied treatment from the surfaces over 3 weeks was also assessed. Discs of three alloys used for dental implants were studied and compared: two types of commercially pure titanium (CpTi)/ (CpTi SLActive) and titanium-zirconia (TiZr). The tested surfaces were: CpTi control (CpC), sandblasted (SB), sandblasted and acid-etched (SBE), and CpTi SLActive®, (TiZr) Roxolid®. Three discs from each group underwent air abrasion with apatite bioceramic powders, 95% hydroxyapatite (HA)/5% calcium oxide (CaO), and 90% hydroxyapatite (HA)/10% calcium oxide (CaO). The treated discs were surface characterized by optical profilometry to obtain surface roughness, scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDS) to compare element weight percentages of titanium, calcium, and phosphate. Dissolution was assessed using inductively coupled plasma optic emission spectrometry (ICP-OES). Bioceramic powders were deposited on all tested surfaces leading to changes in surface characteristics. The only statistically significant differences between the material groups for surface roughness were found with 95% HA/5% CaO powder in the Sp and Rp parameters (p = 0.03 and 0.04, respectively). There were no significant differences in the Ca and P wt% between all groups and powders 95% HA/5% CaO and 90% HA/10% CaO (p = 0.14, 0.18, and p = 0.15, 0.12, respectively). A non-uniform dispersion of the treatment on the surface layer was visible on all treated surfaces. The bioceramic powder continued to dissolute from the tested surfaces for 3 weeks. Bioceramic abrasion modifies implant surface characteristics, although the change in surface characteristics resulting from such treatment was not influenced by the implant material or surface treatment. Air abrasion with hydroxyapatite and calcium oxide bioceramics leaves powder deposits on the treated implant surfaces that could potentially influence the healing of implants affected by peri-implantitis.

Discrimination of geographical origin of Korean and Chinese red pepper paste via inductively coupled plasma atomic emission spectroscopy and mass spectrometry

BackgroundRed pepper paste is a common ingredient used in food in Korea. The discrimination of the geographical origin of agricultural products is important to protect the agricultural industry and customers from the misinformation regarding the product origin. Several studies have attempted to identify the geographical origin of red pepper based on its characteristic features using diverse methods, such as inorganic elemental analysis. However, similar studies on red pepper pastes have not been conducted thus far.ResultsIn, this study, we established methods based on inductively coupled plasma optical emission spectrometry (ICP-AES) and inductively coupled plasma mass spectrometry (ICP-MS) for determining inorganic elements in red pepper pastes. The limit of detection (LOD) of ICP-AES was in the range of 0.006–0.531 mg∙kg−1 and the limit of quantification (LOQ) was 0.017–1.593 mg∙kg−1. In addition, LOD and LOQ ranges for ICP-MS were 0.001–1.553, and 0.002–5.176 μg∙kg−1, respectively. The concentrations of Ca, K, Mg, Na, P, S, Cr, Mn, Co, Ni, Cu, Ga, As, Sr, Zr, Mo, Pd, Cd, Sn, Sb, Ce, Pt, Pb, and U were high in the Korean red pepper paste. All the employed discrimination models could clearly distinguish between Korean and Chinese red pepper pastes. In particular, among the four different models, CDA showed the most accurate ability to discriminate the geological origin of Korean and Chinese red pepper paste compared to that achieved using the other models with 100% accuracy.ConclusionsBased on, the findings of this study, the use of ICP-AES and ICP-MS analyses for discriminating the inorganic elements in food products in combination with the aforementioned statistical analysis models could help the mitigation of issues associated with the misinformation of the geographical origin of agricultural products, aiding customer protection.Graphical

Blood Concentration of Macro- and Microelements in Women Who Are Overweight/Obesity and Their Associations with Serum Biochemistry

Risk elements in blood matrices can affect human health status through associations with biomarkers at multiple levels. The aim of this study was to analyze 15 macro- and microelements in the blood serum of women with overweight (BMI of ≥25 kg/m2) and obesity (BMI of ≥30 kg/m2) and to examine possible associations with biochemical, liver enzymatic parameters, and markers of oxidative stress. Based on the power calculation, the study involved women (in the postmenopausal stage) whom are overweight (n = 26) and obese (n = 22), aged between 50–65 years. Multifrequency bioelectrical impedance analysis was used to measure body composition parameters. Concentrations of elements were determined by inductively coupled plasma optical emission spectrometry, and Hg was measured using cold-vapor atomic absorption spectroscopy. Individuals with obesity, as indicated by a higher BMI, percentage of body fat, and visceral fat area, had elevated serum levels of Ca, Mg, Fe, Al, Sr, Pb, and Hg. Concentrations of Al, Cu, K, Sb, Zn, and Pb significantly affected biochemical and liver function markers in women who were overweight or obese. Elements such as Cu and Al were associated with increased total cholesterol. The correlation analysis between total antioxidant status and Cu, Al, and Ni confirmed associations in both groups. Our findings underscore the importance of addressing excess body weight and obesity in relation to risk elements. The results of the research could be beneficial in identifying potential targets for the treatment or prevention of comorbidities in people with obesity.

Eco-friendly synthesis of fluorescent cobalt-doped manganese ferrites for thermo-therapeutic applications

The synthesis of high-quality nanoparticles for biomedical applications through environmentally friendly methods is a major challenging task. In this work, oxidative precipitation and a novel method, oxidative hydrothermal synthesis, are explored as one-pot eco-friendly synthesis routes to obtain single phase multicore-like and single-core citrate-stabilized cobalt and/or manganese-doped ferrite (CoxMn1-xFe2O4, 0 ≤ x ≤ 1) nanoparticles, respectively. The Co2+/Mn2+ ratio and synthesis method were found to influence the nanoparticles' morphology and structure, with oxidative precipitation producing multicore-like structures and hydrothermal synthesis yielding single-core particles with crystalline sizes in the range of 2 − 10 nm and 4 − 11 nm, respectively. Inductively coupled plasma optical emission spectrometry (ICP-OES) indicated a composition near the expected values. Mixed ferrites displayed improved saturation magnetization up to 60 A.m2/kg, exhibiting superparamagnetism at room temperature. The particles’ stability was evaluated in physiological pH, and the mixed ferrites displayed intrinsic fluorescence emission in the violet-green range with a maximum wavelength near 425 nm. The cobalt and/or manganese-doped ferrites were evaluated for magnetic hyperthermia and photothermia, displaying high heating efficiency for several alternating magnetic field conditions (up to ∼2.5 nHm2/kg) compatible with biological applications, and high light-to-heat conversion efficiency (up to ∼53%) with near infrared (NIR) laser irradiation at 808 nm. Hereby, the oxidative precipitation and oxidative hydrothermal synthesis are promising eco-friendly methods for the development of crystalline citrate-stabilized cobalt and/or manganese-doped ferrites with multicore-like and single-core spherical morphology, respectively, without requiring additional post-synthesis treatments and with suitable properties for biomedical applications, such as magnetic hyperthermia, photothermia and as prospective fluorescent probes for bio-imaging.

Assessment of potentially toxic and mineral elements in paddy soils and their uptake by rice (Oryza sativa L.) with associated health hazards in district Malakand, Pakistan

Rice, a primary food source in many countries of the world accumulate potentially harmful elements which pose a significant health hazard to consumers. The current study aimed to evaluate potentially toxic and mineral elements in both paddy soils and rice grains associated with allied health risks in Malakand, Pakistan. Rice plants with intact root soil were randomly collected from paddy fields and analyzed for mineral and potentially toxic elements (PTEs) through inductively coupled plasma optical emission spectrometry (ICP‒OES). Through deterministic and probabilistic risk assessment models, the daily intake of PTEs with allied health risks from consumption of rice were estimated for children and adults. The results of soil pH (<8.5) and electrical conductivity (EC > 400 μs/cm), indicated slightly saline nature. The mean phosphorus concentration of 291.50 (mg/kg) in soil samples exceeded FAO/WHO permissible limits. The normalized variation matrix of soil pH with respect to Ni (0.05), Ca (0.05), EC (0.08), and Mg (0.09), indicated significant influence of pH on PTEs mobility. In rice grains, the mean concentrations (mg/kg) of Mg (463.81), Al (70.40), As (1.23), Cr (12.53), Cu (36.07), Fe (144.32), Mn (13.89), and Ni (1.60) exceeded FAO/WHO safety limits. The transfer factor >1 for K, Cu, P and Zn indicated bioavailability and transfer of these elements from soil to rice grains. Monte Carlo simulations of hazard index >1 for Cr, Zn, As, and Cu with certainties of 89.93% and 90.17%, indicated significant noncarcinogenic risks for children and adults from rice consumption. The total carcinogenic risk (TCR) for adults and children exceeded the USEPA acceptable limits of 1.0E-06 and 1.0E-04, respectively. The sensitivity analysis showed that the ingestion rate was a key risk factor. Arsenic (As) primarily influenced total cancer risk (TCR) in children, while chromium (Cr) significantly impacted adults. Deterministic cancer risk values slightly exceeded probabilistic values due to inherent uncertainties in deterministic analysis. Rice consumption poses health risks, mainly from exposure to Cr, Ni and As in the investigated area.

Preparation and evaluation of magnetic iron oxide-MgCeAl lamellar composite-TiO2 in the photocatalytic degradation of methylene blue dye

A new photocatalyst prepared from ternary lamellar double hydroxides (Mg, Ce, Al) by coprecipitation method and impregnated with TiO2 and magnetic properties was successfully synthesized. Different molar ratios between the trivalent cations were used, varying the proportion of Ce3+ in the Ce3+/(Ce3++Al3+) ratio. The synergistic effect between Ce3+ and TiO2 led to a significant increase in the photocatalytic and kinetic activity of MgCeAl-TiO2 for the photodegradation of the dye Methylene Blue (MB) at a concentration of 20mgL-1, using UV-visible radiation (filter cut-off for λ > 300nm). The materials studied were characterized by the techniques of IR Spectroscopy (FT-IR), Raman Spectroscopy, X-Ray Diffraction (XRD), Energy Dispersive Spectroscopy (EDS), Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES), Scanning Electron Microscope (SEM), determination of Zeta Potential and Differential Pulse Voltammetry (DPV). The synthesized photocatalyst that showed the highest efficiency was the one with a composition of Ce3+ = 5% and Al3+ = 95%, besides having 5% of its weight composed of magnetic iron oxide (5Fe/MgCe5Al-TiO2), presenting high photocatalytic activity, completely degrading (~100%) the dye in the time of 90minutes.

Evaluation of Heavy Metal Concentrations in Enzyme Embedded Poly Lactic Acid (EPLA) by ICP-OES: Lipase from Candida Rugosa.

Abstract: Enzymes like lipases are essential for catalyzing important reactions in the fields of biotechnology and industrial operations. For quality control and safety evaluations, however, the quantification of these contaminants is crucial because the presence of heavy metals in enzyme preparations can negatively affect their activity and stability. Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES), a key component of this investigation, is used to measure the levels of heavy metals in lipase enzyme preparations embedded in polylactic acid (PLA). The lipase enzyme being studied comes from Candida rugosa, which is well-known for its considerable industrial applications. According to preliminary findings, the lipase enzyme is successfully protected from external heavy metal pollutants by the encapsulating technique, maintaining its enzymatic activity and stability. The lipase-PLA composite had only minimal quantities of heavy metals, according to the ICP-OES study. The research's conclusions show great potential for the creation of reliable and contaminant-free lipase enzyme preparations, which will increase their suitability for usage in a variety of industrial processes and encourage the use of biodegradable polymers, supporting environmental sustainability. By highlighting the significance of quality control and safety assessment through the determination of heavy metal concentrations, this research contributes to the larger field of enzyme biotechnology. It also highlights the potential of Candida Rugosa lipase implanted in PLA matrices for eco-friendly and sustainable biocatalytic applications in sectors ranging from food and pharmaceuticals to biofuel generation and other biodegradable polymers.

STUDIES TO ESTABLISH THE SCALING FACTOR METHODOLOGY FOR LIQUID RADIOACTIVE WASTE GENERATED BY TRIGA REACTOR

During TRIGA reactor operation significant amounts of liquid radioactive waste are generated requiring appropriate management to ensure their safe disposal. Radiological characterization is an important activity needed to accomplish the waste acceptance criteria for different management steps including disposal. The purpose of this paper is to assess the activity concentrations of the (_1^3)H , (_38^90)Sr, (_28^63)Ni (difficult-to-measure), and gamma emitters (easy-to-measure) radionuclides in liquid radioactive waste generated by the TRIGA reactor operation and to establish a correlation among them to determine the scaling factors for this waste category. The radiological protocols applied for (_28^63)Ni and (_38^90)Sr, separation and purification involve extraction chromatography using selective resins, while for (_1^3)H separation the distillation technique was applied. The assessment of gamma emitters was carried out using gamma-ray spectrometry and the detection of (_1^3)H , (_38^90)Sr, and (_28^63)Ni was performed by liquid scintillation counting. The chemical yield of each experiment was determined by measuring the carrier added in each test by inductively coupled plasma optical emission spectrometry. The activity concentrations of (_38^90)Sr, and (_28^63)Ni obtained were correlated with the activity concentration of (_27^60)Co for establishing the scaling factor for the liquid radioactive waste stream. There were obtained good correlations but more experimental data are needed to determine the relevant scaling factors for these difficult-to-measure radionuclides. The scaling factors, once established, will improve and optimize the radiological characterization methodology applied for liquid radioactive waste as an easy and rapid method for assessment of concentration activities of difficult-to-measure radionuclides. Until now, no scaling factors data were reported for this liquid radioactive waste generated by TRIGA reactor operated by Institute for Nuclear Research Pitesti. The results obtained in this work represent preliminary data for establishing correlations between difficult-to-measure and easy-to-measure radionuclides and will be used for developing a scaling factor methodology. This will further be used to determine the inventory of difficult-to-measure radionuclides in different waste streams generated by TRIGA operation and decommissioning (foreseen after 2035).

Exploring the Nutritional and Bioactive Potential of Olive Leaf Residues: A Focus on Minerals and Polyphenols in the Context of Spain's Olive Oil Production.

Lyophilized plant-origin extracts are rich in highly potent antioxidant polyphenols. In order to incorporate them into food products, it is necessary to protect these phytochemicals from atmospheric factors such as heat, light, moisture, or pH, and to enhance their bioavailability due to their low solubility. To address these challenges, recent studies have focused on the development of encapsulation techniques for antioxidant compounds within polymeric structures. In this study, lyophilized olive leaf extracts were microencapsulated with the aim of overcoming the aforementioned challenges. The method used for the preparation of the studied microparticles involves external ionic gelation carried out within a water-oil (W/O) emulsion at room temperature. HPLC analysis demonstrates a high content of polyphenols, with 90% of the bioactive compounds encapsulated. Meanwhile, quantification by inductively coupled plasma optical emission spectroscopy (ICP-OES) reveals that the dried leaves, lyophilized extract, and microencapsulated form contain satisfactory levels of macro- and micro-minerals (calcium, potassium, sodium). The microencapsulation technique could be a novel strategy to harness the polyphenols and minerals of olive leaves, thus enriching food products and leveraging the antioxidant properties of the polyphenolic compounds found in the lyophilized extract.

Nutritional profile and risk assessment of inorganic elements in enteral and parenteral nutrition formulas

The contents of essential (Ca, Fe, K, Na, P, and Zn) and potentially toxic inorganic elements (As, Al, Cd, Cr, Cu, Mn, and Pb) in enteral and parenteral nutrition formulas were evaluated by inductively coupled plasma optical emission spectrometry (ICP OES) and graphite furnace atomic absorption spectrometry (GFAAS). A total of 30 enteral formulas, 23 parenteral solution components, and 3 parenteral solutions were analyzed. The elements Ca and K presented the higher contents (72–2918 mg L−1 and 235–2760 mg L−1) while the lowest concentration levels were found for As and Cd (<0.68 µg L−1 and <0.01–0.62 µg L−1) in the studied samples. The validated analytical methods presented an accuracy of 75–116% and RSD values lower than 9.8%. Calcium gluconate and magnesium sulfate, which are used as raw materials in parenteral solution, are potential sources of Al and Mn contamination. A Hazard Quotient (HQ) >1 was obtained for Al (27 ± 1 µg L−1) in one of the parenteral samples, whereas the established limit is 25 µg L−1. Enteral samples were considered safe for consumption regarding the Al, As, and Cd levels. One healing-specific and pediatric formula contained Pb at levels above 0.25 µg kg-day−1, too high for safe consumption. The enteral formulas (pediatric, diabetes-specific, renal-specific, healing-specific, and standard formula with addition of fiber) presented risks in relation to the consumption of Cr and Mn (>250 µg day−1 and >11 mg day−1). The results indicate the need for strict monitoring, considering that these formulations are often the single patient’s food source.

Separation and Characterization of Nickel Hydroxide from Waste Solution Using Ca(OH)2 Precipitation in Chloride Media

Nickel hydroxide (Ni(OH)2) is a valuable compound derived from nickel, widely utilized across various fields because of its versatile properties. This study aimed to characterize as-prepared β-Ni(OH)2 via chemical precipitation using various analytical techniques. X-ray diffraction (XRD) analysis confirmed the formation of a β-Ni(OH)2 hexagonal crystalline structure, validating the successful precipitation. Fourier-transform infrared spectroscopy (FTIR) spectra exhibited main characteristic peaks of (υOH) and υ(NiO), corresponding to the formation of nickel hydroxide (Ni(OH)2). Subsequently, X-ray photoelectron spectroscopy (XPS) revealed a prominent peak for Ni2+ oxidation, confirming the successful precipitation of nickel hydroxide at pH 6.5, which identifies the existence of impurities, such as chlorine and calcium, from the waste matrix. Scanning electron microscopy (SEM) micrographs demonstrated stratified granules with a nearly pure brucite crystalline phase, typical of β-Ni(OH)2. Furthermore, the surface morphology revealed a coarse texture and uneven clustering, suggesting possible elevated oxide levels on the Ni surface. Energy-dispersive X-ray spectroscopy (EDX) confirmed the presence of nickel (Ni) and oxygen (O), with Ca impurities attributed to the chemical precipitation process. Particle size distribution analysis estimated an average particle size of 2.0 µm. Additionally, the precipitation of nickel was investigated using inductively coupled plasma optical emission spectroscopy (ICP-OES). Ni was observed in decreasing order, 62.7 g/L, 0.8 g/L, and 0.501 g/L in the pregnant leach, precursor solution, and solid precipitate (cake), respectively. The separation of Ni(OH)2 through the precipitation process from the waste (acidic chloride media) enabled efficient recycling and re-use of nickel, which provides a cost-effective and environmentally friendly method for the highly efficient utilization of waste (acidic chloride media).

Innovative recycling of high purity silver from silicon solar cells by acid leaching and ultrasonication

Precious and scarce silver (Ag) is used as a front electrical contact in silicon solar panels. With massive amounts of solar panel waste coming to end-of-life, it is imperative to recover all the Ag from these modules. In this paper, we propose a novel method to easily reclaim Ag from end-of-life silicon solar cells using low concentration sulfuric acid (H2SO4) leaching followed by ultrasonication. Our process simplifies the Ag recycling procedure by directly recovering the Ag contacts from solar cells, eliminating the need for secondary precipitation/electrodeposition. First, scanning electron microscopy (SEM) with energy dispersive X-ray spectroscopy (EDX) and X-ray photoelectron spectroscopy (XPS) was used to study the leaching and ultrasonication process on rejected solar wafers. Next, a solar panel from landfill was heated in a furnace to burn off the polymer encapsulant. The silicon wafers were then collected from the burning process and leached in 2 M H2SO4 at two different shaking speeds for 48 h at room temperature. Finally, the end-of-life silicon wafer pieces were collected, sonicated in water, and then the sonication water was centrifuged to show a proof-of-concept to recover the Ag contacts. Inductively coupled plasma optical emission spectroscopy (ICPOES) is used to monitor dissolved elements in the leachate as a function of time and shaking speed. XPS is used to evaluate the composition of the silicon cell wafer surface before and after H2SO4 leaching. SEM is used to image the recovered Ag contacts morphology and EDX confirms the recovered particles contain high amounts of Ag. A proposed schematic illustrates the authors’ hypothesis for the peeling mechanism.

Role of Salt Concentration in Stabilizing Charged Ni-Rich Cathode Interfaces in Li-Ion Batteries.

The cathode-electrolyte interphase (CEI) in Li-ion batteries plays a key role in suppressing undesired side reactions while facilitating Li-ion transport. Ni-rich layered cathode materials offer improved energy densities, but their high interfacial reactivities can negatively impact the cycle life and rate performance. Here we investigate the role of electrolyte salt concentration, specifically LiPF6 (0.5-5 m), in altering the interfacial reactivity of charged LiN0.8Mn0.1Co0.1O2 (NMC811) cathodes in standard carbonate-based electrolytes (EC/EMC vol %/vol % 3:7). Extended potential holds of NMC811/Li4Ti5O12 (LTO) cells reveal that the parasitic electrolyte oxidation currents observed are strongly dependent on the electrolyte salt concentration. X-ray photoelectron and absorption spectroscopy (XPS/XAS) reveal that a thicker LixPOyFz-/LiF-rich CEI is formed in the higher concentration electrolytes. This suppresses reactions with solvent molecules resulting in a thinner, or less-dense, reduced surface layer (RSL) with lower charge transfer resistance and lower oxidation currents at high potentials. The thicker CEI also limits access of acidic species to the RSL suppressing transition-metal dissolution into the electrolyte, as confirmed by nuclear magnetic resonance (NMR) spectroscopy and inductively coupled plasma optical emission spectroscopy (ICP-OES). This provides insight into the main degradation processes occurring at Ni-rich cathode interfaces in contact with carbonate-based electrolytes and how electrolyte formulation can help to mitigate these.

Catalytic conversion of crude oil to hydrogen by a one-step process via steam reforming

This work presents a multi-functional NiCoCe-based catalyst for crude oil steam reforming for hydrogen production. Arab Light (AL) and Arab Extra Light (AXL) were centrifuged to reduce the asphaltenes and sequentially steam reformed in a fixed bed reactor. Results showed that the NiCoCe catalyst was stable and highly selective under reaction conditions and in cyclic operation. The physicochemical properties of the catalyst were determined via inductively coupled plasma–optical emission spectrometry, X-ray diffraction, transmission electron microscopy, and scanning electron microscopy. The high dispersion of the NiCo alloy on a Mg–Al support was crucial for ensuring the hydrocarbon reforming in the presence of heteroatomic species.

A Simple Method to Determine Low Metal Concentrations in Naphtha by Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES)

A Simple Method to Determine Low Metal Concentrations in Naphtha by Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES)

Catalytic Transformation of Nitroarenes to Amines over Ba(1-x)SrxTiO3 (0 < x < 1) Perovskites in Water.

This work is focused on the application of lanthanide-free perovskite Ba1-xSrxTiO3 (0 < x < 1) in valorization of toxic pollutants as 4-nitrophenol (4-NPh). The series of perovskites were fabricated by facile, one-step solid-state preparation method and characterized via various techniques: elemental analysis (Inductively Coupled Plasma Optical Emission Spectrometry, ICP-OES), powder X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR) and dielectric properties (impedance spectroscopy, IS). The methods confirmed the assumed composition, structure and high purity of the materials. The results showed that substitution of Ba2+ by Sr2+ in the perovskite crystal lattice influenced the dielectric properties of samples and the size of the grains. The absorption and catalytic properties of Ba(1-x)SrxTiO3 (0 < x < 1) series were evaluated in reduction of 4-NPh in water using NaBH4 as reducing agent. No adsorption of 4-NPh was found for all the materials during 180 min of contact (experiment without reducing agent), and the best catalytic performance was found for the Ba(1-x)SrxTiO3 (x = 0.3) sample. The catalytic transformation of 4-NPh to 4-APh follows a pseudo-first-order model, and the catalysts can be easily regenerated via mild annealing (300 °C).

Participatory assessment of pollution and health risk in artisanal and small-scale gold mining communities in Colombia

The predominantly Afro-descendant communities of Yolombó and La Toma depend on the region's rich natural resources through livelihoods such as farming, fishing, and artisanal and small-scale gold mining (ASGM). Previous studies of the region have identified elevated levels of mercury in several surface and groundwater sites. Furthermore, recent regional studies have identified human health risks associated with mercury exposure through hazard quotient (HQ) modeling and global sensitivity and uncertainty analysis (GSUA). However, there has yet to be a comprehensive analysis of water pollution involving different metals and metalloids potentially present in ASGM-influenced areas to estimate the associated environmental and human health impacts. In this study, we employed a participatory methodology to identify sources of exposure in Colombian ASGM communities through surveys, consumption diaries, and interviews. We then screened for relevant metals and metalloids through groundwater analysis using inductively coupled plasma optical emission spectroscopy (ICP-OES) and cold vapor atomic absorption spectrometry (CV-AAS). Furthermore, we calculated water pollution indices, including heavy metal pollution index (HPI), degree of contamination (Cd), heavy metal toxicity load (HMTL) and heavy metal evaluation index (HEI). Finally, we quantified human health risks related to groundwater consumption through the HQ and hazard index (HI). Although the groundwater assessed in this study generally meets United States and Colombian regulatory standards, heightened Fe, Mn, and Al levels were observed. The pollution indices generally agreed that three of the sites tested showed medium to high pollution levels. The HI showed that the combined effect of all metals tested did not substantiate risk for most participants. However, the HI of one participant, a child, exceeded the 1.00 threshold. Furthermore, the presence of Pb, despite meeting regulatory limits, necessitates further scrutiny due to its substantial impact on pollution and human health hazard indices.