Graphite Furnace Atomic Absorption Spectrometry Research Articles

Arsenic, Cadmium, and Lead Levels in School Meals and Their Risk Assessment in Municipalities in Bahia, Brazil

Background: School meals represent a significant supply of nutrients for children in Brazil, especially those in conditions of social vulnerability. Objectives: This study aimed to assess the levels of arsenic (As), cadmium (Cd), and lead (Pb) in meals served in public elementary schools in four municipalities in the state of Bahia, Brazil, and assess the risk posed to children’s health. Methods: Ninety-six samples were collected from 16 schools, freeze-dried, and subjected to microwave-assisted digestion. The As, Cd, and Pb levels were determined by graphite furnace atomic absorption spectrometry. The risk assessment was based on calculating each element’s hazard quotient (HQ). Results: None of the samples reached or exceeded the tolerable levels for the elements analyzed. Pb was the metal that obtained the most significant result, reaching maximum levels of 39–157 µg·kg−1. Conclusions: No element exceeded the PTWI proposed by JECFA; thus, the toxic metal content in school meals poses a negligible risk to children’s health.

A straightforward deep eutectic solvent-based extraction for the determination of lead in drill cuttings by graphite furnace atomic absorption spectrometry

A straightforward deep eutectic solvent-based extraction for the determination of lead in drill cuttings by graphite furnace atomic absorption spectrometry

Phytochemical Characterization, Antioxidant, and Antimicrobial Activity of the Vegetative Buds from Romanian Spruce, Picea abies (L.) H. Karst.

This study aims to investigate the vegetative buds from Picea abies (spruce), naturally found in a central region of Romania, through a comprehensive analysis of the chemical composition to identify bioactive compounds responsible for pharmacological properties. Using HPLC/derivatization technique of GC-MS and quantitative spectrophotometric assays, the phenolic profile, and main components of an ethanolic extract from the buds were investigated. The essential oil was characterized by GC-MS. Moreover, the antioxidant activity with the DPPH method, and the antimicrobial activity were tested. Heavy metal detection was performed by graphite furnace atomic absorption spectrometry. The main components of the alcoholic extract were astragalin, quercetin, kaempferol, shikimic acid, and quinic acid. A total content of 25.32 ± 2.65 mg gallic acid equivalent per gram of dry plant (mg GAE/g DW) and of 10.54 ± 0.083 mg rutin equivalents/g of dry plant (mg RE/g DW) were found. The essential oil had D-limonene, α-cadinol, δ-cadinene, 13-epimanool, and δ-3-carene as predominant components. The spruce vegetative buds exhibited significant antioxidant activity (IC50 of 53 μg/mL) and antimicrobial effects against Staphylococcus aureus. Furthermore, concentrations of heavy metals Pb and Cd were below detection limits, suggesting that the material was free from potentially harmful contaminants. The results confirmed the potential of this indigenous species to be used as a source of compounds with pharmacological utilities.

An updated ecotoxicological evaluation and health risk assessment of metal contaminants in Perna viridis mussel harvested on March to August 2018 from Pasir Gudang Coastal Area, Malaysia

Perna viridis (P. viridis) is a significant protein source globally but is often contaminated by metals due to its filter-feeding behavior. Given that Kampung Pasir Puteh, Pasir Gudang (Johor) is Malaysia's primary P. viridis harvesting site and the last health risk assessment (2015) was incomplete, the metal contamination status remains uncertain. Graphite furnace-atomic absorption spectroscopy was employed to analyze metal contaminant concentrations in P. viridis samples collected from March to August 2018, as per Malaysian legal requirements. The R2 values varied between 0.9976 and 0.9980 for P. viridis mussels and between 0.9976 and 0.9999 for seawater. The recovery for P. viridis mussels and seawater ranged from 93.95% to 106.80% and 92.73–108.84%, respectively. Precision and accuracy for both intra and inter-day measurements ranged from 0.15% to 5.49% for P. viridis and 0.05–5.58% for seawater. The concentrations of metal contaminants in P. viridis varied significantly among the different months of sampling (p < 0.05). All P. viridis samples had higher concentration of arsenic (3.16–75.80 μg g−1) than that prescribed by the Malaysian law. Higher cadmium concentration was observed during July (2.12 μg g−1) and August (2.05 μg g−1) alone. With target hazard quotients and hazard indices > 1.0, the likelihood of negative health impacts from consuming these mussels cannot be ignored. TCR values for As and Cd exceeded USEPA standards, indicating a potential lifetime carcinogenic risk from continuous P. viridis consumption. Pb (21.20–49.28 µg L−1) in all surface seawater samples was invariably higher than the allowable limit for Class 2 water areas. Metal contaminant concentrations varied significantly between P. viridis and surface seawater (p < 0.05), implying inconsistent bioaccumulation due to pollution differences. Given the significance of P. viridis mussels, concerted scientific efforts are essential to devise effective metal contaminant removal methods.

Rapid and sensitive determination of trace Cd in carbonate samples using direct solid sampling electrothermal vaporization atomic absorption spectrometry

The accurate determination of cadmium (Cd) hosted and accumulated in sedimentary carbonate remains challenging due to its low concentration (ng·g−1) and complex matrix. Conventional methods, such as inductively coupled plasma mass spectrometry (ICP-MS) and graphite furnace atomic absorption spectrometry (GF-AAS), which typically rely on liquid sampling and sample digestion, are tedious, labor-intensive and time-consuming. In this study, a rapid and sensitive method for the direct determination of carbonate-hosted Cd was developed based on solid sampling electrothermal atomic absorption spectrometry (SS-ETV-AAS). This method eliminates the need of acid digestion procedure, allowing the entire analysis, including sample preparation, to be completed within 10 min. To minimize the carbonate matrix effect, ethylene diamine tetra acetic acid disodium salt (EDTA-2Na) was proposed as matrix modifier to facilitate the release of Cd, enabling fast and accurate determination of trace Cd in carbonate samples. Under optimized conditions, the Cd detection limits was found to be as low as 0.17 ng·g−1, and repeatability (relative standard deviation, RSD) was better than 8 % (n = 7). The accuracy of the proposed SS-ETV-AAS was verified by analyzing five carbonate certified reference materials (GBW07127, GBW07129, GBW07130, GBW07135 and JDo-1), two soil certified reference materials (GBW07404a, GBW07405), as well as several actual carbonate samples. All these results demonstrate that the proposed SS-ETV-AAS method provides a simple, rapid and sensitive approach for measuring trace Cd in carbonates.

Evaluation of imprecision in the different detection methods of Zn based on 5 years of data from an external quality assessment program in China

BackgroundThis study examines the imprecision of zinc (Zn) measurements across various clinical detection methods by analyzing the external quality assessment (EQA) data from 2018 to 2022. The findings of this study aim to offer recommendations for enhancing Zn measurements. MethodsParticipating laboratories were grouped into peer categories based on the detection methods. The robust mean and coefficient of variation (CV) of the samples were calculated following ISO 13528 guidelines. The evaluation criteria for optimal, desirable, and minimum allowable imprecision in Zn estimation are2.50%, 5.05%, and 7.55%, respectively, based on biological variation. Furthermore, the study examined inter-lab CVs, inter-method bias, and the passing rate. The impact of sample concentration on CVs and the pass rate was also investigated. ResultsOver the past five years, 4,283 laboratories participated in the EQA program, showing a high pass rate that improved as sample concentration increased. Differential pulse polarography (DPP) demonstrated stable and low CVs (0.61–1.86%). Although differential pulse stripping (DPS) was less stable than DPP, it still exhibited a low CV (0.71–3.10%). Graphite furnace atomic absorption spectrometry (GFAAS) and flame atomic absorption spectrometry (FAAS) performed similarly and displayed stable CVs (2.39–4.42%) within the acceptable range of desirable imprecision (5.05%). However, the CVs for ICP-MS were unacceptable in three out of the five years (5.28–6.20%). In 2022, the number of participating laboratories for DDP, DPS, GFAAS, FAAS and ICP-MS is 131, 35, 35, 820 and 72, respectively. ConclusionThis study provides reliable insights into the imprecision of Zn measurements in clinical laboratories. The findings indicate that additional efforts are required to reduce the imprecision of ICP-MS in Zn measurements.

A new method based on extraction induced by emulsion breaking for determination of Co and Ni in chocolate bars by graphite furnace atomic absorption spectrometry

This paper describes a new experimental configuration of extraction induced by emulsion breaking method to extract and determine Ni and Co in chocolate bars by graphite furnace atomic absorption spectrometry. At optimized conditions, the sample (0.08 g) was mixed with 4 mL of extractant solution (4% m/v Triton X-100 and 10% v/v HNO3) in a plastic syringe to form a solid-oil-water emulsion. Then, emulsion breaking was assisted by membrane filtration. The total extraction procedure took approximately 1 min, in opposition to 25 (centrifugation) and 50 min (heating). Extraction yields ranged from 94.8 to 114.3% for Co and from 85.9 to 108.4% for Ni. The limits of detection and quantification were, respectively, 24.73 and 82.45 μg Kg−1 for Co and 49.05 and 163.5 μg Kg−1 for Ni. Recoveries ranged from 92.1 (Ni) to 105.4% (Co).

The Determination and evaluation of trace elements in the blood of radiography workers using graphite furnace atomic absorption spectrometry

This study aimed to evaluate the potentially toxic effects of trace elements in the blood of Iraqi medical radiography workers by analyzing them through GF-AAS. The study involved 50 male blood radiography workers from the medical imaging field at Al-Shatrah General Hospital in Thi-Qar City, Iraq. All workers were aged between 35-50 years and had worked for less than 10 years. The study compared these workers with 50 healthy men. The study found a significant increase in the levels of Cu, Pb, Cd, and Ca among radiography workers compared to the healthy control group, while Zn and Se levels decreased significantly. Moreover, Specificity and confidence interval (95%) were estimated via the receiver operating characteristic curve (ROC). The study provided conclusive evidence of disturbances in the levels of trace elements in the blood of radiographer workers, which makes them more susceptible to many diseases because of their radiation exposure. which portends the more preventive measures of radiation. The linear range of Cd, Cu, Zn, Se and Pb in human serum were obtained 0.2-6.0 µg dL-1, 6.0-200 µg dL-1, 8.0-200 µg dL-1, 10-250 µg dL-1, 4-120 µg dL-1 by GF-AAS after dilution samples with DW up to 20 (n=10, RSD&lt; 5%).

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.

Accumulation and toxicity of biologically produced gold nanoparticles in different types of specialized mammalian cells.

The biologically produced gold nanoparticles (AuNPs) are novel carriers with promising use in targeted tumor therapy. Still, there are no studies regarding the efficacy of nanoparticle internalization by cancer and noncancer cells. In this study, AuNPs were produced by Fusarium oxysporum and analyzed by spectrophotometry, transmission electron microscopy (TEM), energy dispersive x-ray spectroscopy (EDS), and Zetasizer. Obtained AuNPs were about 15nm in size with a zeta potential of -35.8mV. The AuNPs were added to cancer cells (4T1), noncancer cells (NIH/3T3), and macrophages (RAW264.7). The viability decreased in 4T1 (77 ± 3.74%) in contrast to NIH/3T3 and RAW264.7 cells (89 ± 4.9% and 90 ± 3.5%, respectively). The 4T1 cancer cells also showed the highest uptake and accumulation of Au (∼80% of AuNPs was internalized) as determined by graphite furnace atomic absorption spectroscopy. The lowest amount of AuNPs was internalized by the NIH/3T3 cells (∼30%). The NIH/3T3 cells exhibited prominent reorganization of F-actin filaments as examined by confocal microscopy. In RAW264.7, we analyzed the release of proinflammatory cytokines by flow cytometry and we found the AuNP interaction triggered transient secretion of tumor necrosis factor alpha (TNF-α) and interferon gamma (IFN-γ). In summary, we proved the biologically produced AuNPs entered all the tested cell types and triggered cell-specific responses. High AuNP uptake by tumor cells was related to decreased cell viability, while low nanoparticle uptake by fibroblasts triggered F-actin reorganization without remarkable toxicity. Thus, the biologically produced AuNPs hold promising potential as cancer drug carriers and likely require proper surface functionalization to shield phagocytizing cells.

Effects of Low-Level Inorganic Selenium on Selenium Bioaccumulation in Escherichia coli: A Bioanalytical Study Using Graphite Furnace Atomic Absorption Spectrometry (GFAAS)

This study aimed to assess the bioaccumulation of selenite – Se(IV) – and selenate – Se(VI) – in Escherichia coli ATCC 11775 biomass. Escherichia coli cultures were exposed to low selenium concentrations (0.3–30.0 µM), and subsequent effects on growth and viability were evaluated. Selenium content in biomass was quantified using graphite furnace atomic absorption spectroscopy (GFAAS) and inductively coupled plasma mass spectrometry (ICP-MS), with Se recovery assessed through mass balance analysis. The average percentage of bioaccumulated Se exhibited variability depending on the Se species at different concentrations. At a concentration of 30.0 μM, elemental selenium formation emerged within the Se(IV) assay, leading to a significantly higher mean percentage of bioaccumulated selenium for Se(IV) (41.1%) compared to Se(VI) (15.8%). While the mean percentage of bioaccumulated selenium showed no significant variance across the Se(VI) concentrations, a significant difference was observed across the Se(IV) concentrations (ranging from 6.1% to 41.1%). Considering the percentage of Se recovered in the solid and liquid phases, the mass balance ranged from 82.1% to 94.5%. These findings underscore the ability of Escherichia coli ATCC 11775 to accumulate notable quantities of selenium, with the amount of bioaccumulated Se influenced by Se(IV) concentration but not by Se(VI). Furthermore, bacterial viability remained unaffected by selenium species and concentrations. This study contributes valuable insights into the bioaccumulation dynamics of Se(IV) and Se(VI) in non-genetically modified Escherichia coli, shedding light on factors governing selenium accumulation in bacterial biomass, particularly regarding natural biological representation, standardization, comparability, and applicability to environmental studies.

Recent overview of microextraction of metal ions and pharmaceuticals by solidified floating organic drop microextraction techniques

AbstractThis work presents a comprehensive overview of solidified floating organic drop microextraction, with a particular emphasis on its applications in the analysis of heavy metal ions and different pharmaceutical compounds by sample pretreatment, complexation, and their identification by various analytical techniques. Here, we discussed basic principles, procedures, applications of the technique, and effects of different variables like pH, temperature, stirring rate, extraction time, salts addition, extraction solvent and extraction volume, centrifugation speed, and, vortex time on preconcentration. In brief, the review summarises the various modes of solidified floating organic drop microextraction such as dispersive liquid‐liquid microextraction, ultrasound‐assisted, air‐assisted liquid‐liquid microextraction, and vortex‐assisted solidified floating organic drop microextraction. this review covers the methods combined with analytical techniques such as inductively coupled plasma‐optical emission spectrometry, electrothermal atomic absorption spectrometry, flame atomic absorption spectroscopy, graphite furnace atomic absorption spectrometry, electrothermal vaporization inductively coupled plasma mass spectrometry, high‐performance liquid chromatography, and gas chromatography/mass spectrometry. among these, the incorporation of ultrasonic, vortex, and air agitation improves the dispersion mechanism. The coupling of solidified floating organic drop microextraction with other techniques enhances the selectivity and efficiency of the preconcentration procedure. This review provides a potential overview of the fundamental principles, advancements in various modes, influencing factors, and applications of solidified floating organic drop microextraction, showing its potential for advancements in sample preparation and analytical methodologies across various domains.

Silver carboxylate-TiO2/polydimethyl siloxane is a safe and effective antimicrobial with significant wound care potential.

With the rise in antibiotic resistance, new methodologies are needed to combat musculoskeletal infections. Silver is an antimicrobial that can be synthesized in different forms, but its pharmacokinetics are difficult to control. This study details the antibacterial efficacy and cellular cytotoxicity of a formulation consisting of silver carboxylate (AgCar) released through a titanium dioxide/polydimethylsiloxane matrix with a predictable release profile on Pseudomonas aeruginosa, Acinetobacterium baumannii, and human-derived primary osteoblasts. Through an Institutional Animal Care and Use Committee and IRB-approved protocol, AgCar was applied to live Yucatan porcine skin and histologically analyzed for skin penetration. Graphite Furnace Atomic Absorption Spectroscopy (GFAAS) was used to measure elution of AgCar. Dose-response curves were generated through optical density to assess potency. Finally, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay was used to quantify the cellular cytotoxicity of the novel formulation. The results were subject to statistical analysis using analysis of variance and post hoc Tukey tests. The silver carboxylate coating demonstrated deep penetration into the epithelium at the level of the deep pilosebaceous glands in animal models. GFAAS testing demonstrated the extended elution profile of silver carboxylate over 96 hours, while 100% silver with no titanium dioxide-polydimethylsiloxane matrix fully eluted within 48 hours. 10x silver carboxylate demonstrated superior antimicrobial activity to antibiotics and other silver formulations and showed minimal cytotoxicity compared with other silver formulations. Current antimicrobial therapies in wound care and surgical antisepsis, such as chlorhexidine gluconate, have pitfalls including poor skin penetration and short duration of efficacy. The broad antimicrobial activity, extended elution, and deep skin penetration of this AgCar formulation show great promise for surgical site infection and wound care treatment. Novel technology to fight the growing threat of microbial resistance should be at the forefront of orthopaedic surgical site infection prevention and treatment.

Determination of chromium in foodstuffs by using novel adsorbent in vortex assisted-dispersive solid phase micro-extraction method: An application of multivariate techniques

A new graft copolymer composed of polystyrene and polylinoleic acid (PLinas) with the sodium salt of iminodiacetate (Ida) was synthesized and used as an adsorbent. The vortex-assisted dispersive solid-phase micro-extraction (VA-dSPµE) method was used for the extraction and pre-concentration of chromium. Multivariate methodologies, such as factorial design and 3D surface plots, were applied for screening and optimizing effective extraction parameters. The influence of diverse analytical parameters, such as pH, sample volume, and interfering ions, on the extraction of chromium was studied. The calibration standard curve exhibited a linear range from 0.01 to 0.50 μg L−1. The relative standard deviation and limit of detection were found to be 1.65 % and 0.003 μg L−1, respectively. Extraction recoveries were found in the range of 96 to 99 % by using certified reference materials (CRMs). The adsorbent capacity of PLinas-Ida was found to be 112 mg g−1. The VA-dSPµE method demonstrated its effectiveness in the pre-concentration and determination of chromium within samples of foodstuffs by graphite furnace-atomic absorption spectrometry (GF-AAS).

Microwave Exfoliated Graphene Oxide for Sorption Concentration of Gold and Silver

A method has been reported for determining of Au and Ag in waters using preliminary sorption concentration of these analytes by microwave exfoliated graphene oxide (GO) and quantitative analysis by two-jet arc plasma atomic emission spectrometry (TJP-AES) and graphite furnace atomic absorption spectrometry (GFAAS). The parameters of sorption of analytes such as duration of sorption and pH were optimized for the preliminary concentration of Au and Ag on various carbon sorbents for subsequent TJP-AES and GFAAS analysis. The sorption properties of carbon nanotubes (CNTs), multilayer graphene (MLG) and GO such as sorption capacity and surface area were compared. The content of analytes in sorption materials was defined. The results demonstrated that GO provides the best sorption properties and the use of exfoliated GO for preconcentration decreaces the blank signal from nonselective absorption by 10 to 120 times. The limits of detection (LODs) for Au and Ag are 4·10−1 µg L−1 and 8·10−2 µg L−1 by GFAAS and 5 µg L−1 and 2·10−1 µg L−1 by TJP-AES.

Lead extraction from food samples by combined cloud point-micro solid phase extraction

An economic strategy was investigated for extraction of Pb(II) by merging cloud point extraction (CPE) and micro solid phase extraction (μSPE) using montmorillonite (MMT) as a natural sorbent. In this context, Pb(II) was adsorbed onto MMT as 4-(pyridyl-2-azo)-resorcinol (PAR) complex and transferred into micellar phase of Triton X-114. Subsequently, Pb(II) were eluted from MMT by 0.5 mol L−1 of HNO3 and quantified by graphite furnace atomic absorption spectrometry (GFAAS). The central composite design of response surface methodology was used to study the effects of some experimental parameters such as pH, MMT amount, surfactant concentration, and temperature while the desirability function approach was utilized to define the best conditions for Pb(II) extraction. The calibration curve was linear from 0.02 to 10.0 µg L−1 of and an enrichment factor of 95.6 was obtained for 50.0 mL sample. The limit of detection for was 0.006 µg L−1 and the relative standard deviations for five replicate analysis of 1.0 µg L−1 and 5.0 µg L−1 of Pb(II) were 2.8% and 1.5%, respectively. The method was assessed for its environmental friendliness using the analytical AGREEnness calculator. The applicability of the method were evaluated by determination of Pb(II) in certified reference materials and food samples.

Leaching of catalyst platinum from cured silicone elastomers: A preliminary study for comparing reagents

Addition curing systems involve two-part silicones which require the mixture of a silicone polymer with a catalyst to initiate the cure. Platinum is the most commonly used metal catalyst for addition curing of silicones by hydrosilylation which involves the crosslinking by the addition reaction of silicon hydride species to unsaturated bonds, mainly CC, but also CO or CN double bonds. After crosslinking of the polymers, the platinum catalyst cannot be recovered but remains in the silicone materials throughout the entire product life. In the end, platinum is disposed of together with the silicones and is thus lost to the value chain. The overall objective of this work was to develop a recycling process for the recovery of platinum from addition-cured silicone elastomers. In the first step, this was achieved by efficient digestion methods and by optimizing the leaching processes for exemplary commercial silicone elastomer products. Two different silicone materials were investigated, both of which were crosslinked with a platinum catalyst. The initial Pt content in the tested samples was 12.6 ± 0.2 mg/kg for a commercial silicone impression material and 6.3 ± 0.5 mg/kg for a silicone baking mold, measured by graphite furnace atomic absorption spectrometry (GF-AAS). Samples were first frozen with liquid nitrogen to improve brittleness and then crushed with a simple food processor to obtain a silicone granule. Various acid mixtures, mainly based on sulfuric acid, were investigated as digestion methods in order to extract platinum from the silicone network. These had different effects on the dissolution behavior of silicone samples and the amount of platinum extracted in each case. The amount of platinum leached from the filtrate of the digested samples in each case was measured by ICP-OES to evaluate the efficiency of different leaching mixtures. In addition, the dissolved platinum species present in the solutions was identified by UV/VIS as tetrachloridoplatinate(II) complex. The best platinum leaching results so far were obtained with two methods, both of which used a leaching mixture based on sulfuric acid and hexamethyldisiloxane (M2). In the presence of hydrochloric acid, 9.6 ± 1.6 mg platinum/kg was leached from the silicone impression material and 4.2 ± 0.8 mg platinum/kg from the silicone baking mold. With the additional use of aqua regia instead of hydrochloric acid, 10.4 ± 2.8 mg platinum/kg was extracted from the silicone impression material and 4.8 ± 1.0 mg platinum/kg was extracted from the silicone baking mold. These methods were replicated with n = 3. Using statistical evaluation methods (F-test, t-test, and confidence interval), no significant difference was found between these two best methods. Recovery of platinum(0) from leach mixtures has not yet been achieved due to high dilution and very low platinum concentration in samples and will be part of another study.

Disruption of a three-component solution as a novel strategy for Cu and Ni extraction from vegetable oils for their determination by GF AAS

In this work, we propose a novel approach for extracting Cu and Ni from vegetable oils (which can be expanded to other metals). The method is based on the transference of the analytes to an aqueous acid phase due to the disruption of a three-component solution. The extraction was carried out in two steps. In the first step, a three-component solution was prepared comprising the sample, 1-octanol, and HNO3 solution. Next, the homogeneous system was disrupted by adding 1.0 mL of deionized water, and two phases were formed. The aqueous extract deposited in the bottom of the flask was collected with a micropipette, and Cu and Ni were determined by graphite furnace atomic absorption spectrometry (GF AAS). The developed method presented limits of quantification (LOQ) of 0.25 and 0.17 ng g−1 for Cu and Ni, respectively, and was successfully applied in the analysis of eleven oil samples from different origins.

Interference free ultratrace beryllium determination in alkaline effluents of beryllium processing plants by graphite furnace atomic absorption spectrometry after a novel graphene oxide-assisted dispersive micro solid phase extraction without using a chelating agent

Ultratrace level determination of beryllium is carried out using graphene oxide as a dispersive micro solid phase extractant in alkaline beryllium processing plant effluents.

Boron elemental and isotopic determination via the BF diatomic molecule using high-resolution continuum source graphite furnace molecular absorption spectrometry

A new approach for the elemental and isotopic monitoring of boron via HR CS GFMAS is introduced.