Flame Atomic Absorption Spectrophotometry Research Articles

Microwave-assisted synthesis of γ-alooh nanoflowers as an adsorbent for cadmium removal from domestic wastewater.

In this study, cadmium ions were effectively removed from domestic wastewaters using an adsorptive treatment strategy based on γ-AlOOH nanoflowers. A novel, rapid, and simple procedure was developed for the synthesis of the nanoflowers. Characterization studies were performed using X-ray powder diffraction patterns and scanning electron microscope images. The synthesized nanoflowers were utilized as adsorbent in the batch adsorption experiments. The influential parameters of the adsorption process were optimized, and a flame atomic absorption spectrophotometry (FAAS) system was used to determine maximum percent removal of cadmium ions. Matrix-matched calibration strategy, in which the calibration plot was developed in wastewater medium, was utilized for the accurate and precise quantification of cadmium in the effluent samples. The percentage removal efficiency values were calculated between 84 and 98% for different concentrations of cadmium ions in the wastewater samples. Equilibrium data was fitted to the four different linearization methods of the Langmuir isotherm model, as well as the Freundlich isotherm model and Elovich isotherm model. The best fitting was achieved for the Langmuir model with a high R2 value of 0.9956 and maximum adsorption capacity was calculated as 6.23mg/g.

Assessment of some heavy metals for their potential health implications in the skin whitening creams available in Pakistani cosmetic market

ABSTRACT Skin whitening creams may contain impermissible levels of toxic metals, especially the non-regulated products. The present work aims to check the quality of selected skin whitening products sold in Sargodha, Pakistan for their heavy metals content because these products are in direct and in frequent contact with the skin and mucous membranes causing hazardous effects. Quantification of the metals under study was made using flame atomic absorption spectrophotometry after wet digestion of the samples. The results show that the concentrations of heavy metals are ranked as follows: As (263 ppm) > Pb (26 ppm) > Cr (2 ppm) > Cu (0.7 ppm) > Cd (not detected). The calculated p value of 0.00 (>0.05) depicts a significant difference in the levels of heavy metals in the same creams and for the same metal among different creams. The normality of the data was checked by the Kolmogorov-Smirnov and Shapiro–Wilk tests, while metal-to-metal correlation was determined by the Pearson Correlation Coefficient. Comparison of the results with limitations set by the international regulatory bodies showed that the levels of As, Pb and Cr in these creams are above the safety limits. A strict monitoring is suggested during the manufacturing process to avoid any detrimental effects.

Determination of Trace Elements Content of a Popular Traditional Herbal Medicine Used for Internal Hemorrhoids Treatment in Katsina State, Nigeria

Study’s Excerpt/Novelty Assessment of toxic metal concentrations of a widely used traditional herb in Katsina state, was carried out. Flame atomic absorption spectrophotometry and descriptive statistical analysis was employed in the research. Pb, Cr, and As were found to be beyond WHO/FAO thresholds. Full Abstract There has been an increase in the utilization of traditional herbal drugs for different medications and health care in Katsina state. This is possibly due to the growing need for complementary disease treatment, relative cheapness, availability, and wider distribution. Raw samples of a popularly used traditional herb (locally named - Dan Lambar Rimi) were purchased from local markets, prepared, and analyzed using a flame atomic absorption spectrophotometer for Pb, Cr, As, Co, Ni, and Cd concentrations. The obtained concentrations were then summarized using descriptive statistics in SPSS Version 27. The results for the elements analyzed were Ni (0.83 ± 0.15), Cd (0.20 ± 0.01), Pb (21.5 ± 6.63), As (2.10 ± 0.70), Cr (2.36 ± 0.37), and Co (1.15 ± 0.22) ppm. Cr, Pb and As concentrations were greater than the WHO/FAO threshold limits for herbal medicines, while that of Cd was within the recommended threshold. Furthermore, the concentrations of these metals (As, Cr, and Pb) were greater than the WHO/FAO acceptable threshold in 50% of the herbal samples analyzed. Therefore, these metals can pose a threat to public health, especially considering the conventional way in which this herbal medicine is used. With deliberate improvement in hygiene during its preparation prior to consumption, the risk will be brought to a minimal. Future studies should perform a detailed chemical risk assessment, especially when we look at the increase in the number of diseases of unknown etiology in the region.

Chemometrics, health and environmental risk assessments of commonly consumed biscuits in Lagos and Ibadan metropolises, Southwestern Nigeria

The United Nations' Agenda 2030 for sustainable development calls, amongst others, for universal action toward ending malnutrition and ensuring healthy living and well-being for all. So, efforts have intensified to attain the sustainable development goal-2 targets on stunting and wasting in children. Reported herein, therefore, is the quantification of metals in biscuits. Biscuits are commonly consumed snacks world-over and have become sources of nourishment for children and adults due to growing sedentary lifestyles and hectic school/work schedules. Nine metals (Pb, Ni, Cu, Co, Zn, Fe, Na, Mg and Ca) were assayed in six biscuit types (crackers, cookies, shortcakes, digestives, cabins and wafers) via wet digestion and flame atomic absorption spectrophotometry, and the ensuing data subjected to multivariate analyses (analysis of variance, Tukey's test, Pearson correlation, and principal component and hierarchical cluster analyses). The highest concentrations of macrominerals were found in the wafers (Ca), crackers (Na) and cabins (Mg) whereas the micronutrients peaked in the cookies (Fe, Zn), crackers (Cu), shortcake (Co) and wafers (Ni), respectively. The metal levels in the sampled biscuits were all safe for consumption, except for Pb at 0.83 ± 0.76–2.3 ± 1.3 mg/kg. Similarly, the health risk assessments of ingesting metals from the biscuits exposed Pb as potentially liable to cause adverse non-carcinogenic and carcinogenic health effects in children (aged 4–20 years) but Co and Ni exhibited borderline non-carcinogenic and carcinogenic health risks, respectively, in children. Gratifyingly, the ecological risk assessments to evaluate the likelihood of wastes, from expired and/or egested potentially toxic metals-contaminated biscuits, to cause damage to ecology were categorized as low. Nonetheless, constant evaluation and monitoring remain germane.

Comparison of Phosphogypsum-Steel Slag-Based cement and Portland cement for stabilization of heavy metals in oil-based drillings cuttings

This research compared Portland cement and Phosphogypsum-Steel Slag-Based (PSSB) cement in terms of their capabilities to stabilize heavy metals (specifically lead and nickel) in Oil-Based Drill Cuttings (OBDC). In the experimental section, the qualitative analysis of heavy metal constituents in OBDC was captured by X-ray Photoelectron Spectroscopy (XPS). Additionally, an acetic acid leaching test was implemented for the heavy metal leaching concentration to evaluate the ceramsite stabilization effect on OBDC. In the simulation phase, cement models, heavy metal ion models, and stabilization models were constructed to explore the stabilization mechanism of heavy metals. Results demonstrated that PSSB cement exhibits superior stabilization effects on OBDC compared to Portland cement. Flame Atomic Absorption Spectrophotometry (FAAS) tests showed that PSSB cement reduced Ni and Pb leaching by 21.87 % and 47.32 %, respectively, compared to Portland cement. In PSSB cement, the diffusion coefficients for Ni and Pb ions were observed to decrease by 42.92 % and 79.63 %, respectively, as revealed through Mean Square Displacement (MSD) analysis. The cohesive energy of PSSB cement was 76.73 % lower than that of Portland cement, and its interaction energies for stabilizing Ni and Pb ions were 59.43 % and 76.22 % lower, respectively, demonstrating greater stability and efficiency in metal stabilization. PSSB cement exhibited lower heavy metal concentration and better structural stability than Portland cement.

Composition of heavy metals in sediment, water, and fish of the Ganga and Yamuna Rivers in two major cities of India.

The rapid industrial development in the Indian capital region has led to significant waste generation, which, despite undergoing treatment prior to disposal, contributes substantially to water body contamination. Given the diverse nature of these wastes and their potential repercussions across the food chain, a study was conducted to evaluate heavy metal contamination levels in the Ganga and Yamuna Rivers of two major cities. Six heavy metals (Pb, Cd, Hg, Cu, Cr, and Zn) were analyzed in fish, water, and sediment samples by utilizing flame atomic absorption spectrophotometry (Avanta Σ) from March 2019 to February 2020. Results revealed distinct heavy metal distribution patterns, with Cr > Zn > Pb > Cu > Cd > Hg in the Ganga River and Zn > Cr > Pb > Cu > Cd > Hg in the Yamuna River for fish samples. Additionally, levels of Hg in Cyprinus carpio and Sperata oar from the Ganga River, and Pb, Cd, Hg, and Cr in Salmophasia bacaila and Mystus cavasius from the Yamuna River exceeded WHO/FAO permissible limits. In water samples, the predominant heavy metal sequences were Pb > Cu > Zn > Cr > Cd > Hg for the Ganga River and Cr > Zn > Pb > Cu > Cd > Hg for the Yamuna River, with Pb, Cr, Zn, and Cd surpassing WHO standards. Sediment analysis revealed varying heavy metal compositions, with Zn > Cr > Pb > Cu > Cd > Hg in the Ganga River and Cr > Zn > Pb > Cu > Cd > Hg in the Yamuna River. While drinking water and fish from the Ganga River were deemed safe for consumption, those from the Yamuna River were not. Given the toxic nature of heavy metals and their detrimental health impacts, regular monitoring and effective management strategies are imperative.

Comparison among native floating aquatic macrophytes for bioconcentration of heavy metals

This work was aimed to show the development of a comparative study of the capability of bioindicators to reveal the presence of heavy metals among species of floating aquatic macrophytes such as Spirodela sp (giant duckweed), Pistia stratiotes (water lettuce), Salvinia sp used as a parameter for bioconcentration factors plant / sediment. We performed a simple sampling at six sites in the region of Pelotas, southern Brazil, in which it was collected sediments and plants. The plants experienced the nitric perchloric acid digestion method, while the sediment suffered pseudo total acid digestion method. The determination of Cr, Cu, Pb and Zn in the extracts was conducted by atomic absorption spectrophotometry in flame. In general, the floating aquatic macrophytes studied showed better bioconcentration factor for metals from the sediment in the following order: Cu>Zn>Pb>Cr. For copper, the figures obtained with Pistia stratiots ranged from 5.7 to 82.8. The BCF for Zn ranged from 3.0 to 11.6 and Salvinia sp. For the Pb bioconcentration factor, it ranged from 5.4 to 0.6 in Spirodela sp. The in situ study showed that all species had high bioaccumulation potential, especially Pistia stratiotes that was employed to remove copper.

Preparation and investigation of green and cheap deep eutectic solvents for determination of essential and toxic metal ions at trace levels in different coffee products

In this research, a vortex-assisted hydrophobic deep eutectic solvent-based dispersive liquid phase microextraction (VA-HDES-DLPME) method was developed to extract some essential (Fe, Mn and Zn) and toxic (Cd and Pb) metal ions from coffee products. After the VA-HDES-DLPME method, the amounts of the metal ions in the HDES-phase were determined by flame atomic absorption spectrophotometry (FAAS). For selective extraction of metal ions, five HDESs (as extraction solvent) were prepared and tested according to the ultrasonic-assisted procedure. Some dispersive solvents were investigated to ensure the dispersion of HDES in the sample solution. In the VA-HDES-DLPME method, heating and centrifugation steps were not required to separate the HDES-phase from the sample solution. Key factors were investigated and optimized to achieve selective and rapid extraction of metal ions. Under optimized conditions, the working range of the VA-HDES-DLPME method for metal ions ranged from 0.03 to 280 μg kg−1. The detection limits of Fe(II), Mn(II), Zn(II), Cd(II), and Pb(II) ions were 0.01, 0.27, 0.02, 0.015, and 0.18 μg kg−1, respectively. Relative standard deviation and extraction recovery for five replicate runs of 5 μg kg−1 of metal ions were in the range of 1.3%–1.9% and 94 ± 4%-98 ± 2%, respectively. Validation of the VA-HDES-DLPME method was tested by studies on three reference materials. In the final step, the VA-HDES-DLPME method was successfully applied to microwave digestion of coffee samples using a standard addition method. The obtained quantitative recoveries showed the good accuracy of the method.

Rapid preconcentration and determination of Co (II) ions in aqueous medium using ultrasound assisted cloud point extraction method

A flame atomic absorption spectrophotometric technique was studied for the preconcentration and determination of of Co2+ ions in trace amounts after ultrasound enhanced enrichment of its 1-(2-pyridylazo)-2-naphthol (PAN) complexes by cloud point extraction. The Co2+ ions were firstly complexed with PAN molecules at pH 4 and the complex transferred to a surfactant (Tergitol NP-7) rich phase with a very small volume under ultrasound waves. The surfactant rich phase was separated and dissolved by 1 mL, 1.0 M HNO3 in ethanol prior to determination of Co2+ concentration by flame atomic absorption spectrophotometry. The optimization steps of ultrasound interaction time, solution pH and surfactant volumes were achieved by response surface methodology (RSM) which is a combination of statistical approaches. Sample volume, PAN concentration and and possible interfering ions were optimized conventionally. The Co2+ ions were extracted only in 150 s at pH 4 quantitatively under optimum conditions (˃95%). The accuracy and validity of developed UA-CPE was granted by employing a certified reference material wastewater UME CRM 1204. The technique was applied to wastewater and natural water with satisfactory results.

Heavy metal contamination and environmental risk assessment: a case study of surface water in the Bahr Mouse stream, East Nile Delta, Egypt

Water, as an indispensable constituent of life, serves as the primary source of sustenance for all living things on Earth. The contamination of surface water with heavy metals poses a significant global health risk to humans, animals, and plants. Sharkiya Governorate, situated in the East Nile Delta region of Egypt, is particularly susceptible to surface water pollution due to various industrial, agricultural, and urban activities. The Bahr Mouse Stream, crucial for providing potable water and supporting irrigation activities in Sharkiya Governorate, caters to a population of approximately 7.7 million inhabitants. Unfortunately, this vital water source is exposed to many illegal encroachments that may cause pollution and deteriorate the water resource quality. In a comprehensive study conducted over two consecutive seasons (2019–2020), a total of 38 surface water samples were taken to assess the quantity of heavy metals in surface water destined for human consumption and other applications, supported by indices and statistics. The assessment utilized flame atomic absorption spectrophotometry to determine the concentration of key heavy metals including iron (Fe), manganese (Mn), cadmium (Cd), copper (Cu), lead (Pb), zinc (Zn), nickel (Ni), cobalt (Co), and chromium (Cr). The calculated mean value of the Water Quality Index (WQI) was found to be 39.1 during the winter season and 28.05 during the summer season. This value suggests that the surface water maintains good quality and is suitable for drinking purposes. Furthermore, the analysis indicated that the concentrations of heavy metals in the study area were below the recommended limits set by the World Health Organization and fell within the safe threshold prescribed by Egyptian legislation. Despite the identification of localized instances of illegal activities in certain areas, such as unauthorized discharges, the findings affirm that the Bahr Mouse stream is devoid of heavy metal pollution. This underscores the importance of continued vigilance and regulatory enforcement to preserve the integrity of these vital water resources.

Analytical Compatibility between Various Techniques for Determining Dissolved Manganese in Produced Water

Petroleum-produced water is the primary effluent generated during the oil extraction process, presenting high flow rates, and containing a series of chemical components that are harmful to the environment, such as dissolved manganese. The proof of metrological compatibility between laboratories and different test methods or techniques is an analytical challenge when complying with environmental laws and regulations, which is the aim of this study. The first step of this study was to compare the results of manganese content in real test samples of produced water between some laboratories that used different test methods, that is, flame atomic absorption spectrophotometry, inductively coupled plasma optical emission spectroscopy, and inductively coupled plasma mass spectrometry. Based on one-way analysis of variance, systematic errors were found. The following step was to visit a specific lab, where one could confirm the relevance of the wavelength parameters, operating conditions for the view configuration, and effects of the saline matrices. Finally, a compatibility assessment between the reference laboratory and a new laboratory, which implemented and validated its analytical methodology based on these analytical adjustments, and the experiences and lessons learned in the previous step, was undertaken by a paired t-test.

Method Development and Optimization of Liquid-Liquid Microextraction Based on the Decomposition of Deep Eutectic Solvent for the Determination of Chromium (VI) in Spinach: Assessment of the Greenness Profile Using Eco-scale, AGREE, and AGREEprep

A simple, effective, and ligandless liquid-liquid microextraction (LLME) procedure based on the decomposition of hydrophobic deep eutectic solvents (HDES) was developed for the separation and pre-concentration of chromium (VI) ions in spinach leaves, before the determination by flame atomic absorption spectrophotometry. In the proposed study, the first stage involved the leaching of chromium (VI) from spinach leaves with 0.1 M Na2CO3, and in the second stage, chromium (VI) extract was preconcentrated with the LLME procedure using a DES prepared from the combination of DL-menthol and formic acid as a chelating agent and extraction solvent. The DES decomposed in an aqueous donor phase resulting in the dispersion of menthol and extraction of Cr (VI) ions. Under optimal experimental conditions, the limits of detection (LOD) and quantification (LOQ) were 0.63 and 2.1 µg L−1, respectively. The relative standard deviation (RSD) was less than 7%, and the pre-concentration factor (PF) was found to be 31.25. The accuracy of the present methodology was tested by recovery experiments. The greenness of the developed method was assessed using three quantitative green metrics tools: Analytical Eco-scale, AGREE, and AGREEprep, with only Analytical Eco-scale qualifying the proposed method as green.

A simple and effective graphene oxide-zinc oxide nanocomposite based solid phase extraction method for the determination of cadmium in tea matrix at trace levels by flame atomic absorption spectrophotometry

In this study, an easy, environmentally friendly and fast approach was introduced for the synthesis of GO-ZnO nanocomposite (NC). Characterization tools including X-ray Diffraction (XRD) and Scanning Electron Microscopy (SEM) were used to verify the synthesized nanomaterial. Afterward, the combination of GO-ZnO NC based dispersive solid phase microextraction (dSPME) and flame atomic absorption spectrophotometry (FAAS) was used to preconcentrate and determine Cd with high precision and accuracy. In the optimization experiments, all parameters that affecting extraction yield were optimized. Limit of quantification (LOQ) and detection (LOD) values for the GO-ZnO NC-dSPME-FAAS system were calculated as 12.76 µg L−1 and 3.83 µg L−1, respectively. In order to check the applicability and accuracy of the developed method, recovery experiments were performed on three different hibiscus tea samples. The percent recovery values calculated from the spike experiments were in the range of 84 – 111%.

Metal concentrations (Fe and Zn) in Macrobrachium amazonicum from Brazilian Amazon rivers

The objective of this work was to analyze the contamination by iron (Fe) and zinc (Zn) in the shrimp Macrobrachcium amazonicum in the region of the mouth of the Amazon River in the State of Amapá, taking into account aquaculture and fishing activities. 90 shrimp were used, 45 females and 45 males of M. amazonicum. The animals (30) were found in three different points, being Mazagão Velho in Mazagão, a community on Ilha de Santana, a district in the Brazilian municipality of Santana and Arquipélago do Bailique. Fe and Zn determinations were performed by conventional flame atomic absorption spectrophotometry. The greatest accumulation of Zn in the organs and the lowest concentration of Zn in the muscle and exoskeleton of M. amazonicum was observed. Fe had the highest accumulation in organs, followed by exoskeleton and muscle. Zn accumulation in male organs was greater than in muscle and exoskeleton while Fe concentrations were greater in organs, followed by exoskeleton and muscle. In females, Zn accumulation was greater in our organs, with no difference between muscle and exoskeleton. According to the present study, to maintain levels of food security, the consumption of freshwater shrimp caught and farmed in Mazagão, Bailique Archipelago and community of Ilha de Santana should be limited to a daily shrimp intake dose of 96. 52 g for Fe and 226.81 g for Zn.

Maternal Serum Copper and Some Metabolic Indexes in Late Second Trimester of Gestational Diabetes Mellitus Pregnancy.

Copper (Cu) is a physiologically important trace element during pregnancy. The study aim is to assess the altered level of serum Cu and its association with some metabolic indexes in Gestational Diabetes Mellitus (GDM). A total of 108 pregnant women (aged 18 - 40, second trimester) are included in the study and divided into two groups (GDM n = 54; pregnant with normal glucose tolerance (NGT), n = 54) after performing a 2-hour 75-g oral glucose tolerance test (OGTT). Maternal blood samples are collected at 26 - 28 gestational week. All biochemical parameters are measured in serum from fasting venous blood. Serum Cu levels are analyzed by flame atomic absorption spectrophotometry (Perkin Elmer AAnalyst 300, USA). Body Mass Index (BMI), insulin sensitivity/resistance, triglyceride-glucose (TyG), TyG-BMI (triglyceride glucose-body mass) indexes are calculated by formulas. The following data were observed: significantly higher levels of serum Cu (p = 0.009), pre-pregnancy BMI (pre-pBMI), BMI at the GDM diagnosis (pBMI), TyG, pregnancy TyG-BMI (pTyG-BMI) p < 0.001, and triglycerides (Tgl) (p = 0.02) in GDM compared to NGT pregnancy. The study presents a positive correlation between serum Cu and pre-pBMI (p < 0.02), pBMI and pTyG-BMI (p < 0.001). Besides, pre-pBMI (mean ≥ 25 kg/m2), pBMI (mean ≥ 30 kg/m2), and pTyG-BMI are associated with 14.5% (OR 1.145, 95% CI: 1.064 - 1.232; p < 0.001), 15.3% (OR 1.153, 95% CI: 1.070 - 1.243; p < 0.001), and 5.9% (OR 1.059, 95% CI: 1.022 - 1.086; p < 0.001) increased risk for GDM development. No association is found between Cu and Tgl levels, fasting plasma glucose e(FPG) and TyG. ROC analysis suggests the serum Cu as a possible risk factor for GDM development. The analysis shows that at a cutoff point of ≥ 31.9 µmol/L, serum Cu presents a sensitivity and specificity of 64.8% and 66.7% in the prediction of GDM development (AUC = 0.659, p < 0.012). After adjustment for maternal age, gestational age, and family predisposition, the odds ratios (ORs) (95% CIs) still show association of Cu levels with increased GDM risk (OR 1.099, 95% CI 1.018 - 1.184, p = 0.013). pTyG-BMI index exhibits a better interaction than TyG index, Tgl, and glucose separately with serum Cu levels where BMI has a mediator's role.

Determination of copper ion at trace levels in apple tea samples by simultaneous complexation and spray assisted microextraction method prior to detection by flame atomic absorption spectrophotometry

In the present study, a green and sensitive analytical method for the determination of copper ion at trace levels in apple tea samples was developed. Simultaneous complexation/extraction of the analyte were achieved by spraying-based fine droplet formation liquid-phase microextraction (SFDF-LPME). Copper ion was complexed with a Schiff base chelating agent called as N,N′-Bis(salicylidene)-1,2-phenylenediamine (BSP). Under the optimum conditions, the developed SFDF-LPME-FAAS and FAAS system were assessed with respect to limit of detection (LOD), limit of quantitation (LOQ), linearity and percent relative standard deviation (%RSD). LOD and LOQ values for SFDF-LPME-FAAS method were found to be 6.0 and 19.9 µg/kg, respectively. Enhancement in calibration sensitivity for developed method was found as 23 folds. In addition, accuracy/suitability of the developed SFDF-LPME-FAAS method were confirmed by spiking experiments. Two different apple tea samples were spiked to different concentration values and percent recovery results from 91.1 and 123.8 % proved the accuracy/suitability of the method.

Phytochemical Screening, Antioxidant Capacity Measurement, and Mineral Content Determination of Thymus vulgaris L. Extracts

The aim of this study was to evaluate the chemical composition and antioxidant activity of Thymus vulgaris L. extracts. T. vulgaris L. is a medicinal plant that has various bioactive compounds. Four different solvents (ethanol, water, ethyl acetate, and chloroform) were used to extract these compounds from the plant. The phytochemical screening of the extracts showed that the ethanolic extract had the highest diversity of compounds, including coumarins, flavonoids, alkaloids, tannins, phenols, carbohydrates, and proteins. The total phenolic and total antioxidant contents of the ethanolic extract were measured by the Folin–Ciocalteu and phosphomolybdenum methods, respectively. The ethanolic extract had a high phenolic content of 77.7 mg gallic acid equivalent/g dry weight, which indicates its potential antioxidant capacity. The mineral content of T. vulgaris L. was also assessed by flame photometry and atomic absorption spectrophotometry after dry digestion. The plant contained five macroelements (K, Na, Ca, Mg, P) and three microelements (Fe, Cu, Zn) in different concentrations. The highest concentration was found for potassium (15259 mg/kg), followed by calcium (5118 mg/kg) and sodium (4793 mg/kg). The lowest concentration was found for phosphorus (1400 mg/kg), which was still higher than the microelements. Among the microelements, zinc had the highest concentration (24.82 mg/kg), followed by iron (17.44 mg/kg) and copper (14.98 mg/kg). The results of this study provide useful information for the users, collectors and practitioners of medicinal plants from polluted areas, as they can evaluate the quality and safety of T. vulgaris L. for human consumption.

The concentration of Pb, Cd, and Sn in vegetables from ex-tin mining land in Bangka, Indonesia

Utilization of ex-tin mining land as agricultural land is thought to have the potential to contribute heavy metals in agricultural products. The research objective was to obtain data on the metal content of Pb, Cd, and Sn in various vegetable crops such as spinach, cucumber, tomato, cayenne pepper, bitter guard, eggplant, pumpkin, and pepper. In addition to obtaining data on bioconcentration factors (BCFs) of metals in various vegetables. Vegetables were obtained from ex-mining vegetable fields in Jelitik Village, Gunung Pelawan, and Rebo Village, and metal measurements used Analytical Flame Atomic Absorption Spectrophotometry (F-AAS) Jena ContrAA 300. The results showed that the Sn metal in all vegetables analyzed ranged from 4.71 -10.86 mg/kg, Pb ranged from 0 – 5.0 mg/kg, and Cd metal was not found in all the vegetables and soil samples analyzed. The highest of Sn was found in spinach, and Pb in pepper. Generally, the Pb, Cd, and Sn content in vegetables still meets the Indonesian National Standard (SNI) No. 7387:2009, because not exceed the recommended quality standards. Soil from the three villages of ex-tin mining is not categorized as polluted with Pb, Cd, and Sn metals because it does not exceed the target values recommended by WHO. The TFs (Transfer Factors) value of metals in all types of vegetables analyzed was < 1, meaning that the ex-tin mining lands in Jelilik Village, Gunung Pelawan, and Rebo Village, Bangka are still relatively safe for growing vegetables because they do not contribute to the pollution of Pb, Cd, Sn.

Concentration of Heavy Metals in Pollen and Bees Osmia bicornis L. in Three Different Habitats in the Łowicz District in Central Poland

The aim of our research was to compare the levels of pollution in different habitats based on the concentrations of heavy metals found in pollen and the organisms of Osmia bicornis L. bees in three habitats: orchards, berry plantations, and urban habitats (near by power plant, landfill, residential areas, and heavy vehicle traffic). The concentration of Ag, Cd, Cu, Fe, Mn, Ni, Pb and Zn were determined. Samples were quantified using flame atomic absorption spectrophotometry (AAS), with evaluations being carried out three times for each sample. Bee nests were also analyzed concerning reproduction and the presence of parasites. There were no significant differences in the content of heavy metals Ag, Cd, Cu, Fe, Mn, Ni, Pb and Zn in pollen samples between the three habitat types. Bee samples differed only in their Zn content, which was significantly higher in orchards (2.67 mg/kg) than urban habitats (0.80 mg/kg) and berry plantation (0.94 mg/kg). Habitat type had no effect on most bee reproductive parameters (percentage of occupied nest tubes, population growth). Our results show that bees pollinating crops in, for example orchards or berry plantations are exposed to heavy metals to a similar extent to those urban areas.

A green and simplified approach for the quantitative and sensitive analysis of heavy metal ions in sea and stream waters

Abstract Elimination of the matrix effect is a major challenge in developing a method for the quantification of heavy metals (HMs) in water samples. In this regard, the current research describes the simultaneous analyses of Cu(II), Cd(II), and Ni(II) ions in water matrices through flame atomic absorption spectrophotometry (FAAS) after preconcentration with carrier element-free co-precipitation (CEFC) technique by the help of an organic co-precipitant, 3-{[5-(4-Chlorobenzyl)-3-(4-chlorophenyl)-1H-1,2,4-triazol-1-yl]-methyl}-4-[2,4-(dichlorobenzylidene)amino]-1H-1,2,4-triazole-5(4H)-thione (CCMBATT). Based on our literature research, CCMBATT was employed for the first time in this study as an organic co-precipitant for the preconcentration of HMs. Factors such as solution pH, concentration of co-precipitant, sample volume, standing time, centrifugation rate, and time were thoroughly examined and optimized to achieve the highest efficiency in terms of HM recovery. The limits of detection (LODs) (with 10 number of tests) of 0.54, 0.34, and 1.95 μg L−1 and the relative standard deviations (RSD %) of 2.1, 3.3, and 3.0 were determined for Cu(II), Cd(II) and Ni(II) ions, respectively. Recovery results of HMs for the spiked samples were in the range of 92.8–101.0%, demonstrating the trueness of the method and its applicability to the water samples matrix.