Plasma Atomic Emission Spectrometer Research Articles

Evaluation of selected minerals and health risk and proximate analysis of wasawasa (a street food)

This study was carried out to determine the proximate composition and the potential heavy metal health risk that may be associated with the consumption of wasawasa, a dish made from locally milled yam peels, by examining the presence of six metals (iron, nickel, chromium, sodium, and magnesium and potassium) in samples procured. Sixteen (16) samples of ready-to-eat wasawasa were collected from Aboabo, Manhyia, Sawaba, Asawase, Adenyase, and Ayigya in Kumasi, since these are the communities where wasawasa is mainly produced, sold, and consumed. The samples were digested with a nitric, perchloric, and sulfuric acid mixture and analyzed using a microwave plasma atomic emission spectrometer (Agilent 4210 MP-AES). The average concentrations of metals were Na (8506.88 mg/kg), Mg (222.63 mg/kg), Fe (84.45 mg/kg), Cr (2.31 mg/kg), K (1702.08 mg/kg, and Ni (1.12 mg/kg). Proximate analysis was used to determine Protein, fat, ash, moisture, and fiber content of the local wasawasa, which were found to be 15.667 %, 0.45 %, 1.00 %, 27.54 %, and 0.41 %, respectively. The hazard index of the heavy metals (Fe, Ni and Cr) for both adults and children were each greater than one, indicating the population is likely to experience non-carcinogenic effects from the consumption of wasawasa.

Kinetic investigation of dry reforming of methane reaction over Ni–Rh/ZrO2–Al2O3 catalyst using Langmuir-Freundlich isotherm

The study involved conducting kinetic measurements for the dry reforming of methane (DRM) over a Ni–Rh/Al2O3 (85%)-ZrO2(15%) catalyst under a wide range of operating conditions (temperature: 500–900 °C, total flow rate of the inlet feed: 50–100 mL/min). The support material was prepared using the sol-gel method, followed by impregnation of Ni–Rh catalyst on the incipient wetness of the Al2O3–ZrO2 support. The calcined, reduced and spent samples were characterized by X-ray diffraction (XRD), thermal gravimetric analysis (TGA), inductively coupled plasma atomic emission spectrometer (ICP-AES), N2 adsorption/desorption and CHNS analyzer, and tested for activity, yield and stability in DRM reaction. Furthermore, kinetic behavior of Ni–Rh/Al2O3–ZrO2 catalyst in DRM process was investigated by assuming DRM and reverse water-gas shift (RWGS) reactions take place on two kinds of different active sites. Experimental data were fitted using rate expressions based on the Langmuir-Freundlich (LF) isotherm for DRM and RWGS reactions. The activation energy for the DRM reaction was optimized at 43.62 kJ/mol, falling within the reported literature range of 24.73–108.9 kJ/mol. Statistical indices indicated that the kinetic model accurately predicted CO2 conversion compared to other responses, with an error of 12.054%. The computed and experimental trends for CH4 and CO2 conversions, H2 and Co yield in terms of temperature were similar with each other and the difference between the calculated and experimental trends was lower for conversions compared to yields.

Determination of rare earth elements in ferrocarbonatite using ICP-AES and ICP-MS

AbstractA method has been developed for the determination of Rare Earth Elements (REEs) in ferrocarbonatite using Inductively Coupled Plasma—Atomic Emission Spectrometer (ICP-AES) and Inductively Coupled Plasma—Mass Spectrometer (ICP-MS). The conventional dissolution procedures are tedious, with large measurement uncertainty and are thus not suitable for certified reference material (CRM) production and exploration of REEs. The described method involves leaching of sample using 3 M HCl followed by dissolution of residue (silica and REEs) by HF then determined REEs using ICP-AES and ICP-MS. The leaching step prevents formation of fluoride precipitates of matrix (Ca, Mg, Ba and Al). The method has been validated using CRMs.

Removal of Arsenic from Contaminated Water by Polypyrrole-Based Adsorbents

Worldwide, there is growing concern over the toxicity of arsenic in drinking water. The US Environmental Protection Agency and Central Pollution Control Board (India) have set a safe limit of 50 parts per billion for arsenic in drinking water. Millions of people are at immediate risk due to high concentrations of arsenic in drinking water, particularly in developing nations where arsenic poisoning symptoms have been observed. One of the essential techniques described in this article is the absorption of arsenic from contaminated water by sustainable cellulosic materials like jute and wood sawdust after suitable modification. Jute and sawdust are cheap and abundantly available in South Asia. They are functionalized with polypyrrole coating by in situ chemical polymerization of pyrrole in aqueous medium in the presence of ferric chloride. Polypyrrole-coated jute fabric (with 11.28% polypyrrole add-on) and polypyrrole-coated sawdust (with 5.28% polypyrrole add-on) are found to be excellent adsorbers of arsenic ion (As3+) from water. The effect of dosage of polypyrrole-coated adsorbents, treatment time and pyrrole concentration on the As removal efficiency have been investigated in this work. The arsenic concentration in water is determined using a microwave plasma atomic emission spectrometer with the highest level of accuracy. Maximum As removal efficiency by the polypyrrole-coated sawdust and polypyrrole-coated jute fabric is found to be 80.90% and 97.3%, respectively, from a 50 mL, 7.5 parts per million As solution with a dosage of 1 g at neutral pH. The polypyrrole-coated jute and sawdust are characterized by Fourier-transform infrared spectroscopy to understand the chemical interaction between cellulose and polypyrrole molecules. The scanning electron microscope studies reveal a uniform coating of polypyrrole around the surface of jute fibre and sawdust particles. Thermo-gravimetric analysis shows good thermal stability of jute and sawdust after polypyrrole coating.

L-cysteine mediated rapid separation of Hg2+ and MeHg+ by anion-exchange HPLC

Owing to the on-going emission of Hg into the global environment, new insight into their bioinorganic chemistry in mammals is urgently required to better understand their adverse health effects and analytical methods to quantify Hg2+ and MeHg+ in environmental samples are needed. Analytical separations can help to address both of these needs. While Hg2+ and MeHg+ have been most frequently separated by cation and reversed-phase (RP) HPLC, we here report on using anion-exchange (AEX) HPLC in conjunction with a flame atomic absorption spectrometer (FAAS) to observe the retention behavior of these mercury species in the pH range 5.0–8.0 using mobile phases comprised of 10 mM l-cysteine (Cys) in 100 mM phosphate buffer. The results obtained for pH 5.0 served as a starting point to develop a rapid HPLC separation for these mercurials. The addition of 5–20 % methanol (MeOH) to this mobile phase revealed that MeOH did not appreciably change the retention of Hg2+, but significantly reduced the retention of MeHg+. A 15 % MeOH-containing mobile phase offered the best compromise between achieving a rapid baseline separation in <400 s at affordable costs. To assess the suitability and robustness of the developed AEX-HPLC separation method for the analysis of environmental samples an inductively coupled plasma atomic emission spectrometer (ICP-AES) was employed as the mercury-specific detector. The developed AEX-HPLC-ICP-AES method allowed to achieve detection limits of 1.5 ppm for Hg2+ and 2.9 ppm for MeHg+ and was successfully applied to analyze wastewater that had been spiked with Hg2+ and MeHg+.

Investigation of Heavy Metal Composition and Associated Health Risks from Selected Groundwater Wells in Temeke, Dar-es-Salaam

Water quality continues to be the challenge to residents in Dar es Salaam due to various anthropogenic activities in the city. This study was conducted to assess groundwater quality by determining concentrations of heavy metals. Both probability and Nonprobability sampling techniques were used to collect samples from 40 groundwater wells in 24 wards of Temeke municipal and analysed using Microwave Plasma Atomic Emission Spectrometer (Agilent 4210 MP-AES) at the Geochemistry Laboratory of the University of Dar es Salaam. Results indicated varying heavy metal concentrations ranging from 0.71 ± 0.08 to 6.64 ± 0.21 mg/l for As, 0.02 ± 0.01 to 0.07 ± 0.01 mg/l for Co and 0.16 ± 0.01 to 0.02 ± 0.01 mg/l for Pb. The As, Co and Pb concentrations exceeded (P &amp;lt; 0.05) the recommended TBS standards of 0.05 mg/l, 0.003 mg/l and 0.01 mg/l respectively. Other concentrations ranged from 0.01 ± 0.01 to 0.88 ± 0.01 mg/l for Cu, 0.02 ± 0.01 to 3.55 ± 0.02 mg/l for Fe, 0.00 ± 0.00 to 4.63 ± 0.03 mg/l for Mn and 0.01 ± 0.01 to 3.00 ± 0.01 mg/l for Zn. The Cu, Fe, Mn and Zn concentrations were below (P &amp;gt; 0.05) the allowable TBS limits of 0.05 mg/l, 0.3 mg/l, 0.1 mg/l and 3 mg/l respectively. Health risk analysis revealed potential adverse health effects from long term consumption of As, Mn and Pb with Hazard Quotient exceeding 1 (HQ &amp;gt; 1). The Hazard Index (HI) for all groundwater samples was also above 1 (HI &amp;gt; 1) indicating a higher likelihood of adverse health effects. The study concluded that groundwater wells in Temeke Municipal are affected through natural and anthropogenic activities leading to high levels of heavy metal concentrations. Also, this study provides valuable information on risk associated by continued usage of groundwater in Temeke region and hence informs respective stakeholders on groundwater quality and potential risks thereby emphasizing the need for remedial measures and stricter regulations to safeguard public health. The study recommends the need for regular groundwater quality and safety monitoring to assess the levels of heavy metals concentrations and implement sustainable groundwater management strategies to address the increasing water demand in Temeke municipal, Dar es Salaam.

OBTAINING HUMATE-, NITROGEN AND MOLYBDENUM-CONTAINING LIQUID ORGANOMINERAL FERTILIZERS

The presence of humic substances (HS) and microelements in liquid organomineral fertilizers (LOMF) makes it possible to balance the mineral nutrition of plants and thereby increase the agricultural crops yield. The use of such fertilizers significantly increases the efficiency and reduces the costs of using mineral fertilizers. The aim of this work is to study the patterns of new types LOMF obtaining process, including macro- and microelements and physiologically active humic substances, and its composition and properties. Methods. Chemical analysis, inductively coupled plasma atomic emission spectrometer, infrared spectroscopy. Results and discussion. The processes of synthesis of LOMF through the interaction of sodium humate and ammonium heptamolybdate tetrahydrate were studied. Analysis of obtained results showed the same nature of the composition dependence and properties of the obtained LOMF on time. It was found that increasing the time from 10 to 120 min leads to an increase in the yield of humic acids (HAdaf) to 40.08%, the N content to 4.62% and Mo to 0.17%, the amount of COOH to 1.80 mg-eq/g and OHphen. groups – up to 0.71 mg-eq/g. It has been shown that with an increase in S:L ratio from 0.3:100 to 0.7:100, the HAdaf decreases to 36.97%, and the N and Mo contents increase, respectively, to 6.0 and 0.37%. Conclusion. The regularities of the time influence and S:L ratios on the composition and properties of LOMF samples have been established. It has been shown that an increase in time and S:L ratio contributes to an increase in the content of N and Mo, the carboxyl and phenolic hydroxyl groups. The changes in these parameters have different effects on the HAdaf. The presence of HS, N, Mo, COOH and OHphen groups in the resulting products allows them to be used in agriculture and for restoring soil fertility.

Interaction of carbonic anhydrase I released from red blood cells with human plasma in vitro.

Red blood cells (RBCs) constitute ∼50% of the bloodstream and represent an important target for environmental pollutants and bacterial/viral infections, which can result in their rupture. In addition, diseases such as sickle cell anaemia and paroxysmal nocturnal haemoglobinuria can also result in the rupture of RBCs, which can be potentially life-threatening. With regard to the release of cytosolic metalloproteins from RBCs into the blood-organ system, the biochemical fate of haemoglobin is rather well understood, while comparatively little is known about another highly abundant Zn-metalloprotein, carbonic anhydrase (CA I). To gain insight into the interaction of CA I with human blood plasma constituents, we have employed a metallomics tool comprised of size-exclusion chromatography (SEC) coupled online with an inductively coupled plasma atomic emission spectrometer (ICP-AES), which allows to simultaneously observe all Cu, Fe, and Zn-metalloproteins. After the addition of CA I to human blood plasma incubated at 37°C, the SEC-ICP-AES analysis using phosphate buffered saline (pH 7.4) after 5min, 1h, and 2h revealed that CA I eluted after all endogenous Zn-metalloproteins in the 30kDa range. Matrix-assisted laser desorption-time of flight mass spectrometry analysis of the collected Zn-peak confirmed that CA I eluted from the column intact. Our in vitro results suggest that CA I released from RBCs to plasma remains free and may be actively involved in health-relevant adverse processes that unfold at the bloodstream-endothelial interface, including atherosclerosis and vision loss.

Microstructure and corrosion behaviour of Mg-1Sc alloy with different processing conditions

The microstructure and corrosion resistance of Mg-1Sc alloys in different processing conditions were investigated. The composition was examined by Inductively Coupled Plasma Atomic Emission Spectrometer, the microstructure was analyzed by metallographic microscope. The corrosion behaviour of the alloy was investigated by hydrogen evolution tests and electrochemical tests. The results showed that as-cast and rolled Mg-1Sc possess better corrosion resistance compared with extruded Mg-1Sc alloys, which is due to the fact that the extrusion flow lines and residual stresses caused by machining in extruded Mg-1Sc alloys can lead to easier corrosion. In addition, rolled Mg-1Sc alloy shows better corrosion resistance than as-cast alloy, which is attributed to the finer grain sizes and a denser corrosion product film.

Solidification and Release Characteristics of Heavy Metals in Gypsum from Coal-Fired Power Plants

Heavy metals in flue gas desulfurization (FGD) gypsum from coal-fired power plants are at risk of releaching during the processes of stockpiling and resource utilization. In this study, the effects of organosulfur chelators dithiocarbamate (DTC) and trisodium trithiocyanate-15 (TMT-15) on the solidification characteristics of heavy metals in desulphurized gypsum under different mass fractions, pH values, water contents and reaction times were investigated. The chemical composition and morphology were analyzed by inductively coupled plasma atomic emission spectrometer (ICP-AES) and scanning electron microscope (SEM). The experiments showed that both DTC and TMT-15 were effective at stabilizing the heavy metals in the FGD gypsum, with more than a 50% curing effect for all the heavy metals except Pb. DTC showed a better stabilization for Pb, Hg, Cu, Zn, and Cr, and TMT-15 showed a better curing effect for Cd. The solidified gypsum had good heavy metal stability in low-water-content environments. Increasing the mass fraction, reaction time, and pH decreased the heavy metal leaching, and the mass fraction had the greatest effect on the total heavy metal leaching concentration, followed by the reaction time and pH value.

Nutritional composition and mineral bioavailability of selected root and tuber crops in the Bicol Region, Philippines

Filipinos consume root and tuber crops as inexpensive sources of nourishment. However, the limited information on the nutritional and mineral bioavailability of root and tuber crops inhibits their optimal utilization in what could possibly address nutrient deficiencies among the populations. This study determined the proximate composition of cassava, sweet potato, taro, giant swamp taro, cocoyam, and purple yam through the Association of the Analytical Chemists (AOAC) standard method. The mineral bioavailability was determined in vitro by simulating digestion from the oral up to the intestinal phase. Mineral and trace metal contents were quantified using a Microwave Plasma Atomic Emission Spectrometer (MP-AES). The crops’ ash, protein, fat, and total dietary fiber contents ranged from 1.23-3.53%, 2.01-9.32%, 0.18-0.83%, and 4.23-19.3%, respectively. Taro (9.32%) and purple yam (6.71%) have the highest protein contents among the crops examined and can be considered as sources of protein based on the recommended nutrient intake (RENI) for Filipino adults. Except for cassava, most of the studied crops were high sources of total dietary fiber, with the giant swamp taro (48% RENI) as the highest. Total minerals such as K, Ca, Mg, Na, and considerable quantities of Zn, Mn, Fe, and Cu were detected. The mineral bioavailability varied for Zn (47.0-98.0%), Cu (37.5-86.8%), Mn (31.5-91.8%), Mg (31.9-90.2%), Ca (2.54-31.1%) and Fe (4.7-20.7%). Consumption of 100 g of the examined crops, except for giant swamp taro and cassava, can contribute to the daily Cu for adults aged 19-29. Taro contributes to the daily nutritional requirement for bioavailable Ca and Mg, while giant swamp taro contributes to Zn and Mn requirements. None of the examined crops contained sufficient bioavailable Fe to contribute to Filipinos’ daily requirements. The study can help address the limited information on the nutritional and mineral bioavailability of root and tuber crops, which hampers their utilization to address some nutrient deficiency among the Filipino population, and emphasizes the consumption of these crops to enhance dietary diversification, which can alleviate some nutrient deficiencies in the country.

Effect of sodium chloride on yield, purity, morphology and polymorphs of calcium or magnesium carbonate sequentially precipitated from brine solution

Oilfield brine disposal in marine environments is undesirable due to concentrated salts of calcium, magnesium, sodium, and others which endanger aquatic organisms. Thus, it is paramount to precipitate the dissolved ions into stable carbonates for industrial applications. However, the effect of NaCl in the brine solution on the quantity and quality of precipitated carbonates is not yet reported. In this study, microwave plasma atomic emission spectrometer (MIP AES), x-ray diffraction (XRD), and scanning electron microscopy (SEM) were employed to investigate the effect of 0–2 M NaCl on the yield, purity, polymorph, and morphology of calcium and magnesium carbonates. The yields of 96.2% to 98.9% and 53.7% to 69.6% and the purity of 90.9% to 92.7% and 96% to 99.5% CaCO3 and MgCO3·3H2O were obtained, respectively. Moreover, the maximum yield and purity of carbonates were obtained from a brine solution of 1 M NaCl. The concentration of 0–0.5 M NaCl favored more the formation of aragonite whiskers and rhombohedral calcite whereas the concentration of 1–2 M NaCl favored more the formation of aragonite whiskers, lamella vaterite,and rhombohedral calcite. Nevertheless, only nesquehonite (MgCO3·3H2O) precipitated regardless of brine concentration. The crystal surface and length of the precipitated nesquehonite from 1 to 2 M NaCl brine were affected.

Assessment of trace elements (Cu, Fe, and Zn) in Limnothrissa miodon from Lake Kariba, Zambia: implications for ecological and human health

ABSTRACT This study examined Copper (Cu), Iron (Fe), and Zinc (Zn) levels in Limnothrissa miodon fish from Lake Kariba in Zambia and their potential impact on human health. Two-gram samples from each stratum underwent a 12-hour digestion, and concentrations were determined using Microwave Plasma Atomic Emission Spectrometer. Results indicated that Cu, Fe, and Zn concentrations fell within Food and Agricultural Organization and World Health Organization safety limits. Estimated Daily Intake (EDI) and Hazard Quotient (THQ) values for males and females remained under recommended thresholds, suggesting minimal health risks from consumption. Element concentrations followed the order Fe > Zn > Cu, all below Recommended Daily Allowances (RDAs). THQ values, with Zn posing the highest potential risk followed by Fe and Cu, were under one. Overall, the Hazard Index (HI) was 0.02, signifying a low non-carcinogenic risk from fish consumption. Despite safety, ongoing monitoring of heavy metal accumulation in the ecosystem is advisable for long-term safety. In conclusion, trace element levels in Limnothrissa miodon from Lake Kariba are safe for human consumption with low associated health risks. Nonetheless, continued monitoring of heavy metal levels is vital.

Environmental assessment of Heavy Metals in Sedi - ments of Tigris, Euphrates, Shatt Al-Arab rivers and northern west of Arabian Gulf.

The most prevalent environmental contaminants found in sediments that suggest the presence of effluents from both home and industrial sources are thought to be heavy metals. The aim of this study was to assess the accumulation of heavy metals at surface sediment samples that were collected in order to measure the amounts of Cu, Zn, Pb, Cd, and Fe., to re-evaluate the environmental conditions and concentration of the analyzed elements in the sediment to detect any pollution of heavy metals in the studied area by using contamination factors (CF), Enrichment Factor (EF) and geo accumulation index (I-geo). To ascertain the connection between the sediment’s total organic carbon (TOC) level and heavy metal pollution, measurements were taken in addition of it. Using the inductively coupled plasma atomic emission spectrometer, studies were conducted., The mean values of the element in the sediments ranged as: Cu (13.45 μg/g at location 2 to 32.44 μg/g at location 9), Zn (20.76 μg/g at location 1 to 42.49 μg/g at location 10), Pb (9.78 μg/g at location 2 to 30.04 μg/g at location 9 and 10), Cd (7.89 μg/g at location 2 to 18.72 μg/g at location 7) and Fe (459.89 μg/g at location 1 to 833.83 μg/g at location 7) dry weight. The geochemical results show that the distribution and concentration of the heavy metals in the studied sediments is within the average concentration given for the FAO/WHO reported, and the sediment of the studied area is still free from pollution, except Pb and Cd in some local areas, which shows higher concentrations than those reported for world sediments.

TYPOMORPHISM OF THE CHEMICAL COMPOSITION OF BIOGENIC CARBONATES WITHIN THE PRADNIPROV METHANE ANOMALY ON THE BLACK SEA SHELF

Problem Statement and Purpose. The aim of the article is to study the typomorphism of the chemical composition of biogenic calcium carbonates within methane anomalies formed by deep fluids in the bottom sediments of the Black Sea shelf. Gas chromatography was performed at the «Pradniprovska» study area. The results of the site`s bottom sediments analysis confirmed the content of pure methane and its homologues in the samples. Due to the presence of methane homologues, oxygen and carbon isotope analysis of the sediment shells was performed (it is known that the most stable information about the chemical composition of the mineral formation environment can be stored in biogenic carbonates of benthic organisms’ shells). The values obtained from the analysis had a small spread and did not show any visible variability. Data &amp; Methods. Data on the chemical composition of benthic organisms’ shells can be obtained using inductively coupled plasma atomic emission spectrometry. This method requires large samples by weight, so only the shells of the Mytilus mollusks were taken for the study due to their relatively large size. The gas-geochemical studies were based on the methodology of the NDL‑3 laboratory. The extracted gas was stored in glass tubes under a saturated saline solution, which ensured minimal losses from gas dissolution in the seal fluid, followed by studying it using a «Tsvet‑400» gas chromatograph. The separation of hydrocarbon gases was carried out on a chromatographic column filled with aluminum oxide. The detector is flame ionization. Calibration was carried out before the start of each cycle with calibration gas mixtures of standard composition. The spectrometric analysis was performed on a Thermo Scientific inductively coupled plasma atomic emission spectrometer with a CID or CMOS detector operating in the range of 167–820 nm. The method is based on the dissolution of substances in a mixture of nitric, hydrochloric and hydrofluoric acids at a temperature of at least 125 °C, followed by the determination of elements in solutions by inductively coupled plasma atomic emission. To consider matrix effects and improve measurement accuracy, calibration using internal standard lines is used. Results. The analysis of the obtained material allowed the author to draw the following conclusions: a) chemical elements in shells are unevenly distributed, and this unevenness is determined by two main reasons – the peculiarity of the formation of biogenic carbonate of shells and the ability of the carbonate to isomorphically capture a number of elements from the mineral-forming environment; b) according to the quantitative characteristics, three groups of elements can be distinguished: macroelements, mesoelements and trace elements. The first group of elements (macroelements) includes Na, S, Mg, Sr, Fe, Si, Mn, P, K. Among them, one can clearly distinguish elements that are isomorphically included in the structure of calcite or aragonite (Na, Mg, Sr, Fe, Mn, K) and elements captured as non-structural impurities in the agglutination process during the growth of biogenic carbonate (Si, S and P). The second group (mesoelements) includes Ba, Al, As, Zn, Cu, Ti, among which two groups can also be distinguished. One is associated with the formation of sulfide minerals paragenetic to biogenic calcite (As, Zn, Cu), and the other with agglutination of clay minerals in sediments (Al, Ti), or a feature of isomorphism in the biogenic formation of calcium carbonate (Ba). The third group (trace elements) is associated with elements of low content and uneven distribution (Ni, Mo, Pb, Se). The main group here is Ni, Cr, Co, V. These groups, taking into account the fact that they were found in the areas of penetration of deep-sea fluids into the sedimentary strata, allows to consider them as typomorphic signs of biogenic carbonate formation in the areas of fluid influence, and, consequently, as a search sign of such areas on the Black Sea shelf.

Optimization of the Method for Spectrofluorimetric Determination of Aluminum Impurities in Substances

Introduction. Evaluation of the content of impurities is the most important step in confirming the safety and efficacy in the quality control of the medicinal product. Aluminum, being an acceptable impurity in a number of pharmaceutical substances, can adversely affect the human body, as a result of which its content is normalized. The admixture of aluminum in the State Pharmacopoeia of the Russian Federation XV is determined by the spectrofluorimetric method using the ligand – 8-hydroxyquinoline in chloroform. In the present work, it is proposed to replace 8-hydroxyquinoline with the more accessible rutin, which also forms fluorescent complexes with metals. This approach involves the exclusion of the stage of extraction of the aluminum complex into chloroform from sample preparation, which improves the accuracy of the technique, and the replacement of chloroform has a positive effect on safety.Aim. To create an alternative approach for the spectrofluorimetric determination of aluminum impurities using rutin and "potassium chloride" as an active pharmaceutical ingredient.Materials and methods. The following substances and reagents were used as research materials: CRS of aluminum ion 1 mg/ml (LLC "EKROSHIM", Russia), CRS of iron ion (II) 1 mg/ml (LLC "EKROSHIM", Russia), CRS of zinc ion 1 mg/ml (LLC "EKROSHIM", Russia), CRS of lead-ion 1 mg/ml (LLC "EKROSHIM", Russia), CRS nickel-ion 1 mg/ml (LLC "EKROSHIM", Russia), CRS copper-ion 1 mg/ml (LLC "EKROSHIM", Russia), chromium (III) cation standard 1 mg/ml (imp., Sigma-Aldrich, USA) rutin (imp., Sichuan Guangsong Pharmaceutical Co., Ltd., China), ammonium acetic acid (imp., Molekula GmbH, Germany), glacial acetic acid (chemically pure, JSC "Base No. 1 Himreaktivov", Russia), potassium chloride (pharmaceutical substance, LLC "MZHR", Russia). The spectrofluorimetric study was carried out on an FL 6500 instrument (PerkinElmer Inc., USA). The aluminum impurity content was also evaluated using an Optima 8000 inductively coupled plasma atomic emission spectrometer (ICP AES) (PerkinElmer Inc., USA) and a Multi-Element Solution standard sample (PerkinElmer Inc., USA).Results and discussion. The approach given in the article eliminates the use of 8-hydroxyquinoline in chloroform and replaces it with rutin in 70 % ethyl alcohol. The aluminum-rutin complex has an excitation wavelength at 445 nm and an emission wavelength at 565 nm. The proposed method was tested on the substance "Potassium chloride" to assess the indicator "Aluminum", the content of which should not exceed 0.0001 %. Method validation was carried out according to three parameters "Specificity", "Linearity" and "Limit of detection". Comparison of the data obtained was carried out using atomic emission spectroscopy, during which the relevance of the technique was proved.Conclusion. An ergonomic approach has been developed for the spectrofluorimetric determination of aluminum impurities using rutin with approbation on the substance "Potassium chloride". The results obtained during the experiment were confirmed by the ICP AES method.

N-Acetylcysteine Displaces Glutathionyl-Moieties from Hg2+ and MeHg+ to Form More Hydrophobic Complexes at Near-Physiological Conditions.

The anthropogenic release of Hg is associated with an increased human exposure risk. Since Hg2+ and MeHg+ have a high affinity for thiols, their interaction with L-glutathione (GSH) within mammalian cells is fundamentally involved in their toxicological chemistry and excretion. To gain insight into the interaction of these mercurials with multiple small molecular weight thiols, we have investigated their competitive interactions with GSH and N-acetylcysteine (NAC) at near-physiological conditions, using a liquid chromatographic approach. This approach involved the injection of each mercurial onto a reversed-phase (RP)-HPLC column (37 °C) using a PBS buffer mobile phase containing 5.0 mM GSH to simulate cytosolic conditions with Hg being detected in the column effluent by an inductively coupled plasma atomic emission spectrometer (ICP-AES). When the 5.0 mM GSH mobile phase was amended with up to 10 mM NAC, gradually increasing retention times of both mercurials were observed. To explain this behavior, the experiment with 5.0 mM NAC and 5.0 mM GSH was replicated using 50 mM Tris buffer (pH 7.4), and the Hg-containing fractions were analyzed by electrospray ionization mass spectrometry. The results revealed the presence of Hg(GS)(NAC) and Hg(NAC)2 for Hg2+ and MeHg(GS) and MeHg(NAC) for MeHg+, which suggests that the coordination/displacement of GS-moieties from each mercurial by the more hydrophobic NAC can explain their retention behavior. Since the biotransformations of both mercurials were observed at near-physiological conditions, they are of toxicological relevance as they provide a biomolecular explanation for some results that were obtained when animals were administered with each mercurial and NAC.

Development of Wet Chemical Analysis Technique for Tramp Elements (M = As, Pb, Sb, and Sn) in Silver-M Alloys

Wet chemical analysis techniques for four elements (M = As, Pb, Sb, and Sn) in Ag – M binary alloys were investigated with emphasis on the choice of solvent acid and the characteristic wavelength used in the ICP-AES (Inductively-Coupled Plasma Atomic Emission Spectrometer) analysis. The elements are representative tramp elements in ferrous scrap. The activity of these elements needs to be increased to remove them efficiently during the molten scrap refining process. The activity of these elements in the molten scrap (molten iron alloy) is usually measured by a chemical equilibration technique with molten Ag. Therefore, performing an accurate and reliable chemical analysis of these elements in the molten iron alloy and the molten Ag alloy is important. Preliminary tests using conventional acids (hydrochloric acid, nitric acid) resulted in unreliable results. In the present study, the proper choice of acids as solvents was investigated for each element M in the Ag-M alloys. Several synthesized Ag-M alloys of known compositions were analyzed using two ICP-AES systems independently, for cross-checking. As and Pb in Ag alloys could be successfully dissolved in the nitric acid-based solution. On the other hand, Sb and Sn in Ag alloys did not dissolve in the nitric acid-based solution completely, leaving some precipitates. It was found that the addition of hydrofluoric acid could resolve this problem. In addition to this, the effect of the mass of the Ag-M alloy and wavelength selection during ICP-AES analysis on the accuracy and the reproducibility were investigated. An optimized procedure for the wet chemical analysis of these elements in Ag-M alloys is reported.

Investigation of Defect Structure and Optical Properties of Sc: Yb: Ho: LiNbO3 Crystals with Different [Li]/[Nb] Ratios

Sc: Yb: Ho: LiNbO3 crystals with various [Li]/[Nb] ratios (0.85, 0.94, 1.05, 1.20 and 1.38) were grown by Czochralski method. In this report, the effect of the [Li]/[Nb] ratio dependence of the doped element concentration and segregation coefficient was studied using an inductive coupled plasma-atomic emission spectrometer (ICP-AES). It was found that the change of the [Li]/[Nb] ratio will affect the concentration and the occupancy of the doped ions in the crystal. The structures of the crystals with different [Li]/[Nb] ratios are analyzed using X-ray diffraction patterns (XRD). It was found that doping elements do not change the crystal structure, and the crystal has the least defects when the [Li]/[Nb] ratio is 1.20. The optical uniformity of crystals was measured by birefringence gradient method. The results show that the optical uniformity of the crystal is significantly enhanced as the [Li]/[Nb] ratio increases.

Evaluation of metal pollution related to human health risk in freshwater snail Viviparus contectus (Millet, 1813) as a potential bioindicator species in Lake Habitat (Turkey).

Freshwater mollusks are employed as bioindicators for the assessment of water quality in biomonitoring studies since the water quality of natural resources is crucial for humans. The freshwater snail species known as Viviparus contectus (Viviparidae: Gastropoda) is one that people eat. Here, the levels of heavy metals (Cd, Cr, Pb, As, Zn, and Cu) in water and V. contectus samples were determined. An Inductively Coupled Plasma Atomic Emission Spectrometer (ICP-AES, Spectro Arcos, vertical plasma) was used for the analysing the heavy metal concentrations in water and freshwater snail samples. The results of the current investigation demonstrated that freshwater snails accumulated metals in their water and soft tissues in the following orders: Pb > Cr = Zn = Cu = Cd = As and Zn > Cu > Pb > Cd > As = Cr. Autumn was the time of year when higher amounts of heavy metals (As, Cr, Cu, Zn, and Hg) were found. Pb content in the freshwater snail samples was strongly impacted by seasonal fluctuations (P 0.05). For adults, the EDI (estimated daily intake) values were lower than the TDI (tolerable daily intake) values, and the HI (hazard index) values were below 1. Freshwater snail samples had Zn and Pb levels that were over the FAO/WHO, Turkish Food Codex, JECFA, and EC limit values. Except for Pb, the water study shows mean metal concentrations below the USEPA, Turkish Pollution Control Regulation, and World Health Organisation maximum allowed levels. Aquatic ecosystems were negatively impacted by anthropogenic activities overall, and this study can provide a helpful data set for investigations on metallic contamination in water bodies and biomonitoring in freshwater ecosystems.