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Influence of chemical composition on the bandgap of AlGaInAs deposited on InP is often calculated using models for unstrained composition and then corrected for strain-induced bandgap energy changes using deformation potentials. This method relies on up to 25 coefficients, many of which are burdened with large uncertainty. In this paper, a large set of experimental data is used to verify the accuracy of existing approaches and to search for optimal deformation potentials. It is shown that the main source of inaccuracy is not the deformation potentials, but the unstrained bandgap formulas. Additionally, a novel model is proposed, yielding the highest accuracy on our dataset. For the first time, composition determination of a quaternary alloy on InP is reported using inductively coupled plasma-optical emission spectrometry, which is used as a benchmark for modeling. [ABSTRACT FROM AUTHOR]

The role of ambient oxygen gas (O2) on molecular and nanoparticle formation and agglomeration was studied in laser ablation plumes. As a lab-scale surrogate to a high explosion detonation event, nanosecond laser ablation of an aluminum alloy (AA6061) target was performed in atmospheric pressure conditions. Optical emission spectroscopy and two mass spectrometry techniques were used to monitor the early to late stages of plasma generation to track the evolution of atoms, molecules, clusters, nanoparticles, and agglomerates. The experiments were performed under atmospheric pressure air, atmospheric pressure nitrogen, and 20% and 5% O2 (balance N2), the latter specifically with in situ mass spectrometry. Electron microscopy was performed ex situ to identify crystal structure and elemental distributions in individual nanoparticles. We find that the presence of ≈20% O2 leads to strong AlO emission, whereas in a flowing N2 environment (with trace O2), AlN and strong, unreacted Al emissions are present. In situ mass spectrometry reveals that as O2 availability increases, Al oxide cluster size increases. Nanoparticle agglomerates formed in air are found to be larger than those formed under N2 gas. High-resolution transmission electron microscopy demonstrates that Al2O3 and AlN nanoparticle agglomerates are formed in both environments; indicating that the presence of trace O2 can lead to Al2O3 nanoparticle formation. The present results highlight that the availability of O2 in the ambient gas significantly impacts spectral signatures, cluster size, and nanoparticle agglomeration behavior. These results are relevant to understanding debris formation in an explosion event, and interpreting data from forensic investigations. [ABSTRACT FROM AUTHOR]

Zn:Yb:Tm:LiNbO3 crystals with a range of [Li]/[Nb] ratios (0.94, 1.05, 1.20, and 1.38) were grown by Czochraski technique. The influence of [Li]/[Nb] ratio on the concentration of doped elements in grown crystal was investigated by inductively coupled plasma atomic emission spectrometry (ICP-AES). The defect structures formed at different [Li]/[Nb] ratios were studied by X-ray diffraction and INFRARED spectroscopy. The results show that, when the [Li]/[Nb] ratio increases, the segregation coefficients of Yb 3 + and Tm 3 + ions increase, while the segregation coefficient of Zn 2 + ions decreases. When the [Li]/[Nb] ratio in the melt increases to 1.20, the Zn:Yb:Tm:LiNbO3 crystal approaches the stoichiometric ratio. [ABSTRACT FROM AUTHOR]

This investigation aims to identify sources and assess the concentrations, spatial distribution patterns, and ecological and health risks of Zn, Pb, Cu, Ni, Cr, and Cd from road dust (RD) samples collected from Qom, Iran. Samples were collected from the surface of the roads, and were air-dried for 15 days. Debris including hair and leaves were removed from samples by using 1000-μm nylon sieve. One gram of each dried samples were digested according to US environmental protection agency (USEPA) method using HCl, HNO3, and H2O2 for analysis of heavy metals (HMs), and utilising inductively coupled plasma optical emission spectrometry (ICP-OES). The mean concentrations for all HMs have higher values in the warm season with total mean concentrations of Zn = 227.3 > Pb = 130.1 > Ni = 94.2 > Cu = 78.7 > Cr = 39.5 > Cd = 2 mg/kg. Furthermore, correlations between all concentrations have been investigated using Pearson's method after approving normal distribution for all HMs through Kolmogorov-Smirnov (K-S) test. The spatial distribution of Pb, Zn, and Ni show higher concentrations in the periphery of Qom, while Cu, Cr, and Cd are almost the same for the whole city. The geo-accumulation index (Igeo) categorised all HMs as uncontaminated (average Igeo <0) except for Pb and Zn with average Igeo of 1.52 and 1.01, respectively. Ecological risk (Er) analysis confirms lower risk for all HMs (average Er <40). The warm season exhibits a higher potential ecological risk index (average RI = 81.73) for all components compared to the cold season (average RI = 75.85). Hazard index (HI), and carcinogenic risk assessment (CRA) values ranged lower than 1 and 10−6, respectively, and thus, revealed negligible health risks for individuals. Positive matrix factorisation (PMF) points to four factors for HMs dominantly affected by traffic-related and anthropogenic activities (contributing 38.56%), and natural sources (accounting for 32.45%) in the cold and warm seasons, respectively. [ABSTRACT FROM AUTHOR]

Silver is widely used, but the pollution caused by silver ions is also a problem that cannot be ignored. Detection of heavy metal ions based on bulky and costly analytical instruments had been developed very maturely in the laboratory. At present, the main detection methods of silver ion concentration include inductively coupled plasma mass spectrometry, atomic absorption spectrometry and inductively coupled plasma/atomic emission spectrometry. However, these testing methods have many problems to be solved, such as the high of instruments, high operating cost, numerous operational requirements, long testing time and complex processing technology. Nowadays, with the rapid and powerful development of smartphone technology, the new analytical methods based on smartphones equipped with a camera are being carried in the certain applied ideas. Here, the paper introduces a hand-held detection platform smartphone-based that allows the quantification of silver(I) ions with the detection limit of 0.659 mM. The Colour Grab software of android smartphone was applied to obtain R, G, B values of the photo of Rhodamine B solution remaining fluorescence, and then calculated the corresponding grey values by grey formula. The detection platform based on smart phones has the characteristics of cost-effective design and simple operation, as well as high sensitivity and selectivity. Therefore, compared with other detection methods, this method can be widely and conveniently applied to the detection of silver ions in the environment. [ABSTRACT FROM AUTHOR]

In this study, a simple and efficient eco-friendly procedure for preconcentration of trace amounts of Y, Sm, Eu, Gd, Er and Yb was developed prior to determination by inductively coupled plasma optical emission spectrometry (ICP-OES). The extraction process involved two sequential steps. The first is based on ultrasonic-assisted emulsification solidified floating organic drop microextraction using morin and 1-undecanol as complexing and extraction agents, respectively. The analyte in the solidified floated organic drop was then back-extracted into aqueous solution of HNO3 to prevent the relapsing effect of the organic matrix on the performance of ICP-OES. The effect of various experimental parameters on the extraction efficiency was studied and optimised. The limits of detection were in the range of 0.053 (Y) – 0.086 (Sm) µg L−1 with linear dynamic analytical range of 0.3–1000 µg L−1 at the optimal conditions. The relative standard deviations (C = 20 µg L−1, n = 10) ranged from 1.7% (Eu) to 2.5% (Yb). Finally, the approach represented high efficiency in determining the rare earth elements in certified reference material and phosphite rock samples. [ABSTRACT FROM AUTHOR]

In this study, we prepared Co and Fe nanoparticles supported on a layered double hydroxide abbreviated as CoNPs@LDH and FeNPs@LDH. The nanostructured catalysts were characterized using inductively coupled plasma atomic emission spectroscopy (ICP-AES), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX) analysis, infrared spectroscopy (FTIR), X-ray photoemission spectroscopy (XPS), BET surface area analysis and thermogravimetric analysis (TGA) and tested for the oxidation of cyclohexane to KA oil using tert-butylhydroperoxide (TBHP) under solvent-free conditions. CoNPs@LDH appeared to have higher catalytic efficiency than FeNPs@LDH nanocatalysts. Structural analysis revealed that the transition metal nanoparticles are well anchored on the layered double hydroxide, resulting in a fine dispersion of the Co nanoparticles. The CoNPs@LDH nanocatalyst demonstrated a 45.7% conversion of cyclohexane with 95.8% selectivity of KA oil under optimal reaction conditions. Furthermore, the recycling experiment revealed that CoNPs@LDH was a heterogeneous catalyst that could be recycled at least five times without significant loss of catalytic activity. A possible mechanism following the free radical pathway has been proposed. [ABSTRACT FROM AUTHOR]

Seafood is considered a healthy and nutritious food, but the presence of toxic substances in such foods is a serious problem. The present study aimed to analyze the concentration of some toxic metals in seafood and evaluate their noncarcinogenic risks to consumers. Samples were digested according to the Association of Official Agricultural Chemists (AOAC) standard. The heavy metals concentration of Cd, Ni, Hg, Pb, and Sn in 30 canned tuna samples were determined using an inductively coupled plasma optical emission spectroscopy (ICP-OES). The mean concentrations of Cd, Ni, Sn, Pb, and Hg were 0.7, 0.49, 1.03, 0.31, and 0.12 µg g− 1, respectively. Based on these results, the concentrations of Cd, Sn, and Hg in samples met the required standards. However, the concentrations of Ni and Pb in some samples were higher than the permissible limits. The mean values of Sn, Ni, Pb, Hg, and Cd in samples followed a decreasing order. Since the values of the health risk index for these samples were lower than the HI and HRI risk threshold (<1), they can be consumed without any problems arising. Highlights: The metal concentration was measured in the four most popular brands of canned fish sold in Neyshabur City, Iran. Some samples exceeded the maximum permissible level of nickel (Ni) and lead (Pb). A significant correlation was observed between Ni concentration with Pb and Hg concentrations and Pb concentration with Cd concentration. The values of the health risk index (HRI) for noncarcinogenic health risks were lower than 1. The calculated Hazard index (HI) for adult and child consumers was less than 1. The HI values were greater for children than for adults. [ABSTRACT FROM AUTHOR]

Purpose: The objective of the present work was to test the feasibility of in vivo imaging of hyperpolarized 50‐nm silicon‐29 (29Si) nanoparticles. Methods: Commercially available, crystalline 50‐nm nanoparticles were hyperpolarized using dynamic polarization transfer via the endogenous silicon oxide–silicon defects without the addition of exogenous radicals. Phantom experiments were used to quantify the effect of sample dissolution and various surface coating on T1 and T2 relaxation. The in vivo feasibility of detecting hyperpolarized silicon‐29 was tested following intraperitoneal, intragastric, or intratumoral injection in mice and compared with the results obtained with previously reported, large, micrometer‐size particles. The tissue clearance of SiNPs was quantified in various organs using inductively coupled plasma optical emission spectroscopy. Results: In vivo images obtained after intragastric, intraperitoneal, and intratumoral injection compare favorably between small and large SiNPs. Improved distribution of small SiNPs was observed after intraperitoneal and intragastric injection as compared with micrometer‐size SiNPs. Sufficient clearance of nanometer‐size SiNPs using ex vivo tissue sample analysis was observed after 14 days following injection, indicating their safe use. Conclusion: In vivo MRI of hyperpolarized small 50‐nm SiNPs is feasible with polarization levels and room‐temperature relaxation times comparable to large micrometer‐size particles. [ABSTRACT FROM AUTHOR]

Novel ordered β-ketoimine-palladium(II) multilayers supported on the surface of a silicon wafer (Si@[β-Ki-Pd][L2-Pd]n , n = 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, and 11) were fabricated using layer-by-layer (LbL) self-assembly and characterized using Raman spectroscopy (RS), ultraviolet-visible spectroscopy (UV-vis), X-ray diffraction (XRD), cyclic voltammetry (CV), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and inductively coupled plasma-atomic emission spectrometry (ICP-AES). Their catalytic properties were systematically investigated using the Suzuki–Miyaura cross-coupling reaction as a template. Among these catalytic multilayers, Si@[β-Ki-Pd][L2-Pd]11 exhibited high activity (TOF = 12 903.2 h−1), which was ten times and sixty times higher than that of Si@[β-Ki-Pd] (TOF = 1171.7 h−1) and Li2PdCl4 (TOF = 215.8 h−1), respectively. It also showed good substrate adaptability and could be reused 13 times. Si@[β-Ki-Pd][L2-Pd]11 was a heterogeneous catalyst and catalysis occurred on the surface. Active sites formed in situ on the surface, including Pd(0) and Pd(0)/PdO, which exhibited a synergistic effect, such as electronegative Pd(0), were enhanced via the synergistic action between PdO and Pd(0). This synergistic effect made the oxidative addition of Pd reacting with aryl halide easy and boosted catalytic activity. Oxygen also played a crucial role in the formation of PdO, which not only exhibited important electron transferring synergy with Pd, but acted as a stabilizer for Pd(0). This could maintain the balance ratio of Pd/PdO to prevent Pd from aggregating. The above investigation is essential for the optimal design of highly active catalysts. [ABSTRACT FROM AUTHOR]

AbstractRivers are often contaminated with metals. This study was conducted on the Jempul River in Jengka, Pahang, Malaysia, due to the agricultural activities carried out along this river. The aims are to investigate the levels of certain metals (namely Al, Fe, Mn, and Pb), identify their likely sources, assess their toxicity loads, and estimate the associated health risks. Inductively coupled plasma optical emission spectrometry (ICP-OES) was used to determine metal concentrations. The concentrations were discovered in the following order: Fe > Al > Mn > Pb, for both dry and wet conditions. The highest concentration in water sample was observed for Fe (1.28 mg/l) in the dry condition and the lowest was detected for Pb (0.04 mg/l) in the wet condition. Principal component analysis (PCA) indicated that the metals originate from natural and anthropogenic sources. Based on metal toxicity load (MTL) calculations, it is recommended that approximately 73% of Pb, 60% of Mn, and 58% of Al be eliminated from the river water to ensure its safety. Children are more susceptible to non-cancer and cancer hazards than adults. This study suggests that extensive exposure assessment and detailed monitoring of water quality indicators should be carried out. [ABSTRACT FROM AUTHOR]

Water quality degradation due to heavy metal contamination poses serious threats to both human health and aquatic ecosystems. The rise in the concentration of heavy metals in aquatic environments is largely attributable to anthropogenic activities. These metals accumulate over time in water bodies, necessitating rigorous monitoring to accurately assess pollution levels. The present study is concerned with the assessment of heavy metal pollution in the Styr River (Ukraine) before and after the discharge of water from a nuclear power plant. The assessment is based on three indices: the Heavy Metal Pollution Index, the Heavy Metal Evaluation Index, and the Degree of Contamination. Therefore, heavy metals, including zinc (Zn), cadmium (Cd), lead (Pb), copper (Cu), nickel (Ni), manganese (Mn), arsenic (As) and chromium (Cr), were analyzed in this study. Water samples were collected at two locations on a monthly basis over the course of five years (2018–2022) and subsequently analysed using inductively coupled plasma optical emission spectroscopy. The results indicates a low contamination level at both sampling sites, indicating stable and uniform concentrations of metals across the study area. Moreover, statistical analysis highlights significant associations between certain metals and pollution indices, supporting the indices' utility in tracking pollution trends and assessing environmental impacts. This dataset underscores the importance of ongoing monitoring for effective water quality management. [ABSTRACT FROM AUTHOR]

A 77‐year‐old professional gold craftsman ingested a white powder used in goldsmithing, mistaking the powder for a health supplement. He detected a strange taste and immediately fell sick, reported the incident to 911, and was taken to the emergency room. He died approximately 8.5 h post‐ingestion despite treatment. There were no significant findings in the autopsy, the victim's heart blood sample, gastric contents, and the white powder the victim had taken were submitted to the department of forensic toxicology. Using scanning electron microscopy energy dispersive X‐ray analysis, potassium and gold (Au) were detected in the white powder. Ion chromatography analysis detected cyanide. Concentrations of cyanide were 0.5 mg/L in heart blood and 13.3 mg/L in gastric contents. Qualitative and quantitative analyses of Au in the heart blood sample and gastric contents using inductively coupled plasma‐optical emission spectrometry detected concentrations of 79.8 mg/L and 2010.1 mg/L, respectively. Au and cyanide synergistically enhance cytotoxicity through inhibition of detoxification and increasing intracellular accumulation. In the present case, the detected blood cyanide concentration was sub or minimally lethal, and the blood Au concentration was high. The cause of the victim's death was the combined toxicity of Au and cyanide. [ABSTRACT FROM AUTHOR]

The moss bag technique was applied on Kamchatka to assess the effect of Shiveluch volcano on the air quality. Moss bags were exposed in settlements located at different distances from the volcano and affected by ashfall to varying degrees. The inductively coupled plasma optical emission spectrometry was used for the determination of the content of Al, Ba, Co, Cd, Cr, Cu, Fe, Mn, P, Pb, Sr, S, V, and Zn in both exposed and unexposed moss samples. Relative accumulation factor revealed enrichment of mosses exposed in the area affected by ashfall with Al, Cr, V, and Zn. Correlation and principal component analysis allowed to identify elements of volcanogenic, geogenic, and anthropogenic origin. Ecological risk values less than 150 indicate low potential ecological risk in the region. Active moss biomonitoring can be considered a cheap and efficient tool for in-depth study of the influence of volcanic activity on air quality on the peninsula. [ABSTRACT FROM AUTHOR]

Tourmaline is a widespread borosilicate mineral that is well known for its variable chemistry. Although a major amount of octahedral Al in tourmaline is commonplace, the occurrence of significant amounts of tetrahedral Al is relatively rare. This paper focuses on tourmaline from the collection of the A.E. Fersman Mineralogical Museum (Russia) originated from Italy with up to 25% of Si replaced by Al at the tetrahedral site. The tourmaline is characterized by optical and scanning electron microscopy, Raman spectroscopy, infrared spectroscopy, Mössbauer spectroscopy, energy-dispersive and wavelength-dispersive X-ray analysis, laser ablation inductively coupled plasma optical emission spectrometry and single-crystal X-ray diffraction. The studied tourmaline occurs as transparent dark blue crystals (with equant external morphology) up to 3 mm in size and forms veinlets cutting a (Mg,Al)-rich metamorphosed mafic-ultramafic rock (Mg >> Fe) composed of spinel, pargasite, clinochlore, phlogopite, and hydroxylapatite. The studied tourmaline meets the criteria defining magnesio-lucchesiite and can be compositionally formed via Tschermak-like ([6]Me2+ + [4]Si4+ ↔ [6]Al3+ + [4]Al3+, where [6]Me2+ = Mg,Fe) or plagioclase-like ([9]Ca2+ + [4]Al3+ ↔ [9]Na+ + [4]Si4+) substitutions. Zones with a relatively high Si content (Si-rich) have pronounced indications of dissolution, while silicon-depleted zones (Si-poor) overgrow Si-rich zones, eventually creating a visible replacement zone of the crystal. We suggest that Si-poor tourmaline results from the Si-rich tourmaline losing Si during a metasomatic process. The resulting empirical crystal-chemical formula for the Si-poor zone is: X     C a   0.95     N a   0.03     ◻ 0.02         Σ 1.00     Y     M g   1.08     A l   0.98     F e   0.50   2 +     F e   0.43   3 +         Σ 3.00     Z     A l   5.91     F e   0.09   3 +         Σ 6.00     T     S i   4.57     A l   1.43         Σ 6.00     O   18           (BO3)3V(OH)3W[O0.95(OH)0.05]Σ1.00 [a = 15.9811(2), c = 7.12520(10) Å, R1 = 1.7%] and for the Si-rich zone is: X     C a   0.89     N a   0.11         Σ 1.00     Y     M g   1.55     A l   0.80     F e   0.34   2 +     F e   0.31   3 +         Σ 3.00     Z     A l   5.51     M g   0.44     F e   0.05   3 +         Σ 6.00     T     S i   5.35     A l   0.65         Σ 6.00     O   18           (BO3)3V(OH)3W[O0.93(OH)0.07]Σ1.00 [a = 15.9621(3), c = 7.14110(10) Å, R1 = 1.7%]. According to pressure-temperature (P-T) calculations of mineral assemblage stability and comparable data on synthetic [4]Al-rich tourmalines, the studied tourmaline was formed at 600–750 °C and 0.10–0.20 GPa. The formation of tetrahedral Al-rich tourmalines requires several unusual factors: (1) desilication of primary rocks and (2) high temperatures and relatively low pressures. [ABSTRACT FROM AUTHOR]

The Journal of Analytical Atomic Spectrometry (JAAS) published in 2024 by The Royal Society of Chemistry covers a wide range of topics related to advances in the analysis of metals, chemicals, and materials. The issue includes technical notes on simplified instrumental protocols for trace Nd and Hf isotope measurements, as well as papers on various topics such as uranium measurement in a glass matrix and data fusion techniques for improving accuracy in machining processes. The journal aims to provide a platform for research on analytical atomic spectrometry and its applications in diverse fields. [Extracted from the article]

• Study investigates the physico- & phytochemical properties of bee pollen varieties. • Results confirmed high phenolics & high antioxidant activity of mustard bee pollen. • Health-promoting minerals were present, while toxic minerals (As, Pb) were absent. • Absence of toxic minerals confirms its aptness to be consumed as a functional food. • FTIR identified carbohydrates, protein functional groups, and phenolic compounds. In todayʼs health-conscious era, consumers are inclined towards value-added products that offer the option to substitute conventional food products with high-nutritional value components, thereby enhancing the quality of existing processed products. Bee Pollen is a suitable contender, which is a biologically active food ingredient comprising macronutrients, micronutrients, and phenolic compounds. It has been utilized in traditional medicine for its therapeutic properties including hepatoprotective and wound healing. This study aims to unveil the physicochemical, and phytochemical characteristics of two different varieties of bee pollen (viz. mustard and multifloral) in addition to the color, mineral, and Fourier Transform Infrared Spectroscopy (FTIR) analysis. The results indicate that mustard bee pollen (MSBP) possesses high moisture (15.33 ± 0.36 %), ash (4.3 ± 0.014 %), total phenol (2676 ± 0.58 mg GAE/100 g) and total flavonoid content (14.025 ± 0.25 mg QE/g) which is responsible for its high antioxidant activity (82.6 ± 0.54 %) as compared to multifloral bee pollen (MFBP). It was further confirmed from mineral analysis performed by using Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES) quantification procedure that health-promoting minerals like Ca, Mg, Fe, P, and Zn were present; whereas, the toxic minerals including As, Hg, Co, and Pb were absent in the pollen varieties under study. Moreover, FTIR allowed for the identification of stretching, bending, and vibrations associated with the numerous carbohydrates, protein functional groups as well as phenolic compounds. Therefore, the production of bee pollen can be scaled up to an industrial level due to its functional properties for utilization in food formulations, the pharmaceutical industry, and the nutraceutical sector. [ABSTRACT FROM AUTHOR]

The study focuses on the specific features of zinc determination in dust emissions from gas cleaning systems used in an electrometallurgical plant used to process scrap metal. X-ray powder diffraction, energy-dispersive X-ray fluorescence spectrometry (EDXRF), and inductively coupled plasma atomic emission spectrometry (ICP–AES) were employed to identify the elemental and phase compositions of the dust emissions, including zinc oxide, zinc ferrite, halite, sylvite, and magnetite. Based on these compositions, an analytical procedure was developed. The proposed rapid energy-dispersive X-ray fluorescence spectrometry method for zinc determination in dust emissions involves constructing a calibration curve with matrix effect corrections. The relative deviation for zinc determination using EDXRF with matrix correction was 2.1%, while for ICP–AES it was 2.5%. The zinc determination method was tested on real samples of gas cleaning dust emissions. [ABSTRACT FROM AUTHOR]

In this study, we evaluated the effect of the retarders urea and sodium phosphate on the hydration process and leaching of Cr(VI) in calcium sulfoaluminate cement from solid waste (WCSA). We investigated the mechanical properties and hydration processes of WCSA with varying urea and sodium tripolyphosphate contents using thermogravimetry coupled with differential scanning calorimeter (TG-DSC), X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) analysis, and scanning electron microscopy (SEM); the leaching behavior of the heavy metal Cr(VI) in the cement was analyzed using inductive coupled plasma emission spectrometry (ICP). The experimental results showed that lower urea or sodium tripolyphosphate (STPP) contents (0.2%) improved the compressive strength of cement specimens by 18.31% or 3.125% at 28 days, respectively. After incorporating STPP and urea, the hydration heat flow and total hydration heat of WCSA decreased. The porosity first decreased and then increased with increased STPP and urea content. The involvement of urea in hydration produced carbonate, which destroyed the structure of ettringite and formed a new calcium carbonate phase, leading to the release of Cr(VI). In the presence of STPP, a three-dimensional network structure of hydroxyapatite was generated. Chromium ions entered the three-dimensional network structure of hydroxyapatite, increasing the solidification of Cr(VI) in WCSA. [ABSTRACT FROM AUTHOR]

The silicon-aluminum ratio of the molecular sieves is a crucial control index for the quality of synthetic molecular sieves. Here a fast, simple and reliable sample preparation method, referred to as pouring and curing method, is described for determining the silicon-aluminum ratio of high silicon molecular sieves by energy dispersive x-ray fluorescence (EDXRF). Resin is used as the carrier with the addition of a curing agent, so that the sample powder is embedded in the resin matrix. By measuring sixteen random positions of the same cured sample, the homogeneity of the sample was evaluated to ensure the stability of the results. A double logarithmic calibration curve of the analysis line ratio and the corresponding concentration ratio of silicon and aluminum was established according to the binary ratio method. The results by EDXRF and inductively coupled plasma-optical emission spectrometer (ICP-OES) were compared with a relative standard error from 2.934 to 6.777%. The good precision shows that the pouring and curing method is a suitable for measuring the silicon-aluminum ratio of molecular sieves. [ABSTRACT FROM AUTHOR]

A series of Cu‐based mixed oxides were prepared by calcinations of corresponding CuMgAl‐layered double hydroxides precursors at different temperatures with nominal Cu/Mg/Al ratios of 1 : 1 : 2(Cu‐LDH‐1), 1 : 2 : 1(Cu‐LDH‐2),1 : 1 : 1(Cu‐LDH‐3), and 2 : 1 : 1(Cu‐LDH‐4). The synthesized catalysts were characterized using X‐ray diffraction, high‐resolution transmission electron microscopy, scanning electron microscopy, X‐ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, inductively coupled plasma atomic emission spectroscopy (ICP‐AES), and N2 physisorption analysis techniques. All as‐obtained catalysts showed adequate catalytic performance for the α‐alkylation of ketones with alcohols through a hydrogen autotransfer mechanism. The catalyst CuMgAl‐I‐650 (obtained by calcining Cu‐LDH‐1 at 650 °C) displayed the highest activity and selectivity. Using this catalyst system, a wide range of branched ketones were synthesized in good to excellent isolated yields. Moreover, the catalyst CuMgAl‐I‐650 could be recycled and reutilized for four cycles without any significant loss of activity and selectivity. This study provides a very simple and inexpensive catalysis based on transition metals, which are in abundance on earth. [ABSTRACT FROM AUTHOR]

The study was conducted in Cerritos, San Luis Potosí, México, near the Guaxcama mine, focused on environmental contamination (groundwater and agricultural soil) from antimony (Sb), arsenic (As), lead (Pb), cadmium (Cd), and mercury (Hg). In March 2022, 20 agricultural soil and 16 groundwater samples were collected near the historically cinnabar (HgS)- and arsenopyrite (FeAsS)-rich Guaxcama mine. Hydride generation atomic fluorescence spectrometry (HG-AFS) for As, cold vapor atomic fluorescence spectrometry (CV-AFS) for Hg, and inductively coupled plasma optical emission spectrometry (ICP-OES) for Cd, Pb, and Sb were used for the determinations of potentially toxic elements (PTEs). While concentrations of Cd, Hg, Pb, and Sb in groundwater were below detection limits, As levels exhibited a range from 40.9 ± 1.4 to 576.0 ± 1.0 µg/L, exceeding permissible limits for drinking water (10 µg/L). In agricultural soil, As was between 7.67 ± 0.16 and 24.1 ± 0.4 µg/g, Hg ranged from 0.203 ± 0.018 to 2.33 ± 0.19 µg/g, Cd from 2.53 ± 0.90 to 2.78 ± 0.01 µg/g, and Pb from 11.7 ± 1.2 to 34.3 ± 4.1 µg/g. Only one study area surpassed the Mexican As soil limit of 22 µg/g. Sequential extraction (four-step BCR procedure) indicated significant As bioavailability in soil (fractions 1 and 2) ranging from 3.66 to 10.36%, heightening the risk of crop transfer, in contrast to the low bioavailability of Hg, showing that fractions 1, 2, and 3 were below the limit of quantification (LOQ). Crucial physicochemical parameters in soil, including nitrate levels, pH, and organic matter, were pivotal in understanding contamination dynamics. Principal component analysis highlighted the influence of elements like Fe and Ca on phytoavailable As, while Pb and Cd likely originated from a common source. Ecological risk assessments underscored the significant impact of pollution, primarily due to the concentrations of Cd and Hg. Non-cancer and cancer risks to residents through As poisoning via contaminated water ingestion also were found. The hazard index (HI) values varied between 4.0 and 82.2 for adults and children. The total incremental lifetime cancer risk (TILCAR) values for adults ranged from 7.75E − 04 to 1.06E − 02, whereas for children, the values were from 2.47E − 04 to 3.17E − 03. [ABSTRACT FROM AUTHOR]

Two‐dimensional Molybdenum diselenide is a versatile and promising material used for a wide range of applications and its synthesis in high quality and yield is currently the subject of intense research. Low temperature solution phase synthesis of nanomaterials using designed molecular precursors enjoys tremendous advantages over traditional high‐temperature solid‐state synthesis. However, molecular precursor chemistry of molybdenum selenide nanomaterials is almost non‐existent. We report here synthesis and structural characterization of new molybdenum molecular precursors with selenoether and selenourea ligands, which due to their easy synthesis, desired Mo/Se composition and moderate processing properties, are highly promising as single source precursors for the scale‐up production of 2D molybdenum diselenide materials. This is demonstrated by the solution‐phase decomposition of the Mo‐selenourea precursor which produced Mo‐rich MoSe2‐x ultrathin nanosheets (NSs) in good yield. These NSs were characterized by Inductively Coupled Plasma Optical Emission Spectroscopy (ICP‐OES), Powder X‐ray diffraction (XRD), Raman spectroscopy, Fourier Transform Infrared Spectroscopy (FT‐IR), Thermogravimetric analysis (TGA), Transmission electron microscopy (TEM) and X‐ray photoelectron spectroscopy (XPS) studies. [ABSTRACT FROM AUTHOR]

Biostimulants contribute to the physiological growth of plants by enhancing the quality characteristics of fruit without harming the environment. In addition, biostimulants applied to plants strengthen nutritional efficiency, abiotic stress tolerance, and fruit biochemical traits. We investigated the effectiveness of specific organic biostimulants. Five treatments were tested: (1) control (H2O, no biostimulants); (2) Magnablue + Keyplex 350 (Mgl + Kpl350); (3) Cropobiolife + Keyplex 120 (Cpl + Kpl120); (4) Keyplex 120 (Kpl120); and (5) Magnablue + Cropobiolife + Keyplex 120 (Mgl + Cpl + Kpl120) on the mineral uptake and physiology in black chokeberry (Aronia) plants, as well as the quality of their berries. The different treatments were applied to three-year-old chokeberry plants, and the experimental process in the field lasted from May to September 2022 until the harvest of ripe fruits. Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES) revealed that the fifth treatment significantly increased concentrations of P, Ca, and K. Additionally, the fifth treatment enhanced photochemical efficiency (Fv/Fm), water-splitting efficiency (Fv/Fo) in PSII, and the performance index (PI) of both PSI and PSII in chokeberry leaves. Improvements in photosynthesis, such as CO2 assimilation (A), transpiration (E), and water-use efficiency (A/E), were also noted under biostimulant applications. Upon harvesting the ripe fruits, part of them was placed at room temperature at 25 °C, while the rest were stored at 4 °C, RH 90% for 7 days. The cultivation with biostimulants had beneficial effects on the maintenance of flesh consistency, ascorbic acid concentration, and weight of berries at 4 and 25 °C, especially in the 5th treatment. Moreover, the total antioxidant capacity, anthocyanin concentration, and total phenols of the berries were notably higher in the third and fifth treatments compared to the control. These data suggest that selecting appropriate biostimulants can enhance plant yield and fruit quality by potentially activating secondary metabolite pathways. [ABSTRACT FROM AUTHOR]

Copyright of Chinese Journal of Inorganic Analytical Chemistry / Zhongguo Wuji Fenxi Huaxue is the property of Beijing Research Institute of Mining & Metallurgy Technology Group and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Chinese Journal of Inorganic Analytical Chemistry / Zhongguo Wuji Fenxi Huaxue is the property of Beijing Research Institute of Mining & Metallurgy Technology Group and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The etch rate uniformity in photoresist etching was monitored using multi-channel optical emission spectroscopy (OES) and a spatially resolved etch rate model incorporating radical and ion etching characteristics. The F radical densities at various locations were estimated using 8-channel OES and applied to a radical-spontaneous etch rate model to examine the impact of radicals on the etch rate. The ion fluxes were measured using a scanning floating harmonic probe for an ion-enhanced etch rate model to investigate the effect of ions on the etch rate. A combined etch rate model was proposed to explain the effects on both radical and ion etching characteristics, and the etch rates and etch rate uniformities predicted by the model were quantitatively compared with the measured values. The calculated R-squared score (R2) and the mean absolute percentage error (MAPE) of the etch rates predicted by the model were 0.99 and 1.3%, respectively. The etch rate uniformities predicted by the model showed good accuracy with R2 of 0.99 and MAPE of 12.0% compared to the measured values, and the combined etch rate model also successfully predicted the distribution of the etch rate. This study demonstrates that multi-channel OES and the developed model can quantitatively predict the etch rate distribution of plasma etching processes. [ABSTRACT FROM AUTHOR]

The increasing presence of nanoparticles in food products, especially in those consumed by sensitive populations like infants, raises justified health concerns. The presence of zinc oxide nanoparticles (ZnO-NPs) in three different commercial infant milk formulas were analyzed. In addition, one maternal food supplement was included in this study. Notably, existing regulations lack specificity regarding the size distribution of nanoparticles (NPs) and the maximum permissible concentrations in commercial infant products. Except in one sample, the total zinc content exceeded the reported amount in the nutritional label, which varied from 34 to 119 µg/g. This work validated the cloud point extraction (CPE) technique for the effective isolation of ZnO-NPs from the selected products. CPE was then used to evaluate the ZnO-NPs concentrations in commercially available infant formulas and maternal supplements. Using inductively coupled plasma optical emission spectrometry (ICP-OES), the ZnO-NPs and total Zn concentrations were determined. The ZnO-NPs concentration ranged from 16 to 39 µg/g, representing a considerable portion of the total zinc content. Transmission electron microscopy (TEM) analysis indicated the presence of nanoparticles with an average diameter of 6.3 nm. The NPs size could determine their cell internalization, and thus, the potential cytotoxic effects are discussed. These findings underscore the need for rigorous isolation and quantification of nanoparticles from infant milk formulas, and as an inevitable first step for in vitro and in vivo toxicity studies to address the potential health impact of nanoparticles in food products. [ABSTRACT FROM AUTHOR]

ABSTRACT As the world shifts towards renewable and sustainable energy sources, converting syngas into hydrocarbons using Fischer–Tropsch synthesis (FTS) catalysts is crucial. In this work, a series of copper‐modified iron‐based catalysts with cerium and strontium promoters supported on γ‐Alumina as follows were prepared using a wet‐impregnation method: FCA (18Fe/4Cu/γ‐Al2O3), FCCA (18Fe/4Cu/2Ce/γ‐Al2O3), FCSA (18Fe/4Cu/2Sr/γ‐Al2O3), and FCCSA (18Fe/4Cu/1Ce/1Sr/γ‐Al2O3). The phase, structure, and morphology of the catalysts were characterized using X‐ray diffraction (XRD), Brunauer–Emmett–Teller (BET) specific surface area analysis, field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), inductively coupled plasma–atomic emission spectrometry (ICP‐AES), hydrogen temperature‐programmed reduction (H2‐TPR), and hydrogen temperature‐programmed desorption (H2‐TPD). The impacts of Ce and Sr, individually and in combination, on the structure, adsorption, reduction, and catalytic performance of the catalysts were evaluated in a fixed bed reactor at 300°C, 2.0‐MPa pressure, a time of stream of 168 h, and an H2/CO ratio of 1. The CO conversion and product selectivity were calculated using gas chromatography results, highlighting the synergistic effect of Ce and Sr promoters on hydrocarbon product distribution. The doubly promoted FCCSA catalyst exhibited a high CO conversion rate of 77.65%, CO2 selectivity of 43.5%, C2‐C4 selectivity of 55.89%, C5+ selectivity of 85.62.0%, and a yield of 43.19%, surpassing FCA, FCCA, and FCSA catalysts. Similar characteristics, CO conversion, and product selectivity were achieved for FCCSA during long‐term 336‐h FTS runs, indicating stability. [ABSTRACT FROM AUTHOR]

This study was designed to evaluate the health risks faced by inhabitants living in the slum areas of Addis Ababa, Ethiopia. The levels of PM2.5 and PM10 and elemental composition of the PM10 were measured in indoors (in the kitchen and living room) and outdoors (at the roadside). A total of 75 sampling locations (45 indoor and 30 outdoor) were selected for the study. The levels of PM2.5 and PM10 were determined using an AROCET531S instrument, while an universal air pump was used for the sampling of PM10 for the determination of trace elements by inductively coupled plasma-optical emission spectroscopy (ICP‒OES). The health impacts of PMs on the inhabitants of twelve microenvironments (MEs), where they spend much of their daily time, were estimated. The total amounts of PM2.5 and PM10, and trace metals in PM10 found in the nine or twelve MEs ranged from 10.6–119, 128–185, and 0.007–0.197 μg m-3, respectively. According to the United States Environment Protection Agency (USEPA) guidelines, ten of the twelve MEs can cause significant health problems for inhabitants (HI > 1) due to PM2.5 and PM10. Thus, special attention should be given by stakeholders/inhabitants to minimize the health impacts on long-term exposure. This study assessed the risk of levels of trace elements on the inhabitants who spend most of their daily lives. The study revealed that the lifetime cancer risk values for the individual and cumulative trace elements were within the tolerable range set by the USEPA guidelines. [ABSTRACT FROM AUTHOR]

Beach pollution can impact the health of people living in or visiting coastal areas. The primary goal of this research was to investigate the presence of heavy metal pollutants and associated health risks in three distinct coastal cities, Jeddah, Al-Lith, and Al-Qunfudhah, located along Saudi Arabia's Red Sea coast. Forty-three soil samples were collected from different locations, heavy metals including Fe, Zn, Mn, Cu, Cd, and Pb were isolated, and analyzed using inductively coupled plasma optical emission spectroscopy. Various metrics such as pollution indices (PI), integrated pollution indices (IPI), enrichment factors (EF), daily dose averages (ADD), hazard quotients (HQ), and hazard indices (HI), as well as principal component analysis (PCA) and cluster analysis were employed to evaluate the environmental impacts and health risks posed by these heavy metals. The results revealed that Fe, Pb, Cu, Mn, and Zn concentrations in beach zones were below their respective background levels, while concentrations of Cd exceeded corresponding background levels. PCA revealed the highest levels of Pb, Fe, and Mn on Al-Qundudah beach, while Cd and Cu were highest on Al-Lith beach, and Zn was highest on Jeddah beach. PI values highlighted extremely high levels of Cd pollution on all designated beaches. The findings provide a foundational basis for further investigations into health problems potentially related to Cd contamination, such as chronic kidney disease (CKD), osteomalacia, and osteoporosis. [ABSTRACT FROM AUTHOR]

Chronic inflammation significantly contributes to the progression of osteoarthritis (OA), and an anti‐inflammatory small molecule derived from medicinal herbs could be a potential drug candidate for OA. Herein, we investigated the function and mechanism of Evodiamine (EAE), the active ingredient from Evodia rutaecarpa, in chondrocytes and macrophages in vitro and in vivo. The cytotoxicity of EAE was determined using an MTT assay. And the anti‐inflammatory and anti‐extracellular matrix (ECM) degradation effects of EAE were investigated using qRT‐PCR, western blot (WB), immunofluorescence (IF). Inductively Coupled Plasma Atomic Emission Spectrometry (ICP‐AES), Fluo‐4 AM, IF and AutoDock were used to elucidate the molecular mechanisms and signalling pathways of the reducing‐inflammatory properties of EAE on chondrocytes in vitro. Moreover, the effect of EAE on macrophage polarization was detected by IF and flow cytometry (FC). Ultimately, we explored the in vivo therapeutic efficacy of EAE in an anterior cruciate ligament transection (ACLT)‐induced OA model. The finding demonstrated that EAE blocked the phosphorylation of IKBα and Ca2+ influx, thereby curbing inflammation and ECM degradation. Additionally, EAE can prevent the polarization towards the M1 phenotype. Thus, our findings suggest that EAE has great potential as a therapeutic drug for the treatment of OA. [ABSTRACT FROM AUTHOR]

The current investigation involved the development of activated carbon, juglans regia activated carbon (JRACs), from walnut shells, scientifically known as Juglans regia. The ZnO nanorods were loaded on the activated carbon and referred to as ZnO@JRACs. Desulfurization efficiency was assessed through batch adsorption and compared to commercial activated carbon known as DARCO. The materials were characterized using PXRD (powder X-ray diffraction), FTIR (Fourier-transform infrared spectroscopy), ICP-AES (inductively coupled plasma atomic emission spectroscopy), BET (Brunauer–Emmett–Teller) surface area analysis, TEM (transmission electron microscopy) imaging, and TGA (thermal gravimetric analysis). The findings indicated that the materials have oxygen functionalities, a porous morphology, and a substantial specific surface area (BET) of 1269.92 m2/g for ZnO@JRACs. Zn atom concentration in the ZnO@JRACs surface was determined to be 1.16 atomic percent using ICP-AES. Desulfurization experiments were conducted on three liquid fuels, namely a single component model fuel, MSF (multicomponent simulated fuel), and commercial fuel (kerosene), under optimized conditions (8 g/L adsorbent dosage in 10 mL of fuel, 15 min of contact time at room temperature). The conditions effectively removed ~ 98.9% of dibenzothiophene (DBT) from the single component model fuel. The observed order for adsorption capacity is as follows: ZnO@JRACs (63.6 mg g−1) > JRACs (46.3 mg g−1) > DARCO (26.1 mg g−1). The analysis of multicomponent simulated fuel (MSF) using gas chromatography-flame photometric detector (GC-FPD) revealed significant removal percentages for different types of thiophenic sulfur. Specifically, the removal percentages were ~ 46.2%, 97.6%, and 99.4% for benzothiophene, dibenzothiophene, and 4, 6-dimethyldibenzothiophene, respectively. Kinetic studies have shown that the adsorption process is governed by a pseudo second-order reaction. Additional thermodynamic studies were conducted to further investigate the mechanism of adsorption. The spent synthesized composite ZnO@JRACs were thermally regenerated and can be reused for up to four cycles. [ABSTRACT FROM AUTHOR]

Environmental pollution from heavy metals such as zinc (Zn), lead (Pb), and cadmium (Cd) poses serious risks to human health and ecosystems. This study examines the bioaccumulation of these metals in the livers of house sparrows (Passer domesticus) in Meknes, Morocco, using them as bioindicators of pollution. Fifty adult sparrows were collected from five areas: The Industrial Zone (IZ), Town Centre (TC), Sidi Said Bus Station (SS), Fes-Meknes Main Road (MR), and a Rural Site (Ref). Liver samples were analysed with Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES). The highest Zn concentrations were found at IZ (111.43 µg/g) and Ref (90.66 µg/g), Pb at TC (4.17 µg/g), and Cd at IZ and TC (0.70 µg/g and 0.71 µg/g). Statistical analyses revealed significant correlations between metal levels. Clustering techniques identified three distinct contamination profiles. These results highlight house sparrows as reliable bioindicators for monitoring heavy metal pollution. [ABSTRACT FROM AUTHOR]

The treatment of damaged enamel surfaces involves modification of the enamel surface with artificial materials or the development of a pseudo-enamel, with research focusing on bioactive and biomimetic materials. In this study, a bioactive auto-polymerizing resin (APR) was developed by adding surface-pre-reacted glass ionomer (S-PRG) fillers of different quantities to APR. Its bioactive effects were evaluated via pH neutralization, ion release, and inhibition of enamel demineralization studies. The pH and fluoride ion release were measured using ion-specific electrodes, revealing that the APR disk with the S-PRG filler immediately neutralized the lactic acid solution (pH 4.0) through ion release. Inductively coupled plasma atomic emission spectrometry revealed that the Sr ion release peaked on the first day, with the other ions following the order F > B > Si > Al > Na, exhibiting a weekly decrease in the same order. Scanning electron microscopy was used to examine the enamel block morphology of the disks after 7 d of incubation, revealing enamel demineralization in disks without the S-PRG filler, whereas no demineralization occurred in disks with the S-PRG filler. APR containing the S-PRG filler demonstrated acid buffering suppressed enamel demineralization and bioactive properties. [ABSTRACT FROM AUTHOR]

A three‐step synthetic route is established for the synthesis of a phosphorus‐containing ε‐caprolactam derivative, starting from cyclohex‐2‐enone and diphenylphosphinous chloride, followed by a Beckmann rearrangement. 2D NMR spectroscopy reveals that the phosphorus moiety is selectively localized at the 4‐position of the caprolactam ring. Different amounts of the phosphorus‐containing comonomer are systematically incorporated into polyamide 6 by anionic ring‐opening copolymerization with ε‐caprolactam at elevated temperatures. Polymerization reactions are initiated by a latent, CO2 protected N‐heterocyclic carbene in the presence of N‐acetyl caprolactam and MgCl2. The phosphorus content is determined by inductively‐coupled plasma‐optical emission spectroscopy (ICP‐OES) analysis. Limiting oxygen indices up to 23.5 are found for polymers containing ≈1 wt.‐% of phosphorus. The thermal properties of the copolymers are determined and compared to those of polyamide 6. [ABSTRACT FROM AUTHOR]

This study investigates the magnetic response of Ho3+ doped Ni 0.4 Cu 0.6 Ho y Fe 2-y O 4 (y = 0.0, 0.02, 0.04, 0.06, and 0.08) spinel ferrites (SFs) and their correlation with crystallite size. The synthesis was achieved using a sol-gel auto-combustion (SGAC) route and performed different characterizations, including X-ray diffraction (XRD), Scanning electron microscope (SEM), Energy dispersive x-ray (EDX), Inductively coupled plasma atomic emission spectroscopy (ICP-AES), and vibrating sample magnetometer (VSM) analysis. The cubic spinel phase was verified via XRD in pure NCF and Ho3+ doped NCF samples. The lattice constant (a) was improved from 8.344 Å to 8.378 Å. The substitution of Ho3+ ions led to a decrease in porosity from 42.22 % to 39.54 %. The introduction of Ho3+ ions also reduced the crystallite size (D) from 37.05 nm to 27.72 nm. The specific surface area (S) was increased from 27.44 g/cm2 to 36.14 g/cm2 with the doping of Ho3+. The average particle size (D S) was decreased from 54 nm to 35 nm. The EDX and ICP-AES analyses confirmed the good agreement with the theoretical composition. The VSM measurements provided insights into their magnetic properties. Furthermore, the doping of Ho3+ ions enhanced coercivity (H C), while reducing saturation magnetization (M S) from 64.35 emu/g to 16.22 emu/g. The decrease in crystalline anisotropy (K) observed at higher concentrations of Ho3+ may result from the increase in coercivity, potentially attributable to the smaller crystallite size of the single-domain SFs particles. The single-phase matrix and their magnetic behaviour showed that the Ho3+ doped Ni–Cu SFs samples are suitable for high-frequency applications. [Display omitted] • Ni 0.4 Cu 0.6 Ho y Fe 2-y O 4 was prepared via the sol-gel auto-combustion technique. • The crystallite size was the minimum (27.72 nm) for the y = 0.08 (NCHF4) sample. • The sample has y = 0.08 (NCHF4) and contains maximum coercivity (1031.44 Oe). • The sample has y = 0.08 (NCHF4) and is best-suitable for high-frequency applications. [ABSTRACT FROM AUTHOR]

Household cleaning products (HCPs) are widely used; however, their airborne emissions and hazards have not been thoroughly studied. This study is aimed at evaluating the concentrations of volatile organic compounds (VOCs) and metals present in HCPs and the hazards associated with them. A total of 23 VOCs and 19 metals from 75 HCPs (four spray types and 14 intended usage categories) were analyzed using gas chromatography–mass spectrometry and inductively coupled plasma‐mass spectrometry/optical emission spectroscopy. The largest number of VOCs (21 of 23 ingredients) were detected in spray‐type and had the highest frequency (176). d‐Limonene was found in almost all products (69 of 75) and had the highest concentration. Benzene, a carcinogen, was detected in six spray‐type products. Only three of the 23 VOCs—d‐limonene, ethyl acetate, and heptane—appeared in three, one, and one product labels, respectively. Eight of 19 metals were primarily detected in spray‐type and spray foam‐type products, with sodium, magnesium, and calcium as the main components. Nickel, another carcinogen, was detected in both spray‐type and trigger‐type products. Caution is required when using spray‐type products, especially sticker/glue/tar/oil removers containing benzene and nickel. The study discovered that the VOCs and metals varied by their spray type and lacked sufficient harmful information. [ABSTRACT FROM AUTHOR]

Inaouen wadi is the second largest tributary of the Sebou river, one of Morocco's major rivers, which holds significant economic and social importance. Unfortunately, this watercourse is severely impacted by pollution from various human activities, particularly industrial sources. However, available data on the presence of potentially toxic elements (PTEs) that could harm human health in this region remain limited. PTEs pose major environmental risks due to their toxicity, persistence, and bioaccumulation. This study aimed to assess the concentrations of PTEs in the sediments of Inaouen wadi and its main tributaries based on sediment samples collected from 12 locations in 2019. The concentrations of Cd, Pb, Cr, Ag, Al, Cu, Fe, and Zn were measured using inductively coupled plasma atomic emission spectroscopy (ICP–AES), and sediment contamination levels were evaluated using multiple indices: the enrichment factor (EF), the geo-accumulation index (Igeo), the potential ecological hazard index (RI), and the modified ecological risk index (MRI). The results indicate that concentrations of Pb, Cd, Cr, Cu, Fe, and Zn are significantly influenced by urban discharges, particularly at sites S1, S3, and S5 near the cities of Taza and Oued-Amlil. The maximum values recorded were 7.01 g/kg for Pb, 0.9 g/kg for Cd, 0.1 g/kg for Cr, 19.9 g/kg for Fe and 1.9 g/kg for Zn. The enrichment factor (EF) revealed anthropogenic sources of Fe and Pb, confirming the human origin of these elements. The geo-accumulation index (Igeo) showed that the areas around stations S1, S3, and S5 are highly contaminated by Pb, Cd, and Fe, a finding also supported by the MRI. The study identified potential ecological risks at stations S1, S3, and S5, highlighting the urgent need for improved pollution management practices to mitigate environmental risks. [ABSTRACT FROM AUTHOR]

Medicinal plants (MPs) have long been used for their therapeutic properties in traditional forms of medicine. However, the presence of potentially toxic elements (PTEs) in MPs raises concerns about their safety, efficacy, and potential adverse effects on human health. The current study aimed to determine the level of potentially toxic and essential elements (PTEEs) in commonly consumed MPs in Zabol, Iran, along with their health risk assessments. To conduct the present study, 10 types of MPs widely used in Zabol, Iran, were selected, and 15 samples of each type (150 samples in total) were taken. Each sample was analyzed for the presence of various PTEEs using Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES) for Lead (Pb), cadmium (Cd), chrome (Cr), nickel (Ni), copper (Cu), zinc (Zn), iron (Fe), aluminum (Al) and manganese (Mn); and Atomic Absorption Spectrometry (AAS) for arsenic (As) and mercury (Hg). Finally, to better comprehend the scope of exposure and its possible effects, the Monte Carlo simulation method is successfully applied to assess human health risks related to PTEs in MPs. Statistical analysis revealed statistically significant (P < 0.001) variations in PTE averages among MP types. Furthermore, all samples' overall PTE mean concentration (range: 0.18 to 215.5 µg/kg) was below the World Health Organization's (WHO) regulatory standards. Probabilistic health risks, including non-carcinogenic-target hazard quotient (THQ) for each element, total target hazard quotient (TTHQ) for all elements, and carcinogenic-incremental lifetime cancer risk (ILCR) for each element, and total carcinogenic risk (TCR) for all elements, were significantly lower than the acceptable limit for children and adults. Accordingly, it can be said that consuming MPs sold in Zabol is safe for children and adults regarding carcinogenic (ILCR/TCR = 10− 4) and non-carcinogenic (THQ/TTHQ = 1) effects. In light of the findings presented here, and to our understanding, the primary factor contributing to lower levels of PTEs in MPs in Zabol City markets is the cultivation of plants in nonindustrialized areas, separate from urban and industrial zones. This practice keeps them from environmental contaminations, including soil quality and water sources. It is recommended that it is essential to regulate the sources that enhance the transfer of PTEs and other harmful pollutants from surroundings to the soil and, consequently, MPs. It is also suggested that, like chemical drugs, MPs should undergo rigorous testing by quality control agencies before being made available to the market. [ABSTRACT FROM AUTHOR]

Considering the urgency of resource utilization and environmental protection, the geochemistry of anomalous trace transition metal elements in coal formed in terrestrial environments has been studied using methods such as inductively coupled plasma atomic emission spectrometry analysis, electron probe micro-area analysis, sequential chemical extraction procedures, and correlation analysis. The results indicate that minerals in the coal samples included pyrite, kaolinite, quartz, dolomite, calcite, and celestite. Furthermore, compared with the average values of coals in China and the upper continental crust, the coal samples were rich in transition metal trace elements such as Ni, Cr, and Sr and were deficient in Be, Cd, Cu, Co, Ga, Mo, Sb, Tl, V, Zn, and Ti. We found that Ni preferentially occurred in the organic matter over minerals, while Cr primarily bonded with sulfide minerals and to a lesser extent with the iron-manganese oxide minerals. Sr had a low correlation with organic matter but adhered to clay minerals and celestite. Ni enrichment in coal samples was the result of terrigenous input, while the Cr enrichment was related to intrusion of magmatic hydrothermal fluids. Sr enrichment was caused by the presence of SO42- in the terrigenous debris and the influence of Sr-rich water underground. [ABSTRACT FROM AUTHOR]

Conventional energy sources emit huge amounts of carbon dioxide (CO 2) into the atmosphere causing global warming. Hydrogen (H 2) is an alternative clean energy carrier that produces only heat and water vapor upon combustion. In this work, we utilized industrial waste material (Red Mud, RM) to develop a cost-effective and efficient catalyst for steam reforming of diesel (n-dodecane as a model compound) for hydrogen production. We impregnated nickel (Ni), a prudent and effective metal, in red mud (RM) in varied proportions to employ as a catalyst for hydrogen production. The catalysts' structure was characterized by powdered X-ray Diffraction (PXRD), Fourier Transform Infrared spectroscopy (FTIR), and X-ray Photoelectron Spectroscopy (XPS). Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES) and Electron Dispersive Spectroscopy (EDS) were used to measure the elemental composition while Scanning Electron Microscopy (SEM) was used to investigate the catalysts' morphology. Surface area and porosity were analyzed using the N 2 adsorption/desorption isotherms, and H 2 -Temperature Programmed Reduction (H 2 -TPR) to study the reducibility and interaction of Ni species to the RM. The catalysts were then evaluated for hydrogen production by the steam reforming process of n-dodecane (SRD). It was found that the catalyst with 20% Ni loading (20% Ni@RM) can produce hydrogen with selectivity as high as 75%, and stability for 20 h with a negligible decline in the catalyst performance. • Red Mud-impregnated nickel was developed as an efficient catalyst for steam reforming of diesel for hydrogen production. • The catalyst with 20% Ni loading (20% Ni@RM) in Red Mud can produce hydrogen with selectivity as high as 75%. • The catalysts showed stability for 20 h with a negligible decline in the catalyst performance. • The 20%Ni@RM catalysts show the highest yields 75.61%, 15.62%, and 6.07 of H 2, CO, H 2 /CO ratio correspondingly. [ABSTRACT FROM AUTHOR]

AbstractDue to the worldwide growth in population, agricultural and industrial activities are expanding quickly, which pollutes the air, water, and soil and leads to the buildup of potentially hazardous substances in medicinal plants. The current study sought to determine the concentrations of various metals in Silybum marianum plants and soils in order to highlight the level of pollution in a Turkish Organized Industrial Zone in Dilovasi District, Kocaeli, and to investigate the effects of these heavy metals on plants. In order to determine the concentrations of elements evaluated within the scope of this study inductively coupled plasma optical emission spectroscopy was employed, due to the benefits of ICP that provides few or no organic molecules, few ionization interferences, as well as the ability to analyze many elements sequentially. Furthermore, in order to evaluate elemental analysis in terms of nutritional values, risk assessments using RDA, EDI, THQ, and HI parameters were conducted. The value of heavy metals in co-located soil samples is relatively high. However, except for Co, Mn, and Ni, it has stayed within the World Health Organization’s permitted limits. The evaluation of the co-located soil samples found that the highest contents (mg kg−1) of Al, Ca, Cd, Cr, Cu, Fe, K, Mn, Na, Ni, Pb, and Zn, were recorded as 7825.10, 4365.86, 4768.59, 2.50, 30.45, 38.49, 8352.00, 17452.26, 1495.82, 1495.82, 163.53, 1452.23, 28.67, 136.55 and 125.45, respectively, belonging to Location 1. These findings are in accordance with the Industrial Status Report since the place specified as Location 1 in the current study is characterized by its pronounced industrial activity and the robust electrical plant station with an industrial facility for generating electric power. Furthermore, the hazard index, the estimated daily intake and target hazard quotient for potentially harmful components and recommended daily allowance values for mineral nutrients were computed. Therefore, even though mineral nutritional values in some areas were found to be higher than Buyukada control location, this should be ignored. Consequently, this study warns against using S. marianum plants as food or medicine collected from current regions. As a result, ongoing inspection is necessary to prevent an excessive buildup of metals in the area and other places with similar human life-related features. [ABSTRACT FROM AUTHOR]

We studied cytotoxicity and accumulation of boron and lithium by cultured human fibroblasts and human and mouse skin melanoma cell cultures. The cytotoxicity of boron and lithium drugs was assessed by MTT tests in the boron and lithium concentration range of 10-640 μg/ml. Cell viability was significantly reduced after incubation with boron and lithium at concentrations >160 μg/ml. To assess accumulation of boron and lithium, the concentration of elements was measured using inductively coupled plasma atomic emission spectrometry. Melanoma cells more intensively accumulated lithium in comparison with boron. The results indicate the possibility of safe application of lithium salts in concentrations minimally required for successful neutron capture therapy. [ABSTRACT FROM AUTHOR]

The antibacterial performance of biocomposite films prepared from lignocellulosic waste (hazelnut husk or hazelnut leafy green cover) modified with silver nanoparticles and polylactic acid (PLA) was determined. The amount of hazelnut husk in the PLA matrix ranged from 10 to 40% by weight in 10% increments. The composite pellets were produced using a twin-screw extruder. Biocomposite films of 0.6 mm x 40 mm x 200 mm were produced from the pellets in a laboratory hydraulic hot press. The surfaces of the modified hazelnut husk and biocomposite specimens were analyzed by scanning electron microscopy (SEM) and inductively coupled plasma optical emission spectrometry (ICP-OES). The antibacterial activity of the biocomposite films against Staphylococcus aureus bacteria was determined using the ASTM E 2149 (2020) method. The antibacterial activity of the biocomposite films increased noticeably with the addition of hazelnut husk modified with the silver nanoparticles. Compared to the pure PLA film, the biocomposite films with 10 wt% modified husk flour showed the lowest antibacterial activity (31.3%) against S. aureus over 24-h while the films with 40 wt% showed the highest antibacterial activity (99.9%). The biocomposite films made of hazelnut husk flour with silver nanoparticles and PLA matrix could be considered for food packaging applications. [ABSTRACT FROM AUTHOR]

This study aimed to determine the most suitable woody species that can be used to reduce the pollution of Sr, Mo, and Sn, which are heavy metals that are harmful to the ecosystem and human and environmental health. Within the study's scope, samples were taken from the wood parts of 16 woody species growing under similar conditions in Düzce province, which is among the five cities with the most polluted air in Europe. The wood part is the largest organ of higher plants in terms of mass; it traps heavy metals within itself for many years and can remove heavy metals to a great extent. Therefore, plants with a high potential for heavy metal accumulation in the wood part are among the most suitable plants for phytoremediation studies. The study determined Sr, Mo, and Sn concentrations in the wood parts of 16 tree species via inductively coupled plasma optical emission spectroscopy and compared them using statistical methods. Results indicate that Robinia pseudoacacia and Cedrus atlantica species were suitable for reducing pollution by Mo and Sn, while Platanus orientalis and Populus alba species were suitable for reducing Sr pollution. [ABSTRACT FROM AUTHOR]

The ammonium sulphate roasting process involves reacting mineral-bearing materials with ammonium sulphate via a solid–solid roasting process and subjecting the resulting roast residue to aqueous leaching. This process enables the simultaneous, non-selective co-extraction of strategic metals from the starting materials. However, effective separation of the extracted metals is often mandatory to produce quality products of high purity. In this study, the combined application of thermogravimetric analysis, X-ray powder diffraction and inductively coupled plasma optical emission spectrometry confirmed the non-selectivity of the process when applied to a South African diamond mine residue residue roasted with ammonium sulphate in a 1:2 mass ratio (m/m) at 450 °C for 2 h, with magnesium, iron and aluminium being co-extracted into water-soluble metal sulphates. Thermogravimetry was then applied to develop a multi-step, multi-temperature selective roasting process using mixtures of pure commercial metal sulphate salts. The first step of the modified process successfully separated iron and aluminium sulphates from magnesium-sulphates in the roast residues by thermally decomposing soluble iron and aluminium sulphates into insoluble oxides via calcination at 750 °C for 2 h. This temperature was lower than the one at which magnesium sulphates convert into magnesium oxide. In the second and final step, iron and aluminium were recovered from the oxide minerals via solid–solid re-roasting with ammonium sulphate at 450 °C for 1 h, causing the oxides to revert back to their water-soluble sulphate forms. The effectiveness of the modified process was subsequently verified using a diamond mine residue, showing that the soluble iron and aluminium contents in the magnesium-bearing leachate could be reduced by over 90%. [ABSTRACT FROM AUTHOR]

The traditional usage of salt taken from vegetables for the treatment of blood pressure and diabetes is seen in several regions of Ethiopia, particularly in Gambella. The aim of the study was to investigate the mineral content, anti‐hypertensive properties, and sensory attributes of salt obtained from the Hygrophilia schulli. The salt was extracted from the ashing of stems of Hygrophilia schulli. Optical Emission Spectroscopy with Inductively Coupled Plasma was used to identify macro‐minerals, micro‐minerals, and some toxic metals. Flame Atomic Absorption Spectroscopy was used to assess the levels of arsenic and mercury. The anti‐hypertensive property of the salt was determined in vivo using the Wistar rats. The extracted salt was rich in potassium and was deficient in sodium from the analyzed macro‐minerals. It was free from mercury, cadmium, chromium, and arsenic. Lead and nickel were below the Tolerable Weekly Intake Provisional specified by the European Union. Among carbonate and sulfate, chloride was the main anion in this salt. The salt was discovered to have a low taste characteristic compared to common salt. However, the taste attribute of the combination of vegetable and common salt in different proportions was better than common salt. Rats fed with salt from Hygrophilia schulli showed a statistically significant lower systolic, diastolic, and mean blood pressure compared to normal‐fed and common salt‐fed rat groups. Generally, this study suggests that Hygrophilia schulli salt has the potential to be a viable alternative to common salt, particularly for those suffering from hypertension and other related chronic conditions. [ABSTRACT FROM AUTHOR]

Biochar is a carbon-rich material that has recently received attention due to its increasing agronomical potential. The agricultural utilization of biochar relates to its potential to act in the soil as a soil conditioner; nevertheless, complex information on the direct dependence of biochar's physical properties (texture, particle size) and corresponding leaching and availability of organic molecules (e.g., the polycyclic and heterocyclic organic compounds) and inorganic mineral salts (based on micro- and macroelements) is still inconsistent. Multi-elemental analysis by using inductively coupled plasma atomic emission spectroscopy (ICP-OES) was used to assess the information on the contents and availability of macro- and microelements in studied commercial biochar samples. The results showed a statistically significant indirect relation between an increase in the size fraction of biochar and the content of aqueous-extractable K and Na and the direct relation with the aqueous-extractable Ca, Mg, and P. Compared to the macroelements, the detected contents of aqueous-extractable microelements were almost three orders lower, and the dependence on fraction size was not consistent or statistically significant. In addition, gas chromatography (GC) coupled with mass spectroscopy (MS) was further used to reveal the concentrations of available polycyclic aromatic and heterocyclic compounds in biochar samples. The detected concentrations of these types of organic compounds were far below the certified limits, and a statistically significant indirect correlation with particle size was also observed for all the studied biochar samples. The proposed methodological concept could provide the necessary insights into the description of biochar mineral content and its connection to biochar texture, the physicochemical properties, and the potential of biochar to release nutrients into the soil. These findings could help in the further assessment of biochar as a soil conditioner in modern agriculture. [ABSTRACT FROM AUTHOR]