Search Results (25)

Rock-forming minerals, olivine and pyroxene, from three ore-bearing intrusions in the Norilsk districts were studied. They are the Norilsk 1 and the Northern and Southern Maslovsky massifs with PGE-Cu-Ni ores, located in the Norilsk syncline. Trace elements such as Al, Ti, Co, Cu, Nd, Sm, Ce, Cr, V, Dy, Y, Yb, Er, Sr, and Eu were determined by LA-ICP-MS. The authors found differences in mineral compositions between picritic gabbro-dolerites from these intrusions. The parental melt of the Southern Maslovsky intrusion corresponded to tholeiitic basalt containing (wt.%) H₂O—0.65, CO₂—0.16, and B—0.004. It was concluded that parental magmas for ore-bearing intrusions had no specific features and were closed to intraplate basalts. Full article

Inatlar limestone, which is dated to the Middle Jurassic–Lower Cretaceous, is exposed between the villages of Kabulbaba and Söğütalan in the Mustafakemalpaşa district of Bursa, Turkey. This study investigates its mineralogical, petrographic, and geochemical characteristics, focusing on major, trace, and rare earth element (REEs) compositions to interpret the depositional environment, paleoenvironmental conditions, and diagenetic processes. Petrographic analysis identified four main limestone types: siliceous, micritic, fossiliferous, and dolomitic. REEs geochemistry indicates enrichment in heavy REEs (HREEs), depletion in light REEs (LREEs), and characteristic anomalies with negative Ce and Eu and positive La, suggesting an open marine depositional environment and early diagenesis. Trace element data point to deposition in settings ranging from continental margins to open marine environments. Ni and V concentrations reflect a spectrum of depositional conditions, including terrestrial, transitional (oxic–dysoxic), and marine anoxic settings. Z values support the theory that the limestones have a marine origin. δ¹³C and δ¹⁸O isotope values indicate deposition in both hydrothermal and typical marine carbonate environments. Y/Ho and Er/Nd ratios reveal the influence of terrestrial input, as well as diagenetic and detrital material. Furthermore, V/(V + Ni) ratios reflect fluctuating oxic to suboxic/anoxic conditions, while Ni/Co ratios indicate predominantly euxinic and, to a lesser extent, anoxic conditions. Altogether, these geochemical signatures suggest that the Inatlar limestone was deposited in a dynamic marine system characterized by variable redox states and salinity fluctuations. Full article

Petrological knowledge on weathering processes controlling the mobility of chemical elements is still limited in the dry tropical zone of Cameroon. This study aims to investigate the mobility of major and trace elements during rhyolite weathering and soil formation in Mobono by understanding the mineralogical and elemental vertical variation. The studied soil was classified as Cambisols containing mainly quartz, K-feldspar, plagioclase, smectite, kaolinite, illite, calcite, lepidocrocite, goethite, sepiolite, and interstratified clay minerals. pH values ranging between 6.11 and 8.77 indicated that hydrolysis, superimposed on oxidation and carbonation, is the main process responsible for the formation of secondary minerals, leading to the formation of iron oxides and calcite. The bedrock was mainly constituted of SiO₂, Al₂O₃, Na₂O, Fe₂O₃, Ba, Zr, Sr, Y, Ga, and Rb. Ce and Eu anomalies, and chondrite-normalized La/Yb ratios were 0.98, 0.67, and 2.86, respectively. SiO₂, Al₂O₃, Fe₂O₃, Na₂O, and K₂O were major elements in soil horizons. Trace elements revealed high levels of Ba (385 to 1320 mg kg⁻¹), Zr (158 to 429 mg kg⁻¹), Zn (61 to 151 mg kg⁻¹), Sr (62 to 243 mg kg⁻¹), Y (55 to 81 mg kg⁻¹), Rb (1102 to 58 mg kg⁻¹), and Ga (17.70 to 35 mg kg⁻¹). LREEs were more abundant than HREEs, with LREE/HREE ratio ranging between 2.60 and 6.24. Ce and Eu anomalies ranged from 1.08 to 1.21 and 0.58 to 1.24 respectively. The rhyolite-normalized La/Yb ratios varied between 0.56 and 0.96. Mass balance revealed the depletion of Si, Ca, Na, Mn, Sr, Ta, W, U, La, Ce, Pr, Nd, Sm, Gd and Lu, and the accumulation of Al, Fe, K, Mg, P, Sc, V, Co, Ni, Cu, Zn, Ga, Ge, Rb, Y, Zr, Nb, Cs, Ba, Hf, Pb, Th, Eu, Tb, Dy, Ho, Er, Tm and Yb during weathering along the soil profile. Full article

For the first time, inductively coupled plasma mass spectrometry (ICP-MS) was developed for determining the target elemental composition of gadolinium–aluminum garnets with the varying composition Gd_3–xCe_xSc_yAl_5–yO₁₂, where x = 0.01–0.16 and y = 0.25–1.75. This fact has a fundamental importance for obtaining optical ceramics with predictable properties. Using the proposed acid mixture and temperature-time program, microwave digestion of these materials and complete transfer of the sample’s components into solution were possible. Moreover, we estimated the influence of the matrix composition, sample introduction system and collision cell on the limits of determination (LOD) of impurity elements by ICP-MS (Mg, Si, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Y, La, Pr, Nd, Sm, Eu, Tb, Er, Ho, Tm, Yb, and Lu). It has been shown that the conditions of mass spectral analysis proposed in this work provide LOD of target analytes in the range of 1∙10⁻⁶–4.15∙10⁻³ wt.%. The accuracy of the obtained results has been confirmed by the added-found method and by analyzing samples with known chemical composition. The standard deviation of repeatability (S_r) of the developed technique lies in the range from 1 to 6%. The developed analysis method is characterized by sensitivity, robustness and multi-elementality. It has application potential for other optical and ceramic materials of similar composition. Full article

We synthesized Pr₂NiMnO₆, Gd₂NiMnO₆, and Er₂NiMnO₆ double perovskites in a nano-ceramic form by a sol–gel method. By means of room-temperature X-ray powder diffraction measurements, we determined the crystal structure of the three compounds, which is monoclinic, corresponding to a double perovskite structure, described by space group P2₁/n structure. From the determined structures, the bulk moduli were estimated to be 173–179 GPa. The average size particle of nanoparticles was determined from X-ray diffraction by the Langford method plot and by the Scherrer formula. The morphology and homogeneity of nanoparticles were analyzed by scanning electron microscopy. We found that they form compact agglomerations of approximately 200 nm in diameter. Fourier transform infrared spectroscopy measurements were performed, determining the absorption spectrum. The assignment of the measured infrared absorption bands is discussed. Full article

To create materials that interact effectively with electromagnetic (EM) radiation, new nanosized substituted ferrites (NiZn)_1−xMn_xFe₂O₄ (x = 0, 0.5, and 1) anchored on the surface of multi-walled carbon nanotubes (CNTs) have been synthesized. The concentration of CNTs in the (NiZn)_1−xMn_xFe₂O₄/CNT system was from 0.05 to 0.07 vol. fractions. The dielectric and magnetic characteristics of both pristine (NiZn)_1−xMn_xFe₂O₄ ferrites and (NiZn)_1−xMn_xFe₂O₄/CNT composite systems were studied. The introduction of (NiZn)_1−xMn_xFe₂O₄/CNT composites into the amorphous epoxy matrix allows to tailor absorbing properties at the high-frequency by effectively shifting the maximum peak values of the absorption and reflection coefficient to a region of lower frequencies (20–30 GHz). The microwave adsorption properties of (NiZn)_1−xMnxFe₂O₄/0.07CNT–ER (x = 0.5) systems showed that the maximum absorption bandwidth with reflection loss below −10 dB is about 11 GHz. Full article

A zinc supracluster [Zn₂₄(ATZ)₁₈(AcO)₃₀(H₂O)_1.5]·(H₂O)_3.5 (Zn₂₄), and a 1D zinc supracluster chain {[Zn₂₄(ATZ)₁₈(AcO)₃₀(C₂H₅OH)₂(H₂O)₃]·(H₂O)_2.5}_n (1-D⊂Zn₂₄) with molecular diameters of 2 nm were synthesized under regulatory solvothermal conditions or the micro bottle method. In an N,N-dimethylformamide solution of Zn₂₄, Fe³⁺, Ni²⁺, Cu²⁺, Cr²⁺ and Co²⁺ ions exhibited fluorescence-quenching effects, while the rare earth ions Ce³⁺, Dy³⁺, Er³⁺, Eu³⁺, Gd³⁺, Ho³⁺, La³⁺, Nd³⁺, Sm³⁺, and Tb³⁺showed no obvious fluorescence quenching. In ethanol solution, the Zn₂₄ supracluster can be used to selectively detect Ce³⁺ ions with excellent efficiency (limit of detection (LOD) = 8.51 × 10⁻⁷ mol/L). The Zn₂₄ supracluster can also detect wavelengths between 302 and 332 nm using the intensity of the emitted light. Full article

The composition of the filler electrodes, as well as the shielding gases, has a strong impact on the static and dynamic properties of welded joints in HSLA steels. The content of Cr, Ni, and Mo, along with the shielding gases, helps maintain the hardness values in the HAZ of HSLA steels welded using the GMAW process, resulting in a positive impact on the fatigue life of the joints. Maintaining fatigue properties in the regions of the heat-affected zone is crucial. The increase in the size of the HAZ, coupled with microstructural changes, leads to a reduction in the hardness values in this region, contributing to a decrease in the fatigue life of welded joints. In this study, the effects of using different filler electrodes and shielding gases on the fatigue properties of welded joints in LNE 600 steel with a thickness of 4.75 mm, welded using the GMAW process, were evaluated. It was possible to observe a reduction in the hardness values in the HAZ region and a similar static resistance behavior for all evaluated conditions, except for the ER70S-6 electrode with 5% O₂ gas, where the fatigue life showed better results with the application of the ER120S-G electrode. Full article

The purpose of this study is to evaluate the bio-accumulation of different soil-crop systems (SCSs) for heavy metals (HMs) and the geo-accumulation of different agricultural growing regions. The ecological risk (ER) assessment was conducted to understand the impact of intensive agricultural production on the environment. To achieve this aim, four typical crops, wheat, corn, potatoes, and leeks grown in the Jiao River Basin (JRB), were selected as the research objects. The concentrations of eight HMs, including copper (Cu), lead (Pb), zinc (Zn), nickel (Ni), chromium (Cr), cadmium (Cd), arsenic (As), and mercury (Hg) in crop tissue and soil were detected. The statistical analysis, including the geo-accumulation index ($I_{geo}$), geostatistical analysis, correlation and cluster analysis were then used to evaluate soil contamination and determine the source types of HMs. The results show that the average concentrations of eight HMs in the soil follow the order: Zn > Cr > Ni > Pb > Cu > As > Cd > Hg and the calculated concentration coefficients (K) vary from 0.41–1.12, indicating relative scarcity in sources of HMs. All the $I_{geo}$ values of HMs are less than 0 except the $I_{geo}$ of Cr within potato-farmland is from 0 to 1, illustrating that the soil in JRB is uncontaminated. The correlation and cluster analysis reveal that Cu, Zn, and Cd have a strong relationship with each other and the relationship between Pb, Ni, and Cr is general. The content of eight HMs in different crops varies greatly and most of them are within the scope of National Food Safety Standards—Limit of Pollutants in food of China. The bioconcentration factors (BCF) indicate that wheat, corn, potato, and leek have strong bio-accumulation ability of Cu, Zn, and Cd. The ecological risk factor (Er) shows that JRB is in low risk of Cu, Pb, Zn, Ni, Cr, and As; however, the risk of Cr and Hg are mostly low, characterized by partially dotted moderate risk. The risk index (RI) is mainly moderate with partially low risk distributed in planar and high risk distributed in point. Full article

In this work, Li⁺-doped NiO:Yb,Er thin films are obtained via pulsed laser deposition. It was found that the films exhibit high transparency in the visible region and clearly red up-conversion luminescence under 980 nm excitation. Doping with Li⁺ can adjust the up-conversion emission intensity of the films. Moreover, all the films have p-type conductivity with a single activation energy of around 360 meV. The sheet resistivity of the films can be improved through changing the doping concentration of Li⁺ ions. Taken together, 5% is the best doping concentration for the potential application of this kind of film. Full article

In this study, the formation of thin-film barrier coatings based on a highly conductive Bi_1.60Er_0.4O₃ (EDB) solid electrolyte on supporting Ce_0.8Sm_0.2O_1.9 (SDC) electrolyte substrates was implemented for the first time using electrophoretic deposition (EPD). The electrokinetic properties of EDB-based suspensions in a non-aqueous dispersion medium of isopropanol modified with small additions of polyethyleneimine (PEI, 0.26 g/L) and acetylacetone (0.15 g/L), as well as in a mixed isopropanol/acetylacetone (70/30 vol.%) medium, were studied. The dependences of the thickness of the EDB coatings on voltage and deposition time were obtained using deposition on a model Ni foil electrode. Preliminary synthesis of a conductive polypyrrole (PPy) polymer film was used to create surface conductivity on non-conductive SDC substrates. The efficiency of using a modified dispersion medium based on isopropanol to obtain a continuous EDB coating 12 μm thick, sintered at a temperature of 850 °C for 5 h, is shown. The microstructure and morphology of the surface of the EDB coating were studied. A Pt/SDC/EDB/Pt cell was used to characterize the coating’s conductivity. The EPD method is shown to be promising for the formation of barrier coatings based on doped bismuth oxide. The developed method can be used for creating cathode barrier layers in SOFC technology. Full article

Metal aromatic substances play a unique and important role in both experimental and theoretical aspects, and they have made tremendous progress in the past few decades. The new aromaticity system has posed a significant challenge and expansion to the concept of aromaticity. From this perspective, based on spin-polarized density functional theory (DFT) calculations, we systematically investigated the doping effects on the reduction reactions of N₂O catalyzed by CO for M₁₃@Cu₄₂ (M = Cu, Co, Ni, Zn, Ru, Rh, Pd, Pt) core–shell clusters from aromatic-like inorganic and metal compounds. It was found that compared with the pure Cu₅₅ cluster, the strong M–Cu bonds provide more structural stability for M₁₃@Cu₄₂ clusters. Electrons that transferred from the M₁₃@Cu₄₂ to N₂O promoted the activation and dissociation of the N–O bond. Two possible reaction modes of co-adsorption (L-H) and stepwise adsorption (E-R) mechanisms over M₁₃@Cu₄₂ clusters were thoroughly discovered. The results showed that the exothermic phenomenon was accompanied with the decomposition process of N₂O via L-H mechanisms for all of the considered M₁₃@Cu₄₂ clusters and via E-R mechanisms for most of the M₁₃@Cu₄₂ clusters. Furthermore, the rate-limiting step of the whole reactions for the M₁₃@Cu₄₂ clusters were examined as the CO oxidation process. Our numerical calculations suggested that the Ni₁₃@Cu₄₂ cluster and Co₁₃@Cu₄₂ clusters exhibited superior potential in the reduction reactions of N₂O by CO; especially, Ni₁₃@Cu₄₂ clusters are highly active, with very low free energy barriers of 9.68 kcal/mol under the L-H mechanism. This work demonstrates that the transition metal core encapsulated M₁₃@Cu₄₂ clusters can present superior catalytic activities towards N₂O reduction by CO. Full article

Generally, our ecosystem is continuously contaminated as a result of anthropogenic activities that form the basis of our comfort in our routine life. Thus, most scientists are engaged in the development of new technologies that can be used in environmental remediation. Herein, highly calcined binary metal oxide (Er₂O₃@NiO) semiconductor nanocomposite (NC) was synthesized using a classical wet chemical process with the intention to both detect and degrade the toxic chemicals in an aqueous medium using a novel electrochemical current–potential (I–V) approach for the first time. Optical, morphological, and structural properties of the newly synthesized semiconductor NC were also studied in detail using FT-IR, UV/Vis., FESEM-EDS, XPS, BET, EIS, and XRD techniques. Then, a modified glassy carbon electrode (GCE) based on the newly synthesized semiconductor nanocomposite (Er₂O₃@NiO-NC/Nafion/GCE) as a selective electrochemical sensor was fabricated with the help of 5% ethanolic-Nafion as the conducting polymer binder in order to both detect and electro-hydrolyze toxic chemicals in an aqueous medium. Comparative study showed that this newly developed Er₂O₃@NiO-NC/Nafion/GCE was found to be very selective against m-tolyl hydrazine (m-Tolyl HDZN) and to have good affinity in the presence of other interfering toxic chemicals. Analytical parameters were also studied in this approach to optimize the newly designed Er₂O₃@NiO-NC/Nafion/GCE as an efficient and selective m-Tolyl HDZN sensor. Its limit of detection (LOD) at an SNR of 3 was calculated as 0.066 pM over the linear dynamic range (LDR) of our target analyte concentration (0.1 pM–0.1 mM). The limit of quantification (LOQ) and sensitivity were also calculated as 0.22 pM and 14.50 µAµM⁻¹cm⁻², respectively. m-Tolyl HDZN is among the toxic chemicals in our ecosystem that have lethal effects in living beings. Therefore, this newly designed electrochemical sensor based on semiconductor nanostructure material offers, for the first time, a cost-effective technique, in addition to long-term stability, that can be used as an alternative for efficiently probing other toxic chemicals in real samples. Full article

As one of the main fossil fuels globally, coal can be enriched with a variety of critical metal elements in specific geological conditions. This paper investigates the mineral compositions and concentrations of major and minor element oxides and trace elements in the No. 9 coal from the Xinyuan mine of the northern Qinshui coalfield, China, and discusses the modes of occurrence and enrichment mechanisms of critical metal elements such as Li, Ga, Th and REY. The mineral compositions of the No. 9 coal are primarily represented by clay minerals and quartz, with a small amount of calcite, siderite, anatase, etc. The major element oxides in the No. 9 coal are dominated by SiO₂ and Al₂O₃. Compared with world hard coal, the No. 9 coal of the Xinyuan mine is rich in Li (CC = 8.00) and Th, slightly enriched with Pb, Sc, Ga, Y, La, Ce, Tb, Dy, Er, Yb and Hg, and depleted in Mn, Co, Ni, Rb, Cs and Tl. The critical metal elements such as Li, Ga, Th and REY that enriched No. 9 coal mainly occur in aluminum silicates. The genetic type of the critical metal elements in the No. 9 coal from the Xinyuan mine is source rock-controlled type. The critical metal minerals and solutions from the source area were transported to the study area by the action of water. Due to the change of swamp water conditions, the critical metal elements were combined with clay minerals and enriched the coal. Full article

The property of persistent luminescence shows great potential for anti-counterfeiting technology and imaging by taking advantage of a background-free signal. Current anti-counterfeiting technologies face the challenge of low security and the inconvenience of being limited to visible light emission, as emitters in the NIR optical windows are required for such applications. Here, we report the preparation of a series of Zn_1+xGa_2−2xSn_xO₄ nanoparticles (ZGSO NPs) with persistent luminescence in the first and second near-infrared window to overcome these challenges. ZGSO NPs, doped with transition-metal (Cr³⁺ and/or Ni²⁺) and in some cases co-doped with rare-earth (Er³⁺) ions, were successfully prepared using an improved solid-state method with a subsequent milling process to reach sub-200 nm size particles. X-ray diffraction and absorption spectroscopy were used for the analysis of the structure and local crystal field around the dopant ions at different Sn⁴⁺/Ga³⁺ ratios. The size of the NPs was ~150 nm, measured by DLS. Doped ZGSO NPs exhibited intense photoluminescence in the range from red, NIR-I to NIR-II, and even NIR-III, under UV radiation, and showed persistent luminescence at 700 nm (NIR-I) and 1300 nm (NIR-II) after excitation removal. Hence, these NPs were evaluated for multi-level anti-counterfeiting technology. Full article