Search Results (8)

The six platinum group elements (PGE) are among the rarest elements in the upper continental crust of the earth. Higher values of PGE have been detected in the upper mantle and in chondrite meteorites. The PGE are siderophile and chalcophile elements and are divided into the following: (1) the Ir subgroup (IPGE) = Os, Ir, and Ru and (2) the Pd subgroup (PPGE) = Rh, Pt, and Pd. The IPGE are more refractory and less chalcophile than the PPGE. High concentrations of PGE led, in rare cases, to the formation of mineral deposits. The PGE are carried in discrete phases, the platinum group minerals (PGM), and are included as trace elements into the structure of base metal sulphides (BM), such as pentlandite, chalcopyrite, pyrite, and pyrrhotite. Similarly to PGE, the PGM are also divided into two main groups, i.e., IPGM composed of Os, Ir, and Ru and PPGM containing Rh, Pt, and Pd. The PGM occur both in mafic and ultramafic rocks and are mainly hosted in stratiform reefs, sulphide-rich lenses, and placer deposits. Presently, there are only 169 valid PGM that represent about 2.7% of all 6176 minerals discovered so far. However, 496 PGM are listed among the valid species that have not yet been officially accepted, while a further 641 are considered as invalid or discredited species. The main reason for the incomplete characterization of PGM resides in their mode of occurrence, i.e., as grains in composite aggregates of a few microns in size, which makes it difficult to determine their crystallography. Among the PGM officially accepted by the IMA, only 13 (8%) were discovered before 1958, the year when the IMA was established. The highest number of PGM was discovered between 1970 and 1979, and 99 PGM have been accepted from 1980 until now. Of the 169 PGM accepted by the IMA, 44% are named in honour of a person, typically a scientist or geologist, and 31% are named after their discovery localities. The nomenclature of 25% of the PGM is based on their chemical composition and/or their physical properties. PGM have been discovered in 25 countries throughout the world, with 64 from Russia, 17 from Canada and South Africa (each), 15 from China, 12 from the USA, 8 from Brazil, 6 from Japan, 5 from Congo, 3 from Finland and Germany (each), 2 from the Dominican Republic, Greenland, Malaysia, and Papua New Guinea each, and only 1 from Argentine, Australia, Bulgaria, Colombia, Czech Republic, England, Ethiopia, Guyana, Mexico, Serbia, and Tanzania each. Most PGM phases contain Pd (82 phases, 48% of all accepted PGM), followed, in decreasing order of abundances, by those of Pt 35 phases (21%), Rh 23 phases (14%), Ir 18 phases (11%), Ru 7 phases (4%), and Os 4 phases (2%). The six PGE forming the PGM are bonded to other elements such as Fe, Ni, Cu, S, As, Te, Bi, Sb, Se, Sn, Hg, Ag, Zn, Si, Pb, Ge, In, Mo, and O. Thirty-two percent of the 169 valid PGM crystallize in the cubic system, 17% are orthorhombic, 16% hexagonal, 14% tetragonal, 11% trigonal, 3% monoclinic, and only 1% triclinic. Some PGM are members of a solid-solution series, which may be complete or contain a miscibility gap, providing information concerning the chemical and physical environment in which the mineral was formed. The refractory IPGM precipitate principally in primitive, high-temperature, mantle-hosted rocks such as podiform and layered chromitites. Being more chalcophile, PPGE are preferentially collected and concentrated in an immiscible sulphide liquid, and, under appropriate conditions, the PPGM can precipitate in a thermal range of about 900–300 °C in the presence of fluids and a progressive increase of oxygen fugacity (fO₂). Thus, a great number of Pt and Pd minerals have been described in Ni-Cu sulphide deposits. Two main genetic models have been proposed for the formation of PGM nuggets: (1) Detrital PGM represent magmatic grains that were mechanically liberated from their primary source by weathering and erosion with or without minor alteration processes, and (2) PGM reprecipitated in the supergene environment through a complex process that comprises solubility, the leaching of PGE from the primary PGM, and variation in Eh-pH and microbial activity. These two models do not exclude each other, and alluvial deposits may contain contributions from both processes. Full article

This paper presents the results of the influence of variation of the synthesis conditions of CuBi/CuBi₂O₄ films with a change in the applied potential difference, as well as a change in electrolyte solutions (in the case of adding cobalt or nickel sulfates to the electrolyte solution) on changes in the phase composition, structural parameters and strength characteristics of films obtained using the electrochemical deposition method. During the experiments, it was found that, in the case of the addition of cobalt or nickel to the electrolyte solutions, the formation of films with a spinel-type tetragonal CuBi₂O₄ phase is observed. In this case, a growth in the applied potential difference leads to the substitution of copper with cobalt (nickel), which in turn leads to an increase in the structural ordering degree. It should be noted that, during the formation of CuBi/CuBi₂O₄ films from solution–electrolyte №1, the formation of the CuBi₂O₄ phase is observed only with an applied potential difference of 4.0 V, while the addition of cobalt or nickel sulfates to the electrolyte solution results in the formation of the tetragonal CuBi₂O₄ phase over the entire range of the applied potential difference (from 2.0 to 4.0 V). Studies have been carried out on the strength and tribological characteristics of synthesized films depending on the conditions of their production. It has been established that the addition of cobalt or nickel sulfates to electrolyte solutions leads to an increase in the strength of the resulting films from 20 to 80%, depending on the production conditions (with variations in the applied potential difference). During the studies, it was established that substitution of copper with cobalt or nickel in the composition of CuBi₂O₄ films results in a rise in the shielding efficiency of low-energy gamma radiation by 3.0–4.0 times in comparison with copper films, and 1.5–2.0 times for high-energy gamma rays, in which case the decrease in efficiency is due to differences in the mechanisms of interaction of gamma quanta, as well as the occurrence of secondary radiation as a result of the formation of electron–positron pairs and the Compton effect. Full article

In this research, the formation processes of CuBi₂O₄ films were examined using atomic force microscopy, energy dispersive analysis and X-ray diffraction analysis methods. The films were synthesized through electrochemical deposition from sulfuric acid solutions at a potential difference of 3.5 V. The duration of film growth was set to between 10 and 90 min to assess the possibility of controlled film growth and preserve the stability of their structural properties during growth over an extended period. An analysis of the data obtained by X-ray diffraction revealed that the resulting film samples are highly ordered structures with a tetragonal CuBi₂O₄ phase. The results of the connection between the thickness of CuBi₂O₄ films and strength properties depending on the time of film deposition were obtained. The results of the shielding efficiency of low-energy γ-quanta using CuBi₂O₄ films were obtained. Full article

The problem of industrial dyes depollution has pushed the scientific research community to identify novel photocatalysts with high performance. Herein, new photocatalysts composed of BaTiO₃, BaTi_0.96Cu_0.04O₃, BaTi_0.96Cu_0.02V_0.02O₃ and BaTi_0.96Cu_0.02Nb_0.02O₃ powders were prepared by solid-state reaction. The structural analysis of the samples confirmed the formation of the BaTiO₃ structure. The splitting of (002) and (200) planes verified the formation of the tetragonal phase. The XRD peaks shifted, and the unit cell volume expansion verified the substitution of the Ti⁴⁺ site by Cu²⁺, V⁴⁺ and Nb⁵⁺ ions. The morphological measurements showed that the addition of (Cu, V) and (Cu, Nb) ions changes the particles’ morphology of BaTiO₃, reducing its grains size. After the incorporation of (Cu, V) and (Cu, Nb) ions, the band gap of BaTiO₃ was reduced from 3.2 to 2.84 and 2.72 eV, respectively. The modification of BaTiO₃ by (Cu, Nb) ions induced superior photocatalytic properties for methyl green and methyl orange with degradation efficiencies of 97% and 94% during 60 and 90 min under sunlight irradiation, respectively. The total organic carbon results indicated that the BaTi_0.96Cu_0.02Nb_0.02O₃ catalyst has a high mineralization efficiency. In addition, it possesses a high stability during three cycles. The high photodegradation efficiency of Bi_0.96La_0.02Gd_0.02FeO₃ was related to the wide-ranging visible light absorption. Full article

While the CuBi₂O₄-based photocathode has emerged as an ideal candidate for photoelectrochemical water splitting, it is still far from its theoretical values due to poor charge carrier transport, poor electron–hole separation, and instability caused by self-photoelectric-corrosion with electrolytes. Establishing synthesis methods to produce a CuBi₂O₄ photocathode with sufficient cocatalyst sites would be highly beneficial for water splitting. Here, the platinum-enriched porous CuBi₂O₄ nanofiber (CuBi₂O₄/Pt) with uniform coverage and high surface area was prepared as a photocathode through an electrospinning and electrodeposition process for water splitting. The prepared photocathode material was composed of a CuBi₂O₄ nanofiber array, which has a freestanding porous structure, and the Pt nanoparticle is firmly embedded on the rough surface. The highly porous nanofiber structures allow the cocatalyst (Pt) better alignment on the surface of CuBi₂O₄, which can effectively suppress the electron–hole recombination at the electrolyte interface. The as-fabricated CuBi₂O₄ nanofiber has a tetragonal crystal structure, and its band gap was determined to be 1.8 eV. The self-supporting porous structure and electrocatalytic activity of Pt can effectively promote the separation of electron–hole pairs, thus obtaining high photocurrent density (0.21 mA/cm² at 0.6 V vs. RHE) and incident photon-to-current conversion efficiency (IPCE, 4% at 380 nm). This work shows a new view for integrating an amount of Pt nanoparticles with CuBi₂O₄ nanofibers and demonstrates the synergistic effect of cocatalysts for future solar water splitting. Full article

A new two-dimensional (2D) coordination polymer of the formula {Cu(ox)(4-Hmpz)·1/3H₂O}_n (1) (ox = oxalate and 4-Hmpz = 4-methyl-1H-pyrazole) has been prepared, and its structure has been determined by single-crystal X-ray diffraction. It consists of corrugated oxalato-bridged copper(II) neutral layers featuring two alternating bridging modes of the oxalate group within each layer, the symmetric bis-bidentate (μ-κ²O¹,O²:κ²O^2′,O^1′) and the asymmetric bis(bidentate/monodentate) (μ₄-κO¹:κ²O¹,O²:κO^2′:κ²O^2′,O^1′) coordination modes. The three crystallographically independent six-coordinate copper(II) ions that occur in 1 have tetragonally elongated surroundings with three oxygen atoms from two oxalate ligands, a methylpyrazole-nitrogen defining the equatorial plane, and two other oxalate-oxygen atoms occupying the axial positions. The monodentate 4-Hmpz ligands alternatively extrude above and below each oxalate-bridged copper(II) layer, and the water molecules of crystallization are located between the layers. Compound 1 exhibits a fast and selective adsorption of methylamine vapors to afford the adsorbate of formula {Cu(ox)(4-Hmpz)·3MeNH₂·1/3H₂O}_n (2), which is accompanied by a concomitant color change from cyan to deep blue. Compound 2 transforms into {Cu(ox)(4-Hmpz)·MeNH₂·1/3H₂O}_n (3) under vacuum for three hours. The cryomagnetic study of 1–3 revealed a unique switching from strong (1) to weak (2 and 3) antiferromagnetic interactions. The external control of the optical and magnetic properties along this series of compounds might make them suitable candidates for switching optical and magnetic devices for chemical sensing. Full article

Tetragonal CuBi₂O₄/amorphous BiFeO₃ (T-CBO/A-BFO) composites are prepared via a one-step solvothermal method at mild conditions. The T-CBO/A-BFO composites show expanded visible light absorption, suppressed charge recombination, and consequently improved photocatalytic activity than T-CBO or A-BFO alone. The T-CBO/A-BFO with an optimal T-CBO to A-BFO ratio of 1:1 demonstrates the lowest photoluminescence signal and highest photocatalytic activity. It shows a removal rate of 78.3% for the photodegradation of methylene orange under visible light irradiation for 1 h. XPS test after the cycle test revealed the reduction of Bi³⁺ during the photocatalytic reaction. Moreover, the as prepared T-CBO/A-BFO show fundamentally higher photocatalytic activity than their calcinated counterparts. The one-step synthesis is completed within 30 min and does not require post annealing process, which may be easily applied for the fast and cost-effective preparation of photoactive metal oxide heterojunctions. Full article

In this article, a short-time hydrothermal method is developed to prepare CuBi₂O₄ nanocolumn arrays. By using Bi(NO₃)₃·5H₂O in acetic acid and Cu(NO₃)₂·3H₂O in ethanol as precursor solutions, tetragonal CuBi₂O₄ with good visible light absorption can be fabricated within 0.5 h at 120 °C. Tetragonal structured CuBi₂O₄ can be formed after 15 min hydrothermal treatment, however it possesses poor visible light absorption and low photocatalytic activity. Extending the hydrothermal treatment duration to 0.5 h results in a significant improvement invisible light absorption of the tetragonal CuBi₂O₄. The CuBi₂O₄ obtained through 0.5 h hydrothermal synthesis shows a band gap of 1.75 eV and exhibits the highest photocatalytic performance among the CuBi₂O₄ prepared with various hydrothermal time. The removal rate of methylene blue by the 0.5 h CuBi₂O₄ reaches 91% under visible light irradiation for 0.5 h. This study proposes a novel strategy to prepare photoactive CuBi₂O₄ nanocolumn arrays within 0.5 h at a moderate temperature of 120 °C. The hydrothermal method provides a facile strategy for the fast synthesis of metal-oxide-based photocatalysts at mild reaction conditions. Full article