Merohedral Mechanism Twining Growth of Natural Cation-Ordered Tetragonal Grossular

Garnet supergroup minerals are in the interest of different applications in geology, mineralogy, and petrology and as optical material for material science. The growth twins of natural tetragonal grossular from the Wiluy River, Yakutia, Russia, were investigated using single-crystal X-ray diffraction, optical studies, Raman spectroscopy, microprobe, and scanning electron microscopy. The studied grossular is pseudo-cubic (a = 11.9390 (4), c = 11.9469 (6) Å) and birefringent (0.01). Its structure was refined in the Ia3¯d, I41/acd, I41/a, and I4¯2d space groups. The I41/a space group was chosen as the most possible one due to the absence of violating reflections and ordering of Mg2+ and Fe3+ in two independent octahedral sites, which cause the symmetry breaking according to the group–subgroup relation Ia3¯d → I41/a. Octahedral crystals of (H4O4)4−-substituted grossular are merohedrally twinned by twofold axis along [110]. The mechanism of twining growth led to the generation of stacking faults on the (110) plane and results in the formation of crystals with a long prismatic habit

A Rare Au-Sb Telluride Pampaloite from the Svetlinsk Gold-Telluride Deposit, South Urals, Russia

Pampaloite AuSbTe, a rare gold-antimony telluride that was first described in 2019 from the Pampalo gold mine, Finland, was found in samples from the large Svetlinsk gold-telluride deposit, South Urals, Russia. Optical microscopy, scanning electron microscopy, electron microprobe analysis, reflectance measurements, electron backscatter diffraction and Raman spectroscopy were used to study eight grains of pampaloite. Pampaloite forms inclusions (5–30 μm) in quartz together with other tellurides (typically petzite), native gold and, less often, sulfides. In reflected light, pampaloite is white or creamy white in color with weak anisotropism and without internal reflections. The empirical formula calculated on the basis of 3 apfu is Au0.97–1.07Ag0–0.02Sb0.96–1.04Te0.96–1.04 (n = 18). The holotype pampaloite structure was used as a reference and provided the perfect match for an experimental EBSD pattern (12 bands out of 12, mean angle deviation 0.19°). Raman spectra are reported for the first time for this mineral. All studied pampaloite grains exhibit vibrational modes in the range 60–180 cm−1. Average peak positions are 71, 108, 125, 147 and 159 cm−1. According to experimental data for the Au-Sb-Te system, we estimate the upper temperature range of pampaloite crystallization at the Svetlinsk deposit to be 350–430 °C

Synthesis of Catalytic Microswimmers Based on Anisotropic Platinum Sorption on Melamine Barbiturate Supramolecular Structures

Herein, a straightforward synthesis approach for the formation of anisotropic microswimmers is proposed as an alternative to a top–down fabrication for asymmetric artificial swimmers. Melamine barbiturate (MBA)–self‐assembled supramolecular crystals are utilized as an asymmetric matrix for selective chemical platinum deposition. Surface functional groups of prevalent crystallographic planes for platinum sorption are presented by acidic sites of the assembly. The formed platinum catalytic layer is separated from the bulk MBA and investigated using X‐Ray photoelectron spectroscopy and scanning electron microscope energy‐dispersive X‐Ray spectroscopy analysis. Both methods confirm platinum adsorption and reduction of platinum ions during the deposition process. The MBA asymmetric swimmers show directional motion in a fuel environment, proved by the mean‐squared displacement study. Previously reported pH‐dependency and encapsulation capacity of MBA opens wide opportunities for functional materials formation

Montbrayite from the Svetlinsk Gold–Telluride Deposit (South Urals, Russia): Composition Variability and Decomposition

A rare gold–telluride montbrayite from the large Svetlinsk gold–telluride deposit (South Urals, Russia) was comprehensively studied using optical microscopy, scanning electron microscopy, electron microprobe analysis, reflectance measurements, electron backscatter diffraction, and Raman spectroscopy. Significant variations in the composition of the mineral were revealed (in wt%): Au 36.98–48.66, Te 43.35–56.53, Sb 2.49–8.10, Ag up to 4.56, Pb up to 2.04, Bi up to 0.33, Cu up to 1.42. There are two distinct groups with much more-limited variation within the observed compositional interval (in wt%): (1) Au 36.98–41.22, Te 49.35–56.53, Sb 2.49–5.57; (2) Au 47.86–48.66, Te 43.35–44.92, Sb 7.15–8.10. The empirical formula calculated on the basis of 61 apfu is Au16.43–23.28Sb1.79–6.09Te32.01–38.89Ag0–3.69Bi0–0.14Pb0–0.90Cu0–1.96. Two substitution mechanisms for antimony are proposed in the studied montbrayite grains: Sb→Au (2.5–5.6 wt% Sb) and Sb→Te (7–8 wt% Sb). The dependence of the reflection spectra and Raman spectra on the antimony content and its substitution mechanism, respectively, was found in the mineral. The slope of the reflectance spectra decreases and the curve in the blue–green region of the spectrum disappears with increasing Sb content in montbrayite. Raman spectra are reported for the first time for this mineral. The average positions of the peak with high-intensity are ~64 cm−1 and ~90 cm−1 for montbrayite with Sb→Te and Sb→Au, respectively. Two grains of montbrayite demonstrate decomposition according to two schemes: (1) montbrayite (7 wt% Sb) → native gold + calaverite ± altaite, and (2) montbrayite (5 wt% Sb) → native gold + tellurantimony ± altaite. A combination of melting and dissolution–precipitation processes may be responsible for the formation of these decomposition textures

Silicates from Lherzolites in the South-Eastern Part of the Kempirsay Massif as the Source for Giant Chromitite Deposits (the Southern Urals, Kazakhstan)

We provide results of a comprehensive mineralogical and microstructural study of relict lherzolites of the main ore field and fresh rocks from a deep structural borehole drilled in the south-eastern part of the Kempirsay massif. Olivine and orthopyroxene from lherzolites contain numerous pieces of evidence of material redistribution at different scales caused mainly by solid-state processes, such as plastic flow of mantle, syntectonic recrystallization, and annealing. The results of deformation-induced processes at the submicron scale are recorded by optical and electronic microscopy. In olivine, the plastic deformation caused segregation of impurities at structural defects. As a result, abundant tiny rods of newly formed Cr-spinels occurred inside its grains. Moreover, in enstatite, deformation caused partial or complete chemical decomposition with exsolution of diopside, pargasite and spinel lamellae up to the formation of a “fibrous” structure. In other cases, it provided partial or complete recrystallization to form new phases of enstatite-2, forsterite, diopside, pargasite, and spinel. Petrographic observations are validated by geochemical data, i.e., regularly decreasing concentrations of minor elements in neoblasts compared to large grains (porphyroclasts). Further redistribution of spinel grains with the formation of chromitite bodies is witnessed by their permanent association with the most mobile phase of the upper mantle, i.e., olivine, which is the only mineral that remains stable under the intense plastic flow. An increased concentration of Cr-spinel grains during formation of massive chromitites could appear under conditions close to pressure sintering, as evidenced by stressed textures of ores and an increased grain size compared to disseminated chromitites. The formation of unique chromitite deposits is associated with integration of numerous disparate podiform bodies into “ore bunches” due to the tectonic impact in the shear-compression regime. This was most likely associated with transition of the rifting (spreading) regime to that of the upper mantle of the fore-arc basin

Vesuvianite from the somma-vesuvius complex: New data and revised formula

At present, the vesuvianite group of minerals consists of eight members, six of which are distinguished by the dominant cation in the Y1(A,B) five-coordinated site. We investigated two vesuvianite samples from the type locality by electron microprobe analysis, Mössbauer and infrared spectroscopy, TGA/DSC, MAS NMR, single-crystal and powder X-ray diffraction. The crystal structures of these samples (# 27844 and 51062 from the Vesuvius collection, Fersman Mineralogical Museum, Moscow) have been refined to R1 = 0.027 and R1 = 0.035, respectively. Both samples have the space group P4/nnc; a = 15.5720(3) and 15.5459(3), c = 11.8158(5) and 11.7988(4), respectively. In both samples low-occupied T1 and T2 sites are populated by minor B and Al, which agrees with their high-temperature origin. According to our experimental results, the general revised crystal-chemical formula of vesuvianite can be written as VIIIXX19 VY1 VIY12(Z2O7)4(ZO4)10(W)10, where X are sevento nine-coordinated sites of Ca with minor Na, K, Fe2+ and REE impurities; VY has a square pyramidal coordination and is occupied predominantly by Fe3+ with subordinate Mg, Al, Fe2+ and Cu2+; VIY has octahedral coordination and is predominantly occupied by Al with subordinate Mg, Fe2+, Fe3+, Mn2+, Mn3+, Ti, Cr and Zn; ZO4 = SiO4, sometimes with subordinate AlO4 and/or (OH)4, and W = OH, F, with minor O and Cl. The idealized charge-balanced formula of the vesuvianite end-member without subordinate cations is Ca19Fe3+(Al10Me2+ 2)(Si2O7)4(SiO4)10O(OH)9, where Me = Fe2+, Mg2+, Mn2+