Molybdenite in the Aitik deposit and its southern extension was studied through mineralogical/chemical analysis and laboratory flotation tests. It is demonstrated that molybdenite varies considerably in grain size, ranging from coarse (>20 μm) to very fine (<2 μm) and occurs predominantly as single grains in the groundmass of the rocks, as grain aggregates, and intergrown with chalcopyrite and pyrite. The dominating molybdenite-bearing rocks are the mica schists, the quartz-monzodiorite, and the Salmijärvi biotite-amphibole gneiss, the latter containing mostly medium-coarsegrained molybdenite. Later geological features, such as garnet-magnetite-anhydrite-K feldspar alteration and pegmatite dikes appear to be responsible for a significant part of the distribution pattern of molybdenite. Molybdenite grains contain up to 1587 ppm Re, with an average of 211 ± 10 ppm in Aitik molybdenite and 452 ± 33 ppm in Salmijärvi molybdenite. The higher Re concentrations are found in molybdenite associated with sericite- and quartz-amphibole-magnetite altered rocks, whereas low Re values occur in rocks in which potassic alteration is prominent. Molybdenite recovery is influenced by the mineralogy of the host rock and the alteration grade; hence both of these factors will have an impact on potential recoveries. The recovery of molybdenite was lower from flotation feeds with significant amounts of Mg-bearing clay-micas. Full article

Extremely Re-rich molybdenite occurs with pyrite in sodic–calcic, sodic–sericitic and sericitic-altered porphyritic stocks of granodioritic–tonalitic and granitic composition in the Sapes–Kirki–Esymi, Melitena and Maronia areas, northeastern Greece. Molybdenite in the Pagoni Rachi and Sapes deposits is spatially associated with rheniite, as well as with intermediate (Mo,Re)S₂ and (Re,Mo)S₂ phases, with up to 46 wt % Re. Nanodomains and/or microinclusions of rheniite may produce the observed Re enrichment in the intermediate molybdenite–rheniite phases. The extreme Re content in molybdenite and the unique presence of rheniite in porphyry-type mineralization, combined with preliminary geochemical data (Cu/Mo ratio, Au grades) may indicate that these deposits have affinities with Cu–Au deposits, and should be considered potential targets for gold mineralization in the porphyry environment. In the post-subduction tectonic regime of northern Greece, the extreme Re and Te enrichments in the magmatic-hydrothermal systems over a large areal extent are attributed to an anomalous source (e.g., chemical inhomogenities in the mantle-wedge triggered magmatism), although local scale processes cannot be underestimated. Full article

The review presents synthetic approaches to modern rhenium-based catalysts. Creation of an active center is considered as a process of obtaining a nanoparticle or a molecule, immobilized within a matrix of the substrate. Selective chemical routes to preparation of particles of rhenium alloys, rhenium oxides and the molecules of alkyltrioxorhenium, and their insertion into porous structure of zeolites, ordered mesoporous MCM matrices, anodic mesoporous alumina, and porous transition metal oxides are considered. Structure-property relationships are traced for these catalysts in relation to such processes as alkylation and isomerization, olefin metathesis, selective oxidation of olefins, methanol to formaldehyde conversion, etc. Full article