Search results for "sulfide"
showing 10 items of 388 documents
Atmospheric aging and surface degradation in As2S3 fibers in relation with suspended-core profile
2015
Abstract Microstructured optical fibers (MOF) can be seen as next generation fiber of significance in advancing the compact optics because of its excellent compatibility in integrated optics. However, the degradation of their physicochemical properties limits their efficiency and lifetime. Atmospheric moisture is responsible for the degradation of amorphous systems especially chalcogenide glasses. In the light of previously reported studies, in order to clarify the aging process continuously evolving in sulfide microstructured optical fiber over time, a detailed investigation of this phenomenon has been conducted. The time-dependent transmission and glass chemical deterioration have been st…
Chalcogenide Fibers for Mid-IR Light Generation: Potentialities and Drawbacks of the Microstructured Design in Sulfide Waveguides
2014
We study optical and structural aging in As2S3 microstructured optical fibers, submitted to room atmosphere that may have, among others, an impact on mid-infrared supercontinuum generation.
Chemical evolution of ore-forming brines – Basement leaching, metal provenance, and the redox link between barren and ore-bearing hydrothermal veins.…
2019
Abstract Six mineralogically exemplary barren and mineralized hydrothermal veins (with Pb and Zn ores) of Jurassic-Cretaceous and Cenozoic age in the Schwarzwald mining district, SW Germany were chosen to shed light on the origin of their mineralogical diversity. The selection of the veins was guided by the fact that they represent the largest number of veins in the region, are very well known mineralogically and geochemically, and they provide nice examples of barren and mineralized veins of similar age. Fluid inclusion data from the individual veins overlap implying their diverse mineralogy is not caused by different fluid compositions participating during fluid mixing. LA-ICPMS data of s…
Some observations on the determination of sulfite by reduction to sulfide with sodium borohydride
1987
Abstract Sodium borohydride is studied as an agent for reducing sulfite to sulfide. Rapid reductions are attained with greater than 97% recovery in the range 700–1200 μg of S/50 ml. Sulfate is not reduced.
Sulfide ore facies, fluid inclusion and sulfur isotope characteristics of the Tappehsorkh Zn-Pb ( ± Ag-Ba) deposit, South Esfahan, Iran
2020
International audience; The stratiform, stratabound Tappehsorkh Zn-Pb (± Ag-Ba) deposit, located in the southeastern part of the Malayer-Esfahan Metallogenic Belt of Iran, formed during Lower Cretaceous back-arc extension. Sulfide mi-neralization occurs within dolostone, black siltstone, and crystal lithic tuff and andesite associated with the Gushfil-Baghabrisham synsedimentary normal fault. Three sulfide ore facies (massive, bedded, and stockwork) occur in the deposit. Sulfide minerals are sphalerite, galena, tetrahedrite and pyrite with minor chalcopyrite and bornite, and gangue minerals are barite, dolomite and quartz. Sulfide mineralization textures are massive, replacement , vein-vein…
Trapping Rare and Elusive Phosphinidene Chalcogenides
2017
Four-membered rings with a P2Ch2 core (Ch=S, Se) and phosphorus in the +3 oxidation state have been synthesized. The utility of these rings as a source of monomeric phosphinidene chalcogenides was probed by the addition of an N-heterocyclic carbene, resulting in a base-stabilized phosphinidene sulfide. Similarly, persistence of the phosphinidene selenide in solution was shown through cycloaddition chemistry with 2,3-dimethylbutadiene at elevated temperatures. The observed reactivity was explained by detailed computational work that established the conditions upon which the P2Ch2 rings can liberate phosphinidene chalcogenides. peerReviewed
Biogas Cleaning by Hydrogen Sulfide Scrubbing and Bio-oxidation of Captured Sulfides
2015
Hydrogen sulfide and partially carbon dioxide can be absorbed into alkaline washing liquid with nitrates for upgrading a quality of biogas. Sulfides captured into the washing liquid are consequently biologically oxidized in an anoxic bioreactor by autotrophic denitrifying bacteria. Nitrates in the washing liquid serve as electron acceptors for sulfide bio-oxidation. Washing of hydrogen sulfide from biogas was examined in a lab-scale countercurrent scrubber that was packed with plastic carriers and operated at different biogas and washing liquid flows. The hydrogen sulfide concentration in treated biogas was investigated in the range from 3 to 12.3 g m–3. The influence of the hydrogen sulfid…
Solvothermal synthesis, crystal structure and magnetic properties of homometallic Co(II) and Cu(II) chains with double di(4-pyridyl)sulfide as bridges
2012
Abstract Two new coordination polymers {[Co(μ-4,4′-dps)2(H2O)2](NO3)2·2(4,4′-dps)·4H2O}n (1) and {[Cu(μ-4,4′-dps)2(H2O)2](NO3)2·2H2O}n (2) [4,4′-dps = di(4-pyridyl)sulfide] have been synthesized by solvothermal reactions between the nitrate salts of cobalt(II) (1) and copper(II) (2) and the 4,4′-dps molecule. Compounds 1 and 2 have been characterized by elemental analysis, thermal analysis (TG/DTA), vibrational spectroscopy, single crystal X-ray diffraction analysis and variable-temperature magnetic measurements. Compounds 1 and 2 are cationic chain compounds of formula {[M(μ-4,4′-dps)2(H2O)2]n2n+ [M = Co(II) (1) and Cu(II) (2)] with double 4,4′-dps bridges, uncoordinated nitrate anions, an…
Fragmentation reactions of realgar caused by early transition metal hydrides
2012
Abstract The reaction of realgar with [Cp′2MH3] in boiling toluene gave [Cp′2M2As2S6] (Cp′ = t-BuC5H4; M = Nb: 1; Ta: 2), while [Cp2WH2] (Cp = C5H5) reacted with As4S4 to give [Cp2W(H)(η1-As5S2)] (6). The structures were determined by X-ray crystallography. Compounds 1 and 2 are dimers in which two Cp′M units are symmetrically bridged by a μ,η2:2-AsS3 ligand, a sulfide ligand and a heteroallylic μ,η2:2-AsS2 ligand. The structure of 6 belongs to the type of bent metallocenes in which tungsten is surrounded tetrahedrally by two Cp ligands, a crystallographically found hydride atom and the new As5S2 cage. The reaction of 1 with W(CO)5THF gave [Cp′2Nb2As2S6·W(CO)5] (3) and [Cp′2Nb2As2S6W(CO)3·W…
Metallocene sulfide chemistry of niobium and tantalum: new insights into the formation of niobium-polysulfido complexes and synthesis, structure, and…
1992
The previously described reaction of Cp'2NbH3 (Cp' = t-BuC5H4) with S8 was investigated with regard to the kinetic stabilization of as yet elusive intermediates during the formation of the polysulfide complex Cp'4Nb2S9 (1). Therefore, the permethylated complex Cp*2NbS3H (2; Cp* = C5Me5) and the Ta complex Cp'2TaS2H (3) were synthesized in a related reaction and structurally investigated. Despite the problematic localization of the hydride atom during X-ray crystallographic studies, the molecules can be described in a proper manner: Characteristic of 2 and 3 are M(eta(2)-S2) cores to which either an SH (2) or a H (3) ligand is attached. Complex 3 is the first known tantalocene sulfide. It re…