Adsorption of Tetrathiomolybdate to Iron Sulfides and Its Impact on Iron Sulfide Transformations

2020 ◽  
Vol 4 (12) ◽  
pp. 2246-2260
Author(s):  
Nathan Miller ◽  
Maura Dougherty ◽  
Ruochen Du ◽  
Tyler Sauers ◽  
Candice Yan ◽  
...  
Keyword(s):  
2020 ◽  
Vol 22 (40) ◽  
pp. 23258-23267
Author(s):  
Miroslav Kolos ◽  
Daniel Tunega ◽  
František Karlický

The adsorption properties of two iron sulfide minerals (mackinawite and pyrite) and zero-valent iron with respect to two small polar molecules (H2O and H2S) and trichloroethylene (TCE) were modeled.


2019 ◽  
Vol 116 (41) ◽  
pp. 20376-20381 ◽  
Author(s):  
Satoshi Okada ◽  
Chong Chen ◽  
Tomo-o Watsuji ◽  
Manabu Nishizawa ◽  
Yohey Suzuki ◽  
...  

Biomineralization in animals exclusively features oxygen-based minerals with a single exception of the scaly-foot gastropod Chrysomallon squamiferum, the only metazoan with an iron sulfide skeleton. This unique snail inhabits deep-sea hot vents and possesses scales infused with iron sulfide nanoparticles, including pyrite, giving it a characteristic metallic black sheen. Since the scaly-foot is capable of making iron sulfide nanoparticles in its natural habitat at a relatively low temperature (∼15 °C) and in a chemically dynamic vent environment, elucidating its biomineralization pathways is expected to have significant industrial applications for the production of metal chalcogenide nanoparticles. Nevertheless, this biomineralization has remained a mystery for decades since the snail’s discovery, except that it requires the environment to be rich in iron, with a white population lacking in iron sulfide known from a naturally iron-poor locality. Here, we reveal a biologically controlled mineralization mechanism employed by the scaly-foot snail to achieve this nanoparticle biomineralization, through δ34 S measurements and detailed electron-microscopic investigations of both natural scales and scales from the white population artificially incubated in an iron-rich environment. We show that the scaly-foot snail mediates biomineralization in its scales by supplying sulfur through channel-like columns in which reaction with iron ions diffusing inward from the surrounding vent fluid mineralizes iron sulfides.


2018 ◽  
Vol 6 (35) ◽  
pp. 17111-17119 ◽  
Author(s):  
Natalia Voronina ◽  
Hitoshi Yashiro ◽  
Seung-Taek Myung

Iron sulfides have attracted significant attention as promising electrode materials for sodium-ion batteries (SIBs) owing to their low electronegativity, high theoretical capacity, and cost-effectiveness.


2019 ◽  
Author(s):  
Noah E. Horwitz ◽  
Elena V. Shevchenko ◽  
Jehee Park ◽  
Eungje Lee ◽  
Jiaze Xie ◽  
...  

Transition metal chalcogenides with layered structures have emerged as promising materials for energy storage, catalysis, and electronics, among other areas. We have identified a new layered phase of iron sulfide containing interlayer solvated cations. We present an optimized synthesis for the Li+-containing material from an Fe(III) xanthate complex. Structure and composition data indicate the material consists of poorly-ordered iron sulfide layers separated by solvated cations. The lamellar spacing in these materials can be tuned by changing the identity of the cation. Furthermore, the lamellar spacing can also be reversibly tuned by the degree of solvation of the material. The material is electrically conductive and can serve as a pseudocapacitor with comparable performance to commercial materials such as MnO<sub>2</sub>. Furthermore, these materials also show promise as lithium or sodium ion battery cathodes with good capacity and reversibility.


2011 ◽  
Vol 2011 ◽  
pp. 1-12
Author(s):  
Arun Kumar Singh

The reaction products of sulfurized Mohwa oil with iron powder in hydrocarbon medium at 150°C for 8 h were studied to investigate the type of lubricant films formed during their application as antiwear and extreme pressure additives. The main reaction product was isolated on the basis of its solubility in mixed solvent. Surface characterization was carried out using ultraviolet-visible spectroscopy (UV), fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR), X-ray diffraction spectroscopy (XRD), scanning electron microscope (SEM), and high frequency reciprocal rig (HFRR). An examination of their elemental analysis and instrumental analysis data reveals that there is reduction in the length of the alkyl chains and carbonyl ester groups with formation of inorganic iron sulfides. Polymerized product with a number of ketonic and aldehydic groups containing iron and sulfur in the polymeric films in the form of unsaturated cyclic rings was also formed. The films are organo-inorganic in nature, unlike the purely inorganic iron sulfide type. The load-carrying characteristic of this product is strongly influenced by the type of the film formed on the iron surfaces.


1998 ◽  
Vol 4 (S2) ◽  
pp. 562-563
Author(s):  
S. C. Cheng ◽  
R. T. Wilkin

The white lines on the L2,3 absorption edges of the transition metals and on the M4,5 absorption edges of the rare earth elements are the most prominent feature in electron-energy-loss spectra (EELS). The white lines of these elements have been studied and used to determine valance and coordination of atoms in various systems. Fe-O compounds with valence 2, 3 and mixed valence states, for example, have been carefully examined and characterized. However, in spite of the importance of iron sulfides in geochemistry and environmental science, the EELS data of these compounds are not available. Pyrite (FeS2) is widespread in hydrothermal ores, modern sediments, and sedimentary rocks deposited throughout the geologic record. The ferromagnetic iron sulfide greigite (Fe3S4) is another important compound. It has been recognized as a carrier of magnetic remanence in young sediments. Sedimentary greigite may be precipitated inorganically or biogenically by magnetotactic bacteria.


1992 ◽  
Vol 38 (12) ◽  
pp. 1320-1324 ◽  
Author(s):  
F. G. Ferris ◽  
T. R. Jack ◽  
B. J. Bramhill

Attached populations of corrosion enhancing sulfate-reducing bacteria (SRB) and organic acid-producing bacteria (APB) were measured on steel plugs at an oil field water injection plant near Wainwright, Alberta. The sample plugs were colonized to ca. 106 SRB/cm2. Counts for APB ranged from 102 to 10/cm2. Scanning electron microscopic examination of the sample plugs revealed an uneven distribution of surface corrosion deposits. A thin iron sulfide layer covered most of the exposed areas. Thicker sulfur-enriched deposits occurred randomly. The bulk of the thicker deposits were smooth, whereas peripheral regions exhibited a porous texture. The elemental composition of the different regions was the same; however, bacterial cells were concentrated in the porous areas and were not found in the thinner deposits. In transmission electron microscopic thin sections cut perpendicularly through corrosion deposits, bacterial cells were found mineralized in successive stages by iron sulfides. The corrosion deposit matrix also generated strong Cl peaks in energy dispersive X-ray spectra. This entrainment of bacterial cells within a corrosion deposit matrix is consistent with the concept of bacterial enhancement of corrosion by removal of reducing power from iron sulfides galvanically coupled to the steel surface. Key words: microbial corrosion, iron sulfide, cathodic hydrogen, electron microscopy.


2007 ◽  
Vol 561-565 ◽  
pp. 2099-2102 ◽  
Author(s):  
Chung Kwei Lin ◽  
Chin Yi Chen ◽  
Pee Yew Lee ◽  
Chih Chieh Chan

In the present study, pure elemental powders of Fe and S were mixed to give the desired compositions of Fe50S50. A SPEX 8000D high-energy ball mill was used to synthesize iron sulfide powders under an Ar-filled atmosphere. The prepared powders were examined by conventional X-ray diffractometry and synchrotron X-ray absorption spectroscopy. The experimental results revealed that mechanochemical reactions occurred during the ball milling process for all the compositions. The Fe50S50 phase was obtained after ball milling for 20 h. Extended X-ray absorption fine structure (EXAFS) results revealed that the nearest neighbor bond lengths of the radial distribution function (RDF) for iron decreased when iron sulfides formed. X-ray absorption near edge structure (XANES) of S K-edges distinguished better the structural evolution of these iron sulfides.


1992 ◽  
Vol 62 (9) ◽  
pp. 516-521 ◽  
Author(s):  
John R. McLaughlin ◽  
Margaret M. Leonard

We propose that iron sulfides can be formed in the first bowl of a commercial wool scour. Under the low redox conditions recorded, ferric iron, a ubiquitous component of minerals on the fleece, is dissolved reductively to the ferrous form, which reacts with sulfide present either as residual depilatory on slipe wool or from degraded wool protein. The black iron sulfide may deposit on the scoured wool, making it dull and gray. The observation that some scoured wools become brighter and more yellow with time is consistent with the expected behavior of deposited iron sulfides, which slowly oxidize in air.


2021 ◽  
Vol 55 (1) ◽  
Author(s):  
Franco Zunino ◽  
Karen Scrivener

AbstractValorisation of locally available clays for producing blended cements is crucial for a widespread adoption of sustainable binders incorporating these materials. In some places, clays can be intermixed with small amounts of iron sulfides, which could eventually expand in the alkaline media of concrete and lead to cracking if clay particles are sufficiently fine. This study explored the stability of iron sulfides, namely troilite and pyrite, during calcination of clays and their influence in reactivity. It was found that both troilite and pyrite decompose and oxidize into hematite under typical calcination conditions for clays. Furthermore, there is no negative influence of the presence of iron sulfide phases on the reactivity of calcined clays. This shows that these clays are suitable for use in blended cements, provided that adequate quality control is conducted to ensure a complete decomposition of the iron sulfide phases.


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