scholarly journals Inorganic Polysulfides and Related Reactive Sulfur–Selenium Species from the Perspective of Chemistry

Molecules ◽  
2019 ◽  
Vol 24 (7) ◽  
pp. 1359 ◽  
Author(s):  
Ammar Kharma ◽  
Marian Grman ◽  
Anton Misak ◽  
Enrique Domínguez-Álvarez ◽  
Muhammad Nasim ◽  
...  

Polysulfides (H2Sx) represent a class of reactive sulfur species (RSS) which includes molecules such as H2S2, H2S3, H2S4, and H2S5, and whose presence and impact in biological systems, when compared to other sulfur compounds, has only recently attracted the wider attention of researchers. Studies in this field have revealed a facet-rich chemistry and biological activity associated with such chemically simple, still unusual inorganic molecules. Despite their chemical simplicity, these inorganic species, as reductants and oxidants, metal binders, surfactant-like “cork screws” for membranes, components of perthiol signalling and reservoirs for inorganic hydrogen sulfide (H2S), are at the centre of complicated formation and transformation pathways which affect numerous cellular processes. Starting from their chemistry, the hidden presence and various roles of polysulfides in biology may become more apparent, despite their lack of clear analytical fingerprints and often murky biochemical footprints. Indeed, the biological chemistry of H2Sx follows many unexplored paths and today, the relationship between H2S and its oxidized H2Sx species needs to be clarified as a matter of “unmistaken identity”. Simultaneously, emerging species, such as HSSeSH and SenS8−n, also need to be considered in earnest.

1992 ◽  
Vol 150 ◽  
pp. 459-460
Author(s):  
D. Despois ◽  
J. Crovisier ◽  
D. Bockelee-Morvan ◽  
P. Colom

Recent determinations of H2S and other sulfur compounds abundances in comets and in Orion KL bring new tests of the origin of cometary matter.


CORROSION ◽  
1960 ◽  
Vol 16 (10) ◽  
pp. 503t-506t ◽  
Author(s):  
KENNETH L. MOORE

Abstract Various corrosion problems are described which have occurred in a large diethanolamine (DEA) system that removes hydrogen sulfide from refinery gas streams and a liquid propane-butane stream. These include reboiler corrosion, rich DEA corrosion, stress corrosion cracking, and corrosion-erosion. The effect of the problems on system operation is discussed, as well as the means of minimizing the problems. Electrical resistance measuring device data indicate the importance of keeping the solution loading below 0.34 mol of acid gas (H2S + CO2) per mol of DEA to minimize the corrosion in the rich DEA. Data from this source also show the relationship between general reboiler corrosion and solution contamination. 8.4.3


2011 ◽  
Vol 29 (6) ◽  
pp. 711-741 ◽  
Author(s):  
Sumei Li ◽  
Xiongqi Pang ◽  
Quan Shi ◽  
Baoshou Zhang ◽  
Haizu Zhang ◽  
...  

Nine marine and two terrestrial oils from the Tarim Basin in Western China were analyzed by Fourier transform ion cyclotron resonance mass spectrometry. Sulfur compounds with 8–47 carbon atoms and double-bond equivalent (DBE) values of 0–21 are abundant in the crude oils. The most abundant sulfur species in Tazhong marine oils are S1 species (80.57–85.22%), followed by O1S1 (6.95–14.78%) and S2 (0.71–6.69%) species. The dominant species in Yingmaili terrestrial oils are S1 (51.41–52.76%), O1S1 (26.83–35.27%) and O2S1 (11.97–21.76%) species; no S2 species were detected. The results suggest that the sulfur compounds present in oil vary with the oil type. For the S1 and S2 species, as the thermal maturity increased, the degree of condensation increased, and the median and range of the number of carbon atoms decreased. Compounds with DBE values of 9, which are most likely dibenzothiophenes, became concentrated as the thermal maturity increased. Therefore, the unusually high abundance of dibenzothiophenes in the Lower Ordovician oils could be related to the thermal maturity. The TZ83 (O1) oil has an abnormal distribution of S1 species, and is characterized by sulfur species with relatively low DBE values (0–7). This abnormal distribution could be caused by thermochemical sulfate reduction, and a relatively high content of H2S in the associated gases and abundant sulfo-diamantane in the oil supported this theory. In conclusion, the thermal maturity, organic facies, paleoenvironment of the source rock, and possibly thermochemical sulfate reduction have a large impact on the sulfur compounds present in the oils. The O1S1/S1 and S2/S1 ratios could be used as indicators of the precursors/paleoenvironment, and C10–19/C20–50 DBE9 and DBE1,3,6 /DBE9 could be used as indicators of thermal maturity. Fourier transform ion cyclotron resonance mass spectrometry is very useful for detecting sulfur compounds, especially those with high molecular weights, in the crude oils. This technique has potential for determining the formation mechanisms of some unusual oils and the geochemical implications of the sulfur compounds they contain.


Redox Biology ◽  
2018 ◽  
Vol 15 ◽  
pp. 74-85 ◽  
Author(s):  
Kenneth R. Olson ◽  
Yan Gao ◽  
Faihaan Arif ◽  
Kanika Arora ◽  
Shivali Patel ◽  
...  

Minerals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 114
Author(s):  
Kadriann Tamm ◽  
Zeinab Arab Zadeh ◽  
Rein Kuusik ◽  
Juha Kallas ◽  
Jason Yang ◽  
...  

Phosphorus is an essential and non-substitutable element for the cellular processes of all living organisms. The main source of phosphorus in the biosphere is phosphate rock. With more than 700 Mt phosphate rock, Estonia holds the largest sedimentary phosphate rock deposits in the European Union. Estonian phosphate rock is particularly outstanding due to its remarkably low content of hazardous heavy metals such as Cadmium (<5 ppm) and trace elements of Uranium (<50 ppm). It is also a reliable source of valuable elements such as rear earth elements (REEs). The aim of this study was to investigate the distribution of the main minerals (apatite and quartz) between slimes, tailings, and concentrates that formed at the froth flotation of Estonian phosphate rock with the up-to-date level of know-how and techniques. Subsequently, the relationship between the obtained grades and recovery levels in concentrates was determined based on the collector dosage and flotation duration. It was observed that the fine fraction of the tailings contains 17.9–33.49 wt% P2O5 that can be added to the final product. Moreover, it was found that, with the lower dosage of the collector, the extended flotation time does not influence the phosphate grade and a high amount of quartz remains in the concentrates. It was also shown that, by raising the collector dosage and setting the flotation time, an adequate grade (>32 wt% P2O5) and recovery (up to 98%) can be gained. The results showed that Estonian phosphate rock can be beneficiated to produce a high-quality concentrate at high recovery levels by modifying the main flotation parameters depending on the properties of the ore.


2012 ◽  
Vol 12 (1) ◽  
pp. 527-543 ◽  
Author(s):  
S. L. Capps ◽  
D. K. Henze ◽  
A. Hakami ◽  
A. G. Russell ◽  
A. Nenes

Abstract. We present the development of ANISORROPIA, the discrete adjoint of the ISORROPIA thermodynamic equilibrium model that treats the Na+-SO42−- HSO4−-NH4+ -NO3−-Cl−-H2O aerosol system, and we demonstrate its sensitivity analysis capabilities. ANISORROPIA calculates sensitivities of an inorganic species in aerosol or gas phase with respect to the total concentrations of each species present with less than a two-fold increase in computational time over the concentration calculations. Due to the highly nonlinear and discontinuous solution surface of ISORROPIA, evaluation of the adjoint required a new, complex-variable version of the model, which determines first-order sensitivities with machine precision and avoids cancellation errors arising from finite difference calculations. The adjoint is verified over an atmospherically relevant range of concentrations, temperature, and relative humidity. We apply ANISORROPIA to recent field campaign results from Atlanta, GA, USA, and Mexico City, Mexico, to characterize the inorganic aerosol sensitivities of these distinct urban air masses. The variability in the relationship between fine mode inorganic aerosol mass and precursor concentrations shown has important implications for air quality and climate.


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