Oxygen-converter reduction of iron and manganese from their oxides by components dissolved in liquid iron

2009 ◽  
Vol 39 (6) ◽  
pp. 445-449 ◽  
Author(s):  
M. K. Shakirov ◽  
I. A. Zhibinova ◽  
K. M. Shakirov ◽  
E. V. Protopopov
2019 ◽  
Vol 1153 ◽  
pp. 012078
Author(s):  
La Aba ◽  
Agung Prasetyo ◽  
Wa Ode Sitti Ilmawati ◽  
La Ode Ahmad ◽  
La Ode Sahidin

2021 ◽  
Vol 10 ◽  
pp. 56-64
Author(s):  
R. I. Gulyaeva ◽  
◽  
S. V. Sergeeva ◽  
S. A. Petrova ◽  
L. Yu. Udoeva ◽  
...  

Processes of calciothermal reduction of metals from iron (FeTa2O6) and manganese (MnTa2O6) tantalates as well as tantalum oxide (Ta2O5) were studied in this work. According to the results of thermodynamic analysis performed in the temperature range 373 – 2773 К, the interaction of FeTa2O6 and MnTa2O6 with calcium proceeds with complete reduction of metals. By the calculation and comparison of the lgK equilibrium constants for the reactions of alumino- and calciothermal reduction of iron and manganese tantalates were showed the thermodynamic advantage of using metallic calcium as a reducing agent. Experimental investigations of calciothermal reduction on samples of synthesized oxides were carried out by the method of combined thermogravimetry and differential thermal analysis in the mode of non-isothermal heating to 1473 K in an argon flow. X-ray powder diffraction was used to determine the phase composition of the initial samples and interaction products. It was shown that the calciothermal reduction of metals from the synthesized manganese tantalate proceeds actively at temperatures above 1196 K, while iron tantalate and tantalum oxide with the appearance of molten calcium. Tantalum and its solid solutions with iron or manganese, corresponding to the structural type Ta7Fe6, were included in the main metal components of the products of the interaction of FeTa2O6 and MnTa2O6 with calcium.


2017 ◽  
Vol 115 (2) ◽  
pp. 296-301 ◽  
Author(s):  
Gilian Schout ◽  
Niels Hartog ◽  
S. Majid Hassanizadeh ◽  
Jasper Griffioen

Blowouts present a small but genuine risk when drilling into the deep subsurface and can have an immediate and significant impact on the surrounding environment. Nevertheless, studies that document their long-term impact are scarce. In 1965, a catastrophic underground blowout occurred during the drilling of a gas well in The Netherlands, which led to the uncontrolled release of large amounts of natural gas from the reservoir to the surface. In this study, the remaining impact on methane chemistry in the overlying aquifers was investigated. Methane concentrations higher than 10 mg/L (n = 12) were all found to have δ13C-CH4 values larger than −30‰, typical of a thermogenic origin. Both δ13C-CH4 and δD-CH4 correspond to the isotopic composition of the gas reservoir. Based on analysis of local groundwater flow conditions, this methane is not a remnant but most likely the result of ongoing leakage from the reservoir as a result of the blowout. Progressive enrichment of both δ13C-CH4 and δD-CH4 is observed with increasing distance and decreasing methane concentrations. The calculated isotopic fractionation factors of εC = 3 and εD = 54 suggest anaerobic methane oxidation is partly responsible for the observed decrease in concentrations. Elevated dissolved iron and manganese concentrations at the fringe of the methane plume show that oxidation is primarily mediated by the reduction of iron and manganese oxides. Combined, the data reveal the long-term impact that underground gas well blowouts may have on groundwater chemistry, as well as the important role of anaerobic oxidation in controlling the fate of dissolved methane.


Author(s):  
J. Thieme ◽  
J. Niemeyer ◽  
P. Guttman

In soil science the fraction of colloids in soils is understood as particles with diameters smaller than 2μm. Clay minerals, aquoxides of iron and manganese, humic substances, and other polymeric materials are found in this fraction. The spatial arrangement (microstructure) is controlled by the substantial structure of the colloids, by the chemical composition of the soil solution, and by thesoil biota. This microstructure determines among other things the diffusive mass flow within the soils and as a result the availability of substances for chemical and microbiological reactions. The turnover of nutrients, the adsorption of toxicants and the weathering of soil clay minerals are examples of these surface mediated reactions. Due to their high specific surface area, the soil colloids are the most reactive species in this respect. Under the chemical conditions in soils, these minerals are associated in larger aggregates. The accessibility of reactive sites for these reactions on the surface of the colloids is reduced by this aggregation. To determine the turnover rates of chemicals within these aggregates it is highly desirable to visualize directly these aggregation phenomena.


2008 ◽  
Vol 21 (1) ◽  
pp. 77-80
Author(s):  
Andrzej Kot ◽  
Stanisław Zaręba

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