scholarly journals Phosphate coprecipitation affects reactivity of iron (oxyhydr)oxides towards dissolved iron and sulfide

Author(s):  
Peter Kraal ◽  
Case M. van Genuchten ◽  
Thilo Behrends
Keyword(s):  
Author(s):  
Donald Eugene Canfield

This chapter considers the aftermath of the great oxidation event (GOE). It suggests that there was a substantial rise in oxygen defining the GOE, which may, in turn have led to the Lomagundi isotope excursion, which was associated with high rates of organic matter burial and perhaps even higher concentrations of oxygen. This excursion was soon followed by a crash in oxygen to very low levels and a return to banded iron formation deposition. When the massive amounts of organic carbon buried during the excursion were brought into the weathering environment, they would have represented a huge oxygen sink, drawing down levels of atmospheric oxygen. There appeared to be a veritable seesaw in oxygen concentrations, apparently triggered initially by the GOE. The GOE did not produce enough oxygen to oxygenate the oceans. Dissolved iron was removed from the oceans not by reaction with oxygen but rather by reaction with sulfide. Thus, the deep oceans remained anoxic and became rich in sulfide, instead of becoming well oxygenated.


Author(s):  
Yuri Fedorov ◽  
Yuri Fedorov ◽  
Irina Dotsenko ◽  
Irina Dotsenko ◽  
Leonid Dmitrik ◽  
...  

The distribution and behavior of certain of trace elements in sea water is greatly affected by both physical, chemical and hydrometeorological conditions that are showed in the scientific works of prof. Yu.A. Fedorov with coauthors (1999-2015). Due to the shallow waters last factor is one of the dominant, during the different wind situation changes significantly the dynamics of water masses and interaction in the system “water – suspended matter – bottom sediments”.Therefore, the study of the behavior of the total iron in the water of the sea at different wind situation is relevant. The content of dissolved iron forms migration in The Sea of Azov water (open area) varies from 0.017 to 0.21 mg /dm3 (mean 0.053 mg /dm3) and in Taganrog Bay from 0.035 to 0.58 mg /dm3 (mean 0.11 mg /dm3) and it is not depending on weather conditions.The reduction in the overall iron concentration in the direction of the Taganrog Bay → The Sea of Azov (open area) is observed on average more than twice. The dissolved iron content exceeding TLV levels and their frequency of occurrence in the estuary, respectively, were higher compared with The Sea of Azov (open area).There is an increase in the overall iron concentration in the water of the Azov Sea on average 1.5 times during the storm conditions, due to the destruction of the structure of the upper layer and resuspension of bottom sediments, intensifying the transition of iron compounds in the solution.


Author(s):  
Daria Boglaienko ◽  
Odeta Qafoku ◽  
Ravi K. Kukkadapu ◽  
Libor Kovarik ◽  
Yelena P. Katsenovich ◽  
...  

Enhanced TcO4− reduction by metallic Fe0 in the presence of particulate and structural Si. Rhythmical precipitation of dissolved iron leads to formation of layered structures related to geological phenomena such as orbicular rocks and Liesegang rings.


2009 ◽  
Vol 71-73 ◽  
pp. 437-440
Author(s):  
Lasse Ahonen ◽  
Pauliina Nurmi ◽  
Olli H. Tuovinen

Geochemical modeling program PHREEQC was used to simulate generic bioleaching processes. Carbonate minerals (e.g., calcite) dissolve in acid solution, increasing the solution pH and Ca concentration while the concentration of CO2 may be controlled by the equilibrium with the atmospheric CO2. Non-oxidative dissolution of Fe-monosulphides was demonstrated to release H2S and increase the pH. In the absence of ferric iron precipitation (goethite), the oxidation of pyrite decreased the solution pH from 2 to ~1.4, while the oxidation of Fe-monosulphide and chalcopyrite increased the solution pH to ~3.2-3.4. Assuming equilibrium precipitation of goethite, oxidative leaching decreased the solution pH for all three minerals from pH ~2 to ~0.9-1.2. Adjustment of the solution pH to 1.8 or 2.0 with KOH with concurrent equilibrium precipitation of K-jarosite resulted in low dissolved iron concentrations.


Chemosphere ◽  
2011 ◽  
Vol 82 (8) ◽  
pp. 1161-1167 ◽  
Author(s):  
Hiroshi Hasegawa ◽  
Ismail M.M. Rahman ◽  
Sanae Kinoshita ◽  
Teruya Maki ◽  
Yoshiaki Furusho

2005 ◽  
Vol 32 (19) ◽  
pp. n/a-n/a ◽  
Author(s):  
Cécile Guieu ◽  
Sophie Bonnet ◽  
Thibaut Wagener ◽  
Marie-Dominique Loÿe-Pilot

1976 ◽  
Vol 29 (10) ◽  
pp. 2149 ◽  
Author(s):  
RJ Atkinson

FeC2O4,2H2O(s) suspensions in sodium hydroxide solutions were oxidized by a fast air-bubble flow at room temperature until complete reaction had occurred. With amounts of NaOH in the range OH/Fe initial mole ratio ≤1.0, the reaction is FeC2O4, 2H2(s)+ OH-(aq)+ �O2(g) → ⅔γFeOOH(s)+1/3Fe(C2O4)33-(aq)+13/6H2O With OH/Fe mole ratio ≥ 2.0 the reaction is FeC2O4, 2H2(s)+ 2OH-(aq)+ �O2(g) → αFeOOH(s)+(C2O4)33-(aq)+ 5/2 H2O Mixtures of goethite (α-FeOOH) and lepidocrocite (γ-FeOOH) form at intermediate OH/Fe mole ratio. The oxidation process occurs in a solid-phase intermediate product. Comparisons with similar oxidations of iron(11)sulphate solutions showed that γ-FeOOH formation was favoured and α-FeOOH formation inhibited in the iron(11) oxalate oxidation. These differences are related to pH and dissolved iron concentrations.


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