Iron(III) solubility and speciation in aqueous solutions. experimental study and modelling: part 1. hematite solubility from 60 to 300°C in NaOH–NaCl solutions and thermodynamic properties of Fe(OH)4−(aq)
“…[16] [16] (DG°3 83K [110°C] < À36.49 kJ/mol). [48][49][50][51][52] In addition, a few small powdery electroreduction-generated iron grains are found in the reaction interface (the inset in Figure 14(a)), which suggests that the solid state electroreduction mechanism (Reactions [1] and [2]), i.e., Fe 2 O 3 fi Fe 3 O 4 fi Fe, is likely to present in the electroreduction process. The electroreduction-generated oxygen ion could then react with H 2 O to form OH À , i.e., O 2À + H 2 O fi 2OH À .…”
Section: Influence Of the Electroreduction Time On The Electroredumentioning
confidence: 99%
“…[15] The theoretical decomposition potentials (E°) for Reactions [1] through [3] have been calculated from the reported thermodynamic data. [48][49][50][51][52] …”
Section: Influence Of the Electroreduction Time On The Electroredumentioning
confidence: 99%
“…The standard Gibbs free energy changes (DG°) or the theoretical decomposition potentials (E°) for Reactions [4] through [9] have been calculated based on the reported thermodynamic data. [48][49][50][51][52] More details about the reaction mechanisms of the electrodeposition of iron from Fe 2 O 3 and NaFeO 2 precursors in aqueous NaOH solution can be found in our recent work. [56] Therefore, during the electroreduction process in this experiment, Fe 2 O 3 precursor and the electroreduction-generated Fe 3 O 4 and/or NaFeO 2 intermediates surrounded by aqueous NaOH solution would dissolve in the nearby electrolyte simultaneously, and then redeposit on the preformed iron to form dendritic crystals in the reaction front area immediately (as schematically shown in Figure 14(b)).…”
Section: Solid State Electroreduction Mechanismmentioning
Low temperature electrochemical reduction of iron(III) oxide to iron in a strongly alkaline solution has been systematically investigated in this article. The facile electrochemical process was carried out in 50 to 70 wt pct aqueous NaOH solution at 383 K (110°C) and 1.7 V. The preformed spherical Fe 2 O 3 pellets with porous structures were used directly as precursors for the electrolytic production of iron. The influences of the experimental parameters on the electroreduction process and the characteristics of the iron products as well as the reaction mechanisms were investigated. The results show that the precursor's pre-sintering process and the concentration of NaOH aqueous electrolyte have significant influences on the electroreduction process. The electroreduction-generated spherical metallic iron layer comprising dendritic iron crystals is first formed on the surface of Fe 2 O 3 pellet precursor and then extends gradually into the pellet's interior along the radial direction. The electroreduction process is confirmed to be a typical shrinking-core reaction process. The direct solid state electroreduction mechanism and the dissolution-electrodeposition mechanism coexist in the electrochemical process. The experimental observations suggest that the dissolution-electrodeposition mechanism appears to be the dominant mechanism under the experimental conditions employed in this study. This facile process may open a new green electricitybased route for the production of dendritic iron crystals from iron(III) oxide in alkaline media.
“…[16] [16] (DG°3 83K [110°C] < À36.49 kJ/mol). [48][49][50][51][52] In addition, a few small powdery electroreduction-generated iron grains are found in the reaction interface (the inset in Figure 14(a)), which suggests that the solid state electroreduction mechanism (Reactions [1] and [2]), i.e., Fe 2 O 3 fi Fe 3 O 4 fi Fe, is likely to present in the electroreduction process. The electroreduction-generated oxygen ion could then react with H 2 O to form OH À , i.e., O 2À + H 2 O fi 2OH À .…”
Section: Influence Of the Electroreduction Time On The Electroredumentioning
confidence: 99%
“…[15] The theoretical decomposition potentials (E°) for Reactions [1] through [3] have been calculated from the reported thermodynamic data. [48][49][50][51][52] …”
Section: Influence Of the Electroreduction Time On The Electroredumentioning
confidence: 99%
“…The standard Gibbs free energy changes (DG°) or the theoretical decomposition potentials (E°) for Reactions [4] through [9] have been calculated based on the reported thermodynamic data. [48][49][50][51][52] More details about the reaction mechanisms of the electrodeposition of iron from Fe 2 O 3 and NaFeO 2 precursors in aqueous NaOH solution can be found in our recent work. [56] Therefore, during the electroreduction process in this experiment, Fe 2 O 3 precursor and the electroreduction-generated Fe 3 O 4 and/or NaFeO 2 intermediates surrounded by aqueous NaOH solution would dissolve in the nearby electrolyte simultaneously, and then redeposit on the preformed iron to form dendritic crystals in the reaction front area immediately (as schematically shown in Figure 14(b)).…”
Section: Solid State Electroreduction Mechanismmentioning
Low temperature electrochemical reduction of iron(III) oxide to iron in a strongly alkaline solution has been systematically investigated in this article. The facile electrochemical process was carried out in 50 to 70 wt pct aqueous NaOH solution at 383 K (110°C) and 1.7 V. The preformed spherical Fe 2 O 3 pellets with porous structures were used directly as precursors for the electrolytic production of iron. The influences of the experimental parameters on the electroreduction process and the characteristics of the iron products as well as the reaction mechanisms were investigated. The results show that the precursor's pre-sintering process and the concentration of NaOH aqueous electrolyte have significant influences on the electroreduction process. The electroreduction-generated spherical metallic iron layer comprising dendritic iron crystals is first formed on the surface of Fe 2 O 3 pellet precursor and then extends gradually into the pellet's interior along the radial direction. The electroreduction process is confirmed to be a typical shrinking-core reaction process. The direct solid state electroreduction mechanism and the dissolution-electrodeposition mechanism coexist in the electrochemical process. The experimental observations suggest that the dissolution-electrodeposition mechanism appears to be the dominant mechanism under the experimental conditions employed in this study. This facile process may open a new green electricitybased route for the production of dendritic iron crystals from iron(III) oxide in alkaline media.
“…It is worthy to note that the ferric-hydroxo complexes Fe(OH) 2+ and Fe(OH) 2 + were included in the model. According to Diakonov et al [9], these species form as pH increases at room temperature. Since at high temperatures the pH of a sulphate solution also increases, one may assume that these hydroxide complexes also form.…”
Section: Resultsmentioning
confidence: 97%
“…The speciation of aluminum sulfate and magnesium sulfate in sulfuric acid solution are given by Baghalha and Papangelakis [2] as follows: The speciation of ferric sulfate in sulfuric acid solution at high temperature was given by Diakonov et al [9] and Liu et al [8]:…”
Section: Speciation Reactions Of Al In Aqueous Hmentioning
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