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Forced hydrolysis of FeCl3 solutions in the presence of Cr3+ ions
Forced hydrolyses of FeCl3 solutions in the presence of Cr3+ ions without alkali addition were investigated at 160 and 200 °C. These precipitation systems were compared to corresponding reference systems. The isolated precipitates were characterized with XRD, 57Fe Mössbauer, FT-IR, FE SEM and photoc...
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Published in: | The Journal of physics and chemistry of solids 2021-09, Vol.156, p.110166, Article 110166 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Forced hydrolyses of FeCl3 solutions in the presence of Cr3+ ions without alkali addition were investigated at 160 and 200 °C. These precipitation systems were compared to corresponding reference systems. The isolated precipitates were characterized with XRD, 57Fe Mössbauer, FT-IR, FE SEM and photocatalytic measurements. Although chromium was not detected by EDS (Energy Dispersive X-ray Spectroscopy), the analysis of samples precipitated in the presence of Cr3+ ions showed several effects which can be attributed to the presence of these ions in the starting solutions. These effects are specifically well pronounced for samples obtained at 200 °C. For the highest concentration of Cr3+ ions and upon heating at 200 °C the transformation kinetics β-FeOOH to α-Fe2O3 was impeded. Relative intensities of prominent diffraction lines 104 and 110 of α-Fe2O3 changed as a result of the presence of Cr3+ ions. Changes in the size and formation of lemon-like particles instead of cube-like α-Fe2O3 particles were also noticed. The presence of Cr3+ ions in hydrolysing FeCl3 solution influenced the photocatalytic degradation of rhodamine B. Since no specific adsorption of Cr3+ ions occurred in the acidic pH medium, it was inferred that traces of Cr3+ ions enter into the structural tunnels of β-FeOOH crystals. The associates Cl−-Cr3+ are formed, which in the next step destabilize the crystal structure of β-FeOOH particles. Cr3+ ions leave the crystal structure upon dissolution of β-FeOOH. It can be assumed that α-Fe2O3 crystals start to grow on very fine and thin β-FeOOH crystallites which were not completely dissolved, but were previously affected by Cr3+ ions.
•Cr3+ ions influenced forced hydrolysis of FeCl3 solutions at pH |
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ISSN: | 0022-3697 1879-2553 |
DOI: | 10.1016/j.jpcs.2021.110166 |