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Synthesis of Alpha Ferrous Oxalate Dihydrate from Ferrotitaniferous Mineral Sands via Hot Pressurized Aqueous Oxalic Acid: Kinetics and Characterization.

Authors :
Valdivieso-Ramírez, Carla S.
Galeas, Salomé
Saldaña, Marleny D. A.
Pontón, Patricia I.
Guerrero, Víctor H.
Vizuete, Karla
Debut, Alexis
Marinkovic, Bojan A.
Source :
Minerals (2075-163X). Sep2024, Vol. 14 Issue 9, p891. 19p.
Publication Year :
2024

Abstract

Ferrous oxalate dihydrate is a versatile organic mineral with applications across fields. However, little is known about the feasibility of its synthesis directly from iron-bearing minerals using binary subcritical water (sCW) systems and its associated kinetics. In this study, the sCW+oxalic acid system at either 115 °C or 135 °C was investigated as a reaction medium for ferrous oxalate dihydrate (α-FeC2O4∙2H2O) synthesis, starting from ferrotitaniferous sands. The kinetics of the synthesis reaction were studied, and the physicochemical characterization of the as-synthetized ferrous oxalates was performed. Overall, the sCW synthesis was temperature-dependent, following second-order reaction kinetics according to the proposed precipitation pathway. A high reaction rate constant, significantly high yields (up to 89%), and reduced reaction times (2–8 h) were evident at 135 °C. The as-synthetized product corresponded to the monoclinic α-FeC2O4∙2H2O, showed relatively high specific surface areas (from 31.9 to 33.7 m2∙g−1), and exhibited band gap energies within the visible light range (~2.77 eV). These results suggest that α-FeC2O4∙2H2O can be synthesized using an organic dicarboxylic acid and iron-rich, widely available, low-cost mineral precursors. In addition, the as-prepared α-FeC2O4∙2H2O could be further optimized and tested for catalytic and visible light photocatalytic applications. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
2075163X
Volume :
14
Issue :
9
Database :
Academic Search Index
Journal :
Minerals (2075-163X)
Publication Type :
Academic Journal
Accession number :
180010275
Full Text :
https://doi.org/10.3390/min14090891