2019
DOI: 10.1007/s42452-019-0218-9
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Characterization studies on Agbaja iron ore: a high-phosphorus content ore

Abstract: Characterization of Agbaja iron ore was carried out using optical microscopy, scanning electron microscopy with energydispersive X-ray spectroscopy, X-ray fluorescence spectrometry, powder X-ray diffraction, thermal gravimetry, and differential scanning calorimetry. The ore consists of a matrix of gangue minerals composed principally of aluminosilicates and iron-rich concentric cored structures characteristic of oolitic ores. Chemical analyses of the ore indicate that it is principally composed of 53.1 wt% Fe,… Show more

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Cited by 14 publications
(11 citation statements)
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References 63 publications
(71 reference statements)
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“…However, looking at the upper limits of phosphorus contents reported for high-phosphorus iron ores in which distinct phosphorus minerals are yet to be identified (0.8% [41,42] to −1.395% [20]), with the maximum plausible substitution of Fe cations with P cations calculated assuming the non-plausible equality of charge, and the maximum hydroxyl ion substitution with phosphate ligand that permits the maintenance of the stability of the respective structures (in P solid solution with goethite and phosphate ligand substitution of hydroxyl groups in goethite), it might be argued that both theories may not fully account for the full range of phosphorus content in iron ores. In light of the known affinity of iron oxide/hydroxide surfaces for phosphorus/phosphate anions which permits their use as adsorbents for phosphorus removal [49,[72][73][74][75][76][77][78][79][80][81][82][83][84][85][86][87][88][89], it stands to reason that a significant proportion of phosphorus in high-phosphorus iron ores, especially in goethite ores, might be present as adsorbed species on the mineral surface.…”
Section: Phosphorus In Iron Ores and Theories On Its Existence In Iromentioning
confidence: 99%
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“…However, looking at the upper limits of phosphorus contents reported for high-phosphorus iron ores in which distinct phosphorus minerals are yet to be identified (0.8% [41,42] to −1.395% [20]), with the maximum plausible substitution of Fe cations with P cations calculated assuming the non-plausible equality of charge, and the maximum hydroxyl ion substitution with phosphate ligand that permits the maintenance of the stability of the respective structures (in P solid solution with goethite and phosphate ligand substitution of hydroxyl groups in goethite), it might be argued that both theories may not fully account for the full range of phosphorus content in iron ores. In light of the known affinity of iron oxide/hydroxide surfaces for phosphorus/phosphate anions which permits their use as adsorbents for phosphorus removal [49,[72][73][74][75][76][77][78][79][80][81][82][83][84][85][86][87][88][89], it stands to reason that a significant proportion of phosphorus in high-phosphorus iron ores, especially in goethite ores, might be present as adsorbed species on the mineral surface.…”
Section: Phosphorus In Iron Ores and Theories On Its Existence In Iromentioning
confidence: 99%
“…This report suggests that the thermal treatment of iron ores can influence their interaction with phosphate. On the other hand, iron ores are known to be associated with various other phases like kaolinite, as in the Agbaja ore from Nigeria [20], dolomite, clinochlore, and quartz, as in the ore from Hubei province (China) [257], kaolinite, as in the ore from Pilbara area of Western Australia [258], quartz and chamosite as in the ore from Aswan area of Egypt [38], clay-like minerals such as carbonates, chlorite, other aluminosilicates, and quartz as in the ore from Lisakovsk, North Kazakhstan [41,107], and silica and alumina, as in the ore from Moncorvo in north-east Portugal [45,[259][260][261]. Wei et al [234] studied the surface properties and phosphate adsorption of goethite, kaolinite, goethite-kaolinite association (GKA) and goethite-kaolinite mixture (GKM), and established their respective pHs at a point of zero charge (PZC) to be around 8.2, 4.1, 7.0, and 6.1 respectively, and their surface charges at pH 5 to be 0.561, −0.092, 0.097, and 0.041 mmol/g, respectively.…”
Section: Plausible Reasons For Differences In the Ease Of Phosphorus mentioning
confidence: 99%
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