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Indian low grade iron ores mostly contain quartz, gibbsite, and clay as the major impurities. Depending upon the ore characteristics, in many instances froth flotation has to be used to recover the hematite and other iron oxides from the ground ores. In this context, the difference in silica and alumina content in low grade iron ores is brought to bear on the prospects of iron ore flotation. For this purpose, pure minerals like hematite, quartz, gibbsite, and clay have been used to prepare synthetic mixtures and analyzed to determine the difference in floatability. The results are compared against natural iron ores with variations in silica and alumina content. The flotation results with oleic acid and dodecylamine show better recovery of iron values in the hematite–quartz mixture as well as in the naturally occurring high silica ore compared to the hematite–clay mixture and the high alumina ore respectively. Similarly results on a variety of iron ores show that high silica content as quartz in the ore causes less hindrance in the flotation of iron ore, whereas the presence of silica as clay inhibits the flotation response of iron ore. The scanning electron microscopic (SEM) studies indicate that clay particles cover the surface of hematite, making it less selective for interaction with the collector. The surface potential studies of clay and quartz suggest that charge reversal takes place for quartz treated with dodecylamine (DDA), but for the DDA adsorption on clay, negative potential values are noted beyond a pH of 4.6. [ABSTRACT FROM AUTHOR]

This study illustrates a density functional theory (DFT) based approach to design the amine collectors with regards to their interaction with the quartz surface. Mechanism of interaction of primary aliphatic amines and their ether and ester derivatives with the quartz surface has been established. Hydrogen bond geometries and adsorption energies as calculated using DFT reveal that ester amines are stronger surfactants compared to the ether amines and primary alkyl amines. Simulation studies carried out for the different amines with number of carbon atoms varying from 10 to 18 suggest that increasing the number of carbon atoms in the alkyl chain enhances the interaction, but not beyond C 14 for primary amines and C 16 for its ether and ester derivatives. Presence of both ether and ester group in the alkyl chain facilitates its interaction strength. Adsorption strength of C 12 amine containing both ether and ester amine is almost equivalent to that of C 16 ester amine. [ABSTRACT FROM AUTHOR]