4.7 Article

Effect of siderite dissolution on mineral particles interaction in aqueous suspension

Journal

POWDER TECHNOLOGY
Volume 382, Issue -, Pages 189-198

Publisher

ELSEVIER
DOI: 10.1016/j.powtec.2020.12.067

Keywords

Siderite; Mineral dissolution; Interfacial interaction; Hetero-aggregation

Funding

  1. National Natural Science Foundation of China [51904020]
  2. China Postdoctoral Science Foundation [2019M660466]
  3. Fundamental Research Funds for the Central Universities [FRF-TP-18-082A1]

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The study investigated the dissolution of siderite and its effects on the interaction with quartz particles using real-time particle characterization tools and theoretical calculations. The results showed that siderite dissolution at pH 5.0 weakened the electrostatic attraction energies between siderite and quartz, resulting in the suppression of hetero-aggregation.
Siderite dissolution and its effects on the interaction between siderite and quartz particle was investigated through focused beam reflectance measurement (FBRM) particle size analysis (a real-time particle characterization tool), zeta potential distribution measurement, and DLVO theoretical calculations, supplemented by dissolution tests, solution chemistry calculation, and X-ray photoelectron spectroscopy (XPS) analysis. The results of FBRM and zeta potential distribution measurement showed that the hetero-aggregation scarcely formed in the siderite-quartz mixture system, which was contrary with the calculated attraction energies (VTD) between siderite and quartz at pH 5.0. Dissolution test and solution chemistry calculation indicated that siderite could dissolve lattice ions, beside compression effects on the double electrode layer, the dissolved ferrous ions can also adsorb onto the negatively charged surface of quartz, which was confirmed by the results of zeta potential and XPS analysis. These would weaken the electrostatic attraction energies (VE) between siderite and quartz at pH 5.0, resulting in depressing the hetero-aggregation. (C) 2020 Elsevier B.V. All rights reserved.

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