Tao Long , Qubing Li , Wei Yang , Sha Deng , Xiangyu Peng , Jianping Jin
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DFT calculation revealed that the adsorption of H<sub>4</sub>SiO<sub>4</sub> and [H<sub>3</sub>SiO<sub>4</sub>]<sup>−</sup> on the talc surface is relatively weak, with adsorption energies of −7.71 kJ/mol and −23.15 kJ/mol. Following the adsorption of Al<sup>3+</sup> onto the talc surface, the adsorption energies of H<sub>4</sub>SiO<sub>4</sub> and [H<sub>3</sub>SiO<sub>4</sub>]<sup>−</sup> were further decreased to −78.41 kJ/mol and −119.63 kJ/mol. The presence of Al<sup>3+</sup> significantly enhanced the interaction between water glass and the talc surface. This enhancement was attributed to the formation of hydrogen bonds between water glass and the Al<sup>3+</sup> water complex–Al(OH)<sub>3</sub>·H<sub>2</sub>O, which augmented the interaction with the talc surface.</div></div>","PeriodicalId":18594,"journal":{"name":"Minerals Engineering","volume":"222 ","pages":"Article 109127"},"PeriodicalIF":4.9000,"publicationDate":"2024-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mechanism of synergistic effect of aluminum ions and water glass on talc flotation depression\",\"authors\":\"Tao Long , Qubing Li , Wei Yang , Sha Deng , Xiangyu Peng , Jianping Jin\",\"doi\":\"10.1016/j.mineng.2024.109127\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Talc, a prevalent gangue mineral in sulfide ores, poses a significant challenge in the flotation process due to its good floatability. The application of water glass as a standalone reagent has been found to be less effective in suppressing talc. In this study, we delve into the synergistic inhibitory mechanism of Al<sup>3+</sup> in conjunction with water glass on talc through a series of micro-flotation tests, wettability tests, ICP-MS tests and FTIR spectroscopy tests. Our findings demonstrated that the presence of Al<sup>3+</sup> significantly enhanced the adsorption capacity of water glass on talc surface. Talc recovery was 23.34 % with the addition of both inhibitors, which was lower than the recovery of 55.82 % with the addition of water glass only. DFT calculation revealed that the adsorption of H<sub>4</sub>SiO<sub>4</sub> and [H<sub>3</sub>SiO<sub>4</sub>]<sup>−</sup> on the talc surface is relatively weak, with adsorption energies of −7.71 kJ/mol and −23.15 kJ/mol. Following the adsorption of Al<sup>3+</sup> onto the talc surface, the adsorption energies of H<sub>4</sub>SiO<sub>4</sub> and [H<sub>3</sub>SiO<sub>4</sub>]<sup>−</sup> were further decreased to −78.41 kJ/mol and −119.63 kJ/mol. The presence of Al<sup>3+</sup> significantly enhanced the interaction between water glass and the talc surface. 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引用次数: 0
摘要
滑石是硫化物矿石中常见的脉石矿物,由于其良好的可浮性,给浮选工艺带来了很大的挑战。用水玻璃作为单独的试剂抑制滑石的效果较差。本研究通过一系列的微浮选试验、润湿性试验、ICP-MS试验和FTIR光谱试验,探讨了Al3+与水玻璃对滑石的协同抑制机理。研究结果表明,Al3+的存在显著增强了水玻璃在滑石表面的吸附能力。添加两种抑制剂时,滑石回收率为23.34%,低于仅添加水玻璃时的55.82%。DFT计算表明,H4SiO4和[H3SiO4]−在滑石表面的吸附较弱,吸附能分别为−7.71 kJ/mol和−23.15 kJ/mol。Al3+在滑石表面吸附后,H4SiO4和[H3SiO4] -的吸附能进一步降低至- 78.41 kJ/mol和- 119.63 kJ/mol。Al3+的存在显著增强了水玻璃与滑石表面的相互作用。这种增强是由于水玻璃与Al3+水络合物- al (OH)3·H2O之间形成氢键,增强了与滑石表面的相互作用。
Mechanism of synergistic effect of aluminum ions and water glass on talc flotation depression
Talc, a prevalent gangue mineral in sulfide ores, poses a significant challenge in the flotation process due to its good floatability. The application of water glass as a standalone reagent has been found to be less effective in suppressing talc. In this study, we delve into the synergistic inhibitory mechanism of Al3+ in conjunction with water glass on talc through a series of micro-flotation tests, wettability tests, ICP-MS tests and FTIR spectroscopy tests. Our findings demonstrated that the presence of Al3+ significantly enhanced the adsorption capacity of water glass on talc surface. Talc recovery was 23.34 % with the addition of both inhibitors, which was lower than the recovery of 55.82 % with the addition of water glass only. DFT calculation revealed that the adsorption of H4SiO4 and [H3SiO4]− on the talc surface is relatively weak, with adsorption energies of −7.71 kJ/mol and −23.15 kJ/mol. Following the adsorption of Al3+ onto the talc surface, the adsorption energies of H4SiO4 and [H3SiO4]− were further decreased to −78.41 kJ/mol and −119.63 kJ/mol. The presence of Al3+ significantly enhanced the interaction between water glass and the talc surface. This enhancement was attributed to the formation of hydrogen bonds between water glass and the Al3+ water complex–Al(OH)3·H2O, which augmented the interaction with the talc surface.
期刊介绍:
The purpose of the journal is to provide for the rapid publication of topical papers featuring the latest developments in the allied fields of mineral processing and extractive metallurgy. Its wide ranging coverage of research and practical (operating) topics includes physical separation methods, such as comminution, flotation concentration and dewatering, chemical methods such as bio-, hydro-, and electro-metallurgy, analytical techniques, process control, simulation and instrumentation, and mineralogical aspects of processing. Environmental issues, particularly those pertaining to sustainable development, will also be strongly covered.