Elucidating the mechanism of ball milling on surface reconstruction of arsenopyrite: XPS property and theoretical studies

IF 4.9 2区 工程技术 Q1 ENGINEERING, CHEMICAL Minerals Engineering Pub Date : 2024-10-30 DOI:10.1016/j.mineng.2024.109077
Manjiao Chen , Xinjun Hu , Jianping Tian
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Abstract

The surface composition, coordination environment, and chemical state of arsenopyrite dictate the propensity of the mineral to undergo oxidation, leaching, and flotation separation. Because of this, it is of great significance to study the mechanism by which mechanical ball milling affects the composition and coordination of the surface atoms. In this study, the arsenopyrite powder was ground using ball milling under argon. Then, the composition and oxidation state of the Fe, As, and S atoms on the arsenopyrite surface were characterized by XPS after different ball milling durations. A surface reconstruction model was constructed using density functional theory (DFT) calculations by adsorption of single atoms and multiple atoms onto the (001) surface of arsenopyrite, and the atomic configuration, binding energy, and formation energy of the reconstructed surface were calculated. The results showed that the relative content of Fe atoms raised from 30.3 % to 36.3 % as the duration of ball milling increased from 0 to 2 h, while the relative content of S atoms reduced from 33.33 % to 28.47 % under the same conditions. Furthermore, as the duration of ball milling was extended, there was an enhancement in the oxidation state of the atoms on the surface. In particular, S atoms under prolonged ball milling were converted to S0 (S monomer polymer). The binding energy between S atoms and the ideal surface was significantly greater than the energies between Fe and As atoms and the surface. Furthermore, the binding energy between the reconstruction layer and the ideal surface was positively correlated with the ratio of Fe atoms, with the 1Fe + 3As + 2S structure having the lowest binding energy and the 3Fe + 1As + 2S and 3Fe + 2As + 1S structures having the highest binding energies. When the surface was rich in S atoms, the formation energy of the reconstructed surface was the most negative, indicating the highest surface stability.

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阐明球磨对砷黄铁矿表面重构的作用机理:XPS 特性与理论研究
黄铜砷矿的表面组成、配位环境和化学状态决定了该矿物的氧化、浸出和浮选分离倾向。因此,研究机械球磨对表面原子组成和配位的影响机制具有重要意义。本研究在氩气环境下使用球磨法研磨砷黄铁矿粉末。然后,用 XPS 表征了不同球磨持续时间后砷黄铁矿表面铁、砷和 S 原子的组成和氧化态。利用密度泛函理论(DFT)计算,通过单原子和多原子在黄铜砷矿(001)表面的吸附,构建了表面重构模型,并计算了重构表面的原子构型、结合能和形成能。结果表明,随着球磨时间从 0 小时增加到 2 小时,Fe 原子的相对含量从 30.3% 增加到 36.3%,而在相同条件下,S 原子的相对含量从 33.33% 降低到 28.47%。此外,随着球磨时间的延长,表面原子的氧化态也有所增强。特别是,S 原子在长时间的球磨过程中转化为 S0(S 单体聚合物)。S 原子与理想表面之间的结合能明显高于铁原子和砷原子与表面之间的结合能。此外,重构层与理想表面之间的结合能与铁原子的比例呈正相关,其中 1Fe + 3As + 2S 结构的结合能最低,而 3Fe + 1As + 2S 和 3Fe + 2As + 1S 结构的结合能最高。当表面富含 S 原子时,重构表面的形成能最负,表明表面稳定性最高。
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来源期刊
Minerals Engineering
Minerals Engineering 工程技术-工程:化工
CiteScore
8.70
自引率
18.80%
发文量
519
审稿时长
81 days
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.
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