Study of the adsorption of Nickel ions on local natural clays in hydrometallurgical effluents

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Abstract

This research focuses on the treatment of hydrometallurgical effluents, specifically studying the adsorption of metallic ions such as Nickel, Copper, Cobalt, Mercury, and lead on natural clays from the Democratic Republic of Congo (DRC). Twelve clay samples, six activated with a strong acid and six non-activated, were characterized using various techniques including X-Ray Diffraction, Fourier Transform Infrared Spectroscopy, X-Ray Fluorescence, Transmission Electron Microscopy, and chemical dosage. The characterization revealed that the clays are mixed with several clayey minerals, enriched in aluminum silicate; contain absorption and water retention sites, and exhibit heterogeneities at the interfaces between grains and exchangeable ions. Activating the clays increased their cation exchange capacities, removed impurities, and increased pore size and specific area. Two aqueous solutions were used in the experiments: a laboratory-prepared nickel sulfate solution and a hydrometallurgical aqueous solution from a factory, both initially containing 15 mgL-1 of Ni2+ ions. Results showed that the adsorption of Ni2+ ions increased with the quantity of clay in the solution. The activated clays adsorbed more ions than non-activated clays at the same Ni2+ ion concentration. Additionally, adsorption was weaker in the hydrometallurgical solution compared to the nickel sulfate solution, suggesting competition from other metallic ions. The optimal adsorption occurred with chemically activated clays containing high Na+, Fe2+, and Al3+ ion content and low K+ ion content. The Hill-Langmuir model was used to describe the adsorption results, revealing that minimal quantities of activated clay were needed to adsorb a large quantity of Ni2+ ions in the solution, whereas large quantities of non-activated clays were insufficient. In conclusion, the research demonstrates the potential of natural clays from the DRC to adsorb metallic ions from hydrometallurgical effluents, providing insights for effective treatment methods in the future. The model revealed that the clay samples A2a clay, A6a and A3na have the very elevated reactional sites concentrations.
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水冶废水中当地天然粘土对镍离子的吸附研究
本研究侧重于湿法冶金废水的处理,特别是研究刚果民主共和国(DRC)天然粘土对镍、铜、钴、汞和铅等金属离子的吸附。利用各种技术,包括 X 射线衍射、傅立叶变换红外光谱、X 射线荧光、透射电子显微镜和化学剂量,对 12 种粘土样品(6 种用强酸活化,6 种未活化)进行了表征。表征结果表明,粘土中混有多种粘土矿物,富含硅酸铝;含有吸水和保水位点,并在晶粒和可交换离子的界面处表现出异质性。活化粘土可提高其阳离子交换能力,去除杂质,增大孔径和比面积。实验中使用了两种水溶液:一种是实验室制备的硫酸镍溶液,另一种是来自工厂的湿法冶金水溶液,两者最初都含有 15 mgL-1 的 Ni2+ 离子。结果表明,Ni2+ 离子的吸附量随溶液中粘土数量的增加而增加。在 Ni2+ 离子浓度相同的情况下,活化粘土比非活化粘土吸附更多的离子。此外,与硫酸镍溶液相比,湿法冶金溶液中的吸附力较弱,这表明存在其他金属离子的竞争。Na+、Fe2+ 和 Al3+ 离子含量高、K+ 离子含量低的化学活化粘土的吸附效果最佳。希尔-朗穆尔模型用于描述吸附结果,结果表明,要吸附溶液中大量的 Ni2+ 离子,只需要极少量的活化粘土,而大量的非活化粘土是不够的。总之,这项研究表明刚果民主共和国的天然粘土具有吸附湿法冶金废水中金属离子的潜力,为今后采用有效的处理方法提供了启示。模型显示,粘土样本 A2a 粘土、A6a 和 A3na 的反应位点浓度非常高。
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