碳酸钙含量为20%和25%的常压红土矿浸出液除铁工艺产物的表征

Muhammad Nibras Azza Adhikara, R. M. Ulum, A. F. Madsuha, F. Abidin
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摘要

摘要电动汽车通过提供更加环保和可持续的能源,成为解决气候变化和全球变暖问题的替代方案。随着对可持续汽车需求的增加,电池的功能变得至关重要。电池内部的一个重要方面是镍。镍在锂离子电池中发挥着重要作用,它能提供更大的能量密度和更高的存储容量,这意味着它能提高电池的效率。然而,优化镍提取的尝试仍然是一个挑战。为此,采用湿法研究了红土矿高效提镍工艺,即常压条件下混合氢氧化物(MHP)脱铁工艺。以pH为(1、2、3)的碳酸钙(CaCO3)试剂溶液(20% w/w和25% w/w)为添加剂。采用x射线衍射(XRD)和扫描电子显微镜-能量色散x射线(SEM-EDS)对PLS析出物进行了表征,并用电感耦合等离子体发射光谱(ICP-OES)对滤液进行了表征。基于析出物的分析表明,酸中和过程发生时,析出物中铁含量充足,镍含量最少。此外,所有沉淀物的pH值和浓度定性地说明了涉及钙和硫的相同中和过程。从本研究中通过ICP测试的滤液结果来看,与pH 2和3相比,pH 1在20%和25%浓度下提供了最低的回收率以及最小的ppm;因此,铁沉淀形成硫化铁和/或硫酸铁。综上所述,最佳参数为碳酸钙浓度为25%,pH为1,90oC,搅拌2小时,以减少溶液中铁的含量。
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Characterization of Iron Removal Process Products from Atmospheric Lateritic Ore Leaching Solution by using 20 and 25% of Calcium Carbonate
AbstractElectric vehicles become the alternative to solve the climate change and global warming problems by providing a more eco-friendly and sustainable source of energy. As the demand for sustainable vehicles increased, the functionality of batteries become crucial. One of the important aspects inside the batteries is nickel. Nickel plays a big role in lithium-ion batteries by delivering greater amounts of energy density with a higher storage capacity, which means it provides bigger efficiency to the batteries. Yet, the attempt of optimizing nickel extraction remains a challenge. Therfore, nickel extraction process of lateritic ore with high efficiency is investigated by using hydrometellurgy process, specifically the iron removal process in atmospheric condition in mixed hydroxide precipitates (MHP) route.The reagent solution of (20% w/w and 25%  w/w) calcium carbonate (CaCO3) at pH (1, 2, 3) were utilized as additive in this process. The precipitates resulted from PLS were characterized by x-ray diffraction (XRD) and Scanning Electron Microscopy - Energy Dispersive X-Ray (SEM–EDS), while the filtrates were investigated by Inductively Coupled Plasma-Optical Emission Spectrometry (ICP-OES). Analysis based on precipitates demonstrates that the acid neutralization process took place with a sufficient amount of iron in the precipitates with the least amount of nickel. In addition, all pH and concentration of precipitates qualitatively illustrate the same neutralization process involving calcium and sulfur. From the results of filtrate through ICP testing in this study, pH 1 for both 20% and 25% concentration provides the lowest recovery rate alongside the smallest ppm compare to pH 2 and 3; thus, the iron precipitates in the formation of iron sulfide and/or iron sulfate. Overall, the optimum parameter is 25% of calcium carbonate, pH 1, 90oC for 2 hours of agitation to reduce the amount of iron in the solution.
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