印度尼西亚东南苏拉威西 Wolo 矿区褐铁矿石的常压盐酸和硝酸浸出过程

Sufriadin, Malyanus Yepta, I. Nur, Purwanto, Rizky Amalia, U. R. Irfan, Djabal Nur Basir, Tsubasa Otake
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摘要

我们使用盐酸(HCl)和硝酸(HNO3)对印度尼西亚东南苏拉威西省沃洛矿区的褐铁矿样本进行了常压酸浸出研究。这些研究的目的是比较金属(镍、钴、铁和铝)的浸出程度,并分析矿物在不同酸浓度下的溶解行为。使用光学显微镜、扫描电子显微镜(SEM)和 X 射线衍射法对矿石样本进行了矿物学表征,并分别使用 X 射线荧光光谱法(XRF)和原子吸收光谱法(AAS)测定了化学成分。在酸浓度、浸出时间为 90 分钟、浸出温度为 100℃的条件下,进行了常压浸出试验。褐铁矿矿石样品中含有鹅卵石、吉比石、滑石、石英和蜥蜴石。结果表明,使用 3 M HCl 可以浸出高达 92.22% 的镍和 90.14% 的铁,而使用 3 M HNO3 只能从褐铁矿中提取 63.14% 的镍和 38.74% 的铁。在盐酸中铁的浸出率较高,说明镍的选择性较低,可能会污染孕浸溶液(PLS),导致提纯过程更加复杂。浸出实验的结果表明,与在 HNO3 中相比,在 HCl 中更容易溶解高铁锰矿。
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Atmospheric hydrochloric and nitric acid leaching of a limonite ore from the Wolo mine area, Southeast Sulawesi, Indonesia
The atmospheric acid leaching studies of a limonite ore sample from the Wolo mine area, Southeast Sulawesi, Indonesia, have been performed using hydrochloric acid (HCl) and nitric acid (HNO3). The objectives of these studies were to compare the leaching degree of metals (Ni, Co, Fe, and Al) and to analyze the dissolution behavior of minerals under different acid concentrations. Mineralogical characterization of the ore sample was conducted using optical microscopy, scanning electron microscopy (SEM), and X-ray diffraction, whereas chemical composition was determined by X-ray fluorescence (XRF) spectrometry and atomic absorption spectroscopy (AAS), respectively. An atmospheric leaching test was done with the variables of acid concentration, leaching duration of 90 min, and leaching temperature of 100℃. Limonite ore samples contain goethite, gibbsite, talc, quartz, and lizardite. It was revealed that as much as 92.22% of Ni and 90.14% of Fe could be leached using 3 M HCl, whereas only 63.14% of Ni and 38.74% of Fe could be extracted from limonite ore using 3 M HNO3. The higher leaching degree of Fe in HCl indicates low selectivity with Ni, which might contaminate pregnant leach solution (PLS), leading to further complications in the purification process. Results of the leaching experiment show that goethite was more easily dissolved in HCl than in HNO3.
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