THE ROLE OF SCANDIUM CHLORIDE AND HYDROXIDE COMPLEXES IN THE FORMATION OF SCANDIUM DEPOSITS: INSIGHTS FROM EXPERIMENTS AND MODELING

IF 5.5 1区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS Economic Geology Pub Date : 2023-10-09 DOI:10.5382/econgeo.5026
Jiaxin Wang, A. E. Williams-Jones, A. Timofeev, Xueni Zhang, Jiajun Liu, Shunda Yuan
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Abstract

Abstract Although scandium is commonly concentrated to economic levels by magmatic processes, hydrothermal fluids also play an important role in its concentration. Indeed, the most important source of scandium is currently the Bayan Obo deposit in China, where scandium is extracted from hydrothermally produced aegirine. To know how and why scandium is concentrated by hydrothermal fluids, it is necessary to understand the speciation of scandium in hydrothermal fluids. In a recently published study, we showed that scandium forms stable species with fluoride ions and proposed that such species may have been responsible for the hydrothermal transport of scandium in deposits like Bayan Obo. Chloride ions, which have been shown to form stable complexes with the other rare earth elements (REE), however, are much more abundant in most hydrothermal fluids than fluoride ions, as are hydroxide ions, particularly at high pH. We, therefore, conducted solubility experiments designed to investigate the stability of scandium chloride and hydroxide complexes in hydrothermal fluids. The experiments investigating the role of chloride species considered the solubility of Sc2O3(s) in the H2O-NaCl-HCl system at 100°, 150°, 300°, and 350°C and saturated water vapor pressure. These experiments showed that scandium concentration is independent of chloride concentration over the range of chlorinity investigated, i.e., up to 3.6 mol Cl– and that scandium, therefore, does not form stable complexes with chloride ions. To evaluate the role of hydroxide species in scandium transport and avoid the effect of chloride ions in the complexation, a second set of experiments was conducted that determined the solubility of Sc2O3(s) in H2O-NaClO4-HClO4 solutions at 100°, 150°, 200°, and 250°C, and saturated water vapor pressure. The results of these experiments showed that the solubility of Sc2O3(s) depends on pH and temperature. Based on the former dependence, two scandium hydroxide complexes, Sc(OH)2+ and Sc(OH)3°, were identified at low and higher pH, respectively. The formation constant (log β) determined for Sc(OH)2+ is 10.29 ± 0.07, 10.32 ± 0.07, 10.35 ± 0.19, and 10.91 ± 0.20 at 100°, 150°, 200°, and 250°C, respectively. That of Sc(OH)3° is 27.22 ± 0.68, 26.66 ± 1.35, 27.04 ± 0.13, and 28.02 ± 0.14 at the same temperatures, respectively. These results demonstrate that, unlike the case for the other rare earth elements, chloride plays a negligible role in transporting scandium in hydrothermal fluids. Instead, they show that scandium hydroxide complexes can be important in the transport of scandium and could have contributed significantly to the formation of deposits like those at Bayan Obo.
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氯化钪和氢氧化物配合物在钪矿床形成中的作用:来自实验和建模的见解
虽然钪通常是通过岩浆过程浓缩到经济水平,但热液流体在其浓缩过程中也起着重要作用。事实上,目前最重要的钪来源是中国的白云鄂博矿床,那里的钪是从水热生产的铝中提取的。要了解热液中钪的富集机理和原因,就必须了解热液中钪的形态。在最近发表的一项研究中,我们发现钪与氟离子形成稳定的物种,并提出这些物种可能是巴彦敖包等矿床中钪热液运输的原因。氯离子,已被证明与其他稀土元素(REE)形成稳定的配合物,然而,在大多数热液流体中比氟离子丰富得多,氢氧化物离子也是如此,特别是在高ph时。因此,我们进行了溶解度实验,旨在研究热液流体中氯化钪和氢氧化物配合物的稳定性。实验考察了Sc2O3在H2O-NaCl-HCl体系中在100°、150°、300°和350°C和饱和水蒸气压下的溶解度。这些实验表明,在所研究的氯度范围内,即高达3.6 mol Cl -,钪浓度与氯离子浓度无关,因此,钪不会与氯离子形成稳定的配合物。为了评估氢氧化物在钪输运中的作用,避免氯离子对络合的影响,我们进行了第二组实验,测定了Sc2O3在100°、150°、200°和250°C的H2O-NaClO4-HClO4溶液中的溶解度,以及饱和水蒸气压。实验结果表明,Sc2O3的溶解度与pH和温度有关。基于前一依赖性,在低pH和高pH条件下分别鉴定出了两种氢氧化钪配合物Sc(OH)2+和Sc(OH)3°。Sc(OH)2+在100°,150°,200°和250°C时的形成常数(log β)分别为10.29±0.07,10.32±0.07,10.35±0.19和10.91±0.20。在相同温度下,Sc(OH)3°的温度分别为27.22±0.68、26.66±1.35、27.04±0.13和28.02±0.14。这些结果表明,与其他稀土元素的情况不同,氯化物在热液流体中运输钪的作用可以忽略不计。相反,他们表明,氢氧化钪络合物在钪的运输中可能是重要的,并且可能对巴彦敖包等矿床的形成做出了重大贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Economic Geology
Economic Geology 地学-地球化学与地球物理
CiteScore
10.00
自引率
6.90%
发文量
120
审稿时长
6 months
期刊介绍: The journal, now published semi-quarterly, was first published in 1905 by the Economic Geology Publishing Company (PUBCO), a not-for-profit company established for the purpose of publishing a periodical devoted to economic geology. On the founding of SEG in 1920, a cooperative arrangement between PUBCO and SEG made the journal the official organ of the Society, and PUBCO agreed to carry the Society''s name on the front cover under the heading "Bulletin of the Society of Economic Geologists". PUBCO and SEG continued to operate as cooperating but separate entities until 2001, when the Board of Directors of PUBCO and the Council of SEG, by unanimous consent, approved a formal agreement of merger. The former activities of the PUBCO Board of Directors are now carried out by a Publications Board, a new self-governing unit within SEG.
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