汞和相关挥发性金属在岩浆温度下的挥发性

IF 3.6 2区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS
Julien Boulliung , Bernard J. Wood , Tamsin A. Mather
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引用次数: 0

摘要

火成岩系统中金属的挥发性是岩浆脱气、矿石沉积以及地球和其他行星的挥发性预算的重要制约因素。为了对这种挥发性有系统的了解,我们对高温下熔融玄武岩中Hg的挥发性进行了首次实验测量,并将其与其他挥发性微量元素(即Ag、As、Cd、Cr、Cs、Cu、Ga、Ge、In、Li、Pb、Rb、Sb、Sn、Tl和Zn)进行了直接比较。我们把100 毫克的碎玄武岩,包含93 ppm的Hg和 ~ 500 ppm的大多数其他挥发性金属铝坩埚被密封在真空的石英玻璃管体积 ~ 4.4 × 10−6 m3。在高温(1250、1300或1400 °C)下保持5 min至24 h后,样品在空气中淬火。使用直接汞分析仪对淬火玻璃进行分析表明,在最初的几分钟内,几乎所有的汞(>99 %)都丢失了,汞的总压力为150 Pa(根据系统中已知的汞质量和安瓿体积计算)。在1400 °C和1300 °C下,分别在1和6 h后获得~40 ppb Hg和 ~ 100 ppb Hg的表观稳态浓度。XANES测定了产物中Fe的氧化态,结果表明实验过程中Fe3+/(Fe3++Fe2+)保持在~0.1的恒定值。用电子探针和激光烧蚀ICP-MS测定了玻璃中除汞外元素的行为。在我们的实验中我们发现,每个元素的一部分失去了大气层减少按照以下顺序:Hg> 祝辞 Tl 祝辞 Cd 祝辞 In>锌* 祝辞 李 祝辞 Cs 祝辞 铜* 祝辞 As> Ag 祝辞 Pb ~ Sn ~ Ga 祝辞 Ge ~ 某人(带星号的元素的位置不确定性和最大可能的波动采用)。这些结果显示出与熔岩中气体/气溶胶浓度的野外测量所估计的挥发性有广泛的相似之处,但也有重要的差异。它们还显示出与开放系统实验获得的挥发物和从原行星气体盘相对减少的环境中元素的冷凝温度估计的挥发物的重要差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Volatility of mercury and related volatile metals at magmatic temperatures
The volatilities of metals in igneous systems are important constraints in the contexts of magmatic degassing, ore deposition and the volatile budgets of the Earth and other planets. In order to develop a systematic understanding of such volatilities, we have made the first experimental measurements of the volatility of Hg from molten basalt at high temperatures and compared it directly with other volatile trace elements (i.e., Ag, As, Cd, Cr, Cs, Cu, Ga, Ge, In, Li, Pb, Rb, Sb, Sn, Tl and Zn). We placed 100 mg of crushed basalt, containing 93 ppm of Hg and ∼ 500 ppm of most of the other volatile metals in an alumina crucible which was sealed under vacuum inside a silica glass tube of volume ∼ 4.4 × 10−6 m3. After holding them at high temperature (1250, 1300 or 1400 °C) between 5 min and 24 h, samples were quenched in air. Analysis of the quenched glasses using a Direct Mercury Analyser shows that almost all Hg (>99 %) is lost within the first few minutes, establishing a total pressure of Hg species of 150 Pa (calculated from the known mass of Hg in the system and the ampoule volume). Apparent steady-state concentrations of ∼40 ppb Hg at 1400 °C and ∼ 100 ppb Hg at 1300 °C are achieved after 1 and 6 h respectively. The oxidation state of Fe in the products, measured by XANES, indicates that Fe3+/(Fe3++Fe2+) remains constant at ∼0.1 during the experiments. The behavior of elements other than Hg in the glasses were determined by Electron Microprobe and Laser Ablation ICP-MS. In our experiments we find that the fraction of each element lost to the atmosphere decreases in the following order: Hg>>Tl>Cd>In>Zn*>Li>Cs>Cu*>As>Ag>Pb∼Sn∼Ga>Ge∼Sb (with the position of asterisked elements uncertain and maximum possible volatilities adopted). These results show broad similarities to, but also important differences from volatilities estimated from field measurements of gas/aerosol compared to concentrations in lava. They also show important differences from volatilities obtained from open-system experiments and those estimated from the condensation temperatures of elements in the relatively reduced environment of a protoplanetary gas disc.
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来源期刊
Chemical Geology
Chemical Geology 地学-地球化学与地球物理
CiteScore
7.20
自引率
10.30%
发文量
374
审稿时长
3.6 months
期刊介绍: Chemical Geology is an international journal that publishes original research papers on isotopic and elemental geochemistry, geochronology and cosmochemistry. The Journal focuses on chemical processes in igneous, metamorphic, and sedimentary petrology, low- and high-temperature aqueous solutions, biogeochemistry, the environment and cosmochemistry. Papers that are field, experimentally, or computationally based are appropriate if they are of broad international interest. The Journal generally does not publish papers that are primarily of regional or local interest, or which are primarily focused on remediation and applied geochemistry. The Journal also welcomes innovative papers dealing with significant analytical advances that are of wide interest in the community and extend significantly beyond the scope of what would be included in the methods section of a standard research paper.
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