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Experimental study on the speciation and solubility of sulfur, and the behavior of highly siderophile elements in sulfide- and sulfate-saturated basaltic melts and 1300°C and 1 GPa.

机译:硫的形态和溶解度以及在1300°C和1 GPa的硫化物和硫酸盐饱和的玄武质熔体中高铁亲元素的行为的实验研究。

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摘要

The speciation and solubility of sulfur, and the solubilities of Pd, Ir, Pt, and Au were investigated in sulfide- and sulfate-saturated basaltic melts between 1300 to 1355°C and 1.0 to 1.2 GPa. Sulfur solubilities (as wt. % S) of 0.14 ± 0.02 wt.% and of 1.5 ± 0.2 wt.% were determined for sulfide-saturated and sulfate-saturated experiments, respectively.; Sulfur speciation in the melt changed from S2−-dominated (X(S6+) = molar S6+/[S6+ + S 2−]) = 0.03 ± 0.04) in sulfide-saturated experiments to S6+-dominated (X(S6+) = 0.81 ± 0.06) in sulfate-saturated experiments. This change in speciation was combined with previous data on sulfur speciation in basalts to derive an expression for the change in sulfur speciation as a function of oxygen fugacity.; Models for the change in sulfur solubility as a function of oxygen fugacity were derived. These models predict a decrease in the degree of partial melting required to produce sulfur-undersaturated melts with increasing oxygen fugacity in supra-subduction zone settings. Thus, if the source region is oxidized, the magmas generated can be both sulfur-rich and sulfur-undersaturated at relatively low degrees of partial melting.; Concentrations of [Pd]melt = 11.9 ± 1.2 ppm and [Au] melt = 4.7 ± 0.9 ppm in glasses from sulfate-saturated experiments were much higher than in sulfide-saturated experiments ([Pd]melt = 0.63 ± 0.31 ppm; [Au]melt = 0.52 ± 0.08 ppm). In contrast, platinum concentrations were not affected by oxidation state and were similar in oxidized ([Pt]melt = 1.6 ± 0.3 ppm) and reduced experiments ([Pt]melt = 1.23 ± 0.46 ppm). Iridium concentrations decreased with increasing oxidation state (from [Ir]melt = 0.24 ± 0.08 ppm in sulfide-saturated experiments to [Ir] melt = 0.07 ± 0.02 ppm in sulfate-saturated experiments).; The results of this work support the hypothesis that oxidation of mantle sulfides in suprasubduction zone settings favors Au-enrichment in the generated magmas, which translates to potentially higher Au-content in associated porphyry and epithermal deposits. Reduction of a relatively oxidized magma by assimilation of carbon-bearing country rocks can trigger sulfide saturation and produce orthomagmatic ore deposits.; Because the solubility of sulfur in oxidized melts decreases significantly with decompression, oxidized, water- and sulfur-rich basaltic magmas are likely to exsolve water- and sulfur-rich volatile phases upon ascent. Therefore, the results are consistent with the contribution of a volatile phase exsolved from basaltic magmas at depth to explain the high-sulfur degassing in some arc-related volcanoes.
机译:在1300至1355°C和1.0至1.2 GPa的硫化物和硫酸盐饱和的玄武质熔体中研究了硫的形态和溶解度以及Pd,Ir,Pt和Au的溶解度。对于硫化物饱和和硫酸盐饱和的实验,分别确定了0.14±0.02重量%和1.5±0.2重量%的硫溶解度(以重量%S计)。熔体中的硫形态从S 2-为主(X(S 6 + )=摩尔S 6 + / [S 6 + + S 2 − ])= 0.03±0.04)在硫化物饱和的实验中,以S 6 + 为主(X(S 在硫酸盐饱和的实验中,6 + )= 0.81±0.06)。这种形态变化与先前关于玄武岩中硫形态变化的数据结合,得出了硫形态变化与氧气逸度的关系表达式。得出了硫溶解度随氧逸度变化的模型。这些模型预测,在超俯冲带环境中,随着氧气逸度的增加,产生硫不饱和熔体所需的部分熔融程度会降低。因此,如果源区被氧化,则产生的岩浆可以在相对较低的部分熔融度下富含硫和不饱和硫。硫酸盐饱和实验的玻璃中[Pd] melt 的浓度为11.9±1.2 ppm,[Au] 熔融 = 4.7±0.9 ppm的浓度比硫化物饱和的玻璃高得多实验([Pd] <熔体 = 0.63±0.31 ppm; [Au] <熔体 = 0.52±0.08 ppm)。相反,铂浓度不受氧化态的影响,并且在氧化([Pt] melt = 1.6±0.3 ppm)和还原实验([Pt] melt = 1.23±0.46 ppm)。铱浓度随着氧化态的增加而降低(从硫化物饱和实验中的[Ir] melt = 0.24±0.08 ppm到硫酸盐溶液中的[Ir] 熔体 = 0.07±0.02 ppm饱和实验)。这项工作的结果支持这样的假说,即在超俯冲带环境中,地幔硫化物的氧化有利于生成的岩浆中金的富集,这转化为相关斑岩和超热矿床中潜在的更高的金含量。通过含碳乡村岩石的同化而还原相对氧化的岩浆会触发硫化物饱和并产生正岩浆矿床。由于减压后硫在氧化熔体中的溶解度显着降低,因此氧化的富含水和硫的玄武岩浆在上升时很可能会溶解富含水和硫的挥发性相。因此,结果与从玄武岩浆深度溶出的挥发性相的贡献相一致,以解释某些与弧有关的火山中的高硫脱气。

著录项

  • 作者

    Jugo, Pedro J.;

  • 作者单位

    University of Alberta (Canada).;

  • 授予单位 University of Alberta (Canada).;
  • 学科 Geochemistry.; Geology.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 p.123
  • 总页数 190
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 地质学;
  • 关键词

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