首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Solubility of gold in oxidized, sulfur-bearing fluids at 500-850 degrees C and 200-230 MPa: A synthetic fluid inclusion study
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Solubility of gold in oxidized, sulfur-bearing fluids at 500-850 degrees C and 200-230 MPa: A synthetic fluid inclusion study

机译:金在500-850℃和200-230MPa的氧化,含硫流体中的溶解度:合成液体包裹性研究

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Although Au solubility in magmatic-hydrothermal fluids has been investigated by numerous previous studies, there is a dearth of data on oxidized (log fO(2) FMQ+2.5 - FMQ fayalite-magnetite-quartz buffer), sulfur-bearing fluids such as those that formed porphyry Cu-Au (-Mo) deposits. We performed experiments to constrain the effects of fluid salinity, HCl content, sulfur content, fO(2) and temperature on Au solubility in such oxidized, sulfur-bearing fluids. For this purpose, small aliquots of fluids equilibrated with Au metal were trapped at high pressure and temperature in the form of synthetic fluid inclusions in quartz and were subsequently analyzed by LA-ICP-MS. Additionally, Raman spectra were collected from quartz-hosted fluid inclusions at up to 600 degrees C to help to identify the nature of dissolved gold and sulfur species. Gold solubility was found to be affected most strongly by the HCl content of the fluid, followed by fO(2), fluid salinity and temperature. Compared to these factors the sulfur content of the fluid has relatively little influence. At 600 degrees C and 100 MPa, fluids with geologically realistic HCl contents (similar to 1.1 wt%) and salinities (7-50 wt% NaClequiv) dissolve similar to 1000-3000 ppm Au at oxygen fugacities controlled by the magnetite-hematite buffer. At even more oxidized conditions (three log units above the hematite-magnetite fO(2) buffer), HCl-, NaCl- and H2SO4-rich fluids can dissolve up to 5 wt% Au at 800 degrees C and 200 MPa. The observed Au solubility trends are controlled by HCl0 species in the Na-H-Cl-SO4 fluid and are quantitatively reproduced by existing thermodynamic data for Au-Cl complexes. In all experiments, AuCl0 and AuCl2- species are predicted to occur in comparable although variable concentrations, and account for more than 95% of Au solutes. Natural, high-temperature (500 degrees C) brine inclusions from porphyry Cu-Au (-Mo) deposits contain significantly less Au than gold-saturated brines tha
机译:尽管通过许多先前的研究已经研究了岩浆 - 水热流体中的溶解度,但氧化的数据很少(Log Fo(2)& FMQ + 2.5 - FMQ fayalite-mariage-Stumets),含硫流体作为形成斑岩Cu-Au(-mo)沉积物的那些。我们进行了实验,以限制流体盐度,HCl含量,硫含量,氟(2)和温度对如此氧化的硫的液体中的溶解度的影响。为此目的,用Au金属平衡的小等分试样在石英中以高压和高压的温度捕获,并且随后通过La-ICP-MS进行分析。另外,从石英托管的流体夹杂物收集拉曼光谱,高达600℃,以帮助识别溶解的金和硫种类的性质。发现金溶解度受到流体的HCl含量最强烈的影响,然后是FO(2),流体盐度和温度。与这些因素相比,流体的硫含量具有相对较小的影响。在600摄氏度和100MPa的情况下,具有地质逼真的HCl含量的流体(类似于1.1wt%)和盐度(7-50wt%的浊度)溶解于由磁铁矿 - 赤铁矿缓冲液控制的氧气逃逸的1000-3000ppm Au。在更具氧化条件下(赤铁矿 - 磁铁矿上方的三个对数单元(2)缓冲液),HCl-,NaCl-和H 2 SO 4的流体可以在800℃和200MPa下溶解高达5wt%的Au。观察到的Au溶解度趋势由Na-H-C1-SO4流体中的HCl0物种控制,并通过现有的Au-Cl复合物定量再现。在所有实验中,预测AuCl0和AuCl 2-含量在可比性浓度虽然可变浓度,并且占95%以上的Au溶质。自然,高温(& 500℃)斑卟啉Cu-au(-mo)沉积物的盐水夹杂物含有比金饱和盐水的含量显着更少

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