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Aqueous geochemistry at subduction zone conditions: Experimental constraints.

机译:俯冲带条件下的含水地球化学:实验约束。

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摘要

Despite the importance of fluids in high pressure environments, the behavior of most solutes in H2O-rich solutions at the relevant pressures and temperatures has not been measured. The revised Helgeson-Kirkham-Flowers equations of state (HKF-EOS) depends on empirical solute data and is the method the most widely used for calculating the thermodynamic properties of aqueous species at elevated pressures and temperatures. There are, however, empirical data on only a few species over the entire interval over which the HKF model may be used; it is necessary to support this predictive approach through experiments. This dissertation provides experimental data on the solubility of major rock forming elements at 0.5–2.0 GPa, 350–500°C and on the dissociation of H2Saq and HCl at elevated pressures and temperatures.; This study's diaspore solubility measurements greatly increase the range of conditions where the solubility of aluminum has been measured. In this system, the neutral aluminum species, Al(OH)30 predominates and an expression: GJ AlOH 03=-98 2552-24799.4PGPa+ -285+76PGPa TK was derived to allow calculation of aluminum solubility in near-neutral solutions over a range of pressures and temperatures and demonstrate that aluminum is fairly mobile in near-neutral solutions.; Albite-paragonite-quartz solubility experiments probe the mobility of silica, sodium and aluminum in these high pressure environments. The measured solubilities were high and increase with both pressure and temperature. These results corroborate the strong increase in solubility with high pressures expected from lower pressure experiments.; As natural solutions are seldom pure H2O, the dissociation of H2Saq at 0.5 GPa, 350°C and of HClaq at 1.0 GPa, 470°C and 1.2 GPa, 450°C were measured. The dissociation constant of H2Saq was found to be much lower than predicted, indicating that HS dominates under more basic conditions than previously believed. The dissociation of HCl was determined to be about ten times lower than some predictions, agreeing with the lowest predicted values.; The results from these experiments demonstrate that mineral solubilities are comparatively high at elevated pressures. These experiments also demonstrate that the dissociation of the acids HClaq and H 2Saq are considerably more associated than predicted and will therefore play a less significant role in mass transport at high pressures than has been believed.
机译:尽管在高压环境中流体很重要,但尚未测量到大多数H2 O O溶液在相关压力和温度下的大多数溶质的行为。修改后的Helgeson-Kirkham-Flowers状态方程(HKF-EOS)取决于经验溶质数据,是最广泛用于计算高温和高压下水族物质热力学性质的方法。但是,在可以使用HKF模型的整个时间间隔内,只有少数物种的经验数据。有必要通过实验来支持这种预测方法。本论文提供了主要岩石形成元素在0.5–2.0 GPa,350–500°C下的溶解度以及H 2 S aq 和HCl在60℃下的解离的实验数据。压力和温度升高。这项研究的渗铝溶解度测量极大地增加了测量铝溶解度的条件范围。在此系统中,中性铝物种Al(OH) 3 0 占主导地位,其表达式为: <?Eqn TeX style =“ script”> G J Al OH 0 3 =-98 2552-24799.4 P GPa + -285 + 76P GPa T K < / fen> <?Eqn TeX endstyle =“ script”> 可以在一定压力和一定压力下计算铝在近中性溶液中的溶解度并证明铝在接近中性的溶液中具有很好的流动性。阿尔比特石蜡石-石英的溶解度实验探讨了在这些高压环境中二氧化硅,钠和铝的迁移率。测得的溶解度很高,并且随着压力和温度的升高而增加。这些结果证实了低压实验所预期的高压下溶解度的强烈增加。由于天然溶液很少是纯H 2 O,因此H 2 S aq 在0.5 GPa,350°C时会解离,而HCl 在1.0 GPa,470°C和1.2 GPa,450°C下测量> aq 。发现H 2 S aq 的解离常数比预期的低得多,这表明HS -在比以前认为的更基本的条件下占主导地位。 。 HCl的解离被确定为比一些预测低约十倍,与最低预测值相符。这些实验的结果表明,在较高的压力下,矿物的溶解度较高。这些实验还表明,酸HCl aq 和H 2 S aq 的解离作用远比预期的多,因此发挥的作用较小。高压在大众运输中起着重要作用。

著录项

  • 作者

    Lin, Heather Ann.;

  • 作者单位

    University of California, Los Angeles.;

  • 授予单位 University of California, Los Angeles.;
  • 学科 Geochemistry.; Geology.
  • 学位 Ph.D.
  • 年度 2001
  • 页码 247 p.
  • 总页数 247
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 地质学;地质学;
  • 关键词

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