首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Rb and Sr partitioning between haplogranitic melts and aqueous solutions
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Rb and Sr partitioning between haplogranitic melts and aqueous solutions

机译:Rb和Sr在触变熔体和水溶液之间的分配

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Rubidium and strontium partitioning experiments between haplogranitic melts and aqueous fluids (water or 1.16–3.56 m (NaCl + KCl) ± HCl) were conducted at 750–950 C and 0.2–1.4 GPa to investigate the effects of melt and fluid composition, pressure, and temperature. In addition, we studied if the applied technique (rapid and slow quench, and in-situ determination of trace element concentration in the fluid) has a bearing on the obtained data. There is good agreement of the data from different techniques for chloridic solutions, whereas back reactions between fluid and melt upon cooling have a significant effect on results from the experiments with water. The Rb fluid–melt partition coefficient shows no recognizable dependence on melt composition and temperature. For chloridic solutions, it is 0.4, independent of pressure. In experiments with water, it is one to two orders of magnitude lower and increases with pressure. The strontium fluid–melt partition coefficient does not depend on temperature. It increases slightly with pressure in Cl free experiments. In chloridic fluids, there is a sharp increase in the Sr partition coefficient with the alumina saturation index (ASI) from 0.003 at an ASI of 0.8 to a maximum of 0.3 at an ASI of 1.05. At higher ASI, it decreases slightly to 0.2 at an ASI of 1.6. It is one to two orders of magnitude higher in chloridic fluids compared to those found in H2O experiments. The Rb/Sr ratio in non-chloridic solutions in equilibrium with metaluminous melts increases with pressure, whereas the Rb/Sr ratio in chloridic fluids is independent of pressure and decreases with fluid salinity. The obtained fluid–melt partition coefficients are in good agreement with data from natural cogenetic fluid and melt inclusions. Numerical modeling shows that although the Rb/Sr ratio in the residual melt is particularly sensitive to the degree of fractional crystallization, exsolution of a fluid phase, and associated fluid–melt partitioning is not a significant factor controlling Rb and Sr concentrations in the residual melt during crystallization of most granitoids.
机译:在750–950 C和0.2–1.4 GPa下进行石质熔体和水性流体(水或1.16–3.56 m(NaCl + KCl)±HCl)之间的和锶分配实验,以研究熔体和流体组成,压力,和温度。此外,我们研究了所应用的技术(快速和慢速淬火,以及流体中微量元素浓度的现场测定)是否对获得的数据有影响。对于氯化物溶液,来自不同技术的数据有很好的一致性,而冷却后流体和熔体之间的逆反应对水实验的结果有重大影响。 Rb的熔体分配系数对熔体组成和温度没有明显的依赖性。对于氯化物溶液,它是0.4,与压力无关。在水的实验中,它会降低一到两个数量级,并随压力而增加。锶流体-熔体分配系数不取决于温度。在无氯实验中,它随压力而略有增加。在含氯流体中,随着氧化铝饱和指数(ASI)从0.83的ASI的0.003到在1.05的ASI的最大值0.3,Sr分配系数急剧增加。在较高的ASI下,在ASI为1.6时,它会稍微降低到0.2。与在H2O实验中发现的相比,含氯流体的含量要高一到两个数量级。与金属熔体平衡的非氯化物溶液中的Rb / Sr比值随压力而增加,而氯化液中的Rb / Sr比值与压力无关,而随盐度的增加而降低。所得的熔体分配系数与天然共生流体和熔体包裹体的数据非常吻合。数值模型表明,尽管残余熔体中的Rb / Sr比对分步结晶度特别敏感,但液相的析出以及相关的熔体分配并不是控制残余熔体中Rb和Sr浓度的重要因素。在大多数类固醇的结晶过程中。

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