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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Apatite solubility in carbonatitic liquids and trace element partitioning between apatite and carbonatite at high pressure
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Apatite solubility in carbonatitic liquids and trace element partitioning between apatite and carbonatite at high pressure

机译:磷灰石在碳酸盐液体中的溶解度和高压下磷灰石与碳酸盐之间的微量元素分配

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摘要

We have measured apatite solubility in calcic carbonatitic liquids and determined apatite/melt partition coefficients for a series of trace elements, including the rare earth elements (REE), high field strength elements (HFSE), Rb, Sr, U-Th-Pb. Experiments were performed between 4 and 6. GPa, from 1200 to 1380 °C, using the multianvil apparatus. Trace element concentrations were determined by laser ablation ICP-MS and electron microprobe. In addition, a specific protocol was designed to measure carbon concentration in the apatites, using the electron microprobe. Two starting apatite samples were used in order to test for the effect of apatite chemistry on partitioning behavior.Apatite solubility is lower in calcitic melts by a factor 3-5 compared to dolomitic melts (3-5.5 vs. 10-18wt.% P_2O_5 in melt). We interpret this difference in terms of solubility product in the liquid and propose an empirical model for apatite saturation that takes into account melt calcium content. We conclude that calcitic melts that may form by melting of carbonated eclogites could be saturated with residual apatite, contrary to dolomitic melts formed in carbonated peridotites.Compatibility behavior of the REE depends on apatite silica content: REE are compatible in apatites containing 3.5-5wt.% SiO_2, with DREEapatite/carbonatite values between 1.5 and 4, whereas REE are incompatible in apatites containing 0.2wt.% SiO_2. HFSE, U, Th, and Y are compatible in silica-rich apatite, with DThapatite/carbonatite≥5 while DYapatite/carbonatite≥2. Strontium is always retained in the melt, with DSrapatite/carbonatite of the order of 0.5. Lead appears to be incompatible in apatite, although this finding is weakened by almost complete Pb loss to sample container. High silica concentration favors REE incorporation in apatite by allowing for charged balanced coupled substitution. Sulfur and carbonate may also favor REE incorporation in apatite. Our results allow to reconcile previously published experimental determinations of REE partitioning. We use our experimentally determined partition coefficients to investigate the impact of residual apatite during partial melting of recycled carbonated material (eclogite+sediments) and discuss how the chemical characteristics of the produced liquids can be affected by residual apatite.
机译:我们已经测量了磷灰石在钙碳酸盐液体中的溶解度,并确定了一系列微量元素的磷灰石/熔体分配系数,包括稀土元素(REE),高场强元素(HFSE),Rb,Sr,U-Th-Pb。使用多砧装置在1200至1380°C的4至6 GPa之间进行了实验。痕量元素浓度通过激光烧蚀ICP-MS和电子探针测定。此外,还设计了一种特定的协议,使用电子探针测量磷灰石中的碳浓度。为了测试磷灰石化学对分配行为的影响,使用了两个初始磷灰石样品。与白云石熔体相比,钙钛矿熔体中磷灰石的溶解度要低3-5倍(3-5.5%vs.10-18wt。%P_2O_5熔化)。我们根据在液体中的溶解度产物来解释这种差异,并提出了考虑到熔融钙含量的磷灰石饱和度的经验模型。我们得出的结论是,与碳酸钙橄榄岩中形成的白云岩熔体相反,碳酸钙榴石熔融可能形成的钙熔体可能会被残留的磷灰石饱和.REE的相容性取决于磷灰石二氧化硅含量:REE与3.5-5wt%的磷灰石相容。 %的SiO_2,DREE磷灰石/碳酸盐的值在1.5和4之间,而REE在含有0.2wt。%SiO_2的磷灰石中不相容。 HFSE,U,Th和Y在富含二氧化硅的磷灰石中相容,DThapatite /碳酸盐≥5,而DYapatite /碳酸盐≥2。锶总是保留在熔体中,DSrapatite /碳酸盐大约为0.5。铅在磷灰石中似乎是不相容的,尽管由于几乎完全失去了样品容器中的铅而削弱了这一发现。高二氧化硅浓度通过允许带电平衡偶联取代而促进磷灰石中稀土元素的掺入。硫和碳酸盐也可能促进磷灰石中稀土元素的掺入。我们的结果可以调和以前发布的REE分区的实验确定。我们使用实验确定的分配系数来研究残余磷灰石在回收碳酸碳材料(榴辉岩+沉积物)的部分熔融过程中的影响,并讨论残余磷灰石如何影响采出液的化学特性。

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