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Experimental tests on achieving equilibrium in synthetic fluid inclusions: Results for scheelite, molybdenite, and gold solubility at 800 °C and 200 MPa

机译:在合成流体包裹体中达到平衡的实验测试:800°C和200 MPa下白钨矿,辉钼矿和金的溶解度结果

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摘要

Synthetic fluid inclusions formed in high P-T experiments, which are subsequently analyzed with LA-ICP-MS, enable us to collect thermodynamic data to constrain metal transport in aqueous fluids as well as partitioning of metals between coexisting phases. The most essential prerequisite for such studies is to ensure that equilibrium conditions between liquid and solid phases are reached prior to the formation of synthetic fluid inclusions in the host mineral. Various methods have been proposed by different authors to achieve this goal, but to this point our knowledge on the best approach to synthesize equilibrated fluid inclusions under constrained pressure, temperature, and compositional (P, T, and X) conditions remains poor. In addition, information on the time needed to reach equilibrium metal concentrations in the fluid as well as on the timing of the onset of fluid inclusion formation in the host mineral are scarce.The latter has been tested in a series of time-dependent experiments at 800 °C and 200 MPa using scheelite (CaWO4), molybdenite (MoS2) and metallic gold as dissolving phases and using different approaches to optimize the formation of equilibrated fluid inclusions. Both Embedded Image and Embedded Image were fixed during all experiments using the pyrite-pyrrhotite-magnetite buffer (PPM). As an intermediate in situ quenching of the sample charge plays an important role in the synthesis of fluid inclusions, we further tested the efficiency of such an intermediate quench for re-opening fluid inclusions formed at 600 °C and 200 MPa. Our results reveal that fluid inclusions start forming almost instantaneously and that equilibrium between fluid and solid phases occurs in the timescale of less than two hours for molybdenite and gold up to ca. 10 h for scheelite. The best approach to synthesize equilibrated fluid inclusions at 800 °C was obtained by using an intermediate quench on a previously unfractured quartz host. Experiments at 600 °C showed similar results and illustrate that this should be the method of choice down to this temperature. Below 600 °C pre-treatment of the quartz host (HF etching and/or thermal fracturing) becomes important to produce large enough fluid inclusions for the analyses via LA-ICP-MS and special care must be taken to prevent premature entrapment of the fluid.Fluids with 8 wt% NaCl in equilibrium with scheelite, molybdenite and gold at 800 °C and 200 MPa have concentrations of ca. 7300 ppm W, 1300 ppm Mo, and 300 ppm Au, respectively, which is in good agreement with results from other studies or extrapolation from lower temperatures. It can be concluded that the formation of synthetic fluid inclusions from an equilibrated fluid is possible, but different experimental designs are required, depending on the investigated temperature. In general, dissolution of solid phases seems to be much faster than previously assumed, so that experimental run durations can be designed considerably shorter, which is of great advantage when using fast-consuming mineral buffers.
机译:在高P-T实验中形成的合成流体夹杂物,随后用LA-ICP-MS进行分析,使我们能够收集热力学数据,以限制金属在水性流体中的传输以及金属在共存相之间的分配。进行此类研究的最基本前提是确保在主体矿物中形成合成流体包裹体之前,达到液相和固相之间的平衡条件。不同的作者已经提出了各种方法来实现该目标,但是到目前为止,我们在受限的压力,温度和成分(P,T和X)条件下合成平衡流体包裹体的最佳方法的知识仍然很少。此外,关于在流体中达到平衡金属浓度所需的时间以及主体矿物中形成流体夹杂物的时间的信息很少,后者在一系列与时间有关的实验中得到了验证使用白钨矿(CaWO4),辉钼矿(MoS2)和金属金作为溶解相,并使用不同方法优化平衡流体包裹体的形成,在800°C和200 MPa下进行。在所有实验过程中,均使用黄铁矿-硫铁矿-磁铁矿缓冲液(PPM)固定了嵌入式图像和嵌入式图像。由于样品装料的中间原位淬火在流体包裹体的合成中起着重要作用,因此我们进一步测试了这种中间淬火对于重新打开在600°C和200 MPa下形成的流体包裹体的效率。我们的结果表明,流体夹杂物几乎立即开始形成,并且液相和固相之间的平衡在不到两个小时的时间内就发生了辉钼矿和金矿,直至大约。白钨矿10小时。通过在先前未破裂的石英主体上使用中间淬火,可获得在800°C下合成平衡流体夹杂物的最佳方法。在600°C下进行的实验显示了相似的结果,并说明了在低至此温度的情况下应该选择的方法。在600°C以下,石英主体的预处理(HF蚀刻和/或热压裂)对于通过LA-ICP-MS进行分析产生足够大的流体夹杂物至关重要,必须特别注意防止流体过早夹带在800°C和200 MPa压力下,与白钨矿,辉钼矿和金保持平衡的8%NaCl流体的浓度约为。分别为7300 ppm W,1300 ppm Mo和300 ppm Au,这与其他研究的结果或较低温度的外推结果非常吻合。可以得出结论,由平衡的流体形成合成流体包裹体是可能的,但是根据所研究的温度,需要不同的实验设计。通常,固相的溶解似乎比以前设想的要快得多,因此可以将实验运行时间设计得更短,这在使用快速消耗的矿物缓冲剂时具有很大的优势。

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