埃里伯斯火山含水空纹岩中氯化物的分配和溶解度:对多组分脱气模型的贡献

GeoResJ Pub Date : 2014-09-01 DOI:10.1016/j.grj.2014.09.003
Marina Alletti , Alain Burgisser , Bruno Scaillet , Clive Oppenheimer
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引用次数: 15

摘要

我们提出了一系列关于氯在含水流体相和声母熔体之间分配的实验结果,然后我们用这些结果来模拟火山脱气的具体方面。实验在南极Erebus熔岩湖的一块phonolite上进行,温度为250 ~ 10 MPa,温度为1000℃,靠近QFM固体缓冲液。48个实验样品中只有1个样品在流体相中显示低密度蒸汽和高密度盐水共存,而35个样品在蒸汽场中明确存在。在考虑的P-T处的H2O-NaCl相图中的大不确定性使我们无法为剩余样品分配可靠的相行为。我们选择我们的数据集蒸汽为主的子集,以建立经验的HCl溶解度定律在低压和盐度有效。这一定律被纳入了脱气的热力学模型,我们用它来计算2010年在埃里伯斯进行的气体测量的平衡温度。静止湖活动特征为温度在1000 ~ 1050℃之间循环变化,这与浅层管道系统内的热对流一致。对代表性气体组成和温度的回溯显示了气体中SO2/HCl的摩尔比随压力的变化,这是一个经常在火山羽流中测量的量。模型输出表明,当压力从大气压变化到100兆帕时,这一比率可以变化多达一个数量级,这取决于脱气方式(气体和熔体的耦合或非耦合上升)。
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Chloride partitioning and solubility in hydrous phonolites from Erebus volcano: A contribution towards a multi-component degassing model

We present results from a series of experiments on the partitioning of chlorine between a hydrous fluid phase and a phonolitic melt that we then use to model specific aspects of volcanic degassing. Experiments were performed from 250 to 10 MPa on a phonolite from Erebus lava lake, Antarctica, at 1000 °C near the QFM solid buffer. Only one of 48 experimental samples shows coexistence of low-density vapour and high-density brine in the fluid phase while 35 samples are unambiguously in the vapour field. Large uncertainties in the H2O–NaCl phase diagram at the PT considered do not allow us to assign reliable phase behaviour to the remaining samples. We select a vapour-dominated subset of our dataset to establish an empirical HCl solubility law valid at low pressures and salinities. This law is incorporated into a thermodynamical model of degassing, which we use to compute equilibrium temperatures from gas measurements made at Erebus in 2010. The quiescent lake activity features cyclic temperature variations between 1000 and 1050 °C, which is consistent with thermal convection within the shallow plumbing system. Backward tracking of representative gas compositions and temperatures shows the evolution with pressure of the molar ratio of SO2/HCl in the gas, a quantity that is often measured in volcanic plumes. Model outputs suggest that this ratio can vary by up to an order of magnitude when the pressure changes from atmospheric to 100 MPa, depending on degassing style (coupled vs. decoupled ascent of gas and melt).

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