In situ study of the reaction phase A plus high-P clinoenstatite to forsterite plus water at reduced water activity

IF 1.8 3区 地球科学 Q2 MINERALOGY European Journal of Mineralogy Pub Date : 2023-12-22 DOI:10.5194/ejm-35-1149-2023
Christian Lathe, M. Koch‐Müller, Bernd Wunder, Oona Appelt, Melanie Sieber, S. Bhat, R. Farla
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Abstract

Abstract. We examined the reaction phase A plus high-P clinoenstatite to forsterite plus water (Reaction R1) by means of in situ X-ray diffraction measurements with the large volume press at the synchrotron PETRA III, Hamburg. Contrary to the study of Lathe et al. (2022), in which all experiments on Reaction (R1) were performed at a water activity of 1, the reversed experiments presented in this study were performed at reduced water activity with mole fractions of about XH2O= XCO2=0.5. The intention of this investigation was to test the observation made by Perrillat et al. (2005), which was that dehydration reactions are kinetically faster at reduced than under water-saturated conditions. The position of Reaction (R1) at the reduced conditions was determined by reversal brackets at 9.1 and 9.5 GPa (630 and 700 ∘C), at 9.7 and 10.0 GPa (725 and 700 ∘C), at 9.8 and 10.2 GPa (675 and 750 ∘C), and at 10.5 GPa (675 and 740 ∘C). Additionally, we performed two offline experiments with brackets at 10.0 and 10.6 GPa (750 and 700 ∘C, respectively) that are in agreement with the results of the in situ experiments. We do not observe any “intermediate” precursor phase in our experiments. The equilibrium of Reaction (R1) is shifted by about 100 ∘C to lower temperature compared to the results under water-saturated conditions. Thus, at a water activity (aH2O) below 1 the phase A plus clinoenstatite dehydration reaction can only occur in extremely cold subduction slabs. The kinetics of Reaction (R1) dehydration at reduced water activity is slower than that determined previously by Lathe et al. (2022) under water-saturated conditions. Thus, the above-mentioned hypothesis of Perrillat et al. (2005) could not be confirmed. However, in both of our studies on Reaction (R1), the newly formed dehydration product forsterite was of nanometer size, which supports earlier experimental observations, which is that product phases of dehydration reactions are generally very fine-grained and might promote the concept that intermediate-depth earthquakes in subduction zones are initiated by mechanical instabilities from extremely fine-grained materials formed during dehydration reactions.
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在水活度降低的条件下,将 A 相加高磷钙钛矿转化为绿泥石加水的反应相的原位研究
摘要。我们利用汉堡同步加速器 PETRA III 的大体积压机,通过原位 X 射线衍射测量,研究了 A 相加高 P 值clinoenstatite 到 forsterite 加水的反应(反应 R1)。Lathe 等人(2022 年)的研究中,反应 (R1) 的所有实验都是在水活度为 1 的条件下进行的,与此相反,本研究中的反向实验是在水活度降低、摩尔分数约为 XH2O= XCO2=0.5 的条件下进行的。这项研究的目的是检验 Perrillat 等人(2005 年)的观察结果,即在水活度降低的条件下,脱水反应的动力学速度要快于水饱和条件下的脱水反应。反应 (R1) 在还原条件下的位置是在 9.1 和 9.5 GPa(630 和 700 ∘C)、9.7 和 10.0 GPa(725 和 700 ∘C)、9.8 和 10.2 GPa(675 和 750 ∘C)以及 10.5 GPa(675 和 740 ∘C)下通过反转括号确定的。此外,我们还在 10.0 和 10.6 GPa(分别为 750 和 700 ∘C)条件下进行了两次支架离线实验,实验结果与原位实验结果一致。我们在实验中没有观察到任何 "中间 "前体相。与水饱和条件下的结果相比,反应 (R1) 的平衡温度降低了约 100 ∘C。因此,在水活度(aH2O)低于 1 的条件下,A 相加闪长岩的脱水反应只能发生在极冷的俯冲板块中。在水活度降低的条件下,反应(R1)的脱水动力学比 Lathe 等人(2022 年)之前在水饱和条件下测定的要慢。因此,Perrillat 等人(2005 年)的上述假设无法得到证实。不过,在我们对反应(R1)的两次研究中,新形成的脱水产物紫翠石的粒度都是纳米级的,这支持了早先的实验观察结果,即脱水反应的产物相一般都是非常细粒的,这可能会促进俯冲带中深层地震是由脱水反应过程中形成的极细粒物质的机械不稳定性引发的这一概念。
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来源期刊
CiteScore
2.80
自引率
9.50%
发文量
40
审稿时长
6-12 weeks
期刊介绍: EJM was founded to reach a large audience on an international scale and also for achieving closer cooperation of European countries in the publication of scientific results. The founding societies have set themselves the task of publishing a journal of the highest standard open to all scientists performing mineralogical research in the widest sense of the term, all over the world. Contributions will therefore be published primarily in English. EJM publishes original papers, review articles and letters dealing with the mineralogical sciences s.l., primarily mineralogy, petrology, geochemistry, crystallography and ore deposits, but also biomineralogy, environmental, applied and technical mineralogy. Nevertheless, papers in any related field, including cultural heritage, will be considered.
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