论文标题

在100kPa处辉石和熔体之间的铁铁分配的实验测定

Experimental determination of ferric iron partitioning between pyroxene and melt at 100KPa

论文作者

Rudra, Avishek, Hirschmann, Marc M.

论文摘要

Pyroxene是玄武岩源区域中Fe $^{3+} $的主要主持人,分别在Spinel和Garnet Lherzolite中占79%和81%的Fe $^{3+} $,分别为OPX和CPX,分别为48%和31%,总托管48%和31%,总计Fe $^{3+} $ spinel per per,为了更好地了解pyroxene和熔体之间的Fe $^{3 +} $的分区,我们以100 kpa进行了实验,由f $ _ {o2} $控制由Co -Co $ _2 $ _2 $ _2 $ _2 $ _2 $ _2 $Δ$Δ$ qu qfm -qfm -1.19-1.1.1.1.1.19至+2.06在包含OPX或CPX的系统中 +2.2.06中。为了产生大型(100-150 $ $ m),均质的辉石,我们采用了一种动态冷却技术,其冷却速率为5-10美元$ C/h,以及初始和最终的温度为5-10 $°C和20-30美元$^\ Circ Circ $ c Super和Super-cips super and-Liquidus。产生的辉石晶体在Al $ _2 $ o $ _3 $和TIO $ _2 $ _2 $ <0.05 wt。%和<0.02 wt。%的情况下具有绝对变化。 Fe $^{3+} $/fe $^t $ in Pyroxenes和淬火玻璃通过Xanes测量。我们仅通过在$ 50 \ pm 5^\ circ $上选择X射线振动的光谱,将新开发的XANES校准用于CPX和OPX。 DFE $^{3+}的值从0.03增加到0.53,因为FO2从$δ$ qud $ qfm -0.44增加到2.06,而DFE $^{3+} $ opx/melt保持不变,在0.26之间保持在0.26 $ qfm -1..1..1.1.19 to +1.19 to +1.1.37。与天然的橄榄酸脓性相比,在本研究中结晶的pyroxenes中的Fe $^{3+} $/FET在相似的F $ _ {O2} $下较低,这可能是由于下部Al $^{3+} $ contents。这项研究表明,在pyroxenes中实现的现有热力学模型和Perple_x过度预测Fe $^{3+} $的稳定性,在计算出的病态条件下导致异常的降低特征到尖晶石橄榄岩。

Pyroxene is the principal host of Fe$^{3+}$ in basalt source regions, hosting 79 and 81% of the Fe$^{3+}$ in spinel and garnet lherzolite, respectively, with opx and cpx hosting 48% and 31%, respectively, of the total Fe$^{3+}$ in spinel peridotite. To better understand partitioning of Fe$^{3+}$ between pyroxene and melt we conducted experiments at 100 KPa with f$_{O2}$ controlled by CO-CO$_2$ gas mixes between $Δ$QFM -1.19 to +2.06 in a system containing andesitic melt saturated with opx or cpx only. To produce large (100-150 $μ$m), homogeneous pyroxenes, we employed a dynamic cooling technique with a 5-10$°$C/h cooling rate, and initial and final dwell temperatures 5-10$°$C and 20-30$^\circ$C super and sub-liquidus, respectively. Resulting pyroxene crystals have absolute variation in Al$_2$O$_3$ and TiO$_2$ <0.05 wt.% and <0.02 wt.%, respectively. Fe$^{3+}$/Fe$^T$ in pyroxenes and quenched glass were measured by XANES. We used a newly developed XANES calibration for cpx and opx by only selecting spectra with X-ray vibrating on the optic axial plane at $50 \pm 5^\circ$ to the crystallographic c axis. Values of DFe$^{3+}$ cpx/melt increase from 0.03 to 0.53 as fO2 increases from $Δ$QFM -0.44 to 2.06, while DFe$^{3+}$ opx/melt remains unchanged at 0.26 between $Δ$QFM -1.19 to +1.37. In comparison to natural peridotitic pyroxenes, Fe$^{3+}$/FeT in pyroxenes crystallized in this study are lower at similar f$_{O2}$, presumably owing to lower Al$^{3+}$ contents. This study shows that the existing thermodynamic models implemented in pMELTS and Perple_X over-predict the stability of Fe$^{3+}$ in pyroxenes, causing an anomalous reduced character to spinel peridotites at calculated conditions of MORB genesis.

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