首页> 外文期刊>Earth and Planetary Science Letters: A Letter Journal Devoted to the Development in Time of the Earth and Planetary System >Plastic deformation experiments to high strain on mantle transition zone minerals wadsleyite and ringwoodite in the rotational Drickamer apparatus
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Plastic deformation experiments to high strain on mantle transition zone minerals wadsleyite and ringwoodite in the rotational Drickamer apparatus

机译:旋转Drickamer仪器对地幔过渡带矿物辉绿岩和林榴石进行高应变塑性变形实验。

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摘要

We report the results of plastic deformation experiments on polycrystalline wadsleyite and ringwoodite performed at 15-23GPa and 1300-2100K conducted using the rotational Drickamer apparatus (RDA). Wadsleyite was synthesized from fine-grained (~2μm) San Carlos olivine in a Kawai-type multianvil apparatus; the average grain size of the resulting wadsleyite was 1.2μm. The initial water content of the undeformed wadsleyite was 24,000-26,000H/10~6 Si but the final water content is variable and less than the initial water content. Ringwoodite was synthesized from wadsleyite in situ in the RDA. Both strain and stress were measured in situ using a synchrotron x-ray facility. Determinations of strains and strain rates were made from x-ray radiographs of the sample, using a Mo foil strain marker in the sample assembly. The state of stress was determined from the observed d-spacing of multiple lattice planes as a function of azimuth angle. Samples were deformed at various strain rates at around 10~(-4)-10~(-5)s~(-1). Deformation mechanisms were inferred from the stress exponent and the microstructures. We determined the stress exponent n for wadsleyite to be 6±3, suggesting dislocation creep was the dominant deformation mechanism in wadsleyite. At grain sizes of ~1μm, our samples were still deforming primarily by dislocation creep. However, small dislocation-free grains are also observed suggesting that diffusion creep may operate in some parts of our samples.
机译:我们报告了使用旋转Drickamer仪器(RDA)在15-23GPa和1300-2100K上对多晶硅灰石和菱铁矿进行塑性变形实验的结果。瓦兹利石是在Kawai型多砧装置中由细粒(〜2μm)的圣卡洛斯橄榄石合成的。生成的硅钙石的平均晶粒尺寸为1.2μm。未变形的钙铝石的初始水含量为24,000-26,000H / 10〜6 Si,但最终水含量是可变的并且小于初始水含量。在RDA中由沃兹利石原位合成林伍德石。使用同步加速器X射线设备现场测量应变和应力。使用样品组件中的Mo箔应变标记,根据样品的X射线照片确定应变和应变率。根据观察到的多个晶格平面的d间距确定了应力状态,该d间距是方位角的函数。样品在10〜(-4)-10〜(-5)s〜(-1)附近以不同的应变率变形。从应力指数和微观结构推断出变形机理。我们确定了辉石的应力指数n为6±3,表明位错蠕变是辉石的主要变形机制。在〜1μm的晶粒尺寸下,我们的样品仍然主要是由于位错蠕变而变形。但是,还观察到小的无位错晶粒,这表明扩散蠕变可能在我们样品的某些部分起作用。

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