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Experimental dissolution of molybdenum‐sulphides at low oxygen concentrations: A first‐order approximation of late Archean atmospheric conditions

机译:低氧浓度下硫化钼的实验溶出:太古宙晚期大气条件的一阶近似

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AbstractThe abundance of atmospheric oxygen and its evolution through Earth's history is a highly debated topic. The earliest change of the Mo concentration and isotope composition of marine sediments are interpreted to be linked to the onset of the accumulation of free O2 in Earth's atmosphere. The O2 concentration needed to dissolve significant amounts of Mo in water is not yet quantified, however. We present laboratory experiments on pulverized and surface-cleaned molybdenite (MoS2) and a hydrothermal breccia enriched in Mo-bearing sulphides using a glove box setup. Duration of an experiment was 14 days, and first signs of oxidation and subsequent dissolution of Mo compounds start to occur above an atmospheric oxygen concentration of 72 ± 20 ppmv (i.e., 2.6 to 4.6 × 10−4 present atmospheric level (PAL)). This experimentally determined value coincides with published model calculations supporting atmospheric O2 concentrations between 1 × 10−5 to 3 × 10−4 PAL prior to the Great Oxidation Event and sets an upper limit to the molecular oxygen needed to trigger Mo accumulation and Mo isotope variations recorded in sediments. In combination with the published Mo isotope composition of the rock record, this result implies an atmospheric oxygen concentration prior to 2.76 Ga of below 72 ± 20 ppmv.
机译:摘要大气中氧气的丰富及其在地球历史上的演变是一个备受争议的话题。海洋沉积物中Mo浓度和同位素组成的最早变化被认为与地球大气中游离O 2 的积累有关。然而,尚未确定溶解大量Mo所需的O 2 浓度。我们目前使用手套箱设置对粉磨和表面清洁的辉钼矿(MoS 2 )和富含钼的硫化物的水热角砾岩进行实验室实验。实验时间为14天,在大气氧浓度高于72±20 ppmv(即存在2.6至4.6×10 −4 )时,开始出现Mo化合物氧化和随后溶解的第一个迹象。大气水平(PAL))。该实验确定的值与已发布的模型计算吻合,该模型计算支持大气P <1×10 -5 至3×10 -4 PAL前的O 2 浓度。氧化大事件,并设定了触发沉积物中记录的Mo积累和Mo同位素变化所需的分子氧的上限。结合岩石记录中已公布的Mo同位素组成,该结果表明2.76 Ga之前的大气氧浓度低于72±20 ppmv。

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