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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Carbon isotopic composition of organic acids in oil field waters, San Joaquin Basin, California, USA
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Carbon isotopic composition of organic acids in oil field waters, San Joaquin Basin, California, USA

机译:美国加利福尼亚州圣华金盆地,油田水中有机酸的碳同位素组成

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The carbon isotopic compositions of short-chain organic acids (C-2-C-5) in oilfield waters of the San Joaquin Basin exhibit a wide range of values, from +0.57 to -27.33 parts per thousand (PDB). Most, however, are in the range of -15 to -25 parts per thousand. The bulk isotopic compositions of individual acids generally become isotopically depleted (more negative) with increasing carbon number (chain length) but are consistently more enriched than the isotopic composition of coproduced oils. Relationships between carbon number and isotopic composition of the acids suggest intramolecular isotopic fractionation. Calculated carboxyl carbons (COOH) are isotopically more enriched, typically by 10 to 38 parts per thousand, than aliphatic carbons (CH). Calculated aliphatic carbon isotopic compositions cluster around two values, -23 and - 28 parts per thousand, consistent with the isotopic composition of coproduced oils derived from two different sources, Miocene Monterey-sourced oils (-22 to -25 parts per thousand) and Eocene Kreyenhagen-soureed oils (-28 to -30 parts per thousand). We suggest that the isotopic composition of the aliphatic carbons in the organic acids reflects the carbon isotopic composition of the coproduced oils (or their source kerogen). Isotopic compositions of carboxyl carbons fall within a range of -12.8 to +8.0, consistently heavier than aliphatic carbons. We interpret the enrichment of carboxyl carbons to be inherited from either biological precursors in the source rock kerogen or due to exchange with carbon in dissolved HCO3. The carbon isotopic enrichment of carboxyl carbons is at odds with theories that attribute organic acids to the inorganic oxidation of hydrocarbons in the subsurface. Copyright (C) 2001 Elsevier Science Ltd. [References: 45]
机译:圣华金盆地油田水域中短链有机酸(C-2-C-5)的碳同位素组成显示范围很广,从+0.57到-27.33千分之几(PDB)。但是,大多数含量在每千分之-15至-25之间。随着碳原子数(链长)的增加,单个酸的总同位素组成通常会同位素贫化(更负),但始终比联产油的同位素组成更富集。碳原子数与酸的同位素组成之间的关系表明分子内同位素分级分离。与脂肪族碳(CH)相比,计算出的羧基碳(COOH)在同位素上的富集度通常为千分之10至38。计算得出的脂肪族碳同位素组成大约在两个值(千分之-23和-28)附近,这与衍生自两种不同来源的中生代蒙特雷来源的油(千分之-22至-25)和始新世的共产油的同位素组成一致Kreyenhagen酸化油(-28至-30千分之一)。我们建议,有机酸中脂肪族碳的同位素组成反映了联产油(或其来源干酪根)的碳同位素组成。羧基碳的同位素组成在-12.8至+8.0的范围内,始终比脂肪族碳重。我们解释了源于岩石干酪根的生物前体或由于与溶解的HCO3中的碳交换而继承的羧基碳的富集。羧基碳的碳同位素富集与将有机酸归因于地下碳氢化合物的无机氧化的理论不一致。版权所有(C)2001 Elsevier Science Ltd. [参考:45]

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