Carbon isotopic composition of organic acids in oil field waters, San Joaquin Basin, California, USA

Citation
Sg. Franks et al., Carbon isotopic composition of organic acids in oil field waters, San Joaquin Basin, California, USA, GEOCH COS A, 65(8), 2001, pp. 1301-1310
Citations number
45
Categorie Soggetti
Earth Sciences
Journal title
GEOCHIMICA ET COSMOCHIMICA ACTA
ISSN journal
00167037 → ACNP
Volume
65
Issue
8
Year of publication
2001
Pages
1301 - 1310
Database
ISI
SICI code
0016-7037(200104)65:8<1301:CICOOA>2.0.ZU;2-F
Abstract
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, fr om +0.57 to -27.33 parts per thousand (PDB). Most, however, are in the rang e of -15 to -25 parts per thousand. The bulk isotopic compositions of indiv idual acids generally become isotopically depleted (more negative) with inc reasing carbon number (chain length) but are consistently more enriched tha n the isotopic composition of coproduced oils. Relationships between carbon number and isotopic composition of the acids suggest intramolecular isotop ic fractionation. Calculated carboxyl carbons (COOH) are isotopically more enriched, typicall y by 10 to 38 parts per thousand, than aliphatic carbons (CH). Calculated a liphatic carbon isotopic compositions cluster around two values, -23 and - 28 parts per thousand, consistent with the isotopic composition of coproduc ed 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 al iphatic carbons in the organic acids reflects the carbon isotopic compositi on 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 enrichme nt 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.