69 D32. Geochemistry (Posters)
Sunday, 22 October 2017
9:00 AM - 5:30 PM
Halls 4EF
QUANTIFYING THE ∆63-∆47 OFFSET: DETERMINING MINERAL- AND TEMPERATURE-DEPENDENT ACID FRACTIONATION FACTORS THROUGH MASS SPECTROMETRIC ANALYSES OF STOCHASTICALLY-REORDERED CARBONATES
Paper number: 69-9
Program: Technical Sessions
Time: 9:00 AM – 5:30 PM
Authors
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Jed L. MosenfelderUniversity of Minnesota Twin Cities, Minneapolis, MN
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Aradhna K. TripatiUniversity of California, Los Angeles, Los Angeles, CA
Abstract
Unfortunately, precision mass spectrometric determination of the abundance of isotopologues in solid materials has proven difficult; instead, the isotopic composition of carbonates has traditionally been measured through acid digestion and subsequent analysis of the product CO2 gas. For example, clumped isotope thermometry typically relates formation temperature to ∆47, the abundance of 47-amu isotopologues relative to the predicted stochastic distribution.
As a consequence, the degree of fractionation that occurs between solid (∆63) and gaseous (∆47) phases has largely gone unstudied. By melting calcite and witherite powder at high pressures and temperatures (~1650ºC), we have produced a suite of carbonates predicted to have stochastic distributions of CO32- isotopologues (i.e., ∆63 values of 0‰). Thus, the measured ∆47 values of CO2 produced from these samples through acid digestion should equal the degree of fractionation that occurs.
We perform these measurements at a range of acid temperatures on several digestion apparatuses in order to deduce and quantify controls on acid digestion fractionation factors. We also calculate acid digestion fractionation factors using different sets of constants and compare our results to previously published estimates.
Geological Society of America Abstracts with Programs. Vol. 49, No. 6
doi: 10.1130/abs/2017AM-304811
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