Equilibrium isotope fractionation factors of H exchange between steam and soil clay fractions

Rationale

Steam equilibration overcomes the problem of the traditional measurements of H isotope compositions, which leave an arbitrary amount of adsorbed water in the sample, by controlling for the entire exchangeable H pool, including adsorbed water and hydroxyl-H. However, the use of steam equilibration to determine nonexchangeable stable H isotope compositions in environmental media (expressed as δ
²H_n values) by mathematically eliminating the influence of exchangeable H after sample equilibration with waters of known H-isotopic composition requires the knowledge of the equilibrium isotope fractionation factor between steam-H and exchangeable H of the sample (α_ex-w), which is frequently unknown.

Methods

We developed a new method to determine the α_ex-w values for clay minerals, topsoil clay fractions, and mica by manipulating the contributions of exchangeable H to the total H pool via different degrees of post-equilibration sample drying. We measured the δ
²H values of steam-equilibrated mineral and soil samples using elemental analyzer-pyrolysis-isotope ratio mass spectrometry.

Results

The α_ex-w values of seven clay minerals ranged from 1.071 to 1.140, and those of 19 topsoil clay fractions ranged from 0.885 to 1.216. The α_ex-w value of USGS57 biotite, USGS58 muscovite, and of cellulose was 0.965, 0.871, and 1.175, respectively. The method did not work for kaolinite, because its small exchangeable H pool did not respond to the selected drying conditions. Structurally different mineral groups such as two- and three-layer clay minerals or mica showed systematically different α_ex-w values. The α_ex-w value of the topsoil clay fractions correlated with the soil clay content (r = 0.63, P = 0.004), the local mean annual temperature (r = 0.68, P = 0.001), and the δ
²H values of local precipitation (r = 0.72, P < 0.001), likely to reflect the different clay mineralogy under different weathering regimes.

Conclusions

Our new α_ex-w determination method yielded realistic results in line with the few previously published values for cellulose. The determined α_ex-w values were similar to the widely assumed values of 1.00–1.08 in the literature, suggesting that the adoption of one of these values in steam equilibration approaches is appropriate.