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DIVISION S-2 - SOIL CHEMISTRY

Stability of Reduced Organic Sulfur in Humic Acid as Affected by Aeration and pH

^a Dep. of Soil Science, North Carolina State Univ., Raleigh, NC 27695
^b Dep. of Physics, North Carolina State Univ., Raleigh, NC 27695

Corresponding author (kim_hutchison{at}ncsu.edu)

Reduced S groups in soil organic matter (OM) play an important role in the complexation of heavy metals. These complexation reactions are often studied using the humic acid component of OM. The objective of our study was to determine the effect of pH on humic acid yield and the effect of pH and exposure to O₂ on the oxidation of reduced organic S. Humic acid was extracted at pH levels between 11.5 and 13.0 from a soil collected from a salt marsh. Also, aqueous samples of humic acid at different pH levels were aspirated with CO₂-free air for 4 or 44 h. X-ray absorption near-edge structure (XANES) spectroscopy was used to determine changes in S oxidation states for the various treatments. With increasing pH, the yield of humic acid increased from 1.3 to 4.6 g humic acid kg^-1 soil, and the total S in these samples was 24 ± 1 g kg ^-1 humic acid. Linear-combination fitting of XANES spectra showed that all of these humic acid samples contained 70% (mol/mol) reduced S (modeled as benzyl disulfide) and 30% (mol/mol) oxidized S (modeled as sulfonate and ester sulfate). For humic acid exposed to aeration for 4 h at pH levels between 11.5 and 13.0, reduced organic S was oxidized only at pH 13.0 (15% [mol/mol] of total S). Samples exposed to aeration for 44 h between pH 3.5 and 12.4 showed no detectable change in reduced organic S.

Abbreviations: CV, coefficient of variation • IHSS, International Humic Substance Society • LDPE, low-density polyethylene • OM, organic matter • XANES, x-ray absorption near edge structure • UV, ultra-violet