Journal
CHEMOSPHERE
Volume 119, Issue -, Pages 99-104Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2014.05.066
Keywords
Sorption; Diuron; NMR spectroscopy; Clay-organic matter interactions; Organo-mineral interactions
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Funding
- Natasha Waller of CSIRO Land Water
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Sorption of non-ionic organic compounds to soil is usually expressed as the carbon-normalized partition coefficient (K-OC), because it is assumed that the main factor that influences the amount sorbed is the organic carbon content of the soil. However, K-OC can vary by a factor of at least ten across a range of soils. We investigated two potential causes of variation in diuron K-OC - organic matter-mineral interactions and organic matter chemistry - for a diverse set of 34 soils from Sri Lanka, representing a wide range of soil types. Treatment with hydrofluoric acid (HF-treatment) was used to concentrate soil organic matter. HF-treatment increased K-OC for the majority of soils (average factor 2.4). We attribute this increase to the blocking of organic matter sorption sites in the whole soils by minerals. There was no significant correlation between K-OC for the whole soils and Koc for the HF-treated soils, indicating that the importance of organic matter-mineral interactions varied greatly amongst these soils. There was as much variation in K-OC across the HF-treated soils as there was across the whole soils, indicating that the nature of soil organic matter is also an important contributor to K-OC variability. Organic matter chemistry, determined by solid-state C-13 nuclear magnetic resonance (NMR) spectroscopy, was correlated with Koc for the HF-treated soils. In particular, Koc increased with the aromatic C content (R = 0.64, p =1 x 10(-6)), and decreased with O-alkyl C (R = -0.32, p = 0.03) and alkyl C (R = -0.41, p = 0.004) content. (C) 2014 Elsevier Ltd. All rights reserved.
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