Contributions of partition and adsorption to polycyclic aromatic hydrocarbons sorption by fractionated soil at different particle sizes.

Abstract

Partition and adsorption of polycyclic aromatic hydrocarbons (PAHs) are critical mechanisms determining their fate at the solid-liquid interface. The complexity of soil composition makes it difficult to distinguish between partition and adsorption, and bates the accuracy of the research results. This study found that the composition and structure of the soil particles (SAs) of varying particle sizes were significantly different. Partition contributed significantly to phenanthrene (Phe) sorption in SAs over 0.002mm. However, PAHs had the highest sorption coefficient (Kd) in SA less than 0.002mm (SA-3), and the lower aqueous phase equilibrium concentration of Phe, the greater the adsorption effect. According to morphology and structural analysis, Fourier transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS), interactions of micropores, soil organic matter (SOM) and minerals enhanced the sorption of PAHs. Additionally, thermogravimetry and mass spectrometry (TG-MS) results proved that SOM could inhibit the release of PAHs adsorbed in SAs during heating process. We observed that the Log Koc of PAHs was the most important factor in determining the Kd in SAs applying principal component analyses (PCA), and they have significant linear relationships (R2=0.79-0.93). These findings provide new understandings on interface reactivity of PAHs sorption to soils and the development of interface model.