The soil aqueous phase contains a multitude of dissolved as well as colloidal substances, e.g., organic colloids and clay minerals. Due to their ability to facilitate co-transport, colloids significantly contribute to the fluxes of carbon, nutrients, and contaminants, which renders a thorough consideration of colloids and their mobility a prerequisite for an understanding of soil matter exchange. However, a comprehensive assessment of colloidal transport is often hampered by the heterogeneity of reactions at soil mineral interfaces and the compositional and functional diversity of organic matter in natural soil suspensions. We addressed this challenge by using tailored organic polymers based on poly(ethylene glycol) (PEG) with high reactivity towards clay minerals. Hence, the polymers may be immobilized when clays are exposed on pore walls or mobilized when clay minerals form a colloidal suspension that permits a co-transport of clays and polymers. To unravel the competition between these mechanisms, we investigated the separate and combined transport of PEG and bentonite in column experiments using natural limestone as substrate. Here, PEG was strongly retarded due to adsorption on clay mineral surfaces that were exposed following limestone weathering. In contrast, PEG was highly mobile when transported simultaneously with bentonite and the observed PEG breakthrough resembled that of bentonite, indicating PEG was co-transported. This demonstrates that the application of PEG is promising in the disentanglement of complex transport phenomena in natural porous media, particularly if competition between adsorption sites is decisive for the fate of organic matter.
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Kwarkye et al. (2024) studied this question.
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