Effects of molecular weight-dependent physicochemical heterogeneity of natural organic matter on the aggregation of fullerene nanoparticles in mono- and di-valent electrolyte solutions

• Enhancement of nC60 stability positively correlates with the MW of NOM in NaCl.
• nC60 stability in NOM is electrolyte dependent and follows NaCl > MgCl2> CaCl2.
• High MW NOMs stabilize nC60 in NaCl more effectively than low MW counterparts.
• High MW NOMs promote nC60 attachment and thus aggregation in divalent cations.

Given the wide presence of heterogeneous natural organic matter (NOM) and metal ions (Na+/Ca2+/Mg2+), as well as their significant role in governing nanoparticle stability in aqueous environments, it is of great importance to understand how the molecular weight (MW)-dependent physicochemical properties of NOM impact fundamental transportation processes like the aggregation of engineered nanoparticles (ENPs) in the presence of Na+/Ca2+/Mg2+. Here, we report on the aggregation behavior of a model ENP, fullerene nanoparticles (nC60) in the presence of five MW fractions of Suwannee River NOM (Mf-SRNOMs, separated by ultrafiltration techniques) and three electrolytes (NaCl, CaCl2 and MgCl2). We found that in all NaCl treatments and low concentration CaCl2/MgCl2 treatments, the enhancement of nC60 stability positively correlated with the MW of Mf-SRNOMs. Whereas, the stability efficiency of identical Mf-SRNOM in different electrolytes followed an order of NaCl > MgCl2 > CaCl2, and the enhanced attachment of nC60-SRNOM associations was observed in high MW Mf-SRNOM (SRNOM>100 kD and SRNOM 30–100 kD) at high concentration CaCl2/MgCl2. Our results indicate that although the high MW NOM with large humic-like material is the key component for stabilizing nC60 in monovalent electrolyte, it could play a reversed role in promoting the attachment of nC60, especially in long term aggregations and at high concentrations of divalent cations. Therefore, a detailed understanding of the effects of heterogeneous NOM on the aggregation of ENPs should be highly valued, and properly assessed against different cation species and concentrations.

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