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  4. Aggregation Behavior of Inorganic 2D Nanomaterials beyond Graphene: Insights from Molecular Modeling and Modified DLVO Theory
 
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Aggregation Behavior of Inorganic 2D Nanomaterials beyond Graphene: Insights from Molecular Modeling and Modified DLVO Theory

Source
Environmental Science and Technology
ISSN
0013936X
Date Issued
2019-04-16
Author(s)
Mohona, Tashfia M.
Gupta, Anusha
Masud, Arvid
Chien, Szu Chia
Lin, Li Chiang
Nalam, Prathima C.
Aich, Nirupam
DOI
10.1021/acs.est.8b05180
Volume
53
Issue
8
Abstract
We report the comparative aggregation behavior of three emerging inorganic 2D nanomaterials (NMs): MoS<inf>2</inf>, WS<inf>2</inf>, and h-BN in aquatic media. Their aqueous dispersions were subjected to aggregation under varying concentrations of monovalent (NaCl) and divalent (CaCl<inf>2</inf>) electrolytes. Moreover, Suwanee River Natural Organic Matter (SRNOM) has been used to analyze the effect of natural macromolecules on 2D NM aggregation. An increase in electrolyte concentration resulted in electrical double-layer compression of the negatively charged 2D NMs, thus displaying classical Derjaguin-Landau-Verwey-Overbeek (DLVO)-type interaction. The critical coagulation concentrations (CCC) have been estimated as 37, 60, and 19 mM NaCl and 3, 7.2, and 1.3 mM CaCl<inf>2</inf> for MoS<inf>2</inf>, WS<inf>2</inf>, and h-BN, respectively. Theoretical predictions of CCC by modified DLVO theory have been found comparable to the experimental values when dimensionality of the materials is taken into account and a molecular modeling approach was used for calculating molecular level interaction energies between individual 2D NM nanosheets. Electrostatic repulsion has been found to govern colloidal stability of MoS<inf>2</inf> and WS<inf>2</inf> while the van der Waals attraction has been found to govern that of h-BN. SRNOM stabilizes the 2D NMs significantly possibly by electrosteric repulsion. The presence of SRNOM completely stabilized MoS<inf>2</inf> and WS<inf>2</inf> at both low and high ionic strengths. While h-BN still showed appreciable aggregation in the presence of SRNOM, the aggregation rates were decreased by 2.6- and 3.7-fold at low and high ionic strengths, respectively. Overall, h-BN nanosheets will have higher aggregation potential and thus limited mobility in the natural aquatic environment when compared to MoS<inf>2</inf> and WS<inf>2</inf>. These results can also be used to mechanistically explain fate, transport, transformation, organismal uptake, and toxicity of inorganic 2D NMs in the natural ecosystems.
Publication link
https://doi.org/10.1021/acs.est.8b05180
URI
http://repository.iitgn.ac.in/handle/IITG2025/23308
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