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Structural evolution of salt-free aqueous Laponite dispersions: A study based on low-field NMR relaxometry and rheological investigations

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Abstract The combination of Low-Field NMR relaxometry (LF-NMR) and rheological analyses was used to investigate the kinetics of aging and structural evolution of salt-free aqueous Laponite dispersions with concentrations ranging… Click to show full abstract

Abstract The combination of Low-Field NMR relaxometry (LF-NMR) and rheological analyses was used to investigate the kinetics of aging and structural evolution of salt-free aqueous Laponite dispersions with concentrations ranging from 0.33 to 2.00 wt%. The examination of LF-NMR results reveals that the rate of nanoclay delamination increases with increasing Laponite concentration while its degree decreases. Furthermore, the LF-NMR results were interpreted together with rheological results to assess the kinetics of processes occurring on different length scales reflecting on the time evolution of the three-dimensional structure. The structural evolution is described by the definition and comparison of three different characteristic times. The LF-NMR decay time (tr) designates the time required for Laponite delamination. The induction time (ti) indicates when interparticle edge-face interactions become effective enough for incipient networking. The gelation time (tg) corresponds to sufficiently high degree of interparticle connectivity for the development of a macroscopic gel behavior. The comparison of ti and tg, on one hand, and tr, on the other hand, allows to conclude that for low concentration Laponite dispersions nanoclay delamination is a prerequisite for the formation of the new dispersion structure with a macroscopic gel behavior. Interestingly, the development of the new structure, based on orientation of clay disks into edge-to-face pattern and mutual interparticle attractive interactions, starts when the delamination process is still running.

Keywords: nmr; evolution; low field; time; structural evolution; laponite dispersions

Journal Title: Colloids and Surfaces A: Physicochemical and Engineering Aspects
Year Published: 2020

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