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Wilbert J. Smit

Publications and source records attributed to Wilbert J. Smit.

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Isosbestic points in time resolved SAXS: from spectroscopic analogy to model free structural markers during colloidal gelation

Gelation is the transition from a fluid state into a system-spanning, out of equilibrim soft-solid network through a hierarchical process that couples local particle interactions to mesoscopic clustering and global connectivity. In time-resolved small-angle X-ray scattering (SAXS), isosbestic points -- scattering wavevectors where scattering intensity remains invariant -- emerge during this transformation, yet their physical meaning has remained unclear. Here, we show that two isosbestic points, $q_1$ and $q_2$, observed during salt-induced gelation of Ludox colloids, reflect fundamental structural constraints rather than a two-species interconversion. The high-$q$ point $q_2$ is a universal geometric marker, determined by particle contact distances, while the low-$q$ point $q_1$ arises from Porod invariant conservation and separates rapidly arrested local clusters from the growing mesoscopic network. By decomposing the Porod invariant across the reciprocal-space regions defined by these points, we define a dimensionless parameter, $\Phi(t/t_g)$, whose sigmoidal evolution provides a simple, model-free, scale-resolved fingerprint of gelation. Together with the combined evolution of $S(q_{\min},t)$ and $S(q \rightarrow 0,t)$, these results establish a quantitative model free framework linking local structuring, global connectivity, and scattering signatures, clarifying the role of isosbestic points in soft-matter transformations.

cond-mat.soft

Imprinting Macroscopic Fracture during Gelation: A Mechanism for Tuning Colloidal Gels

Colloidal gels form through the sol-gel transition of attractive particle suspensions, where local aggregation leads to a space-spanning network with solid-like properties. Their microstructure and mechanical properties are highly sensitive to external perturbations, which can substantially alter the pathway of network formation. Here, we investigate how nonlinear oscillatory shear affects the sol-gel transition of colloidal silica suspensions. Using large-amplitude oscillatory shear (LAOS), we vary both the strain amplitude and the duration of oscillatory forcing, varying between one and two times the gelation time. We find that sufficiently large strain amplitudes, or prolonged exposure to oscillations in the nonlinear regime, alter irreversibly the gel properties: the storage modulus $G'$ decreases while its frequency dependence remains unchanged. In contrast, the loss modulus $G''$, which decreases monotonically with frequency under quiescent gelation, exhibits an upturn at high frequencies when the gel is formed under strong oscillatory shear. The viscoelastic spectra of gels formed under quiescent conditions are well captured by a fractional Maxwell model, while gels formed under LAOS require an additional fractional element to account for damage-induced dissipation. Rheo-imaging experiments corroborate this interpretation by revealing the growth of cracks in gels formed under LAOS. We further show that these gels display a progressively more ductile nonlinear response for prolonged exposure to LAOS during gelation. These results demonstrate that the interplay between non-linear shear and gelation can permanently imprint a macroscopic fracture pattern into colloidal gels, offering a route to tune their viscoelastic properties.

cond-mat.soft