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Rheo-acoustic gels: Tuning mechanical and flow properties of colloidal gels with ultrasonic vibrations (1905.07282v3)

Published 17 May 2019 in cond-mat.soft

Abstract: Colloidal gels, where nanoscale particles aggregate into an elastic yet fragile network, are at the heart of materials that combine specific optical, electrical and mechanical properties. Tailoring the viscoelastic features of colloidal gels in real-time thanks to an external stimulus currently appears as a major challenge in the design of "smart" soft materials. Here we introduce "rheo-acoustic" gels, a class of materials that are sensitive to ultrasonic vibrations. By using a combination of rheological and structural characterization, we evidence and quantify a strong softening in three widely different colloidal gels submitted to ultrasonic vibrations (with submicron amplitude and frequency 20-500 kHz). This softening is attributed to micron-sized cracks within the gel network that may or may not fully heal once vibrations are turned off depending on the acoustic intensity. Ultrasonic vibrations are further shown to dramatically decrease the gel yield stress and accelerate shear-induced fluidization. Ultrasound-assisted fluidization dynamics appear to be governed by an effective temperature that depends on the acoustic intensity. Our work opens the way to a full control of elastic and flow properties by ultrasonic vibrations as well as to future theoretical and numerical modeling of such rheo-acoustic gels.

Citations (28)

Summary

  • The paper demonstrates that ultrasonic vibrations significantly soften colloidal gels by inducing micron-sized cracks.
  • The methodology involved applying ultrasound (20–500 kHz) to calcite, silica, and carbon black gels to alter their elasticity and yield stress.
  • The findings highlight potential applications in designing smart materials with tunable properties for industrial and biomedical use.

Rheo-Acoustic Gels: Mechanical and Flow Property Manipulation Through Ultrasonic Vibrations

The paper "Rheo-acoustic gels: Tuning mechanical and flow properties of colloidal gels with ultrasonic vibrations" explores the influence of ultrasonic vibrations on colloidal gel networks. Colloidal gels, pivotal in various industrial and scientific applications, exhibit unique elastic properties due to their nanoscale particulate network. This paper introduces the concept of "rheo-acoustic" gels—colloidal materials that can be mechanically tuned using ultrasound frequencies ranging from 20 to 500 kHz.

Key Findings

The primary accomplishment of this research is the demonstration of notable softening in three distinct colloidal gels (calcite, silica, and carbon black) when subjected to ultrasonic vibrations at submicron amplitudes. The researchers attribute this softening effect to the formation of micron-sized cracks within the gel network. These cracks, dependent on the acoustic intensity, may remain as permanent defects or partially heal, influencing the elasticity and yield stress of the gels.

The implications of this paper extend to the reduced yield stress and accelerated shear-induced fluidization under ultrasonic excitation. This phenomenon correlates to altering an effective temperature parameter that scales with the acoustic intensity applied, posing significant implications for external control over the material's behavior.

Implications

The capability to modify the mechanical response of gels using ultrasonic vibrations opens avenues for designing smart materials that can be precisely controlled in real-time. Such systems find potential applications in enhancing flow processes, lubrications, and material extrusion within industrial and biomedical domains.

On a theoretical level, these findings challenge traditional models of structural response under oscillatory forces and necessitate further exploration into the microscopic mechanisms governing such transformations. They prompt the development of new theoretical frameworks and simulations that account for frequency-dependent structural adaptation in viscoelastic materials.

Future Directions

Future investigations could focus on more comprehensive characterization of the microstructural changes at play through real-time imaging techniques such as advanced scattering or imaging methods. Additionally, the scalability of this method to other gel systems and environmental conditions presents considerable interest.

Integrating numerical simulations with empirical findings will be crucial in understanding the underlying dynamics at both mesoscopic and macroscopic levels. These include exploring model adaptations to mesoscopic elastoplastic frameworks or noise-activated event theories, which present innovative means of understanding gel softening and fluidization through vibrational mechanisms.

Overall, the paper provides a comprehensive foundation for future exploration in the field of material science and offers compelling insight into the manipulation of gel properties without altering physical or chemical composition through innovative non-invasive techniques.

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