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Plastron Regeneration on Submerged Superhydrophobic Surfaces Using In Situ Gas Generation by Chemical Reaction

Author(s)
Panchanathan, Divya; Rajappan, Anoop; Varanasi, Kripa; McKinley, Gareth H
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Abstract
Superhydrophobic surfaces submerged under water appear shiny due to total internal reflection of light from a thin layer of air (plastron) trapped in their surface texture. This entrapped air is advantageous for frictional drag reduction in various applications ranging from microfluidic channels to marine vessels. However, these aerophilic textures are prone to impregnation by water due to turbulent pressure fluctuations from external flows and dissolution of the trapped gas into the water. We demonstrate a novel chemical method to replenish the plastron in situ by using the decomposition reaction of hydrogen peroxide on superhydrophobic surfaces prepared with a catalytic coating. We also provide a thermodynamic framework for designing superhydrophobic surfaces with optimal texture and chemistry for underwater plastron regeneration. We finally demonstrate the practical utility of this method by fabricating periodic microtextures on aluminum surfaces that incorporate a cheap catalyst, manganese dioxide. We perform drag-reduction experiments under turbulent flow conditions in a Taylor-Couette cell (TC cell), which show that more than half of the drag increase ensuing from plastron collapse can be recovered spontaneously by injection of dilute H₂O₂ into the TC cell. Thus, we present a low-cost, scalable method to enable in situ plastron regeneration on large surfaces for marine applications.
Date issued
2018-09
URI
https://hdl.handle.net/1721.1/124202
Department
Massachusetts Institute of Technology. Department of Mechanical Engineering
Journal
ACS Applied Materials & Interfaces
Publisher
American Chemical Society (ACS)
Citation
Panchanathan, Divya et al. "Plastron Regeneration on Submerged Superhydrophobic Surfaces Using In Situ Gas Generation by Chemical Reaction." ACS Applied Materials & Interfaces 10, 39 (September 2018): 33684-33692 © 2018 American Chemical Society
Version: Author's final manuscript
ISSN
1944-8244
1944-8252

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