Issue 43, 2017

pH-responsive superomniphobic nanoparticles as versatile candidates for encapsulating adhesive liquid marbles

Abstract

Conventional adhesives are rarely used in sophisticated applications such as micro-fluidic devices or ‘operations of bonding from a distance’ due to their permanent wetting characteristics. Liquid marbles offer exceptional switching between non-wetting and wetting on demand. In this contribution, we present a novel approach to encapsulate both hydrophilic (epoxy resin) and hydrophobic (siloxane polymer) liquids via wrapping them with superomniphobic nanoparticles. The free energy for marble formation is lower for a hydrophobic liquid (0.931 × 10−16 J), whereas a hydrophilic liquid registers a higher value of 1.86 × 10−16 J. The mechanical bursting energy for hydrophobic marbles (20 μJ) is lower than that for their hydrophilic counterpart (48.6 μJ). The static friction coefficients of epoxy-based liquid marble are between 0.015 and 0.020 on glass, aluminium and stainless steel substrates. As a highlight, the nanoparticle coating is responsive to pH, and the bursting time of the liquid marbles can be tuned from <1 minute to several hours. It is demonstrated that the adhesive strength of cross-linked epoxy obtained by a liquid marble route is higher than that obtained vis-a-vis a conventional wetting route. The liquid marbles presented in this work can be ruptured by changing the pH, have a lower friction coefficient compared to the bare liquids (more rolling distance, which is highly essential for bonding of an intricate space from a distance) and are useful as dry adhesives.

Graphical abstract: pH-responsive superomniphobic nanoparticles as versatile candidates for encapsulating adhesive liquid marbles

Supplementary files

Article information

Article type
Paper
Submitted
27 Aug 2017
Accepted
12 Oct 2017
First published
12 Oct 2017

J. Mater. Chem. A, 2017,5, 22813-22823

pH-responsive superomniphobic nanoparticles as versatile candidates for encapsulating adhesive liquid marbles

S. Chandan, S. Ramakrishna, K. Sunitha, M. S. Chandran, K. S. S. Kumar and D. Mathew, J. Mater. Chem. A, 2017, 5, 22813 DOI: 10.1039/C7TA07562F

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