Issue 10, 2014

An electrochemical and high-speed imaging study of micropore decontamination by acoustic bubble entrapment

Abstract

Electrochemical and high-speed imaging techniques are used to study the abilities of ultrasonically-activated bubbles to clean out micropores. Cylindrical pores with dimensions (diameter × depth) of 500 μm × 400 μm (aspect ratio 0.8), 125 μm × 350 μm (aspect ratio 2.8) and 50 μm × 200 μm (aspect ratio 4.0) are fabricated in glass substrates. Each pore is contaminated by filling it with an electrochemically inactive blocking organic material (thickened methyl salicylate) before the substrate is placed in a solution containing an electroactive species (Fe(CN)63−). An electrode is fabricated at the base of each pore and the Faradaic current is used to monitor the decontamination as a function of time. For the largest pore, decontamination driven by ultrasound (generated by a horn type transducer) and bulk fluid flow are compared. It is shown that ultrasound is much more effective than flow alone, and that bulk fluid flow at the rates used cannot decontaminate the pore completely, but that ultrasound can. In the case of the 125 μm pore, high-speed imaging is used to elucidate the cleaning mechanisms involved in ultrasonic decontamination and reveals that acoustic bubble entrapment is a key feature. The smallest pore is used to explore the limits of decontamination and it is found that ultrasound is still effective at this size under the conditions employed.

Graphical abstract: An electrochemical and high-speed imaging study of micropore decontamination by acoustic bubble entrapment

Supplementary files

Article information

Article type
Paper
Submitted
03 Dec 2013
Accepted
21 Jan 2014
First published
21 Jan 2014
This article is Open Access
Creative Commons BY license

Phys. Chem. Chem. Phys., 2014,16, 4982-4989

An electrochemical and high-speed imaging study of micropore decontamination by acoustic bubble entrapment

D. G. Offin, P. R. Birkin and T. G. Leighton, Phys. Chem. Chem. Phys., 2014, 16, 4982 DOI: 10.1039/C3CP55088E

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