- Title
- Electrostatic Adsorption Behaviors of Polymer Plates to a Droplet
- Creator
- Takeuchi, Kazusa; Ireland, Peter M.; Webber, Grant B.; Wanless, Erica J.; Hayashi, Masaki; Sakabe, Ryuga; Fujii, Syuji
- Relation
- ARC.DP170100578 http://purl.org/au-research/grants/arc/DP170100578
- Relation
- Langmuir Vol. 39, Issue 28, p. 9617-9626
- Publisher Link
- http://dx.doi.org/10.1021/acs.langmuir.3c00485
- Publisher
- American Chemical Society
- Resource Type
- journal article
- Date
- 2023
- Description
- Electrostatic transfer and adsorption of electrically conductive polymer-coated poly(ethylene terephthalate) plates from a particle bed to a water droplet were studied, with the influence of plate thickness and shape observed. After synthesis and confirmation of the particles' properties using stereo and scanning electron microscopies, elemental microanalysis, and water contact angle measurement, the electric field strength and droplet-bed separation distance required for transfer were measured. An electrometer and high-speed video footage were used to measure the charge transferred by each particle, and its orientation and adsorption behavior during transfer and at the droplet interface. The use of plates of consistent square cross section allowed the impact of contact-area-dependent particle cohesion and gravity on the electrostatic transfer of particles to be decoupled for the first time. The electrostatic force required to extract a plate was directly proportional to the plate mass (thickness), a trend very different from that previously observed for spherical particles of varied diameter (mass). This reflected the different relationship between mass, surface area, and cohesive forces for spherical and plate-shaped particles of different sizes. Thicker plates transferred more charge to the droplet, probably due to their remaining at the bed at higher field strengths. The impact of plate cross-sectional geometry was also assessed. Differences in the ease of transfer of square, hexagonal, and circular plates seemed to depend only on their mass, while other aspects of their comparative behavior are attributed to the more concentrated charge distribution present on particles with sharper vertices.
- Subject
- electric fields; liquids; nanoparticles; organic polymers; thickness
- Identifier
- http://hdl.handle.net/1959.13/1479612
- Identifier
- uon:50339
- Identifier
- ISSN:0743-7463
- Rights
- This document is the Accepted Manuscript version of a Published Work that appeared in final form in Industrial and Engineering Chemistry Research, ©2021 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://dx.doi.org/10.1021/acs.iecr.1c01504.
- Language
- eng
- Full Text
- Reviewed
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