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Adhesion of alumina surfaces through confined water layers containing various molecules

Rossetto, Hebert L.; Bowen, James and Kendall, Kevin (2012). Adhesion of alumina surfaces through confined water layers containing various molecules. Langmuir, 28(10) pp. 4648–4653.

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DOI (Digital Object Identifier) Link: https://doi.org/10.1021/la2045064
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Abstract

When two surfaces confine water layers between them at the nanoscale, the behaviour of these confined water molecules can deviate significantly from the behaviour of bulk water and it could reflect on the adhesion of such surfaces. Thus, the aim of this study is to assess the role of confined water layers on the adhesion of hydrophilic surfaces and how sensitive this adhesion is to the presence of contaminants. Our methodology used under water AFM force measurements with an alumina sputtered sphere-tipped cantilever and a flat alumina single crystal, then added fractions of ethanol, dimethylformamide, formamide, trimethylamine, and trehalose to water, as contaminants. Such solutions were designed to illuminate the influences of dielectric constant, molecular size, refractive index and number of hydrogen bonds from donors and acceptors of solutes to water. Apart from very dilute solutions of dimethylformamide, all solutions decreased the ability of confined water to give adhesion of the alumina surfaces. The predicted theoretical contribution of van der Waals and electrostatic forces was not observed when the contaminants distorted the way water organizes itself in confinement. The conclusion was that adhesion was sensitive mostly to hydrogen bonding network within water layers confined by the hydrophilic alumina surfaces.

Item Type: Journal Item
Copyright Holders: 2012 American Chemical Society
ISSN: 1520-5827
Academic Unit/School: Faculty of Science, Technology, Engineering and Mathematics (STEM) > Engineering and Innovation
Faculty of Science, Technology, Engineering and Mathematics (STEM)
Item ID: 43176
Depositing User: James Bowen
Date Deposited: 04 Jun 2015 10:27
Last Modified: 22 Nov 2016 17:24
URI: http://oro.open.ac.uk/id/eprint/43176
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