Tension at the surface: Which phase is more important, liquid or vapor?
dc.contributor.author | Prpich, Andrew M. | |
dc.contributor.author | Sheng, Yuebiao | |
dc.contributor.author | Wang, Wei | |
dc.contributor.author | Biswas, M. Elias | |
dc.contributor.author | Chen, P. | |
dc.date.accessioned | 2025-07-03T18:10:39Z | |
dc.date.available | 2025-07-03T18:10:39Z | |
dc.date.issued | 2009 | |
dc.description | © 2009 Prpich et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | |
dc.description.abstract | Tension at the surface is a most fundamental physicochemical property of a liquid surface. The concept of surface tension has widespread implications in numerous natural, engineering and biomedical processes. Research to date has been largely focused on the liquid side; little attention has been paid to the vapor—the other side of the surface, despite over 100 years of study. However, the question remains as to whether the vapor plays any role, and to what extent it affects the surface tension of the liquid. Here we show a systematic study of the effect of vapor on the surface tension and in particular, a surprising observation that the vapor, not the liquid, plays a dominant role in determining the surface tension of a range of common volatile organic solutions. This is in stark contrast to results of common surfactants where the concentration in the liquid plays the major role. We further confirmed our results with a modified adsorption isotherm and molecular dynamics simulations, where highly structured, hydrogen bonded networks, and in particular a solute depletion layer just beneath the Gibbs dividing surface, were revealed. | |
dc.description.sponsorship | Natural Sciences and Engineering Research Council of Canada (NSERC) || Canada Research Chairs (CRC) || Ontario Graduate Scholarships (OGS). | |
dc.identifier.uri | https://doi.org/10.1371/journal.pone.0008281 | |
dc.identifier.uri | https://hdl.handle.net/10012/21962 | |
dc.language.iso | en | |
dc.publisher | Public Library of Science (PLOS) | |
dc.relation.ispartofseries | PLOS One; 4(12); e8281 | |
dc.rights | Attribution 4.0 International | en |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject | surface tension | |
dc.subject | vapors | |
dc.subject | aqueous solutions | |
dc.subject | surfactants | |
dc.subject | adsorption | |
dc.subject | liquids | |
dc.subject | solutions | |
dc.subject | hydrogen bonding | |
dc.title | Tension at the surface: Which phase is more important, liquid or vapor? | |
dc.type | Article | |
dcterms.bibliographicCitation | Prpich, A. M., Sheng, Y., Wang, W., Biswas, M. E., & Chen, P. (2009). Tension at the surface: Which phase is more important, liquid or vapor? PLoS ONE, 4(12). https://doi.org/10.1371/journal.pone.0008281 | |
uws.contributor.affiliation1 | Faculty of Engineering | |
uws.contributor.affiliation2 | Chemical Engineering | |
uws.peerReviewStatus | Reviewed | |
uws.scholarLevel | Faculty | |
uws.typeOfResource | Text | en |