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The Effect of Isopropyl Alcohol and Non-Ionic Surfactant Mixtures on the Wetting of Porous Coated Paper
Authors:C.-M. T?g  M. Toiviainen  M. Juuti  J. B. Rosenholm  K. Backfolk  P. A. C. Gane
Affiliation:1. Laboratory of Physical Chemistry, Center for Functional Materials, ?bo Akademi University, 20500, ?bo, Finland
2. Forest Pilot Center Oy, Kerrolankatu 2, 21200, Raisio, Finland
3. VTT Technical Research Centre of Finland, P.O. Box 1199, 70211, Kuopio, Finland
4. Laboratory of Fiber and Paper Technology, Department of Chemical Technology, Lappeenranta University of Technology, P.O. Box 20, 53851, Lappeenranta, Finland
5. Department of Forest Products Technology, School of Chemical Technology, Aalto University, 00076, Aalto, Helsinki, Finland
6. Omya Development AG, Baslerstrasse 42, 4665, Oftringen, Switzerland
Abstract:The influence of isopropyl alcohol and non-ionic surfactant solutions on aqueous droplet wetting behaviour on porous coated paper was determined. Paper coatings provide a micro- and nano-porous surface structure, which strictly speaking cannot be described in simple roughness terms as sub-surface lateral absorption directly impacts on the apparent contact angle. It is this very deviation from an idealised system that leads to novel wetting phenomena. Isopropyl alcohol and surfactant-based systems, both of which are commonly used in the printing industry, show differences in wetting behaviour, on both short and long timescales, with changes in the relative composition of the mixtures. Small variations of 0.1?wt% in surfactant concentration have a dramatic influence on the dynamic surface tension, and thus the wetting. It was observed that the wetting kinetics for isopropyl alcohol and surfactant solutions were different in terms of both wetting area and the penetration rate, even in cases where the dynamic surface tension of the solutions was kept the same. Different stages in the wetting and following drying processes could be observed with near infrared spectral imaging. In addition, the surfactant chemistries such as their degrees of hydrophilicity and molecular weights generated comparative differences in the wetting kinetics. The dominating factor affecting the wetting was, as expected, the solid?Cliquid interfacial energy defined on the practical porous substrate, which differed from the direct comparison with dynamic surface tension, thus exemplifying the deviation from idealised surface roughness behaviour when considering porous materials. An apparent ??equivalent?? surface roughness value for the porous material was determined, and it was seen that an increase in this equivalent parameter enhanced the rate of wetting behaviour with decreasing solution surface tension, and so also affected the wetting evolution. The wetting was enhanced by cavities in the coating layer, which were enlarged by the penetrating liquids.
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