Open Access
Open access
volume 12 issue 17 pages 3334

Dynamic Viscosity, Surface Tension and Wetting Behavior Studies of Paraffin–in–Water Nano–Emulsions

David R Cabaleiro 1, 2, 3
Samah Hamze 1
Filippo Agresti 4
Patrice Estelle 1
Simona Barison 4
Laura Fedele 2
Sergio Bobbo 2
2
 
Institute of Construction Technologies, National Research Council, I–35127 Padova, Italy
4
 
Institute of Condensed Matter Chemistry and Technologies for Energy, National Research Council, I–35127 Padova, Italy
Publication typeJournal Article
Publication date2019-08-29
scimago Q1
wos Q3
SJR0.713
CiteScore7.3
Impact factor3.2
ISSN19961073
Electrical and Electronic Engineering
Energy Engineering and Power Technology
Renewable Energy, Sustainability and the Environment
Control and Optimization
Engineering (miscellaneous)
Energy (miscellaneous)
Abstract

This work analyzes the dynamic viscosity, surface tension and wetting behavior of phase change material nano–emulsions (PCMEs) formulated at dispersed phase concentrations of 2, 4 and 10 wt.%. Paraffin–in–water samples were produced using a solvent–assisted route, starting from RT21HC technical grade paraffin with a nominal melting point at ~293–294 K. In order to evaluate the possible effect of paraffinic nucleating agents on those three properties, a nano–emulsion with 3.6% of RT21HC and 0.4% of RT55 (a paraffin wax with melting temperature at ~328 K) was also investigated. Dynamic viscosity strongly rose with increasing dispersed phase concentration, showing a maximum increase of 151% for the sample containing 10 wt.% of paraffin at 278 K. For that same nano–emulsion, a melting temperature of ~292.4 K and a recrystallization temperature of ~283.7 K (which agree with previous calorimetric results of that emulsion) were determined from rheological temperature sweeps. Nano–emulsions exhibited surface tensions considerably lower than those of water. Nevertheless, at some concentrations and temperatures, PCME values are slightly higher than surface tensions obtained for the corresponding water+SDS mixtures used to produce the nano–emulsions. This may be attributed to the fact that a portion of the surfactant is taking part of the interface between dispersed and continuous phase. Finally, although RT21HC–emulsions exhibited contact angles considerably inferior than those of distilled water, PCME sessile droplets did not rapidly spread as it happened for water+SDS with similar surfactant contents or for bulk–RT21HC.

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GOST Copy
Cabaleiro D. R. et al. Dynamic Viscosity, Surface Tension and Wetting Behavior Studies of Paraffin–in–Water Nano–Emulsions // Energies. 2019. Vol. 12. No. 17. p. 3334.
GOST all authors (up to 50) Copy
Cabaleiro D. R., Hamze S., Agresti F., Estelle P., Barison S., Fedele L., Bobbo S. Dynamic Viscosity, Surface Tension and Wetting Behavior Studies of Paraffin–in–Water Nano–Emulsions // Energies. 2019. Vol. 12. No. 17. p. 3334.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.3390/en12173334
UR - https://doi.org/10.3390/en12173334
TI - Dynamic Viscosity, Surface Tension and Wetting Behavior Studies of Paraffin–in–Water Nano–Emulsions
T2 - Energies
AU - Cabaleiro, David R
AU - Hamze, Samah
AU - Agresti, Filippo
AU - Estelle, Patrice
AU - Barison, Simona
AU - Fedele, Laura
AU - Bobbo, Sergio
PY - 2019
DA - 2019/08/29
PB - MDPI
SP - 3334
IS - 17
VL - 12
SN - 1996-1073
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2019_Cabaleiro,
author = {David R Cabaleiro and Samah Hamze and Filippo Agresti and Patrice Estelle and Simona Barison and Laura Fedele and Sergio Bobbo},
title = {Dynamic Viscosity, Surface Tension and Wetting Behavior Studies of Paraffin–in–Water Nano–Emulsions},
journal = {Energies},
year = {2019},
volume = {12},
publisher = {MDPI},
month = {aug},
url = {https://doi.org/10.3390/en12173334},
number = {17},
pages = {3334},
doi = {10.3390/en12173334}
}
MLA
Cite this
MLA Copy
Cabaleiro, David R., et al. “Dynamic Viscosity, Surface Tension and Wetting Behavior Studies of Paraffin–in–Water Nano–Emulsions.” Energies, vol. 12, no. 17, Aug. 2019, p. 3334. https://doi.org/10.3390/en12173334.