Study of nanosuspension droplets free evaporation and electrowetting
dc.contributor.advisor
Sefiane, Khellil
en
dc.contributor.advisor
Walton, Anthony
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dc.contributor.author
Orejon, Daniel
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dc.contributor.sponsor
Engineering and Physical Sciences Research Council (EPSRC)
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dc.date.accessioned
2013-12-11T09:57:46Z
dc.date.available
2013-12-11T09:57:46Z
dc.date.issued
2013-11-28
dc.description.abstract
Evaporation and wetting of droplets are a phenomena present in everyday life and in
many industrial, biological or medical applications; thus controlling and
understanding the underlying mechanisms governing this phenomena becomes of
paramount importance. More recently, breakthroughs in the fabrication of new
materials and nanomaterials have led to the synthesis of novel nanoscale particulates
that dispersed into a base fluid modify the properties of this latter. Enhancement in
heat transfer or the self-assembly of the particles in suspension during evaporation,
are some of the areas in which nanofluids excel. Since it is a relatively new area of
study, the interplay particle-particle, particle-fluid or particle-substrate at the macro-,
micro-, and nanoscale is yet poorly understood. This work is an essay to elucidate the
fundamental physics and mechanisms of these fluids during free evaporation, of
great importance for the manipulation and precise control of the deposits.
The evaporative behaviour of pure fluids on substrates varying in hydrophobicity has
been studied and an unbalance Young’s force is proposed to explain the effect of
substrate hydrophilicity on the pinning and the depinning forces involved during
droplet evaporation. On other hand, the addition of nanoparticles to a base fluid
modifies the evaporative behaviour of the latter and: a more marked “stick-slip”
behaviour is observed when increasing concentration on hydrophobic substrates,
besides the longer pinning of the contact line reported on hydrophilic ones when
adding nanoparticles. A deposition theory to explain the final deposits observed, for
the outermost ring, after the complete vanishing of a 0.1% TiO2-ethanol nanofluid
droplet has also been developed. In addition, the evaporation of pinned nanofluid
droplets on rough substrates at reduced pressures has been systematically studied.
A revisited Young-Lippmann equation is proposed as one of the main findings to
explain the enhancement on electrowetting performance of nanoparticle laden fluid
droplets when compared to the pure fluid case. On the other hand, of relevant
importance is the absence of “stick-slip” behaviour and the more homogeneous
deposits found after the complete evaporation of a nanofluid droplet under an
external electric field applied when compared to free evaporation of these fluids.
en
dc.identifier.uri
http://hdl.handle.net/1842/8272
dc.language.iso
en
dc.publisher
The University of Edinburgh
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dc.relation.hasversion
Evaporation of nanofluid droplets with applied DC potential. Orejon, D., K. Sefiane and M.E. R. Shanahan. Journal of Colloids and Interface Science, Volume 407, Pages 29-38, 2013.
en
dc.relation.hasversion
Young-Lippmann equation revisited for nano-suspensions. Orejon, D., K. Sefiane and M.E. R. Shanahan. Applied Physics Letters, Volume 102, Issue 20, Pages 201601-1 to 201601-3, 2013.
en
dc.relation.hasversion
Stick-slip of evaporating droplets: substrate hydrophobicity and nanoparticle concentration. Orejon, D., K. Sefiane and M.E. R. Shanahan. Langmuir, Volume 27, Pages 12834-12843, 2011.
en
dc.relation.hasversion
Nanoparticle deposits near the contact line of pinned volatile droplets: size, and shape revealed by atomic force microscopy. Askounis, A., D. Orejon, V. Koutsos, K. Sefiane and M.E. R. Shanahan. Soft Matter, Volume 7, Pages 4152-4155, 2011.
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dc.subject
droplet evaporation
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dc.subject
nanofluids
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dc.subject
patterning
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dc.subject
electrowetting
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dc.subject
interfacial phenomena
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dc.title
Study of nanosuspension droplets free evaporation and electrowetting
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dc.type
Thesis or Dissertation
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dc.type.qualificationlevel
Doctoral
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dc.type.qualificationname
PhD Doctor of Philosophy
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