Thin films of amphiphilic polyelectrolytes. Soft materials characterized by Kelvin probe force microscopy
Author
dc.contributor.author
Briones, X. G.
Author
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Urzúa Acevedo, Marcela
es_CL
Author
dc.contributor.author
Ríos, H. E.
es_CL
Author
dc.contributor.author
Espinoza Beltrán, F. J.
es_CL
Author
dc.contributor.author
Dabirian, R.
es_CL
Author
dc.contributor.author
Yazdani-Pedram Zobeiri, Mehrdad
es_CL
Admission date
dc.date.accessioned
2014-01-13T14:57:36Z
Available date
dc.date.available
2014-01-13T14:57:36Z
Publication date
dc.date.issued
2013
Cita de ítem
dc.identifier.citation
Polymer 54 (2013) 5733e5740
en_US
Identifier
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DOI: 10.1016/j.polymer.2013.07.066
Identifier
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https://repositorio.uchile.cl/handle/2250/119687
General note
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Artículo de publicación ISI
en_US
Abstract
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Hydrophobically modified amphiphilic polyelectrolyte films derived from poly (maleic anhydride-altstyrene)
containing hydrophobic aryl-alkyl type side chains such as phenyl-ethyl, phenyl-butyl,
naphthyl-ethyl and naphthyl-butyl were studied by Kelvin probe force microscopy. These films were
adsorbed from polyelectrolyte solutions at 0.001 mol/L and 0.1 mol/L NaCl onto silicon wafers modified
with 3-aminopropyltrimethoxysilane. At high ionic strength, the work function was dependent on the
hydrophobic character of the side chain. At low ionic strength this behavior was determined by the
spacer group in the side chain. The fractal analysis of the films indicated self-affinity surfaces whereas
the fractal dimensions of the surface topography follow a similar trend as the electronic work function
with the ionic strength. This behavior can be explained by the increasing hydrophobic character of the
side chain with naphthyl moieties. Relationship between the molecular structure and the fractal dimensions
with the work function of the adsorbed polyelectrolytes was found.