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Complex polyion-surfactant ion salts in equilibrium with water: Changing aggregate shape and size by adding oil

Bernardes, Juliana LU ; Norrman, Jens LU ; Piculell, Lennart LU and Loh, Watson LU (2006) In The Journal of Physical Chemistry Part B 110(46). p.23433-23442
Abstract
The phase behavior of ternary mixtures containing an alkyltrimethylammonium polyacrylate complex salt, water, and a nonpolar "oil" (n-decanol, p-xylene or cyclohexane) is investigated. The complex salts were prepared with short or long polyacrylates (30 or 6000 repeating units) and with hexadecyltrimethylammonium or dodecyltrimethylammonium surfactant ions. Phase diagrams and structures were determined by visual inspection and small-angle X-ray scattering analyses. Systems containing decanol display a predominance of lamellar phases, while hexagonal phases prevail in systems containing p-xylene or cyclohexane. The difference is interpreted as a result of the different locations of the oils within the surfactant aggregates. Decanol is... (More)
The phase behavior of ternary mixtures containing an alkyltrimethylammonium polyacrylate complex salt, water, and a nonpolar "oil" (n-decanol, p-xylene or cyclohexane) is investigated. The complex salts were prepared with short or long polyacrylates (30 or 6000 repeating units) and with hexadecyltrimethylammonium or dodecyltrimethylammonium surfactant ions. Phase diagrams and structures were determined by visual inspection and small-angle X-ray scattering analyses. Systems containing decanol display a predominance of lamellar phases, while hexagonal phases prevail in systems containing p-xylene or cyclohexane. The difference is interpreted as a result of the different locations of the oils within the surfactant aggregates. Decanol is incorporated at the aggregate interface, leading to a decrease in its curvature, which favors the appearance of lamellar structures. p-Xylene and cyclohexane, on the other hand, are mostly incorporated in the interior of the cylindrical aggregate, as reflected by its swelling as the oil content increases. The comparison of these results with those reported for similar systems with monovalent (bromide) counterions indicates a much more limited swelling of the lamellar phases with polymeric counterions by water. This limited swelling behavior is predominantly ascribed to bridging due to the polyions. (Less)
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author
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organization
publishing date
type
Contribution to journal
publication status
published
subject
in
The Journal of Physical Chemistry Part B
volume
110
issue
46
pages
23433 - 23442
publisher
The American Chemical Society (ACS)
external identifiers
  • wos:000242045900072
  • scopus:33846038711
ISSN
1520-5207
DOI
10.1021/jp0636165
language
English
LU publication?
yes
id
a1046250-5272-4ea9-b171-39b58df6eb8d (old id 376938)
date added to LUP
2016-04-01 15:33:26
date last changed
2022-04-06 23:35:11
@article{a1046250-5272-4ea9-b171-39b58df6eb8d,
  abstract     = {{The phase behavior of ternary mixtures containing an alkyltrimethylammonium polyacrylate complex salt, water, and a nonpolar "oil" (n-decanol, p-xylene or cyclohexane) is investigated. The complex salts were prepared with short or long polyacrylates (30 or 6000 repeating units) and with hexadecyltrimethylammonium or dodecyltrimethylammonium surfactant ions. Phase diagrams and structures were determined by visual inspection and small-angle X-ray scattering analyses. Systems containing decanol display a predominance of lamellar phases, while hexagonal phases prevail in systems containing p-xylene or cyclohexane. The difference is interpreted as a result of the different locations of the oils within the surfactant aggregates. Decanol is incorporated at the aggregate interface, leading to a decrease in its curvature, which favors the appearance of lamellar structures. p-Xylene and cyclohexane, on the other hand, are mostly incorporated in the interior of the cylindrical aggregate, as reflected by its swelling as the oil content increases. The comparison of these results with those reported for similar systems with monovalent (bromide) counterions indicates a much more limited swelling of the lamellar phases with polymeric counterions by water. This limited swelling behavior is predominantly ascribed to bridging due to the polyions.}},
  author       = {{Bernardes, Juliana and Norrman, Jens and Piculell, Lennart and Loh, Watson}},
  issn         = {{1520-5207}},
  language     = {{eng}},
  number       = {{46}},
  pages        = {{23433--23442}},
  publisher    = {{The American Chemical Society (ACS)}},
  series       = {{The Journal of Physical Chemistry Part B}},
  title        = {{Complex polyion-surfactant ion salts in equilibrium with water: Changing aggregate shape and size by adding oil}},
  url          = {{http://dx.doi.org/10.1021/jp0636165}},
  doi          = {{10.1021/jp0636165}},
  volume       = {{110}},
  year         = {{2006}},
}