The aqueous phase behavior of polyion-surfactant ion complex salts mixed with nonionic surfactants.
Janiak, John LU ; Piculell, Lennart LU ; Olofsson, Gerd LU and Schillén, Karin LU
(2011)
In Physical chemistry chemical physics : PCCP
13.
p.3126-3138
- Abstract
- The aim of this work was to study intermolecular interactions in systems containing charged polyion (polyacrylate, PA(-)), charged surfactant (C(16)TA(+)) and nonionic surfactant (C(12)E(5) or C(12)E(8)). To achieve this we have created four different phase diagrams using two different so-called complex salts, C(16)TAPA(25) and C(16)TAPA(6000), both consisting of positively charged surfactant (C(16)TA(+)) with polyacrylate (PA(-)) as counterions (no simple salt). The difference between the salts is the length of the polyion (25 or 6000 monomers). Both are insoluble in water. The results revealed that decreasing polyion length and increasing the PEO chain length of the nonionic surfactant were important factors for increasing the solubility... (More)
- The aim of this work was to study intermolecular interactions in systems containing charged polyion (polyacrylate, PA(-)), charged surfactant (C(16)TA(+)) and nonionic surfactant (C(12)E(5) or C(12)E(8)). To achieve this we have created four different phase diagrams using two different so-called complex salts, C(16)TAPA(25) and C(16)TAPA(6000), both consisting of positively charged surfactant (C(16)TA(+)) with polyacrylate (PA(-)) as counterions (no simple salt). The difference between the salts is the length of the polyion (25 or 6000 monomers). Both are insoluble in water. The results revealed that decreasing polyion length and increasing the PEO chain length of the nonionic surfactant were important factors for increasing the solubility of the complex salt. We also found that the curvature effects are quite small at low water content when gradually exchanging C(12)E(8) for either one of the complex salts while there is a gradual change in curvature for the systems containing C(12)E(5). Another interesting observation was the possibility for relatively large amounts of complex salt to be incorporated into a V(1) (Ia3d, bicontinuous) phase in the C(12)E(8)-containing systems. This gives rise to several questions regarding arrangements and dynamics of the polyion in this phase. In the dilute regime several different liquid crystalline phases can coexist with a dilute liquid phase containing the nonionic surfactant. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1711290
- author
- Janiak, John
LU
; Piculell, Lennart
LU
; Olofsson, Gerd
LU
and Schillén, Karin
LU
- organization
- publishing date
- 2011
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Physical chemistry chemical physics : PCCP
- volume
- 13
- pages
- 3126 - 3138
- publisher
- Royal Society of Chemistry
- external identifiers
-
- wos:000287041700016
- pmid:20938517
- scopus:79951499366
- pmid:20938517
- ISSN
- 1463-9084
- DOI
- 10.1039/c0cp01031f
- language
- English
- LU publication?
- yes
- id
- 02d50ae9-d956-48ce-a73d-f3f81dfb4fe4 (old id 1711290)
- date added to LUP
- 2016-04-01 15:03:14
- date last changed
- 2022-01-28 03:54:05
@article{02d50ae9-d956-48ce-a73d-f3f81dfb4fe4,
abstract = {{The aim of this work was to study intermolecular interactions in systems containing charged polyion (polyacrylate, PA(-)), charged surfactant (C(16)TA(+)) and nonionic surfactant (C(12)E(5) or C(12)E(8)). To achieve this we have created four different phase diagrams using two different so-called complex salts, C(16)TAPA(25) and C(16)TAPA(6000), both consisting of positively charged surfactant (C(16)TA(+)) with polyacrylate (PA(-)) as counterions (no simple salt). The difference between the salts is the length of the polyion (25 or 6000 monomers). Both are insoluble in water. The results revealed that decreasing polyion length and increasing the PEO chain length of the nonionic surfactant were important factors for increasing the solubility of the complex salt. We also found that the curvature effects are quite small at low water content when gradually exchanging C(12)E(8) for either one of the complex salts while there is a gradual change in curvature for the systems containing C(12)E(5). Another interesting observation was the possibility for relatively large amounts of complex salt to be incorporated into a V(1) (Ia3d, bicontinuous) phase in the C(12)E(8)-containing systems. This gives rise to several questions regarding arrangements and dynamics of the polyion in this phase. In the dilute regime several different liquid crystalline phases can coexist with a dilute liquid phase containing the nonionic surfactant.}},
author = {{Janiak, John and Piculell, Lennart and Olofsson, Gerd and Schillén, Karin}},
issn = {{1463-9084}},
language = {{eng}},
pages = {{3126--3138}},
publisher = {{Royal Society of Chemistry}},
series = {{Physical chemistry chemical physics : PCCP}},
title = {{The aqueous phase behavior of polyion-surfactant ion complex salts mixed with nonionic surfactants.}},
url = {{http://dx.doi.org/10.1039/c0cp01031f}},
doi = {{10.1039/c0cp01031f}},
volume = {{13}},
year = {{2011}},
}