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Aggregation of tetrameric acids in aqueous media studied by small-angle neutron scattering
[Display omitted] ► Determination of the aggregated structure of two tetrameric acids (sodium form). ► Determination of structure in aqueous media by SANS. ► Different structures formed in solution as function of the structure of the acids. This article presents the characterization of two self-asso...
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Published in: | Journal of colloid and interface science 2013-03, Vol.394, p.277-283 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
► Determination of the aggregated structure of two tetrameric acids (sodium form). ► Determination of structure in aqueous media by SANS. ► Different structures formed in solution as function of the structure of the acids.
This article presents the characterization of two self-associated structures, a C80-tetraacid (also known as ARN), which is an aliphatic molecule present in crude oil and responsible for the formation of deposits, and BP-10, a molecule designed to model the properties of the C80-tetraacid. These molecules have four carboxylic functions at the end of four interconnected hydrocarbon chains and can be dissolved in aqueous solution and in basic media. In this paper we have used small-angle neutron scattering (SANS) as the main method to study the tetrameric acids in solution.
SANS measurements show that the two molecules (in sodium form) exhibit very different types of aggregation properties in aqueous solution. More specifically, Na4BP-10 forms nanometer-sized micelles with an aggregation number close to 5 (at concentrations above the critical micellar concentration) in both 20mM NaCl and 0.9wt.% 1-butanol media. On the contrary fully ionised C80-TA forms very large structures in pure D2O and NaCl 20mM, so large that their exact dimensions could not be determined by SANS. |
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ISSN: | 0021-9797 1095-7103 |
DOI: | 10.1016/j.jcis.2012.12.012 |