Properties of aqueous solutions of hydrophobically modified polyethylene imines in the absence and presence of sodium dodecylsulfate

[Display omitted] ► Polyethylene imines with pendant alkyl groups show pronounced surface activity. ► Polyelectrolyte hydrophobicity can be tuned by increasing the alkyl chain length. ► Hydrophobic polyethylene imines interact strongly with sodium dodecylsulfate (SDS). ► At high c(SDS), polyethylene...

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Veröffentlicht in:Journal of colloid and interface science 2012-03, Vol.370 (1), p.94-101
Hauptverfasser: Bellettini, Ismael C., Nandi, Leandro G., Eising, Renato, Domingos, Josiel B., Machado, Vanderlei G., Minatti, Edson
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Sprache:eng
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Zusammenfassung:[Display omitted] ► Polyethylene imines with pendant alkyl groups show pronounced surface activity. ► Polyelectrolyte hydrophobicity can be tuned by increasing the alkyl chain length. ► Hydrophobic polyethylene imines interact strongly with sodium dodecylsulfate (SDS). ► At high c(SDS), polyethylene imines form aggregated and random-coil polymer chains. Four modified hyperbranched polyethylene imines (PEIs) were synthesized by means of the alkylation of PEI. SAXS, viscosity, surface tension, and pyrene fluorescence emission were then used as techniques to examine the conformation and aggregation of the modified PEIs in aqueous solution, in the absence and presence of sodium dodecylsulfate (SDS). Analysis of the SAXS data showed that the radius of gyration decreases with an increase in the alkyl chain length of the polymer, while the viscosity data indicated a decrease in the intrinsic viscosity under the same conditions. The nonmodified PEI was not surface active, while the hydrophobically modified samples showed pronounced surface activity and the presence of hydrophobic domains. On addition of SDS, the onset of the formation of polymer–surfactant complexes was determined, indicating a decrease in the critical aggregate concentration with an increase in the alkyl chain length of the polymer backbone.
ISSN:0021-9797
1095-7103
DOI:10.1016/j.jcis.2011.12.049