ASSOCIATION OF BRANCHED POLYETHYLENE IMINE WITH SURFACTANTS IN AQUEOUS SOLUTION

Química Nova

Ismael C. Bellettini¹  Renato Eising¹  Arlindo C. Felippe¹  Josiel B. Domingos¹  Edson Minatti¹  Vanderlei G. Machado¹ 

关键词: polymer-surfactant interactions;    pyrene fluorescence;    polyelectrolytes;   

DOI  :  10.5935/0100-4042.20150085

来源: SciELO

【 摘 要 】

Three polymer-surfactant systems comprised of branched polyethylene imine (PEI) with an anionic surfactant (sodium dodecylsulfate; SDS), a cationic surfactant (tetradecyltrimethylammonium bromide; TTAB), and a zwitterionic surfactant (N-tetradecyl-N,N-dimethyl-3-ammonio-1-propanesulfonate; SB3-14) were studied based on the properties of surface tension, pyrene fluorescence emission, dynamic light scattering, pH, and zeta potential measurements. The critical aggregation concentration (cac) and polymer saturation point (psp) were determined for all three systems. The effect of these surfactants on the physico-chemical characteristics (diameter and surface charge) of the complexes formed was determined. Polymer-surfactant interactions occurred in all of the systems studied, with the strongest interactions, electrostatic in nature, occurring in the SDS-PEI system. After the neutralization of the polymer charges with the addition of the surfactant, the hydrophobic effect started to control the interlacing of the polymer chains. For the PEI-TTAB system, a very dense film was formed at surfactant concentrations above 2.0 mmol L^-1. In this case, the bromide counter-ion interacted with both the positively-charged PEI and the head of the surfactant, which is responsible for the formation of double layer coordination complexes. For the system composed of PEI and the zwitterionic surfactant, less cooperative associations occurred in comparison with the other systems.

【 授权许可】

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