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Rhamnolipids biosurfactants as potential modulators of phase and partitioning behavior in micellar systems of aliphatic alcohol ethoxylate surfactants

Haidar, Carla Nahir et al · Elsevier Science · 2020

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The impact of rhamnolipids (RL) biosurfactants presence on the phase-separation equilibrium, micellar properties and partitioning behavior of systems containing the aliphatic non-ionic surfactant Tergitol 15-S-7 (Tg7) was studied in this work. The cloud points of Tg7 solutions (1- 10% w/w) in water and sodium citrate (NaCit) buffers pH 7.00 were increased after the RL addition (0.25% w/w) while they were decreased in NaCit pH 5.00. The most marked changes were verified for those systems with low Tg7 concentrations (< 4% w/w) and high RL/Tg7 mass ratio (>7°). As expected, the zeta potential (ζ) of non-ionic Tg7 systems was close to zero; however, ζ became clearly negative (≅ −20 mV) in NaCit pH 7.00 after the addition of RL. This finding suggested that RL, which is negatively charged at pH 7.00, self-incorporated into Tg7 micelles and conferred them its charge. Hydrodynamic diameter (Dh) was either increased (in citrate media) or decreased (in water) by the RL, depending on the changes caused in the critical packing parameter of mixed micelles. Interestingly, an exponential decay equation, useful for predictive purpose, was found to correlate the cloud point with the hydrodynamic diameter, thus evidencing the crucial role of micelle size/shape on the phase separation. The partitioning behavior of cibacron blue (CB) and malaquite green (MG), negatively and positively charged dyes respectively, in Tg7 aqueous micellar two-phase systems (AMTPS) was significantly affected by the RL 0.25% w/w. In AMTPS with pH 7.00, the RL induced opposite effects, either duplicating the partition coefficient of MG or reducing it to a half for CB. Attractive and repulsive electrostatic interactions between the negatively charged mixed micelles and the partitioned molecules would be responsible of these trends. These results demonstrate the role of RL as a modulator of partitioning behavior of charged molecules and its potential use to improve recoveries and selectivity in a purification protocol. Fil: Haidar, Carla Nahir. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Procesos Biotecnológicos y Químicos Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Procesos Biotecnológicos y Químicos Rosario; Argentina Fil: Martini, Georgina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Procesos Biotecnológicos y Químicos Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Procesos Biotecnológicos y Químicos Rosario; Argentina

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APA 7

Haidar, C. N. E. A. (2020). Rhamnolipids biosurfactants as potential modulators of phase and partitioning behavior in micellar systems of aliphatic alcohol ethoxylate surfactants. http://hdl.handle.net/11336/166742

MLA

Haidar, Carla Nahir et al. "Rhamnolipids biosurfactants as potential modulators of phase and partitioning behavior in micellar systems of aliphatic alcohol ethoxylate surfactants." 2020. http://hdl.handle.net/11336/166742.

Chicago

Haidar, Carla Nahir et al. 2020. "Rhamnolipids biosurfactants as potential modulators of phase and partitioning behavior in micellar systems of aliphatic alcohol ethoxylate surfactants.". http://hdl.handle.net/11336/166742.

Harvard

Haidar, C. N. E. A. 2020, Rhamnolipids biosurfactants as potential modulators of phase and partitioning behavior in micellar systems of aliphatic alcohol ethoxylate surfactants, Elsevier Science, available at: http://hdl.handle.net/11336/166742 [Accessed 8 Aug. 2026].

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Título
Rhamnolipids biosurfactants as potential modulators of phase and partitioning behavior in micellar systems of aliphatic alcohol ethoxylate surfactants
Autor / colaboradores
Haidar, Carla Nahir et al
Editora
Elsevier Science
Ano de publicação
2020
ISSN
0167-7322
ISSN
0167-7322
Idioma
Inglés

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