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The understanding of molecular interactions that control phase separation in polymer/polymer aqueous two-phase systems (ATPS) has been a subject of debate up to this day. In light of this, we set out to investigate the molecular interactions occurring in ternary mixtures composed of polyethylene glycol (PEG600), polypropylene glycol (PPG400) and water. The ternary phase diagram was plotted at two temperatures (298 K and 323 K), revealing a transition from a type 0 to a type I diagram. Molecular dynamics (MD) simulations were performed to elucidate the polymer–polymer and polymer–water interactions occurring at different temperatures and water concentrations. COnductor-like Screening Model for Realistic Solvents (COSMO-RS) was used to assess the thermodynamic properties of the polymer–water binary mixtures and their correlation with ATPS formation. The MD simulations clearly demonstrate the effect of segregation/separation with increasing water content and temperature, highlighting a significant reduction in PPG–water interactions compared to PEG–water counterparts. Polymer–water interactions were identified as those controlling the phase separation mechanism, and the thermodynamic properties determined with COSMO-RS for the polymer–water binary systems further support this view. [ABSTRACT FROM AUTHOR]

Hypothesis: Semifluorinated alkanes amphiphiles spontaneously form highly monodispersed hemimicelles at the surface of water. The origin of the formation and complex structure of these surprising supramolecular aggregates were only recently clarified using molecular dynamics simulations (MD). The existence of a pit at the center of these aggregates made up of almost 3000 molecules was indeed reproduced by the MD simulations, but not understood., Method: A careful strategy of atomistic MD simulations comparing non-electrostatic force fields with force fields that include electrostatic forces, thus bearing an implicit or explicit dipole, allowed demonstrating the roles of dipolar interactions and interactions with the liquid subphase on the morphology of the aggregates., Findings: The simulation results clearly show that within the hemimicelles the strong molecular dipoles located at the CH 2 -CF 2 junctions tend to align, leading to a collective shift of the PFAA molecules relatively to each other. This shift is responsible for the curvature of the hemimicelles and originates the central pit, provided the possibility of deforming the surface of the water sub-phase. Comparisons with non-electrostatic force field results further contribute to understand the origin of the self-assembling process. The results directly connect for the first time a molecular property with a mesoscopic structural feature. Given the molecular simplicity of these "primitive" amphiphiles compared to the common hydrophilic/hydrophobic surfactants, the results contribute to understand self-assembly in general., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.)

Hypothesis: Aqueous solutions of mixtures of hydrogenated and perfluorinated ionic surfactants are known to display anomalous aggregation behavior due to the mutual phobicity between hydrogenated and perfluorinated chains. Despite all efforts, different experimental limitations prevented so far a definite interpretation of the existing experimental results: both intermicellar and intramicellar segregation remain acceptable possibilities., Method: The potential for segregation of mixtures of fluorinated and hydrogenated ionic surfactants in water was assessed using atomistic molecular dynamics simulations. Aqueous mixtures of hydrogenated and perfluorinated ionic surfactants were studied: mixtures of anionic surfactants (sodium dodecylsulfate (SDS) + sodium perfluoro-octanoate (SPFO)) and catanionic surfactants (decyltrimethylammonium bromide (DeTAB) + SPFO) were simulated., Findings: The mixture of anionic surfactants, SDS + SPFO, exhibits clear intramicellar segregation between fluorinated and hydrogenated chains, displaying hydrogenous-rich and fluorous-rich regions. Compartmentalized micelles are thus clearly formed. The simulation results also suggest the possibility of intermicellar segregation. Conversely, catanionic mixtures of DeTAB and SPFO in water solution assemble into a large oblate structure, containing all available molecules in the simulation box, resembling a double layer membrane or a vesicle wall. In this case mixing between fluorinated and hydrogenated surfactants is dictated by charge alternation., Competing Interests: Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Eduardo J. M. Filipe reports financial support was provided by Foundation for Science and Technology., (Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.)