Modification of deeply buried hydrophobic interfaces by ionic surfactants
Author(s) -
L. Tamam,
Diego Pontoni,
Zvi Sapir,
Shai Yefet,
Eli Sloutskin,
B. M. Ocko,
H. Reichert,
Moshe Deutsch
Publication year - 2011
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1014100108
Subject(s) - monolayer , alkane , pulmonary surfactant , phase diagram , ionic bonding , molecule , phase transition , phase (matter) , chemistry , chemical engineering , materials science , crystallography , chemical physics , organic chemistry , thermodynamics , hydrocarbon , nanotechnology , ion , engineering , biochemistry , physics
Hydrophobicity, the spontaneous segregation of oil and water, can be modified by surfactants. The way this modification occurs is studied at the oil-water interface for a range of alkanes and two ionic surfactants. A liquid interfacial monolayer, consisting of a mixture of alkane molecules and surfactant tails, is found. Upon cooling, it freezes at T(s), well above the alkane's bulk freezing temperature, T(b). The monolayer's phase diagram, derived by surface tensiometry, is accounted for by a mixtures-based theory. The monolayer's structure is measured by high-energy X-ray reflectivity above and below T(s). A solid-solid transition in the frozen monolayer, occurring approximately 3 °C below T(s), is discovered and tentatively suggested to be a rotator-to-crystal transition.
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