Adhesive transitions in Newton black films: A computer simulation study

被引:27
作者
Bresme, Fernando [1 ]
Chacon, Enrique [2 ,3 ]
Martinez, Hector [4 ]
Tarazona, Pedro [3 ,4 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England
[2] CSIC, Inst Ciencia Mat Madrid, E-28049 Madrid, Spain
[3] Univ Autonoma Madrid, Inst Ciencia Mat Nicolas Cabrera, E-28049 Madrid, Spain
[4] Univ Autonoma Madrid, Dept Fis Teor Mat Condensada, E-28049 Madrid, Spain
关键词
LIQUID-VAPOR INTERFACE; MOLECULAR-DYNAMICS; FOAM FILMS; DISJOINING PRESSURE; FORCE-FIELD; WATER; HYDRATION; DEPENDENCE; STABILITY; EMULSIONS;
D O I
10.1063/1.3596752
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report molecular dynamics simulations of Newton black films (NBFs), ultra thin films of aqueous solutions stabilized with two monolayers of ionic surfactants, sodium dodecyl sulfate. We show that at low water content conditions and areas per surfactant corresponding to experimental estimates in NBFs, homogeneous films undergo an adhesion "transition," which results in a very thin adhesive film coexisting with a thicker film. We identify the adhesive film with the equilibrium structure of the Newton black film. We provide here a direct microscopic view of the formation of these important structures, which have been observed in experimental studies of emulsions and foams. We also report a detailed investigation of the structural properties and interfacial fluctuation spectrum of the adhesive film. Our analysis relies on the definition of an "intrinsic surface," which is used to remove the averaging effect that the capillary waves have on the film properties. c 2011 American Institute of Physics. [doi:10.1063/1.3596752]
引用
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页数:12
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