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017 _ _ |a This version is available at the following Publisher URL: http://jcp.aip.org
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024 7 _ |a 2128/1455
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037 _ _ |a PreJuSER-53859
041 _ _ |a eng
082 _ _ |a 540
084 _ _ |2 WoS
|a Physics, Atomic, Molecular & Chemical
100 1 _ |a Tartaglino, U.
|b 0
|0 P:(DE-HGF)0
245 _ _ |a Impact of molecular structure on the lubricant squeeze-out between curved surfaces with long range elasticity
260 _ _ |a Melville, NY
|b American Institute of Physics
|c 2006
300 _ _ |a 014704
336 7 _ |a Journal Article
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440 _ 0 |a Journal of Chemical Physics
|x 0021-9606
|0 3145
|v 125
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a The properties of butane (C4H10) lubricants confined between two approaching solids are investigated by a model that accounts for the curvature and elastic properties of the solid surfaces. We consider the linear n-butane and the branched isobutane. For the linear molecule, well defined molecular layers develop in the lubricant film when the width is of the order of a few atomic diameters. The branched isobutane forms more disordered structures which permit it to stay liquidlike at smaller surface separations. During squeezing the solvation forces show oscillations corresponding to the width of a molecule. At low speeds (<0.1 ms) the last layers of isobutane are squeezed out before those of n-butane. Since the (interfacial) squeezing velocity in most practical applications is very low when the lubricant layer has molecular thickness, one expects n-butane to be a better boundary lubricant than isobutane. With n-butane possessing a slightly lower viscosity at high pressures, our result refutes the view that squeeze-out should be harder for higher viscosities; on the other hand our results are consistent with wear experiments in which n-butane were shown to protect steel surfaces better than isobutane.
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700 1 _ |a Sivebaek, I. M.
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700 1 _ |a Persson, B. N. J.
|b 2
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|0 P:(DE-Juel1)130885
700 1 _ |a Tosatti, E.
|b 3
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773 _ _ |a 10.1063/1.2210008
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856 7 _ |u http://dx.doi.org/10.1063/1.2210008
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