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  • 1
    ISSN: 1573-2711
    Keywords: friction modifiers ; thin film lubrication ; nanorheology ; molecular tribology ; surface forces apparatus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Dilute solutions of two polar end‐functionalized linear alkanes (1‐hexadecylamine and palmitic acid), each dissolved in tetradecane, were confined between two mica surfaces and investigated using a surface forces apparatus modified to study shear nanorheology. These two solutions showed similar nanorheological properties that differed from those observed for pure n‐alkanes. In static measurements, a “hard wall”, rather than an oscillatory force, was observed as a function of film thickness. The polar alkane component formed a weakly adsorbed single layer at each mica surface, disrupting the layered structures found in neat n‐tetradecane. In dynamic experiments at low shear amplitude, the storage modulus G' exceeded the loss modulus G" at low frequencies; above some characteristic frequencies G' increased such that g' ≈ G", indicating significantly more energy loss through viscous modes at higher frequency. When the amplitude was varied at fixed frequency, no stick–slip was observed and the limiting value of the shear stress at high effective shear rate was an order of magnitude less than for unfunctionalized n‐alkanes at similar loads. Together, these results show that the addition of a small amount of polar alkane component, by disrupting the layered structures that would have been formed in the neat n‐alkane, is effective in suppressing static friction and reducing kinetic friction in the boundary lubrication regime.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 2429-2437 
    ISSN: 0887-6266
    Keywords: surface ; adsorption ; exchange ; FTIR-ATR ; histogram ; hydrogen-bond ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polarized infrared spectroscopy in attenuated total reflection was used to investigate the adsorption of PMMA (polymethylmethacrylate) onto PS (polystyrene) that was previously adsorbed onto oxidized silicon from dilute solution in carbon tetrachloride at 30°C. The carbonyl group of PMMA forms hydrogen bonds with surface silanol groups, giving segment-surface interaction energy of 4 kT as against 1 kT for PS (k is the Boltzmann constant, T the absolute temperature). The formation of hydrogen-bonding by PMMA was unaffected, in rate or amount, by preadsorbed PS, but a lesser total amount of PMMA adsorbed onto PS, resulting in a higher average bound fraction. The histogram of the mass adsorbed, attributable to subpopulations of chains with different bound fractions, was inferred by subtracting infrared spectra acquired at successive times. Whereas this histogram was broad and bimodal for adsorption onto bare surface, it was narrower and unimodal for adsorption onto preadsorbed PS. © 1995 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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