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Adsorption thermodynamics fractional surface coverage

A MC study of adsorption of living polymers [28] at hard walls has been carried out in a grand canonical ensemble for semiflexible o- 0 polymer chains and adsorbing interaction e < 0 at the walls of a box of size C. A number of thermodynamic quantities, such as internal energy (per lattice site) U, bulk density (f), surface coverage (the fraction of the wall that is directly covered with segments) 9, specific heat C = C /[k T ]) U ) — U) ), bulk isothermal compressibility... [Pg.532]

As this subject was covered in detail in Chapter 5, only a summary will be provided at this point. Surfactant adsorption is usually reversible, and hence thermodynamics can be applied for deriving the adsorption isotherm. Eor example, the adsorption of ionic surfactants onto hydrophobic surfaces may be represented by the Stern-Langmuir isotherm [13]. Consider a substrate containing sites (molm ) on which F molm of surfactant ions are adsorbed. The surface coverage 0 is (F/NJ and the fraction of uncovered surface is (1 — 0). The Stern-Langmuir... [Pg.139]

The Langmuir adsorption isotherm was developed by Irving Langmuir in 1916 from kinetic considerations to describe the dependence of the surface fractional coverage of an adsorbed gas on the pressure of the same gas above the adsorbent surface at a constant temperature. The Langmuir isotherm expression was re-derived thermodynamically by Volmer and statistically mechanically by Fowler. In his original treatment, Langmuir made several assumptions for his model ... [Pg.297]


See other pages where Adsorption thermodynamics fractional surface coverage is mentioned: [Pg.338]    [Pg.58]    [Pg.211]    [Pg.248]    [Pg.159]    [Pg.304]    [Pg.465]    [Pg.32]    [Pg.670]    [Pg.119]    [Pg.183]   
See also in sourсe #XX -- [ Pg.123 ]




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