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Chemical potential surface energy

The surface chemical and morphological characteristics of inorganic sorbents such as silicas, aluminas, talc, micas define both their chemical and physical adsorption potentials (surface energy). But the existence of mineral and organic surface pollutants will indeed strongly influence those properties. [Pg.479]

Note that H20(l) is formed in the low-temperature fuel cells when temperature is below 100°C and pressure is 1 bar. If temperature is above I00°C and pressure is ambient, H20(g) is formed instead of H20(I). A mixture of H20(g) and H20(l) can also be formed when the temperature is around 100°C. In these half-reactions, Pt/C represents carbon support slurry with particles of about a micron in size with Pt nanoparticles deposited on the carbon. Nanoparticles are used to increase the surface area of the electrode. In the H+(m) symbol, m represents a proton conductive membrane. While the properties of H+(m) and H+(aq) might be different, this fact is usually ignored in most of the studies because the chemical potential (Gibbs energy of formation) of proton in membrane is not known. [Pg.163]

Energy balances can be more difficult because energy and work can take so many different forms. Internal, kinetic, potential, chemical, and surface energies are all important. Work can involve forces of pressure, gravity, and electrical potential. As a result, a truly general energy balance is extraordinarily complicated, so much so that it is difficult to use. [Pg.575]

Ultimately, the surface energy is used to produce a cohesive body during sintering. As such, surface energy, which is also referred to as surface tension, y, is obviously very important in ceramic powder processing. Surface tension causes liquids to fonn spherical drops, and allows solids to preferentially adsorb atoms to lower tire free energy of tire system. Also, surface tension creates pressure differences and chemical potential differences across curved surfaces tlrat cause matter to move. [Pg.2761]

Reality suggests that a quantum dynamics rather than classical dynamics computation on the surface would be desirable, but much of chemistry is expected to be explainable with classical mechanics only, having derived a potential energy surface with quantum mechanics. This is because we are now only interested in the motion of atoms rather than electrons. Since atoms are much heavier than electrons it is possible to treat their motion classically. Quantum scattering approaches for small systems are available now, but most chemical phenomena is still treated by a classical approach. A chemical reaction or interaction is a classical trajectory on a potential surface. Such treatments leave out phenomena such as tunneling but are still the state of the art in much of computational chemistry. [Pg.310]

AB diblock copolymers in the presence of a selective surface can form an adsorbed layer, which is a planar form of aggregation or self-assembly. This is very useful in the manipulation of the surface properties of solid surfaces, especially those that are employed in liquid media. Several situations have been studied both theoretically and experimentally, among them the case of a selective surface but a nonselective solvent [75] which results in swelling of both the anchor and the buoy layers. However, we concentrate on the situation most closely related to the micelle conditions just discussed, namely, adsorption from a selective solvent. Our theoretical discussion is adapted and abbreviated from that of Marques et al. [76], who considered many features not discussed here. They began their analysis from the grand canonical free energy of a block copolymer layer in equilibrium with a reservoir containing soluble block copolymer at chemical potential peK. They also considered the possible effects of micellization in solution on the adsorption process [61]. We assume in this presentation that the anchor layer is in a solvent-free, melt state above Tg. The anchor layer is assumed to be thin and smooth, with a sharp interface between it and the solvent swollen buoy layer. [Pg.50]


See other pages where Chemical potential surface energy is mentioned: [Pg.1120]    [Pg.1120]    [Pg.524]    [Pg.148]    [Pg.84]    [Pg.194]    [Pg.96]    [Pg.93]    [Pg.2456]    [Pg.2771]    [Pg.2772]    [Pg.220]    [Pg.339]    [Pg.477]    [Pg.310]    [Pg.301]    [Pg.328]    [Pg.330]    [Pg.128]    [Pg.200]    [Pg.249]    [Pg.373]    [Pg.122]    [Pg.536]    [Pg.161]    [Pg.247]    [Pg.252]    [Pg.277]    [Pg.281]    [Pg.283]    [Pg.365]    [Pg.485]    [Pg.668]    [Pg.768]    [Pg.866]    [Pg.121]    [Pg.88]    [Pg.339]    [Pg.1094]    [Pg.1130]    [Pg.1131]    [Pg.1132]    [Pg.1160]    [Pg.103]    [Pg.46]    [Pg.31]   
See also in sourсe #XX -- [ Pg.423 , Pg.423 ]




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