Adsorption organic species

Hydrophilic and Hydrophobic Surfaces. Water is a small, highly polar molecular and it is therefore strongly adsorbed on a polar surface as a result of the large contribution from the electrostatic forces. Polar adsorbents such as most zeoHtes, siUca gel, or activated alumina therefore adsorb water more strongly than they adsorb organic species, and, as a result, such adsorbents are commonly called hydrophilic. In contrast, on a nonpolar surface where there is no electrostatic interaction water is held only very weakly and is easily displaced by organics. Such adsorbents, which are the only practical choice for adsorption of organics from aqueous solutions, are termed hydrophobic. 

The reaction shown above for the steam reforming of methatie led to die formation of a mixture of CO and H2, die so-called synthesis gas. The mixture was given this name since it can be used for the preparation of a large number of organic species with the use of an appropriate catalyst. The simplest example of this is the coupling reaction in which medrane is converted to ethane. The process occurs by the dissociative adsorption of methane on the catalyst, followed by the coupling of two methyl radicals to form ethane, which is then desorbed into the gas phase. 

Breiter, M. W. Adsorption of Organic Species on Platinum Metal Electrodes 10... 

Many organic species are adsorbed on platinum at potentials ranging from approximately 0.1 to 0.7 V (RHE). At more positive potentials they desorb because of oxidation or of displacement from the surface by adsorbing oxygen. The extent of adsorption of the organic substances can be considerable, and they can take up as many as 70% of the surface sites. 

The synergistic elfect seen in Pt-Rn alloys has aronsed great interest, since it opened perspectives for their nse in efficient methanol fnel cells. Many studies were performed to elucidate the origins of this effect. Some workers believe that it is due to changes in the electron strnctnre of platinnm npon alloy formation with ruthenium. A popular interpretation is the bifunctional mechanism, according to which the organic species are preferentially chemisorbed on platinnm sites while the ruthenium sites facilitate the adsorption of the species needed for oxidation of the orgaiuc species. 

The creation of additional sites with an enhanced adsorption of active forms of the oxygen-containing species involved in the slow oxidation step of the organic species chemisorbed on the platinnm snrface (bifnnctional mechanism of catalytic action) ... 

Gomez-Sainero et al. (11) reported X-ray photoelectron spectroscopy results on their Pd/C catalysts prepared by an incipient wetness method. XPS showed that Pd° (metallic) and Pdn+ (electron-deficient) species are present on the catalyst surface and the properties depend on the reduction temperature and nature of the palladium precursor. With this understanding of the dual sites nature of Pd, it is believed that organic species S and A are chemisorbed on to Pdn+ (SI) and H2 is chemisorbed dissociatively on to Pd°(S2) in a noncompetitive manner. In the catalytic cycle, quasi-equilibrium ( ) was assumed for adsorption of reactants, SM and hydrogen in liquid phase and the product A (12). Applying Horiuti s concept of rate determining step (13,14), the surface reaction between the adsorbed SM on site SI and adsorbed hydrogen on S2 is the key step in the rate equation. 

Adsorption of Organic Species on Uncalcined and Calcined LDHs. 205... 

Mordand MM (1970) Clay-organic complexes and interactions. Adv Agron 22 75-117 Mordamd MM (1986) Mechanism of adsorption of nonhumic organic species by clays. In Huang PM, Schnitzer M (eds) Interaction of soil minerals with natural organics and microbes. Soil Sci Soc Amer, Madison, Wisconsin, pp 59-76... 

The study of the adsorption phenomena of ions and organic species on nickel electrodes may contribute to a better understanding of the electrode processes occurring at the nickel/electrolyte interface. 

Fig. 6.117. Adsorption isotherms for various organic species on platinum in 0.01 N HCI solution, obtained with the radiotracer technique valeric acid (a), butanol ( ), benzoic acid (a), naphtoic acid ( ), naphtol (O). All the data are taken at the maximum adsorption potential. (Reprinted from J. Jeng, dissertation, Texas A M University, 1991.)...

Derivatization and absorption are being used for collection of polar and reactive organic species that do not behave well when collected by the whole-air, cryogenic, or adsorption techniques. 

The earliest NMR studies of oxide surfaces (362-364) involved wide-line proton NMR of adsorbed organic species. For example, Petrakis and Kiviat (363), who studied the adsorption of pyridine and thiophene on molybdena-modified alumina, found that chemisorbed and physisorbed species can be readily distinguished. When physically adsorbed, both compounds exhibited liquid-like NMR behavior with high molecular mobility even at low temperatures. Chemisorbed pyridine was much more rigidly held with essentially only a rotation about the C2 molecular axis persisting to - 130°C. Pyridine was sorbed both physically and chemically, and pretreatment of the surface was not particularly significant in this respect. By contrast, thiophene was physisorbed only on surfaces previously reduced with hydrogen, and underwent a reaction on calcined but unreduced surfaces. 

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