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Crown density

The total concentration of sugars in sap varies due to several factors. Variation between individual trees may be quite large due to differences in genetics, growth rate, and crown density. However, the ranking of any one tree relative to its neighbors tends to remain relatively constant both within a season and from season to season (Taylor, 1956). [Pg.111]

Forests collect more pollutants than do surrounding surfaces with lower vegetation. For example, the forest edge will disturb the vertical wind profde and induce air turbulence that will in turn increase the dry deposition. The deposition at the front is considerably higher compared to that in the open field (by a factor of between 5 and 20), and also to that within the forest (a factor of 2 to 4). The increased deposition affects the vitality of the trees at the edge. Forest structures (tree species, crown density, stem density) differ widely in terms of aerodynamic roughness and leaf area, and these factors will each influence deposition. [Pg.60]

One of the most important factors affecting Qsei [76, 78, 87] is graphite-anode exfoliation, as a result of intercalation of solvated lithium ions. Factors that are reported to decrease (9lR are increasing the EC content in organic carbonates or di-oxolane solutions [98, 991 addition of C02 [31, 87, 99] or crown ethers [8, 71, 78] and increasing the current density [73] (this also lowers <2SE [14] as a result of decrease in (2s P ) ... [Pg.436]

Interestingly, the energy difference is smallest for S7O which as a heterocycle forms a crown-shaped eight-membered ring similar to and isoelec-tronic with the well known 8 structure of 04a symmetry. The transformation of the heterocycle S7O into the homocyclic isomer 7=0 was studied by the molecular dynamics/density functional method but the unrealistically high barrier of 5 eV calculated for this transformation indicates that the system was far from equilibrium during most of the simulation [66]. [Pg.228]

When a membrane based on a derivative of azobis(benzo-15-crown-5) in contact with a solution of a primary cation is exposed to visible light, we assume that the iono-phore within the membrane phase is exclusively in the trans isomer and forms a 1 1 ionophore (I)-cation (M+) complex with a stability constant, trans. According to Eq. (10), the corresponding charge density at the membrane side of the interface, o is > can be expressed as... [Pg.459]

Pelletier and Reber315 present new luminescence and low-energy excitation spectra of Pd(SCN)42 in three different crystalline environments, K2Pd(SCN)4, [K(18-crown-6)]2Pd(SCN)4, and (2-diethylammonium A -(2,6-dimethylphcnyl)acetamide)2Pd(SCN)4, and analyze the vibronic structure of the luminescence spectra, their intensities, and lifetimes as a function of temperature. The spectroscopic results are compared to the HOMO and LUMO orbitals obtained from density functional calculations to qualitatively illustrate the importance of the bending modes in the vibronic structure of the luminescence spectra. [Pg.582]

Further considerations. It needs to be noted that the stoichiometry of a given crown-metal complex is not only influenced by ring size a range of other factors which include the charge density on the metal, the nature of the anion, and the relative strain energies of the crown in different conformations may all make a contribution. [Pg.98]

With a view to producing catalysts that can easily be removed from reaction products, typical phase-transfer catalysts such as onium salts, crown ethers, and cryptands have been immobilized on polymer supports. The use of such catalysts in liquid-liquid and liquid-solid two-phase systems has been described as triphase catalysis (Regen, 1975, 1977). Cinquini et al. (1976) have compared the activities of catalysts consisting of ligands bound to chloromethylated polystyrene cross-linked with 2 or 4% divinylbenzene and having different densities of catalytic sites ([126], [127], [ 132]—[ 135]) in the... [Pg.333]

Interestingly, the sulfur-linked bis-crown ligand [8] shows an unprecedented cathodic potential shift upon addition of K+ cations to the electrochemical solution (Table 3). It is believed to be a conformational process that causes the anomalous shift of the ferrocene/ferrocenium redox couple and not a through-space or through-bond interaction, as these effects would produce the expected anodic potential shift of the ferrocene redox couple. The origin of the effect may be a redirection of the lone pairs of the sulfur donor atoms towards the iron centre upon complexation. This would increase the electron density... [Pg.13]

In coronal caries, the enamel of the tooth crown is affected. With lasting caries, the lesion deepens and acquires a conical shape. In polarized light microscopy, zones with different mineral densities can be distinguished, such as the lesion body and the mineralized surface layer... [Pg.9]

Thermodynamically stable sulfur forms deep yellow, nonodorous orthorhombic crystals with a space group Fddd-D, containing 16 molecules, i.e., 128 atoms in the unit cell. It has a density of 2.069 gm/cm and is well soluble in CS2. Its molecular unit is Sg, cyclooctasulfur, a crown-shaped molecule with a symmetry of i>4d. The pale flowers of sulfur, prepared by alchemist by distillation, are insoluble in CS2, and the structure is not yet fully understood. Another form, plastic sulfur, is obtained by melting sulfur to about 180°C, where it forms as highly... [Pg.287]


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See also in sourсe #XX -- [ Pg.56 ]




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