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Polarization surface charge

Despite the simple form of Equation (1.83), the detailed formulation of an extended Lagrangian for CPCM is not a straightforward matter and its implementation remains challenging from the technical point of view. Nevertheless, is has been attempted with some success by Senn and co-workers [31] for the COSMO-ASC model in the framework of the Car-Parrinello ab initio MD method. They were able to ensure the continuity of the cavity discretization with respect to the atomic positions, but they stopped short of providing a truly continuous description of the polarization surface charge as suggested,... [Pg.69]

Fig. 3.12. Edge wetting angle of pentaplast coatings by glycerin as a function of the coating s polarization surface charge... Fig. 3.12. Edge wetting angle of pentaplast coatings by glycerin as a function of the coating s polarization surface charge...
In particular, in polar solvents, the surface of a colloidal particle tends to be charged. As will be discussed in section C2.6.4.2, this has a large influence on particle interactions. A few key concepts are introduced here. For more details, see [32] (eh 13), [33] (eh 7), [36] (eh 4) and [34] (eh 12). The presence of these surface charges gives rise to a number of electrokinetic phenomena, in particular electrophoresis. [Pg.2674]

By using an effective, distance-dependent dielectric constant, the ability of bulk water to reduce electrostatic interactions can be mimicked without the presence of explicit solvent molecules. One disadvantage of aU vacuum simulations, corrected for shielding effects or not, is the fact that they cannot account for the ability of water molecules to form hydrogen bonds with charged and polar surface residues of a protein. As a result, adjacent polar side chains interact with each other and not with the solvent, thus introducing additional errors. [Pg.364]

The MEP at the molecular surface has been used for many QSAR and QSPR applications. Quantum mechanically calculated MEPs are more detailed and accurate at the important areas of the surface than those derived from net atomic charges and are therefore usually preferable [Ij. However, any of the techniques based on MEPs calculated from net atomic charges can be used for full quantum mechanical calculations, and vice versa. The best-known descriptors based on the statistics of the MEP at the molecular surface are those introduced by Murray and Politzer [44]. These were originally formulated for DFT calculations using an isodensity surface. They have also been used very extensively with semi-empirical MO techniques and solvent-accessible surfaces [1, 2]. The charged polar surface area (CPSA) descriptors proposed by Stanton and Jurs [45] are also based on charges derived from semi-empirical MO calculations. [Pg.393]

Water-soluble globular proteins usually have an interior composed almost entirely of non polar, hydrophobic amino acids such as phenylalanine, tryptophan, valine and leucine witl polar and charged amino acids such as lysine and arginine located on the surface of thi molecule. This packing of hydrophobic residues is a consequence of the hydrophobic effeci which is the most important factor that contributes to protein stability. The molecula basis for the hydrophobic effect continues to be the subject of some debate but is general considered to be entropic in origin. Moreover, it is the entropy change of the solvent that i... [Pg.531]

Monovalent cations are good deflocculants for clay—water sHps and produce deflocculation by a cation exchange process, eg, Na" for Ca ". Low molecular weight polymer electrolytes and polyelectrolytes such as ammonium salts (see Ammonium compounds) are also good deflocculants for polar Hquids. Acids and bases can be used to control pH, surface charge, and the interparticle forces in most oxide ceramic—water suspensions. [Pg.307]

Pyroelectrics. Pyroelectric ceramics are materials that possess a uoique polar axis and are spontaneously polarized ia the abseace of an electric field. Pyroelectrics are also a subset of piezoelectric materials. Ten of the 20 crystal classes of materials that display the piezoelectric effect also possess a unique polar axis, and thus exhibit pyroelectricity. In addition to the iaduced charge resultiag from the direct pyroelectric effect, a change ia temperature also iaduces a surface charge (polarizatioa) from the piezoelectric aature of the material, and the strain resultiag from thermal expansioa. [Pg.343]

The electrostatic behavior of intrinsically nonconductive substances, such as most pure thermoplastics and saturated hydrocarbons, is generally governed by chemical species regarded as trace contaminants. These are components that are not deliberately added and which may be present at less than detectable concentrations. Since charge separation occurs at interfaces, both the magnitude and polarity of charge transfer can be determined by contaminants that are surface active. This is particularly important for nonconductive liquids, where the electrostatic behavior can be governed by contaminants present at much less than 1 ppm (2-1.3). [Pg.9]

A particular problem is determination of surface charge density on a nonconductor which has charges of opposite polarity on either side (bipolar... [Pg.53]

Based on the preceding local history, the boundaries at the elastic and plastic wave fronts are characterized by bound surface charges of equal magnitude and opposite sign to the initial piezoelectric states. The polarization in the region behind the plastic wave E3, has magnitude equal to the change... [Pg.100]

FIG. 11 Cation (full), anion (dashed), and oxygen (dotted) radial density distributions in polar pores with embedded surface charges. Top NaCl solution bottom KCl solution. [Pg.371]

In the polar pores, the diffusion coefficient of all ions is strongly reduced relative to the bulk values. No counterion dependence is observed for the SDC of CP. A more detailed analysis shows that the ion SDC depends on the ion s relative position in the pore [174]. In the case of the K ion, this dependence is particularly strong. K ions forming contact pairs with the surface charges are almost completely immobilized on the time scale of the simulations. The few remaining ions in the center of the pore are almost unaffected by the (screened) surface charges. The fact that most of the K ions form contact pairs substantially reduces the average value of the normalized K SDC to 0.2. The behavior of CP is similar to that of K. The SDC of sodium ions, which... [Pg.372]

FIGURE 6.24 (a) The alpha helix consisting of residues 153-166 (red) in flavodoxin from Anahaena is a surface helix and is amphipathic. (b) The two helices (yellow and blue) in the interior of the citrate synthase dimer (residues 260-270 in each monomer) are mostly hydrophobic, (c) The exposed helix (residues 74-87—red) of calmodulin is entirely accessible to solvent and consists mainly of polar and charged residues. [Pg.180]

In globular protein structures, it is common for one face of an a-helix to be exposed to the water solvent, with the other face toward the hydrophobic interior of the protein. The outward face of such an amphiphilic helix consists mainly of polar and charged residues, whereas the inward face contains mostly nonpolar, hydrophobic residues. A good example of such a surface helix is that of residues 153 to 166 of flavodoxin from Anabaena (Figure 6.24). Note that the helical wheel presentation of this helix readily shows that one face contains four hydrophobic residues and that the other is almost entirely polar and charged. [Pg.181]


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See also in sourсe #XX -- [ Pg.269 ]




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Charged surfaces

Polar surface

Polarity charge

Polarization charge

Surface charge

Surface charges surfaces

Surface charging

Surface polarization

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