Polar and nonpolar surfaces

Many biomolecules are amphipathic proteins, pigments, certain vitamins, and the sterols and phospholipids of membranes all have polar and nonpolar surface regions. Structures composed of these molecules are stabilized by hydrophobic interactions among the non-... 

Healy et al. (134) studied experimentally the heats of adsorption of many polar and nonpolar gases on polar and nonpolar surfaces by means of their heats of immersion. It was found that the heat of immersion of rutile on a series of straight-chain compounds was a linear function of the dipole moment of the wetting liquid. In a later article (135)- this work was extended and it is shown that nearly the entire heat effect on immersion of the clean solid surface is due to adsorption of molecules in the first layer. From the slope of the line, giving the values found for the net heat of adsorption as a function of the dipole moments, the average field strength, F, of rutile can be found by means of Eq. (22). The experimental value found by these investigators is... 

The adsorption of nonionic surfactants on polar and nonpolar surfaces also exhibits various features, depending on the nature of the surfactant and the substrate. Three types of isotherms may be distinguished, as illustrated in Fig. 7. These isotherms can be accounted for by the different surfactant orientations and their association at the solid/liquid interface as illustrated in Fig. 8. Again, bilayers, hemimicelles, and micelles can be identified on various substrates. 

Determination of surface atom density on nanocrystals can be difficult, and imprecise, especially for very small particles that cannot be easily characterized microscopically. Nevertheless, reasonable accuracy can be obtained by using theoretical calculations informed by empirical data. In this work, the CdTe nanocrystals that were prepared (2.5-6 nm diameter) were found to be in the zinc blende crystal structure, allowing the use of the bulk density and interplanar distances of zinc blende CdTe in these calculations. It is likely that a variety of crystalline facets are exposed on individual nanocrystals, each with a range of planar densities of atoms. It is also likely that there is a distribution of different facets exposed across an assembly of nanocrystals. Therefore, one may obtain an effective average number of surface atoms per nanocrystal by averaging the surface densities of commonly exposed facets in zinc blende nanocrystals over the calculated surface area of the nanocrystal. In this work we chose to use the commonly observed (Iff), (100), and (110) zinc blende planes, which are representative of the lattice structure, with both polar and nonpolar surfaces. For this calculation, we defined a surface atom as an atom (either Cd or Te ) located on a nanocrystal facet with one or more unpassivated orbitals. Some facets, such as Cd -terminated 111 faces, have closely underlying Te atoms that are less than 1 A beneath the surface plane. These atoms reside in the voids between Cd atoms, and thus are likely to be sterically accessible from the surface, but because they are completely passivated, they were not included in this definition. 

Geometrical 3D structure of molecule (molecular volume, solvent accessible surface area, polar and nonpolar surface area)... 

In dishwashing, one must consider soil and surfactant adsorption to both polar and nonpolar surfaces. Metals (aluminum, stainless steel, carbon steel, cast iron, silver, and tin), siliceous surfaces (china, glass, and pottery), and organics (polyethylene, polypropylene, polyethylene terephthalate (PET), polytetrafluoroethylene (PTFE), and wood) present a wide variety of surface characteristics. They span the range of high interfacial free energy (metals and many ceramics) to low interfacial free energy (hydrocarbon polymers) surfaces [27,28],... 

An average residue buries about half of its potential accessible surface ( 80A ) in going from an extended conformation to an a-helix or two stranded P-sheet. On folding, both polar and nonpolar surfaces are reduced by a similar amount, approximately three-quarters. 

Surfactants are molecules that have both hydrophilic and hydrophobic sections that impart partial affinity toward both polar and nonpolar surfaces. The hydrophobic section of surfactant molecules consists of nonpolar moieties such as repeating carbon-hydrogen (CHj) units or carbon-fluorine (CFj) units. The hydrophilic sections of surfactant molecules contain ionic functional groups such as ammonium (NH4+) or carboxylate (C02"), or they consist of nonionic polar groups such as the hydroxyl portion of alcohol molecules. Thus, surfactants are at least partially soluble in polar liquids such as water as well as nonpolar media such as hexane. 

Subsequent SFA force measurements were taken between mica surfaces coated in a variety of surfactant monolayers in symmetric and asymmetric organic liquids. These measurements showed oscillatory force profiles between molecularly smooth polar and nonpolar surfaces in symmetric liquids only, indicating that the oscillatory forces in these cases were due to geometric packing of the molecules on the approach of the surfaces a summary of these results is shown in Fig. 1.7. 

The HVPE growth in H2 atmosphere at otherwise the same conditions on almost dislocation-free high-pressure substrates allows obtaining of almost dislocation-free HVPE material also for crystallization rates exceeding 100 gm h h Bulk crystals with thicknesses of about 1 mm have been grown in this way on n-type high-pressure substrates. Very low dislocation densities (<10 cm ) were observed by DSE of both (0001) polar and nonpolar surfaces of such crystals. 

The gradient model has been combined with two equations of state to successfully model the temperature dependence of the surface tension of polar and nonpolar fluids [54]. Widom and Tavan have modeled the surface tension of liquid He near the X transition with a modified van der Waals theory [55]. 

Hydrophobic bonds, or, more accurately, interactions, form because nonpolar side chains of amino acids and other nonpolar solutes prefer to cluster in a nonpolar environment rather than to intercalate in a polar solvent such as water. The forming of hydrophobic bonds minimizes the interaction of nonpolar residues with water and is therefore highly favorable. Such clustering is entropically driven. The side chains of the amino acids in the interior or core of the protein structure are almost exclusively hydrophobic. Polar amino acids are almost never found in the interior of a protein, but the protein surface may consist of both polar and nonpolar residues. 

The characteristic coiled-coil motifs found in proteins share an (abcdefg) heptad repeat of polar and nonpolar amino acid residues (Fig. 1). In this motif, positions a, d, e, and g are responsible for directing the dimer interface, whereas positions b, c, and f are exposed on the surfaces of coiled-coil assemblies. Positions a and d are usually occupied by hydrophobic residues responsible for interhelical hydrophobic interactions. Tailoring positions a, d, e, and g facilitates responsiveness to environmental conditions. Two or more a-helix peptides can self-assemble with one another and exclude hydrophobic regions from the aqueous environment [74]. Seven-helix coiled-coil geometries have also been demonstrated [75]. 

Methods of controlling surface behavior are to 1. create polar and nonpolar regions in the molecule thus producing a hydrophilic-lipophilic balance in the molecule, 2. charge the... 

Fontes tt al. [224,225 addressed the acid—base effects of the zeolites on enzymes in nonaqueous media by looking at how these materials affected the catalytic activity of cross-linked subtilisin microcrystals in supercritical fluids (C02, ethane) and in polar and nonpolar organic solvents (acetonitrile, hexane) at controlled water activity (aw). They were interested in how immobilization of subtilisin on zeolite could affected its ionization state and hence their catalytic performances. Transesterification activity of substilisin supported on NaA zeolite is improved up to 10-fold and 100-fold when performed under low aw values in supercritical-C02 and supercritical-ethane respectively. The increase is also observed when increasing the amount of zeolite due not only to a dehydrating effect but also to a cation exchange process between the surface proton of the enzyme and the sodium ions of the zeolite. The resulting basic form of the enzyme enhances the catalytic activity. In organic solvent the activity was even more enhanced than in sc-hexane, 10-fold and 20-fold for acetonitrile and hexane, respectively, probably due to a difference in the solubility of the acid byproduct. 

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