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Surface solvent

Film pressure is often measured directly by means of a film balance. The principle of the method involves the direct measurement of the horizontal force on a float separating the film from clean solvent surface. The film balance has been considerably refined since the crude model used by Langmuir and in many... [Pg.114]

These equations imply that A132 will exceed A12 if A33 is larger than A13 + A23. This effect, termed lyophobic bonding, occurs if the solvent-surface interaction is weaker than that between the solvent molecules. More interestingly, the dispersion interaction will be repulsive (A 132 < 0) when An and/or A23 are sufficiently large. Israelachvili [1] tabulates a number of Am values Awhw Ahwh 0-4X 10 erg, Apwp 1 x 10" erg, and Aqwq = O.SX -IO erg, where W, H, P, and Q denote water, hydrocarbon, polystyrene and quartz respectively. [Pg.240]

In section 8.2 we described the solvophobic effect, which theory leads us to expect is related to the solvent surface tension. Abraham et al. have developed a different measure of solvophobicity by relating the transfer free energy W)... [Pg.427]

Electron flow across the solute-solvent surface. [Pg.321]

Type Composition Character Average Pore Diameter (nm) Specific Specific Solvent Surface Pore Uptake Area Volurc. (g/g) of ( /g) (Ml/g) resin ... [Pg.399]

Recent experimental and theoretical studies on crystal growth, especially in the presence of tailor-made inhibitors, provide a link between macroscopic and microscopic chirality. We shall discuss these principles in some detail for chiral molecules. Furthermore, we shall examine whether it is indeed feasible today to establish the absolute configuration of a chiral crystal from an analysis of solvent-surface interactions. Since these analyses are based on understanding the interactions between a growing crystal and inhibitors present in solution, we shall first illustrate the general mechanism of this effect in various chiral and nonchiral systems. [Pg.11]

Some of the difficulties encountered in establishing the effect of solvent on crystal growth may be circumvented by focusing on polar crystals. This is because the difference in the rates of growth of opposite faces (hid) and (hkl) along a polar direction must arise primarily from differences in their solvent-surface interactions. Thus, one generally does not have to be concerned with faces other than the hemihedral ones in question. We illustrate below an approach to understanding solvent-surface interactions in the polar crystals of resorcinol (102). [Pg.68]

This approach to studying solvent-surface interactions is encouraging. We intend to apply it to the crystals of enantiomers in order to assign their absolute configurations and so close the circle started by Waser. [Pg.70]

GOSUB1310 INPUT"Input solvent surface tension" ... [Pg.73]

Table 1. Grafting of 3-aminopropyl groups on mesoporous silica obtained in polar-protic, polar-aprotic and non-polar solvents, surface area and catalytic efficiency for Nitroaldol condensation of 4-hydroxybenzaldehyde and nitromethane [22]. [Pg.92]

The coating (ingredients, solvents, surface chemistry, rheology, tackiness, etc.)... [Pg.264]

Specifications and Standards. Borax stability is an important property in adhesives, paper, and textile applications. Ollier emulsion properties tabulated by manufacturers include tolerance to specific solvents, surface tension, minimum film-forming temperature, dilution stability, freeze-thaw stability, percent soluble polymer, and molecular weight. [Pg.1678]

We shall now consider the solvent properties in a more quantitative way by applying the COSMOSPACE thermodynamics to an ensemble of solvent surface segments of composition... [Pg.96]

Molecules on a solvent surface (interface), in solution versus on solution. Thomas LL, Tirado-Rives J, Jorgenson WL, J Am Chem Soc, (2010), 132 3097... [Pg.557]

Keywords Interface Langmuir monolayer Adsorption process Spreading solvent Surface tension Surface isotherm Langmuir-Blodgett film Collapse pressure Amphiphilic polymer... [Pg.163]

Approximate solutions can be obtained by considering only the interaction between the solute charge and the reaction charge density generated in the solvent on solvent-surface boundary [58],... [Pg.516]


See other pages where Surface solvent is mentioned: [Pg.47]    [Pg.191]    [Pg.494]    [Pg.468]    [Pg.395]    [Pg.15]    [Pg.388]    [Pg.55]    [Pg.149]    [Pg.353]    [Pg.54]    [Pg.721]    [Pg.11]    [Pg.67]    [Pg.79]    [Pg.293]    [Pg.92]    [Pg.168]    [Pg.18]    [Pg.226]    [Pg.277]    [Pg.184]    [Pg.440]    [Pg.646]    [Pg.494]    [Pg.21]    [Pg.47]    [Pg.45]    [Pg.193]    [Pg.240]    [Pg.367]    [Pg.75]    [Pg.8]    [Pg.17]   
See also in sourсe #XX -- [ Pg.236 ]




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