Attractive hydrophobic potential

The slight compression noted in the torsions above is primarily due to the attractive hydrophobic forces that favor compaction. In both models, this force is balanced by the torsional potential that favors extended conformations. Significant differences exist,... 

Hydrophobic interactions are rather typical for organic colloidal particles (e.g., the particles of latex) dissolved in water. They produce a net attractive contribution. The hydrophobic potential for two equal spherical colloidal particles is expressed as [13] ... 

Sorption of nonionic, nonpolar hydrophobic compounds occurs by weak attractive interactions such as van der Waals forces. Net attraction is the result of dispersion forces the strength of these weak forces is about 4 to 8 kj/mol ( 1 2 kcal/mol). Electrostatic interactions can also be important, especially when a molecule is polar in nature. Attraction potential can develop between polar molecules and the heterogeneous sod surface that has ionic and polar sites, resulting in stronger sorption. 

The exponential dependence is indicative of hydrophobic attractive forces between the glycerol-air interface and the glycerol-mica interface. This potential gives a negative disjoining pressnre of 1 atm at z close to 0. The strength of the force appears to be 100 times lower than that typical for water between hydrophobic surfaces [6]. 

Here we present and discuss an example calculation to make some of the concepts discussed above more definite. We treat a model for methane (CH4) solute at infinite dilution in liquid under conventional conditions. This model would be of interest to conceptual issues of hydrophobic effects, and general hydration effects in molecular biosciences [1,9], but the specific calculation here serves only as an illustration of these methods. An important element of this method is that nothing depends restric-tively on the representation of the mechanical potential energy function. In contrast, the problem of methane dissolved in liquid water would typically be treated from the perspective of the van der Waals model of liquids, adopting a reference system characterized by the pairwise-additive repulsive forces between the methane and water molecules, and then correcting for methane-water molecule attractive interactions. In the present circumstance this should be satisfactory in fact. Nevertheless, the question frequently arises whether the attractive interactions substantially affect the statistical problems [60-62], and the present methods avoid such a limitation. 

This paper has provided the reader with an introduction to a class of polymers that show great potential as reverse osmosis membrane materials — poly(aryl ethers). Resistance to degradation and hydrolysis as well as resistance to stress Induced creep make membranes of these polymers particularly attractive. It has been demonstrated that through sulfonation the hydrophilic/hydrophobic, flux/separation, and structural stability characteristics of these membranes can be altered to suit the specific application. It has been Illustrated that the nature of the counter-ion of the sulfonation plays a role in determining performance characteristics. In the preliminary studies reported here, one particular poly(aryl ether) has been studied — the sulfonated derivative of Blsphenol A - polysulfone. This polymer was selected to serve as a model for the development of experimental techniques as well as to permit the investigation of variables... 

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