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Acid/base attraction forces

Fillers and additives may interact by covalent bonding van der Waals forces ionic forces hydrogen bonding acid-base attraction forces absorption. [Pg.89]

According to this equation, the solubility of the polymer molecules in a liquid will increase with increasing positive values of AC n. as the polymer molecules will increasingly repel each other and thereby tend to disperse. If AG n < 0. solubility decreases due to molecular attraction. In most pharmaceutical systems, molecular contributions to AG2T2 will be from apolar Lifshitz-van der Waals (AG212) forces and from Lewis acid/base (AGm) forces. Hence, AG2T2 is represented by... [Pg.603]

Schreiber and Ouhlal [98] annealed a number of polymer pairs in contact for up to 72 h at 60-160°C and found substantial increases in adhesive strength for polypropy-lene/linear low density polyethylene and polystyrene/PVC, but not with polystyrene/ PMMA and PVC/polyvinylidene chloride. With the two polyolefins in contact only dispersion forces are available, and only in the case of polystyrene/PVC are there favourable acid-base attractions. The data point to significant contributions to bond... [Pg.43]

Until surface contact, the force between molecules is always one of attraction, although this attraction has different origins in different systems. London forces, dipole-dipole attractions, acid-base interactions, and hydrogen bonds are some of the types of attraction we have in mind. In the foregoing list, London forces are universal and also the weakest of the attractions listed. The interactions increase in strength and also in specificity in the order listed. [Pg.521]

It can be seen from the figure that the electrostatic repulsive forces between the macrocations are overwhelmed, probably by hydrophobic attractive forces between their hydrophobic side groups. It should be noted that the complimentary base-base pairing is unimportant in the present case. If this is not the case, the mixtures of APVP and TPVP should show the largest hypochromicity. This, however, is not the case. The importance of the hydrophobic interactions between nucleic acid bases has been proposed by Ts o et al.I9 from thermodynamic parameters of various nucleic acid bases or nucleosides in aqueous media. [Pg.140]

The attraction of coloring matter by charcoal is denominated mechanical, while the attraction of sulphuric acid by baryta is classed with chemical effects. But animal charcoal does not only attract coloring matter it aho decomposes metallic salts, and fixes their base by that same power of retention., Now it is known that chemical combinations and decompositions are produced by differences in intensity of one only chemical attractive force eollod affinity. It is evident that the same force is inherent in animal charcoal. This view is corroborated by the fact thot animal charcoal absorbs different compounds in different bnt determined quantities. Niepce has shown that iodine and chlorine gas ore condensed by the Inked portion of printed paper, while the white portion of the paper dees not retain any of the gases. Charcoal absorbs heat and light most readily.. It.Condenses... [Pg.1184]

Probably the most useful method for preparing polymeric materials through unsupported metallophilic interactions is an acid-base reaction. In these, basic gold(I) precursors react with metallic Lewis acids, forming supramolecular networks via acid-base stacking. The stability of these systems can be related to the ionic interactions nevertheless, the dispersion forces and relativistic effects can also be invoked to explain the formation of these systems, and in some occasions, these effects are even more important than the electrostatic attractions in determining the structural motifs. [Pg.333]

A study of the interaction of Lewis acids and bases (or electron acceptors and donors) in surface dynamics has led to new insight into interactions with various solid surfaces [26,64,99,100,104,110,130-142], as well as interactions at interfaces between two different substances. It is noted that the acid-base interactions of Lewis, including the orientational properties of charge transfer forces of Mulliken [143], occur between specific (or polar) groups in substances. These interactions are quite dependent on the Stockmayer degree of polarity, <5, [126] as measured by dipole moment in Eq. (58). Furthermore, it can be found that a concept of acids attract bases may be substituted... [Pg.410]

By far the dominant adhesion mechanism, particularly in the absence of covalent linkages, is the electrostatic attraction of the polar groups of the adhesive to polar groups of the adherends. These are mainly forces arising from the interaction of permanent dipoles, including the special cases of hydrogen bonding (10-25 kJ/mol) and Lewis acid-base interactions (<80 kJ/mole).25 26 These forces provide much of the attraction between the... [Pg.594]

As seen in Chapters 4 and 5, aqueous cations and anions are formed by the dissolution of metal oxides and acid phosphates. Electrostatic (Coulomb) force attracts the oppositely charged ions to each other and stacks them in periodic configurations. That results in an ionic crystal structure. Thus, the ionic bond is one of the main mechanisms that is responsible for forming the acid-base reaction products. [Pg.86]

Morgado, C. A. Jurecka, R Svozil, D. Hobza, R Sponer, J. 1. Balance of attraction and repulsion in nucleic-acid base stacking CCSD(T)/complete-basis-set-limit calculations on uracil dimer and a comparison with the force-field description, J. Chem. Theor. Comput. 2009, 5, 1524-1544. [Pg.502]

Attracted by the wealth and accuracy of the information provided by X-ray crystallographic analysis, organic chemists utilize this powerful tool to infer mechanistic and conformational hypotheses based on structural data [20J, though it seems implausible that static, crystalline species could reveal any information regarding the dynamics of transition states. This attitude has been particularly fruitful in the study of weak intermolecular forces such as hydrogen bonding f2l and Lewis acid-base interactions [22, 23], and obviously carbony 1-Lewis acid complexation is not the exception. [Pg.13]


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See also in sourсe #XX -- [ Pg.89 ]




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Attractive forces

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