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Bonding systems application

Modern bonding systems usually consist of a primer coat, often with a secondary tie coat, plus a tacky solution to assist in the application of the rubber. The bonding systems currently in use are usually suitable both for autoclave vulcanisation and vulcanisation at 100°C with atmospheric pressure steam or hot water. Ambient vulcanisation bonding systems have to be chemically active at the lower temperatures and are therefore specialist in nature. [Pg.945]

Guo, H., Sirois, S., Proynov, E. I., Salahub, D. R., 1997, Density Functional Theory and its Applications to Hydrogen-bonded Systems in Theoretical Treatments of Hydrogen Bonding, Hadzi, D. (ed.), Wiley, New York. [Pg.289]

Gresh N, Claverie P, Pullman A (1982) Computations of intermolecular interactions Expansion of a charge-transfer energy contribution in the framework of an additive procedure. Applications to hydrogen-bonded systems. Int J Quant Chem 22 199... [Pg.171]

Latajka, Z., and Y. Bautellier. 1994. Application of density functional methods for the study of hydrogen-bonded systems The hydrogen flouride dimer. J. Chem. Phys. 101, 9793. [Pg.126]

Csajka, F. S. Chandler, D., Transition pathways in a many-body system application to hydrogen-bond breaking in water, J. Chem. Phys. 1998,109, 1125-1133... [Pg.276]

Low-pressure thermal dissociation, ZTRID, is only at the threshold of application to bond strength problems. It is inherently best suited to weakly bonded systems. Room temperature studies are appropriate to bond strengths in the 0.5 to 1.0 eV region. [Pg.116]

In this chapter we will mainly concentrate on hydrogen-bonded ferroelectrics, which were the first class of ferroelectrics where the coexistence of the different dynamics was postulated and observed [26,27]. In Chap. 2 of this volume (by Dalai et al. [51]) new experimental techniques and their advantages over conventional ones will be described together with their applications to hydrogen-bonded systems. The theoretical concept of bihnear... [Pg.5]

Carbon materials provide electrical conduction through the pi bonding system that exists between adjacent carbon atoms in the graphite structure [182]. Electrical properties of nanocomposites based on conducting nanofillers such as EG [183-187], CNTs [188-190], and CNFs [191], dispersed in insulating polymer matrix have found widespread applications in industrial sectors. [Pg.51]

The application of Stepanov s theory to intramolecular F bonded systems has been criticized [42], In this case the low frequency vibration described above as vXH Y is also partly constrained by a more nearly harmonic vibration involving skeletal bending motions of the rest of the molecule, and the X, H, and Y atoms are not collinear. These factors would seem to suggest that (I) the vXll Y type of vibration will be of higher frequency than in the usual case (perhaps 200-300 cm"1 rather than 100-200 cm"1) so that the sub-bands will be more widely spaced and may not be recognised as part of the rXH band (2) the motion of the H atom will have less effect on rXY and (3) H-bond bending vibrations may also couple considerably with vXH. The observation of rather smaller frequency shifts for vXR and narrower absorption bands w such cases are in reasonable agreement with this picture,... [Pg.96]

D"cjbihg the last few years many investigations have been carried out upon the problems of hydrogen bonding, Many experimental data obtained from the application of different methods with a variety of hydrogen bonded systems have been published, and several theoretical... [Pg.579]

Another approach for the ring expansion of epoxides uses low-valent iron complexes which open epoxides under reductive conditions, as reported by Hilt et al. [106]. The iron complexes are reduced and after coordination of the epoxide to the iron center an electron transfer initiates the radical-type ring opening of the epoxide. Under formal insertion of an alkene, regioselective formation of tetrahy-drofurans was observed (Scheme 9.46). The reaction is applicable to a broad range of acceptor-substituted alkenes bearing another double or triple bond system in conjugation with the inserted carbon-carbon double bond. [Pg.265]


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See also in sourсe #XX -- [ Pg.129 ]




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