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Applications bond strength

The primary challenge facing adhesive bonding of metals is to obtain sufficient durability of a bonded structure. Initial bond strength in metal-polymer adhesive joints is almost invariably excellent. Challenging the application of adhesives in polymer-polymer joining, however, is the problem of obtaining a joint that is... [Pg.459]

Theoretically, these intermolecular interactions could provide adhesion energy in the order of mJ/m. This should be sufficient to provide adhesion between the adhesive and the substrate. However, the energy of adhesion required in many applications is in the order of kJ/m. Therefore, the intermolecular forces across the interface are not enough to sustain a high stress under severe environmental conditions. It is generally accepted that chemisorption plays a significant role and thus, physisorption and chemisorption mechanisms of adhesion both account for bond strength. [Pg.689]

For most applications the strength requirements for steel bonding may not be as demanding as for aluminum and titanium so some sacrifice in bondment... [Pg.963]

Temperature resistance, i.e. a combination of melting point and oxidation resistance, may be of prime importance. A general correlation exists between melting point and hardness since both reflect the bond strength of the atoms in the crystal lattice, and the preferred order of coating metals for use in high temperature applications as temperature is increased is silver, aluminium, nickel, rhenium, chromium, palladium, platinum and rhodium. [Pg.455]

Can one further enhance the performance of this classically promoted Rh catalyst by using electrochemical promotion The promoted Rh catalyst, is, after all, already deposited on YSZ and one can directly examine what additional effect may have the application of an external voltage UWR ( 1 V) and the concomitant supply (+1 V) or removal (-1 V) of O2 to or from the promoted Rh surface. The result is shown in Fig. 2.3 with the curves labeled electrochemical promotion of a promoted catalyst . It is clear that positive potentials, i.e. supply of O2 to the catalyst surface, further enhances its performance. The light-off temperature is further decreased and the selectivity is further enhanced. Why This we will see in subsequent chapters when we examine the effect of catalyst potential UWR on the chemisorptive bond strength of various adsorbates, such as NO, N, CO and O. But the fact is that positive potentials (+1V) can further significantly enhance the performance of an already promoted catalyst. So one can electrochemically promote an already classically promoted catalyst. [Pg.19]

Hertwig, R.H., Hrusak, J., Schroder, D., Koch, W. and Schwarz, H. (1995) The metal-ligand bond strengths in cationic gold(l) complexes. Application of approximate density functional theory. Chemical Physics Letters, 236, 194-200. [Pg.236]

Methods can be based on some preconceived concept of bonding, with ionic and covalent extremes, or on pattern recognition based on the periodic table. Miscellaneous methods of limited applicability link bond strength with other physical properties. The a priori calculation of heats of formation by wave mechanics is possible in theory. In practice, the most widely applied method incorporates experimental data to derive atom or bond parameters which can then be used for calculations on closely related compounds. [Pg.31]

In the chemistry of main-group element sulfoxide complexes, a relationship between Aj/(S=0) and the enthalpy of formation of the sulfoxide complex has been derived (159). The applicability of the equation has only been examined for O-l SO complexes, and the constraints on using Ai (S=0) as a measure of metal-ligand bond strength should be borne in mind during its application. [Pg.140]

The application of 170 NMR spectroscopy to obtain structural information about polyoxoanions, mainly in nonaqueous solution, had been examined and discussed in detail (99). A very useful finding was that chemical shifts are determined largely by metal-oxygen bond strengths. An inverse correlation exists between the 170 shift and the shortest bond length to a given metal. In aqueous solution the existence of [Mo7024]6 could be confirmed by the use of 170 and "Mo NMR spectroscopy (100-104). Evidence for the existence of the three... [Pg.151]


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See also in sourсe #XX -- [ Pg.156 ]




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