Energy-power relationship, mechanical initiators

The initial objective of our work was to quantify solvent effects (particularly solvent nucleophilicity) by adapting the Grunwald-Winstein equation (2) (5). In equation 2, k is the rate of solvolysis of a substrate (RX) in any solvent relative to 80% v/v ethanol-water (k0) and Y is the solvent ionizing power defined by m = 1.000 for solvolyses of tert-butyl chloride at 25 °C. In this chapter, a discussion of equation 2 and similar free-energy relationships is presented. At the time our work began (1969), in collaboration with Schleyer, mechanisms of solvolytic reactions were close to a high in controversy (6-8). More recent mechanistic developments (9-13) are not reviewed in detail here, but increased recognition of the importance of nucleophilic solvent assistance should be noted. 

With the rapid increase in numerical computing power, there have been attempts to formalize the different environmental contributions in order to provide a procedure to predict assembly durability (Crocombe 1997 Loh et al. 2002 Bordes et al. 2009). PigMre4S.IS shows a simple scheme. This is based on an initial identification of diffusion coefficients and mechanical parameters. The relationships between water content and properties such as tensile modulus, tensile strength, and interfacial fracture energy are then established. A coupled numerical model for the joint of interest is then constructed. This allows local water content to be defined and resulting changes in adhesive and interface properties to be predicted. At present, there are... 

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