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The behavior of substances in solutions may not be adequately
characterized by the effect of any single physicochemical parameter
of solvents, nor are numerous semi-empirical scales of the solvent
effect (their 'polarity') suitable for their limited selections
only. In recent decades, it has been found that the variation of
reaction rate constants in solutions or that spectral parameters of
dissolved substances are determined by the total effect of
different solvation processes. This monograph presents numerous
examples of such an approach and characterizes various empirical
and semi-empirical scales of solvent properties. It is shown that
additional consideration of some structural parameters of solvents,
namely, their cohesive energy and the molar volume, may provide for
spreading this approach on homolytical and catalytic reaction.
The main focus in this monograph is on models of the kinetics of photo-initiated polymerization of mono- and bi-functional monomers up to the high conversion stage, their derivation, analysis and comparison with the experimental data. This monograph can be useful for scientists, engineers, post-graduate training students and students who are interested in problems both of the polymerization kinetics and general chemical kinetics.
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