This paper addresses the origin, structure and properties of the inter
phase in adhesion. By interphase is meant that interfacial region betw
een bulk adhesive and bulk adherend over which the local density displ
ays a spatial gradient. In such a region all the local thermodynamic p
roperties, including the mechanical properties, will be a function of
distance from the surface. The question of how large these variations
may be both in terms of magnitude and range is clearly a matter of som
e import in adhesive technology. The term ''local'' is a key considera
tion because meaningful discussion of the interphase can hardly be con
templated without explicit recognition that matter in the interphase s
hould be regarded properly as existing in a thermodynamically metastab
le small system of low dimensionality. The results of a number of our
numerical and theoretical studies, namely molecular dynamics simulatio
n of realistic interfaces and nonlinear dynamical analysis, have been
used to investigate the nature of materials close to surfaces. It has
been found that the form and range of the density profile are indeed s
ensitive to the chemical nature of the surface but it has not been pos
sible to rationalize the existence of the macroscopic long-range inter
phase on the basis of the usual type of spatial correlation. Recognizi
ng that many adhesive bonds are formed using a reactive resin system w
e have investigated the effects of nonlinearities in the reaction kine
tics on the structure and morphology of the interphase. When these fac
tors are taken into account, a theoretical description of the interpha
se is possible in which the coupling between the various distance scal
es arises in a very natural fashion.