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a) b - École Polytechnique de Montréal

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2.1.2.1 Binary Polymer Blends<br />

2.1.2.1.1 Co-continuous Morphology<br />

There is currently an increasing interest in techniques used to control interfacial properties of<br />

polymeric materials. Through controlling morphology of polymer blends, novel materials for<br />

different applications can be <strong>de</strong>signed. For immiscible polymer binary blends, two types of<br />

morphologies, namely matrix/dispersed structure and co-continuous morphologies, have been<br />

realized. At low concentration of one phase, dispersed droplets of that phase in the other<br />

component is observed. By increasing the concentration of the minor phase, phase inversion<br />

occurs and a dual phase region is reached in which various levels of co-continuous structure coexist.<br />

At concentrations near the phase inversion region, blends with two fully interconnected<br />

and interpenetrating structures in three dimensions are observed. In other words, a binary blend<br />

is formed of two polymers in which the surface of each phase is an exact topological replica of<br />

the other (antitropic). Generally, in polymer blends, the matrix dominates the properties of blend;<br />

thus, in binary co-continuous blends both polymers have approximately equal contributions to<br />

the blend properties. Moreover, their interpenetrating assembly can lead to synergistic<br />

improvement of specific conductivity, permeability, and mechanical properties. A process in<br />

which two phases switch their functions is <strong>de</strong>fined as phase inversion. In a certain concentration<br />

range around the phase inversion concentration, which is <strong>de</strong>fined as the co-continuity interval,<br />

co-continuous morphologies are formed. The phase inversion concentration is regar<strong>de</strong>d as the<br />

center of this area and its correct <strong>de</strong>termination is of great importance in which the former<br />

dispersed phase becomes the matrix and vice-versa. Consequently, the position and width of the<br />

phase inversion concentration are influenced by many rheophysical material parameters of the<br />

blend’s constituents, such as interfacial tension. Willemse et al.(Willemse, Posthuma <strong>de</strong> Boer,<br />

van Dam, & Gotsis, 1999) showed that for different blends with various matrix viscosities and<br />

viscosity ratios, the composition range within which fully co-continuous polymer blend<br />

structures form is influenced by interfacial tension. It was found(He, Bu, & Zeng, 1997) that<br />

phase co-continuity occurs in a wi<strong>de</strong> composition range at a short mixing time, but with<br />

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