Our recent experimental results have shown that a miscible blend containing a liquid
crystalline polymer (LCP) and an amorphous copolymer, both capable of self-association and interassociation by hydrogen-bonding, can be created by slight structural modification of the amorphous polymer.
The results also show that an optimum amount of intermolecular H-bonding can be formed in the blend
by systematically varying the distance between the hydrogen-bonding groups on the copolymer chain. It
was found that the system with the optimum amount of intermolecular hydrogen-bonding is also the
system with the broadest miscibility window. In this paper, this work is extended by examining the effect
of elimination of self-associating hydrogen bonds in the LCP on the intermolecular hydrogen-bonding
and on the phase behavior of these blends. FTIR and phase behavior results show that this modification
results in increased intermolecular hydrogen-bonding and a broader miscibility window than the blend
that contains the original liquid crystalline polymer. In agreement with our previous results, the optimum
amount of intermolecular H-bonding is formed in the blend by systematically varying the distance between
the hydrogen-bonding groups on the amorphous copolymer. DSC and optical microscopy correlate these
data to the blend phase behavior to show that the optimum amount of intermolecular hydrogen-bonding
correlates to the system with the broadest miscibility window. Finally, thermodynamic analysis of these
blends provides insight and guidelines regarding the applicability of this scheme to create a miscibility
window in other polymer blends.