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Synthesis and characterization of ionomeric poly(vinyl butyral)
Author(s) -
Dasgupta A. M.,
David D. J.,
Misra A.
Publication year - 1992
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.1992.070440711
Subject(s) - materials science , polymer , dynamic mechanical analysis , polymer chemistry , vinyl alcohol , differential scanning calorimetry , ionomer , chemical engineering , ionic bonding , polymerization , composite material , copolymer , chemistry , organic chemistry , thermodynamics , ion , physics , engineering
A route to synthesizing novel poly(vinyl butyral) ionomers (IPVB), via a condensation polymerization process, has been developed. In the process, ionic groups were permanently incorporated into the poly(vinyl butyral) backbone by using an ion‐containing aldehyde in addition to butyraldehyde during the acetalization of poly(vinyl alcohol). The resulting polymers demonstrated properties typical of ionomer systems, i.e., they behaved as “thermally reversible crosslinked thermoplastics” due to the presence of ionic associations present in the polymers. The ionic associations enabled the polymers to behave as crosslinked materials at ambient temperatures, whereas, at higher temperatures (processing temperatures), the ionic associations were lost, thus allowing the polymers to flow. Consequently, at ambient temperatures, the IPVBs demonstrated increased stiffness as determined from the storage modulus of the polymers, whereas, at higher temperatures, the IPVBs demonstrated moduli and stress‐relaxation properties comparable to those of conventional poly(vinyl butyral). The IPVBs were characterized by a number of techniques including, high resolution NMR spectroscopy ( 1 H, 13 C), dilute solution viscometry, dynamic mechanical analysis, and differential scanning calorimetry (DSC). Characterization was done on plasticized and unplasticized IPVBs.