Abstract
Vinyl pivalate (VPi) was solution-polymerized in tertiary butyl alcohol (TBA) and in dimethyl sulfoxide (DMSO) with low chain transfer constant using a low temperature initiator, 2,2′-azobis(2,4-dimethylvaleronitrile) (ADMVN). TBA was absolutely superior to DMSO in increasing the syndiotacticity and molecular weight of poly(vinyl alcohol) (PVA). Low-temperature solution polymerization of VPi in TBA or DMSO by adopting ADMVN proved to be successful in obtaining PVA of ultrahigh molecular weight (maximum number-average degree of polymerization (Pn): 13,500–17,000) and of high yield (ultimate conversion of VPi into PVPi: 55–80%) to a much higher conversion than that from bulk polymerization. Moreover, PVA from TBA system were fibrous, with a high degree of orientation of the crystallites, indicating the syndiotactic nature of TBA polymerization.
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