1986•Bulletin of the Korean Chemical SocietyRequires access

Complex Formation of Syndiotactic Poly(methacrylic acid) with Complementary Polymers through Hydrogen Bonding

Bum Sung Kim, Seung-Ho Jeon, Taikyue Ree

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Abstract

Complex formations between syndiotactic poly(methacrylic acid) (st-PMAA) and poly(N-vinyl pyrrolidone) (PVP), and that between st-PMAA and polyethyleneoxide (PEO) through hydrogen bonding were studied by viscometry and potentiometry. Reduced viscosity () was measured at various mole fraction of PVP or PEO with respect to a constant amount of st-PMAA. Observation shows a sharp minimum at the 1:1 mole ratio of st-PMAA:PVP or st-PMAA:PEO, which shows that the complexation becomes optimal and the complex has a compact structure in this ratio. Variation of pH also supports this conclusion. This is the case of the system of st-PMAA and PVP in water as well as in DMF. Also the complexation is much enhanced when the molecular weight of PVP is high. Meanwhile, the system of st-PMAA and PEO shows a little different behavior, i.e., this system does not form the complex in DMF and does only in water. It is because the interaction st-PMAA with PEO is weaker than that with PVP.

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What this paper is about

Complex formations between syndiotactic poly(methacrylic acid) (st-PMAA) and poly(N-vinyl pyrrolidone) (PVP), and that between st-PMAA and polyethyleneoxide (PEO) through hydrogen bonding were studied by viscometry and potentiometry. Reduced viscosity () was measured at various mole fraction of PVP or PEO with respect to a constant amount of st-PMAA. Observation shows a sharp minimum at the 1:1 mole ratio of st-PMAA:PVP or st-PMAA:PEO, which shows that the complexation becomes optimal and the complex has a compact structure in this ratio. Variation of pH also supports this conclusion. This is the case of the system of st-PMAA and PVP in water as well as in DMF. Also the complexation is much enhanced when the molecular weight of PVP is high. Meanwhile, the system of st-PMAA and PEO shows a little different behavior, i.e., this system does not form the complex in DMF and does only in water. It is because the interaction st-PMAA with PEO is weaker than that with PVP.

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Available abstract

Complex formations between syndiotactic poly(methacrylic acid) (st-PMAA) and poly(N-vinyl pyrrolidone) (PVP), and that between st-PMAA and polyethyleneoxide (PEO) through hydrogen bonding were studied by viscometry and potentiometry. Reduced viscosity () was measured at various mole fraction of PVP or PEO with respect to a constant amount of st-PMAA. Observation shows a sharp minimum at the 1:1 mole ratio of st-PMAA:PVP or st-PMAA:PEO, which shows that the complexation becomes optimal and the complex has a compact structure in this ratio. Variation of pH also supports this conclusion. This is the case of the system of st-PMAA and PVP in water as well as in DMF. Also the complexation is much enhanced when the molecular weight of PVP is high. Meanwhile, the system of st-PMAA and PEO shows a little different behavior, i.e., this system does not form the complex in DMF and does only in water. It is because the interaction st-PMAA with PEO is weaker than that with PVP.

Key concepts: Poly(methacrylic acid), Methacrylic acid, Hydrogen bond, Polymer chemistry, Tacticity, Polymer, Viscometer, Intrinsic viscosity

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