Journal of Polymer Science Polymer Chemistry Edition · 1976 · 30 citations · 14 references
Natural SciencesChemical EngineeringChemistryPhysical ChemistryPolymer ChemistryPolymer MaterialsAcid-base ChemistryIonic PolymersOrganic AcidsPolymer Physical ChemistryPolymerization ChemistryPolymerization KineticsCopolymerizationCopolymerization BehaviorCopolymerization KineticsElectrostatic InteractionsElectrostatic Interactions In PolymersMonomer Reactivity RatiosPh DependenceReactivity
Abstract Acrylic acid (AA) and N ‐vinylpyrrolidone (NVP) were copolymerized in aqueous solution at 30°C in the pH range 4–9 and the monomer reactivity ratios ( r 1 for AA and r 2 for NVP) were determined as a function of pH from the high conversion data by using both the differential (YBR) and the integrated copolymerization equations. The value of r 1 decreased from 5.2 at pH 4 to a minimum of 1.3 at pH 5 and then increased to 8.1, 6.6, and 7.2 at pH 7, 8, and 9, respectively. Addition of 1 M NaCl at pH 6.5 restored the r 1 nearly to that at pH 4, the predominantly un‐ionized acid. The r 2 values for NVP were nearly zero at all pH values except at pH 5. The variation of the reactivity ratios with pH was examined in terms of the electrostatic interactions between the ionized monomer molecules, the rate of homopolymerization of acrylic acid, and the cation binding to the poly(acrylic acid) molecules. The r 2 values for NVP compared favorably with the literature values reported in bulk and organic solvent systems, although r 1 values are much higher.
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J. R. Huizenga, Philip F. Grieger, Frederick T. Wall · Journal of the American Chemical Society · 1950 · 216 citations