Abstract

Carbon-centered radicals have been randomly generated on the chains of poly(acrylic acid), PAA, the simplest synthetic anionic polyelectrolyte, by pulse-irradiating its dilute, oxygen-free aqueous solutions by 6 MeV electron beam. In some experiments, oligo(acrylic acid), OAA, and propionic acid, PA, were used as PAA models. Recombination kinetics of PAA radicals has been followed by fast spectrophotometry. A strong pH dependence of radical lifetime on pH, and thus on the linear charge density due to deprotonated carboxylate groups, has been confirmed, while a weaker amplitude of pH dependence was observed for OAA and PA. Decay kinetics of PAA radicals in the protonated state, at pH 2, have been studied in some detail. At moderate doses of ionizing radiation, resulting in a moderate average initial number of radicals per chain, ZR0, the decay can be satisfactorily described by a second-order kinetic model, but a somewhat better fit is obtained by using a dispersive kinetics approach. While for a constant polymer concentration the reciprocal half-lives are proportional to the initial radical concentrations, such a data series for different PAA concentrations do not overlap, indicating that the overall radical concentration is not the decisive factor controlling the kinetics. Arranging all data, in the form of second-order rate constants, as a function of the average initial number of radicals per chain allows one to obtain a common dependence. The latter seems to consist of two parts: a horizontal one at low ZR0 and another one of positive slope at higher ZR0. This is interpreted as two kinetic regimes where two distinct reactions dominate, intermolecular and intramolecular recombination, respectively. Comparison of the low ZR0 data with calculations based on the translational diffusion model indicate that the latter is not the rate-controlling process in intermolecular recombination of polymer radicals; segmental diffusion is the more likely candidate.

Highlights

  • Introduction published maps and institutional affilChanges in public awareness and the related drive to move from an economy based on fossil resources to the new one, based on renewable materials, are reflected in the field of polymers and plastics

  • In this study we focus on protonated PAA since this is the form that allows to obtain nanogels upon irradiation, and because the kinetic results obtained for the non-ionized form are of broader relevance for free radical reactions in non-ionic polymers

  • Recombination of radicals derived from poly(acrylic acid) and model compounds in oxygen-free dilute aqueous solutions has been studied by pulse radiolysis with spectrophotometric detection

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Summary

Introduction

Changes in public awareness and the related drive to move from an economy based on fossil resources to the new one, based on renewable materials, are reflected in the field of polymers and plastics. Specialty polymers, used in new organic electronics and photovoltaics, biomaterials, drug delivery systems, etc., will definitely make use of the extraordinary properties that synthetic polymers can provide. These applications require the possibilities of synthesizing polymers of precisely known and well-controlled architecture, such as can be provided by modern synthetic methods based, for instance, on controlled radical polymerization [1,2,3,4,5]. To achieve full control over the processes involved in the synthesis of these specialty polymers and products, it is desirable to know the detailed kinetics and mechanisms of the involved elementary iations.

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