Abstract
Water-soluble, carboxylic acid monomers are known to exhibit peculiar kinetics when polymerized in aqueous solution. Namely, their free-radical polymerization rate is affected by several parameters such as monomer concentration, ionic strength, and pH. Focusing on methacrylic acid (MAA), even though this monomer has been largely addressed, a systematic investigation of the effects of the above-mentioned parameters on its polymerization rate is missing, in particular in the fully ionized case. In this work, the kinetics of non-ionized and fully ionized MAA are characterized by in-situ nuclear magnetic resonance (NMR). Such accurate monitoring of the reaction rate enables the identification of relevant but substantially different effects of the monomer and electrolyte concentration on polymerization rate in the two ionization cases. For non-ionized MAA, the development of a kinetic model based on literature rate coefficients allows us to nicely simulate the experimental data of conversion versus time at a high monomer concentration. For fully ionized MAA, a novel propagation rate law accounting for the electrostatic interactions is proposed: the corresponding model is capable of predicting reasonably well the electrolyte concentration effect on polymerization rate. Nevertheless, further kinetic information in a wider range of monomer concentrations would be welcome to increase the reliability of the model predictions.
Highlights
Water soluble polymers are very attractive materials which have applications in many different fields: they are employed in the manufacturing of pharmaceuticals and cosmetics, in enhanced oil separation and water purification processes, and as additives for thickening, flocculation, coating, etc. [1,2,3]
In addition to the effect on the material properties, these interactions involving monomer and polymer moieties have an impact on the reaction kinetics during aqueous radical polymerization, which is the usual method of synthesis of water-soluble polymers
We propose a rate law of propagation of fully ionized methacrylic acid (MAA) composed of an intrinsic kinetics term and a diffusion term, the latter being driven by electrostatic interactions and a function of the electrolyte concentration, similar to the equation developed in a previous work [11]: kp =
Summary
Water soluble polymers are very attractive materials which have applications in many different fields: they are employed in the manufacturing of pharmaceuticals and cosmetics, in enhanced oil separation and water purification processes, and as additives for thickening, flocculation, coating, etc. [1,2,3]. The peculiar properties of such polymers come from their building blocks, namely water soluble vinyl monomers exhibiting polarizable, ionizable, or charged moieties. Typical examples of such monomers are acrylic and methacrylic acid as well as their esters, acrylamides and vinyl amides, and ammonium salts. The solution and surface properties of the polymer as well as the viscoelastic behavior of the material are affected by such interactions, determining the peculiar features of water-soluble polymers which make them so interesting and versatile [4,5]. In addition to the effect on the material properties, these interactions involving monomer and polymer moieties have an impact on the reaction kinetics during aqueous radical polymerization, which is the usual method of synthesis of water-soluble polymers. The presence of charges or dipoles can induce interactions of various nature between the reacting species, and they can in Processes 2017, 5, 23; doi:10.3390/pr5020023 www.mdpi.com/journal/processes
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