Volume 216, Issue 4 pp. 400-416
Full Paper

Comparison of Particle Size Techniques to Investigate Secondary Nucleation in HEMA-Rich Latexes

Martin Ocepek

Martin Ocepek

Helios Domzˇale d.d., Central R&D of HELIOS Group, Kolicˇevo 2, SI-1230 Domzˇale, Slovenia

Centre of Excellence for Polymer Materials and Technologies, Tehnolosˇki park 24, SI-1000 Ljubljana, Slovenia

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Mark D. Soucek

Corresponding Author

Mark D. Soucek

Department of Polymer Engineering, The University of Akron, 250 S. Forge St., Akron, OH, 44325 USA

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Peter Berce

Peter Berce

Helios Domzˇale d.d., Central R&D of HELIOS Group, Kolicˇevo 2, SI-1230 Domzˇale, Slovenia

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Lei Meng

Lei Meng

Department of Polymer Engineering, The University of Akron, 250 S. Forge St., Akron, OH, 44325 USA

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First published: 02 January 2015
Citations: 12

Abstract

2-Hydroxyethyl methacrylate (HEMA)-rich latex is synthesized via a semibatch mono­mer-starved emulsion polymerization process. Six emulsion polymerizations, containing 0–40 mol% HEMA in monomer composition, are synthesized and compared. Calculations of mass balances are made in order to predict final particle size and particle size development during the course of polymerization. Average particle sizes obtained by dynamic light scattering (DLS) are compared to ultrasound acoustic attenuation spectroscopy (UAAS) and transmission electron microscopy (TEM). The influence of HEMA on polymerization on the onset of secondary nucleation is evaluated using each technique. The DLS, TEM, and UAAS secondary nucleation data are compared to physical latex blends of small and large particles. The blend data are consistent with the secondary nucleation data. Additionally, conductivity and surface tension are monitored. TEM, atomic force microscope (AFM), and UAAS are found to be more appropriate methods than the widely used DLS for particle size and particle size distribution characterization in this system. Increasing HEMA content to 20 mol% results in formation of significant amount of secondary particles via proposed homogeneous nucleation of HEMA-rich oligomers.

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