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Updated: Jun 10, 2026

Preparation and Friction Force Microscopy Measurements of Immiscible, Opposing Polymer Brushes
Published on: December 24, 2014
Direct observations of three nucleation/growth processes of charge-stabilized dispersion polymerizations with varying
Fen Zhang1, Yuhong Ma, Lianying Liu
1Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, College of Material Science and Engineering, Beijing University of Chemical Technology, Beijing, 100029, PR China.
Abstract:
This article presents observations of three polymerization modes of a self-developed cation-charge-stabilized styrene/water/methanol dispersion polymerization system: (1) a water/methanol (20/80) system, corresponding to a typical dispersion polymerization mode where the particle nucleation occurred in the solution phase and growth in the particle phase; (2) a pure CH(3)OH system, including a first nucleation in the solution phase with growth by absorption of the small particles and polymers formed in this phase, and a secondary nucleation with growth in the particle phase, when high molecular weight copolymers appeared in the solution phase; and (3) a water/methanol (5/95) system, similar to the conventional dispersion polymerization mode during the first 90 min, with subsequent epitaxial growth. Interestingly, the metastable state of the nucleation stage, including minuscule 6-nm particles, their aggregates, and the aggregating process, was first observed experimentally. By quantitatively following the relationship of the deposited molecular weight and the nucleation/growth process in the three systems, it was proposed that the molecular weight of the deposited polymer had to reach a specific high value before they could absorb or capture monomer to form smooth/spherical nuclei or particles.
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