Bimodal molecular mass distribution in surfactant-free emulsion polymerization as a consequence of coagulative nucleation
Marta Dobrowolska, Ger J. M. Koper

TL;DR
This paper explains the bimodal molecular weight distribution in surfactant-free emulsion polymerization as a result of multistage kinetics, including primary particle formation and coagulative nucleation, which lead to distinct molecular weight modes.
Contribution
It identifies the multistage kinetic process as the cause of bimodal molecular weight distribution, linking different polymerization phases to specific molecular weight modes.
Findings
Bimodal distributions observed for ionic and non-ionic initiators.
The initial stage produces larger molecular weights than the coagulative nucleation stage.
Prolonging initial formation kinetics reveals the distinct modes in molecular weight distribution.
Abstract
It is demonstrated that the often observed broadness of the molecular weight distribution obtained from latex particles synthesized by means of surfactant-free emulsion polymerization results from the multistage kinetics. The initial stage of the polymerization, by which the primary particles are formed, is of the 01-kind which means that it can be assumed that the particles are so small that at any moment of time there is no more than one radical chain per particle. After the aggregation of primary particles into secondary particles, the so called coagulative nucleation step, the polymerization kinetics in the subsequently coalesced secondary particles is of the pseudo-bulk kind which means that there are so many radicals in the particles that the polymerization process proceeds as in bulk. The important consequence is that the molecular weight of the 01-process is about one order of…
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Taxonomy
TopicsAdvanced Polymer Synthesis and Characterization · Analytical Chemistry and Chromatography · Surfactants and Colloidal Systems
