Confinement effects in the step-growth polymerization within AAO templates and modeling

Confinement effects in the step-growth polymerization within AAO templates and modeling Nanostructured polyurethanes have attracted substantial interest for the generation of “smart” surfaces, but step-growth polymerization at the nanoscale has scarcely been reported. In this work, the synthesis of polyurethanes by step-growth polymerization in the nanocavities of anodized aluminum oxide (AAO) templates is studied, finding that the kinetics of the reaction was faster than in bulk, while the molecular weight and the dispersity were reduced. A mathematical model was developed to explain these differences, taking into account the chemical and physical interactions encountered in the reaction between the monomers (diisocyanate and dialcohol) for nanoconfined in AAO and bulk. In nanoconfinement, the polyaddition is catalyzed by hydroxyl groups on the pore wall, resulting in an increase in the rate of polymerization during the early stages of the reaction. At high conversions, the limited diffusion of the polymer chains results in a slower polymerization and a dispersity lower than that expected from bulk. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Polymer Elsevier

Confinement effects in the step-growth polymerization within AAO templates and modeling

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Publisher
Elsevier
Copyright
Copyright © 2018 Elsevier Ltd
ISSN
0032-3861
D.O.I.
10.1016/j.polymer.2018.02.041
Publisher site
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Abstract

Nanostructured polyurethanes have attracted substantial interest for the generation of “smart” surfaces, but step-growth polymerization at the nanoscale has scarcely been reported. In this work, the synthesis of polyurethanes by step-growth polymerization in the nanocavities of anodized aluminum oxide (AAO) templates is studied, finding that the kinetics of the reaction was faster than in bulk, while the molecular weight and the dispersity were reduced. A mathematical model was developed to explain these differences, taking into account the chemical and physical interactions encountered in the reaction between the monomers (diisocyanate and dialcohol) for nanoconfined in AAO and bulk. In nanoconfinement, the polyaddition is catalyzed by hydroxyl groups on the pore wall, resulting in an increase in the rate of polymerization during the early stages of the reaction. At high conversions, the limited diffusion of the polymer chains results in a slower polymerization and a dispersity lower than that expected from bulk.

Journal

PolymerElsevier

Published: Mar 28, 2018

References

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