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Probing interfacial interactions and dynamics of polymers enclosed in boron nitride nanotubes

Authors :
Niskanen, Jukka
Xue, Yanming
Golberg, Dmitri
Winnik, Francoise
Pellerin, Christian
Vapaavuori, Jaana
Niskanen, Jukka
Xue, Yanming
Golberg, Dmitri
Winnik, Francoise
Pellerin, Christian
Vapaavuori, Jaana
Source :
Journal of Polymer Science, Part A: Polymer Chemistry
Publication Year :
2022

Abstract

Understanding interfacial interactions in polymer systems is crucial for their applicability for instance in adhesives and coatings. Enclosing polymers in a cylindrical volume provides a system for studying interactions dictated by a continuous interfacial layer and a bulk-like volume in the middle of the cylinders. Here, we describe a simple method for enclosing polymers into boron nitride nanotubes (BNNTs) and establishing the effect of the interfacial interactions on the glass transition temperature (Tg) of the polymers by infrared spectroscopy. The volume of the inner channel is large in comparison to the volume of the loaded polymer coils, allowing the polymer to expand along the inner channel, resulting in the effect of interfacial interactions on polymer dynamics dominating over confinement effects. As examples, we loaded poly(4-vinyl pyridine), poly(methyl methacrylate), poly(vinyl pyrrolidone), and poly(disperse red 1 acrylate) in BNNTs. The strongest interaction between the studied polymer and BNNTs was observed for poly(4-vinyl pyridine), which also caused a significant increase of Tg. In addition to characterizing the effect of interfacial interactions on the thermal transitions of the polymers, this method, which is generalizable to most soluble polymer materials, can be used for studying photoinduced transitions in photoactive polymers thanks to the transparency of the BNNTs at visible wavelengths.

Details

Database :
OAIster
Journal :
Journal of Polymer Science, Part A: Polymer Chemistry
Notes :
application/pdf
Publication Type :
Electronic Resource
Accession number :
edsoai.on1287976909
Document Type :
Electronic Resource