Please use this identifier to cite or link to this item: https://doi.org/10.1002/pola.24872
Title: Polymer brushes on multiwalled carbon nanotubes by activators regenerated by electron transfer for atom transfer radical polymerization
Authors: Aitchison, T.J.
Ginic-Markovic, M.
Saunders, M.
Fredericks, P.
Valiyaveettil, S. 
Matisons, J.G.
Simon, G.P.
Keywords: ARGET ATRP
composite
living radical polymerization
multiwalled carbon nanotube
nanocomposites
nanoparticles
polymer brushes
polystyrene
Issue Date: 1-Oct-2011
Citation: Aitchison, T.J., Ginic-Markovic, M., Saunders, M., Fredericks, P., Valiyaveettil, S., Matisons, J.G., Simon, G.P. (2011-10-01). Polymer brushes on multiwalled carbon nanotubes by activators regenerated by electron transfer for atom transfer radical polymerization. Journal of Polymer Science, Part A: Polymer Chemistry 49 (19) : 4283-4291. ScholarBank@NUS Repository. https://doi.org/10.1002/pola.24872
Abstract: The synthesis and characterization of multiwalled carbon nanotube (MWCNT) polymer brushes produced by activators regenerated by electron transfer (ARGET) in atom-transfer radical polymerization (ATRP) was discussed. The polymer brushes were synthesized by esterification of the MWCNT carboxylic acid groups with hydroxyethyl-2-bromoisobutyrate and subsequently used in ARGET ATRP. This created a well defined living polymer brush carbon nanotube of comparatively low polydispersity and a polymer layer 10 nm thick. As, ARGET ATRP uses only minute concentrations of copper (II) catalyst, and is less sensitive to air compared to other living polymerization techniques, this process is a more industry-compatible route for the commercialization of such materials. The structural and chemical properties were explored by a range of techniques including high resolution transmission electron microscopy, gel permeation chromatography, elemental analysis, Fourier transform infrared spectroscopy, thermogravimetric analysis, and differential scanning calorimetry. In addition, the polymer brush nanotubes were explored for their potential use in films and as fillers. © 2011 Wiley Periodicals, Inc.
Source Title: Journal of Polymer Science, Part A: Polymer Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/76776
ISSN: 0887624X
DOI: 10.1002/pola.24872
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