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Novel preparation of self-assembled HCl-doped polyaniline nanotubes using compressed CO2-assisted polymerization.

Authors :
Noby, H.
El-Shazly, A.H.
Elkady, M.F.
Ohshima, M.
Source :
Polymer. Nov2018, Vol. 156, p71-75. 5p.
Publication Year :
2018

Abstract

Abstract Recently, extraordinary attention has been given to the preparation of strong acid-doped polyaniline in distinct morphologies, such as nanofibers, nanotubes, and nanoflowers, while seeking proper and cheap energy polymeric materials. This work introduces the CO 2 -supported polymerization process as an advanced and novel polymerization technique to prepare rectangular cross-sectional self-assembled HCl-doped polyaniline nanotubes (HCl-PANNT) without the need to use any surfactants for the first time. Based on the scanning electron microscopy (SEM) and transmission electron microscopy (TEM) results, a rectangular cross-sectional HCl-PANNT with an average outer diameter and wall thickness of 110 and 35 nm, respectively, was prepared. Furthermore, X-ray powder diffraction (XRD) and Fourier-transform infrared spectroscopy (FT-IR) were employed to reveal the crystallinity and the chemical structure of the prepared polyaniline, respectively. Accordingly, the produced PANNT has a partial crystalline structure and emeraldine salt form. Moreover, the produced HCl-PANNT showed a high electrical conductivity of 1.5 S/cm. Graphical abstract Image Highlights • Strong acid-doped polyaniline nanotubes preparation is highly desired. • Compressed CO 2 was used for polyaniline nanotubes preparation without surfactants. • The synthesized nanotubes have a rectangular cross-sectional area. • The prepared polyaniline nanotubes have a significant electrical conductivity. • CO 2 -assisted polymerization is promising in advance polyaniline morphologies production. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00323861
Volume :
156
Database :
Academic Search Index
Journal :
Polymer
Publication Type :
Academic Journal
Accession number :
132826669
Full Text :
https://doi.org/10.1016/j.polymer.2018.09.060