Effect of protonation media on chemically and electrochemically synthesized polyaniline

Citation
Rc. Patil et al., Effect of protonation media on chemically and electrochemically synthesized polyaniline, POLYM INT, 49(2), 2000, pp. 189-196
Citations number
28
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
POLYMER INTERNATIONAL
ISSN journal
09598103 → ACNP
Volume
49
Issue
2
Year of publication
2000
Pages
189 - 196
Database
ISI
SICI code
0959-8103(200002)49:2<189:EOPMOC>2.0.ZU;2-9
Abstract
Polyaniline films have been prepared both chemically and electrochemically using formic ('Pani-Formic'), boric ('Pani-Boric') or acetic acid ('Pani-Ac etic') as protonation media. Among the three, formic acid seems to be a bet ter protonating medium because it selectively yields the conducting phase o f polyaniline. The variation of potential with the amount of oxidizing agen t suggests one dimensional growth of polymer chain, which proceeds through a PG/EM mechanism as indicated by spectral data. The Pani-Boric and Pani-Ac etic acid demonstrate three- and four-step decomposition patterns, respecti vely, with complete decomposition at about 760 degrees C. Pani-Formic acid, in contrast, reveals a three-step decomposition pattern with 90% weight lo ss at about 900 degrees C and shows a tendency to react with the Pt sample holder. The films of polyaniline generated electrochemically also suggest f ormic acid to be a better protonating medium for achieving a relatively gre ater fraction of conducting emeraldine salt. However, boric acid produces e xcellent quality adherent films with very high deposition rate. Morphologic al features give strong support to this observation. The films of Pani-Form ic and Pani-Acetic acids show a spongy network and globular morphology, res pectively, while Pani-Boric acid yields an extremely uniform surface coatin g. Furthermore, cyclic voltammetry reveals different patterns depending upo n the formation of different oxidation states and the results are in accord ance with optical absorption studies. (C) 2000 Society of Chemical Industry .