Open main menu
Home
Random
Recent changes
Special pages
Community portal
Preferences
About Wikipedia
Disclaimers
Incubator escapee wiki
Search
User menu
Talk
Dark mode
Contributions
Create account
Log in
Editing
Polyaniline
(section)
Warning:
You are not logged in. Your IP address will be publicly visible if you make any edits. If you
log in
or
create an account
, your edits will be attributed to your username, along with other benefits.
Anti-spam check. Do
not
fill this in!
===Synthesis=== Although the synthetic methods to produce polyaniline are quite simple, the mechanism of polymerization is probably complex. The formation of leucoemeraldine can be described as follows, where [O] is a generic oxidant:<ref name=Chiang>{{cite journal|last=Chiang|first=J.C.|author2=MacDiarmid, A. G. |title='Polyaniline': Protonic Acid Doping of the Emeraldine Form to the Metallic Regime|doi=10.1016/0379-6779(86)90070-6|journal=Synthetic Metals|year=1986|volume=1|issue=13|page=193}}</ref> :n C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub> + [O] β [C<sub>6</sub>H<sub>4</sub>NH]<sub>n</sub> + H<sub>2</sub>O A common oxidant is [[ammonium persulfate]] in 1 M [[hydrochloric acid]] (other acids can be used). The polymer precipitates as an unstable [[Dispersion (chemistry)|dispersion]] with micrometer-scale particulates. (Per)nigraniline is prepared by oxidation of the emeraldine base with a [[peracid]]:<ref>{{cite journal|doi=10.1016/0379-6779(91)91145-Z|title=Polyaniline: Synthesis and properties of pernigraniline base|journal=Synthetic Metals|volume=41|issue=1β2|pages=621β626|year=1991|last1=MacDiarmid|first1=A.G.|last2=Manohar|first2=S.K.|last3=Masters|first3=J.G.|last4=Sun|first4=Y.|last5=Weiss|first5=H.|last6=Epstein|first6=A.J.|doi-access=free}}</ref> :{[C<sub>6</sub>H<sub>4</sub>NH]<sub>2</sub>[C<sub>6</sub>H<sub>4</sub>N]<sub>2</sub>}<sub>n</sub> + RCO<sub>3</sub>H β [C<sub>6</sub>H<sub>4</sub>N]<sub>n</sub> + H<sub>2</sub>O + RCO<sub>2</sub>H Aniline can also be electrochemically polymerised directly onto conductive surfaces without the use of a chemical oxidant.<ref>{{Cite journal |last1=Boeva |first1=Zh. A. |last2=Sergeyev |first2=V. G. |date=September 2014 |title=Polyaniline: Synthesis, properties, and application |url=http://link.springer.com/10.1134/S1811238214010032 |journal=Polymer Science Series C |language=en |volume=56 |issue=1 |pages=144β153 |doi=10.1134/S1811238214010032 |issn=1811-2382|url-access=subscription }}</ref><ref>{{Cite journal |last1=Li |first1=Chun |last2=Bai |first2=Hua |last3=Shi |first3=Gaoquan |date=2009 |title=Conducting polymer nanomaterials: electrosynthesis and applications |url=https://xlink.rsc.org/?DOI=b816681c |journal=Chemical Society Reviews |language=en |volume=38 |issue=8 |pages=2397β2709 |doi=10.1039/b816681c |pmid=19623357 |issn=0306-0012|url-access=subscription }}</ref>
Edit summary
(Briefly describe your changes)
By publishing changes, you agree to the
Terms of Use
, and you irrevocably agree to release your contribution under the
CC BY-SA 4.0 License
and the
GFDL
. You agree that a hyperlink or URL is sufficient attribution under the Creative Commons license.
Cancel
Editing help
(opens in new window)