Polyaniline

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Polyaniline (PANI) is a conducting polymer of the semi-flexible rod polymer family. Although the compound itself was discovered over 150 years ago, only since the early 1980s has polyaniline captured the intense attention of the scientific community. This interest is due to the rediscovery of high electrical conductivity. Amongst the family of conducting polymers and organic semiconductors, polyaniline has many attractive processing properties. Because of its rich chemistry, polyaniline is one of the most studied conducting polymers of the past 50 years.[1][2]

Historical development[edit]

Polyaniline was discovered in the early 1860s by Lightfoot in his studies on the oxidation of aniline, which had been isolated only 20 years before. He developed the first commercially successful route to the dye called Aniline Black.[3][4] The first definitive report of polyaniline did not occur until 1862, which included an electrochemical method for the determination of small quantities of aniline.[5]

From the early 20th century on, occasional reports about the structure of PANI were published.

Figure 1. Main polyaniline structures n+m = 1, x = half degree of polymerization

Polymerized from the inexpensive aniline, polyaniline can be found in one of three idealized oxidation states:[6]

  • leucoemeraldine – white/clear & colorless (C6H4NH)n
  • emeraldine – green for the emeraldine salt, blue for the emeraldine base ([C6H4NH]2[C6H4N]2)n
  • (per)nigraniline – blue/violet (C6H4N)n

In figure 1, x equals half the degree of polymerization (DP). Leucoemeraldine with n = 1, m = 0 is the fully reduced state. Pernigraniline is the fully oxidized state (n = 0, m = 1) with imine links instead of amine links. Studies have shown that most forms of polyaniline are one of the three states or physical mixtures of these components. The emeraldine (n = m = 0.5) form of polyaniline, often referred to as emeraldine base (EB), is neutral, if doped (protonated) it is called emeraldine salt (ES), with the imine nitrogens protonated by an acid. Protonation helps to delocalize the otherwise trapped diiminoquinone-diaminobenzene state. Emeraldine base is regarded as the most useful form of polyaniline due to its high stability at room temperature and the fact that, upon doping with acid, the resulting emeraldine salt form of polyaniline is highly electrically conducting.[4] Leucoemeraldine and pernigraniline are poor conductors, even when doped with an acid.

The colour change associated with polyaniline in different oxidation states can be used in sensors and electrochromic devices.[7] Polyaniline sensors typically exploit changes in electrical conductivity between the different oxidation states or doping levels.[8] Treatment of emeraldine with acids increases the electrical conductivity by up to ten orders of magnitude. Undoped polyaniline has a conductivity of 6.28×10−9 S/m, whereas conductivities of 4.60×10−5 S/m can be achieved by doping to 4% HBr.[9] The same material can be prepared by oxidation of leucoemeraldine.

Synthesis[edit]

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:[10]

n C6H5NH2 + [O] → [C6H4NH]n + H2O

A common oxidant is ammonium persulfate in 1 M hydrochloric acid (other acids can be used). The reaction is exothermic. The polymer precipitates as an unstable dispersion with micrometer-scale particulates.

(per)nigraniline is prepared by oxidation of the emeraldine base, one typical oxidant being meta-chloroperoxybenzoic acid:[11]

{[C6H4NH]2[C6H4N]2}n + RCO3H → [C6H4N]n + H2O + RCO2H

Processing[edit]

The synthesis of polyaniline nanostructures is facile.[12]

Using special polymerisation procedures and surfactant dopants, the obtained polyaniline powder can be made dispersible and hence useful for practical applications. Bulk synthesis of polyaniline nanofibers has led to a highly scalable and commercially applicable form of polyaniline that has been researched extensively since their discovery in 2002.[13]

A multi-stage model for the formation of emeraldine base is proposed. In the first stage of the reaction the pernigraniline PS salt oxidation state is formed. In the second stage pernigraniline is reduced to the emeraldine salt as aniline monomer gets oxidized to the radical cation.[6] In the third stage this radical cation couples with ES salt. This process can be followed by light scattering analysis which allows the determination of the absolute molar mass. According to one study in the first step a DP of 265 is reached with the DP of the final polymer at 319. Approximately 19% of the final polymer is made up of the aniline radical cation which is formed during the reaction.[14]

Polyaniline is typically produced in the form of long-chain polymer aggregates, surfactant (or dopant) stabilized nanoparticle dispersions, or stabilizer-free nanofiber dispersions depending on the supplier and synthetic route. Surfactant or dopant stabilized polyaniline dispersions have been available for commercial sale since the late 1990s.[15]

Potential applications[edit]

The major applications are printed circuit board manufacturing: final finishes, used in millions of m² every year, antistatic and ESD coatings, and corrosion protection.[3][15]

References[edit]

  1. ^ Okamoto, Yoshikuko; Brenner, Walter (1964). "Ch. 7: Organic Semiconductors". Polymers. Reinhold. pp. 125–158.
  2. ^ Heeger, Alan (2001). "Nobel Lecture: Semiconducting and metallic polymers: The fourth generation of polymeric materials". Reviews of Modern Physics. 73 (3): 681. Bibcode:2001RvMP...73..681H. CiteSeerX 10.1.1.208.7569. doi:10.1103/RevModPhys.73.681.
  3. ^ a b Horst Berneth (2002). "Azine Dyes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_213.pub2.
  4. ^ a b MacDiarmid, Alan G. (2001). ""Synthetic Metals": A Novel Role for Organic Polymers (Nobel Lecture)". Angewandte Chemie International Edition. 40 (14): 2581. doi:10.1002/1521-3773(20010716)40:14<2581::AID-ANIE2581>3.0.CO;2-2.
  5. ^ Letheby, H. (1862). "XXIX.-On the production of a blue substance by the electrolysis of sulphate of aniline". Journal of the Chemical Society. 15: 161. doi:10.1039/JS8621500161.
  6. ^ a b Feast, W.J.; Tsibouklis, J.; Pouwer, K.L.; Groenendaal, L.; Meijer, E.W. (1996). "Synthesis, processing and material properties of conjugated polymers". Polymer. 37 (22): 5017. doi:10.1016/0032-3861(96)00439-9.
  7. ^ Huang, Li-Ming; Chen, Cheng-Hou; Wen, Ten-Chin (2006). "Development and characterization of flexible electrochromic devices based on polyaniline and poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonic acid)". Electrochimica Acta. 51 (26): 5858. doi:10.1016/j.electacta.2006.03.031.
  8. ^ Virji, Shabnam; Huang, Jiaxing; Kaner, Richard B.; Weiller, Bruce H. (2004). "Polyaniline Nanofiber Gas Sensors: Examination of Response Mechanisms". Nano Letters. 4 (3): 491. Bibcode:2004NanoL...4..491V. doi:10.1021/nl035122e.
  9. ^ Hammo, Shamil M. (2012). "Effect of Acidic Dopants properties on the Electrical Conductivity of Poly aniline". Tikrit Journal of Pure Science. 17 (2).
  10. ^ Chiang, J.C.; MacDiarmid, A. G. (1986). "'Polyaniline': Protonic Acid Doping of the Emeraldine Form to the Metallic Regime". Synthetic Metals. 1 (13): 193. doi:10.1016/0379-6779(86)90070-6.
  11. ^ Sapurina, I. Yu. and Shishov, M. A. (2012) "Oxidative Polymerization of Aniline: Molecular Synthesis of Polyaniline and the Formation of Supramolecular Structures", in New Polymers for Special Applications, Ailton De Souza Gomes (Ed.), ISBN 978-953-51-0744-6, InTech, doi:10.5772/48758.
  12. ^ Ćirić-Marjanović, G. Polyaniline Nanostructures, in Nanostructured Conductive Polymers (ed A. Eftekhari), 2010, John Wiley & Sons, Ltd, Chichester, UK. doi:10.1002/9780470661338.ch2 PDF
  13. ^ Huang, Jiaxing; Virji, Shabnam; Weiller, Bruce H.; Kaner, Richard B. (2003). "Polyaniline Nanofibers: Facile Synthesis and Chemical Sensors" (PDF). Journal of the American Chemical Society. 125 (2): 314–5. doi:10.1021/ja028371y. PMID 12517126. Archived from the original (PDF) on July 22, 2010.
  14. ^ Kolla, Harsha S.; Surwade, Sumedh P.; Zhang, Xinyu; MacDiarmid, Alan G.; Manohar, Sanjeev K. (2005). "Absolute Molecular Weight of Polyaniline". Journal of the American Chemical Society. 127 (48): 16770–1. doi:10.1021/ja055327k. PMID 16316207.
  15. ^ a b Wessling, Bernhard (2010). "New Insight into Organic Metal Polyaniline Morphology and Structure". Polymers. 2 (4): 786. doi:10.3390/polym2040786.