Faculty of Chemical Engineering and Environmental Protection, Gheorghe Asachi Technical University of Iasi, 73 Prof. dr. docent Dimitrie Mangeron, 700050, Iasi, Romania
Faculty of Chemical Engineering and Environmental Protection, Gheorghe Asachi Technical University of Iasi, 73 Prof. dr. docent Dimitrie Mangeron, 700050, Iasi, Romania
Faculty of Chemical Engineering and Environmental Protection, Gheorghe Asachi Technical University of Iasi, 73 Prof. dr. docent Dimitrie Mangeron, 700050, Iasi, Romania
References
[1] Perento J., Inherently Conductive Polyaniline for Electronics Applications, In: Polymers in Electronics, Conference Proceedings, (30-31 January 2007, Munich, Germany), Smithers-Rapra Ltd., 2007, 1-8.
[2] MacDiarmid, A.G., Synthetics Metals: a novel role for organic polymer (Nobel lecture), Synth. Met., 2002, 1, 11-12.
[3] Bhadra, S., Singha, N.K., Khastgir, D., Effect of aromatic substitution in aniline on the properties of Polyaniline,Eur. Polym. J., 2008, 44, 1763-1770.[Crossref][WoS]
[4] Chevalier, J.W., Bergeron, J.Y., Dao, L.H., Synthesis, characterization, and properties of poly (N-alkylanilines), Macromolecules, 1992, 25, 3325-3331.[Crossref]
[6] Bhadra, S., Singha, N.K., Khastgir, D., Effect of aromatic substitution in aniline on the properties of Polyaniline, Eur. Polym. J., 2008, 44, 1763-1770.[Crossref][WoS]
[7] Cao, Y., Smith, P., Heeger, A., Counterion induced processability of conducting polyaniline and of conducting polyblends of polyaniline in bulk polymers, Synth. Met., 1992, 48, 91-97.
[8] Armes, S.P., Aldissi, M., Agnew, S., Gottesfeld, S., Synthesis and characterization of aqueous colloidal dispersions of poly(vinyl alcohol)/polyaniline particles, Mol. Cryst. Liq. Cryst., 1990, 190, 63-74.
[9] Armes, S.P., Aldissi, M., Agnew, S., Gottesfeld, S., Aqueous colloidal dispersions of polyaniline formed by using poly(vinylpyridine)-based steric stabilizers, Langmuir, 1990, 6, 1745-1749.[Crossref]
[10] Amarnath, C.A., Palaniappan, S., Puzari, A., Rannou, P., Pron, A., Solution processible and conductive polyaniline via protonation with 4,4-bis(4-hydroxy phenyl)-valeric acid: preparation and characterization, Mater. Lett., 2007, 61, 4204-4207.[WoS]
[11] Olinga, T.E., Fraysse, J., Travers, J.P., Dufresne, A., Pron, A., Highly conducting and solution-processable polyaniline obtained via protonation with a new sulfonic acid containing plasticizing functional groups, Macromolecules, 2000, 33, 2107-2113.
[12] Xie, H.Q., Ma, Y.M., Feng, D.S., Preparation of organosoluble conductive polyaniline via precipitation polymerization and study of its conductivity, Eur. Polym. J., 2000, 36, 2201-2206.[Crossref]
[13] Hwang, J.H., Yang, S.C., Morphological modification of polyaniline using polyelectrolyte template molecules, Synth. Met., 1989, 29, 271-276.
[14] Li, S., Dong, H., Cao, Y., Synthesis and characterization of soluble polyaniline, Synth. Met., 1989, 29, 329-336.[WoS]
[15] Kim, J.W., Kim, S.G., Choi, H.J., Jhon, M.S., Synthesis and electrorheological properties of polyaniline-Na+-montmorillonite suspensions, Macromol. Rapid Commun., 1999, 20, 450-452.
[16] Choi, H.J., Park, S.J., Kim, S.T., Jhon, M.S., Electrorheological application of polyaniline/multi-walled carbon nanotube composites, Diamond Relat. Mater., 2005, 14, 766-769.
[17] Yue, J., Epstein, A.J., Synthesis of self-doped conducting poly- aniline, J. Am. Chem. Soc., 1990, 112, 2800-2801.
[18] Li, D., Jiang, Y., Wu, Z., Chen, X., Li, Y., Fabrication of self-assembled polyaniline films by doping-induced deposition, Thin Solid Films, 2000, 360, 24-27.
[20] Bekri-Abbes, I., Bayoudh, S., Baklouti, M., Converting waste polystyrene into adsorbent: Potential use in the removal of lead and cadmium ions from aqueous solution, J. Polym. Environ., 2006, 14, 249-256.[Crossref]
[21] El-kharouf, A., Chandan, A., Hattenberger, M., Pollet, B.G., Proton exchange membrane fuel cell degradation and testing: review, J. Energ. Inst., 2012, 85, 188–200.[WoS]
[22] Ping, Z., In situ FTIR-attenuated total reflection spectroscopic investigations on the baseeacid transitions of polyaniline. Base-acid transition in the emeraldine form of Polyaniline, J. Chem. Soc. Faraday Trans., 1996, 92, 3063-3067.[Crossref]
[23] Cochet, M., Louarn, G., Quillard, S., Boyer, M.I., Buisson, J.P., Lefrant, S., Theoretical and experimental vibrational study of polyaniline in base forms: non-planar analysis. Part I., J. Raman Spectrosc., 2000, 31, 1029-1039.[Crossref]
[24] Blomquist, M., Bobacka, J., Ivaska, A., Levon, K., Electrochemical and spectroscopic study on thiolation of polyaniline, Electrochim. Acta., 2013, 90, 604-614.[WoS]
[25] Tarver, J., Yoo, J.E., Loo Y.L., Organic Electronic Devices with Water-Dispersible Conducting Polymers, In: Wiederrecht G. (ed), Handbook of Nanoscale Optics and Electronics, Elsevier BV, Amsterdam, 2010
[26] Boonpoo-nga, R., Sriring, M., Nijpanich, S., Wongbuth, L., Martwiset, S., Semi-interpenetrating Polymer Networks of Poly(4-styrenesulfonic acid) and Poly(acrylic acid) for Fuel Cell Applications, KKU Res. J., 2011, 16, 757-763.
[27] Gomes, E.C., Oliveira, M.A.S., Chemical Polymerization of Aniline in Hydrochloric Acid (HCl) and Formic Acid (HCOOH) Media. Differences Between the Two Synthesized Polyanilines, Am. J. Polym. Sci., 2012, 2, 5-13.
[28] Shakoor, A., Rizvi T.Z., Nawaz, A., Raman spectroscopy and AC conductivity of polyaniline montmorillonite (PANI–MMT) nanocomposites, J. Mater. Sci. Mater. Electron., 2011, 22, 1076-1080.[WoS][Crossref]
[29] Claudio, H.B., Ferreira, S.D.C, Constantino, V.R.L., Temperin, M.L.A., Characterization of the products of aniline peroxydisulfate oligo/polymerization in media with different pH by resonance Raman spectroscopy at 413.1 and 1064 nm excitation wavelengths, J. Raman Spectrosc., 2011, 42, 1653–1659.[WoS]
[30] Gupta, N., Kumar, D., Tomar, S.K., Thermal Behaviour of Chemically Synthesized Polyanilines/Polystyrene Sulphonic Acid Composites, Int. J. Mater. Chem., 2012, 2, 79-85