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Abstrakty
Powdered polyaniline (PANI) was synthesised chemically with different doping anions namely hydrochloric acid, sulphuric acid and para-toluenesulfonic acid (pTSA). Two-step synthetic procedure was utilised at low temperature. The highest reaction efficiency was found for chlorine-doped PANI. Structural characterization with FTIR revealed the vibration bands characteristicto formation of the emeraldine salt. The surface morphology of doped PANIs was studied by SEM images which showed near globular shape and porous structures with different size of the aggregated particles. They were smaller for Cl-- or pTS--doped PANI while for SO42- the size was markedly larger. The XRD patterns revealed that there are ordered regions especially for pTS- doped PANI, while the highest conductivity value was recorded for Cl- doped one followed by organic pTS- doped and SO42- doped one.
Słowa kluczowe
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Czasopismo
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Tom
Strony
1023--1028
Opis fizyczny
Bibliogr. 18 poz., fot., rys., tab.
Twórcy
autor
- University of Silesia, Institute of Materials Science, 1A 75 Pulku Piechoty Str., 41-500 Chorzow, Poland
autor
- University of Silesia, Institute of Materials Science, 1A 75 Pulku Piechoty Str., 41-500 Chorzow, Poland
autor
- University of Silesia, Institute of Materials Science, 1A 75 Pulku Piechoty Str., 41-500 Chorzow, Poland
autor
- University of Silesia, Institute of Materials Science, 1A 75 Pulku Piechoty Str., 41-500 Chorzow, Poland
autor
- University of Silesia, Institute of Materials Science, 1A 75 Pulku Piechoty Str., 41-500 Chorzow, Poland
Bibliografia
- [1] H. Zhang, X. Wang, J. Li, F. Wang, Synth. Met. 159, 1508-1511 (2009).
- [2] Y. Yang, S. Chen, L. Xu, Macromol. Rapid Commun. 32 (7), 593-597 (2011).
- [3] J. Jin, Q. Wang, M. A. Haque, J. Phys. D 43 (205302), 1-5 (2010).
- [4] J. Stejskal, D. Hlavata, P. Holler, M. Trchova, J. Proles, I. Sapurina, Polym. Int. 53, 294-300 (2004).
- [5] Y. Wang, H. D. Tran, L. Liao, X. Duan, R. B. Kaner, J. Am. Chem. Soc. 132, 10365-10373 (2010).
- [6] N. S. Sariciftci, H. Kuzmany, H. Neugebauer, A. Neckel, The Journal of Chemical Physics 92, 4530-4539 (1990).
- [7] P. N. Adams, P. J. Laughlin, A. P. Monkman, Synth. Met. 76, 157-160 (1996).
- [8] I. Y. Sapurina, M. A. Shishov, Oxidative Polymerization of Aniline: Molecular Synthesis of Polyaniline and the Formation of Supramolecular Structures, in: New Polymers for Special Applications (Chapter 9) (2012).
- [9] Y. Gawli, A. Banerjee, D. Dhakras, M. Deo, D. Bulani, P. Wadgaonkar, M. Shelke, S. Ogale, Sci. Rep. 6, 21002: 1-10 (2016), doi: 10.1038/srep21002.
- [10] G. Ciric-Marjanovic, L. Dragicevic, M. Milojevic, M. Mojovic, S. Mentus, B. Dojcinovic, B. Marjanovic, J. Stejskal, J. Phys. Chem. B 113 (20), 7116-7127 (2009).
- [11] G. Ciric-Marjanovic, V. Dondur, M. Milojevic, M. Mojovic, S. Mentus, A. Radulovic, Z. Vukovic, J. Stejskal, Langmuir 25(5), 3122-3131 (2009).
- [12] A. Mostafaei, F. Nasirpouri, Prog. Org. Coat. 77, 146-159 (2014).
- [13] X. Du, Y. Xu, L. Xiong, Y. Bai, J. Zhu, S. Mao, J. Appl. Polym. Sci. 131, 40827-40837 (2014).
- [14] M. Trchová, J. Stejskal, Pure Appl. Chem. 83 (10), 1803-1817 (2011).
- [15] J. Stejskal, I. Sapurinab, M. Trchová, Prog. Polym. Sci. 35, 1420-1481 (2010).
- [16] J. Stejskal, I. Sapurina, J. Prokes, J. Zemek, Synth. Met. 105, 195-202 (1999).
- [17] J. Bhadra, N. K. Madi, N. J. Al-Thani, M. A. Al-Maadeed, Synth. Met. 191, 126-134 (2014).
- [18] J. Vivekanandan, V. Ponnusamy, A. Mahudeswaran, P. S. Vijayanand, Arch. Appl. Sci. Res. 3 (6), 147-153 (2011).
Uwagi
PL
Opracowanie rekordu w ramach umowy 509/P-DUN/2018 ze środków MNiSW przeznaczonych na działalność upowszechniającą naukę (2019).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-2a6ac0de-22d3-4214-b6d5-dfabffe95ad9