2006
DOI: 10.1021/la060173n
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New Renewable Resource Amphiphilic Molecular Design for Size-Controlled and Highly Ordered Polyaniline Nanofibers

Abstract: We demonstrate here, for the first time, a unique strategy for conducting polyaniline nanofibers based on renewable resources. Naturally available cardanol, which is an industrial waste and main pollutant from the cashew nut industry, is utilized for producing well-defined polyaniline nanofibers. A new amphiphilic molecule is designed and developed from cardanol, which forms a stable emulsion with aniline for a wide composition range in water (1:1 to 1:100 dopant/aniline mole ratio) to produce polyaniline nano… Show more

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Cited by 82 publications
(110 citation statements)
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“…The peaks appearing within the small diffraction angle for PANI doped with different acids have been previously observed by many researchers: for example, the diffraction peaks at 6.4 o and 6.7 o correspond to the doping of cardanol [26] and 12-tungstophosphoric acid [27], respectively. For our samples, it is believed that the peak near 7.5 o is related to the existence of molybdate counter-ions in PANI, since the XRD pattern of ES does not show any peak around this position.…”
Section: Materials Characterizationsupporting
confidence: 55%
“…The peaks appearing within the small diffraction angle for PANI doped with different acids have been previously observed by many researchers: for example, the diffraction peaks at 6.4 o and 6.7 o correspond to the doping of cardanol [26] and 12-tungstophosphoric acid [27], respectively. For our samples, it is believed that the peak near 7.5 o is related to the existence of molybdate counter-ions in PANI, since the XRD pattern of ES does not show any peak around this position.…”
Section: Materials Characterizationsupporting
confidence: 55%
“…[25,26] The peak centered at 2u ¼ 18.88 is ascribed to periodicity parallel to the polymer chain and the peak centered at 2u ¼ 25.58 is attributable to the periodicity perpendicular to the polymer chain. [27][28][29] Compared with previously reported results, [25][26][27][28][29][30][31] there are no significant differences between the structural order of the PANI nanosheets and that of conventional PANI powders or films. The formation mechanism of sheet-like PANI appears to be related to the following three issues.…”
Section: Resultsmentioning
confidence: 52%
“…For doped PANI, three peaks are shown at 1302, 1037, and 816 cm À1 that correspond to the O = S = O (sym), NH + ···SO 3 À interactions between the polymers chain and dopant, and the C À S stretching vibrations, respectively. [28] Peaks at 1249 and 1139 cm À1 were assigned to C À N and in-plane bending of C À H. These results indicate that doped PANI was successfully synthesized. Moreover, in addition to the characteristic PANI bands, 1727 and 1602 cm À1 stretch vibrations assigned to C=O and C=C, respectively, appear in the spectrum of FUN-PANI (Figure 1A b), which clearly indicates that the carbonyl and vinyl groups of CH 2 =CHCOCl were successfully introduced onto the PANI surface.…”
Section: Resultsmentioning
confidence: 70%
“…[28] First the dopant was synthesized. A solution of sulfanilic acid (0.036 mol) and sodium carbonate (0.016 mol) in water (40 mL) was heated to 75 8C, then cooled to 5 8C and nitrite (0.032 mol) in water (6 mL) was added.…”
Section: Instruments and Measurementsmentioning
confidence: 99%
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