2010
DOI: 10.1016/j.jallcom.2010.04.032
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Multiwall carbon nanotubes purification and oxidation by nitric acid studied by the FTIR and electron spectroscopy methods

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Cited by 510 publications
(287 citation statements)
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“…It is also observed from Figure 3(b) that the individual nanotubes are clearly visible after acid functionalization, being easier to differentiate from one to another. It is expected that acid functionalization also dissolve eventual amorphous regions present in the MWCNT 42,43 . Samples of TiO 2 -coated MWCNT, obtained after the sol-gel process using different titanium isopropoxide (TTIP) to H 2 O molar ratios, are shown in Figure 4.…”
Section: Resultsmentioning
confidence: 99%
“…It is also observed from Figure 3(b) that the individual nanotubes are clearly visible after acid functionalization, being easier to differentiate from one to another. It is expected that acid functionalization also dissolve eventual amorphous regions present in the MWCNT 42,43 . Samples of TiO 2 -coated MWCNT, obtained after the sol-gel process using different titanium isopropoxide (TTIP) to H 2 O molar ratios, are shown in Figure 4.…”
Section: Resultsmentioning
confidence: 99%
“…Both peaks centred at 1380 and 2920 cm -1 are assigned as bending and stretching vibrations of C-H. The intense bands at 3400 cm −1 indicate stretching vibrations of isolated surface -OH moieties and/or -OH in carboxyl groups in absorbed water [29]. From FTIR spectra we can conclude the oxygen functional groups are attached to the carbon in the ICNS film, changing the surface wettability of the sample.…”
Section: Accepted M Manuscriptmentioning
confidence: 86%
“…is attributed to C=O bands characteristic of carboxyl functional groups (-COOH) and of ketone/quinine [14][15][16]. It has also been reported [13] that the band in the range of 1590-1570 cm −1 can be assigned to a combined band due to the aromatic ring mode of conjugated systems (diketone, ketoester, and carboxylate structures) and the absorption band at 1150 cm -1 is assigned to -C-O and -OH bonds in ether lactones, carboxyl, and phenolic structures.…”
Section: Methodsmentioning
confidence: 99%