1981
DOI: 10.1016/0008-6223(81)90023-3
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Surface oxide structures on a commercial activated carbon

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Cited by 139 publications
(55 citation statements)
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“…The spectrum of the char also shows an intensification of the band at 1600 cm -1 that can be associated to quinone groups [27,28]. This band, together with the overlapping bands between 1000 and 1500 cm -1 have also been attributed to carboxylcarbonate structures [29,30]. The presence of these basic oxides helps to explain the basicity of the char and its relatively high oxygen content.…”
Section: Resultsmentioning
confidence: 86%
See 1 more Smart Citation
“…The spectrum of the char also shows an intensification of the band at 1600 cm -1 that can be associated to quinone groups [27,28]. This band, together with the overlapping bands between 1000 and 1500 cm -1 have also been attributed to carboxylcarbonate structures [29,30]. The presence of these basic oxides helps to explain the basicity of the char and its relatively high oxygen content.…”
Section: Resultsmentioning
confidence: 86%
“…However, as previously discussed, the DRIFT spectrum of GKOS does not show any characteristic band at 1750 cm -1 , typical of those species. The presence of carboxyl-carbonates was also reported [29,30]. These groups could release CO 2 upon heating, which would explain the CO 2 emissions from GKOS.…”
Section: Characterisation Of the Activated Samplesmentioning
confidence: 75%
“…Even though a cluster of functional groups were present on the carbon surface, the prominent among them was a sharp and intense band centered around 1,691.51 cm −1 which was attributed to the carbonyl (-C=O) stretching vibration of quinine or quinone or conjugated ketone (Ji et al 2007;Biniak et al 1997;Yu et al 2008;Ishizaki and Marti 1981;Shin et al 1997;Moreno-Castilla et al 1998;Starsinic et al 1983;Zawadzki 1989). The carbon surface is oxidized by treatment with concentrated HNO 3 leading to the generation of such quinone type carbon functional groups which bear significance in the redox chemistry of carbon materials.…”
Section: Ftir Spectroscopy Of Nvnc Before and After Defluoridationmentioning
confidence: 99%
“…Although CO 2 evolution in that temperature range is commonly assigned to decomposition of carboxyls and lactones, the DRIFT (diffuse reflectance infrared Fourier transform) spectrum of A ( Figure 2) does not show the characteristic band in the nearby of 1700 cm -1 . However, it does present a sharp band at 1600 cm -1 and a group of overlapping bands between 1100 and 1500 cm -1 that have been related to carboxylcarbonate structures [28,29]. AA750 presents CO 2 evolution at lower temperature, with maximum at 145 ºC, which might come from the decomposition of labile carboxyls formed upon exposure to air after the activation process [30].…”
Section: Chemical Characterisationmentioning
confidence: 99%