1983
DOI: 10.1016/0008-6223(83)90155-0
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Functional groups in carbon black by FTIR spectroscopy

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Cited by 191 publications
(83 citation statements)
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“…The fresh material showed a strong absorbance at 1787 cm −1 and a band at 1262 cm −1 , assigned to the carboxylic acid groups [27] and [28], both being not observed after reaction. This was attributed to the thermal instability of the carboxylic acid surface groups, known to decompose for temperatures higher than 540 K. The absorption maximum at 1106 cm −1 and the shoulder at 1053 cm −1 observed on the fresh UDD, was located in the spectral region corresponding to C-O stretching vibrations of ether-type groups and alcohols [25] and [29]. After reaction, these features disappeared or at least reduced in intensity.…”
Section: Characterizationmentioning
confidence: 93%
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“…The fresh material showed a strong absorbance at 1787 cm −1 and a band at 1262 cm −1 , assigned to the carboxylic acid groups [27] and [28], both being not observed after reaction. This was attributed to the thermal instability of the carboxylic acid surface groups, known to decompose for temperatures higher than 540 K. The absorption maximum at 1106 cm −1 and the shoulder at 1053 cm −1 observed on the fresh UDD, was located in the spectral region corresponding to C-O stretching vibrations of ether-type groups and alcohols [25] and [29]. After reaction, these features disappeared or at least reduced in intensity.…”
Section: Characterizationmentioning
confidence: 93%
“…By contrast, at 870-970 K, the (111) facet was also clean from any forms of carbon deposits with a similar measured activation energy of combustion for this plane at 230 ± 10 kJ mol −1 . Hence, it can be assumed that the UDD surfaces free of graphitic deposits might consist of (100) facets, while (111) facets might be covered by more reactive graphitic deposits according to [29]. This explained the remaining significant benzene yield of 8% on UDD at steady-state, due to the incomplete coverage of the UDD nanoparticles with sp 2 -carbon.…”
Section: Discussionmentioning
confidence: 99%
“…Finally, the peaks at 1352 and 1230 cm -1 correspond to the C-C and C-OH stretching vibration of carboxylic groups. 27 Relating to Vulcan-CBZ spectrum ( Figure S1b) the presence of characteristic stretches of thiosemicarbazide functional groups can be clearly observed ( Figure S1c): 22,28,29 u(C=S) 840-730 cm -1 , u(N-N) 1037-840 cm -1 and u(N-H) 3368-3175 cm -1 . It is also noted that the peak assigned to N-H centered at 3363 cm -1 underwent a slight change.…”
Section: Characterization Of Materialsmentioning
confidence: 88%
“…There is a little contribution of: (i) symmetrical and anti-symmetrical CH 2 stretching vibrations in the 2900-2800 cm -1 region; and (ii) the peak at 1714 cm -1 resulting from the stretching of the carbonyl bond of the COOH group. 27 Also, in the medium frequency region, there is a broad band in the range of 1665-1500 cm -1 due to the contribution of the angular deformation of the OH group conjugated with the CO stretch. Finally, the peaks at 1352 and 1230 cm -1 correspond to the C-C and C-OH stretching vibration of carboxylic groups.…”
Section: Characterization Of Materialsmentioning
confidence: 99%
“…The absorption peaks at around 1649 cm À1 , 1109 cm À1 and 802 cm À1 may be assigned to SiO 2 . 18,19 Furthermore, the morphology and microstructure of the as-prepared N-HCS are identi¯ed by SEM and TEM measurements. Observation from the SEM image in Fig.…”
Section: -3mentioning
confidence: 99%