1999
DOI: 10.1016/s0008-6223(98)00328-5
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Effect of different oxidizing agent treatments on the surface properties of activated carbons

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Cited by 495 publications
(230 citation statements)
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“…Thus, the activity of CI and CII depends to some extent upon their ash content. It was also reported that the retention of some chemisorbed chlorine could decrease the pore size thereby influencing the catalytic performance of the carbon [182]. However, other factors should play a role since oxidation treatments for example of CI carbon comparably suppressed the ash content (<1 wt.%), but not the phenol conversion (between 35 and 38%) as can be depicted from figure 3.…”
Section: Preparation and Characterisationmentioning
confidence: 93%
See 1 more Smart Citation
“…Thus, the activity of CI and CII depends to some extent upon their ash content. It was also reported that the retention of some chemisorbed chlorine could decrease the pore size thereby influencing the catalytic performance of the carbon [182]. However, other factors should play a role since oxidation treatments for example of CI carbon comparably suppressed the ash content (<1 wt.%), but not the phenol conversion (between 35 and 38%) as can be depicted from figure 3.…”
Section: Preparation and Characterisationmentioning
confidence: 93%
“…According to the manufactureres, the carbons were prepared from wood (CI) and coconut shell (CII) precursors. Following previously tested procedures [182], modification of parent carbons was performed by liquid phase oxidation with H 2 O 2 , (NH 4 ) 2 S 2 O 8 or HNO 3 and demineralisation with HCl. The treated activated carbons were characterised by means of N 2 -adsorption isotherms, elemental and TG analysis, Boehm titration, oxic phenol adsorption at 20°C, slurry pH and ability for generating oxygenated radicals from dissolved molecular oxygen.…”
Section: Preparation and Characterisationmentioning
confidence: 99%
“…The FT-IR spectra of GAC and PAC (Fig. 5b) also showed the presence of the carbonyl (1,682 cm -1 ), C=C bond of aromatic rings (1,477 cm -1 ), and hydroxyl functional group (2,400-2,700 cm -1 ), respectively (Jiang et al 2008;Njoku and Hameed 2011;Pradhan and Sandle 1999).…”
Section: Identification Of Surface Functional Groups By Ft-irmentioning
confidence: 91%
“…The absorption peaks at 1,680, 1,583, and 874 cm -1 were characteristics of carbonyl stretching vibrations, N-H bending vibration of primary amines, and C-H bending vibrations of benzenes, respectively (Juan and Ke-Qiang 2009;Pradhan and Sandle 1999;Shen et al 2008). The broad absorption band in the region of 3,400-2,500 cm -1 was related to the stretching vibration of O-H groups (Jiang et al 2008;Njoku and Hameed 2011;Pradhan and Sandle 1999). The FT-IR spectra of GAC and PAC (Fig.…”
Section: Identification Of Surface Functional Groups By Ft-irmentioning
confidence: 92%
“…However, the majority of activated carbons do not contain such admixtures, which is related to their lack or very low content in the precursor used for the production of activated carbons. The solution proposed was development of effective methods of modification of the activated carbons (such as oxidation or ammoxidation) permitting introduction of different functional groups into the activated carbon structures Pradhan and Sandle 1999;Moreno-Castilla et al 2000;Aguilar et al 2003;Przepiórski 2006).…”
Section: Introductionmentioning
confidence: 99%