2008
DOI: 10.1016/j.carbon.2008.06.045
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Characterization of the surface chemistry of carbon materials by potentiometric titrations and temperature-programmed desorption

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Cited by 168 publications
(87 citation statements)
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“…Two functional groups on the surface in the carboxylate region (pK 2.0-5.0) [20] with pK a = 3.40 ± 0.05 (number of sites = 900 ± 30 mmol/g) and pK a = 5.5 ± 0.1 (number of sites = 240 ± 30 mmol/g) respectively, have been identified. The higher pK a value (5.5) is ascribable to the presence of lactones and carboxylic anhydride groups that tend to hydrolyze in the presence of acids and bases [21]. It is noteworthy that the number of sites attributable to carboxylic acid sites is significantly higher with respect to the value estimated by the THA method and more consistent with literature data referring to related materials such as graphite oxide [22].…”
Section: Resultssupporting
confidence: 71%
“…Two functional groups on the surface in the carboxylate region (pK 2.0-5.0) [20] with pK a = 3.40 ± 0.05 (number of sites = 900 ± 30 mmol/g) and pK a = 5.5 ± 0.1 (number of sites = 240 ± 30 mmol/g) respectively, have been identified. The higher pK a value (5.5) is ascribable to the presence of lactones and carboxylic anhydride groups that tend to hydrolyze in the presence of acids and bases [21]. It is noteworthy that the number of sites attributable to carboxylic acid sites is significantly higher with respect to the value estimated by the THA method and more consistent with literature data referring to related materials such as graphite oxide [22].…”
Section: Resultssupporting
confidence: 71%
“…Table 1 presents the results of proximate and ultimate analysis along with the textural characteristics of the samples. It is observed from the table that amine grafting decreases surface area and pore volume of the samples, as widely reported by others (Gorgulho et al 2008;Marcoux et al 2007;Pittman et al 1997a, b, c;Torres et al 2006). This can be interpreted in terms of pore blockage by functional groups attached on the surface.…”
Section: Co 2 Capture Measurementssupporting
confidence: 73%
“…Scheme 1 shows the main functional groups identified on CNT surfaces after the HNO 3 treatment. [18,[27][28][29][30] Among them, phenolic, lactonic, quinonic, and carboxylic groups are usually present in large amounts, both on SWCNTs and MWCNTs.…”
Section: Introductionmentioning
confidence: 99%
“…[4,6] Many experimental studies have been devoted to the oxidation of CNT surface by nitric acid in order to 1) identify the nature of the oxygenated surface functionalities and to quantify them, 2) evaluate the physicochemical properties of the oxidized CNTs, and 3) control the kinetics of formation of oxygenated surface groups. Several techniques, often in combination, such as chemical titration, [9,17] thermal analysis/mass spectroscopy, [18,19] X-ray photoelectron spectroscopy (XPS), [20][21][22][23] FTIR spectroscopy, [21,24] and X-ray absorption near edge structure (XANES) analysis [25,26] have been used to elucidate the chemical nature of the oxygenated surface groups. Scheme 1 shows the main functional groups identified on CNT surfaces after the HNO 3 treatment.…”
Section: Introductionmentioning
confidence: 99%