1968
DOI: 10.1021/es60016a002
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Role of surface acidity in the adsorption of organic pollutants on the surface of carbon

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Cited by 530 publications
(249 citation statements)
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References 15 publications
(23 reference statements)
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“…Langmuir and Freundlich models fit the sorption isotherms well (Table 4), and the values of 1/n were generally lower than 0.5 (Table 4), consistent with the adsorption onto other carbon materials such as activated carbon [27,28] and black carbon [29,30]. Three main mechanisms have been proposed for the sorption of nondissociable aromatic compounds onto carbon materials, (1) π-π dispersion interaction, (2) hydrogen bonding [12], and (3) electron donor-acceptor complex formation [13]. Of the three proposed mechanisms, π-π dispersion interaction is the most widely accepted mechanism for the adsorption of aromatic compounds on activated carbon [11,14].…”
Section: Sorption Kinetics Of Nacssupporting
confidence: 67%
See 1 more Smart Citation
“…Langmuir and Freundlich models fit the sorption isotherms well (Table 4), and the values of 1/n were generally lower than 0.5 (Table 4), consistent with the adsorption onto other carbon materials such as activated carbon [27,28] and black carbon [29,30]. Three main mechanisms have been proposed for the sorption of nondissociable aromatic compounds onto carbon materials, (1) π-π dispersion interaction, (2) hydrogen bonding [12], and (3) electron donor-acceptor complex formation [13]. Of the three proposed mechanisms, π-π dispersion interaction is the most widely accepted mechanism for the adsorption of aromatic compounds on activated carbon [11,14].…”
Section: Sorption Kinetics Of Nacssupporting
confidence: 67%
“…Sorption properties of NACs on activated carbon have been studied for many years and involve electrostatic and dispersive interactions between the adsorbate and the activated carbon [10,11]. Electrostatic interactions dominate when the adsorbate is dissociated under the experimental conditions, while three mecha- nisms are proposed for nonelectrostatic interactions, (1) π-π dispersion interaction, (2) hydrogen bonding [12], and (3) electron donor-acceptor complex formation [13]. Of theses the π-π dispersion interaction mechanism is the most widely accepted [11,14].…”
Section: Introductionmentioning
confidence: 99%
“…1). The functional groups most often suggested are carboxyl groups, phenolic hydroxyl groups, and quinone carbonyl groups [6][7][8][9][10]. Less often suggested are ether, peroxide, and ester groups in the forms of normal and fluorescein-like lactones [11], carboxylic acid anhydrides [12], and cyclic peroxide [13].…”
Section: Surface Complexesmentioning
confidence: 99%
“…6). When the solution pH was close to the pH pzc , the surface electrostatic on ACs was zero, and phenol remained in molecular forms (pH<9), the ʌ-ʌ dispersion interaction strengthened [24], which leaded to the best adsorption capacity of AC and MAC. When the solution pH<pH pzc , the charge of activated carbon was positive, the dispersion interaction between the activated carbons and the phenol molecular was reduced, then the adsorption capacity was decreased.…”
Section: Langmuir Linear Equationmentioning
confidence: 99%